Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Nov;81(11):1945-50.
doi: 10.1002/jmv.21602.

Development of a consensus microarray method for identification of some highly pathogenic viruses

Affiliations

Development of a consensus microarray method for identification of some highly pathogenic viruses

Kang Xiao-Ping et al. J Med Virol. 2009 Nov.

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.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Albrecht V, Chevallier A, Magnone V, Barbry P, Vandenbos F, Bongain A, Lefebvre JC, Giordanengo V. 2006. Easy and fast detection and genotyping of high‐risk human papillomavirus by dedicated DNA microarrays. J Virol Methods 137: 236–244. - PubMed
    1. Bohlander SK, Espinosa R III, Le Beau MM, Rowley JD, Diaz MO. 1992. A method for the rapid sequence‐independent amplification of microdissected chromosomal material. Genomics 13: 1322–1324. - PubMed
    1. Calvario A, Bozzi A, Scarasciulli M, Ventola C, Seccia R, Stomati D, Brancasi B. 2002. Herpes Consensus PCR test: A useful diagnostic approach to the screening of viral diseases of the central nervous system. J Clin Virol 5: S71–S78. - PubMed
    1. Casas JA, García‐Ochoa F. 1999. Sophorolipid production by Candida bombicola: Medium composition and culture methods. J Biosci Bioeng 88: 488–494. - PubMed
    1. Chang PC, Peck K. 2003. Design and assessment of a fast algorithm for identifying specific probes for human and mouse genes. Bioinformatics 19: 1311–1317. - PubMed

Publication types

MeSH terms

Substances