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dc.contributor.authorGarcia, Alexis
dc.contributor.authorMuthupalani, Sureshkumar
dc.contributor.authorSwennes, Alton G.
dc.contributor.authorFox, James G.
dc.contributor.authorShringi, Smriti
dc.contributor.authorLahmers, Kevin K.
dc.contributor.authorPotter, Kathleen A.
dc.contributor.authorHovde, Carolyn J.
dc.contributor.authorCall, Douglas R.
dc.contributor.authorBesser, Thomas E.
dc.date.accessioned2013-03-27T19:59:26Z
dc.date.available2013-03-27T19:59:26Z
dc.date.issued2011-10
dc.date.submitted2011-06
dc.identifier.issn0019-9567
dc.identifier.urihttp://hdl.handle.net/1721.1/78007
dc.description.abstractEnterohemorrhagic Escherichia coli O157:H7 (EHEC O157) is an important cause of food and waterborne illness in the developed countries. Cattle are a reservoir host of EHEC O157 and a major source of human exposure through contaminated meat products. Shiga toxins (Stxs) are an important pathogenicity trait of EHEC O157. The insertion sites of the Stx-encoding bacteriophages differentiate EHEC O157 isolates into genogroups commonly isolated from cattle but rarely from sick humans (bovine-biased genotypes [BBG]) and those commonly isolated from both cattle and human patients (clinical genotypes [CG]). Since BBG and CG share the cardinal virulence factors of EHEC O157 and are carried by cattle at similar prevalences, the infrequent occurrence of BBG among human disease isolates suggests that they may be less virulent than CG. We compared the virulence potentials of human and bovine isolates of CG and BBG in newborn conventional pig and weaned Dutch Belted rabbit models. CG-challenged piglets experienced severe disease accompanied by early and high mortality compared to BBG-challenged piglets. Similarly, CG-challenged rabbits were likely to develop lesions in kidney and intestine compared with the BBG-challenged rabbits. The CG strains used in this study carried stx2 and produced significantly higher amounts of Stx, whereas the BBG strains carried the stx2c gene variant only. These results suggest that BBG are less virulent than CG and that this difference in virulence potential is associated with the Stx2 subtype(s) carried and/or the amount of Stx produced.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Contract N01-AI-30055)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Contract R21AI073803)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Contract T32 RR007036-24)en_US
dc.language.isoen_US
dc.publisherAmerican Society for Microbiologyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1128/iai.05470-11en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceProf. Fox via Howard Silveren_US
dc.titleDifferential Virulence of Clinical and Bovine-Biased Enterohemorrhagic Escherichia coli O157:H7 Genotypes in Piglet and Dutch Belted Rabbit Modelsen_US
dc.typeArticleen_US
dc.identifier.citationShringi, S. et al. “Differential Virulence of Clinical and Bovine-Biased Enterohemorrhagic Escherichia Coli O157:H7 Genotypes in Piglet and Dutch Belted Rabbit Models.” Infection and Immunity 80.1 (2011): 369–380. © 2011 American Society for Microbiologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.approverFox, James G.
dc.contributor.mitauthorGarcia, Alexis
dc.contributor.mitauthorMuthupalani, Sureshkumar
dc.contributor.mitauthorSwennes, Alton G.
dc.contributor.mitauthorFox, James G.
dc.relation.journalInfection and Immunityen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsShringi, S.; Garcia, A.; Lahmers, K. K.; Potter, K. A.; Muthupalani, S.; Swennes, A. G.; Hovde, C. J.; Call, D. R.; Fox, J. G.; Besser, T. E.en
dc.identifier.orcidhttps://orcid.org/0000-0001-9307-6116
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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