Pathogenesis of coxsackievirus B2 in mice: characterization of clinical isolates of the coxsackievirus B2 from patients with myocarditis and aseptic meningitis in Korea.
10.4142/jvs.2017.18.4.457
- Author:
Jiyoung HONG
1
;
Bunghak KANG
;
Sanggu YEO
;
Youngmee JEE
;
Jae Hak PARK
Author Information
1. Laboratory Animal Medicine, College of Veterinary Medicine, Seoul National University, Seoul 08826, Korea. pjhak@snu.ac.kr
- Publication Type:Original Article
- Keywords:
cardiovirulence;
coxsackievirus B2;
myocarditis;
pathogenesis
- MeSH:
Animals;
Base Sequence;
Enterovirus;
Genome;
Heart Failure;
Humans;
Inflammation;
Korea*;
Male;
Meningitis, Aseptic*;
Mice*;
Myocarditis*;
Pathology;
Phenotype;
Virology
- From:Journal of Veterinary Science
2017;18(4):457-464
- CountryRepublic of Korea
- Language:English
-
Abstract:
Group B coxsackieviruses (CVBs) are a group of common human pathogens producing various clinical symptoms. Although the virology of CVB is well known, there is limited information on viral pathogenesis and the relationship between clinical symptoms and viral phenotype, particularly for CVB type 2 (CVB2). In 2004 in Korea, two CVB2 strains were isolated: CB2/04/279 from stool of an acute myocarditis patient with heart failure and CB2/04/243 from an aseptic meningitis patient. In this study, a high degree of homology was observed between the CB2/04/279 and CB2/04/243 full genome sequences. The two Korean CVB2 isolates had 93.1% homology compared to 82.1%–82.5% nucleotide sequence identity with the cardiovirulence-associated reference CVB strain Ohio-1 (CVB/O). CVB2-induced pathogenesis was analyzed, focusing on virus-induced pathology of various tissues in 4-week-old BALB/c inbred male mice. Myocarditis developed and extensive pancreatic inflammation was observed in all mice infected with CB2/04/279 or CVB/O, but not in animals infected with CB2/04/243. This is the first report of the full-genomic sequence and pathogenesis of the CVB2 strain isolated from an acute myocarditis patient in Korea.
