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The Red Tide Toxin, Brevetoxin, Induces Embryo Toxicity and Developmental Abnormalities.

Brevetoxins are lipophilic polyether toxins produced by the red tide dinoflagellate Gymnodinium breve, and their neurotoxic effects on adult animals have been documented. In this study, we characterized adverse developmental effects of brevetoxin-1 (PbTx-1) using an exposure paradigm that parallels the maternal oocyte transfer of toxin. Medaka fish (Oryzias latipes) embryos were exposed to PbTx-1 via microinjection of toxin reconstituted in a triolein oil droplet. Embryos microinjected with doses of 0.1-8.0 ng/egg (ppm) of brevetoxin-1 exhibited pronounced muscular activity (hyperkinesis) after embryonic day 4. Upon hatching, morphologic abnormalities were commonly found in embryos at the following lowest adverse effect levels: 1.0-3.0 ppm, lateral curvature of the spinal column; 3.1-3.4 ppm, herniation of brain meninges through defects in the skull; and 3.4-4.0 ppm, malpositioned eye. Hatching abnormalities were also commonly observed at brevetoxin doses of 2.0 ppm and higher with head-first, as opposed to the normal tail-first, hatching, and doses [is greater than] 4.1 ng/egg produced embryos that developed but failed to hatch. Given the similarity of developmental processes found between higher and lower vertebrates, teratogenic effects of brevetoxins have the potential to occur among different phylogenetic classes. The observation of developmental abnormalities after PbTx-1 exposure identifies a new spectrum of adverse effects that may be expected to occur following exposure to G. breve red tide events. Key words: brevetoxin, red tides, teratogenicity. Environ Health Perspect 109:377-381 (2001). [Online 16 March 2001]

http://ehpnet1.niehs.nih.gov/docs/2001/109p377-381kimm-brinson /abstract.html

Brevetoxins are lipid-soluble, polyether, marine toxins that have an excitatory action on voltage-sensitive sodium channels (1). Brevetoxins are produced by the marine dinoflagellate Gymnodinium breve (2,3), an organism responsible for toxic red tides in the Gulf of Mexico (4). Nine brevetoxins (PbTx1-9) are known to be produced by G. breve, with PbTx-3, PbTx-1, and PbTx-2 being the predominate forms (5). PbTx-1 is the most potent of the brevetoxins, with a median lethal dose ([LD.sub.50]) of 180 [micro]g/kg in the mouse and 4 ng/mL in the fish (6).

Brevetoxins bioaccumulate in various filter-feeding organisms, particularly shellfish (7). Shellfish contaminated with brevetoxins are toxic to humans and are responsible for neurotoxic shellfish poisoning (NSP). NSP is characterized by gastrointestinal and neurologic symptoms, which include tingling sensations in the mouth and extremities, motor incoordination, hot-cold flashes, slowed pulse, pupil dilation, and mild diarrhea (8). These symptoms may persist for several days.

G. breve red tides were first documented along the Gulf Coast of Florida in the 1530s, and the first report of an associated marine animal mortality event was published in 1844 (9). Fish are the primary organisms affected, especially bottom-dwelling species; however, larger fish and marine mammals are commonly susceptible during moderate and severe red tides (10). The most common routes of brevetoxin exposure in aquatic species is by absorption of the toxin from lysed cells across gill epithelium and direct ingestion of G. breve and absorption of its toxins across gastrointestinal epithelia. Although finfish account for most common animal mortalities associated with red tide events, brevetoxin accumulation in fin fish has not been well characterized. The adverse effects that have been characterized in striped mullet (Mugil cephalus) and mosquito fish (Gambusia affinis) include vigorous twisting and corkscrew swimming, contractions, tail curvature, loss of equilibrium, slow and irregular opercular movements, quiescence, and sudden convolutions leading to death (11,12).

