II. Existing variations on the gene structure of hepatitis E virus strains from some regions of China
The isolation and identification of the 87A strain of hepatitis E virus (HEV) by means of cell culture have been described previously. This paper reports the nucleotide sequence of a portion of this HEV strain. The RNA extracted from the supernatants of the different passages of the 87A strain cultu...
Gespeichert in:
Veröffentlicht in: | Journal of medical virology 1995-12, Vol.47 (4), p.303-308 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The isolation and identification of the 87A strain of hepatitis E virus (HEV) by means of cell culture have been described previously. This paper reports the nucleotide sequence of a portion of this HEV strain. The RNA extracted from the supernatants of the different passages of the 87A strain cultured in the A549 cell line was reverse‐transcribed (RT) to cDNA, and then the polymerase chain reaction (PCR) amplification was carried out using the primers of HEV ET1.l region. The PCR products from 1) the supernatant of the infected cells at the fourth passage, 2) the virus concentrated by polyethylene glycol (PEG) precipitation at the tenth passage, and 3) the virus purified by a sucrose gradient at the tenth pas sage were sequenced. In addition, three other PCR products obtained from sera of acute hepa titis E patients in Beijing (B‐9) and Guangzhou (G‐9 and G‐20) were also sequenced. The nucle otide sequences of the above four strains of HEV (located in the genome from positions 4545–4754) were compared to those of some reported HEV strains. The nucleotide sequences of the B‐9 strain and the 87A strain were similar to the Burmese strain and may belong to the same branch of HEV. The nucleotide sequences of the G‐9 strain and the G‐20 strain were a novel and unique branch. The Chinese HEV strains are multiplex and variable in gene structure. © Wiley‐Liss, Inc. |
---|---|
ISSN: | 0146-6615 1096-9071 |
DOI: | 10.1002/jmv.1890470403 |