艰难梭菌毒素产生和毒素基因存在的微生物组特征:霰弹枪宏基因组方法。

IF 3.1 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-09-25 DOI:10.1128/msphere.00435-25
Jiye Kwon, Maria A Correa, Yong Kong, William Pelletiers, Martina Wade, Danyel Olson, Melinda M Pettigrew
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引用次数: 0

摘要

艰难梭菌是一种机会性胃肠道病原体,能够无症状定植,引起从腹泻到假膜性结肠炎等疾病。艰难梭菌感染(CDI)的准确诊断具有挑战性,对治疗和控制至关重要。我们假设肠道微生物组谱可以帮助区分难辨梭菌定殖腹泻患者和真正的CDI患者。我们分析了172例难辨梭菌谷氨酸脱氢酶阳性个体的粪便样本。参与者根据毒素状态(即毒素阳性或阴性)进行分类,然后根据毒素的产生进一步分为三个毒素组,如果不产生,则艰难梭菌菌株是否携带毒素编码基因。我们研究了患者特征、既往抗生素暴露、微生物群落结构和功能以及毒素类别之间的关系。35%的毒素阴性参与者接受了抗生素治疗,尽管他们没有达到真正CDI的标准。各组肠球菌种类丰富。粪肠杆菌的相对丰度在有抗生素暴露史的个体中较高。α和β多样性在不同毒素组间没有差异。在控制了既往抗生素暴露和既往CDI发作后,嗜粘液阿克曼氏菌、多黄酮因子和青少年双歧杆菌的丰度区分了毒素阳性艰难梭菌个体。艰难梭菌的丰度并不能区分真正的CDI患者和被定植的患者。我们确定了肠道微生物群与艰难梭菌毒素基因存在和毒素产生之间的关联。这些结果突出了微生物组诊断在提高CDI准确性和指导治疗决策方面的潜力。艰难梭状芽胞杆菌在社区和医院环境中定植人类并引起腹泻。艰难梭菌感染(CDI)是一种毒素介导的疾病,其诊断具有挑战性。这项研究的目的是确定肠道微生物组的差异是否有助于区分定植个体和CDI患者。我们检查了172个个体的粪便样本和数据,根据毒素的检测,如果没有检测到,是否存在艰难梭菌菌株中的毒素编码基因,将其分为三组。我们发现,粪肠球菌等细菌在使用抗生素的人群中含量更高。虽然肠道微生物组的多样性没有因毒素组而异,但特定的肠道细菌、抗生素抗性基因和代谢途径与毒素组相关。我们的研究结果表明,考虑完整的肠道微生物群和过去使用抗生素等因素可能有助于改善CDI的诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microbiome signatures of Clostridioides difficile toxin production and toxin gene presence: a shotgun metagenomic approach.

Clostridioides difficile is an opportunistic gastrointestinal pathogen capable of asymptomatic colonization and causes diseases ranging from diarrhea to pseudomembranous colitis. Accurate diagnosis of C. difficile infection (CDI) is challenging and critical for treatment and control. We hypothesized that gut microbiome profiles could help distinguish C. difficile colonized patients with diarrhea from those with true CDI. We analyzed 172 stool samples from individuals who tested glutamate dehydrogenase positive for C. difficile. Participants were categorized by toxin status (i.e., toxin positive or negative) and then further classified into three toxin groups based on the production of toxin, and if not produced, whether the C. difficile strain carried toxin-encoding genes. We examined associations between patient characteristics, prior antibiotics exposure, microbiome community structure and function, and toxin categories. Thirty-five percent of toxin-negative participants received antibiotics despite not meeting the criteria for true CDI. Enterococcus species were abundant in all groups. The relative abundance of E. faecalis was higher among individuals with prior antibiotics exposure. Alpha and beta diversity did not differ by toxin group. After controlling for prior antibiotics exposure and previous CDI episode, the abundance of Akkermansia muciniphila, Flavonifractor plautii, and Bifidobacterium adolescentis distinguished individuals with toxin-positive C. difficile. C. difficile abundance did not differentiate participants with true CDI from those who were colonized. We identified associations between the gut microbiome and C. difficile toxin gene presence and toxin production. These results highlight the potential for microbiome-informed diagnostics to improve CDI accuracy and guide treatment decisions.IMPORTANCEClostridioides difficile colonizes humans and causes diarrhea in community and hospital settings. C. difficile infection (CDI) is a toxin-mediated disease, and its diagnosis is challenging. The goal of this study was to determine whether differences in the gut microbiome could help distinguish between colonized individuals and those with CDI. We examined stool samples and data from 172 individuals categorized into three groups based on the detection of toxin and, if not detected, whether toxin-encoding genes were present in the C. difficile strain. We identified bacteria, such as Enterococcus faecalis, that were more abundant in people who had used antibiotics. While the diversity of the gut microbiome did not differ by toxin group, specific gut bacteria, antibiotic resistance genes, and metabolic pathways were associated with toxin group. Our findings suggest that considering the full gut microbiome and factors like past antibiotic use could help improve the diagnosis and treatment of CDI.

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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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