I. Rabauschstarz et al., PERSISTENCE OF VIRUS AND VIRAL GENOME IN MYOCARDIUM AFTER COXSACKIEVIRUS B3-INDUCED MURINE MYOCARDITIS, Clinical and experimental immunology, 96(1), 1994, pp. 69-74
Following infection with Coxsackievirus B3 (CVB3), A-strain mice devel
op ongoing myocarditis that persists after the virus ceases to be cult
ivatable from heart tissue. We studied the natural history of this vir
us-induced but apparently autoimmune inflammation by means of in situ
hybridization (ISH) and by polymerase chain reaction (PCR). Both ISH a
nd culture allowed detection of virus up to 2 weeks post-infection in
virtually all heart tissues. In contrast, PCR revealed the presence of
viral genome for a substantially longer period of time, i.e. at least
34 days after CVB3 infection. Similarly, the majority of mice showed
myocardial inflammation at this time point. However, the persistence o
f virus did not correlate with ongoing myocarditis, and vice versa. Mo
st mice with ongoing myocarditis produced heart myosin autoantibodies,
most probably as a result of tissue damage. The lack of correlation b
etween presence of ongoing inflammation and persistence of virus suppo
rts our previous view that the late phase of CVB3-induced myocarditis
is mediated by autoimmunological mechanisms.