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Histological findings, cadmium bioaccumulation, and isolation of expressed sequence tags (ESTS) in cadmium-exposed, specific pathogen-free shrimp, Litopenaeus vannamei postlarvae.

ABSTRACT Cadmium (Cd) is an ubiquitous environmental pollutant of increasing worldwide concern. It has become one of the most hazardous heavy metals heavy metals, metallic compounds, such as aluminum, arsenic, cadmium, lead, mercury, and nickel. Exposure to these metals has been linked to immune, kidney, and neurotic disorders.
 in aquatic environments and could threaten aquatic organisms, including marine shrimp. Shrimp are sensitive to Cd and have been found to accumulate it in their bodies in proportion to environmental concentrations. The effects of Cd on the biology and gene expression of the commercially important Litopenaeus vannamei are unknown. The overall hypothesis is that Cd exerts effects on shrimp at both biological and molecular levels. These changes may provide a way to identify genes responsible for toxicity, detoxification Detoxification Definition

Detoxification is one of the more widely used treatments and concepts in alternative medicine. It is based on the principle that illnesses can be caused by the accumulation of toxic substances (toxins) in the body.
 and/or tolerance to Cd exposure both acute and chronic. To test the hypothesis, a small-scale pilot project was initiated to obtain baseline information on histological changes associated with Cd treatment and to develop the genomics tools needed to identify genes associated with Cd exposure. The specific objectives of this study were to (1) observe histopathologic changes in control- and Cd-treated postlarvae (PL) during a 48-h period, (2) measure Cd concentrations in Cd-exposed and untreated PLs, and (3) isolate expressed sequence tags (ESTs) from control and Cd-treated PLs for future genomics studies. Specific pathogen-free L. vannamei PLs at stage 42 (PL42, from the Kona Line of the United States Marine Shrimp Farming Program) were used in a waterborne bioassay Bioassay

A method for the quantitation of the effects on a biological system by its exposure to a substance, as well as the quantitation of the concentration of a substance by some observable effect on a biological system.
 to determine histological changes in PLs exposed to a range of concentrations of Cd[Cl.sub.2] (0, 0.01, 0.1, 1.0, and 10.0 ppm) for 48 h. Results for objective (1) indicated variable response of individual shrimp to Cd exposure at different concentrations. All but 2 animals from 10-ppm group died by 24 h. Histological lesions were limited to the integument integument

Covering of the body, which protects it from the outside world and from drying out. In humans and other mammals it consists of the skin (including outer epidermis and inner dermis) and its related structures, including hair, nails, and sebaceous and sweat glands.
, musculature musculature /mus·cu·la·ture/ (mus´kul-ah-cher) the muscular apparatus of the body or of a part.

The arrangement of the muscles in a part or in the body as a whole.
, gills, hepatopancreas The hepatopancreas is an organ of the digestive tract of arthropods, gastropods and fish. It provides the functions which in mammals are provided separately by the liver and pancreas. , and midgut-hindgut. For objective (2), results showed that the Cd levels in control PLs at 0 h were low and remained relatively low throughout the study. There was a dose- and time-dependent relationship of waterborne Cd exposure and accumulation. Results from objective (3) suggested differential gene expression in control- and Cd-treated PLs as reflected by the number of ESTs homologous to genes with different molecular function isolated from approximately 1,100 clones each from the control and Cd- exposed (1 ppm) cDNA libraries. These ESTs contributed to the establishment of an EST EST electroshock therapy.

electroshock therapy
 database for L. vannamei (ShrimpESTBase). Homology searches of the nucleotide and translated amino acid amino acid (əmē`nō), any one of a class of simple organic compounds containing carbon, hydrogen, oxygen, nitrogen, and in certain cases sulfur. These compounds are the building blocks of proteins.  sequences of ESTs isolated from the control and Cd-treated (1 ppm) eDNA libraries identified a significant number of clones similar to (a) known housekeeping genes and genes involved in immune recognition, signal transduction and effector effector /ef·fec·tor/ (e-fek´ter)
1. an agent that mediates a specific effect.

2. an organ that produces an effect in response to nerve stimulation.
 function, (b) other shrimp ESTs of unknown function, (c) ESTs from other species, (d) predicted, unknown or unnamed proteins from other species, and (e) no homology to any sequente in the GenBank database. Some ESTs (~30%) from the Cd-treated library showed homology to unique sequences representing potential transposable transposable /trans·pos·a·ble/ (trans-poz´ah-b'l) capable of being interchanged or put in a different place or order.  elements. The results provide baseline information on the potential effects of Cd on shrimp health and growth and suggest a complex interaction between environmental conditions, water, feed, stress, and genetic background of PLs and should be further investigated under both laboratory and commercial conditions. Moreover, data suggest L. vannamei may be useful as bioindicators for the condition of their natural environment.

KEY WORDS: Litopenaeus vannamei, shrimp, postlarvae stage 42, cadmium bioaccumulation bi·o·ac·cu·mu·la·tion
The increase in the concentration of a substance, especially a contaminant, in an organism or in the food chain over time.
, acute toxicity acute toxicity Pharmacology Illness caused by a single exposure to a toxic substance , histology, ESTs, transposable elements, immune- and stress-related genes


Because of human activities, cadmium (Cd) has become one of the most hazardous heavy metals in aquatic environments and could threaten aquatic organisms, including marine shrimp. Cd is a naturally occurring toxic heavy metal with no known biological function in humans and animals and therefore considered nonessential non·es·sen·tial
Being a substance required for normal functioning but not needed in the diet because the body can synthesize it.
Food and Drug Administration

FDA, See Food and Drug Administration.

FDA, the abbreviation for the Food and Drug Administration.
 1993, Pinot et al. 2000). Although levels found in nature are believed to be nontoxic, human activities have generated up to 3,700 tons of Cd per year (Pinot et al. 2000 and references therein). Recent studies have indicated that chronic exposure to sublethal sublethal /sub·le·thal/ (-le´thal) insufficient to cause death.

Not sufficient to cause death.
 levels of Cd can be detrimental to humans (Satarug & Moore 2004). Cd has been shown to be a developmental toxicant toxicant /tox·i·cant/ (tok´si-kant)
1. poisonous.

2. poison.

1. A poison or poisonous agent.

2. An intoxicant.

 in animals, resulting in fetal malformations and other effects, but no conclusive evidence CONCLUSIVE EVIDENCE. That which cannot be contradicted by any other evidence,; for example, a record, unless impeached for fraud, is conclusive evidence between the parties. 3 Bouv. Inst. n. 3061-62.  exists in humans (Calabrese & Kenyon 1991, USDHHS USDHHS, See United States Department of Health and Human Services.
 1993, USFDA USFDA United States Food & Drug Administration  1993, USEPA USEPA United States Environmental Protection Agency  2000, Zhou et al. 2004). Cd is known to be a carcinogen carcinogen: see cancer.

Agent that can cause cancer. Exposure to one or more carcinogens, including certain chemicals, radiation, and certain viruses, can initiate cancer under conditions not completely understood.
 in animals and suspected to be a human carcinogen of increasing environmental and occupational concern (Mikhailova et al. 1997), it has been classified as a Group B1, probable human carcinogen (USEPA 2000) yet the mechanisms underlying Cd's carcinogenicity carcinogenicity /car·ci·no·ge·nic·i·ty/ (kahr?si-no-je-nis´i-te) the ability or tendency to produce cancer.


the ability or tendency to produce cancer.
 remain unclear (Kasprzak & Bialkowski 2000). Heavy metal cations, including Cd, have the ability to bind to to contract; as, to bind one's self to a wife s>.

See also: Bind
 DNA DNA: see nucleic acid.
 or deoxyribonucleic acid

One of two types of nucleic acid (the other is RNA); a complex organic compound found in all living cells and many viruses. It is the chemical substance of genes.
, accumulate within the nuclear chromatin chromatin: see chromosome.  and cause a heritable her·i·ta·ble
1. Capable of being passed from one generation to the next; hereditary.

2. Capable of inheriting or taking by inheritance.
 alteration in the genetic information of the exposed cell(s), leading to transformation of the cell that may ultimately lead to cancer (Kasprzak & Bialkowski 2000, Klaassen et al. 1999, Mikhailova et al. 1997). Targets of Cd include liver, testes testes
 or testicles

Male reproductive organs (see reproductive system). Humans have two oval-shaped testes 1.5–2 in. (4–5 cm) long that produce sperm and androgens (mainly testosterone), contained in a sac (scrotum) behind the penis.
, and renal epithelial cells Epithelial cells
Cells that form a thin surface coating on the outside of a body structure.

Mentioned in: Corneal Transplantation
 with one study concluding that as much as 10% of the general human population may exhibit Cd-dependent renal dysfunction (Bonham et al. 2003 and references therein). In Japan, Cd is believed to cause a condition known as "Itai-Itai" (ouch-ouch) disease in humans; symptoms include nephrotoxicity neph·ro·tox·ic·i·ty
The quality or state of being toxic to kidney cells.

