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首页> 外文期刊>Journal of infection and public health. >Evaluation of different methods to detect methicillin resistance in Staphylococcus aureus (MRSA)
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Evaluation of different methods to detect methicillin resistance in Staphylococcus aureus (MRSA)

机译:评价不同方法检测金黄色葡萄球菌(MRSA)中的甲氧西林耐药性

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摘要

The studies suggest that dogs living with human are potential risk of becoming MRSA carrier and increased risk of infections caused by MRSA. Phenotypic methods to detect methicillin resistance in Staphylococcus aureus (MRSA) are inadequate. The objective of the present study was to determine methicillin resistance in S. aureus by phenotypic susceptibility test (oxacillin disk diffusion, cefoxitin disk diffusion, oxacillin screen agar) and molecular methods (PCR as a gold standard) and the latex agglutination test for the detection of PBP2a and to evaluate the results of these tests for its sensitivity and specificity. A total of 100 swab samples were taken from muzzle site, in more contact with human, of dogs and MRSA were isolated. Oxacillin (1. μg), cefoxitin (30. μg) disk diffusion and oxacillin screen agar method were used. The isolates were also subjected to latex agglutination test for detection of PBP2a and PCR to detect mecA gene. By PCR 37% of isolates show the presence of mecA. Latex agglutination was found to be the most sensitive (97.29%) and cefoxitin disk diffusion to be the most specific (96.82%) tests for detection of MRSA. Our finding showed that combining oxacillin screen agar or cefoxitin disk diffusion with latex agglutination improves sensitivity and specificity to detect methicillin resistance S. aureus (MRSA) isolates.
机译:研究表明,与人同住的狗有成为MRSA携带者的潜在风险,并增加了由MRSA引起的感染的风险。在金黄色葡萄球菌(MRSA)中检测甲氧西林抗药性的表型方法不足。本研究的目的是通过表型药敏试验(奥沙西林盘扩散,头孢西丁盘扩散,奥沙西林筛选琼脂)和分子方法(以PCR为金标准)和乳胶凝集试验确定金黄色葡萄球菌对甲氧西林的耐药性评估PBP2a的敏感性和特异性。从与人更多接触的枪口部位采集了总共100只拭子样品,并分离了MRSA。使用奥沙西林(1.μg),头孢西丁(30.μg)纸片扩散法和奥沙西林筛选琼脂法。还对分离物进行乳胶凝集试验以检测PBP2a,并进行PCR以检测mecA基因。通过PCR 37%的分离物显示出mecA的存在。发现乳胶凝集是检测MRSA的最灵敏方法(97.29%),头孢西丁盘扩散法是最特异性的检测方法(96.82%)。我们的发现表明,将奥沙西林筛选琼脂或头孢西丁盘扩散与乳胶凝集相结合,可提高检测耐甲氧西林金黄色葡萄球菌(MRSA)菌株的敏感性和特异性。

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