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日本 15A 型多药耐药肺炎链球菌的全基因组测序分析及高度耐药 15A-ST9084 克隆的出现。

Whole-Genome Sequencing Analysis of Multidrug-Resistant Serotype 15A Streptococcus pneumoniae in Japan and the Emergence of a Highly Resistant Serotype 15A-ST9084 Clone.

机构信息

Kyoto University Graduate School of Medicine, Kyoto, Japan

National Hospital Organization Mie National Hospital, Tsu, Japan.

出版信息

Antimicrob Agents Chemother. 2019 Apr 25;63(5). doi: 10.1128/AAC.02579-18. Print 2019 May.

DOI:10.1128/AAC.02579-18
PMID:30803976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6496056/
Abstract

Since the introduction of pneumococcal conjugate vaccines (PCVs), an increase in the incidence of disease attributable to serotype 15A-ST63 (sequence type 63) pneumococci has been observed in many regions worldwide. We conducted a nationwide pediatric pneumococcal infection surveillance study between 2012 and 2014 in Japan. In the surveillance study, we detected multidrug-resistant serotype 15A-CC63 (clonal complex 63) strains (resistant to macrolides, penicillin, cefotaxime, and meropenem); in this study, we analyzed these resistant isolates to determine the dynamics and mechanism of resistance using whole-genome sequencing. In most of the penicillin-, cefotaxime-, and meropenem-resistant strains, recombination occurred in the region, resulting in the acquisition of cefotaxime resistance in addition to penicillin and meropenem resistance. In the multidrug-resistant serotype 15A-CC63 strains, we identified a specific clone with ST9084, and all of the isolates were recovered from the Yamaguchi prefecture in Japan. All of the serotype 15A-ST9084 isolates had a novel type (-JP3) that was inserted by recombination events. The conserved amino acid motif profiles of , , and of the strains were identical to those of serotype 19A-ST320. A Bayesian analysis-based date estimation suggested that this clone emerged in approximately 2002 before the introduction of the PCV in Japan. This clone should be monitored because serotype 15A is not contained in the currently used 13-valent PCV (PCV13), and it was resistant to beta-lactams, which are often used in a clinical setting.

摘要

自从肺炎球菌结合疫苗(PCV)问世以来,在世界许多地区都观察到了血清型 15A-ST63(序列型 63)肺炎球菌引起的疾病发病率增加。我们在 2012 年至 2014 年期间在日本进行了一项全国性儿科肺炎球菌感染监测研究。在监测研究中,我们检测到了耐多药血清型 15A-CC63(克隆群 63)菌株(对大环内酯类、青霉素、头孢噻肟和美罗培南耐药);在本研究中,我们分析了这些耐药分离株,使用全基因组测序来确定耐药性的动态和机制。在大多数青霉素、头孢噻肟和美罗培南耐药株中, 区发生了重组,导致除了青霉素和美罗培南耐药外,还获得了头孢噻肟耐药性。在多药耐药血清型 15A-CC63 菌株中,我们鉴定出了一个具有 ST9084 的特定克隆,所有分离株均来自日本山口县。所有血清型 15A-ST9084 分离株都有一个新的 类型(-JP3),是通过重组事件插入的。这些菌株的 、 和 的保守氨基酸基序图谱与血清型 19A-ST320 的图谱相同。基于贝叶斯分析的日期估计表明,该克隆大约在 2002 年日本引入 PCV 之前出现。由于血清型 15A 不包含在目前使用的 13 价 PCV(PCV13)中,并且对临床常用的β-内酰胺类药物耐药,因此应监测该克隆。

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