Frontiers in Microbiology (Mar 2020)

Featured Gut Microbiomes Associated With the Progression of Chronic Hepatitis B Disease

  • Zhangran Chen,
  • Zhangran Chen,
  • Zhangran Chen,
  • Yurou Xie,
  • Yurou Xie,
  • Fei Zhou,
  • Bangzhou Zhang,
  • Bangzhou Zhang,
  • Jingtong Wu,
  • Jingtong Wu,
  • Luxi Yang,
  • Shuangbin Xu,
  • Robert Stedtfeld,
  • Qiongyun Chen,
  • Qiongyun Chen,
  • Jingjing Liu,
  • Xiang Zhang,
  • Hongzhi Xu,
  • Hongzhi Xu,
  • Jianlin Ren,
  • Jianlin Ren

DOI
https://doi.org/10.3389/fmicb.2020.00383
Journal volume & issue
Vol. 11

Abstract

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Dysbiosis of gut microbiota during the progression of HBV-related liver disease is not well understood, as there are very few reports that discuss the featured bacterial taxa in different stages. The aim of this study was to reveal the featured bacterial species whose abundances are directly associated with HBV disease progression, that is, progression from healthy subjects to, chronic HBV infection, chronic hepatitis B to liver cirrhosis. Approximately 400 fecal samples were collected, and 97 samples were subjected to 16S rRNA gene sequencing after age and BMI matching. Compared with the healthy individuals, significant gut microbiota alterations were associated with the progression of liver disease. LEfSe results showed that the HBV infected patients had higher Fusobacteria, Veillonella, and Haemophilus abundance while the healthy individuals had higher levels of Prevotella and Phascolarctobacterium. Indicator analysis revealed that 57 OTUs changed as the disease progressed, and their combination produced an AUC value of 90% (95% CI: 86–94%) between the LC and non-LC groups. In addition, the abundances of OTU51 (Dialister succinatiphilus) and OTU50 (Alistipes onderdonkii) decreased as the disease progressed, and these results were further verified by qPCR. The LC patients had the higher bacterial network complexity, which was accompanied with a lower abundance of potential beneficial bacterial taxa, such as Dialister and Alistipes, while they had a higher abundance of pathogenic species within Actinobacteria. The compositional and network changes in the gut microbiota in varied CHB stages, suggest the potential contributions of gut microbiota in CHB disease progression.

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