Webb Julia, Cella Eleonora, Sutcliffe Catherine G, Johnston Catherine, Hassouneh Sayf Al-Deen, Jubair Mohammad, Riley Dennie Parker, Tso Carol, Weatherholtz Robert C, Hammitt Laura L, Azarian Taj
Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, USA.
Present address: University of North Carolina at Chapel Hill School of Medicine, Raleigh-Durham, Chapel Hill, USA.
Microb Genom. 2025 Mar;11(3). doi: 10.1099/mgen.0.001367.
(SA) is an opportunistic pathogen and human commensal that is frequently present in the upper respiratory tract, gastrointestinal tract and skin. While SA can cause diseases ranging from minor skin infections to life-threatening bacteraemia, it can also be carried asymptomatically. Indigenous individuals in the Southwest USA experience high rates of invasive SA disease. As carriage is the most significant risk factor for disease, understanding the dynamics of SA carriage, and in particular co-carriage of multiple strains, is important to develop strategies to prevent transmission in vulnerable communities. Here, we investigated SA co-carriage and intrahost evolution by sampling several colonies from multiple anatomical sites and whole-genome sequencing (WGS) on 310 SA isolates collected from 60 Indigenous adults participating in a cross-sectional carriage study. We assessed the richness and diversity of SA isolates differences in multilocus sequence type, core-genome SNPs and genome content. Using WGS data, we identified 95 distinct SA intra-subject lineages (ISLs) among 60 participants; co-carriage was detected in 42% (25/60). Notably, two participants each carried four distinct SA ISLs. Variation in antibiotic resistance determinants among carried strains was identified among 42% (25/60) of participants. Lastly, we found unequal distribution of clonal complex by body site, suggesting that certain lineages may be adapted to specific anatomical sites. Together, these findings suggest that co-carriage may occur more frequently than previously appreciated and further our understanding of SA intrahost diversity during carriage, which has implications for surveillance activities and epidemiological investigations.
金黄色葡萄球菌(SA)是一种机会致病菌和人体共生菌,常存在于上呼吸道、胃肠道和皮肤中。虽然SA可引起从轻微皮肤感染到危及生命的菌血症等多种疾病,但也可无症状携带。美国西南部的原住民侵袭性SA疾病发病率很高。由于携带是疾病的最重要危险因素,了解SA携带的动态变化,尤其是多种菌株的共同携带情况,对于制定在脆弱社区预防传播的策略很重要。在此,我们通过从多个解剖部位采集多个菌落样本,并对参与横断面携带研究的60名原住民成年人收集的310株SA分离株进行全基因组测序(WGS),来调查SA的共同携带情况和宿主内进化。我们评估了SA分离株的丰富度和多样性——多位点序列类型、核心基因组单核苷酸多态性和基因组内容的差异。利用WGS数据,我们在60名参与者中鉴定出95个不同的SA个体内谱系(ISL);42%(25/60)检测到共同携带。值得注意的是,两名参与者各自携带四种不同的SA ISL。在42%(25/60)的参与者中发现携带菌株之间抗生素耐药决定因素存在差异。最后,我们发现克隆复合体在身体部位的分布不均,这表明某些谱系可能适应特定的解剖部位。总之,这些发现表明共同携带可能比之前认为的更频繁发生,并加深了我们对携带期间SA宿主内多样性的理解,这对监测活动和流行病学调查具有重要意义。