{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,21]],"date-time":"2026-04-21T04:17:32Z","timestamp":1776745052924,"version":"3.51.2"},"reference-count":36,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2011,2,15]],"date-time":"2011-02-15T00:00:00Z","timestamp":1297728000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Zoonoses and Public Health"],"published-print":{"date-parts":[[2011,11]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p><jats:italic>Staphylococcus aureus<\/jats:italic> is one of the most common causes of infection in people and is increasingly recognized in dogs. The increasing prevalence of methicillin resistant <jats:italic>S.\u2003aureus<\/jats:italic> (MRSA) is complicating the treatment of these infections. Panton Valentine leukocidin (PVL), a toxin involved in the pathogenesis of necrotic syndromes in people may be partially responsible for the rise of MRSA. Canine and human <jats:italic>S.\u2003aureus<\/jats:italic> from the same geographic area are genetically similar, indicating a common population and likely transmission. The implications of increasing antimicrobial resistance complicated by interspecies transmission, necessitates including both dogs and humans in <jats:italic>S.\u2003aureus<\/jats:italic> resistance surveillance studies. A collection of 126 <jats:italic>S.\u2003aureus<\/jats:italic> isolates from people (<jats:italic>n\u2003<\/jats:italic>=\u200399) and dogs (<jats:italic>n\u2003<\/jats:italic>=\u200327) were included, minimum inhibitor concentrations to a panel of 33 antimicrobials used in human and veterinary medicine were determined. No resistance to vancomycin, linezolid, daptomycin, quinupristin\/dalfopristin or nitrofurantoin was found. A wide range of antibiograms were found; including resistance to 0\u201312 drugs (0\u20136 drug classes). Outstanding antibiograms included a canine MRSA resistant to rifampin and a human MRSA resistant to chloramphenicol. Inducible clindamycin resistance was found among 78% and 4% of canine and human MRSA and 17% and 25% of canine colonizing and human methicillin susceptible <jats:italic>S.\u2003aureus<\/jats:italic> (MSSA), respectively. Resistance to mupirocin was only found among human isolates including 20% of MRSA and 4% of MSSA. While no canine isolates were PVL positive, 39% of human MRSA and 2% of MSSA carried the gene. The bidirectional transmission of <jats:italic>S.\u2003aureus<\/jats:italic> between people and dogs necessitates the inclusion of isolates from both species in future studies.<\/jats:p>","DOI":"10.1111\/j.1863-2378.2011.01392.x","type":"journal-article","created":{"date-parts":[[2011,2,15]],"date-time":"2011-02-15T11:58:08Z","timestamp":1297771088000},"page":"454-462","source":"Crossref","is-referenced-by-count":16,"title":["Antimicrobial Susceptibility of Canine and Human <i>Staphylococcus aureus<\/i> Collected in Saskatoon, Canada"],"prefix":"10.1111","volume":"58","author":[{"given":"J. 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