Journal
VIROLOGY
Volume 375, Issue 2, Pages 480-491Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2008.02.030
Keywords
coxsackievirus; human myocarditis; defective enterovirus; 5' terminal deletion
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Funding
- NCRR NIH HHS [P20 RR018788-010002, P20 RR018788] Funding Source: Medline
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Enteroviruses can induce human myocarditis, which can be modeled in mice inoculated with group B coxsackieviruses (CVB) and in which CVB evolve to produce defective, terminally deleted genomes. The 51 non-translated region (NTR) was enzymatically amplified from heart tissue of a fatal case of enterovirus-associated myocarditis in Japan in 2002. While no intact 51 viral genomic termini were detected, 51 terminal deletions ranged in size from 22 to 36 nucleotides. Sequence of the 5' third of this viral genome is of a modern strain, closely related to CVB2 strains isolated in Japan in 2002. A CVB3 chimera containing the 5' NTR with a 22 nt deletion produced progeny virus upon transfection of HeLa cells. When the 51 22 nucleotide deletion was repaired, the virus induced myrocarditis in mice and replicated like wild type virus in murine heart cells. This is the first report of these naturally-occurring defective enteroviral genomes in human myocarditis. (c) 2008 Elsevier Inc. All rights reserved.
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