Cited 17 time in
Prevalence and Microbiological Characteristics of qacA/B-Positive Methicillin-Resistant Staphylococcus aureus Isolates in a Surgical Intensive Care Unit
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Cho, Oh-Hyun | - |
| dc.contributor.author | Park, Ki-Ho | - |
| dc.contributor.author | Song, Ji Young | - |
| dc.contributor.author | Hong, Jeong Min | - |
| dc.contributor.author | Kim, Taeeun | - |
| dc.contributor.author | Hong, Sun In | - |
| dc.contributor.author | Kim, Sunjoo | - |
| dc.contributor.author | Bae, In-Gyu | - |
| dc.date.accessioned | 2022-12-26T17:03:41Z | - |
| dc.date.available | 2022-12-26T17:03:41Z | - |
| dc.date.issued | 2018-04 | - |
| dc.identifier.issn | 1076-6294 | - |
| dc.identifier.issn | 1931-8448 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/11743 | - |
| dc.description.abstract | The increasing use of chlorhexidine for methicillin-resistant Staphylococcus aureus (MRSA) decolonization has raised concerns about the emergence of resistance to or tolerance of this antiseptic. We examined the frequency and characteristics of qacA/B chlorhexidine tolerance genes among MRSA isolates in a surgical intensive care unit (ICU) where MRSA-colonized patients are decolonized by chlorhexidine bathing. The MRSA isolates were evaluated for chlorhexidine susceptibility, mupirocin resistance, molecular typing, agr functionality, and the heterogeneous vancomycin-intermediate S. aureus (hVISA) phenotype according to the presence of the qacA/B genes. Overall, 119 MRSA isolates were obtained from active surveillance cultures (93, 78.2%) and clinical cultures (26, 21.8%) between 2012 and 2014. Among these isolates, 39 (32.8%) carried the qacA/B genes, and 23 (19.3%) exhibited mupirocin resistance. Most qacA/B-positive isolates (36/39, 92.3%) were identified as ST5-SCCmecII (69.2%) and ST239-SCCmecIII (23.1%), which are common healthcare-associated (HA)-MRSA strains in Korea. Multivariate analysis found that qacA/B-positive MRSA isolates were associated with agr dysfunction (OR, 4.87; 95% CI, 1.71-13.87) and the hVISA phenotype (OR, 4.09; 95% CI, 1.48-11.34). In conclusion, our study showed that qacA/B carriage was common among MRSA isolates in an ICU where chlorhexidine is commonly used for decolonization. qacA/B carriage was significantly associated with agr dysfunction and the hVISA phenotype. These features may confer a selective advantage on HA-MRSA strains, including ST5-SCCmecII and ST239-SCCmecIII, in the ICU setting. | - |
| dc.format.extent | 7 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | MARY ANN LIEBERT, INC | - |
| dc.title | Prevalence and Microbiological Characteristics of qacA/B-Positive Methicillin-Resistant Staphylococcus aureus Isolates in a Surgical Intensive Care Unit | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1089/mdr.2017.0072 | - |
| dc.identifier.scopusid | 2-s2.0-85045472801 | - |
| dc.identifier.wosid | 000430016900008 | - |
| dc.identifier.bibliographicCitation | MICROBIAL DRUG RESISTANCE, v.24, no.3, pp 283 - 289 | - |
| dc.citation.title | MICROBIAL DRUG RESISTANCE | - |
| dc.citation.volume | 24 | - |
| dc.citation.number | 3 | - |
| dc.citation.startPage | 283 | - |
| dc.citation.endPage | 289 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Infectious Diseases | - |
| dc.relation.journalResearchArea | Microbiology | - |
| dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
| dc.relation.journalWebOfScienceCategory | Infectious Diseases | - |
| dc.relation.journalWebOfScienceCategory | Microbiology | - |
| dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
| dc.subject.keywordPlus | CHLORHEXIDINE SUSCEPTIBILITY | - |
| dc.subject.keywordPlus | ANTISEPTIC-RESISTANCE | - |
| dc.subject.keywordPlus | AGR DYSFUNCTION | - |
| dc.subject.keywordPlus | MUPIROCIN | - |
| dc.subject.keywordPlus | TRANSMISSION | - |
| dc.subject.keywordPlus | ACQUISITION | - |
| dc.subject.keywordPlus | INFECTION | - |
| dc.subject.keywordPlus | COMMUNITY | - |
| dc.subject.keywordPlus | GENES | - |
| dc.subject.keywordPlus | COLONIZATION | - |
| dc.subject.keywordAuthor | Staphylococcus aureus | - |
| dc.subject.keywordAuthor | chlorhexidine | - |
| dc.subject.keywordAuthor | microbial drug resistance | - |
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