Humans are also susceptible to adverse effects from G. breve through direct inhalation of brevetoxins and its absorption across respiratory epithelia during red tide events. G. breve cells are unarmored dinoflagellates that lyse easily, releasing their toxins into the water, which easily forms aerosols (13,14). Reports of respiratory irritation occurred as early as 1917 (15) and were later confirmed experimentally (16). Because of the fragile nature of G. breve and the aerosolization of its toxins as a result of wave action, brevetoxin exposures can occur in areas of surf and nearby beach areas. The effects have been described as an abrupt irritant attack that begins with paroxysmal coughing, accompanied by tearing and rhinorrhea from irritated eyes and nasal passages, all of which cease promptly after leaving the beach areas (17).

Given the multiple routes of exposure and the frequency and duration of G. breve red tides along the coastal areas of the Gulf of Mexico, we decided to investigate the potential for adverse developmental effects of brevetoxins. We chose to use a route of exposure different from those described above, proposing a route that presents a high risk to aquatic species: maternal oocyte transfer (18). To evaluate the hazard of maternal oocyte transfer, we used microinjection to transfer known amounts of toxin in an oil droplet into freshly fertilized fish eggs. This method has previously been used to characterize the adverse effects of ciguatoxin and chemical contaminants such as DDT (19,20). Both ciguatoxin and DDT bioaccumulate in fish and are found in the gonads; however, to date comparable data has not been reported for brevetoxin. We chose to investigate brevetoxin because of the common occurrence and persistence of red tides in the Gulf of Mexico and their potential effects on resident and migratory species that inhabit the estuaries to breed and progress through early life phases (13). PbTx-1 was chosen as the test compound, because it is the most lipophillic of the brevetoxins and hence has the greatest potential for biomagnification.

Materials and Methods

Medaka fish (Oryzias latipes) (Carolina Science and Math, Burlington, NC) were maintained in a balanced salt solution (17.0 mM NaCl, 0.4 mM KCl, 0.2 Ca[Cl.sub.2], 0.3 mM Mg[SO.sub.4], 0.24 mM Na[HCO.sub.3]), with a 14 hr light:10 hr dark cycle and a 25-28 [degrees] C day: 22-25 [degrees] C night, which has been determined optimal for breeding (21). Each 10-gallon aquarium had four mature female and two mature male fish. Fertilization occurs externally, with the eggs attached to the abdomen of the female. Eggs were collected each morning from breeding females and kept in embryo-rearing solution (133 mM NaCl, 2.7 mM KCl, 2.1 mM Ca[Cl.sub.2], 0.2 mM Na[HCO.sub.3]), where they were separated and inspected for fertilization. Eggs were placed in 2% agarose in 12.5% Hank's solution (w/v) for stabilization during injection.

Aluminosilicate micropipettes (O.D. 1 mm; Sutter Instrument Co., Navato, CA) were pulled with a micropipette puller (P-87; Sutter) and beveled using a micropipette beveler (BV-10; Sutter). Individual micropipettes were front loaded with either triolein oil (95% pure; Sigma, St. Louis, MO) or with PbTx-1 (Calbiochem, La Jolla, CA) reconstituted into triolein oil. PbTx-1 was concentrated into triolein oil by layering the PbTx-1 (100 [micro]g/mL in methanol) on top of the triolein and evaporating the MeOH under nitrogen to yield a final concentration of 3 [micro]g/[Mu]L. Injections were made into the yolk space with the aid of a gas pico-injector system using an injection pressure of 7.8 psi (PLI-100; Harvard Apparatus, Holliston, MA). Balance pressure was maintained at 0.3 psi and increased to 3.2 psi before insertion through egg chorion to compensate for increased pressure within the egg. Eggs were placed in 2% agarose prepared with 12.5% Hank's balanced salts before injection. Eggs were injected 6-8 hr after fertilization, and both vehicle-injected controls (the same amount of methanol without PbTx-1 in triolein oil) as well as noninjected controls were performed along with the PbTx-1 injections. We injected 20-30 eggs per treatment group. Injected droplet diameters were measured via micrometer and the injected volumes calculated. We calculated the concentration of PbTx-1 injected as the product of the concentration of the toxin in the oil droplet and the volume of the oil droplet. After injections, the eggs were removed from the stabilizing agarose and washed in 12.5% Hank's balanced salts for 1 min. Eggs were then placed in 24-well plates containing 1.5 mi rearing solution and maintained in a 16 hr light: 8 hr dark cycle at 26 [degrees] C. Embryos were observed for development daily for 2 weeks with the aid of a stereomicroscope (MZ12; Leica), and spinal hyperkinetic events were recorded on embryonic day 4 over a 3-min time interval. Digital images were captured with an autoexposure CCD camera (MicroImage Video Systems Co., Boyertown, PA).

