High prevalence of enteroviral genomic sequences in myocardium from cases of endemic cardiomyopathy (Keshan disease) in China

被引:34
作者
Li, Y
Peng, T
Yang, Y
Niu, C
Archard, LC
Zhang, H
机构
[1] Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, Mol Pathol Sect, London SW7 2AZ, England
[2] Shanghai Med Univ, Zhongshan Hosp, Shanghai Inst Cardiovasc Dis, Minist Publ Hlth,Key Lab Viral Heart Dis, Shanghai 200032, Peoples R China
[3] Chuxiong Inst Keshan Dis, Chuxiong, Yunnan, Peoples R China
关键词
enterovirus; coxsackievirus; cardiomyopathy; Keshan disease;
D O I
10.1136/heart.83.6.696
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-To verify the aetiological involvement of enterovirus and identify the viral genomic sequences in Keshan disease. Design-Formalin fixed, paraffin embedded myocardial necropsy tissue samples were collected in Keshan disease endemic regions. Fourteen cases with a histologically confirmed diagnosis of subacute or chronic Keshan disease were studied. Control tissue included 10 samples of myocardium from cases of cerebral trauma and one from accidental acid intoxication. One sample from a case of enteroviral myocarditis was used as a positive control. The presence of viral genomic RNA was investigated using an established reverse transcription nested polymerase chain reaction (PCR) coupled with direct nucleotide sequencing. Further investigations of PCR positive samples included in situ antigen detection or hybridisation to confirm positive results. Results-Nine of 14 myocardial samples from Keshan disease cases and the positive control were positive for the enteroviral RNA. All the controls were negative. Six of the PCR positive samples were investigated further by in situ enteroviral antigen or RNA detection and all were positive. DNA sequencing of six representative PCR products confirmed that they were homologous to the 5' non-translated region of enteroviral genomic RNA. Five had highest homology to coxsackievirus B genotypes and one was identical to poliovirus type 3. Conclusions-These results support an aetiological role for enteroviral infection in Keshan disease. Nucleotide sequence data suggest that coxsackievirus B or coxsackie B like viruses are often involved in Keshan disease.
引用
收藏
页码:696 / 701
页数:6
相关论文
共 41 条
[1]   MOLECULAR PROBES FOR DETECTION OF PERSISTING ENTEROVIRUS INFECTION OF HUMAN HEART AND THEIR PROGNOSTIC VALUE [J].
ARCHARD, LC ;
BOWLES, NE ;
CUNNINGHAM, L ;
FREEKE, CA ;
OLSEN, EGJ ;
ROSE, ML ;
MEANY, B ;
WHY, HJF ;
RICHARDSON, PJ .
EUROPEAN HEART JOURNAL, 1991, 12 :56-59
[2]   Characterization of Coxsackie B virus RNA in myocardium from patients with dilated cardiomyopathy by nucleotide sequencing of reverse transcription-nested polymerase chain reaction products [J].
Archard, LC ;
Khan, MA ;
Soteriou, BA ;
Zhang, HY ;
Why, HJF ;
Robinson, NMK ;
Richardson, PJ .
HUMAN PATHOLOGY, 1998, 29 (06) :578-584
[3]   Enteroviral protease 2A cleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy [J].
Badorff, C ;
Lee, GH ;
Lamphear, BJ ;
Martone, ME ;
Campbell, KP ;
Rhoads, RE ;
Knowlton, KU .
NATURE MEDICINE, 1999, 5 (03) :320-326
[4]   RAPID GENOMIC EVOLUTION OF A NONVIRULENT COXSACKIEVIRUS B3 IN SELENIUM-DEFICIENT MICE RESULTS IN SELECTION OF IDENTICAL VIRULENT ISOLATES [J].
BECK, MA ;
SHI, Q ;
MORRIS, VC ;
LEVANDER, OA .
NATURE MEDICINE, 1995, 1 (05) :433-436
[5]  
Becker K, 1998, J CARDIOTHOR VASC AN, V12, P13
[6]  
BOWLES NE, 1986, LANCET, V1, P1120
[7]   REVERSION TO NEUROVIRULENCE OF THE LIVE-ATTENUATED SABIN TYPE-3 ORAL POLIOVIRUS VACCINE [J].
CANN, AJ ;
STANWAY, G ;
HUGHES, PJ ;
MINOR, PD ;
EVANS, DMA ;
SCHILD, GC ;
ALMOND, JW .
NUCLEIC ACIDS RESEARCH, 1984, 12 (20) :7787-7792
[8]  
*CHUX KESH DIS SCI, 1988, P COMPR SCI INV KD C, P1
[9]   PERSISTENCE OF ENTEROVIRAL RNA IN CHRONIC FATIGUE SYNDROME IS ASSOCIATED WITH THE ABNORMAL PRODUCTION OF EQUAL AMOUNTS OF POSITIVE AND NEGATIVE STRANDS OF ENTEROVIRAL RNA [J].
CUNNINGHAM, L ;
BOWLES, NE ;
LANE, RJM ;
DUBOWITZ, V ;
ARCHARD, LC .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :1399-1402
[10]  
*DEP MICR, 1978, J CHONGQING MED COLL, V2, P1