Gut microbiota as prognosis markers for patients with HBV-related acute-on-chronic liver failure

被引:41
作者
Wang, Ke [1 ,2 ]
Zhang, Zhao [3 ]
Mo, Zhi-Shuo [1 ,2 ]
Yang, Xiao-Hua [1 ,2 ]
Lin, Bing-Liang [1 ,2 ]
Peng, Liang [1 ,2 ]
Xu, Yang [3 ]
Lei, Chun-Yan [3 ]
Zhuang, Xiao-Dong [4 ]
Lu, Ling [5 ]
Yang, Rui-Fu [6 ]
Chen, Tao [3 ]
Gao, Zhi-Liang [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Dept Infect Dis, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 3, Guangdong Key Lab Liver Dis Res, Key Lab Trop Dis Control,Minist Educ, Guangzhou, Guangdong, Peoples R China
[3] Guangdong Longsee Biomed Corp, Res & Dev Dept, Guangzhou, Guangdong, Peoples R China
[4] Univ Oxford, Nuffield Dept Med, Oxford, England
[5] Nanjing Med Univ, Hepatobiliary Ctr, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[6] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatitis B; acute-on-chronic liver failure; gut microbiota; 16S rRNA sequencing; metagenomic sequencing; CHRONIC HEPATITIS-B; BUTYRATE-PRODUCING BACTERIA; HEALTH; FLORA; DYSFUNCTION; MODULATION; CIRRHOSIS; IMPACT; MODEL;
D O I
10.1080/19490976.2021.1921925
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:1 / 15
页数:15
相关论文
共 44 条
  • [1] Host-bacterial mutualism in the human intestine
    Bäckhed, F
    Ley, RE
    Sonnenburg, JL
    Peterson, DA
    Gordon, JI
    [J]. SCIENCE, 2005, 307 (5717) : 1915 - 1920
  • [2] Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer
    Balamurugan, Ramadass
    Rajendiran, Ethendhar
    George, Sarah
    Samuel, G. Vijay
    Ramakrishna, Balakrishnan S.
    [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2008, 23 (08) : 1298 - 1303
  • [3] The gut microbiota of centenarians: Signatures of longevity in the gut microbiota profile
    Biagi, Elena
    Rampelli, Simone
    Turroni, Silvia
    Quercia, Sara
    Candela, Marco
    Brigidi, Patrizia
    [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 2017, 165 : 180 - 184
  • [4] Secretory IgA-Mediated Neutralization of Shigella flexneri Prevents Intestinal Tissue Destruction by Down-Regulating Inflammatory Circuits
    Boullier, Severine
    Tanguy, Myriam
    Kadaoui, Khalil A.
    Caubet, Cecile
    Sansonetti, Philippe
    Corthesy, Blaise
    Phalipon, Armelle
    [J]. JOURNAL OF IMMUNOLOGY, 2009, 183 (09) : 5879 - 5885
  • [5] Microbiota, Liver Diseases, and Alcohol
    Cassard, Anne-Marie
    Gerard, Philippe
    Perlemuter, Gabriel
    [J]. MICROBIOLOGY SPECTRUM, 2017, 5 (04):
  • [6] Gene expression profiling gut microbiota in different races of humans
    Chen, Lei
    Zhang, Yu-Hang
    Huang, Tao
    Cai, Yu-Dong
    [J]. SCIENTIFIC REPORTS, 2016, 6
  • [7] Gut dysbiosis in acute-on-chronic liver failure and its predictive value for mortality
    Chen, Yanfei
    Guo, Jing
    Qian, Guirong
    Fang, Daiqiong
    Shi, Ding
    Guo, Lihua
    Li, Lanjuan
    [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2015, 30 (09) : 1429 - 1437
  • [8] The Impact of the Gut Microbiota on Human Health: An Integrative View
    Clemente, Jose C.
    Ursell, Luke K.
    Parfrey, Laura Wegener
    Knight, Rob
    [J]. CELL, 2012, 148 (06) : 1258 - 1270
  • [9] Intestinal dysbiosis and reduced immunoglobulin-coated bacteria associated with coeliac disease in children
    De Palma, Giada
    Nadal, Inmaculada
    Medina, Marcela
    Donat, Ester
    Ribes-Koninckx, Carmen
    Calabuig, Miguel
    Sanz, Yolanda
    [J]. BMC MICROBIOLOGY, 2010, 10
  • [10] Interactions and competition within the microbial community of the human colon: links between diet and health
    Flint, Harry J.
    Duncan, Sylvia H.
    Scott, Karen P.
    Louis, Petra
    [J]. ENVIRONMENTAL MICROBIOLOGY, 2007, 9 (05) : 1101 - 1111