Chinese journal of virology 

About: Chinese journal of virology is an academic journal. The journal publishes majorly in the area(s): Virus & Gene. It has an ISSN identifier of 1000-8721. Over the lifetime, 669 publications have been published receiving 2103 citations.

Porcine aminopeptidase N is a functional receptor for the PEDV coronavirus

Abstract: Porcine epidemic diarrhea virus (PEDV) causes lethal diarrhea in piglets that leads to great economic losses in East Asia. It was reported that aminopeptidase N (APN) was the receptor for Transmissible gastroenteritis virus (TGEV), Human coronavirus 229E (HCoV-229E) and Feline coronavirus (FeCoV) which all belonged to group I coronavirus including PEDV. It was also confirmed previously that porcine aminopeptidase N (pAPN) could bind to PEDV, and anti-pAPN antibodies could inhibit the combination. To investigate whether pAPN was a receptor for PEDV, we transfected MDCK cells with porcine aminopeptidase (pAPN) cDNA and this enabled non-susceptible cells to support PEDV replication and serial viral propagation. Moreover, the infection was blocked by antibodies against pAPN, implying the critical role of pAPN during virus entry. In addition, immunofluorescence assays for detection of pAPN and PEDV antigens, together with neutralization assays using antibodies against pAPN, further confirmed the correlation between pAPN expression and viral replication in pAPN-transfected MDCK cells. These results indicated that pAPN is a functional receptor for PEDV.

Detection and sequences analysis of bovine hepatitis E virus RNA in Xinjiang Autonomous Region

Abstract: Reverse transcription-nested polymerase chain reaction (RT-nPCR) was used to detect HEV (Hepatitis E virus, HEV) RNA in dung or anus-swab samples collected from the cows with the positive anti-HEV antibodies in dairy farms in Xinjiang Autonomous Region. 7 of 60 (11.67%) cows were positive for HEV RNA in one farm. 1 of 31 (3.23%) cows was positive in the other farm. PCR amplification products were cloned, sequenced and analyzed. The result showed that the homology among the 8 bovine HEV ORF2 189bp nucleotide amplification sequences was 96.3%-100.0%, suggesting the same genotype. Compared with HEV genotype 1, 2, 3 and 4 corresponding 189 bp nucleotide sequences, the average homology was 78.5%-86.4%, 81.7%-83.8%, 79.1%-85.3% and 84.3%-95.8% respectively. The maximum homology between 8 nucleotide amplification sequences and one sequence of genotype 4 was 93.2%-95.8%. Based on the sequence of the nucleic acid fragments, a phylogenetic tree was constructed. It was illustrated that 8 bovine HEV ORF2 189bp nucleotide amplification sequences in this study and human C5 strain, swine swC3, swXJ strain belonged to genotype 4. The finding suggested that infection of HEV probably existed in the cow group in Xinjiang Autonomous Region and the cow might be a new animal host except swine in origin of HEV infection.

[Isolation, identification and characterization of SFTS bunyavirus from ticks collected on the surface of domestic animals].

Abstract: To understand the maintenance and transmission of SFTS virus, the potential vector ticks were collected from sheep, cattle and dogs in the endemic areas of SFTSV in Shandong Province. Among the collected ticks, the dominant species was H. longicornis ticks. Real-time PCR for RNA detection, virus isolation and characterization, genomic sequencing, phylogenetic and antigenic analysis were performed in this investigation. The results showed that the SFTS viral RNA was detected in 2.14% H. longicornis, and a SFTS virus was isolated from one of viral RNA positive ticks collected from sheep. Whole genome analysis of the SFTSV isolates with 11 human-origin SFTS virus revealed a highly pairwise similarity, and the growth curve analysis showed nearly identical in virus yield and the dynamic of virus reproduction compared to human derived viral isolates. Immunofluorescence and neutralization test showed identical serological reaction character of the two different origin viral strains. In this study, the characters of a SFTSV isolate was firstly described, which suggested that the tick species H. longicornis acting important vector role in the transmission of SFTS virus.

Identification of a new subgroup of avian leukosis virus isolated from Chinese indigenous chicken breeds

Abstract: In order to clarify Avian leukosis virus (ALV) characteristics from Chinese native chicken breeds, three ALV JS11C1, JS11C2 and JS11C3 were isolated from Chinese native breed "luhua" by inoculation of DF1 cell culture and detection of p27 antigen. Using PCR amplification of env gene, the amplified gp85 genes were analyzed and compared to all six chicken ALV subgroups reported. The gp85 genes of these three viruses were 1 005bp in length and encoded 335 amino acids, and the gp37 genes were 609bp and encoded 203 amino acids. The homology of gp85 among these three isolated strains was 91.9%-97.0%. Comparing to 18 stains of subgroup A, B, C, D, E published in GenBank, the homology was only in the range of 77.7%-84.6%, significantly lower than the gp85 homology observed within the common chicken subgroups A (88.2%-98.5%), B (91.6%-98.8%), and E (97.9%-99.4%). The gp85 homology compared with subgroup J was only 34.2%-36.5%. These results suggested that three isolated strains from Chinese native breed "luhua" belong to a new subgroup different from all six known subgroups from Chickens, and thus designated as subgroup K.