, hepatotoxicity hepatotoxicity (hepˑ··tō·t , nervous system damage, and high frequency of chromatid chromatid (krō`mətəd): see chromosome; crossing over.  aberrations (Nordberg 2004, Uetani et al. 2006).

Marine shrimp are also sensitive to Cd and have been found to accumulate it in their bodies in proportion to environmental concentrations (Nimmo et al. 1977), however research is limited on Cd effects on shrimp, specifically the Pacific whiteleg Litopenaeus vannamei (Paez-Osuna & Tron-Mayen 1995, Paez-Osuna & Ruiz-Fernandez 1995, Alcivar-Warren et al. 1999, Alcivar-Warren et ai. 200la, Alcivar-Warren et al. 2001b, Alcivar-Warren et al. 2004, Alcivar-Warren & Meehan 2001, Wu & Chen 2004, Wu & Chen 2005a, Wu & Chen 2005b), particularly considering that they may cause indirect adverse effects indirect adverse effects, unfavorable outcomes due to the practitioner's failure to properly perform a diagnostic procedure or administer a therapeutic approach.
 on human beings through the food chain and even spread these effects globally through commercial importation and exportation (Wu & Chen 2005b). Litopenaeus vannamei is an important species in commercial fisheries along its natural range from northern Mexico to northern Peru and is today the principle species farmed worldwide, including the United States and Asia.

Little is known about the relationship between Cd and its effects on the biology, growth, and gene expression in L. vannamei (Vanegas et al. 1997, Wu & Chen 2005b, Wu et al. 2005, Frias-Espericueta et al. 2001). To better understand these relationships, and gain insight on the cellular and molecular mechanisms of Cd toxicity, carcinogenicity and/or tolerance, modern genomics tools need to be developed. These tools include (a) construction of a high-density linkage map for shrimp, (b) cloning of cDNA libraries to isolate expressed sequence tags (ESTs) from Cd-exposed and unexposed shrimp for marker development, mapping and microarray studies, and (c) production of resource families needed to identify candidate genes or quantitative trait quantitative trait
A phenotype that is influenced by multiple genes.
 loci (QTLs) associated with Cd bioaccumulation and/or tolerance, toxicity, detoxification, and carcinogenicity in shrimp. Currently, a low-density linkage map for specific pathogen-free (SPF (1) (Stateful Packet Firewall) See stateful inspection.

(2) (Sender Policy Framework) An e-mail authentication system that verifies that the message came from an authorized mail server.
) L. vannamei (ShrimpMap) has been constructed based mostly on simple sequence repeat (SSRs) or microsatellite See miniaturized satellite.  genetic markers isolated from genomic libraries (Alcivar-Warren et al. 2007a). Efforts are now directed to increase density of the shrimp linkage map using microsatellite-containing ESTs (EST-SSR) markers that would directly sample variation in the transcribed regions of the shrimp genome and enhance their utility in comparative genomics, as well as for conservation and exploitation of shrimp genetic resources. To date, no ESTs from Cd-exposed L. vannamei have been reported.

Histology can be used as an additional tool to monitor the impact of aquatic pollutants on shrimp in their natural environments and aquaculture aquaculture, the raising and harvesting of fresh- and saltwater plants and animals. The most economically important form of aquaculture is fish farming, an industry that accounts for an ever increasing share of world fisheries production.  (Nimmo et al. 1975, Nimmo et al. 1977, Vogt 1987 and references therein). For instance, the midgut midgut /mid·gut/ (mid´gut) the region of the embryonic digestive tube into which the yolk sac opens and which gives rise to most of the intestines; ahead of it is the foregut and caudal to it is the hindgut.  gland of Penaeus monodon was found heavily damaged after exposure to 1 ppm of "Perfekthion" (a dimethoate-based insecticide). Nimmo et al. (1975) observed that P. duorarum developed crystalloids in hepatopancreatic nuclei after exposure to low levels of Arochlor R-1254. Nimmo et al. (1977) observed lesions in gills of P. duorarum exposed to 1-5 ppm of Cd. As suggested by Vogt (1987), structural alterations represent a highly sensitive overall response of shrimp to the synergistic effect Synergistic effect

A violation of value-additivity in that the value of a combination is greater than the sum of the individual values.
 of their nutritional and physiological condition and the quality of the water. Moreover, Johnson & Bergmann (1984) and Moore (1985) suggested that the impact of pollutants in an organism should be realized as perturbations at different levels of functional complexity, by measuring the severity of a toxicant at different levels: molecular, cellular, tissue, organ, individual, or population level; and histological diagnosis should be used as a highly sensitive methods to show the response of an animal to the impact of a toxicant. The specific goals of this study are to (1) observe histological changes in control- and Cd-treated PLs during a 48 h period, (2) measure Cd concentrations in Cd-exposed and untreated PL42s, and (3) isolate expressed sequence tags (ESTs) from control and Cd-treated PLs for future genomics studies. We report here baseline information on histological changes, Cd bioaccumulation, and expressed genes identified in control and Cd-exposed SPF L. vannamei postlarvae.


Experimental Animals and Laboratory Facilities

Specific pathogen-free (SPF) L. vannamei postlarvae (PL) from the United States Marine Shrimp Farming Program (USMSFP USMSFP United States Marine Shrimp Farming Program ) (Carr et al. 1997, Wolfus et al. 1997, Moss et al. 1999, Xu et al. 2003, Hennig et al. 2004) were used in this study. PLs originated from a batch of 10 families of the USMSFP's Research (Kona) Line (Xu et al. 2003, Hennig et al. 2004). PLs at developmental stage 31 (PL31) were shipped from The Oceanic Institute (OI, Kona, HI) to Tufts Cummings School of Veterinary Medicine The Cummings School of Veterinary Medicine is one of the eight colleges and schools that comprise Tufts University and is the only school of veterinary medicine in New England.  (TCSVM TCSVM Tufts Cummings School of Veterinary Medicine (North Grafton, Massachusetts) , North Grafton, MA) and maintained at the wet laboratory at 25[degrees]C under a 12:12 h lightdark photoperiod photoperiod /pho·to·pe·ri·od/ (fo´to-per?e-od) the period of time per day that an organism is exposed to daylight (or to artificial light).photoperiod´ic

. The wet laboratory is equipped with three Aquaneering Zebrafish 9.0-L tanks (Allentown Caging Equipment Company, Inc., Allentown, N J) filled with Instant Ocean (Premium Aquatics, Inc., Indianapolis, IN) artificial seawater at salinity range of 23-26 ppt ppt
1. parts per thousand

2. parts per trillion
. Water quality was maintained at an average pH of 8.0 ([+ or -] 0.4) anal ammonia levels within normal limits (<1.0 mg/L). On arrival, PLs were first placed into a 40 gal glass tank for 24 h. Shrimp were fed twice daily Ziegler Aqua, 35% protein, shrimp grower w 5% squid, and feed #1 and #2. Because of problems with artificial seawater maintaining pH and buffering capacity buffering capacity,
n the body's ability to neutralize the acids that play a role in the demineralization of teeth; may be enhanced by eating firmly textured foods, which improve chewing and stimulate the flow of saliva.
, some of the shrimp were separated into the two Aquaneering systems to decrease biomass in the 40 gal glass tank. Animals were acclimated for 11 days and all surviving shrimp (PL42) were combined (n = 1001) the day the experiment began. A total of 900 animals were used in the experiment (60 PLs/treatment/three replicates). Body weights were measured from randomly selected shrimp (n = 9) at time 0 and averaged 0.051 g (range 0.013-0.102 g). The remaining 101 animals were taken 1 h before treatment began for histology (n = 9), measurement of Cd concentration (n = 2l) and total RNA RNA: see nucleic acid.
 in full ribonucleic acid

One of the two main types of nucleic acid (the other being DNA), which functions in cellular protein synthesis in all living cells and replaces DNA as the carrier of genetic
 isolation and other genomics studies (n--71) and stored at -80[degrees]C until analyses were performed. Postlarvae were starved for 24 h before experimentation. Tufts University's Safety Office, protocol #20044)62CB, approved this study.

Preparation of Cadmium Stocks for Waterborne Assay

Cadmium chloride (Cd[Cl.sub.2], CAS #10108642) was purchased from Fisher Scientific, Pittsburg, PA (catalog #C10-100, lot #041504). A stock solution (1,000 ppm Cd) was prepared using molecular biology grade water and Cd[Cl.sub.2] (1.63 1g/L). Selected experimental concentrations were made by addition of proper volumes of the stock solution in seawater and then added directly to the PL-containing tanks.

Different groups of PL42s were exposed to a range of concentrations of Cd (0, 0.01, 0.10, 1.00, and 10.00 ppm) for 48 h. The range of Cd concentrations was determined based on the published literature for different penaeid shrimp species, which indicated that median lethal concentration or [LC.sub.50] (48 h30 days) for nauplii to juvenile stages ranged from 0.124-5.500 ppm (Nimmo et al. 1977, Bambang et al. 1994, Wu & Chen 2004), whereas the [LC.sub.50] (96 h) for adult is 3.5 ppm (Nimmo et al. 1977). Each group had three replicates in 9.0-L tanks filled with 8.0 L seawater and 60 shrimp each (Table 1). During the two-day experiment, no water was exchanged in any of the treatment tanks.