Results

PbTx-1 was administered to medaka eggs at 6 hr postfertilization by microinjection (Figure 1). Larval survivability at embryonic day 4 was 91% in noninjected animals and 90% of animals injected with triolein. A dose of PbTx-1 caused a dose-dependent effect on larval survivability, with a half maximal effect at approximately 4.5 ng/egg (Figure 2). Hatching of medaka normally occurred on embryonic days 9-12 and occurred successfully in 79% of noninjected embryos and 75% of embryos injected with triolein. A dose of PbTx-1 caused a dose-dependent inhibition of hatching with a half maximal effect at approximately 3 ng/egg (Figure 2).

[ILLUSTRATIONS OMITTED]

PbTx-1 also elicited a hyperkinetic activity, observed on embryonic day 4. This hyperkinesis was manifested as tail and body twitching and was monitored over a 3-min interval. Fewer than five spinal hyperkinetic twitches per 3 min were observed in both the noninjected and triolein-injected vehicle control groups. A concentration-dependent increase was observed for PbTx-1 in the frequency of events. The lowest observable effect occurred in the range of 0.1-0.9 ng/egg (ppm), and a maximal effect of 50 twitches over the 3-min time interval was observed at the dosing range of 5.0-5.9 ng/egg (Figure 3). Hyperkinesis declined at doses [is greater than] 6.0 ng.

[ILLUSTRATION OMITTED]

Increasing concentrations of 0.1-7.9 ng/egg PbTx-1 elicited several morphologic effects on the embryos, some of which affected hatching success. PbTx-1, given at doses in the range of 0.1-3.0 ng/egg induced a lateral curvature of the spinal column in embryos, the severity of which was dependent on the concentration of the dose. Figure 4A shows an embryo hatched from an egg injected with 1.1 ng PbTx-1, and Figure 4B shows an embryo hatched from an egg injected with 1.5 ng PbTx-1. Although this degree of anatomical deformity did not interfere with the hatching success of these embryos, their swimming ability was greatly impaired, leading to their inability to survive longer than 10 days. Concentrations of PbTx-1 between 1.5 and 3.0 ng/egg led to the development of embryos with an even greater degree of spinal curvature. In these cases, the embryos seemed to no longer be able to hatch out in the normal tail-first fashion, but instead hatched out in an abnormal head-first fashion (Figure 5). Although these embryos survived the hatching process, they too were unable to survive due to their greatly impaired swimming ability. Eggs that were injected with [is greater than] 4.0 ng PbTx-1 showed progressing embryonic development but failed to hatch.

[ILLUSTRATIONS OMITTED]

A more severe developmental effect of PbTx-1 on medaka embryos was seen at doses [is greater than] 3.0 ng/egg. Eggs injected with doses from 3.1-3.4 ng/egg of PbTx-1 produced embryos that suffered from herniation of the brain and meninges, possibly through skeletal defects in the skull (Figure 6). It is unknown whether the cranial herniation was due in part to the abnormal head-first hatching of this embryo. However, eggs injected with lower concentrations did not produce embryos with similar defects, even though the embryos had also hatched out head first. Eggs injected with 3.5 5.0 ng of PbTx-1 or higher produced embryos that exhibited malpositioned eyes, and an apparent lack of a frontal skull (Figure 7). A summary of the effects at the different doses is provided in Table 1.

