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14th International AIDS ConferenceBarcelona, Spain - July 7-12, 2002 |
Int Conf AIDS 2002 Jul 7-12; 14:(abstract no. B10176)
Gomes VM, Hirata RD, Hirata MH, Yamamoto YI, Soares CL, Kanashiro CK, Daher MA, Souza AM, Yokio S
Clinic and Toxicology Analysis Department of The School of Pharmaceutical Sciences of The University of Sao Paulo, Sao Paulo, Brazil
INTRODUCTION: The reactivation of latent T. gondii cysts is one of the most common opportunistic infection in patients with AIDS.
METHOD: In this study, we have developed a hemi-nested PCR (Henes-PCR) procedure for detection of T. gondii in blood samples of 38 seropositive and 21 seronegative individuals. DNA was extracted by salting-out and chaotropic methods. DNA was carried out by amplification of the TGR1E sequence by PCR and Henes-PCR procedures.
RESULTS: The analytical sensibility of Henes-PCR was greater (102 parasites/ml) than that of PCR (104 parasites/ml). The analysis of blood samples revealed that both amplification procedures showed high specificity (100%). In T. gondii seropositive patients, 84% (32/38) were also positive for HIV, characterized as: 7 - A1, 12 - A2, 1 - A3, 1 - B3, 3 - C2 and 9 patients in C3 clinical category (MMWR 41: RR - 17, Dec. 18, 1992). PCR and Henes-PCR was positive blood samples from 1 of 4 patients from C2 and C3 groups that had not received parasite prophylaxis.
CONCLUSION: These preliminary data indicates that Henes-PCR procedure is a useful tool for the detection of toxoplasma reactivation in HIV- infected individuals.
020707
B10176
Copyright © 2002 - International AIDS Society (IAS). Reproduction of this abstract (other than one copy for personal reference) must be cleared through the IAS.