期刊论文详细信息
BMC Veterinary Research
Bison and bovine rectoanal junctions exhibit similar cellular architecture and Escherichia coli O157 adherence patterns
Judith A Stasko1  Indira T Kudva2 
[1] Microscopy Services Laboratory, National Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Ames, IA 50010, USA;Food Safety and Enteric Pathogens Research Unit, National Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Ames, IA 50010, USA
关键词: Adherence;    Markers;    Epithelia;    Tissue;    Bison;    Bovine;    O157:H7;   
Others  :  1119372
DOI  :  10.1186/1746-6148-9-266
 received in 2013-10-21, accepted in 2013-12-18,  发布年份 2013
【 摘 要 】

Background

Escherichia coli O157 (E. coli O157) has been isolated from bison retail meat, a fact that is important given that bison meat has been implicated in an E. coli O157-multistate outbreak. In addition, E. coli O157 has also been isolated from bison feces at slaughter and on farms. Cattle are well documented as E. coli O157 reservoirs, and the primary site of E. coli O157 persistence in such reservoirs is the rectoanal junction (RAJ), located at the distal end of the bovine gastrointestinal tract. Since bison and cattle share many genetic similarities manifested as common lineage, susceptibility to infection and the nature of immune responses to infectious agents, we decided to evaluate whether the RAJ of these animals were comparable both in terms of cellular architecture and as sites for adherence of E. coli O157. Specifically, we compared the histo-morphologies of the RAJ and evaluated the E. coli O157 adherence characteristics to the RAJ squamous epithelial (RSE) cells, from these two species.

Results

We found that the RAJ of both bison and cattle demonstrated similar distribution of epithelial cell markers villin, vimentin, cytokeratin, E-cadherin and N-cadherin. Interestingly, N-cadherin predominated in the stratified squamous epithelium reflecting its proliferative nature. E. coli O157 strains 86–24 SmR and EDL 933 adhered to RSE cells from both animals with similar diffuse and aggregative patterns, respectively.

Conclusion

Our observations further support the fact that bison are likely ‘wildlife’ reservoirs for E. coli O157, harboring these bacteria in their gastrointestinal tract. Our results also extend the utility of the RSE-cell assay, previously developed to elucidate E. coli O157-cattle RAJ interactions, to studies in bison, which are warranted to determine whether these observations in vitro correlate with those occurring in vivo at the RAJ within the bison gastrointestinal tract.

