Development of a consensus microarray method for identification of some highly pathogenic viruses
- 22 September 2009
- journal article
- research article
- Published by Wiley in Journal of Medical Virology
- Vol. 81 (11) , 1945-1950
- https://doi.org/10.1002/jmv.21602
Abstract
Some highly pathogenic viruses, such as Chikungunya virus, Japanese encephalitis virus, Yellow fever virus, Dengue virus, Hanta virus, SARS‐CoV, and H5N1 avian influenza virus can cause severe infectious diseases. However, the consensus method for detecting these viruses has not been well established. A rapid and sensitive microarray approach for detection of these viruses and a panel of specific probes covering nine genera and 16 virus species were designed. 70‐mer oligonucleotides were used at the genus level and 50‐mer oligonucleotides were at the species level, respectively. To decrease the interference of the host genome in hybridization, the consensus genus primers were designed and used to reverse transcribe only virus genome. The synthesis of the second strand was carried out with a random primer sequence (5′‐GTTTCCCAGTAGGTCTCNNNNNNNN‐3′). The amplified products were labeled and processed for microarray analyses. This microarray‐based method used the highly conserved consensus primers to synthesize specifically the virus cDNA and could identify effectively Chikungunya virus, Japanese encephalitis virus, Yellow fever virus, Dengue virus, Tick borne encephalitis virus, and H5N1 avian influenza virus. Using this method, one unknown virus isolated from pig brain in Shanxi Province, China was identified. This method may have an important potential application for the diagnosis of virus infection. J. Med. Virol. 81:1945–1950, 2009.Keywords
This publication has 20 references indexed in Scilit:
- Using a Resequencing Microarray as a Multiple Respiratory Pathogen Detection AssayJournal of Clinical Microbiology, 2007
- Microarray assay for detection and discrimination of Orthopoxvirus speciesJournal of Medical Virology, 2006
- Application of DNA microarray technology for detection, identification, and characterization of food-borne pathogensCanadian Journal of Microbiology, 2006
- DNA Probe Array for the Simultaneous Identification of Herpesviruses, Enteroviruses, and FlavivirusesJournal of Clinical Microbiology, 2005
- Development and Clinical Evaluation of a Highly Sensitive DNA Microarray for Detection and Genotyping of Human PapillomavirusesJournal of Clinical Microbiology, 2004
- Use of the DNA Flow-Thru Chip, a Three-Dimensional Biochip, for Typing and Subtyping of Influenza VirusesJournal of Clinical Microbiology, 2004
- Viral Discovery and Sequence Recovery Using DNA MicroarraysPLoS Biology, 2003
- Simultaneous detection of influenza A, B, and C viruses, respiratory syncytial virus, and adenoviruses in clinical samples by multiplex reverse transcription nested‐PCR assayJournal of Medical Virology, 2002
- Multiplex PCR: Optimization and Application in Diagnostic VirologyClinical Microbiology Reviews, 2000
- A method for the rapid sequence-independent amplification of microdissected chromosomal materialGenomics, 1992