[ILLUSTRATIONS OMITTED]
Table 1. Summary of adverse effects of brevetoxin-1 by dose.

Dose Characteristic adverse effect

Noninjected Hatched normally between days 9 and 12
Triolein Hatched normally between days 9 and 12
0.1-0.9 Hatched normally between days 9 and 12
1.0-1.9 Hatched normally, but delayed to days 10-15; spinal
 curvature present
2.0-2.9 Hatched abnormally head first with spinal curvature,
 delayed to days 10-15 or HD; clumping of erythrocytes
 in vessels at day 4
3.0-3.9 Hatched abnormally head first; brain herniation/
 malpositioned eyes present; hatching delayed to days
 12-16 and usually HD; clumping of erythrocytes in
 vessels
4.0-4.9 Abnormally hatched dead (herniation); hatching delayed to
 days 12-16, or NH; heart continued to pump up to day
 18; clumping of erythrocytes in vessels
5.0-5.9 NH; heart continued to pump up to day 18; clumping of
 erythrocytes in vessels
6.0-6.9 NH; often failed to develop to later stages; clumping of
 erythrocytes in vessels
7.0-7.9 NH; often failed to develop to later stages; clumping of
 erythrocytes in vessels

Abbreviations: HD, hatched dead; NH, did not hatch.


Discussion

The objective of this study was to quantify the adverse developmental effects of PbTx-1 using an exposure paradigm that parallels the maternal oocyte transfer of toxin. We have previously used this paradigm to examine the developmental effects of a related polyether toxin, ciguatoxin. Through the use of microinjection, we were able to determine that the lowest observable adverse effect level of PbTx-1 was 0.8-1.0 ng/egg, which is equal to 0.8-1.0 ppm (wet weight embryo = 1.0 mg). With increasing toxin loads of 1.0-3.0 ng/egg, we saw a direct increase in the incidence of lethal spinal defects and an increase in the occurrence of abnormal hatching. Embryos exposed to 3.1-4.0 ng of PbTx-1 exhibited deleterious morphologic abnormalities such as herniation of the brain and meninges and malpositioning of the eyes. Embryos exposed to [is greater than] 4.0 ng/egg exhibited embryonic development, but failed to hatch. Although we calculated the reported toxin dosages administered at the time of injection, we did not know the exact amounts absorbed by the embryos. Injected oil droplets may have different solubility properties from natural oil droplets. Microinjection of the toxin directly into the natural oil droplet may increase absorption efficiency. Accordingly, PbTx-1 may have even more potent effects than described in this report.

Red tide effects have been reported to affect larval stages of finfish. Riley et al. (22) found that that the density of red drum larvae (Scianops ocellatus) declined precipitiously in the Aranasas Pass Channel (Port Aransas, TX) after the September 1989 red tide. These investigators also examined the effects of G. breve on the hatching and larval survivability of laboratory spawned red drum. No effects on hatch rate were found at cell concentrations up to 5,600 cells/mL; however a cell concentration of 23 cells/mL was lethal to larvae. These results indicate that the larvae, but not the eggs, are susceptible to G. breve.

In contrast, an earlier study with the sea urchin (Lytechinus variegatus) reported that lysates of G. breve administered to eggs did induce developmental abnormalities (23). This study found that sperm motility, egg fertilization, and development through the blastula stage were unaffected; however, mortality and developmental (axial) abnormalities occurred in about 50% of the gastrula-stage embryos and 80% of pluteus-stage embryos. The reason for the difference between the study with the red drum eggs and the sea urchin eggs may result from the use of G. breve cells and lysates.

