AI Article Synopsis

  • Korea experienced a nationwide outbreak of hepatitis A from 2006 to 2008, focusing on genotypes IA and IIIA among 595 symptomatic patients.
  • Out of 556 participants, genotypic analysis showed that both IA and IIIA genotypes were equally prevalent, but there was a shift from predominantly IA to IIIA over the study period.
  • Patients with genotype IIIA exhibited more severe symptoms and higher liver enzyme levels compared to those infected with genotype IA, indicating potentially worse clinical outcomes for IIIA infections.

Article Abstract

Korea has recently experienced a nationwide outbreak of hepatitis A. This study aimed to investigate hepatitis A virus (HAV) genotypes and to compare clinical features between patients infected with HAV genotype IA and those with genotype IIIA. From September 2006 to August 2008, 595 patients with symptomatic hepatitis A were enrolled prospectively in four hospitals in Korea. Among them, 556 patients participated in this study by providing serum or stool samples for genotypic analysis. HAV RNA was detected in 499 patients (89.7%). Major genotypes included IA (n = 244, 48.9%) and IIIA (n = 244, 48.9%), and the remaining genotype was IB (n = 11, 2.2%). From September 2006 to August 2007, the distribution of genotypes IA and IIIA were 64.6% and 35.6%, respectively, which changed to 42.3% and 54.6%, respectively, from September 2007 to August 2008, indicating change of circulating HAV genotypes in the study period from IA to IIIA. Major patterns of amino acid substitution in the VP3/VP1 junction region were observed at position 512 (P → L) in genotype IA and at 520 (R → K) in genotype IIIA. Patients with genotype IIIA infection showed significantly higher aminotransferase levels, prothrombin time, and leukocyte count, with more severe symptoms than those with genotype IA at the time of admission. These results suggest the occurrence of a change of circulating HAV genotypes in recent community-wide outbreaks of hepatitis A in Korea, and genotype IIIA infection, compared with genotype IA infection, might show more severe clinical manifestations.

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http://dx.doi.org/10.1002/jmv.22229DOI Listing

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