ONGOING ENTEROVIRUS-INDUCED MYOCARDITIS IS ASSOCIATED WITH PERSISTENT HEART-MUSCLE INFECTION - QUANTITATIVE-ANALYSIS OF VIRUS-REPLICATION, TISSUE-DAMAGE, AND INFLAMMATION
被引:396
作者:
KLINGEL, K
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机构:UNITE FORMAT RECH SCI PHARMACEUT,DEPT MICROBIOL,F-14000 CAEN,FRANCE
KLINGEL, K
HOHENADL, C
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机构:UNITE FORMAT RECH SCI PHARMACEUT,DEPT MICROBIOL,F-14000 CAEN,FRANCE
HOHENADL, C
CANU, A
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机构:UNITE FORMAT RECH SCI PHARMACEUT,DEPT MICROBIOL,F-14000 CAEN,FRANCE
CANU, A
ALBRECHT, M
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机构:UNITE FORMAT RECH SCI PHARMACEUT,DEPT MICROBIOL,F-14000 CAEN,FRANCE
ALBRECHT, M
SEEMANN, M
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SEEMANN, M
MALL, G
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MALL, G
KANDOLF, R
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机构:UNITE FORMAT RECH SCI PHARMACEUT,DEPT MICROBIOL,F-14000 CAEN,FRANCE
KANDOLF, R
机构:
[1] UNITE FORMAT RECH SCI PHARMACEUT,DEPT MICROBIOL,F-14000 CAEN,FRANCE
COXSACKIEVIRUS B3;
PICORNAVIRUS;
INSITU HYBRIDIZATION;
MOUSE MODEL;
DIGITAL IMAGE ANALYSIS;
D O I:
10.1073/pnas.89.1.314
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Coxsackievirus B3-induced myocarditis in different immunocompetent mouse strains was used as a model to investigate interrelationships between virus replication and development of chronic enteroviral heart disease. Using in situ hybridization to detect enteroviral RNA, we show that heart muscle infection is not only detected in acute myocarditis but is also detected during the chronic phase of the disease. Coxsackievirus B3 could evade immunological surveillance in a host-dependent fashion, thus inducing a persistent infection of the myocardium in association with ongoing inflammation. Patterns of acute and persistent myocardial infection were quantitatively assessed in one representative mouse strain (A.CA/SnJ, H-2f) by applying computer-assisted digital image processing; these patterns were then related to the extent of myocardial tissue damage as well as to inflammation. We observed a strong correlation, both spatial and temporal, between viral replication and development of myocardial lesions, indicating that acute and chronic myocardial injuries are a consequence of multifocal organ infection. Analysis of strand-specific in situ hybridization revealed that viral replication in persistent infection is restricted at the level of RNA synthesis. The described procedure for quantitating organ infection provides a powerful tool for evaluating virus-host interactions and will be of particular interest to those studying human enterovirus-induced cardiomyopathies.