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首页> 外文期刊>Journal of Clinical Microbiology >Utility of Sequencing the erm(41) Gene in Isolates of Mycobacterium abscessus subsp. abscessus with Low and Intermediate Clarithromycin MICs
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Utility of Sequencing the erm(41) Gene in Isolates of Mycobacterium abscessus subsp. abscessus with Low and Intermediate Clarithromycin MICs

机译:脓肿分枝杆菌亚种分离物中erm(41)基因测序的效用。低和中级克拉霉素霉素脓肿

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The erm(41) gene confers inducible macrolide resistance in Mycobacterium abscessus subsp. abscessus, calling into question the usefulness of macrolides for treating M. abscessus subsp. abscessus infections. With an extended incubation (14 days), isolates with MICs of ≥8 μg/ml are considered macrolide resistant by current CLSI guidelines. Our goals were to determine the incidence of macrolide susceptibility in U.S. isolates, the validity of currently accepted MIC breakpoints, and the erm(41) sequences associated with susceptibility. Of 349 isolates (excluding those with 23S rRNA gene mutations), 85 (24%) had clarithromycin MICs of ≤8 μg/ml. Sequencing of the erm(41) genes from these isolates, as well as from isolates with MICs of ≥16 μg/ml, including ATCC 19977T, revealed 10 sequevars. The sequence in ATCC 19977T was designated sequevar (type) 1; most macrolide-resistant isolates were of this type. Seven sequevars contained isolates with MICs of >16 μg/ml. The T28C substitution in erm(41), previously associated with macrolide susceptibility, was identified in 62 isolates (18%) comprising three sequevars, with MICs of ≤2 (80%), 4 (10%), and 8 (10%) μg/ml. No other nucleotide substitution was associated with macrolide susceptibility. We recommend that clarithromycin susceptibility breakpoints for M. abscessus subsp. abscessus be changed from ≤2 to ≤4 μg/ml and that isolates with an MIC of 8 μg/ml have repeat MIC testing or erm sequencing performed. Our studies suggest that macrolides are useful for treating approximately 20% of U.S. isolates of M. abscessus subsp. abscessus. Sequencing of the erm gene of M. abscessus subsp. abscessus will predict inducible macrolide susceptibility.
机译: erm (41)基因在脓肿分枝杆菌亚种中赋予可诱导的大环内酯类抗药性。脓肿,质疑大环内酯类药物在治疗脓肿分支杆菌亚种中的作用。脓肿感染。延长孵育时间(14天)后,当前的CLSI指南认为MIC≥8μg/ ml的分离株具有大环内酯抗性。我们的目标是确定美国分离株中大环内酯类药物的敏感性,当前公认的MIC断点的有效性以及与敏感性相关的 erm (41)序列。在349个分离株(不包括具有23S rRNA基因突变的分离株)中,有85个(24%)的克拉霉素MIC≤8μg/ ml。从这些分离株以及MIC≥16μg/ ml的分离株(包括ATCC 19977 T )对 erm (41)基因的测序揭示了10个序列。 ATCC 19977 T 中的序列命名为sequevar(type)1;大多数耐大环内酯的分离株都是这种类型。七个分离液包含的MIC≥16μg/ ml的分离株。在以前与大环内酯易感性相关的 erm (41)中的T28C取代在62个分离株(占18%)中鉴定出,包括三个序列,MIC≤2(80%),4(10%) ,以及8(10%)μg/ ml。没有其他核苷酸取代与大环内酯易感性相关。我们建议脓肿分支杆菌亚种的克拉霉素敏感性转折点。将脓肿从≤2μg/ ml更改为≤4μg/ ml,MIC为8μg/ ml的分离株需进行重复MIC测试或 erm 测序。我们的研究表明大环内酯类药物可用于治疗约20%的脓肿分支杆菌亚种美国分离株。脓肿。脓肿亚种 erm 基因的测序脓肿将预测诱导型大环内酯药的敏感性。

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