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dc.contributor.authorLebreton, Francois
dc.contributor.authorDzink-Fox, Joanne
dc.contributor.authorGilmore, Michael S.
dc.contributor.authorWoods, Stephanie
dc.contributor.authorLieberman, Mia
dc.contributor.authorTrowel, Elise
dc.contributor.authorde la Fuente Nunez, Cesar
dc.contributor.authorFox, James G
dc.date.accessioned2017-06-16T18:42:24Z
dc.date.available2017-06-16T18:42:24Z
dc.date.issued2017-01
dc.date.submitted2016-09
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/109972
dc.description.abstractNonhuman primates are commonly used for cognitive neuroscience research and often surgically implanted with cephalic recording chambers for electrophysiological recording. Aerobic bacterial cultures from 25 macaques identified 72 bacterial isolates, including 15 Enterococcus faecalis isolates. The E. faecalis isolates displayed multi-drug resistant phenotypes, with resistance to ciprofloxacin, enrofloxacin, trimethoprim-sulfamethoxazole, tetracycline, chloramphenicol, bacitracin, and erythromycin, as well as high-level aminoglycoside resistance. Multi-locus sequence typing showed that most belonged to two E. faecalis sequence types (ST): ST 4 and ST 55. The genomes of three representative isolates were sequenced to identify genes encoding antimicrobial resistances and other traits. Antimicrobial resistance genes identified included aac(6’)-aph(2”), aph(3’)-III, str, ant(6)-Ia, tetM, tetS, tetL, ermB, bcrABR, cat, and dfrG, and polymorphisms in parC (S80I) and gyrA (S83I) were observed. These isolates also harbored virulence factors including the cytolysin toxin genes in ST 4 isolates, as well as multiple biofilm-associated genes (esp, agg, ace, SrtA, gelE, ebpABC), hyaluronidases (hylA, hylB), and other survival genes (ElrA, tpx). Crystal violet biofilm assays confirmed that ST 4 isolates produced more biofilm than ST 55 isolates. The abundance of antimicrobial resistance and virulence factor genes in the ST 4 isolates likely relates to the loss of CRISPR-cas. This macaque colony represents a unique model for studying E. faecalis infection associated with indwelling devices, and provides an opportunity to understand the basis of persistence of this pathogen in a healthcare setting.en_US
dc.description.sponsorshipUnited States. National Institutes of Health (T32 OD010978)en_US
dc.description.sponsorshipUnited States. National Institutes of Health (P30 ES02109)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0169293en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourcePLoSen_US
dc.titleCharacterization of Multi-Drug Resistant Enterococcus faecalis Isolated from Cephalic Recording Chambers in Research Macaques (Macaca spp.)en_US
dc.typeArticleen_US
dc.identifier.citationWoods, Stephanie E.; Lieberman, Mia T.; Lebreton, Francois; Trowel, Elise; de la Fuente-Núñez, César; Dzink-Fox, Joanne; Gilmore, Michael S. and Fox, James G. “Characterization of Multi-Drug Resistant Enterococcus Faecalis Isolated from Cephalic Recording Chambers in Research Macaques (Macaca Spp.).” Edited by Lynn E. Hancock. PLOS ONE 12, no. 1 (January 2017): e0169293 © 2017 Woods et alen_US
dc.contributor.departmentMIT Synthetic Biology Centeren_US
dc.contributor.departmentBroad Institute of MIT and Harvarden_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.contributor.mitauthorWoods, Stephanie
dc.contributor.mitauthorLieberman, Mia
dc.contributor.mitauthorTrowel, Elise
dc.contributor.mitauthorde la Fuente Nunez, Cesar
dc.contributor.mitauthorFox, James G
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.orderedauthorsWoods, Stephanie E.; Lieberman, Mia T.; Lebreton, Francois; Trowel, Elise; de la Fuente-Núñez, César; Dzink-Fox, Joanne; Gilmore, Michael S.; Fox, James G.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2993-5198
dc.identifier.orcidhttps://orcid.org/0000-0001-9307-6116
mit.licensePUBLISHER_CCen_US


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