Institute for Medical Microbiology and Hygiene, Technical University of Dresden, Dresden, Germany.
Antimicrob Agents Chemother. 2012 Nov;56(11):5547-54. doi: 10.1128/AAC.00574-12. Epub 2012 Aug 13.
To screen isolates and to identify mecA alleles, published mecA sequences were analyzed, and a microarray for the rapid discrimination of mecA alleles was designed. A GenBank analysis yielded 135 full-length gene sequences annotated as mecA. These sequences clustered into 32 different alleles corresponding to 28 unique amino acid sequences and to 15 distinct hybridization patterns on this microarray. A collection of 78 clinical and veterinary isolates of Staphylococcus spp. was characterized using this assay. Nine of the 15 expected patterns, as well as one as-yet-unknown pattern, were identified. These patterns were detected in various epidemic methicillin-resistant Staphylococcus aureus strains, in S. pseudintermedius, and in coagulase-negative species such as S. epidermidis, S. fleurettii, or S. haemolyticus. There was no correlation between the different mecA hybridization patterns and the SCCmec type. Determination of MICs showed that mecA alleles corresponding to only four of these nine patterns were associated with β-lactam resistance. The mecA alleles that did not confer β-lactam resistance were largely restricted to coagulase-negative staphylococci of animal origin, such as S. sciuri and S. vitulinus. Because of the diversity of sequences and the different impact on β-lactam susceptibility, the existence of different mecA alleles needs to be taken into account when designing diagnostic assays for the detection of mecA.
为了筛选分离株并鉴定 mecA 等位基因,我们分析了已发表的 mecA 序列,并设计了一种用于快速区分 mecA 等位基因的微阵列。GenBank 分析产生了 135 条全长基因序列,注释为 mecA。这些序列聚类为 32 个不同的等位基因,对应于 28 个独特的氨基酸序列和该微阵列上的 15 个不同的杂交模式。使用该检测方法对 78 株临床和兽医分离的葡萄球菌进行了特征分析。鉴定出了 15 个预期模式中的 9 个,以及一个未知模式。这些模式在各种流行的耐甲氧西林金黄色葡萄球菌菌株、中间葡萄球菌以及凝固酶阴性的葡萄球菌物种中被检测到,如表皮葡萄球菌、藤黄微球菌或溶血葡萄球菌。不同的 mecA 杂交模式与 SCCmec 类型之间没有相关性。MIC 的测定表明,与这 9 个模式中的 4 个相对应的 mecA 等位基因与β-内酰胺耐药相关。而不赋予β-内酰胺耐药性的 mecA 等位基因主要局限于动物来源的凝固酶阴性葡萄球菌,如松鼠葡萄球菌和牛葡萄球菌。由于序列的多样性以及对β-内酰胺敏感性的不同影响,在设计用于检测 mecA 的诊断检测时,需要考虑不同的 mecA 等位基因的存在。