COMPARISON OF PROCEDURES FOR THE DETECTION OF ENTEROVIRUSES IN MURINEHEART SAMPLES BY IN-SITU POLYMERASE-CHAIN-REACTION

A protocol for the in situ polymerase chain reaction (IS-PCR) detectio n of viral nucleic acid in the heart tissue of four-to-five-week-old C D1 mice infected with coxsackievirus B3 (CBV3) Nancy strain is describ ed. To compare the effects of formalin concentration on the IS-PCR pro cess, two different concentrations (10 and 37%) were employed. Using 3 7% formalin, 25 PCR cycles were sufficient and a permeabilization step could be omitted. However, postfixation of tissues with 4% paraformal dehyde and 100% ethanol after the deparaffinization, reverse transcrip tase and amplification steps was required in order to minimize artefac ts. When the tissues were fixed in 10% formalin, postfixation with 4% paraformaldehyde was not required, but a permeabilization step had to be employed and 40 cycles of PCR amplification were needed. To detect the PCR product in the 10% formalin-fixed samples, incubation with 0.3 U/ml of an anti-digoxigenin antibody conjugated to alkaline phosphata se was performed for 90 min. When 37% formalin-fixed samples were used , the concentration of the antibody conjugate had to be increased to 3 U/ml and the exposure time was decreased to 30 min. Enterovirus (EV) nucleic acid was detected in the cytoplasm of myocyte's. Thus, IS-PCR was successful in localizing EV nucleic acid in the cytoplasm of myocy tes in mice infected with a cardiotropic strain of CBV3. Using this te chnique, 10% formalin-fixed tissues gave better results than 37% forma lin-fixed tissues.