• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Scientific Publications by FDA Staff

  • Print
  • Share
  • E-mail
-

Search Publications



Fields



Centers











Starting Date


Ending Date


Order by

Entry Details

J Clin Microbiol 2006 Oct;44(10):3752-9

Genotyping of measles virus in clinical specimens on the basis of oligonucleotide microarray hybridization patterns.

Neverov AA, Riddell MA, Moss WJ, Volokhov DV, Rota PA, Lowe LE, Chibo D, Smit SB, Griffin DE, Chumakov KM, Chizhikov VE

Neverov AA (reprint author), US FDA, LMD, CBER, HFM-470,1401 Rockville Pike, Rockville, MD 20852 USA US FDA, LMD, CBER, Rockville, MD 20852 USA Johns Hopkins Univ, Bloomberg Sch Publ Hlth, W Harry Feinstone Dept Mol Microbiol & Immunol, Baltimore, MD USA WHO, Ctr Dis Control & Prevent, Measles Mumps Rubella & Herpesvirus Branch, Global Measles Ref Lab, Atlanta, GA USA WHO, Victorian Infect Dis Ref Lab, Western Pacif Reg Measles Ref Lab, Melbourne, Vic Australia Natl Inst Communicable Dis, Vaccine Preventable Virus Infect Unit, Johannesburg, South Africa State Res Ctr Virol & Biotechnol, Inst Mol Biol, Koltsov, Novosibirsk Reg Russia

Abstract

An oligonucleotide microarray hybridization method for identification of most known measles virus (MV) genotypes was developed. Like the conventional genotyping method, the microarray relied on detecting sequence differences in the 450-nucleotide region coding for the COOH-terminal 150 amino acids of the nucleoprotein (N). This region was amplified using PCR primers binding to all known MV genotypes. The microarray included 71 pairs of oligonucleotide probes (oligoprobes) immobilized on glass slides. Each pair consisted of a genotype-specific oligoprobe, which matched the sequence of only one target genotype, and a control oligoprobe, which contained mismatches at the nucleotide positions unique to this genotype. A pattern recognition algorithm based on cluster analysis of the ratios of hybridization signals from specific and control oligoprobes was used to identify the specific MV genotype. Following the initial validation, the method was used for rapid genotyping of two panels of coded samples. The results of this study showed good sensitivity (90.7%), specificity (100%), and genotype agreement (91.8%) for the new method compared to the results of genotyping conducted using phylogenetic analysis of viral sequences of the C terminus of the N gene. In addition, the microarray demonstrated the ability to identify potential new genotypes of MV based on the similarity of their hybridization patterns with those of known MV genotypes.


Category: Journal Article
PubMed ID: #17021105
PubMed Central ID: #PMC1594792
Includes FDA Authors from Scientific Area(s): Biologics
Entry Created: 2011-10-04 Entry Last Modified: 2012-08-29
Feedback
-
-