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dc.contributor.authorProulx, Megan K.
dc.contributor.authorPalace, Samantha G.
dc.contributor.authorGandra, Sumanth
dc.contributor.authorTorres, Brenda
dc.contributor.authorWeir, Susan
dc.contributor.authorStiles, Tracy
dc.contributor.authorEllison, Richard T. III
dc.contributor.authorGoguen, Jon D.
dc.date2022-08-11T08:09:09.000
dc.date.accessioned2022-08-23T16:19:13Z
dc.date.available2022-08-23T16:19:13Z
dc.date.issued2015-10-26
dc.date.submitted2015-12-07
dc.identifier.citationJ Infect Dis. 2015 Oct 26. pii: jiv512. <a href="http://dx.doi.org/10.1093/infdis/jiv512">Link to article on publisher's site</a>
dc.identifier.issn0022-1899 (Linking)
dc.identifier.doi10.1093/infdis/jiv512
dc.identifier.pmid26503983
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34994
dc.description.abstractApproximately 3% of Staphylococcus aureus strains that, according to results of conventional phenotypic methods, are highly susceptible to methicillin-like antibiotics also have polymerase chain reaction (PCR) results positive for mecA. The genetic nature of these mecA-positive methicillin-susceptible S. aureus (MSSA) strains has not been investigated. We report the first clearly defined case of reversion from methicillin susceptibility to methicillin resistance among mecA-positive MSSA within a patient during antibiotic therapy. We describe the mechanism of reversion for this strain and for a second clinical isolate that reverts at a similar frequency. The rates of reversion are of the same order of magnitude as spontaneous resistance to drugs like rifampicin. When mecA is detected by PCR in the clinical laboratory, current guidelines recommend that these strains be reported as resistant. Because combination therapy using both a beta-lactam and a second antibiotic suppressing the small revertant population may be superior to alternatives such as vancomycin, the benefits of distinguishing between mecA-positive MSSA and MRSA in clinical reports should be evaluated.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26503983&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1093/infdis/jiv512
dc.subjectImmunology of Infectious Disease
dc.subjectInfectious Disease
dc.titleReversion From Methicillin Susceptibility to Methicillin Resistance in Staphylococcus aureus During Treatment of Bacteremia
dc.typeJournal Article
dc.source.journaltitleThe Journal of infectious diseases
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/infdis_pp/213
dc.identifier.contextkey7910528
html.description.abstract<p>Approximately 3% of Staphylococcus aureus strains that, according to results of conventional phenotypic methods, are highly susceptible to methicillin-like antibiotics also have polymerase chain reaction (PCR) results positive for mecA. The genetic nature of these mecA-positive methicillin-susceptible S. aureus (MSSA) strains has not been investigated. We report the first clearly defined case of reversion from methicillin susceptibility to methicillin resistance among mecA-positive MSSA within a patient during antibiotic therapy. We describe the mechanism of reversion for this strain and for a second clinical isolate that reverts at a similar frequency. The rates of reversion are of the same order of magnitude as spontaneous resistance to drugs like rifampicin. When mecA is detected by PCR in the clinical laboratory, current guidelines recommend that these strains be reported as resistant. Because combination therapy using both a beta-lactam and a second antibiotic suppressing the small revertant population may be superior to alternatives such as vancomycin, the benefits of distinguishing between mecA-positive MSSA and MRSA in clinical reports should be evaluated.</p>
dc.identifier.submissionpathinfdis_pp/213
dc.contributor.departmentClinical Microbiology Laboratory
dc.contributor.departmentDepartment of Microbiology and Physiological Systems
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology


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