A method based on DNA amplification and hybridization has been used fo
r the rapid detection of Mycobacterium tuberculosis in blood samples f
rom 38 hospitalized patients (15 human immunodeficiency virus [HIV] po
sitive and 23 HIV negative) in whom localized or disseminated forms of
tuberculosis were suspected. In 32 of these patients, the diagnosis o
f tuberculosis was eventually confirmed by conventional bacteriologica
l or histological procedures, M. tuberculosis DNA was detected with th
e PCR technique in the peripheral blood mononuclear cells from 9 of 11
(82%) HIV-infected patients and in 7 of 21 (33%) HIV-negative patient
s (P < 0.01), while M. tuberculosis blood cultures were positive in 1
of 8 (12.5%) and 1 of 18 (5.5%) patients, respectively. PCR was positi
ve in all cases with disseminated disease in both HIV-negative and HIV
-positive patients and also in the HIV-positive patients with extrapul
monary tuberculosis. Seven samples from patients with documented illne
ss other than tuberculosis and 12 specimens from healthy volunteers, i
ncluding seven volunteers with a recent positive purified protein deri
vative test, were used as controls and had a negative PCR. These resul
ts suggest that detection of M. tuberculosis DNA in peripheral blood m
ononuclear cells may be a useful tool for rapid diagnosis of dissemina
ted and extrapulmonary forms of tuberculosis, especially in an HIV-pos
itive population.