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dc.contributor.authorFeng, Yan
dc.contributor.authorMannion, Anthony
dc.contributor.authorMadden, Carolyn
dc.contributor.authorSwennes, Alton G.
dc.contributor.authorTownes, Catherine
dc.contributor.authorByrd, Charles
dc.contributor.authorMarini, Robert P
dc.contributor.authorFox, James G
dc.date.accessioned2018-01-30T15:33:46Z
dc.date.available2018-01-30T15:33:46Z
dc.date.issued2017-12
dc.date.submitted2017-10
dc.identifier.issn1757-4749
dc.identifier.urihttp://hdl.handle.net/1721.1/113343
dc.description.abstractBackground: Many Escherichia coli strains are considered to be a component of the normal flora found in the human and animal intestinal tracts. While most E. coli strains are commensal, some strains encode virulence factors that enable the bacteria to cause intestinal and extra-intestinal clinically-relevant infections. Colibactin, encoded by a genomic island (pks island), and cytotoxic necrotizing factor (CNF), encoded by the cnf gene, are genotoxic and can modulate cellular differentiation, apoptosis and proliferation. Some commensal and pathogenic pks+ and cnf+ E. coli strains have been associated with inflammation and cancer in humans and animals. Results: In the present study, E. coli strains encoding colibactin and CNF were identified in macaque samples. We performed bacterial cultures utilizing rectal swabs and extra-intestinal samples from clinically normal macaques. A total of 239 E. coli strains were isolated from 266 macaques. The strains were identified biochemically and selected isolates were serotyped as O88:H4, O25:H4, O7:H7, OM:H14, and OM:H16. Specific PCR for pks and cnf1 gene amplification, and phylogenetic group identification were performed on all E. coli strains. Among the 239 isolates, 41 (17.2%) were pks+/cnf1−, 19 (7.9%) were pks−/cnf1+, and 31 (13.0%) were pks+/cnf1+. One hundred forty-eight (61.9%) E. coli isolates were negative for both genes (pks−/cnf1−). In total, 72 (30.1%) were positive for pks genes, and 50 (20.9%) were positive for cnf1. No cnf2+ isolates were detected. Both pks+ and cnf1+ E. coli strains belonged mainly to phylogenetic group B2, including B21. Colibactin and CNF cytotoxic activities were observed using a HeLa cell cytotoxicity assay in representative isolates. Whole genome sequencing of 10 representative E. coli strains confirmed the presence of virulence factors and antibiotic resistance genes in rhesus macaque E. coli isolates. Conclusions: Our findings indicate that colibactin- and CNF-encoding E. coli colonize laboratory macaques and can potentially cause clinical and subclinical diseases that impact macaque models.en_US
dc.publisherBioMed Centralen_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/s13099-017-0220-yen_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceBioMed Centralen_US
dc.titleCytotoxic Escherichia coli strains encoding colibactin and cytotoxic necrotizing factor (CNF) colonize laboratory macaquesen_US
dc.typeArticleen_US
dc.identifier.citationFeng, Yan, et al. “Cytotoxic Escherichia Coli Strains Encoding Colibactin and Cytotoxic Necrotizing Factor (CNF) Colonize Laboratory Macaques.” Gut Pathogens, vol. 9, no. 1, Dec. 2017.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_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.mitauthorFeng, Yan
dc.contributor.mitauthorMannion, Anthony
dc.contributor.mitauthorMadden, Carolyn
dc.contributor.mitauthorSwennes, Alton G.
dc.contributor.mitauthorTownes, Catherine
dc.contributor.mitauthorByrd, Charles
dc.contributor.mitauthorMarini, Robert P
dc.contributor.mitauthorFox, James G
dc.relation.journalGut Pathogensen_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.updated2017-12-10T04:58:12Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dspace.orderedauthorsFeng, Yan; Mannion, Anthony; Madden, Carolyn M.; Swennes, Alton G.; Townes, Catherine; Byrd, Charles; Marini, Robert P.; Fox, James G.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9307-6116
mit.licensePUBLISHER_CCen_US


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