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dc.contributor.authorMcCoy, Colleen S
dc.contributor.authorMannion, Anthony
dc.contributor.authorFeng, Yan
dc.contributor.authorMadden, Carolyn
dc.contributor.authorArtim, Stephen C
dc.contributor.authorAu, Gina G
dc.contributor.authorDolan, Mikayla
dc.contributor.authorHaupt, Jennifer
dc.contributor.authorBurns, Monika
dc.contributor.authorSheh, Alexander
dc.contributor.authorFox, James G
dc.date.accessioned2022-06-30T18:12:47Z
dc.date.available2021-10-27T19:54:01Z
dc.date.available2022-06-30T18:12:47Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/133657.2
dc.description.abstract© 2021, The Author(s). Cyclomodulins are virulence factors that modulate cellular differentiation, apoptosis, and proliferation. These include colibactin (pks), cytotoxic necrotizing factor (cnf), and cytolethal distending toxin (cdt). Pathogenic pks+, cnf+, and cdt+ E. coli strains are associated with inflammatory bowel disease (IBD) and colorectal cancer in humans and animals. Captive marmosets are frequently afflicted with IBD-like disease, and its association with cyclomodulins is unknown. Cyclomodulin-encoding E. coli rectal isolates were characterized using PCR-based assays in healthy and clinically affected marmosets originating from three different captive sources. 139 E. coli isolates were cultured from 122 of 143 marmosets. The pks gene was detected in 56 isolates (40%), cnf in 47 isolates (34%), and cdt in 1 isolate (0.7%). The prevalences of pks+ and cnf+ E. coli isolates were significantly different between the three marmoset colonies. 98% of cyclomodulin-positive E. coli belonged to phylogenetic group B2. Representative isolates demonstrated cyclomodulin cytotoxicity, and serotyping and whole genome sequencing were consistent with pathogenic E. coli strains. However, the presence of pks+, cnf+, or cdt+ E. coli did not correlate with clinical gastrointestinal disease in marmosets. Cyclomodulin-encoding E. coli colonize laboratory common marmosets in a manner dependent on the source, potentially impacting reproducibility in marmoset models.en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/s41598-020-80000-1en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceScientific Reportsen_US
dc.titleCytotoxic Escherichia coli strains encoding colibactin, cytotoxic necrotizing factor, and cytolethal distending toxin colonize laboratory common marmosets (Callithrix jacchus)en_US
dc.typeArticleen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.relation.journalScientific Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-03-11T15:39:48Z
dspace.orderedauthorsMcCoy, CS; Mannion, AJ; Feng, Y; Madden, CM; Artim, SC; Au, GG; Dolan, M; Haupt, JL; Burns, MA; Sheh, A; Fox, JGen_US
dspace.date.submission2021-03-11T15:39:50Z
mit.journal.volume11en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusPublication Information Neededen_US


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