The effect levels we report for brevetoxin are about one-half to one-fifth the in vitro inhibition constant ([K.sub.i]) and median effective dose ([ED.sub.50]) for binding and voltage-dependent sodium channel-directed cytotoxicity (24). The effect levels are also 1,000 times lower than those we observe for the related toxin ciguatoxin (CTX). CTX injected at 1-9 ppb into medaka eggs increased spinal hyperkinesis and produced induced spinal defects (19). CTX is reported to be 20 times more effective than brevetoxin as an ichthyotoxin (0.5 nM vs. 10 nM for [LD.sub.50]) when administered in the aquarium water (25). The higher relative effect by microinjection may be due to differences in the two routes of administration. An unexpected difference between the developmental toxicity of both ciguatoxins and brevetoxins was that PbTx-1, but not CTX, caused cranial and optic deformities. The reason for this difference has not been elucidated, but it may be due to the biodistribution of microinjected toxin or perhaps to channel subtype specificity.

Red tides in the Gulf of Mexico are dense concentrations of G. breve beginning at 0.1 million cells/L and leading to discoloration at 2.0 million cells/L (13). Blooms containing 0.2 million cells/L kill fish (26). In culture G. breve produces approximately 10-15 pg of brevetoxin/cell (27). Thus, an icthyotoxic bloom would contain approximately 5 nM brevetoxins. This value is dose to the 60-min [LD.sub.50] for Poecilia reticulata for PbTx-1 (4.0 ng/mL) in aquarium water (6). Assuming a maximal tolerable concentration of 5 nM (or approximately 5 ppm) for adult fish, developmental effects such as the ones described in this paper could be expected to occur in animals having a bioaccumulation and oocyte transfer factor of approximately 0.1. Brevetoxin accumulation in fish tissue has not been reported; however, ciguatoxin added to aquarium water has been determined to accumulate 9-fold in fish tissue (24). Radioisotopic distribution studies for brevetoxin have been conducted, but distribution to oocytes cannot be inferred from the analysis of the gonads because these studies were not conducted on sexually mature female fish (28,29). However, oocyte transfer factors of 0.1-1.0 have been reported for organochlorines in salmon and lake trout based on body burden measurements and are generally related to egg lipid content (30).

The observation of developmental abnormalities in fish after PbTx-1 exposure identifies a new spectrum of adverse effects that may be expected to occur after exposure to G. breve red tide events. Adverse effects on larval life stages have been long suspected. The persistence of red tides from the late fall until early spring has suggested that the spawning of some marine species may be subject to the adverse effect of red tide toxins. Steidinger et al. (10) also emphasized the need for attention to the effects of red tide outbreaks on migratory species, as many species seek estuaries for breeding and nursery grounds. However, we also raise the potential of lifetime accumulation of sublethal body burdens of brevetoxins. Based on studies with other classes of fat-soluble contaminants, somatic stores of toxin in fish are transferred during oogenesis and lead to larval toxicity (30). This would be expected to have a more pronounced effect on the first brood; however, such effects may not necessarily impact successful recruitment of fish populations in successive years (31).

G. breve red tides have been associated with mortality events of many aquatic animals including finfish, sea turtles, and sea birds during their adult stages (4,9,10, 15,22,26,32-34). These animals have been known to bioaccumulate substantial body burdens of fat-soluble contaminants at times, and in certain cases transfer toxicity to offspring during oogenesis. Mammals including manatees, bottlenose dolphins, and humans are affected by red tide toxins and also accumulate substantial body burdens of fat-soluble contaminants such as organochlorines. A well-recognized means of contaminant transfer in mammals is by lactation, with placental transfer also being a potential risk (35). As the developmental processes of both higher and lower vertebrates is similar, the potential exists for developmental toxicity and abnormalities to occur among different phylogenetic classes as a result of cumulative exposure to G. breve red tide events.

REFERENCES AND NOTES

(1.) Catterall WA, Risk M. Toxin T48 from Ptychodiscus brevis (formerly Gymnodinium breve) enhances activation of voltage-sensitive sodium channels by veratridine. Mol Pharmacol 19:345-348 (1981).

(2.) Martin DF, Chatterjee AB. Isolation and characterization of a toxin from the Florida red tide organism. Nature 221:59 (1969).

