从无症状妇女或急性乳腺炎妇女乳汁中分离的金黄色葡萄球菌的基因型和表型特征

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-23 Epub Date: 2025-08-15 DOI:10.1128/msystems.00797-25
Rubén Jurado, Alberto Aragón, Natalia Hernando, Josué Jara, Juan Miguel Rodriguez, Belén Orgaz, Leonides Fernández
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引用次数: 0

摘要

急性乳腺炎是哺乳期常见的感染,主要由金黄色葡萄球菌引起,这种细菌以其在乳腺导管内形成生物膜并产生抗生素耐药性而闻名。本研究旨在对急性乳腺炎妇女和健康无症状妇女分离的金黄色葡萄球菌菌株进行基因组表征,以更好地了解金黄色葡萄球菌菌株如何从人乳微生物群的无害成分转变为导致乳腺炎的病原体。对9株金黄色葡萄球菌进行了全基因组测序,其中6株来自患有乳腺炎的女性,3株来自健康女性,随后对核心和辅助基因、抵抗组、病毒组、移动组和次级代谢物合成进行了计算机分析,以确定与毒力、抗生素耐药性、生物膜形成和移动遗传元件(如质粒、噬菌体和致病性岛)相关的基因。采用Sensititre EUST2板、琼脂扩散法、96孔板生物膜形成和Chrome Azurol S法对铁载体的产生进行了评估。结果表明,完整的噬菌体基因组仅存在于从乳腺炎病例中分离的金黄色葡萄球菌菌株中。一些毒力基因,包括fnbB和cna,在来自健康女性的菌株中缺失。两种金黄色葡萄球菌菌株均表现出生物膜形成能力,其中乳腺炎相关菌株SA4和SA5的生物膜生成能力最强。同样,尽管所有菌株都分泌铁载体,但SA4和SA55表现出最强的铁载体产量,表明该性状与乳腺炎相关菌株的毒力之间存在联系。通过对关键基因组特征的分析,包括毒力因子、抗性基因和生物膜形成能力,揭示了金黄色葡萄球菌参与乳腺炎发病的一些机制。急性乳腺炎是哺乳期妇女的一种广泛感染,其主要病因金黄色葡萄球菌已对抗生素产生耐药性,使治疗具有挑战性。这种细菌形成生物膜的能力使其从乳腺中根除变得复杂。了解与乳腺炎相关的金黄色葡萄球菌菌株的基因组和表型特征,与从无症状妇女中分离的金黄色葡萄球菌菌株进行比较,对于制定更好的治疗策略至关重要。这项研究提供了新的见解,遗传特征,如毒力因素,抗生素耐药谱和噬菌体的存在,使金黄色葡萄球菌菌株在乳腺炎致病性。它还强调了生物膜形成和铁载体产生作为乳腺炎进展的关键因素的潜力。这些发现可以指导新的治疗方法的发展,如靶向治疗或益生菌,它们可以更有效地治疗乳腺炎,减少对抗生素的依赖,最终改善母婴健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genotypic and phenotypic characterization of Staphylococcus aureus isolated from human milk of asymptomatic women or women with acute mastitis.

Acute mastitis is a common infection during lactation, primarily caused by Staphylococcus aureus, a bacterium known for its ability to form biofilms within mammary ducts and develop antibiotic resistance. This study aimed to genomically characterize S. aureus strains isolated from women with acute mastitis and healthy asymptomatic women to better understand how S. aureus strains transition from harmless components of the human milk microbiota to pathogenic agents responsible for mastitis. Whole-genome sequencing was performed on nine S. aureus strains-six from women with mastitis and three from healthy women-followed by in silico analyses of core and accessory genes, resistome, virulome, mobilome, and secondary metabolite synthesis to identify genes related to virulence, antibiotic resistance, biofilm formation, and mobile genetic elements such as plasmids, bacteriophages, and pathogenicity islands. Antimicrobial resistance profiles were evaluated using Sensititre EUST2 plates, antimicrobial activity by an agar diffusion method, biofilm formation in 96-well plates, and siderophore production with the Chrome Azurol S assay. Results showed that complete bacteriophage genomes were only present in S. aureus strains isolated from mastitis cases. Some virulence genes, including fnbB and cna, were absent in strains from healthy women. Both types of S. aureus strains exhibited biofilm formation capacity, with mastitis-associated strains SA4 and SA5 being the highest biofilm producers. Similarly, although all strains secreted siderophores, SA4 and SA55 exhibited the strongest siderophore production, indicating a link between this trait and virulence in mastitis-associated strains. The analysis of key genomic features, including virulence factors, resistance genes, and biofilm-forming capabilities, revealed some mechanisms by which S. aureus contributes to the pathogenesis of mastitis.IMPORTANCEAcute mastitis is a widespread infection in lactating women, and its main cause, Staphylococcus aureus, has developed resistance to antibiotics, making treatment challenging. The ability of this bacterium to form biofilms complicates its eradication from the mammary glands. Understanding the genomic and phenotypic characteristics of S. aureus strains associated with mastitis, compared to those isolated from asymtomatic women, is critical for developing better treatment strategies. This study provides new insights into the genetic features, such as virulence factors, antibiotic resistance profiles, and presence of bacteriophages, that make S. aureus strains pathogenic in mastitis. It also highlights the potential of biofilm formation and siderophore production as key factors in mastitis progression. These findings could guide the development of novel therapeutic approaches, such as targeted therapies or probiotics, which can more effectively treat mastitis and reduce reliance on antibiotics, ultimately improving maternal and infant health.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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