Correlation between gastrointestinal fungi and varying degrees of
chronic hepatitis B virus infection
Yu Chen, Zhenjing Chen, Renyong Guo, Nan Chen, Haifeng Lu, Shuai Huang,
Jie Wang, Lanjuan Li
⁎
State Key Laboratory for Diagnosis and Treatment of Infectious Disease, First Affiliated Hospital, College of Medicine,
Zhejiang University, Hangzhou, Zhejiang 310003, PR China
Received 10 December 2009; accepted 9 April 2010
Abstract
This study aims to compare the diversity of intestinal fungal microbiota in patients with different degrees of chronic hepatitis B virus
(HBV) infection. Culture-independent and culture-dependent methods were performed on 38 patients with hepatitis B cirrhosis, 35 patients
with chronic hepatitis B, 33 HBV carriers, and 55 healthy volunteers. An overall fungal biodiversity of 37 different operational taxonomic
units was found in the clone libraries; only Candida spp. and Saccharomyces cerevisiae were obtained by the culture-dependent analysis.
There was a higher richness of fungal species in patients with hepatitis B cirrhosis than in patients with chronic hepatitis B, and the latter was
higher than that in HBV carriers and healthy volunteers. There was little difference in enteric fungal diversity between HBV carriers and
healthy volunteers. The results indicate that the diversity of enteric fungi was positively correlated with the disease progression of patients
with different degrees of chronic HBV infection.
© 2011 Elsevier Inc. All rights reserved.
Keywords: 18S rDNA; Culture-independent method; Diversity; Intestinal fungi; HBV infection
1. Introduction
Hepatitis B is a major global health problem. About 2
billion people have been infected with the hepatitis B virus
(HBV), and more than 350 million have chronic liver
infections. According to the Hepatitis B (2000) Fact Sheet of
the World Health Organization, hepatitis B is endemic in
China and other parts of Asia, where 8% to 10% of the adult
population is chronically infected. Altered intestinal micro-
biota is a common complication in liver disease (Norman and
Pirlich, 2008).
Human intestinal microecology plays an essential role in
metabolic activities, immunity, and trophic function (Blaut
and Clavel, 2007; Guarner and Malagelada, 2003). Human
intestinal microbiota was recently understood to constitute a
novel “organ” integral to human health and disease (Eckburg
et al., 2005; O'Hara and Shanahan, 2006). The adult human
gastrointestinal tract contains bacteria, archaea, yeasts, and
filamentous fungi. To date, most molecular studies have
characterized gastrointestinal bacterial diversity, but the
fungal community has been largely neglected (Guarner and
Malagelada, 2003; Rajilic-Stojanovic et al., 2007; Zoetendal
et al., 2008).
Due to the development of molecular biology instru-
ments, such as polymerase chain reaction (PCR) amplifica-
tion and small subunit ribosomal RNA-based technologies, a
more comprehensive phylogenetic framework exists for
identifying microbial diversity in intestinal microbiota. With
the application of culture-independent methods, the diversity
of bacteria within the human gut was documented to be
approximately 800 species (Backhed et al., 2005) instead of
400 to 500 cultured bacterial species as previously assumed
(Moore and Holdeman, 1974).
The first culture-independent analysis of mammalian
enteric fungi revealed unprecedented diversity and multiple
fungal species in murine gut (Scupham et al., 2006). The
latest research showed that the gastrointestinal eukaryotic
Available online at www.sciencedirect.com
Diagnostic Microbiology and Infectious Disease 70 (2011) 492 – 498
www.elsevier.com/locate/diagmicrobio
⁎
Corresponding author. Tel.: +86-571-87236458; fax: +86-571-
87236459.
E-mail address: ljli@zju.edu.cn (L. Li).
0732-8893/$ – see front matter © 2011 Elsevier Inc. All rights reserved.
doi:10.1016/j.diagmicrobio.2010.04.005