(3.) Lin Y, Risk M, Ray SM, Van Engen D, Clardy J, Golik J, James JC, Nakanishi K. Isolation and structure of brevetoxin B from the "red tide" dinoflagellate Ptychodiscus brevis (Gymnodinium breve). J Am Chem Soc 103:6773 (1981).

(4.) Davis CC. Gymnodinium breve: a cause of discolored water and animal mortality in the Gulf of Mexico. Bet Gaz 109:358-360 (1948).

(5.) Poli MA, Mende TJ, Baden DG. Brevetoxins, unique activators of voltage-sensitive sodium channels, bind to specific sites in rat brain synaptosomes. Mol Pharmacol 30:129-135 (1986).

(6.) Shimizu Y, Chou HN, Bando G, VanDuyne G, Clardy J. Structure of brevetoxin-A (GB-1 toxin), the most potent toxin in the Florida red tide organism Gymnodinium breve (Ptychodiscus brevis). J Am Chem Soc 108:514-515 (1986).

(7.) Cummins JM, Jones AC, Stevens AA. Occurrence of toxic bivalve molluscs during a Gymnodinium breve "red tide". Trans Am Fish Sac 1:112-116 (1971).

(8.) McFarren EF, Tanabe H, Silva FJ, Wilson WB, Campbell JE, Lewis KH. The occurrence of a ciguatera-like poison in oysters, clams, and Gymnodinium breve cultures. Toxicon 3:111-123 (1965).

(9.) Walker ST. Fish mortality in the Gulf of Mexico. Proc U.S. Natl Mus 6(6):105-109 (1884).

(10.) Steidinger KA, Burklew MA, Ingle RM. The effects of Gymnodinium breve toxin on estuarine animals. In: Marine Pharmacognosy (Martin DF, Padilla GM, eds). New York:Academic Press, 1973;179-202.

(11.) Starr TJ. Notes on a toxin from Gymnodinium breve. Tex Rep Biol Meal 16:500-507 (1958).

(12.) Spiegelstein MY, Paster Z, Abbott BC. Purification and biological activity of Gymnodinium breve toxin. Toxicon 11:85-93 (1973).

(13.) Steidinger KA, Joyce EA Jr. Florida red tides. Fla State Board Conserv Educ Ser 17:1-26 (1973).

(14.) Pierce RH, Henry MS, Proffitt LS, Hasbrouck PA. Red tide toxin (brevetoxin) enrichment in marine aerosol. In: Toxic Marine Phytoplankton (Graneli E, Sunstron B, Edler L, Anderson DM, eds). Amsterdam:Elsevier Scientific Publishing, 1990;397-402.

(15.) Taylor HF. Mortality of Fishes on the West Coast of Florida. Report of the U.S. Commissioner of Fisheries. Bureau of Fisheries Document 848. Washington, DC:Government Printing Office, 1917.

(16.) Woodcock AH. Note concerning human respiratory irritation associated with high concentrations of plankton and mass mortality of marine organisms. J Mar Res 7(1):56-62 (1948).

(17.) Music SI, Howell JT, Brumback CL. Red tide, its public health implications. J Fla Med Assoc 60(1):27-29 (1973).

(18.) Hesman T. DDT treatment turns male fish into mothers. Science News 157(6):87 (2000).

(19.) Edmunds JSG, McCarthy RA, Ramsdell JS. Ciguatoxin reduces larval survivability in finfish. Toxicon 37(12):1827-1832 (1999).

(20.) Edmunds JSG, McCarthy RA, Ramsdell JS. Permanent and functional male-to-female sex reversal in d-rR strain medaka (Oryzias latipes) following egg microinjection of o,p'-DDT. Environ Health Perspect 108:219-224 (2000).

(21.) Yamamoto T. Artificially induced sex reversal in genotypic males in the medaka (Oryzias latipes). J Exp Zool 123:571-594 (1953).

(22.) Riley CM, Holt SA, Holt J, Buskey EJ, Arnold CR. Mortality of larval red drum (Sciaenops ocellatus) associated with a Ptychodiscus brevis red tide. Contrib Mar Sci 31:137-146 (1989).

