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dc.contributor.authorLieberman, Mia
dc.contributor.authorVan Tyne, Daria
dc.contributor.authorDzink-Fox, JoAnn
dc.contributor.authorMa, Eric J.
dc.contributor.authorGilmore, Michael S.
dc.contributor.authorFox, James G
dc.date.accessioned2019-10-21T15:50:10Z
dc.date.available2019-10-21T15:50:10Z
dc.date.issued2018-07
dc.date.submitted2018-06
dc.identifier.issn0099-2240
dc.identifier.issn1098-5336
dc.identifier.urihttps://hdl.handle.net/1721.1/122645
dc.description.abstractEnterococcus faecalis is a common opportunistic pathogen that colonizes cephalic recording chambers (CRCs) of macaques used in cognitive neuroscience research. We previously characterized 15 E. faecalis strains isolated from macaques at the Massachusetts Institute of Technology (MIT) in 2011. The goal of this study was to examine how a 2014 protocol change prohibiting the use of antimicrobials within CRCs affected colonizing E. faecalis strains. We collected 20 E. faecalis isolates from 10 macaques between 2013 and 2017 for comparison to 4 isolates previously characterized in 2011 with respect to the sequence type (ST) distribution, antimicrobial resistance, biofilm formation, and changes in genes that might confer a survival advantage. ST4 and ST55 were predominant among the isolates characterized in 2011, whereas the less antimicrobial-resistant lineage ST48 emerged to dominance after 2013. Two macaques remained colonized by ST4 and ST55 strains for 5 and 4 years, respectively. While the antimicrobial resistance and virulence factors identified in these ST4 and ST55 strains remained relatively stable, we detected an increase in biofilm formation ability over time in both isolates. We also found that ST48 strains were typically robust biofilm formers, which could explain why this ST increased in prevalence. Finally, we identified mutations in the DNA mismatch repair genes mutS and mutL in separate ST55 and ST4 strains and confirmed that strains bearing these mutations displayed a hypermutator phenotype. The presence of a hypermutator phenotype may complicate future antimicrobial treatment for clinically relevant E. faecalis infections in macaques.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant T32-OD010978)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant P30-ES002109)en_US
dc.language.isoen
dc.publisherAmerican Society for Microbiologyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1128/aem.01336-18en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceProf. Fox via Howard Silveren_US
dc.titleLong-Term Colonization Dynamics ofEnterococcus faecalisin Implanted Devices in Research Macaquesen_US
dc.typeArticleen_US
dc.identifier.citationLieberman, Mia T. et al. "Long-Term Colonization Dynamics of Enterococcus faecalis in Implanted Devices in Research Macaques." Applied and Environmental Microbiology 84, 18 (July 2018): e01336-18 © 2018 American Society for Microbiologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalApplied and Environmental Microbiologyen_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
dc.date.updated2019-10-17T13:19:09Z
dspace.date.submission2019-10-17T13:19:14Z
mit.journal.volume84en_US
mit.journal.issue18en_US


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