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Gut microbiota as prognosis markers for patients with HBV-related acute-on-chronic liver failure.
Wang, Ke; Zhang, Zhao; Mo, Zhi-Shuo; Yang, Xiao-Hua; Lin, Bing-Liang; Peng, Liang; Xu, Yang; Lei, Chun-Yan; Zhuang, Xiao-Dong; Lu, Ling; Yang, Rui-Fu; Chen, Tao; Gao, Zhi-Liang.
Affiliation
  • Wang K; Department of Infectious Diseases and Guangdong Key Laboratory of Liver Disease Research, Third Affiliated Hospital of Sun Yat-sen University, Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Guangzhou, Guangdong, China.
  • Zhang Z; Research and Development Department, Guangdong Longsee Biomedical Corporation, Guangzhou, Guangdong, China.
  • Mo ZS; Department of Infectious Diseases and Guangdong Key Laboratory of Liver Disease Research, Third Affiliated Hospital of Sun Yat-sen University, Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Guangzhou, Guangdong, China.
  • Yang XH; Department of Infectious Diseases and Guangdong Key Laboratory of Liver Disease Research, Third Affiliated Hospital of Sun Yat-sen University, Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Guangzhou, Guangdong, China.
  • Lin BL; Department of Infectious Diseases and Guangdong Key Laboratory of Liver Disease Research, Third Affiliated Hospital of Sun Yat-sen University, Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Guangzhou, Guangdong, China.
  • Peng L; Department of Infectious Diseases and Guangdong Key Laboratory of Liver Disease Research, Third Affiliated Hospital of Sun Yat-sen University, Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Guangzhou, Guangdong, China.
  • Xu Y; Research and Development Department, Guangdong Longsee Biomedical Corporation, Guangzhou, Guangdong, China.
  • Lei CY; Research and Development Department, Guangdong Longsee Biomedical Corporation, Guangzhou, Guangdong, China.
  • Zhuang XD; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Lu L; Hepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
  • Yang RF; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China.
  • Chen T; Research and Development Department, Guangdong Longsee Biomedical Corporation, Guangzhou, Guangdong, China.
  • Gao ZL; Department of Infectious Diseases and Guangdong Key Laboratory of Liver Disease Research, Third Affiliated Hospital of Sun Yat-sen University, Key Laboratory of Tropical Disease Control (Sun Yat-Sen University), Ministry of Education, Guangzhou, Guangdong, China.
Gut Microbes ; 13(1): 1-15, 2021.
Article in En | MEDLINE | ID: mdl-34006193
ABSTRACT
The gut microbiota in the hepatitis B virus related acute-on-chronic liver failure (HBV-ACLF) is poorly defined. We aim to uncover the characteristics of the gut microbiota in HBV-ACLF and in other HBV associated pathologies. We analyzed the gut microbiome in patients with HBV-ACLF or other HBV associated pathologies and healthy individuals by 16S rRNA sequencing and metagenomic sequencing of fecal samples. 212 patients with HBV-ACLF, 252 with chronic hepatitis B (CHB), 162 with HBV-associated cirrhosis (HBV-LC) and 877 healthy individuals were recruited for the study. CHB and HBV-LC patients are grouped as HBV-Other. We discovered striking differences in the microbiome diversity between the HBV-ACLF, HBV-Other and healthy groups using 16S rRNA sequencing. The ratio of cocci to bacilli was significantly elevated in the HBV-ACLF group compared with healthy group. Further analysis within the HBV-ACLF group identified 52 genera showing distinct richness within the group where Enterococcus was enriched in the progression group whilst Faecalibacterium was enriched in the regression group. Metagenomic sequencing validated these findings and further uncovered an enrichment of Lactobacillus casei paracasei in progression group, while Alistipes senegalensis, Faecalibacterium prausnitzii and Parabacteroides merdae dominated the regression group. Importantly, our analysis revealed that there was a rapid increase of Enterococcus faecium during the progression of HBV-ACLF. The gut microbiota displayed distinct composition at different phases of HBV-ACLF. High abundance of Enterococcus is associated with progression while that of Faecalibacterium is associated with regression of HBV-ACLF. Therefore, the microbiota features hold promising potential as prognostic markers for HBV-ACLF.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacteria / Hepatitis B, Chronic / Acute-On-Chronic Liver Failure / Gastrointestinal Microbiome Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Gut Microbes Year: 2021 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacteria / Hepatitis B, Chronic / Acute-On-Chronic Liver Failure / Gastrointestinal Microbiome Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Gut Microbes Year: 2021 Type: Article Affiliation country: China