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.
J Infect Chemother. 2021 Feb;27(2):211-217. doi: 10.1016/j.jiac.2020.09.014. Epub 2020 Sep 29.
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).
A total of 225 mucoid-type isolates were collected. The serotype, antimicrobial susceptibility, and multilocus sequence type of these isolates were determined.
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).
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.
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。
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。
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。
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。