Fixation Protocol and Gross Lesions

Two PLs of each replicate tank were randomly sampled for histological analysis at 12, 24, and 48 h (Table 1) to observe histological changes in control- and Cd-treated PLs. PLs were examined following published protocols for shrimp (Lightner 1996). PLs were rinsed with artificial seawater and directly immersed into Davidson Alcoholic Formalin formalin /for·ma·lin/ (for´mah-lin) formaldehyde solution.

An aqueous solution of formaldehyde that is 37 percent by weight.
 Acetic Acid Fixative fixative /fix·a·tive/ (fik´sit-iv) an agent used in preserving a histological or pathological specimen so as to maintain the normal structure of its constituent elements.

 and taken to Tufts Pathology Laboratory for processing and histological examination. PLs were sectioned at 3-5 [micro]m, mounted on microscope slides, and stained with Harris' haematoxilin and eosin eosin /eo·sin/ (e´o-sin) any of a class of rose-colored stains or dyes, all being bromine derivatives of fluorescein; eosin Y, the sodium salt of tetrabromofluorescein, is much used in histologic and laboratory procedures.  (H&E).

Two PLs from each sample group were sectioned sagittally and one hall of each shrimp was embedded and sectioned with cut-side down. Given the small size of each shrimp, two shrimp were included in each block. In general, two H&E-stained sections were made from each block (cut at two different levels). Consequently, four sagittal sagittal /sag·it·tal/ (saj´i-t'l)
1. shaped like an arrow.

2. situated in the direction of the sagittal suture; said of an anteroposterior plane or section parallel to the median plane of the body.
 sections of shrimp were examined from each sample (two sections each from two different shrimp). This helped to broaden the types and amount of each tissue/organ available for histological examination.

Histological changes were noted on the basis of tissue/organ affected and the degree of changes present were graded on a scale from 0-3 (0 = absent, 1 = mild/1-5 foci, 2 = moderate/ 5-15 foci, 3 = severe/>15 foci or too numerous to count.) The histological differences in organs/tissues of control PLs and Cd-treated PLs were analyzed by a board-certified veterinary pathologist (JK).

Measurement of Cadmium Concentrations in Shrimp Postlarvae

Cadmium concentrations were determined by Environmental Testing and Research Laboratories (Leominster, MA) using acid/peroxide digestion and Inductively Coupled Plasma An inductively coupled plasma (ICP) is a type of plasma source in which the energy is supplied by electrical currents which are produced by electromagnetic induction, that is, by time-varying magnetic fields.  Mass Spectroscopy (ICP/MS ICP/MS Inductively Coupled Plasma/Mass Spectrometry (chemical analysis) ). Two animals per replicate per time point (at 12, 24, and 48 h, total of 6 animals) were collected, rinsed, and stored at -20[degrees]C until Cd analysis was performed. Twenty PLs from time 0 were also sent for analysis. The replicate samples for each time point were pooled and whole body PLs were homogenized ho·mog·e·nize  
v. ho·mog·e·nized, ho·mog·e·niz·ing, ho·mog·e·niz·es
1. To make homogeneous.

a. To reduce to particles and disperse throughout a fluid.

 before analysis was performed.

Cadmium concentrations were also analyzed in samples of Ziegler Aqua feed used during acclimation acclimation /ac·cli·ma·tion/ (ak?li-ma´shun) the process of becoming accustomed to a new environment.

 period and in stock solutions of 1,000 ppm and 100 ppm Cd[Cl.sub.2]. The stock solutions were maintained at room temperature and tested a year after the study was completed.

cDNA Library Construction

Two cDNA libraries were constructed by Amplicon Express, Inc. (Pullman, WA). The control library was prepared using PLs from the pool of 71 individuals collected in liquid nitrogen and stored at -80[degrees]C before experiment began (0 h). The Cd-treated library was prepared using PLs from the 1.00 ppm 24 h group based on the histological findings (see Results section below). A total of six animals per replicate per time point (12, 24, and 48 h) were collected, except for the 10-ppm treatment group, as they were all dead by 48 h. During collection, live shrimp were taken out of their respective treatment tank, filtered in a tine tine (tin) a prong or pointed projection on an implement, as on a fork.

1. The slender pointed end of an instrument, such as an explorer used in dentistry.

 mesh net, rinsed 3 times in clean artificial seawater at reduced salinity (15 ppt) and placed immediately in liquid nitrogen until they were placed at -80[degrees]C for long-term storage. The rime for the collection process from start to finish ranged from 15-30 sec, except for 12-h samples. The 12-h samples were not candidates for cDNA library construction because of uncertainty of time elapsed e·lapse  
intr.v. e·lapsed, e·laps·ing, e·laps·es
To slip by; pass: Weeks elapsed before we could start renovating.

 of tissue handling and therefore RNA quality. The cDNA libraries were constructed a year later. Samples were shipped overnight in dry ice to Amplicon Express, Inc. Amplicon Express staff was responsible for further sample preparation including separation of head (cephalothorax ceph·a·lo·tho·rax  
The anterior section of arachnids and many crustaceans, consisting of the fused head and thorax.

) from tail and immediate placement of the cephalothorax into their proprietary RNA isolation buffer. The mRNA purification and cDNA library cloning protocols followed standard procedures of Amplicon Express.

DNA Sequencing and BLAST Analysis

An aliquot aliquot (al-ee-kwoh) adj. a definite fractional share, usually applied when dividing and distributing a dead person's estate or trust assets. (See: share)  of the cDNA libraries was shipped from Amplicon Express to Agencourt, Inc. (Beverly, MA) for sequencing. Approximately 1,100 positive recombinant clones each from the control and Cd-treated libraries were sequenced. Sequence comparisons were performed by querying the sequences against the nonredundant and EST databases of Blastn and Blastx in GenBank (, NCBI-GenBank Flat file Release 156.0). Output files were created for easy access to individual sequence information and automatic programming established in the shrimp EST database so that it will continuously update new homologous genes and other known sequences. The statistical significance of DNA sequence homologies was based on reported cut-off values of E value [E0] < 0.001 (Pearson 2000). EST sequences were stored in Tuft's Shrimp EST Database (ShrimpESTbase) for future development of polymorphic markers for linkage mapping (Delaney et al. 2007). ESTs were grouped by molecular function/biological processes and summarized accordingly.


There were survivors at all treatments up to 24 h, however there were only 2 survivors from the 10-ppm treatment at that time. By 36 h, a significant number of animals had died in all treatments. At the end of the experiment (48 h) and after the last sampling sequence (RNA, histology, and Cd whole body), there were 32, 24, 24, 32, and 0 remaining shrimp in control, 0.01, 0.1, 1.0, and 10.0-ppm treatments, respectively. It is possible that complex interaction between insufficient environmental conditions, water, feed, stress, size differences, and genetic background of PLs contributed to these observations. Wu & Chen (2004) reported [LC.sub.50] at 48 h of 1.30 ppm Cd in L. vannamei, yet we did not observe any difference in PL42 survival in control and 1 ppm Cd-treated groups, suggesting that SPF PLs from the Kona line of the USMSFP may respond differently to Cd exposure than other L. vannamei stocks. Considering the limited number of samples, no conclusions regarding survivorship survivorship n. the right to receive full title or ownership due to having survived another person. Survivorship is particularly applied to persons owning real property or other assets, such as bank accounts or stocks, in "joint tenancy.  or growth after Cd exposure can be made from this study. A similar bioassay should be repeated for a longer period of time under laboratory and commercial settings to examine the relationship of Cd levels and shrimp biology and growth performance.

Histological Changes in Control- and Cd-treated Postlarvae in a 48-h Period

Histological analysis indicated variable response of individual shrimp to Cd exposure at different concentrations. Lesions were limited to the integument (oral region and appendages were analyzed), musculature, gills, hepatopancreas, and midgut-hindgut (Table 1). Examples of lesions observed in control PLs and PLs exposed to l0 ppm are shown in Figure 1A to F. None were associated with any evident infectious etiology (i.e., viruses, bacteria, fungi, and protozoa). Detailed histological observations are presented later. Lesions present in control shrimp were limited to gill crusting, melanosis melanosis /mel·a·no·sis/ (mel?ah-no´sis) melanism; disordered production of melanin, with darkening of the skin.

melanosis co´li
, and hypercellularity, whereas Cd-treated PLs exhibited lesions of the gills and other sites (see Table 1).



Histological changes in the gills fell into two categories. More frequent was degeneration and necrosis of superficial/ epithelial layers (Fig. 1A, 1B). Affected lamellae lamellae
n the nearly parallel layers of bone tissue found in compact bone.
 were lined or replaced by crusts (sloughing) of flattened cells that exhibited cytoplasmic cytoplasmic

pertaining to or included in cytoplasm.

cytoplasmic inclusions
include secretory inclusions (enzymes, acids, proteins, mucosubstances), nutritive inclusions (glycogen, lipids), pigment granules (melanin, lipofuscin,
 eosinophilia eosinophilia /eo·sin·o·phil·ia/ (e?o-sin?o-fil´e-ah) abnormally increased eosinophils in the blood.

