Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, Room 543-745 Bannatyne Avenue, Winnipeg, Manitoba, Canada R3E 0J9.
Clinical Microbiology, Shared Health, MS673-820 Sherbrook Street, Winnipeg, Manitoba, Canada R3A 1R9.
J Antimicrob Chemother. 2024 Oct 1;79(10):2653-2661. doi: 10.1093/jac/dkae272.
Lower respiratory infections and invasive disease caused by Streptococcus pneumoniae serotype 3 remain major clinical challenges around the world, despite widespread availability of updated vaccines.
As part of CANWARD, antimicrobial susceptibility testing and serotyping were performed on all S. pneumoniae isolates from 2007 to 2021. A subset of 226/264 (85.6%) serotype 3 isolates were selected for WGS to determine sequence type (ST)/clonal cluster (CC) and correspondence of antimicrobial resistance determinants (erm, mefAE, tetM, cat, folA, folP) with resistance phenotype.
Of the 3,039 S. pneumoniae isolates obtained from 2007 to 2021, 8.7% (n = 264) were serotype 3, with 64.0% of respiratory origin and 36.0% from blood. Of 226 sequenced serotype 3 isolates, 184 (81.4%) were ST180 (GPSC12). The proportion of ST8561 (single locus variant of ST180) increased from 7.2% to 16.6% during the study period. An increasing proportion of serotype 3 isolates had phenotypic resistance (P = 0.0007) and genetic resistance determinants (P = 0.004), comparing 2017-21 to 2007-11, largely due to a recently expanded ST180 clade with cat, tetM and mef determinants.
S. pneumoniae serotype 3 from GPSC12 continues to dominate throughout Canada, with an increase in the proportion of ST8561. The proportion of serotype 3 isolates that are phenotypically resistant and with genetic resistance determinants is increasing over time, reflecting a global increase in GPSC12 genotypes with known resistance determinants. Phylogenomic characterization of isolates collected over time and from around the world may facilitate improved treatment and enhanced prevention strategies, including new vaccines with activity against S. pneumoniae serotype 3.
尽管更新的疫苗已广泛普及,但由肺炎链球菌血清型 3 引起的下呼吸道感染和侵袭性疾病仍是全球范围内的重大临床挑战。
作为 CANWARD 的一部分,对 2007 年至 2021 年期间所有分离的肺炎链球菌进行了抗菌药物敏感性测试和血清分型。选择了 226/264(85.6%)个血清型 3 分离株进行 WGS,以确定序列型(ST)/克隆群(CC)和抗菌药物耐药决定因素(erm、mefAE、tetM、cat、folA、folP)与耐药表型的对应关系。
从 2007 年至 2021 年获得的 3039 株肺炎链球菌中,8.7%(n=264)为血清型 3,其中 64.0%来源于呼吸道,36.0%来源于血液。在 226 株测序的血清型 3 分离株中,184 株(81.4%)为 ST180(GPSC12)。在研究期间,ST8561(ST180 的单一位点变异)的比例从 7.2%增加到 16.6%。与 2007-11 年相比,2017-21 年血清型 3 分离株的表型耐药(P=0.0007)和遗传耐药决定因素(P=0.004)的比例增加,主要原因是最近扩展的 ST180 分支具有 cat、tetM 和 mef 决定因素。
GPSC12 中的肺炎链球菌血清型 3 继续在加拿大各地占主导地位,ST8561 的比例增加。随着时间的推移,血清型 3 分离株的表型耐药和遗传耐药决定因素的比例增加,反映了具有已知耐药决定因素的 GPSC12 基因型在全球范围内的增加。随着时间的推移和来自世界各地的分离株的系统发育特征分析可能有助于改善治疗和加强预防策略,包括针对肺炎链球菌血清型 3 的新型疫苗。