【 授权许可】

   
2013 Kudva and Stasko; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Hedrick PW: Conservation genetics and North American bison (Bison bison). J Hered 2009, 100:411-420.
  • [2]Factsheets: American Bison 2009. http://library.sandiegozoo.org/factsheets/bison/bison.htm webcite
  • [3]Food Safety and Inspection Service (FSIS), Food Safety Fact Sheet: Bison from farm to Table. Washington, DC: United States Department of Agriculture; 2013.
  • [4]Bibi F, Vrba ES: Unraveling bovin phylogeny: accomplishments and challenges. BMC Biol 2010, 8:50. doi:10.1186/1741-7007-8-50 BioMed Central Full Text
  • [5]Stevens MG, Olsen SC, Cheville NF: Comparative effects of bovine cytokines on cattle and bison peripheral blood mononuclear cell proliferation. Comp Immun Microbiol Infect Dis 1997, 20:155-162.
  • [6]Swain SD, Nelson LK, Hanson AJ, Siemsen DW, Quinn MT: Host defense function in neutrophils from the American bison (Bison bison). Comp Biochem Physiol A Mol Integr Physiol 2000, 127:237-247.
  • [7]Mackintosh C, Haigh JC, Griffin F: Bacterial diseases of farmed deer and bison. Rev Sci Tech 2002, 21:249-263.
  • [8]Miller RS, Sweeney SJ: Mycobacterium bovis (bovine tuberculosis) infection in North American wildlife: current status and opportunities for mitigation of risks of further infection in wildlife populations. Epidemiol Infect 2013, 141:1357-1370.
  • [9]Pruvot M, Forde TL, Steele J, Kutz SJ, deBuck JD, van der Meer F, Orsel K: The modification and evaluation of an ELISA test for the surveillance of Mycobacterium avium subsp. paratuberculosis infection in wild ruminants. BMC Vet Res 2013, 9:5. doi: 10.1186/1746-6148-9-5 BioMed Central Full Text
  • [10]Olsen SC: Brucellosis in the United States: role and significance of wildlife reservoirs. Vaccine 2010, 28S:F73-F76.
  • [11]Jay-Russell MT, Langholz JA: Potential role of wildlife in pathogenic contamination of fresh produce. Humn-Wild Interact 2013, 7:140-157.
  • [12]Woodbury MR, Chirino-Trejo M: A survey of the fecal bacteria of bison (Bison bison) for potential pathogens and antimicrobial susceptibility of bison-origin E. coli. Can Vet J 2011, 52:414-418.
  • [13]Sánchez S, Martínez R, Rey J, García A, Blanco J, Blanco M, Blanco JE, Mora A, Herrera-León S, Echeita A, Alonso JM: Pheno-genotypic characterisation of Escherichia coli O157:H7 isolates from domestic and wild ruminants. Vet Microbiol 2010, 142:445-449.
  • [14]Ferens WA, Hovde CJ: Escherichia coli O157:H7: Animal Reservoir and Sources of Human Infection. Food Path Dis 2011, 8:465-486.
  • [15]Osterholm MT: Foodborne disease in 2011 – The rest of the story. NEJM 2011, 364:889-891.
  • [16]Scallan E, Hoekstra RM, Angulo FJ, Tauxe RV, Widdowson M, Roy SL, Jones JL, Griffin PM: Foodborne illness acquired in the United States - Major pathogens. Emerg Infect Dis 2011, 17:7-15.
  • [17]Vital signs: Incidence and trends of infection with pathogens transmitted commonly through food --- Foodborne diseases active surveillance network, 10 U.S. Sites, 1996--2010. MMWR 2011, 60:749-755.
  • [18]Griffin PM, Ostroff SM, Tauxe RV, Greene KD, Wells JG, Lewis JH, Blake PA: Illnesses associated with Escherichia coli 0157:H7 infections. A broad clinical spectrum. Ann Intern Med 1998, 109:705-712.
  • [19]Kaper JB, O’Brien AD: Escherichia coli O157:H7 and other Shiga Toxin-Producing E. coli strains. Washington, D.C: ASM Press; 1998.
  • [20]Gyles CL: Shiga toxin-producing Escherichia coli: an overview. J Anim Sci 2007, 85:E45-E62.
  • [21]Buzby JC, Roberts T: The economics of enteric infections: human foodborne disease costs. Gastroenterol 2009, 136:1851-1862.
  • [22]Batz MB, Hoffmann S, Morris JG: Ranking the disease burden of 14 pathogens in food sources in the United States using attribution data from outbreak investigations and expert elicitation. J Food Protect 2012, 75:1278-1291.
  • [23]Hoffman S, Batz MB, Morris JG: Annual cost of illness and quality-adjusted life year losses in the United States due to 14 foodborne pathogens. J Food Protect 2012, 75:1292-1302.
  • [24]Council of State and Territorial Epidemiologists (CSTE) Report: 13-ID-01: Update to Public Health Reporting for Shiga toxin-producing Escherichia coli (STEC). Atlanta, Georgia: CSTE; 2013.
  • [25]Li Q, Sherwood JS, Logue CM: The prevalence of Listeria, Salmonella, Escherichia coli and E. coli O157:H7 on bison carcasses during processing. Food Microbiol 2004, 21:791-799.
  • [26]Magwedere K, Dang HA, Mills EW, Cutter CN, Roberts EL, DebRoy C: Incidence of Shiga toxin-producing Escherichia coli strains in beef, pork, chicken, deer, boar, bison, and rabbit retail meat. J Vet Diagn Invest 2013, 25:254-258.
  • [27]Food Safety and Inspection Service (FSIS), Food Safety Fact Recall Release: FSIS-RC-043-2010: Colorado firm recalls bison products due to possible E. coli O157:H7 contamination. Washington, DC: United States Department of Agriculture; 2010.
  • [28]Reinstein S, Fox JT, Shi X, Alam MJ, Nagaraja TG: Prevalence of Escherichia coli O157:H7 in the American bison (Bison bison). J Food Protect 2007, 70:2555-2560.