An increase in the number of eosinophils in the blood.
, brown discoloration dis·col·or·a·tion  
a. The act of discoloring.

b. The condition of being discolored.

2. A discolored spot, smudge, or area; a stain.

Noun 1.
 (melanization) and loss of cellular detail. Some gills exhibited more diffuse hypercellularity, presumably pre·sum·a·ble  
That can be presumed or taken for granted; reasonable as a supposition: presumable causes of the disaster.
 because of accumulation of hemocytes with resulting distention dis·ten·tion or dis·ten·sion
The act of distending or the state of being distended.

n a state of dilation.
 of hemolymphatic spaces. The hypercellularity was evident in the primary/secondary filaments and central axis. The gill lesions seen here were similar to those reported in juvenile and subadult P. duorarum by Nimmo et al. (1977) using a waterborne assay for 30 days. An ultrastructural study of lesions in gills of Cd-treated P. duorarum revealed changes in mitochondria morphology (Couch 1977).


Some appendages (maxillipeds and pereiopods) and paragnaths exhibited segmental cuticular cu·ti·cle  
1. The outermost layer of the skin of vertebrates; epidermis.

2. The strip of hardened skin at the base and sides of a fingernail or toenail.

3. Dead or cornified epidermis.

 degeneration and necrosis. Similar to the described gill lesions, these were characterized by cuticular disruption and replacement by crusts of slightly granular, basophilic basophilic /ba·so·phil·ic/ (-fil´ik)
1. pertaining to basophils.

2. staining readily with basic dyes.


staining readily with basic dyes.
 to grey-brown pigmented material with underlying piled-up and flattened epithelial cells, hemocytes, and cellular debris.


Few shrimp exhibited angular, wedge-shaped foci of myofiber degeneration with fibrosis. The lesions typically were found along the distal tail in PLs of 0.1, 1.0 and 10.0 ppm groups.

Midgut and Hindgut hindgut /hind·gut/ (-gut) the embryonic structure from which the caudal intestine, chiefly the colon, is formed.

1. The large intestine, rectum, and anal canal.


There were infrequent lesions involving varying segments of the midgut, from the hepatopancreas to the posterior midgut cecum cecum (sē`kəm): see intestine. . Lesions varied from mild (necrosis and sloughing of scattered epithelial cells) to severe (segmental ulceration with expansion of the lamina propria by hemocytes and distention of gut lumen by sloughed cells) (Fig. 1C, 1D). Other studies with cultured shrimp indicated that the midgut gland (central site of metabolism) is a sensitive organ that could be used to monitor changes in water conditions. For instance, the midgut gland was heavily damaged after exposure of P. monodon to 1 ppm of dimethoate-based insecticide well before significant changes in the behavior of the shrimp could be observed (Vogt 1987).


Rare shrimp exhibited isolated foci of necrosis (Fig. 1E, 1F). No report on histological lesions have been described for marine shrimp hepatopancreas even though it is one of the tissues known to accumulate the highest levels of Cd in P. durarum (Nimmo et al. 1977).

Hemolymphatic System

Only one shrimp (10 ppm group) exhibited very prominent mural thickening of the cranial-dorsal hepatopancreatic vessel by hemocytes.

Hematopoietic hematopoietic /he·ma·to·poi·et·ic/ (-poi-et´ik)
1. pertaining to hematopoiesis.

2. an agent that promotes hematopoiesis.


1. pertaining to or affecting the formation of blood cells.

No histological changes were noted (including necrosis or degeneration).

In general, there was no consistent pattern of histological lesions present that could be reliably attributed to Cd exposure. This may be because of either the small number of animals analyzed to date or genetic differences of the pooled offspring of the 10 families from the Kona Line used for this study. In addition, the small size of the shrimp and sagittal sectioning resulted in inconsistent types and amounts of tissue present on each slide. Examination of multiple slides from a tissue block sometimes reduced this complication, and large and prominent structures such as the integument, gills, hepatopancreas, gut, cardiovascular system, nervous system, and hematopoietic tissue were considered to be adequately evaluated. In some cases, however, some tissues were not present for evaluation indicated as (n/a) in Table 1.

Histological lesions in the gills and integument were present and sometimes prominent in both treatment and control groups, and their severity was unrelated to the Cd treatment concentration. It is possible that the gill and cutaneous cutaneous /cu·ta·ne·ous/ (ku-ta´ne-us) pertaining to the skin.

Of, relating to, or affecting the skin.

Pertaining to the skin.
 lesions seen in this experiment were related to other factors such as water quality or stress as a result of crowding or starvation.

The total number of lesions observed in all treatment groups over 48 h is shown in Figure 2A. Close data analysis shows that PLs sampled later during the experiment (24 and 48 h) had more lesions in the gills than the PLs sampled before the experiment began (0 h) and at 12 h (not shown). The distribution of lesions over 48 h by tissue and Cd treatment is shown in Figure 2B. Data indicates that lesions in the integument (oral region and appendages), hepatopancreas, midgut, and hindgut were only seen in treated PLs and were not found in the control animals. Though there is an ultrastructural study of gill lesions in Cd-exposed P. duorarum (Couch 1977) and the impact of Cd on the structure of gills and epipodites of P. japonicus has been described (Soegianto et al. 1999), this is the first report of histological observations for control and Cd-exposed SPF L. vannamei PL42 under laboratory conditions, and with further analysis under more controlled laboratory and commercial settings, Cd-induced histopathologic changes will be better understood.


Cadmium Concentrations in Control and Cd-treated Postlarvae

The Cd levels in control PL42 from the Kona Line were low at 0 h (0.165 ppm) and remained low throughout the study, with levels reaching 0.350 ppm by 48 h after Cd exposure. Low metal levels were also reported in SPF adult L. vannamei (Alcivar-Warren & Meehan 2001) maintained at different grow-out systems (Moss et al. 2001).

Cadmium concentrations in L. vannamei PLs exposed to various Cd[Cl.sub.2] concentrations during time intervals are shown in Table 2 and Figure 3A. The percentage of change from controls is shown in Figure 3B. Results indicated that there is a dose-dependent as well as a time-dependent relationship of water-borne Cd exposure and accumulation. Cd treatments of 1.0 ppm and 10.0 ppm caused the most accumulation of Cd (Table 2). Linear regression analysis showed a significant correlation ([r.sup.2] = 0.924, P < 0.0001) between Cd treatment concentrations and Cd concentrations found in PLs whole body (Fig. 4).

It is expected that exposure of shrimp to low Cd levels over short or extended period of time will also accumulate at various rates in different tissues. Penaeus duorarum accumulated Cd after 96 h at concentrations proportionate to those present in seawater and this accumulation was tissue-specific, with the hepatopancreas containing the highest levels, followed by exoskeleton exoskeleton /exo·skel·e·ton/ (-skel´e-ton) a hard structure formed on the outside of the body, as a crustacean's shell; in vertebrates, applied to structures produced by the epidermis, as hair, nails, hoofs, teeth, etc. , muscle and serum. In P. duorarum muscle, the maximum Cd concentration measured after exposure to seawater containing 0, 0.079, 0.182, 0.307, 0.586, 0.866, and 1.285 ppm Cd for 30 days in a flow-through bioassay was 0.4, 3.8, 10.4, 17.0, 19.4, 30.1, and 30.5 ppm Cd, respectively (Nimmo et al. 1977). The Cd levels accumulated in whole, cultured SPF L. vannamei PL42 using artificial seawater (Table 3) are lower than those accumulated in muscle of wild P. duorarum from seawater (Nimmo et al. 1977) and may reflect either different environmental conditions (salinity, temperature, etc.), species genetic differences, or the effect of many generations of selective breeding in culture settings. The PL42 used in this study were from the Kona Line, which, in addition to consistently being highly susceptible to Taura Syndrome Virus Taura syndrome virus

cause of severe losses in juvenile prawns Penaeus vanammei.
 (TSV TSV - tab-separated values ); White Spot Syndrome white spot syndrome

a baculovirus complex with probably three baculoviruses involved; clinical signs include a loose cuticle with white or reddish-brown spots; 100% mortality in 3-10 days not uncommon in Penaeus monodon, P. japonicus, P. chinensis, P.
 Virus (WSSV WSSV White Spot Syndrome Virus ); and other pathogens, also perform well under intensive growing conditions and are distributed to local shrimp farmers for grow out purposes (Henning et al. 2004). Ir is unclear if PLs from other SPF lines of the USMSFP would also accumulate Cd as the Kona Line. Considering the sample size and environmental variables that may have affected the outcome of our study, the results should be taken with caution. Considering that the Kona Line contributed to the development of the High Growth Line and the new TSV-resistant line of the USMSFP, and the TSV-resistant line also performs well under intensive raceways conditions, and these lines originated from different geographic regions, it will be important to determine the [LC.sub.50] for Cd in PLs from all the SPF lines in the USMSFP germplasm. It is also possible that accumulation of Cd is genetically determined in L. vannamei, and Cd may act as a positive endocrine regulator stimulating growth of SPF shrimp under some environmental conditions. The association between Cd bioaccumulation and growth performance should be rigorously tested under laboratory and commercial settings.



