The healthy human gut can take it all: vancomycin-variable, linezolid-resistant strains and specific bacteriocin-species interplay in Enterococcus spp.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2025-01-31 Epub Date: 2024-12-19 DOI:10.1128/aem.01699-24
Ana C Almeida-Santos, Bárbara Duarte, Ana P Tedim, Maria J Teixeira, Joana C Prata, Rui M S Azevedo, Carla Novais, Luísa Peixe, Ana R Freitas
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Abstract

Enterococcus spp. are opportunistic human pathogens colonizing the human gut and a significant reservoir for the continuous adaptation of hospital clones. However, studies on the features of enterococci species co-colonizing healthy individuals are scarce. We investigated the prevalence, antibiotic resistance, and bacteriocin profiles of Enterococcus species in fecal samples from healthy adults in Portugal using culture-based methods, WGS, and bacteriocin inhibition assays. Results were compared with data from a 2001 study in the same region. Enterococcus spp. (n = 315; 24% MDR) were recovered from all volunteers. Enterococcus lactis was the prevalent species (75%), followed by Enterococcus faecalis (65%) and Enterococcus faecium (47%). E. lactis prevalence increased 2.5-fold since 2001. Linezolid resistance genes (optrA/poxtA) were detected in E. faecium and Enterococcus thailandicus isolates, while a vancomycin-variable E. faecium was also identified. Virulence and plasmid profiles were diverse across species, with evidence of exchange of virulence markers and plasmid replicons between E. faecium and E. lactis. Bacteriocin gene repertoires were extensive and species-specific. Higher numbers of bacteriocin genes were associated with stronger inhibition profiles, and 25% of E. faecium and E. lactis isolates were capable of inhibiting relevant VRE clones. This study unveils the co-occurrence and ecological dynamics of Enterococcus species in the healthy human gut, reinforcing its role as a reservoir for key antibiotic resistance genes and potentially pathogenic strains. The shift toward E. lactis prevalence and the detection of linezolid resistance genes in healthy individuals underscore the need for ongoing surveillance of the gut microbiome to guide public health strategies and antibiotic stewardship efforts.IMPORTANCEThis study highlights the role of Enterococcus species in the healthy human gut, revealing important insights into their prevalence and antibiotic resistance. It emphasizes that the human gut serves as a significant reservoir for antibiotic-resistant strains and shows a notable increase and prevalence of Enterococcus lactis, which has been underappreciated due to identification challenges. The research also underscores the bacteriocins' role in microbial competition, where commensal strains inhibit clinical VRE, potentially aiding the restoration of the gut microbiota, after antibiotic treatment. The findings accentuate the need for ongoing surveillance to track changes in gut bacteria, especially with the emergence of resistance genes to last resort antibiotics. Such monitoring is crucial for shaping public health strategies and managing the growing threat of antibiotic-resistant infections. Profiling bacteriocins at the species and strain level can identify ecological adaptation factors and inform strategies to target high-risk clones.

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健康的人类肠道可以承受这一切:万古霉素变量,利奈唑胺耐药菌株和特定的细菌素物种在肠球菌中相互作用。
肠球菌是一种机会性的人类病原体,定植于人类肠道,是医院克隆持续适应的重要储存库。然而,关于肠道球菌物种共定域健康个体特征的研究很少。我们使用基于培养的方法、WGS和细菌素抑制试验,调查了葡萄牙健康成人粪便样本中肠球菌的患病率、抗生素耐药性和细菌素谱。研究结果与2001年同一地区的一项研究数据进行了比较。肠球菌(n = 315;24%耐多药(MDR))。以乳肠球菌为主(75%),其次为粪肠球菌(65%)和屎肠球菌(47%)。自2001年以来,乳酸菌的流行率增加了2.5倍。在粪肠球菌和泰国肠球菌分离株中检出利奈唑胺耐药基因(optrA/poxtA),同时检出一株万古霉素可变菌株粪肠球菌。不同物种的毒力和质粒谱存在差异,有证据表明粪肠杆菌和乳肠杆菌之间存在毒力标记和质粒复制子的交换。细菌素基因库广泛且具有物种特异性。较高数量的细菌素基因与较强的抑制谱相关,25%的屎肠杆菌和乳杆菌分离株能够抑制相关的VRE克隆。这项研究揭示了肠球菌物种在健康人类肠道中的共存和生态动力学,加强了其作为关键抗生素耐药基因和潜在致病菌株储存库的作用。在健康个体中,乳酸杆菌的流行和利奈唑胺耐药基因的检测的转变强调了对肠道微生物群进行持续监测的必要性,以指导公共卫生战略和抗生素管理工作。这项研究强调了肠球菌在健康人类肠道中的作用,揭示了其患病率和抗生素耐药性的重要见解。它强调人类肠道是抗生素耐药菌株的重要储存库,并显示乳酸肠球菌的显著增加和流行,由于鉴定方面的挑战,这一点一直未得到充分重视。该研究还强调了细菌素在微生物竞争中的作用,其中共生菌株抑制临床VRE,可能有助于抗生素治疗后肠道微生物群的恢复。这些发现强调了持续监测肠道细菌变化的必要性,特别是随着对最后手段抗生素的抗性基因的出现。这种监测对于制定公共卫生战略和管理日益严重的耐抗生素感染威胁至关重要。在物种和菌株水平上分析细菌素可以确定生态适应因素,为针对高风险克隆的策略提供信息。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
期刊最新文献
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