QUANTITATIVE MOLECULAR METHODS IN VIROLOGY

被引:59
作者
CLEMENTI, M [1 ]
MENZO, S [1 ]
MANZIN, A [1 ]
BAGNARELLI, P [1 ]
机构
[1] UNIV TRIESTE, DIPARTIMENTO SCI BIOMED, TRIESTE, ITALY
关键词
D O I
10.1007/BF01322527
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During the past few years, significant technical effort was made to develop molecular methods for the absolute quantitation of nucleic acids in biological samples. In virology, semi-quantitative and quantitative techniques of different principle, complexity, and reliability were designed, optimized, and applied in basic and clinical researches. The principal data obtained in successful pilot applications in vivo are reported in this paper and show the real usefulness of these methods to understand more details of the natural history of viral diseases and to monitor specific anti-viral treatments in real time. Theoretical considerations and practical applications indicate that the competitive polymerase chain reaction (cPCR) and competitive reverse-transcription PCR (cRT-PCR) assay systems share several advantages over other quantitative molecular methodologies, thus suggesting that these techniques are the methods of choice for the absolute quantitation of viral nucleic acids present in low amounts in biological samples. Although minor obstacles to a wide use of these quantitative methods in clinical virology still remain, further technical evolution is possible, thus making the quantitative procedures easier and apt-to routine applications.
引用
收藏
页码:1523 / 1539
页数:17
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共 105 条
[21]  
Clementi M., Bagnarelli P., Menzo S., Valenza A., Manzin A., Varaldo P.E., Clearance of HIV-1 viremia after seroconversion, Lancet, 341, pp. 315-316, (1993)
[22]  
Clementi M., Menzo S., Bagnarelli P., Manzin A., Valenza A., Varaldo P.E., Quantitative PCR and RT-PCR in virology, PCR Methods Appl, 2, pp. 191-196, (1993)
[23]  
Clementi M., Bagnarelli P., Manzin A., Menzo S., Competitive polymerase chain reaction and analysis of viral activity at the molecular level, Genet Anal Tech Appl, 11, pp. 1-6, (1994)
[24]  
Delassus S., Cheynier R., Wain-Hobson S., Nonhomogeneous distribution of human immunodeficiency virus type 1 provirus in the spleen, J Virol, 66, pp. 5642-5645, (1992)
[25]  
Diviacco S., Norio P., Zentilin L., Menzo S., Clementi M., Biamonti G., Riva S., Falaschi A., Giacca M., A novel procedure for quantitative polymerase chain reaction by coamplification of competitive templates, Gene, 122, pp. 3013-3020, (1992)
[26]  
Epstein L.G., Kuiken C., Blumberg B.M., Hartman B., Sharer L.R., Clement M., Goudsmit J., HIV-1 V3 domain variation in brain and spleen of children with AIDS: tissue-specific evolution with host-determined quasispecies, Virology, 180, pp. 583-590, (1991)
[27]  
Fisher A.G., Ensoli B., Looney D., Rose A., Gallo R.C., Saag, Shaw G.M., Hahn B.H., Wong-Staal F., Biologically diverse molecular variants within a single HIV-1 isolate, Nature, 334, pp. 444-447, (1988)
[28]  
Forster E., An improved general method to generate internal standards for competitive PCR, Biotechniques, 16, pp. 18-20, (1994)
[29]  
Garbuglia A.R., Manzin A., Budkowska A., Taliani G., Clementi M., Delfini C., Carloni G., Levels of pre-S antigens and HBV DNA in sera from high and low viremic HBV carriers, J Med Virol, 35, pp. 273-282, (1991)
[30]  
Garson J.A., Brillanti S., Ring C., Perini P., Miglioli M., Barbara L., Hepatitis C viremia rebound after “successful” interferon therapy in patients with chronic non-A, non-B hepatitis, J Med Virol, 37, pp. 210-214, (1992)