To date, no information is available about the association of heavy metals with viral disease susceptibility. Liu et al. (2006) reported that VP9, a full-length protein of WSSV, binds with both Zn2 + and Cd2+. VP9 was found to adopt a similar fold as the DNA binding domain of the papillomavirus E2 protein suggesting that VP9 might be involved in WSSV expression. Research is needed on the potential association of acute and chronic levels of divalent divalent /di·va·lent/ (di-va´lent) bivalent; carrying a valence of two.


 metal ions and WSSV expression and its transcriptional regulation. Moreover, considering that there were no differences in survival of Kona PL42 individuals after 48 h exposure to Cd concentrations of 0.01, 0.10, and 1.00 ppm, a range of concentrations known to cause differences in mortality rates in other shrimp species, it is tempting to speculate a role for Cd as a positive endocrine regulator of high growth of the Kona line. Research is needed to determine the [LC.sub.50] and bioaccumulation of Cd at different stages of shrimp development using PLs from genetically different shrimp stocks such as the TSV-resistant and High Growth lines maintained by the USMSFP.

Results from this study show that SPF L. vannamei PL42 from the Kona Line are capable of accumulating Cd well above maximum levels (0.5 ppm) accepted by the European Union, FAO FAO,
n See Food and Agriculture Organization.
 and WHO (Joint FAO/WHO FAO/WHO Food and Agriculture Organization of the United Nations and the World Health Organisation  Expert Committee on Food Additives 2006) and approaching FDA standards (3.0 ppm) after low level Cd exposure (Table 3). Cadmium bioaccumulation has been studied in various crustaceans including crabs, lobsters, and shrimp. The hepatopancreas, midgut, gills, and exoskeleton have been found to sequester sequester v. to keep separate or apart. In so-called "high-profile" criminal prosecutions (involving major crimes, events, or persons given wide publicity) the jury is sometimes "sequestered" in a hotel without access to news media, the general public or their  Cd in crustacean crustacean (krŭstā`shən), primarily aquatic arthropod of the subphylum Crustacea. Most of the 44,000 crustacean species are marine, but there are many freshwater forms.  whereas the muscle tissue and serum are not considered sites of significant accumulation (Paez-Osuna & Tron-Mayen 1995, Nimmo et al. 1977). In penaeid shrimp species, the hepatopancreas is the main organ of Cd accumulation, differing by one order of magnitude A change in quantity or volume as measured by the decimal point. For example, from tens to hundreds is one order of magnitude. Tens to thousands is two orders of magnitude; tens to millions is three orders of magnitude, etc.  when compared with exoskeleton and three orders of magnitude when compared with serum (Nimmo et al. 1977). In wild Fenneropenaeus merguiensis, higher Cd levels were found in cephalotorax than in tail muscle (Panutrakul et al. 2007). Cd levels were also found x2-x3 higher in cephalothorax of wild L. vannamei of Ecuador and El Salvador (Alcivar-Warren et al. 200la) and P. monodon of Philippines (Alcivar-Warren et ai. 1999) when compared with levels in tail muscle with and without exoskeleton. Considering the potential for adverse health effects from Cd exposure (Nordberg 2004), even at low Cd levels, molecular epidemiology studies should be performed to assess potential risk to shrimp and human health caused Cd bioaccumulation and provide basis for preventive action.

It is possible that long-term exposure to heavy metals contamination alters both gene expression and allele frequencies in wild and cultured shrimp populations. A continued decline in genetic diversity of fingernail fin·ger·nail
The nail on a finger.
 clams was found associated to pollution (Sloss et al. 1998). Changes in allele frequencies of two genetic markers (phosphoglucomutase and glucose phosphate isomerase isomerase /isom·er·ase/ (i-som´er-as) a major class of enzymes comprising those that catalyze the process of isomerization.

) and levels of metallothionein protein were observed in clams after heavy metal challenges (reviewed in Camara et al. 2005). Genetic diversity and heterozygosity heterozygosity /het·ero·zy·gos·i·ty/ (het?er-o-zi-gos´i-te) the state of possessing different alleles at a given locus in regard to a given character.heterozy´gous

 of marine organisms seems to be related to heterogeneity and environmental stress (Nevo et al. 1983, Nevo et al. 1986). These researchers found that marine gastropods with high genetic diversity were more resistant to organic and inorganic pollutants than their counterparts, suggesting that fitness is positively correlated with heterozygosity. Differential survivorship of shrimp allozyme genotypes specific for Cd, Hg, and their interaction, were also reported (Ben-Schlomo & Nevo 1988), suggesting that rapid and precise changes can follow the effects of pollution. Moreover, exposure to Cd leads to a wide reorganization of S. cerevisiae transcriptome The transcriptome is the set of all messenger RNA (mRNA) molecules, or "transcripts", produced in one or a population of cells. The term can be applied to the total set of transcripts in a given organism, or to the specific subset of transcripts present in a particular cell type.  and proteome pro·te·ome
The complete set of proteins that are produced by the genes of an organism.


the entire complement of proteins produced by a cell.
, resulting in a significant increase in glutathione glutathione: see coenzyme.  synthesis regulated by transcriptional activators of the sulfur metabolism enzymes (Baudouin-Cornu & Labarre 2006) and a complex effect on cell cycle regulation (Yen et al. 2005, Othumpangat et al. 2005). However, different pollutants are expected to affect different genotypes, depending on the population's structure and organization of the genome. Genomics tools such as highly saturated genetic linkage maps and microarrays will facilitate identification of genes or QTLs associated with Cd bioaccumulation and Cd tolerance (Delaney et al. 2007).

Cd Stock Solutions and Shrimp Feed

The Cd levels found in the 100 ppm and 1,000 ppm Cd[Cl.sub.2] stock solutions used to prepare dilutions in the bioassay were 102.5 ppm and 891.0 ppm, respectively. These samples were submitted over a year after the solutions were made, possibly explaining the discrepancy in the Cd concentrations.

The Ziegler Aqua shrimp feed (#1 & #2) used in this waterborne bioassay had Cd levels of 0.780 ppm and 0.290 ppm, respectively. These levels are relatively high. Shrimp feed, in addition to the water, may be a vehicle for Cd accumulation and needs further research. As PLs in our study were not fed during the experiment, this could be a potential reason why our controls had low levels of Cd bioaccumulation. Availability of a semipurified shrimp diet would be most valuable for future Cd research.

Expressed Sequence Tags From cDNA Libraries of Control and Cd-treated Postlarvae

A total of 2,684 recombinant clones from the two cDNA libraries were sequenced. After vector trimming and quality assurance (e.g., deletion of clones with less than 50 nucleotides, too many Ns, etc.), ~2,300 ESTs were useful for further analysis. Homology searches of the nucleotides and translated amino acid sequences of ESTs isolated from the control and Cd-treated (1 ppm) cDNA libraries identified a significant number of clones similar to (a) known genes, (b) other shrimp ESTs of unknown function, (c) ESTs from other species, (d) predicted, unknown or unnamed proteins from other species, and (e) no homology to any sequence in the GenBank database.

The known genes in the control cDNA library included genes with different cellular function including: mitochondrial mitochondrial

pertaining to mitochondria.

mitochondrial RNAs
a unique set of tRNAs, mRNAs, rRNAs, transcribed from mitochondrial DNA by a mitochondrial-specific RNA polymerase, that account for about 4% of the total cell RNA that
 DNA-encoded subunits (mostly 16s rRNA anda few COI, COII, COIII, ATPase, NADH NADH the reduced form of NAD.

The reduced form of NAD.

NADH, a coenzyme that incorporates niacin and involved in the Krebs cycle.
1, and NADH6); 40S and 60S ribosomal proteins and others involved in the translational machinery (S4, S8, S9, L5, L6, L10, Lll, L13A, L21, L26, L27, L34, L37, elongation factor 1-gamma); cytoskeleton cytoskeleton

System of microscopic filaments or fibres, present in the cytoplasm of eukaryotic cells (see eukaryote), that organizes other cell components, maintains cell shape, and is responsible for cell locomotion and for movement of the organelles within it.
 proteins (actin, troponin troponin /tro·po·nin/ (tro´po-nin) a complex of muscle proteins which, when combined with Ca2+, influence tropomyosin to initiate contraction.

, tropmyosin, myosin myosin (mī`əsĭn), one of the two major protein constituents responsible for contraction of muscle. In muscle cells myosin is arranged in long filaments called thick filaments that lie parallel to the microfilaments of actin.  heavy chain, sarcoplasmic sarcoplasmic

pertaining to or emanating from sarcoplasm.

sarcoplasmic organelles
include a number of organelles associated with sarcoplasm.
 calcium-binding protein, and tubulin tubulin /tu·bu·lin/ (too´bu-lin) the constituent protein of microtubules.

