Bm. Eriksson et al., DIAGNOSIS OF CYTOMEGALOVIRUS IN BRONCHOALVEOLAR LAVAGE BY POLYMERASE CHAIN-REACTION, IN COMPARISON WITH VIRUS ISOLATION AND DETECTION OF VIRAL-ANTIGEN, Scandinavian journal of infectious diseases, 25(4), 1993, pp. 421-427
Bronchoalveolar lavage (BAL) products from 52 immunocompromised patien
ts with symptoms of pulmonary infection was examined for cytomegalovir
us (CMV) by virus isolation, polymerase chain reaction (PCR) and detec
tion of CMV antigen by immunofluorescence or immunoperoxidase staining
after short-term incubation in tissue culture and directly in BAL cel
ls. We found that PCR detected all cases positive by virus isolation (
15/52 samples) and the result was obtained within 5 h. PCR detected mo
re cases of CMV than did virus isolation (22/52 samples). Positive PCR
and negative virus isolation were consistent with probable CMV infect
ion in 3/7 patients when other clinical and laboratory parameters of C
MV infection were considered. The negative predictive value of PCR was
high; none of 30 patients negative by PCR developed CMV pneumonia wit
hin the subsequent 2 months. Detection of CMV antigen after short-term
incubation was rapid enough to be used in clinical practice, specific
(100%) and with a sensitivity of 60%. Demonstration of CMV antigen in
alveolar cells was highly specific (100%) but had too low a sensitivi
ty (26.7%) to be used as the only rapid method. Our conclusion is that
a combination of PCR and detection of CMV antigen after short-term in
cubation and directly in alveolar cells is optimal for rapid identific
ation of CMV.