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日本侵袭性肺炎球菌病患者分离的粘液型肺炎链球菌的分子流行病学特征。

Molecular epidemiological characterization in mucoid-type Streptococcus pneumoniae isolates obtained from invasive pneumococcal disease patients in Japan.

机构信息

Department of Infectious Diseases, Keio University School of Medicine, Tokyo, Japan.

Department of Microbiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.

出版信息

J Infect Chemother. 2021 Feb;27(2):211-217. doi: 10.1016/j.jiac.2020.09.014. Epub 2020 Sep 29.

Abstract

INTRODUCTION

Streptococcus pneumoniae with a mucoid-type capsule is associated with invasive pneumococcal diseases (IPDs). Despite the introduction of pneumococcal vaccines, IPDs caused by mucoid-type isolates are still prevalent. The present study aimed to characterize mucoid-type S. pneumoniae isolated from IPD patients throughout Japan in 2017 (post-vaccination era).

METHODS

A total of 225 mucoid-type isolates were collected. The serotype, antimicrobial susceptibility, and multilocus sequence type of these isolates were determined.

RESULTS

The prevalence of IPDs caused by mucoid-type isolates was high in adults, especially in the elderly (≥65 years of age), and prognosis in these patients was significantly poor. Of the mucoid-type isolates, the predominant serotype was serotype 3 (84.4%), and the remaining were serotypes 37 (15.1%) and 8 (0.4%). Antimicrobial susceptibility showed that most mucoid isolates exhibited the penicillin-intermediate resistant S. pneumoniae genotype (gPISP). However, the serotype 3 isolate exhibited the penicillin-resistant S. pneumoniae genotype (gPRSP). This gPRSP isolate was classified into ST166, which is related to serotypes 9 V and 11 strains. Sequence analysis of the capsule-coding regions and its flanking regions indicated that recombination occurred upstream and downstream of the capsule-coding region, suggesting that gPRSP (serotype 9 V/ST166) obtaining the type-3 capsule gene cluster resulted in the emergence of gPRSP (serotype 3/ST166).

CONCLUSIONS

Our findings indicated that IPDs caused by mucoid-type S. pneumoniae are still a serious concern and mucoid-type S. pneumoniae with novel phenotype could emerge via capsular switching in response to environmental changes such as introduction of vaccines and improper use of antimicrobial agents.

摘要

简介

具有黏液型荚膜的肺炎链球菌与侵袭性肺炎球菌病(IPD)有关。尽管已经引入了肺炎球菌疫苗,但由黏液型分离株引起的 IPD 仍然很普遍。本研究旨在描述 2017 年日本(疫苗接种后时代)发生的 IPD 患者中分离的黏液型 S. pneumoniae 的特征。

方法

共收集了 225 株黏液型分离株。确定了这些分离株的血清型、抗菌药物敏感性和多位点序列型。

结果

黏液型分离株引起的 IPD 在成年人中,尤其是老年人(≥65 岁)中发病率较高,且这些患者的预后明显较差。在黏液型分离株中,主要血清型为 3 型(84.4%),其余为 37 型(15.1%)和 8 型(0.4%)。抗菌药物敏感性显示,大多数黏液型分离株表现出青霉素中介耐药的肺炎链球菌基因型(gPISP)。然而,3 型分离株表现出青霉素耐药的肺炎链球菌基因型(gPRSP)。该 gPRSP 分离株被分类为 ST166,与 9V 和 11 型菌株有关。对荚膜编码区及其侧翼区的序列分析表明,荚膜编码区上下游发生了重组,提示 gPRSP(9V/ST166 型)获得了 3 型荚膜基因簇,导致 gPRSP(3/ST166 型)的出现。

结论

我们的研究结果表明,由黏液型 S. pneumoniae 引起的 IPD 仍然是一个严重的问题,并且由于疫苗的引入和抗菌药物的不当使用等环境变化,可能会通过荚膜转换出现新表型的黏液型 S. pneumoniae。

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