Distribution of sasX, mupA, and qacA/B genes and determination of genetic relatedness of epidemic methicillin-resistant Staphylococcus aureus strains associated with bloodstream infections in southern China.

IF 4.8 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2025-01-30 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1491658
Rui Zhao, Bingyu Du, Lingling Hu, Chenxi Li, Fen Xue, Xing Wang, Changhong Jiang, Jinghua Wang, Yanfeng Zhao
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Abstract

Introduction: Methicillin-resistant Staphylococcus aureus (MRSA) exhibits diverse genotypes with varying virulence and resistance profiles, particularly in the context of bloodstream infections (BSI). This study investigates the prevalence of the sasX, mupA, and qacA/B genes among MRSA isolates from bloodstream infections in southern China and analyzes their genetic relatedness.

Methods: A polymerase chain reaction (PCR) assay was developed to detect the presence of the sasX gene, which is associated with nasal colonization, immune evasion, and virulence, the mupirocin resistance gene mupA, and the chlorhexidine tolerance gene qacA/B in a total of 77 MRSA isolates. Multilocus sequence typing (MLST) was performed to determine the sequence types (STs) and assess the genetic relatedness of the isolates. The resistance of these strains to 16 antibiotics was also analyzed. The distribution of these genes and their association with epidemic STs were analyzed.

Results: A total of 26 STs were identified, with notable prevalence in five epidemic clones: ST59, ST5, and ST764. The prevalence of the sasX, mupA, and qacA/B genes across all isolates was 23.4%, 33.8%, and 79.2%, respectively. Specifically, the frequency of the sasX gene was highest in ST59 (29.4%), ST239 (100%), and ST764 (37.5%); mupA was most prevalent in ST5 (66.7%), ST59 (17.6%), ST764 (37.5%), and ST15 (100%); qacA/B was predominantly found in ST59 (88.2%), ST5 (66.7%), ST398 (85.7%), ST764 (50.0%), and ST239 (100%). The gene distribution patterns revealed that sasX+ qacA/B+ mupA+ strains were closely associated with epidemic clones ST6290 and ST88, whereas sasX+ qacA/B+ mupA- strains were linked to ST59, ST239, and ST764.

Discussion: Notably, forty-seven (61%) MRSA BSI strains were multidrug-resistant, with the majority exhibiting resistance to penicillin, erythromycin, and clindamycin. Major MRSA clones in southern China include ST59, ST5, ST764, and ST398. In this study, sasX, mupA and qacA/B genes were present in the MRSA isolates, with the mupA gene being the most prevalent. Variations in the prevalence of virulence and resistance genes among these epidemic strains underscore the need for targeted infection control measures. These findings contribute to a better understanding of the genetic epidemiology of MRSA in the region, facilitating the development of effective prevention and control strategies for BSI.

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sasX、mupA和qacA/B基因在中国南方与血流感染相关的耐甲氧西林金黄色葡萄球菌流行株的分布及遗传相关性测定
耐甲氧西林金黄色葡萄球菌(MRSA)表现出不同的基因型,具有不同的毒力和耐药谱,特别是在血液感染(BSI)的背景下。本研究调查了sasX、mupA和qacA/B基因在中国南方MRSA血液感染分离株中的流行情况,并分析了它们的遗传相关性。方法:采用聚合酶链反应(PCR)法检测77株MRSA分离株中与鼻腔定植、免疫逃逸和毒力相关的sasX基因、莫匹罗星耐药基因mupA和氯己定耐药基因qacA/B的存在。采用多位点序列分型(Multilocus sequence typing, MLST)确定分离菌株的序列类型,并评估其遗传亲缘性。并分析了这些菌株对16种抗生素的耐药性。分析了这些基因的分布及其与流行性STs的关系。结果:共鉴定出26株STs,其中在ST59、ST5和ST764 5个流行克隆中流行率较高。sasX、mupA和qacA/B基因在所有分离株中的感染率分别为23.4%、33.8%和79.2%。其中,sasX基因在ST59(29.4%)、ST239(100%)和ST764(37.5%)中频率最高;mupA在ST5(66.7%)、ST59(17.6%)、ST764(37.5%)和ST15(100%)中最常见;qacA/B主要存在于ST59(88.2%)、ST5(66.7%)、ST398(85.7%)、ST764(50.0%)和ST239(100%)中。基因分布模式显示,sasX+ qacA/B+ mupA+菌株与流行克隆ST6290和ST88密切相关,而sasX+ qacA/B+ mupA-菌株与ST59、ST239和ST764密切相关。讨论:值得注意的是,47株(61%)MRSA BSI菌株具有多重耐药,其中大多数对青霉素、红霉素和克林霉素耐药。中国南方主要的MRSA克隆包括ST59、ST5、ST764和ST398。在本研究中,MRSA分离株中存在sasX、mupA和qacA/B基因,其中mupA基因最为普遍。这些流行毒株中毒力和耐药基因流行率的差异突出表明需要采取有针对性的感染控制措施。这些发现有助于更好地了解该地区MRSA的遗传流行病学,促进制定有效的BSI预防和控制策略。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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