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首页> 外文期刊>Journal of Clinical Microbiology >Branched-DNA Assay for Detection of themecA Gene in Oxacillin-Resistant and Oxacillin-Sensitive Staphylococci
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Branched-DNA Assay for Detection of themecA Gene in Oxacillin-Resistant and Oxacillin-Sensitive Staphylococci

机译:分枝DNA检测法检测耐奥沙西林和奥沙西林敏感的葡萄球菌中的themecA基因

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The identification of methicillin-resistant staphylococcus isolates in the clinical laboratory has typically been performed by using methods that detect phenotypic expression of resistance determinants. However, these methods may be difficult to interpret and some isolates do not express resistance until selective pressure is administered. Assays that detect genetic determinants are not subject to these limitations and have been effective in distinguishing isolates that are capable of expressing the resistance phenotype. In this study, a novel branched-DNA (bDNA) hybridization assay was used to test for themecA gene in 416 clinical staphylococcal isolates. The results were compared with those obtained by a PCR-based assay and oxacillin disk diffusion. For 155 Staphylococcus aureus and 261 coagulase-negative Staphylococcus isolates, the bDNA assay and PCR results were 100% concordant. Among the S. aureus isolates, 20 were MecA+ and 135 were MecA?. For the coagulase-negative staphylococci, 150 were MecA+ and 111 were MecA?. The results from the genotypic detection methods were compared with those obtained by oxacillin disk diffusion. No discrepancies were detected among theS. aureus isolates; however, 10 coagulase-negative isolates were MecA+ but oxacillin sensitive and 1 isolate was MecA? but oxacillin resistant. Oxacillin resistance was induced in 6 of the 10 MecA+ isolates previously classified as oxacillin sensitive. These results suggest that the bDNA method described here is a sensitive and efficient method for detection of methicillin resistance in staphylococci and that genetic detection methods may be useful for detection of potential methicillin resistance in the clinical laboratory.
机译:在临床实验室中,耐甲氧西林葡萄球菌分离株的鉴定通常是通过使用检测抗性决定簇表型表达的方法进行的。但是,这些方法可能难以解释,并且某些分离株在施加选择压力之前不会表达抗性。检测遗传决定因素的测定法不受这些限制,并且在区分能够表达抗性表型的分离株方面已经很有效。在这项研究中,一种新颖的分支DNA(bDNA)杂交测定法用于测试416种临床葡萄球菌分离物中的 mecA 基因。将结果与通过基于PCR的分析和奥沙西林纸片扩散获得的结果进行比较。对于155株金黄色葡萄球菌和261株凝固酶阴性 Staphylococcus 分离株,bDNA测定和PCR结果一致。在 S中。金黄色葡萄球菌分离株,其中20个是MecA + ,另外135个是MecA ?。对于凝固酶阴性葡萄球菌,MecA + 为150,MecA ?为111。将基因型检测方法的结果与通过奥沙西林纸片扩散获得的结果进行比较。在 S之间未检测到差异。金黄色葡萄球菌然而,有10株凝固酶阴性的菌株对MecA + 敏感,但对奥沙西林敏感,有1株对MecA ?具有耐药性,但对奥沙西林耐药。在先前归类为对奥沙西林敏感的10个MecA + 菌株中,有6个对奥沙西林产生了抗药性。这些结果表明,此处描述的bDNA方法是检测葡萄球菌中甲氧西林耐药性的灵敏有效方法,并且遗传检测方法对于临床实验室中潜在的甲氧西林耐药性检测可能有用。

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