Goblet cells and mucin related gene expression in mice infected with Eimeria papillata.
The intestine plays an important role in the digestion and absorption of ingested food and the elimination of undigested food, microbes, and microbial products . The mucus layer coating the gastrointestinal tract is the front line of innate host defense, largely because of the secretory products of intestinal goblet cells .
Intestinal goblet cells are highly polarized secretory cells that are present throughout the intestinal tract. These specialized epithelial cells are thought to play an important protective role in the intestine by synthesizing and secreting several mediators, including the mucin MUC2 .
Indeed, infection with Eimeria parasites has been associated with increase in the incidence of the pathological conditions in poultry . These parasites cause various problems ranging from gastroenteritis, anorexia, abdominal distention, diarrhoea, emaciation, and so forth, all of which result in serious economic losses to the farmer as well as the nation in general . Since coccidioses lead to a significant impact on the livestock industry, we characterized the goblet cells response in mice inoculated with Eimeria papillata that infects enterocytes of the jejunum and shares many biological characteristics with the important pathogen of chickens, E. tenella .
The present study aimed to investigate the goblet cell response and its correlated genes during the infection with E. papillata in mice.
2. Materials and Methods
2.1. Animals. Twenty adult male Swiss albino mice weighing 35-30 g and aged 9-12 weeks were obtained from the animal facilities of King Saud University, Riyadh, Saudi Arabia. The mice were bred under specified pathogen-free conditions and fed a standard diet and water ad libitum. The experiments were approved by state authorities and followed Saudi Arabian rules for animal protection.
2.2. Experimental Design. Two groups of mice, with 10 animals per group, were investigated. The first group was inoculated only with sterile saline and served as the control group. The second group was orally infected with [10.sup.3] sporulated oocysts of E. papillata.
2.3. Infection of Mice. A self-healing strain of E. papillata was kindly provided by Professor Mehlhorn (Heinrich Heine University, Duesseldorf, Germany). Infected mice were orally inoculated with 1000 sporulated oocysts of E. papillata suspended in 100 pL sterile saline. Subsequently, fresh faecal pellets were collected every 24 h. The collected pellets from each mouse were weighed and the bedding was changed to eliminate reinfection. Oocyst output was measured as previously described . Faecal pellets were suspended in 2.5% (wt/vol) potassium dichromate and diluted in saturated sodium chloride for oocyst flotation. Oocysts were counted in a McMaster chamber and expressed as number of oocysts per gram of wet faeces.
2.4. Histological Analysis. Pieces of jejunum were freshly prepared from mice on day 5 postinfection with E. papillata, fixed in 10% neutral buffered formalin, and then embedded in paraffin. Sections were cut and then stained with hematoxylin and eosin. According to Dommels et al. , tissue sections were scored for inflammatory lesions (infiltrations by mononuclear cells, neutrophils, eosinophils, and plasmacytes, for fibrin exudation and lymphangiectasis), for tissue destruction (enterocyte loss, ballooning degeneration, edema, and mucosal atrophy), and for tissue repair (hyperplasia, angiogenesis, granulomas, and fibrosis). A rating score between 0 (no change from normal tissue) and 3 (lesions involved most areas and all the layers of the intestinal section including mucosa, muscle, and omental fat) was given for each aspect of inflammatory lesions, tissue destruction, and tissue repair. The sum of inflammatory lesions, tissue destruction, and tissue repair scores was used to represent the total histological injury score (HIS) for each intestinal section. The sum of the inflammatory lesions was multiplied by 2 to give more weight to this value since the tissue changes were mainly characterized by inflammatory lesions .
2.5. TUNEL Apoptosis Detection. Jejunum was collected on day 5 postinfection and terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) assay staining was performed using a TUNEL Apoptosis Detection Kit (GenScript, Piscataway, NJ, USA) by following the manufacturer's protocol. Briefly, sections of paraffin-embedded jejunum were deparaffinized, rehydrated in gradient ethanol, and then digested with proteinase K. Slides were mounted with 4,6-diamidino-2-phenylindole (DAPI). Using this procedure, positive nuclei of apoptotic cells are stained dark brown. Sections were counterstained with hematoxyline. For each animal, the number of apoptotic cells in the jejunum was counted on at least ten well-orientated villous-crypt units (VCU). Results were expressed as the mean number of apoptotic cells per ten VCU.
