Comparison of phenotypic methods with mecA gene based polymerase chain reaction for Methicillin-resistant Staphylococcus aureus detection

金黄色葡萄球菌 聚合酶链反应 耐甲氧西林金黄色葡萄球菌 SCCmec公司 微生物学 表型 基因 生物 遗传学 细菌
作者
Aneela Khawaja,Faiqa Arshad,Idrees Khan
出处
期刊:Journal of Pakistan Medical Association [Pakistan Medical Association]
卷期号:70 (2): 276-280
标识
DOI:10.47391/jpma.20/290732
摘要

Objective: To determine methicillin resistance in staphylococcus aureus by different phenotypic methods, and toevaluate their accuracy with mecA gene polymerase chain reaction for methicillin-resistant staphylococcus aureusdetection. Methods: The descriptive cross-sectional study was conducted from January to December 2015 at the Post-Graduate Medical Institute, Lahore, Pakistan, and comprised consecutive, non-repetitive clinical isolates ofmethicillin-resistant staphylococcus aureus that were screened with oxacillin disk 1ug and cefoxitin disk 30ug byKirby-Bauer method using Clinical and Laboratory Standards Institute guideline. The isolates were cultured onoxacillin screen and mannitol salt agar, and subjected to latex agglutination for penicillin-binding protein 2aandpolymerase chain reaction for mecA gene. Data was analysed using SPSS 20. Results: All the 105 isolates were resistant on oxacillin and cefoxitin disk diffusion test, but 95(90.47%) were positivefor mecA gene by latex agglutination and polymerase chain reaction. The sensitivity of oxacillin salt agar, mannitolsalt agar and latex agglutination was 94.31%, 96.73% and 98.95%, respectively. Keeping polymerase chain reactionas the gold standard, the specificity and diagnostic accuracy of latex agglutination were 77.77% and 97.14%respectively, which was the highest among all the phenotypic methods. Conclusion: Latex agglutination method can be proposed as a swiftly reliable diagnostic technique for thedetection of mecA gene in methicillin-resistant staphylococcus aureus isolates in resource-constrained settingswhere molecular methods are limited. Keywords: Methicillin resistant staphylococcus aureus, Oxacillin, Cefoxitin, Latex agglutination, PCR.
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