Thomasclavelia ramosa 是与酒精性肝细胞癌相关的肠道菌群失调的标志:首次微生物培养组学研究

Reham Magdy Wasfy, Anissa ABDOULAYE, Patrick BORENTAIN, Babacar MBAYE, Maryam TIDJANI ALOU, Aurelia CAPUTO, Claudia ANDRIEU, Giovanna MOTTOLA, Anthony LEVASSEUR, Matthieu Million, Rene GEROLAMI
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摘要

背景:肠道微生物群的改变与酒精性肝病(ALD)和肝癌的发病机制有关。目前还没有研究通过微生物培养组学来描述与酒精性肝病相关的菌群失调。研究方法对无 HCC 的 ALD 患者(ALD-NoHCC,16 人)、有 HCC 的 ALD 患者(ALD-HCC,19 人)和对照组(24 人)进行病例对照研究。16S rRNA 扩增子测序和微生物培养组学是肠道微生物组图谱分析的互补方法。结果通过微生物培养组学分析,Thomasclavelia ramosa 在所有 ALD 样本中的富集度最高并被检测到(100%),而在对照组中仅有一小部分(20%,p <0.001)被培养到。通过 16S rRNA 扩增子测序和三组线性判别分析,在 ALD-HCC 组中明显增加了 T. ramosa(LDA-score > 5,p < 0.05)。结论通过培养组学和 16 rRNA 测序鉴定出的瘤葡萄球菌与 ALD 和 ALD-HCC 相关。除了最近报道的该物种在结直肠癌中的体外遗传毒性外,该物种还被确定为 ALD-HCC 的候选致癌因子。
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Thomasclavelia ramosa is a Signature of Gut Dysbiosis associated with Alcohol-Related Hepatocellular Carcinoma: A First Microbial Culturomics Study
Background: Gut microbiota alteration is implicated in the pathogenesis of alcoholic liver disease (ALD) and HCC. No study has characterized the dysbiosis associated with ALD by microbial culturomics, an approach that certifies viability and allows the characterization of pathobiont strain candidates. Methods: A case-control study was conducted on patients with ALD without HCC (ALD-NoHCC) (n=16), ALD with HCC (ALD-HCC) (n=19), and controls (n=24). 16S rRNA amplicon sequencing and microbial culturomics were used as complementary methods for gut microbiome profiling. Results: By microbial culturomics, Thomasclavelia ramosa was the most enriched and detected in all ALD samples (100%), while it was cultivated in only a small proportion of controls (20%, p < 0.001). By 16S rRNA amplicon sequencing and 3-groups linear discriminant analysis, T. ramosa was increased explicitly in the ALD-HCC group (LDA-score > 5, p < 0.05). Conclusions: T. ramosa, identified by culturomics and 16 rRNA sequencing, is associated with ALD and ALD-HCC. Alongside the recently reported in vitro genotoxicity of this species in colorectal cancer, this species has been identified as a candidate oncobiont in ALD-HCC.
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