2.6. The Number of Goblet Cells. Sections were stained with Alcian blue for determination of the goblet cells. For each animal, the number of goblet cells in the jejunum was counted on at least ten well-orientated villous-crypt units (VCU). Results were expressed as the mean number of goblet cells pertenVCU 8].
2.7. Quantitative Real-Time PCR. Pieces of jejunum were aseptically removed, rapidly frozen, and stored in liquid nitrogen until use. Total RNA was isolated using Trizol (Invitrogen). RNA samples were treated with DNase (Applied Biosystems, Darmstadt, Germany) for at least 1 h and were then converted into cDNA by following the manufacturer's protocol using the reverse transcription kit (Qiagen, Hilden, Germany). Quantitative real-time PCR (qRT-PCR) was performed using the ABI Prism 7500HT sequence detection system (Applied Biosystems, Darmstadt, Germany) with SYBR green PCR master mix from Qiagen (Hilden, Germany). We investigated the genes encoding the mRNAs for the following proteins: interleukin-1[beta] (IL-1[beta]), interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-[alpha]), interferon-[gamma] (IFN[gamma]), toll-like receptor 4 (TLR4), inducible nitric oxide synthase (iNOS), and mucin 2 (MUC2). All primer assays used for qRT-PCR were obtained commercially from Qiagen. PCRs were performed as follows: 2 min at 50[degrees]C to activate uracil-Nglycosylase (UNG); 95[degrees] C for 10 min to deactivate UNG; and 40 cycles at 94[degrees]C for 15 s, 60[degrees]C for 35 s, and 72[degrees]C for 30 s. Reaction specificity was checked by performing dissociation curves after PCR. mRNA levels were normalized to 18S rRNA. The fold induction of mRNA expression upon infection with E. papillata was determined using the 2-AACT method .
2.8. Statistical Analysis. A two-tailed Student t-test was used for statistical analysis.
The course of E. papillata infections in mice was recently characterized in detail [10, 11]. The number of excreted oocysts varied among the individual mice between 200,000 and 260,000 per gram feces (mean value, 235,000 [+ or -] 24,000).
Light microscopical inspection of hematoxylin-and-eosin-stained sections revealed that the epithelial cells of the jejunum were infected by E. papillata. Concomitantly, there occurred some histological changes which were semi-quantified by applying the scoring according to Dommels et al. . Histological analysis revealed that mice infected with sporulated oocysts of E. papillata suffered a moderate inflammatory injury in jejunum (Figure 1).
Infection of mice with E. papillata induced a significant increase in the number of TUNEL-positive cells of the jejunal crypts compared to the noninfected controls (Figure 2). In addition, there was a significant reduction of the goblet cell numbers seen at the site of the E. papillata infection in the jejunum (Figure 3).
Quantitative real-time PCR was used to detect changes in the mRNA levels of inflammatory and goblet cell associated genes in the intestine. Upon infection with E. papillata, there was a significant increase in the mRNA expression of TNF-[alpha], iNOS, IFN-[gamma], and IL-1[beta]. In contrast, the mRNA expression patterns of IL-6 in response to E. papillata infection did not differ significantly between control and infected mice (Figure 4). The mRNA expression of TLR4 is significantly upregulated, whereas the expression of MUC2 is significantly downregulated upon infection (Figure 5).
Intestinal infection with E. papillata can induce substantial pathological changes in the epithelial compartment , as leads to a dramatic reduction in the number of goblet cells . The mucus released by goblet cells can function as a defensive barrier [12, 13]. Our results demonstrated that goblet cells were most evident in the infected crypt and much less so in the neighboring and other uninfected areas of the intestine. In addition, the parasites were mostly discovered at the bottom of the intracrypt epithelium.
