Objective: To examine the prevalence and the sequence of the genes of new genotypes of hepatitis G virus (HGV) in Guangxi, China.

Methods: Serum samples were collected from 85 intravenous drug abusers (IVDAs), 80 patients with liver diseases (PLDs) and 50 blood donors (BDs). All sera (n=215) were tested by using EIA for HBsAg, anti-HCV and anti-HIV, and by using nested PCR for HGV RNA. In 62 subjects positive for HGV, HGV RNA was sequenced, and a phylogenetic tree was constructed for analyzing genotypes of HGV.

Results: HGV RNA was detected in 85 of 215 serum samples (39.53%). The positivity rates for HBsAg, anti-HCV and anti-HIV were 39.07%, 42.79% and 0, respectively. First, 11 nucleotide sequences were determined and the isolates were grouped into three clusters with HGV. 5 of 11 HGV isolates clustered in a distinct phylogenetic branch (genotype Asia) which was different from the described GBV-C and HGV sequences, suggesting the presence of a new genotype of HGV in this locality. Second, 51 nucleotide sequences were determined and analyzed for their genotypes of HGV, and showed genotype GBV-C (3.23%), genotype HGV 30-65% and new genotype (genotype Asia) 64.51%, respectively.

Conclusions: There were subgenotypes in 3 genotypes of HGV; The predominant genotypes of HGV were genotype Asia and genotype HGV among IVDAs, PLDs, and BDs patients in Guangxi, China.

Download full-text PDF

Source

Publication Analysis

Top Keywords

hgv
14
hgv rna
12
genotype asia
12
genotype hgv
12
genotypes hgv
12
genotype
9
hepatitis virus
8
serum samples
8
hbsag anti-hcv
8
anti-hcv anti-hiv
8

Similar Publications

DSG2, encoding desmoglein-2, is one of the causative genes of arrhythmogenic cardiomyopathy. We previously identified a homozygous DSG2 p.Arg119Ter stop-gain variant in a patient with juvenile-onset cardiomyopathy and advanced biventricular heart failure.

View Article and Find Full Text PDF

Assessment of UK Heavy Goods Vehicle drivers' lifestyle behaviours: a cross-sectional study.

J Occup Environ Med

December 2024

School of Sport, Exercise and Health Sciences, Loughborough University, Loughborough, Leicestershire, United Kingdom.

Objective: Heavy Goods Vehicle (HGV) drivers face difficult working conditions, promoting unhealthy lifestyle behaviours which are associated with an elevated prevalence of long-term health conditions.

Methods: 109 drivers across the UK completed an online survey investigating differences in lifestyle behaviours between drivers with (N = 54) and without obesity (N = 55), including differences on work and non-workdays using an exploratory data analysis approach.

Results: Drivers with obesity (49.

View Article and Find Full Text PDF
Article Synopsis
  • - Familial adenomatous polyposis (FAP) is an inherited condition linked to mutations in the APC gene, leading to many colorectal polyps and a high risk of colorectal cancer, usually diagnosed through colonoscopy.
  • - Recent advancements like whole-genome array comparative genomic hybridization (a-CGH) have improved the detection of genetic imbalances associated with FAP, allowing for more precise patient assessment.
  • - In a study focusing on patients with complete APC gene deletions, researchers found varied genetic loss sizes and identified EPB41L4A as a candidate gene that may be linked to neurodevelopmental issues in some patients.
View Article and Find Full Text PDF
Article Synopsis
  • Bryant-Li-Bhoj syndrome (BLBS) is a genetic disorder linked to mutations in the H3F3A and H3F3B genes, leading to developmental issues and physical abnormalities.
  • A Japanese patient was identified with a new variant (p.A48G) in the H3F3A gene, showcasing additional symptoms not previously associated with BLBS, specifically neonatal myoclonus.
  • This case expands our understanding of the range of symptoms associated with BLBS, highlighting the variability in how the syndrome can manifest.
View Article and Find Full Text PDF

We report a case of a fetus with short-rib thoracic dysplasia (SRTD) with polydactyly that also presented with atypical severe acro-mesomelic ossification defects. Genetic analysis using massively parallel sequencing of a skeletal dysplasia panel revealed compound heterozygous variants in DYNC2H1. This clinical report highlights the challenges associated with diagnosing the diverse phenotypes in the SRTD group and emphasizes the importance of genetic surveillance with a targeted gene panel for accurate diagnosis.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!