  • [29]Li Q, Sherwood JS, Logue CM: The growth and survival of Escherichia coli O157:H7 on minced bison and pieces of bison meat stored at 5°C and 10°C. Food Microbiol 2005, 23:415-421.
  • [30]Quantrell RJO, Naylor SW, Roe AJ, Spears K, Gally DL: EHEC O157:H7-getting to the bottom of the burger bug. Microbiol Today 2004, 31:126-128.
  • [31]Sheng H, Lim JY, Knecht HJ, Li J, Hovde CJ: Role of Escherichia coli O157:H7 virulence factors in colonization at the bovine terminal rectal mucosa. Infect Immun 2006, 74:4685-4693.
  • [32]Dean-Nystrom EA, Stoffregen WC, Bosworth BT, Moon HW, Pohlenz JF: Early attachment sites for Shiga-toxigenic Escherichia coli O157:H7 in experimentally inoculated weaned calves. Appl Environ Microbiol 2008, 74:6378-6384.
  • [33]Kudva IT, Dean-Nystrom E: Bovine recto-anal junction squamous epithelial (RSE) cell adhesion assay for studying Escherichia coli O157 adherence. J App Microbiol 2011, 111:1283-1294.
  • [34]Kudva IT, Griffin RW, Krastins B, Sarracino DA, Calderwood SB, John M: Proteins other than the locus of enterocyte effacement-encoded proteins contribute to Escherichia coli O157:H7 adherence to bovine rectoanal junction stratified squamous epithelial cells. BMC Microbiol 2012, 12:103. BioMed Central Full Text
  • [35]Fischer AH, Jacobson KA, Rose J, Zeller R: Cryosectioning tissues. Cold Spring Harb Protoc 2008., 3(8) doi: 10.1101/pdb.prot4991
  • [36]Shi SR, Key ME, Kalra KL: Antigen retrieval in formalin-fixed, paraffin-embedded tissues: an enhancement method for immunohistochemical staining based on microwave oven heating of tissue Sections. J Histochem Cytochem 1991, 39:741.
  • [37]McDowell EM: Fixation and processing. In Diagnostic Electron Microscopy. 1st edition. Edited by Jones RT, Trump BF. Somerset, NJ: John Wiley and Sons; 1978:130.
  • [38]Knutton S: Electron microscopical methods in adhesion. In Adhesion of microbial pathogens. Edited by Doyle RJ, Ofek I. San Diego, CA: Academic Press; 1995:145-158.
  • [39]Hayat MA, Miller SE: Negative staining. New York: McGraw-Hill Publishing Co; 1990.
  • [40]Skepper JN, Powell JM: Microscopy (TEM)- immunogold staining of epoxy resin sections for transmission electron. Cold Spring Harb Protoc 2008., 3(6) doi: 10.1101/pdb.prot5015
  • [41]Dawes CJ: Biological techniques in electron microscopy. New York: Barnes and Noble; 1971.
  • [42]Pease DC: Histology techniques for electron microscopy. New York: Academic Press; 1964.
  • [43]Mahajan A, Naylor S, Mills AD, Low JC, Mackellar A, Hoey DEE, Currie CG, Gally DL, Huntley J, Smith DGE: Phenotypic and functional characterization of follicle-associated epithelium of rectal lymphoid tissue. Cell Tissue Res 2005, 321:365-374.
  • [44]Kanaya T, Aso H, Miyazawa K, Kido T, Minashima T, Watanabe K, Ohwada S, Kitazawa H, Rose MT, Yamaguchi T: Staining patterns for actin and villin distinguish M cells in bovine follicle-associated epithelium. Res Vet Sci 2007, 82:141-149.
  • [45]Bretscher A, Weber K: Villin is a major protein of the microvillus cytoskeleton, which binds both G- and F-actinin a calcium-dependent manner. Cell 1980, 20:839-847.
  • [46]Rusu D, Loret S, Peulen O, Mainil J, Dandrifosse G: Immunochemical, biomolecular and biochemical characterization of bovine epithelia intestinal primocultures. BMC Cell Biol 2005, 6:42. doi: 10.1186/1471-2121-6-42 BioMed Central Full Text
  • [47]Moll R, Franke WW, Schiller DL: The catalog of human cytokeratins: Patterns of expression in normal epithelia, tumors and cultured cells. Cell 1982, 31:11-24.
  • [48]Heid HW, Moll I, Franke WW: Patterns of expression of trichocytic and epithelial cytokeratins in mammalian tissues II. Concomitant and mutually exclusive synthesis of trichocytic and epithelial cytokeratins in diverse human and bovine tissues (hair follicle, nail bed and matrix, lingual papilla, thymic reticulum). Differentiation 1988, 37:215-230.
  • [49]Angst BD, Marcozzi C, Magee AI: The cadherin superfamily: diversity in form and function. Cell Sci 2001, 114:629-641.
  • [50]Liaw CW, Cannon C, Power MD, Kiboneka PK, Rubin LL: Identification and cloning of two species of cadherins in bovine endothelial cells. EMBO J 1990, 9:2701-2708.
  • [51]Lewis JE, Wahl JK III, Sass KM, Jensen PJ, Johnson KR, Wheelock MJ: Cross-talk between adherens junctions and desmosomes depends on plakoglobin. J Cell Biol 1997, 136:919-934.
  • [52]Kantak SS, Kramer RH: E-cadherin regulates anchorage-independent growth and survival in oral squamous cell carcinoma cells. J Biol Chem 1998, 273:16953-16961.
  • [53]Aho AD, McNulty AM, Coussens PM: Enhanced expression of interleukin-1a and tumor necrosis factor receptor-associated protein 1 in ileal tissues of cattle infected with Mycobacterium avium subsp. Paratuberculosis. Infect Immun 2003, 71:6479-6486.
  • [54]Tsuchiya B, Sato Y, Kameya T, Okayasu I, Mukai K: Differential expression of N-cadherin and E-cadherin in normal human tissues. Arch Histol Cytol 2006, 69:135-145.
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