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Objective: To determine the distribution of genotype IV among hepatitis E virus (HEV) infections in Wuhan by sequencing the open reading frame (ORF) 3 gene of HEV clinical isolates.
Methods: Serum samples were collected from 103 individuals who tested positive for the anti-HEV IgM antibody, and total HEV RNA was extracted for targeted gene sequencing analysis. Reverse transcription-nested polymerase chain reaction (PCR) was used to amplify two fragments of the ORF3 gene (5020 to 5392 nt and 5347 to 5956 nt, EF570133). The two PCR products were sequenced and the sequences were stitched with the ContigExpress program and used to determine the HEV genotype.
Results: Both ORF3 gene fragments were amplified in 18 out of the 103 anti-HEV IgM-positive serum samples. These 18 HEV isolates shared 92.5% to 99.4% identity with each other at the nucleotide level. Nucleotide sequence homology analysis of the HEV genotypes I, II, III, and IV indicated the highest homology was with genotype IV; specifically, homology with genotype I was 83.5% to 86.7%, with genotype II was 83.2% to 85.2%, with genotype III was 84.6% to 87.2%, and with genotype IV was 92.0% to 96.5%.
Conclusion: Targeted sequencing of the HEV ORF3 gene facilitated genotyping of clinical isolates. Using this method, it was determined that nearly 20% of HEV clinical isolates from Wuhan belong to genotype IV.
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http://dx.doi.org/10.3760/cma.j.issn.1007-3418.2012.10.012 | DOI Listing |
Arch Virol
August 2025
Chenzhou Tobacco Company of Hunan Province, 423000, Chenzhou City, Hunan Province, P.R. China.
In this study, a novel double-stranded RNA (dsRNA) mycovirus was isolated from the phytopathogenic fungus Fusarium commune, the causal agent of tobacco root rot, and designated "Fusarium commune chrysovirus 1" (FcCV1). The complete genome of FcCV1 consists of five dsRNA fragments with lengths of 3670 bp, 3242 bp, 2866 bp, 2829 bp, and 1258 bp, designated as dsRNA1 to dsRNA5 according to their size. Each of these five dsRNA segments contains a single open reading frame (ORF), designated ORF1 to ORF5, with strictly conserved termini in their 5' and 3' untranslated regions.
View Article and Find Full Text PDFMicroorganisms
July 2025
Department of Bioprocess Engineering (150k), Institute of Food Science and Biotechnology, University of Hohenheim, Fruwirthstr. 12, 70599 Stuttgart, Germany.
DSM 100043 had been previously proven to produce a novel glucoselipid biosurfactant which has a very low critical micelle concentration (CMC) as well as very good stability against a wide range of pH, temperature, and salinity. In this study, we performed a function-based library screening from a DSM 100043 genome library to identify responsible genes for biosynthesis of this glucoselipid. The identified open reading frames (ORFs) were cloned into several constructs in for gene permutation analysis and the individual products were analyzed using high-performance thin-layer chromatography (HPTLC).
View Article and Find Full Text PDFProc Natl Acad Sci U S A
July 2025
Department for Molecular and Medical Virology, Ruhr University Bochum, Bochum 44801, Germany.
Mycophenolic acid (MPA) is commonly used in immunosuppressive regimens following solid organ transplantation. We demonstrate that MPA treatment reproducibly inhibits the replication of a range of viruses, including severe respiratory syndrome coronavirus 2 (SARS-CoV-2). Mechanistically, we identified cellular guanosine triphosphate pool depletion as a key mediator of this antiviral effect.
View Article and Find Full Text PDFNPJ Vaccines
June 2025
Virology Division, Department of Biomolecular Health Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, 3584 CL, The Netherlands.
Porcine epidemic diarrhea virus (PEDV) causes severe diarrheal disease with high mortality in neonatal piglets. To protect suckling piglets, maternal vaccination strategies that induce lactogenic immunity in sows are crucial. To develop modified live vaccine candidates, we generated recombinant viruses with genome alterations such as deletion of the ORF3 accessory gene (ΔORF3), deletion of the N-terminal sialic acid binding domain of the spike glycoprotein (S), and rearrangement of the spike, envelope, matrix and nucleocapsid genes (SEMN → ESMN) in the viral genome.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
June 2025
Department of Molecular Genetics and Microbiology, Duke Center for Virology, Duke University School of Medicine, Durham, NC 27710.
Herpesviruses, including Epstein-Barr virus (EBV) - a human oncogenic virus and essential trigger of multiple sclerosis - must bypass host DNA-sensing mechanisms to establish lifelong, latent infection. Therefore, herpesviruses encode viral proteins to disrupt key host factors involved in DNA sensing and viral restriction. The first viral latency protein expressed, EBNA-LP, is essential for transformation of naïve B cells and establishment of viral gene expression, yet its role in evading host defenses remains unclear.
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