1. Coxsackievirus B3infection and its mutation in Keshan disease
- Author
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Bo Sun, Zhi-Tao Zhao, Fei Sun, Guang-Sheng Li, Liqun Ren, and Xiang-Jun Li
- Subjects
Adult ,Cardiomyopathy, Dilated ,Male ,Adolescent ,viruses ,Molecular Sequence Data ,Virulence ,Autopsy ,In situ hybridization ,Gene mutation ,Biology ,medicine.disease_cause ,Genome ,Keshan disease ,Enterovirus Infections ,medicine ,Humans ,In Situ Hybridization ,Mutation ,Base Sequence ,Reverse Transcriptase Polymerase Chain Reaction ,Gastroenterology ,virus diseases ,RNA ,General Medicine ,biochemical phenomena, metabolism, and nutrition ,medicine.disease ,Virology ,Enterovirus B, Human ,Basic Research ,Child, Preschool ,RNA, Viral ,Female ,5' Untranslated Regions - Abstract
AIM: To investigate coxsackievirus B3 infection and its gene mutation in Keshan disease. METHODS: The expression of Coxsackievirus B3 RNA was detected in autopsy specimens of acute (12 cases), sub-acute (27 cases) and chronic (15 cases) Keshan disease by in situ hybridization. In sub-acute Keshan disease specimens, 3 cases with positive result by in situ hybridization were selected RT-PCR analysis. The DNA segments were then sequenced. RESULTS: Coxsackievirus B3 RNA was detected in the cytoplasm of myocardiocyte. The positive rate was 83% in acute, 67% in sub-acute and 80% in chronic Keshan disease. In the conservative region of Coxsackievirus B3 genome, there was a mutation in 234 (C-T) compared to the non-cardiovirulent strain, CVB3/0. CONCLUSION: Coxsackievirus B3 RNA can survive and replicate in heart muscle of Keshan disease, which may play an important role in the occurrence of Keshan disease. The possible mechanism of occurrence of Keshan disease is associated with point a mutation in Coxsackievirus B3 genome.
- Published
- 2004
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