Detection and discrimination of orthopoxviruses using microarrays of immobilized oligonucleotides

• Published in: Journal of virological methods Vol. 112; no. 1; pp. 67 - 78
• Main Authors: Laassri, Majid, Chizhikov, Vladimir, Mikheev, Maxim, Shchelkunov, Sergei, Chumakov, Konstantin
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.09.2003
• Subjects: Biodefense; Chickenpox virus; DNA Primers - genetics; DNA, Viral - analysis; DNA, Viral - genetics; DNA, Viral - isolation & purification; Gene Expression Profiling; Monkeypox virus; Nucleic acids diagnostics; Oligonucleotide Array Sequence Analysis - methods; Oligonucleotide Probes - genetics; Orthopoxvirus - classification; Orthopoxvirus - genetics; Orthopoxvirus - isolation & purification; Rapid identification; Vaccinia; Variola virus; Viral Proteins - genetics; Biodefense; Variola virus; Monkeypox virus; Nucleic acids diagnostics; Chickenpox virus; Rapid identification; Vaccinia
• ISSN: 0166-0934; 1879-0984
• DOI: 10.1016/S0166-0934(03)00193-9

Variola virus (VARV), causing smallpox, is a potential biological weapon. Methods to detect VARV rapidly and to differentiate it from other viruses causing similar clinical syndromes are needed urgently. We have developed a new microarray-based method that detects simultaneously and discriminates four orthopoxvirus (OPV) species pathogenic for humans (variola, monkeypox, cowpox, and vaccinia viruses) and distinguishes them from chickenpox virus (varicella-zoster virus or VZV). The OPV gene C23L/B29R, encoding the CC-chemokine binding protein, was sequenced for 41 strains of seven species of orthopox viruses obtained from different geographical regions. Those C23L/B29R sequences and the ORF 62 sequences from 13 strains of VZV (selected from GenBank) were used to design oligonucleotide probes that were immobilized on an aldehyde-coated glass surface (a total of 57 probes). The microchip contained several unique 13–21 bases long oligonucleotide probes specific to each virus species to ensure redundancy and robustness of the assay. A region approximately 1100 bases long was amplified from samples of viral DNA and fluorescently labeled with Cy5-modified dNTPs, and single-stranded DNA was prepared by strand separation. Hybridization was carried out under plastic coverslips, resulting in a fluorescent pattern that was quantified using a confocal laser scanner. 49 known and blinded samples of OPV DNA, representing different OPV species, and two VZV strains were tested. The oligonucleotide microarray hybridization technique identified reliably and correctly all samples. This new procedure takes only 3 h, and it can be used for parallel testing of multiple samples.