A globular protein that is the structural constituent of microtubules.
 beta-1 chain); cell wall proteins (galactomannoproteins,

keratin-associated proteins, calcified Calcified
Hardened by calcium deposits.

Mentioned in: Heart Valve Repair
 cuticle cuticle /cu·ti·cle/ (ku´ti-k'l)
1. a layer of more or less solid substance covering the free surface of an epithelial cell.

2. eponychium (1).

3. a horny secreted layer.
 protein, chitinase, partial TTN TTN Technology Transfer Network
TTN Titin
TTN Transient Tachypnea of the Newborn
TTN Technology Transfer Node
TTN Trenton, NJ, USA - Mercer County (Airport Code)
TTN Total Traffic Network
 for titin); cell cycle related proteins (stromal cell derived factor 2, transcription factor AP2, S-phase response); vision genes (opsin opsin /op·sin/ (op´sin) a protein of the retinal rods (scotopsin) and cones (photopsin) that combines with 11-cis -retinal to form visual pigments.

, rhodopsin rhodopsin
 or visual purple

Light-sensitive, purple-red organic pigment contained in the rod cells of the retina that allows the eye to see in black and white in dim light.
), cell-signaling molecules (cyclophillin, yellow head virus receptor protein, laminin laminin
 receptor, receptor for activated protein kinase C-like, TonB-dependent receptors, wound response gene, peritrophin A, motifs of U88 protein of human herpesvirus herpesvirus, any of the family (Herpesviridae) of common DNA-containing viruses, many of which are associated with human disease. See cytomegalovirus; Epstein-Barr virus; herpes simplex; herpes zoster.  6, antiviral proteins (hemocyanin hemocyanin /he·mo·cy·a·nin/ (-si´ah-nin) a blue copper-containing respiratory pigment occurring in the blood of mollusks and arthropods. , crustacyanin, PMAV); and allergens (Pena 1, arginine arginine (är`jənĭn), organic compound, one of the 20 amino acids commonly found in animal proteins. Only the l-stereoisomer participates in the biosynthesis of proteins.  kinase, tropomyosin tropomyosin /tro·po·my·o·sin/ (-mi´o-sin) a muscle protein of the I band that inhibits contraction by blocking the interaction of actin and myosin, except when influenced by troponin. ), among others. A large number of ESTs had no similarity to any other sequences in the database.

The known genes from the Cd-treated (1 ppm) cDNA library included (a) housekeeping genes such as nuclear DNA-encoded subunits of oxidative phosphorylation; mitochondrial DNA subunits (16s rRNA, COI, COII, COIII, NADH2, NADH3); ribosomal proteins and other genes involved in the translational machinery (S3A, S9, S12, S18, S19, Llp/L10e, L6, L7a, L9, L21, L22(L17a), L23, L26, L27, L34, L37a, internal transcribed spacer ITS (for internal transcribed spacer) refers to a piece of non-functional RNA situated between structural ribosomal RNAs (rRNA) on a common precursor transcript. Read from 5' to 3', this polycistronic rRNA precursor transcript contains the 5' external transcribed sequence (5' ETS),  2, elongation factor 1, translation initiation factor 3 subunit 6, acidic ribosomal proteins 1 and 2, 18s rRNA); (b) cytoskeleton proteins (actin, troponin I, tubulin beta-2, myosin heavy chain, 1-connectin); (c) metal- and stress-related proteins (iron ion binding proteins, metal ion transporter, heat-induced protein, ubiquitin u·biq·ui·tin
A polypeptide found in all eukaryotic cells, including plant cells, that participates in a variety of cellular functions including protein degradation.
, thioredoxin), (d) immune response genes including antibacterial peptides (crustacyanin-C1), antiviral genes (hemocyanin), and allergen allergen /al·ler·gen/ (al´er-jen) an antigenic substance capable of producing immediate hypersensitivity (allergy).allergen´ic

pollen allergen
 genes (arginine kinase); (e) cuticle proteins (BCS-1, keratin-associated protein, calcified cuticle protein CP14.1, carcinin-like protein); (f) cell signaling molecules (high mobility protein, sarcoplasmic calcium-binding protein, cyclophillin RNA-interacting protein, PkB-like, adipose adipose /ad·i·pose/ (ad´i-pos)
1. fatty.

2. the fat present in the cells of adipose tissue.

Of, relating to, or composed of animal fat; fatty.
 enhancer binding protein, zinc finger protein A zinc finger protein is a DNA-binding protein domain comprised of zinc fingers ranging from two in the Drosophila regulator ADR1, the more common three in mammalian Sp1 up to nine in TFIIIA. , profilin); and (g) CG6770 orphan gene, among others. Only a few ESTs had no homology to any sequence in the Genebank database. It is possible that differential expression of some of the housekeeping, and potential growth- and development-related genes (such as those involved in the mitochondrial oxidative phosphorylation and translational regulation pathways) identified here in Kona PLs may relate to Cd accumulation stress. A potential association between susceptibility to viral diseases and high growth performance was also observed in some studies using shrimp from the Kona line (Alcivar-Warren et ai. 1997, Moss et al. 1999, Moss et al. 2001, Moss et al. 2002).

This is the first report of genes associated with Cd exposure in SPF L. vannamei postlarvae and some of the metal- and stress-related genes reported here are known to be induced even with minute amounts of Cd (Wiegant et al. 1997) or a nonlethal dose of Cd (Yamada & Koizumi 2002). In other species, Cd activates gene transcription through signal transduction pathways, mediated by protein kinase C Protein kinase C ('PKC', EC is a family of protein kinases consisting of ~10 isozymes.[1] They are divided into three subfamilies: conventional (or classical), novel, and atypical based on their second messenger requirements. , cAMP-dependent protein kinase cAMP-dependent protein kinase

a tetrameric protein composed of two regulatory subunits that bind cAMP, and two catalytic subunits that catalyze the transfer of a phosphoryl group from ATP to a target enzyme.
, or calmodulin calmodulin /cal·mod·u·lin/ (kal-mod´u-lin) a calcium-binding protein present in all nucleated cells; it mediates a variety of cellular reponses to calcium.

 (Bhattacharyya et al. 2000). In human cells, stress-related genes such as those coding for metallothioneins and heat shock proteins, antioxidant antioxidant, substance that prevents or slows the breakdown of another substance by oxygen. Synthetic and natural antioxidants are used to slow the deterioration of gasoline and rubber, and such antioxidants as vitamin C (ascorbic acid), butylated hydroxytoluene  genes, and ubiquitin pathway genes have been identified (Yamada & Koizumi 2002). In yeast cells, mutants deficient in specific ubiquitin-conjugating enzymes and the proteasome Proteasomes are large protein complexes inside all eukaryotes and archaea, as well as in some bacteria. In eukaryotes, they are located in the nucleus and the cytoplasm.[1]  are hypersensitive hy·per·sen·si·tive
Responding excessively to the stimulus of a foreign agent, such as an allergen; abnormally sensitive.

 to Cd, suggesting that Cd resistance is mediated in part by degradation of abnormal proteins (Jungmann et al. 1993). Metallothioneins, an intracellular protein known to protect against Cd toxicity (Klaassen et al. 1999) and induced after transient exposure of Cd (Brulle et al. 2007), was not identified in any of the EST sequences from the Cd-treated (1 ppm) cDNA library. The translation initiation factor-1 [delta] subunit, a Cd-responsive protooncogene with oncogenic oncogenic /on·co·gen·ic/ (-jen´ik) giving rise to tumors or causing tumor formation; said especially of tumor-inducing viruses.

on·co·gen·ic or on·cog·e·nous
 potential (Joseph et al. 2001), was not identified in these EST sequences. Moreover, the eukaryotic translation initiation factor 4E gene, a cellular target for toxicity and death caused by exposure to cadmium chloride (Othumpangat et al. 2005) was also not identified in our ESTs from the cDNA library of Cd-treated PLs and this may be because of many variables including source of RNA used to clone the cDNA library (i.e. tissue [exoskeleton]) and developmental stage, time of exposure, shrimp line used, etc. Considering that differences in molt frequency and molt cycle duration are associated with growth performance of the Kona line (Moss et al. 2002) more research is needed to understand the mechanisms by which Cd affects growth and early development in PLs from disease susceptible (Kona) and disease resistant (TSV-R) lines from the USMSFP.

