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dc.contributor.authorDarby, Alison
dc.contributor.authorLertpiriyapong, Kvin
dc.contributor.authorSarkar, Ujjal
dc.contributor.authorSeneviratne, Uthpala I.
dc.contributor.authorPark, Danny S.
dc.contributor.authorGamazon, Eric R.
dc.contributor.authorBatchelder, Chara
dc.contributor.authorCheung, Cheryl
dc.contributor.authorBuckley, Ellen Marie
dc.contributor.authorTaylor, Nancy S.
dc.contributor.authorShen, Zeli
dc.contributor.authorTannenbaum, Steven Robert
dc.contributor.authorWishnok, John S.
dc.contributor.authorFox, James G.
dc.date.accessioned2014-09-09T15:10:44Z
dc.date.available2014-09-09T15:10:44Z
dc.date.issued2014-07
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/89226
dc.description.abstractKlebsiella oxytoca is an opportunistic pathogen implicated in various clinical diseases in animals and humans. Studies suggest that in humans K. oxytoca exerts its pathogenicity in part through a cytotoxin. However, cytotoxin production in animal isolates of K. oxytoca and its pathogenic properties have not been characterized. Furthermore, neither the identity of the toxin nor a complete repertoire of genes involved in K. oxytoca pathogenesis have been fully elucidated. Here, we showed that several animal isolates of K. oxytoca, including the clinical isolates, produced secreted products in bacterial culture supernatant that display cytotoxicity on HEp-2 and HeLa cells, indicating the ability to produce cytotoxin. Cytotoxin production appears to be regulated by the environment, and soy based product was found to have a strong toxin induction property. The toxin was identified, by liquid chromatography-mass spectrometry and NMR spectroscopy, as low molecular weight heat labile benzodiazepine, tilivalline, previously shown to cause cytotoxicity in several cell lines, including mouse L1210 leukemic cells. Genome sequencing and analyses of a cytotoxin positive K. oxytoca strain isolated from an abscess of a mouse, identified genes previously shown to promote pathogenesis in other enteric bacterial pathogens including ecotin, several genes encoding for type IV and type VI secretion systems, and proteins that show sequence similarity to known bacterial toxins including cholera toxin. To our knowledge, these results demonstrate for the first time, that animal isolates of K. oxytoca, produces a cytotoxin, and that cytotoxin production is under strict environmental regulation. We also confirmed tilivalline as the cytotoxin present in animal K. oxytoca strains. These findings, along with the discovery of a repertoire of genes with virulence potential, provide important insights into the pathogenesis of K. oxytoca. As a novel diagnostic tool, tilivalline may serve as a biomarker for K oxytoca-induced cytotoxicity in humans and animals through detection in various samples from food to diseased samples using LC-MS/MS. Induction of K. oxytoca cytotoxin by consumption of soy may be in part involved in the pathogenesis of gastrointestinal disease.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant T32-RR007036)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant P30-ES002109)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0100542en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourcePublic Library of Scienceen_US
dc.titleCytotoxic and Pathogenic Properties of Klebsiella oxytoca Isolated from Laboratory Animalsen_US
dc.typeArticleen_US
dc.identifier.citationDarby, Alison, Kvin Lertpiriyapong, Ujjal Sarkar, Uthpala Seneviratne, Danny S. Park, Eric R. Gamazon, Chara Batchelder, et al. “Cytotoxic and Pathogenic Properties of Klebsiella Oxytoca Isolated from Laboratory Animals.” Edited by Stefan Bereswill. PLoS ONE 9, no. 7 (July 24, 2014): e100542.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.mitauthorDarby, Alisonen_US
dc.contributor.mitauthorLertpiriyapong, Kvinen_US
dc.contributor.mitauthorSarkar, Ujjalen_US
dc.contributor.mitauthorSeneviratne, Uthpala I.en_US
dc.contributor.mitauthorBatchelder, Charaen_US
dc.contributor.mitauthorCheung, Cherylen_US
dc.contributor.mitauthorBuckley, Ellen Marieen_US
dc.contributor.mitauthorTaylor, Nancy S.en_US
dc.contributor.mitauthorShen, Zelien_US
dc.contributor.mitauthorTannenbaum, Steven Roberten_US
dc.contributor.mitauthorWishnok, John S.en_US
dc.contributor.mitauthorFox, James G.en_US
dc.relation.journalPLoS ONEen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsDarby, Alison; Lertpiriyapong, Kvin; Sarkar, Ujjal; Seneviratne, Uthpala; Park, Danny S.; Gamazon, Eric R.; Batchelder, Chara; Cheung, Cheryl; Buckley, Ellen M.; Taylor, Nancy S.; Shen, Zeli; Tannenbaum, Steven R.; Wishnok, John S.; Fox, James G.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-6774-9639
dc.identifier.orcidhttps://orcid.org/0000-0001-9307-6116
dc.identifier.orcidhttps://orcid.org/0000-0002-2325-552X
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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