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基于青霉素结合蛋白氨基酸替代的B族链球菌β-内酰胺敏感性降低菌株(GBS-RBS)分类

Classification of group B streptococci with reduced β-lactam susceptibility (GBS-RBS) based on the amino acid substitutions in PBPs.

作者信息

Kimura Kouji, Nagano Noriyuki, Arakawa Yoshichika

机构信息

Department of Bacteriology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan

Department of Health and Medical Sciences, Shinshu University Graduate School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan.

出版信息

J Antimicrob Chemother. 2015;70(6):1601-3. doi: 10.1093/jac/dkv022. Epub 2015 Feb 8.

Abstract

All clinical isolates of group B Streptococcus (GBS; Streptococcus agalactiae) are considered uniformly susceptible to β-lactams, including penicillins. However, GBS with reduced penicillin susceptibility (PRGBS) were first identified by our group in Japan and have also been reported from North America. PRGBS are non-susceptible to penicillin because of acquisition of amino acid substitutions near the conserved active-site motifs in PBP2X. In particular, V405A and Q557E are considered the key amino acid substitutions responsible for penicillin non-susceptibility. We revealed that in addition to the substitutions in PBP2X, an amino acid substitution in PBP1A confers high-level cephalosporin resistance in GBS. As the number of publications on GBS with reduced β-lactam susceptibility (GBS-RBS), especially PRGBS, and concomitantly the need for a systematic classification of GBS-RBS is increasing, we propose here a classification of GBS-RBS based on the amino acid substitutions in their PBPs.

摘要

所有B族链球菌(GBS;无乳链球菌)临床分离株均被认为对包括青霉素在内的β-内酰胺类药物普遍敏感。然而,我们团队在日本首次鉴定出对青霉素敏感性降低的GBS(PRGBS),北美也有相关报道。PRGBS对青霉素不敏感是因为在PBP2X保守活性位点基序附近发生了氨基酸替换。特别是,V405A和Q557E被认为是导致青霉素不敏感的关键氨基酸替换。我们发现,除了PBP2X中的替换外,PBP1A中的一个氨基酸替换赋予GBS高水平头孢菌素耐药性。随着关于β-内酰胺敏感性降低的GBS(GBS-RBS),尤其是PRGBS的出版物数量增加,同时对GBS-RBS进行系统分类的需求也在增加,我们在此基于其PBPs中的氨基酸替换提出一种GBS-RBS分类方法。

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