Unknown

Dataset Information

0

Genetic characteristics and pathogenicity of human hepatitis E virus in Nanjing, China.


ABSTRACT: To investigate the genetic characteristics and pathogenicity of hepatitis E virus (HEV) and assess the potential risk factors for sporadic hepatitis E.Sixty-two serum samples from the patients with acute hepatitis E were collected, including 23 cases coinfected with hepatitis B virus. Anti-HEV detection and partial HEV RNA amplification were performed by enzyme immunoassays and reverse transcription-nested polymerase chain reaction (RT-nPCR) method, respectively, and PCR products were sequenced. The isolated human HEV sequences were analyzed phylogenetically.The positive rate of serum HEV RNA were 21.0% (13/62), including 5 cases of liver failure. All the 13 isolates shared a 82.1%-98.0% nucleotide homology with each other and had identities of 74.7%-81.0%, 75.3%-78.6%, 75.3%-80.0% and 82.1%-96.1% with the corresponding regions of HEV genotypes 1-4, respectively. The human HEV strain GS-NJ-12 shared a 100% nucleotide identity with the swine HEV strain swIM6-43 isolated from Inner Mongolia, China.Swine may be a principal risk factor for occurrence of sporadic hepatitis E in eastern China, and genotype 4 HEV can induce acute liver failure.

SUBMITTER: Geng JB 

PROVIDER: S-EPMC3297057 | biostudies-literature | 2012 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Genetic characteristics and pathogenicity of human hepatitis E virus in Nanjing, China.

Geng Jia-Bao JB   Wang Mao-Rong MR   Wang Ling L   Wang Jie J   Yang Zhi-Guo ZG   Cheng Yan Y   Qiao Fei F   Wang Min M  

World journal of gastroenterology 20120301 9


<h4>Aim</h4>To investigate the genetic characteristics and pathogenicity of hepatitis E virus (HEV) and assess the potential risk factors for sporadic hepatitis E.<h4>Methods</h4>Sixty-two serum samples from the patients with acute hepatitis E were collected, including 23 cases coinfected with hepatitis B virus. Anti-HEV detection and partial HEV RNA amplification were performed by enzyme immunoassays and reverse transcription-nested polymerase chain reaction (RT-nPCR) method, respectively, and  ...[more]

Similar Datasets

| S-EPMC3810912 | biostudies-literature
| S-EPMC4458779 | biostudies-literature
| S-EPMC3026811 | biostudies-literature
| S-EPMC5068972 | biostudies-literature
| S-EPMC6232144 | biostudies-literature
| S-EPMC2815617 | biostudies-literature
| S-EPMC4866570 | biostudies-literature