In accordance with previous studies, the intracellular development of these parasites in the jejunum is rapid thus resulting in fecal output of Eimeria oocysts . Epithelial host cells finally disrupt upon discharging the oocysts, and tissue inflammation is therefore expected to occur during E. papillata infections. Also, our data have revealed that the inflammatory process occurring in mice gut is strong and is exacerbated by protozoal invasion. This is not only recorded by histology but also evidenced by the upregulation of the inflammatory cytokines: TNF-[alpha], iNOS, IFN-[gamma], and IL-1[beta].
Only IFN-[alpha], which is known to activate intracellular cytotoxicity , is strongly increased during the infection suggesting a specific role of IFN-[alpha] in E. papillata infection. Indeed, previous findings have also shown an increased production of IFN-[alpha], mainly by NK-cells, during primary infections with E. papillata . Also, a strong IFN-[alpha] response has been described to occur in the intestine upon infection with E. maxima , E. bovis, and E. alabamensis . It has been suggested that IFN-[alpha] limits the output of oocysts during primary infection with E. papillata . Also, the changes in goblet cell numbers may affect the susceptibility of the parasite-infected host to limit the capacity of opportunistic pathogen from increasing or penetrating the local epithelium .
Apoptosis is normal part of development and tissue homeostasis . Apoptotic cells are present in the intestinal crypts and regulate the total amount of progenitor stem cells . The great increase in the amount of apoptosis within E. papillata infected villi may be due to the complex hostparasite interaction. Moreover, apoptosis is an important regulator of the host's response during various intracellular protozoan infections and helps eliminate damaged or infected cells .
Our results of qRT-PCR revealed that the expression of MUC-2 is significantly reduced, whereas the expression of MUC-4 is not changed. MUC-2 is the first line of innate host defense in preventing pathogen-induced epithelial injury. In the absence of MUC-2, mice are more susceptible to Entamoeba histolytica-induced secretory and proinflammatory responses . Moreover, [MUC2.sup.-/-] mice spontaneously develop colitis, indicating that MUC2 is essential for the protection of the colon . The inhibition of the goblet cell marker MUC-2 correlates with an activation of the toll-like receptor 4 (TLR4) (Figure 5). Recently, it was shown that intestinal epithelial TLR4 regulates goblet cell development . In our study, E. papillata induced an upregulation of TLR4 and a downregulation of MUC2 which is consistent with the previous observation. Moreover, E. papillata induces an upregulation of the four miRNA species: miR-1959, MCMV-miR-M23-1-5P, miR-203, and miR-21 . Unfortunately, in silico analysis using the miRWalk database  revealed that none of our deregulated genes are a validated target of the described miRNAs.
Collectively, our data suggest that infections of mice with E. papillata not only induce pathogenesis in the jejunum, the final target site of E. papillata, but also induced an upregulation of TLR4 and a downregulation of MUC2. Further studies are required to know the mechanism of goblet cells regulated genes during infection with E. papillata.
The authors extend appreciations to the Deanship of Scientific Research at King Saud University for funding the work through the Research Group Project no. RGP-VPP-198.
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Mohamed A. Dkhil, (1,2) Denis Delic, (3) and Saleh Al-Quraishy (1)
(1) Department of Zoology, College of Science, King Saud University, P.O.Box 2455, Riyadh 11451, Saudi Arabia
(2) Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt
(3) Department of Molecular Parasitology, Heinrich Heine University, Duesseldorf, Germany
Correspondence should be addressed to Mohamed A. Dkhil; email@example.com
Received 30 September 2013; Accepted 12 November 2013
Academic Editors: G. Cancrini and A. Criado-Fornelio
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|Title Annotation:||Research Article|
|Author:||Dkhil, Mohamed A.; Delic, Denis; Quraishy, Saleh Al-|
|Publication:||The Scientific World Journal|
|Date:||Jan 1, 2013|
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