Genetic characteristics of invasive pneumococcal disease-derived Streptococcus pneumoniae of serogroup 24 isolated in Tokyo, Japan.

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES Journal of Infection and Chemotherapy Pub Date : 2024-07-31 DOI:10.1016/j.jiac.2024.07.024
Yumi Uchitani, Rumi Okuno, Tsukasa Ariyoshi, Hiroaki Kubota, Jun Suzuki, Kenji Sadamasu
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Abstract

Background: Since the introduction of the national routine vaccination program against Streptococcus pneumoniae in Japan from the early 2010s, the incidence of invasive pneumococcal disease (IPD) caused by non-vaccine serotypes has increased. This study focused on non-vaccine serogroup 24 strains derived from IPD and aimed to clarify their genetic characteristics.

Methods: Between 2013 and 2022, 121 strains identified as serogroup 24 in patients with IPD were collected and applied to multilocus sequence typing and next-generation sequencing. Whole-genome data were used to delineate phylogenetic relationships and to identify virulence and antimicrobial resistance-associated genes.

Results: Recent trends in sequence types (STs) were characterized by an increase in the proportion of ST162 and ST2754 for 24F and 24B, respectively, after 2018. Whole-genome phylogenetic analysis demonstrated that serogroup 24 strains were organized into three clades, closely related to STs but not with serotypes. All ST162 strains were classified as Global Pneumococcal Sequence Cluster (GPSC) 6 and harbored the virulence-associated rlrA islet, with co-trimoxazole-resistance mutations in folA and folP genes. Two ST162 strains with different serotypes 24F and 24B from the same patient were phylogenetically indistinguishable, showing that these strains were derived by serotype conversion during infection.

Conclusion: The recent changes in predominant STs were similar to those previously reported throughout Japan, except Tokyo. Little correlation between whole-genome phylogeny and serotypes and the observed serotype conversion in one patient indicate potentially variable immunogenicity of this serogroup.

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在日本东京分离到的侵袭性肺炎链球菌疾病衍生的血清 24 型肺炎链球菌的遗传特征。
背景:自 2010 年代初日本开始实施肺炎链球菌常规疫苗接种计划以来,由非疫苗血清型引起的侵袭性肺炎球菌疾病(IPD)的发病率有所上升。本研究重点关注由 IPD 衍生的非疫苗血清 24 型菌株,旨在阐明其遗传特征:方法:2013 年至 2022 年间,收集了 121 株在 IPD 患者中被鉴定为血清 24 型的菌株,并对其进行了多焦点序列分型和新一代测序。全基因组数据用于划分系统发育关系,并确定毒力和抗菌药耐药性相关基因:序列类型(ST)的最新趋势表现为:2018 年后,24F 和 24B 的 ST162 和 ST2754 比例分别增加。全基因组系统发育分析表明,血清 24 群菌株分为三个支系,与 ST 密切相关,但与血清型无关。所有ST162菌株都被归入全球肺炎球菌序列群(GPSC)6,并携带与毒力相关的rlrA小体,folA和folP基因发生了共抗三唑突变。来自同一患者的两株血清型分别为24F和24B的ST162菌株在系统发育上无法区分,这表明这些菌株是在感染过程中通过血清型转换而来的:结论:除东京外,近期日本各地主要ST的变化与之前报道的相似。全基因组系统发育与血清型之间的相关性很小,而且在一名患者身上观察到血清型转换,这表明该血清群的免疫原性可能会发生变化。
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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