(23.) Moon RT, Morrill JB. The effects of Gymnodinium breve lysate on the larval development of the sea urchin Lytechinus variegatus. J Environ Sci Health A11(10,11):673-683 (1976).

(24.) Lewis RJ. Ciguatoxins are potent ichthyotoxins. Toxicon 30(2):207-211 (1992).

(25.) Dechraoui M-Y, Naar J, Pauillac S, Legrand A-M. Ciguatoxins and brevetoxins, neurotoxic polyether compounds active on sodium channels. Toxicon 37:125-143 (1999).

(26.) Quick JA, Henderson GE. Evidences of new ichthyointoxicative phenomena in Gymnodinium breve red tides. In: Proceedings of the First International Conference on Toxic Dinoflagellate Blooms (LoCicero BR, ed). Wakefield, MA:Massachusetts Science and Technology Foundation, 1975;413-422.

(27.) Morton SM, personal communication.

(28.) Kennedy CJ, Schulman LS, Baden DG, Walsh PJ. Toxicokinetics of brevetoxin PbTx-3 in the gulf toadfish, Opsanus beta, following intravenous administration. Aquat Toxciol 22:3-14 (1992)

(29.) Washburn BS, Baden DG, Gassman NJ, Walsh PJ. Brevetoxin: tissue distribution and effect on cytochrome P450 enzymes in fish. Toxicon 32:799-805 (1997).

(30.) Miller MA. Maternal transfer of lipophilic contaminants in Salmonines to their eggs. Can J Fish Aquat Sci 49:1405-1413 (1993).

(31.) Warlen SM, Tester PA, Colby DR. Recruitment of larval fishes into a North Carolina estuary during a bloom of the red tide dinoflagellate, Gymnodinium breve. Bull Mar Sci 63:83-95 (1998)

(32.) Gunter G, Williams RH, Davis CC, Smith FGW. Catastrophic mass mortality of marine animals and coincident phytoplankton bloom on the west coast of Florida, November 1946 to August 1947. Ecol Monogr 8:310-324 (1948).

(33.) Forrester DJ, Gaskin JM, White FH, Thompson NP, Quick JA, Henderson GE, Woodard JC, Robertson WD. An epizootic of waterfowl associated with a red tide episode in Florida. J Wildl Dis 13:160-167 (1977).

(34.) Bossart GD, Baden DG, Ewing RY, Roberts B, Wright SD. Brevitoxicosis in manatees (Trichechus manatus latirostris) from the 1996 epizootic: gross, histologic and immunohistochemical features. Toxicol Pathol 26:276-282 (1998).

(35.) Ando M, Saito H, Wakisaka I. Transfer of polychlorinated biphenyls (PCBs) to newborn infants through the placenta and mother's milk. Arch Environ Contain Toxicol 14(1):51-57 (1985).

Karen L. Kimm-Brinson and John S. Ramsdell

Marine Biotoxins Program, Center for Coastal Environmental Health and Biomolecular Research, National Oceanic and Atmospheric Administration-National Ocean Service, Charleston, South Carolina, USA

Address correspondence to J.S. Ramsdell, Coastal Research Branch, Center for Coastal Environmental Health & Biomolecular Research, NOAA-National Ocean Service, 219 Fort Johnson Road, Charleston, SC 29412 USA. Telephone: (843) 762-8510. Fax: (843) 762-8700. E-mail: john.ramsdell@noaa.gov

This work was funded by the National Oceanic and Atmospheric Administration (NOAA-NOS). The National Ocean Service (NOS) does not approve, recommend, or endorse any proprietary product or material mentioned in this publication. No reference shall be made to NOS, or to this publication furnished by NOS, in any advertising or sales promotion which would indicate or imply that NOS approves, recommends, or endorses any proprietary product or proprietary material mentioned herein or which has as its purpose any intent to cause directly or indirectly the advertised product to be used or purchased because of NOS publication.

Received 18 July 2000; accepted 24 October 2000.
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Date:Apr 1, 2001
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