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Chin Med J (Taipei) 1997;59:325-33.

Temperature Effect on the Sensitivity of ELISA, PA and WB to Detect Anti-HIV-1 Antibody and Infectivity of HIV-1

Gong-Ren Wang1,2, Jyh-Yuan Yang2, Tsuey-Li Lin2, Hour-Young Chen2, Chi-Byi Horng2

1Department of Medicine, Taipei Medical College; 2National Institute of Preventive Medicine, Department of Health, Executive Yuan, Taipei, Taiwan, R.O.C.


Abstract

Background. This study is designed to resolve the problem of whether temperature or freeze/thaw cycle will have any impact on the sensitivity for detection of anti-HIV-1 antibody by particle agglutination (PA), enzyme-linked immunosorbent assay (ELISA) and western blotting (WB). To reduce potential risk for laboratory personnel exposed to HIV-infection, it will be useful to determine the temperature effect on HIV infectivity.

Methods. Testing sera were incubated at different temperatures or treated with several cycles of freeze and thaw. PA, ELISA and WB were used to detect anti-HIV-antibodies, whereas syncytia formation assay and polymerase chain reaction (PCR) were applied to detect HIV-infection.

Results. The data showed that certain temperature points (no treatment, 25 0C for 1hr, 2hrs and 4 hrs, 37 0C for 30 minutes and 60 minutes, 56 0C for 30 minutes and 60 minutes, 65 0C for 15 minutes and 30 minutes) had no impact on the testing results of ELISA, PA and WB in detection of anti-HIV-1 antibody. In addition, testing results of 50 normal human serum samples which had been heated to 56 0C for 30 minutes were still negative by ELISA and PA. Only the samples incubated at 65 0C for 60 minutes had slight differences in results. Freeze and thaw treatments of the serum did not alter anti-HIV testing results, either. Treatments of supernatant of HTLV-IIIB culture at 56 0C for 30 minutes and 60 minutes, 65 0C for 15 minutes and 30 minutes could eliminate the syncytia formation caused by HIV-infection. Further analysis of the samples by PCR was able to detect HIV-specific sequences in all the treatments.

Conclusions. Anti-HIV antibody is quite stable in serum, even when it is pre-heated to 56 0C for 30 minutes. Freeze and thaw treatment of serum samples up to seven cycles did not change the results, either. In addition, to minimize the potential risk of laboratory personnel exposed to HIV infection, pre-treatment of serum samples with heat at 56 0C for 30 minutes or 60 minutes can reduce HIV infectivity. However, laboratories still must emphasize the importance of universal precautions rather than heat-inactivation of serum to prevent occupational transmission of HIV.

[Chin Med J (Taipei) 1997;59:325-33.]

Keywords: acquired immunodeficiency syndrome, enzyme-linked immunosorbent assay, human immunodeficiency virus, particle agglutination, western blotting

Received: August 1, 1996.

Accepted: April 21, 1997.

Address reprint requests to:

Gong-Ren Wang
161, Kun Yang St.
Nan Kang Dist.
Taipei, Taiwan, R.O.C.


Copyright: 1997, Chinese Medical Association (Taipei)