Department of Laboratory Medicine and Pathology, University of Alberta, 5-411 Edmonton Clinic Health Academy, Edmonton, Alberta, T6G 1C9 Canada.
Alberta Precision Laboratory - Public Health Laboratory, 8440 112 Street NW, Edmonton, Alberta, T6G 2B7 Canada.
Microb Genom. 2023 Nov;9(11). doi: 10.1099/mgen.0.001141.
In the province of Alberta, Canada, invasive disease caused by serogroup 20 (serotypes 20A/20B) has been increasing in incidence. Here, we characterize provincial invasive serogroup 20 isolates collected from 1993 to 2019 alongside invasive and non-invasive serogroup 20 isolates from the Global Pneumococcal Sequencing (GPS) Project collected from 1998 to 2015. Trends in clinical metadata and geographic location were evaluated, and serogroup 20 isolate genomes were subjected to molecular sequence typing, virulence and antimicrobial resistance factor mining, phylogenetic analysis and pangenome calculation. Two hundred and seventy-four serogroup 20 isolates from Alberta were sequenced, and analysed along with 95 GPS Project genomes. The majority of invasive Alberta serogroup 20 isolates were identified after 2007 in primarily middle-aged adults and typed predominantly as ST235, a sequence type that was rare among GPS Project isolates. Most Alberta isolates carried a full-length capsular gene, suggestive of serotype 20B. All Alberta and GPS Project genomes carried molecular resistance determinants implicated in fluoroquinolone and macrolide resistance, with a few Alberta isolates exhibiting phenotypic resistance to azithromycin, clindamycin, erythromycin, tetracycline and trimethoprim-sulfamethoxazole, as well as non-susceptibility to tigecycline. All isolates carried multiple virulence factors including those involved in adherence, immune modulation and nutrient uptake, as well as exotoxins and exoenzymes. Phylogenetically, Alberta serogroup 20 isolates clustered with predominantly invasive GPS Project isolates from the USA, Israel, Brazil and Nepal. Overall, this study highlights the increasing incidence of invasive serogroup 20 disease in Alberta, Canada, and provides insights into the genetic and clinical characteristics of these isolates within a global context.
在加拿大艾伯塔省,由血清群 20(血清型 20A/20B)引起的侵袭性疾病的发病率一直在上升。在这里,我们对 1993 年至 2019 年间收集的省级侵袭性血清群 20 分离株以及 1998 年至 2015 年间收集的全球肺炎球菌测序(GPS)项目中的侵袭性和非侵袭性血清群 20 分离株进行了特征描述。评估了临床元数据和地理位置的趋势,并对血清群 20 分离株基因组进行了分子序列分型、毒力和抗微生物耐药因子挖掘、系统发育分析和泛基因组计算。对 274 株来自艾伯塔省的血清群 20 分离株进行了测序,并与 95 株 GPS 项目基因组进行了分析。大多数侵袭性艾伯塔血清群 20 分离株于 2007 年后被鉴定,主要发生在中青年人中,且主要为 ST235 型,这是 GPS 项目分离株中罕见的一种序列型。大多数艾伯塔省分离株携带全长荚膜基因,提示血清型 20B。所有艾伯塔省和 GPS 项目基因组均携带与氟喹诺酮类和大环内酯类耐药相关的分子耐药决定因素,少数艾伯塔省分离株对阿奇霉素、克林霉素、红霉素、四环素和甲氧苄啶-磺胺甲恶唑表现出表型耐药性,以及对替加环素的非敏感性。所有分离株均携带多种毒力因子,包括参与黏附、免疫调节和营养摄取的因子,以及外毒素和外肽酶。系统发育上,艾伯塔省血清群 20 分离株与主要来自美国、以色列、巴西和尼泊尔的 GPS 项目侵袭性分离株聚类。总体而言,这项研究强调了加拿大艾伯塔省侵袭性血清群 20 疾病发病率的上升,并提供了在全球背景下对这些分离株的遗传和临床特征的深入了解。