Gut Microbiome Signatures in the Progression of Hepatitis B Virus-Induced Liver Disease
The gut microbiome is associated with hepatitis B virus (HBV)-induced liver disease, which progresses from chronic hepatitis B, to liver cirrhosis, and eventually to hepatocellular carcinoma. Studies have analyzed the gut microbiome at each stage of HBV-induced liver diseases, but a consensus has no...
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Veröffentlicht in: | Frontiers in microbiology 2022-06, Vol.13, p.916061-916061 |
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Sprache: | eng |
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Zusammenfassung: | The gut microbiome is associated with hepatitis B virus (HBV)-induced liver disease, which progresses from chronic hepatitis B, to liver cirrhosis, and eventually to hepatocellular carcinoma. Studies have analyzed the gut microbiome at each stage of HBV-induced liver diseases, but a consensus has not been reached on the microbial signatures across these stages. Here, we conducted by a systematic meta-analysis of 486 fecal samples from publicly available 16S rRNA gene datasets across all disease stages, and validated the results by a gut microbiome characterization on an independent cohort of 15 controls, 23 chronic hepatitis B, 20 liver cirrhosis, and 22 hepatocellular carcinoma patients. The integrative analyses revealed 13 genera consistently altered at each of the disease stages both in public and validation datasets, suggesting highly robust microbiome signatures. Specifically,
Colidextribacter
and
Monoglobus
were enriched in healthy controls. An unclassified
Lachnospiraceae
genus was specifically elevated in chronic hepatitis B, whereas
Bilophia
was depleted.
Prevotella and Oscillibacter
were depleted in liver cirrhosis. And
Coprococcus
and
Faecalibacterium
were depleted in hepatocellular carcinoma. Classifiers established using these 13 genera showed diagnostic power across all disease stages in a cross-validation between public and validation datasets (AUC = 0.65–0.832). The identified microbial taxonomy serves as non-invasive biomarkers for monitoring the progression of HBV-induced liver disease, and may contribute to microbiome-based therapies. |
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ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2022.916061 |