In addition to known and hypothetical genes, a large number of ESTs (~30%) from the Cd-treated cDNA library contained portions of a motif (of up to ~137-150 bp) with no similarity to any sequence in the GenBank database. Some clones contained sequences similar to nucleotides 1-137 of a human sequence (GenBank accession #BC063380) and/or portions of the cloning vector pDNR-Lib (approx. 100-220 bp) followed by either partial sequences of known genes such as 28S rRNA, chloramphenicol chloramphenicol (klōr'ămfĕn`əkŏl'), antibiotic effective against a wide range of gram-negative and gram-positive bacteria (see Gram's stain). It was originally isolated from a species of Streptomyces bacteria.  resistant gene, orphan gene, 16s rRNA, ribosomal protein subunits or sequences of unknown function from plant and other species. Some of the ESTs also contained portions (~30-80 nt) of the PP-CAT gene (accession #BAA03718). It is possible that these sequence rearrangements are caused by either cloning artifacts artifacts

see specimen artifacts.
 or expression of transposable elements. Sequence rearrangements indicating active expression of nonLTR retrotransposons (reverse transcriptase) and other transposable elements have been observed in L. vannamei sequences isolated from either genomic libraries or cDNA libraries (of White Spot Syndrome Virus-and Taura Syndrome Virus-challenged shrimp), which were cloned into vectors different from the one used in this study (Alcivar-Warren et al. 2006, Alcivar-Warren et al. 2007b, Garcia & Alcivar-Warren 2007, Xu & Alcivar-Warren, unpublished results). Genetic rearrangements putatively caused by retrotransposons were also identified in L. stylirostris shrimp 24 h after infection with infectious hypodermal hy·po·der·mal  
1. Of or relating to the hypodermis.

2. Lying below the epidermis.

Adj. 1. hypodermal - of or relating to the hypodermis
 and hematopoietic necrotic virus (IHHNV IHHNV Infectious Hypodermal and Hematopoietic Necrosis Virus ), suggesting that stress induces expression of transposable elements (Hizer et al. 2002, Malfavon-Borja et al. 2006). The presence of putative sequence rearrangements after Cd exposure of shrimp postlarvae also suggests that Cd stress induces the expression of transposable elements.

The ESTs isolated from both the control and Cd-treated cDNA libraries have been added to the Tufts' shrimp EST database (ShrimpESTbase) for future microarrays and linkage mapping studies (Alcivar-Warren et al. 2007a). Availability of a highly saturated linkage map will facilitate (1) identification of candidate genes or QTLs associated with tolerance/susceptibility to Cd bioaccumulation, toxicity, and detoxification; (2) introgression in·tro·gres·sion  
Infiltration of the genes of one species into the gene pool of another through repeated backcrossing of an interspecific hybrid with one of its parents.
 of the Cd resistance/tolerance trait through marker-assisted selection; and (3) selective breeding of shrimp resistant/tolerant to Cd bioaccumulation, similar to the breeding program for oyster aimed at reducing Cd content in the species (Camara et al. 2005).

In summary, the histological, biological, and genomics results presented here provide baseline information to enable testable hypothesis on the potential positive or negative effects of Cd on shrimp health, growth and development. The levels of Cd in Cd-treated PLs are very high and should be repeated under more controlled experimental and commercial conditions before final statements are made about potential risk of Cd levels to environmental, animal, or public health. The ESTs add to the ShrimpESTbase and will be useful not only to develop polymorphic markers to increase density of the shrimp linkage map but provide valuable comparative genomic links between L. vannamei and other penaeid species as well as invertebrate invertebrate (ĭn'vûr`təbrət, –brāt'), any animal lacking a backbone. The invertebrates include the tunicates and lancelets of phylum Chordata, as well as all animal phyla other than Chordata.  and vertebrate genomes. Based on the different genes isolated from unexposed and Cd-exposed PLs, it seems that molecular changes precede cellular changes in cephalotorax of Cd-treated PLs, similar to the effects reported in mouse testis testis (tĕs`tĭs) or testicle (tĕs`tĭkəl), one of a pair of glands that produce the male reproductive cells, or sperm.  using low-dose Cd (Zhou et al. 2004).


This work was partially supported by the National Institute of Health Short Training Grant #T35DK07635 (MD), the United States Department of Agriculture United States Department of Agriculture (USDA), established in 1862, USDA is responsible for the safety of meat, poultry, and egg products. It conducts ongoing research in areas from human nutrition to new crop technologies and also helps ensure open
 (USDA-CSREES) through a grant to the United States Marine Shrimp Farming Program (A-W); the Department of Environmental and Population Health, TCSMV (A-W); Tufts Center for Conservation Medicine (MD), and the Pathology Section of the Clinical Sciences Department at TCSVM (JK). The authors thank Dr. Zhenkang Xu for initial suggestions on experimental design during the planning phase of this study, Drs. Paramananda Das and George Saperstein for providing comments on the manuscript, and Ms. Janine Stuczko for editing the manuscript.


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group of rod-shaped, double-stranded, DNA viruses which infect and kill a large number of different invertebrate species especially insects, including Lepidoptera, Hymenoptera, Diptera, Neuroplera, Trichoptera, Coleoptera and Homoptera, and also prawns; used as
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1. To turn inside out or upside down.

2. To reverse the position, order, or condition of.

3. To subject to inversion.

Something inverted.
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something that causes contamination.
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* Both authors contributed equally.

([dagger]) Corresponding author. E-mail:

(1) Pathology Section, Department of Clinical Sciences; (2) International Marine Shrimp Environmental Genomics Initiative (IMSEGI); (3) Environmental and Comparative Genomics Section, Department of Environmental and Population Health; (4) Tufts Center for Conservation Medicine, Cummings School of Veterinary Medicine at Tufts University, North Grafton, Massachusetts 01536
Histopathological lesions observed before and after cadmium exposure
of SPF Litopenaeus vannamei postlarvae stage 42 for a 48-h period (a).

            Time     Treatment   Gills Crusts/        Gills-
Replicate   (hour)    (ppm)      Melanization    Hypercellularity

Shrimp #                          1        2          1     2
            0           C (b)    n/a (c)   1         n/a    0
Tank 1      12 (d      10        n/a       0         n/a    0
                        1        n/a       1         n/a    1
                        0.1      n/a       1         n/a    2
                        0.01     n/a       0         n/a    0
                        C         0        0          0     0
            24         10         1        0          1     2
                        1        n/a       1         n/a    0
                        0.1       1        3          0     0
                        0.01     n/a       1         n/a    0
                        C        n/a       1         n/a    1
            48         10        n/a       2         n/a    3
                        1         1        3          0     3
                        0.1       0        2          0     1
                        0.01      1        1          0     0
                        C         1        2          0     2
Tank 2      24         10        n/a       3         n/a    2
                        1        n/a       1         n/a    0
                        0.1       1        2          0     1
                        0.01      1        1          0     0
                        C         1        3          0     3
            48         10         2        2          2     1
                        1         1        2          0     1
                        0.1       0        1          0     0
                        0.01      2        1          1     1
                        C         3        3          2     2
Tank 3      24         10         1        2          0     2
                        1         3        3          3     3
                        0.1       0        3          0     1
                        0.01      1        2          0     1
                        C         1        3          0     2
            48         10 (e)    --       --         --    --
                        1         2        3          0     3
                        0.1       1        1          3     0
                        0.01      1       n/a         0    n/a
                        C         1        3          1     2

            Time     Treatment   Integument-
Replicate   (hour)    (ppm)      Oral Region   Hepatopancreas

Shrimp #                           1     2        1    2
            0           C (b)     n/a   n/a       0    0
Tank 1      12 (d      10          2     0        0    0
                        1         n/a   n/a       0    0
                        0.1        0    n/a       0    0
                        0.01       2     2        0    0
                        C          0     0        0    0
            24         10          0     0        0    0
                        1          0    n/a       0    0
                        0.1       n/a    2        0    0
                        0.01       2    n/a       0    0
                        C          0    n/a       0    0
            48         10         n/a   n/a       0    0
                        1         n/a   n/a       0    0
                        0.1       n/a   n/a       0    0
                        0.01      n/a   n/a       0    0
                        C          0    n/a       0    0
Tank 2      24         10          0    n/a       2    0
                        1          2    n/a       1    0
                        0.1       n/a   n/a       0    0
                        0.01      n/a   n/a       0    0
                        C         n/a   n/a       0    0
            48         10         n/a   n/a       0    0
                        1         n/a   n/a       0    0
                        0.1       n/a   n/a       0    0
                        0.01      n/a   n/a       0    0
                        C         n/a   n/a       0    0
Tank 3      24         10         n/a   n/a       0    0
                        1         n/a   n/a       0    0
                        0.1       n/a    0        0    0
                        0.01      n/a   n/a       0    0
                        C         n/a   n/a       0    0
            48         10 (e)     --    --       --   --
                        1          2    n/a       0    0
                        0.1        0     0        0    0
                        0.01       0     0        0    0
                          C       n/a   n/a       0    0

            Time     Treatment                          Integument--
Replicate   (hour)    (ppm)       Midgut      Hindgut   appendages

Shrimp #                          1     2     1     2      1    2
            0           C (b)     0     0     0     0      0    0
Tank 1      12 (d      10         0     0     0     0      0    0
                        1         0     0     0     0      0    0
                        0.1       0     0     0     0      0    0
                        0.01      0     0     0     0      0    0
                        C         0     0     0     0      0    0
            24         10         0     0     0     0      0    0
                        1         0     0     0     0      0    0
                        0.1       0     0     0     0      0    0
                        0.01      0     0     0     0      0    0
                        C         0     0     0     0      0    0
            48         10         0     0     0     0      0    0
                        1         0     0     0     0      0    0
                        0.1       0     0     0     0      0    0
                        0.01     n/a    0    n/a    0      0    0
                        C         0     0     0     0      0    0
Tank 2      24         10         0     0     0     0      0    2
                        1         2     0     0     0      0    0
                        0.1       0     0     0     0      0    I
                        0.01      0     0     0     0      0    0
                        C         0     0     0     0      0    0
            48         10         0     0     0     0      0    0
                        1         0     0     0     0      1    0
                        0.1       0     0     2     0      0    0
                        0.01      2     0     0     0      0    0

                        C         0     0     0     0      0    0
Tank 3      24         10         3     0     0     0      2    2
                        1        n/a   n/a    0     0      0    0
                        0.1       0     0     0     0      2    0
                        0.01      0     0     0     0      0    0
                        C         0     0     0     0      0    0
            48         10 (e)    --    --    --    --     --   --
                        1         0     0     0     0      0    0
                        0.1       2    n/a    0     0      0    0
                        0.01     n/a    0     0     0      2    0
                        C         0    n/a    0     0      0    0

(a) The numbers under each column represent the degree of histological
change in tissues as detailed in the Materials and Methods section. Two
shrimp from each sample group were sectioned saggitallly and one half
of each shrimp was embedded and sectioned with cut-side down. Two
shrimp were included in each block. In general, two H&E-stained
sections were made from each block (cut at two different levels).
Consequently, four sagittal sections of shrimp were examined from
each sample (two sections each from two different shrimp).

