Whole-genome sequencing of clinical methicillin-resistant Staphylococcus aureus isolates across hospitals in Mwanza, Tanzania.

Access microbiology Pub Date : 2026-06-12 eCollection Date: 2026-01-01 DOI:10.1099/acmi.0.001127.v5
Vitus Silago, Lawrence Mapunda, Prisca Damiano, Katarina Oravcova, Louise Matthews, Benson R Kidenya, Stephen E Mshana, Jeremiah Seni, Heike Claus
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Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) is a leading cause of both healthcare-associated and community-acquired infections, characterized by limited treatment options and substantial morbidity and mortality, particularly in low- and middle-income countries such as Tanzania. However, genomic data, which provides valuable insights into the pathogen's genetic landscape, remains scarce. This study utilized whole-genome sequencing (WGS) to examine local molecular epidemiological profiles of 14 MRSA isolates isolated from blood, urine and pus samples during (n=6; June 2019-June 2020) and after (n=8; March-August 2023) the implementation of the National Action Plan on Antimicrobial Resistance in Mwanza, Tanzania. All isolates belonged to sequence type 8 (ST8), and 92.9% (13/14) were spa type t1476. Phenotypic and genotypic antimicrobial resistance results were consistent for all antibiotics tested with the exception of tetracycline. Pairwise SNP analysis revealed genetic diversity, with SNP differences ranging from 0 to 99. Maximum likelihood phylogeny analysis based on SNP data identified two closely related MRSA pairs, one from multiple wards while the other confined within the same ward in the same hospital. In conclusion, WGS revealed that all MRSA isolates belonged to ST8 with substantial genetic diversity and phylogenetic analysis revealed two closely related MRSA pairs, suggesting a transmission event, acquisition from a shared source or circulation of a closely related lineage. These findings highlight the importance of genomic surveillance for uncovering MRSA transmission patterns and guiding infection prevention efforts.

坦桑尼亚姆万扎各医院临床耐甲氧西林金黄色葡萄球菌分离物的全基因组测序
耐甲氧西林金黄色葡萄球菌(MRSA)是卫生保健相关感染和社区获得性感染的主要原因,其特点是治疗选择有限,发病率和死亡率高,特别是在坦桑尼亚等低收入和中等收入国家。然而,基因组数据,提供宝贵的见解病原体的遗传景观,仍然稀缺。本研究利用全基因组测序(WGS)检测了在坦桑尼亚姆万扎实施《抗菌素耐药性国家行动计划》期间(n=6; 2019年6月- 2020年6月)和之后(n=8; 2023年3月- 8月)从血液、尿液和脓液样本中分离出的14株MRSA分离株的当地分子流行病学特征。所有分离株均为序列8型(ST8),其中92.9%(13/14)为spa型t1476。除四环素外,所有抗生素的表型和基因型耐药结果一致。对SNP分析显示遗传多样性,SNP差异范围为0 ~ 99。基于SNP数据的最大似然系统发育分析确定了两个密切相关的MRSA对,一个来自多个病房,另一个局限于同一医院的同一病房。综上所述,WGS显示所有MRSA分离株均属于ST8,具有丰富的遗传多样性,系统发育分析显示两个密切相关的MRSA对,表明存在传播事件,来自共享源或密切相关谱系的循环。这些发现强调了基因组监测对于发现MRSA传播模式和指导感染预防工作的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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