An Oligonucleotide Microarray for Multiplex Real-Time PCR Identification of HIV-1, HBV, and HCV
Author(s) -
Dmitriy A. Khodakov,
Natalia V. Zakharova,
Dmitry Gryadunov,
Felix P. Filatov,
А. С. Заседателев,
V. M. Mikhailovich
Publication year - 2008
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/000112628
Subject(s) - multiplex , virology , real time polymerase chain reaction , microarray , oligonucleotide , multiplex polymerase chain reaction , identification (biology) , biology , polymerase chain reaction , human immunodeficiency virus (hiv) , computational biology , genetics , dna , gene , gene expression , botany
We describe a novel microarray-based approach for simultaneous identification and quantification of human immunodeficiency virus type 1 (HIV-1) and hepatitis B and C viruses (HBV and HCV) in donor plasma specimens. The method is based on multiplex real-time RT-PCR performed within the microarray hydrogel pads. Double-stranded amplification products are simultaneously detected using nonspecific SYBR Green I dye due to the reaction run in separate pads bearing 5'-immobilized specific primers. Both the sensitivity and specificity of the assay, based on 132 blood specimens analyzed, were 100% (56, 26, and 8 specimens were seropositive to HBV HCV and HIV-1, respectively; 22 were positive to both HIV-1 and HCV and 2 positive to all three viruses; 18 samples were pathogen-negative). The dynamic range of the quantitative analysis covered a six-order interval ranging from 100 to 106 genome equivalents per assay. The 95% detection limits were 14 gEq for HIV-1, 10 gEq (1.7 IU) for HBV, and 15 gEq (7.5 IU) for HCV per assay. The proposed approach is considered to be versatile and could be adapted for simultaneous identification and quantification of numerous genetic targets.
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