(b) C = control group (0 ppm).

(c) n/a = tissue did not appear in section for evaluation.

(d) 12 h samples were pooled therefore no replicate samples.

(e) All animals were dead at 10 ppm treatment at 48 h.

Cadmium concentrations in control (0) and Cd-exposed
SPF Litopenaeus vannamei postlarvae stage 42 from
the Kona Line of the USMSFP. (a).

Cadmium     Exposure    Cadmium
Treatment     Time      Concentration
(ppm)        (hours)    (ppm) (a)

 0              0                0.165
 0             12                0.223
 0.01          12                0.353
 0.1           12                0.881
 1.0           12                4.580
10.0           12               13.330
 0             24                0.175
 0.01          24                0.780
 0.1           24                1.370
 1.0           24                6.100
10.0           24               15.600
 0             48                0.350
 0.01          48                0.350
 0.1           48                2.230
 1.0           48               15.820

(a) Cadmium concentrations correspond to a pooled
sample of six whole) L. vannamei PL42 (2 Pls per
replicate). No information available for 10.00 ppm
Cd treatment because all animals were dead by 48 h.

Cadmium concentrations ([micro]g [g.sup.-1]) measured in whole,
cultured, specific pathogen-free Litopenaeus vannamei Postlarvae
stage 42 (PL42) treated with Cd in a waterborne assay using
artificial seawater, and comparison with the Cd levels reported from
[LC.sub.50] studies, found in other penaeid shrimp species, and the
internationally recommended safety limit. (a) Cadmium safety limits
are 2.00, 3.00, and 0.50 [micro]g/g (ppm) based on published
international standards (a-c).

                                   of Cd Detected, [mu]g/g
                                        or ppm  (shrimp
Species (Reference; Objective)           Part, Country)

Bioaccumulation studies
  L. vannamei (this study, to      0.17-0.35 (whole, pooled,
     measure Cd concentrations       cultured, PL42, control no
     in control untreated            Cd exposure, Kona, USA)
     PLs and observe
     histopathologic changes
     for 48 h)
  L. vannamei (this study,         0.35-0.78 * (whole, pooled,
     to measure Cd                   cultured, PL42, 0.01ppm
     concentrations in               Cd-exposed, Kona, USA)
     Cd-exposed and                0.83 *-2.23 * (whole,
     control untreated PLs           pooled PL42, 0.10 ppm
     and observe                     Cd-exposed, Kona, USA)
     histopathologic               4.58 *-15.82 * (whole,
     changes), PLs were              pooled PL42, 1.00 ppm
     exposed to 0.01, 0.10,          Cd-exposed, Kona, USA)
     1.00 ppm Cd for 128 h
  L. vannamei (this study,         13.30 *-15.60 * (whole,
     whole PL42 exposed to           pooled PL42, 10.00 ppm
     10.0 ppm Cd for 24h)            Cd-exposed, Kona, USA)
  L. vannamei (Wu & Chen           0.10 ppm (hepatopancreas,
     2005b, studied Cd               juveniles, 0.10 ppm
     accumulation in                 Cd-exposed, Taiwan)
     hepatopancreas, gills
     and muscle)
  P. durarum (Nimmo et al.         3.80 * (muscle, wild,
     1977, studied Cd                from seawater with
     accumulation in                 0.079 ppm Cd)
     muscle of shrimp              10.40 * (muscle, wild,
     exposed to various              from seawater with
     concentrations of Cd            0.182 ppm Cd)
     in test water for 30          17.00 * (muscle, wild,
     days in a flow-through          from seawater with
     bioassay)                       0.307 ppm Cd)
                                   19.40 * (muscle, wild,
                                     from seawater with
                                     0.586 ppm Cd)
                                   30.10* (muscle, wild,
                                     from seawater with
                                     0.866 ppm Cd)
[LC.sub.50] studies
  Penaeus japonicus                Nauplii: 48h
    (Bambang et al. 1994,            [LC.sub.50]: 0.124
    studied effect                 Zoea 96h [LC.sub.50]:
    of Cd on survival,               0.010-0.030
    tolerance and                  Postlarvae 96 h [LC.sub.50]:
    development)                     0.200-3.500 *
                                   Juveniles 96 h
                                     [LC.sub.50]: 5.500 *
  Penaeus durarum                  Juvenile/subadult, 96 h
    (Nimmo et al. 1977)              [LC.sub.50]: 5.000 *
                                     21-25 days
                                     [LC.sub.50]: 1.000 *
                                   Adult, 96 h
                                     [LC.sub.50]: 3.500*
                                   Adult, 30-day
                                     [LC.sub.50]: 0.720*
  L. vannamei                      Subadult/adult:
    (Wu & Chen. 2004)                [LC.sub.50]: 24h = 2.58 *
                                   48 h = 1.30 *
                                   72 h = 1.14 *
                                   96 h = 1.07 *
  L. vannamei (Frias-              Postlarvae: [LC.sub.50]:
    Espericueta                      96h = 2.49
    et al. 2001)

Trace concentrations in
 wild and cultured shrimp
  L. vannamei (Alcivar-            0.100-0.200 (whole adult,
     Warren & Meehan 2001,           cultured, High Growth
     measured Cd in SPF              line USMSFP, USA)
     broodstock kept in
     recirculating, zero
     discharge system)
  L. vannamei (Alcivar-            0.000-0.030 (whole adult,
     Warren & Meehan 2001,           cultured, High Growth
     measured Cd in broodstock       line USMSFP, USA)
     kept in a flow-through
     earthen pond)
  L. vannamei (Alcivar-            0.310-1.070 * (whole
     Warren et al. 2001b,            adult, wild, El
     measured Cd in wild             Salvador)
     brood stock from El
     Salvador -kept in an
     earthen pond in
     Ecuador for breeding
  L. vannamei (Alcivar-            0.090-0.900 * (whole
     Warren et al. 2001b,            adult,  wild, San
     measured Cd in wild             Pablo, Ecuador)
     brood stock from Ecuador
     kept in earthen pond in
     Ecuador, for breeding
  Ocean and pink shrimp            0.100-0.200 (whole
     (NMFS, survey of wild           pooled, wild fishery
      shrimp)                        resource, USA)
  P. monodon (Alcivar-             0.006-1.000 * (whole,
     Warren et al. 1999,             adult, wild, from
     monitored heavy                 Capiz, Negros Occidental,
     metals in wild shrimp           Quezon, and Palawan,
     from four geographic            Philippines). Shrimp
     regions of Philippines)         from Capiz had highest
                                     Cd levels.
  P. monodon (Alcivar-Warren       0.034-0.248 (whole,
     et al. 1999, monitored          subadult/adult,
     heavy metals in cultured        cultured [F.sub.1]-
     shrimp from SEAFDEC,            [F.sub.3], SEAFDEC,
     Philippines)                    Philippines)
  Fenneropenaeus merguiensis       2.27 * (wild, cephalothorax,
                                     Chantaburi province,
                                     Thailand (d,e)

(a) Australia and New Zealand Food Authority Amendment
No. 53. (2000).

(b) US Food and Drug Administration (1993, 2001).

(c) FAO. Report of the Codex Committee on Food Additives and
Contaminants. Draft Guideline level for Cadmium in Food
Joint FAO/WHO Expert Committee on Food Additives (2006).

* indicate maximum concentration, higher than safety limit
for at least one of the agencies listed.

(d) From Panutrakul et al. (2007).

(e) Cephalothorax and tail muscle from wild shrimp of
Chantaburi and Trat provinces were tested.
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Author:Keating, John; Delaney, Martha; Meehan-Meola, Dawn; Warren, William; Alcivar, Aracelly; Alcivar-Warr
Publication:Journal of Shellfish Research
Article Type:Report
Geographic Code:1USA
Date:Dec 1, 2007
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