A multiplex polymerase chain reaction microarray assay to detect bioterror pathogens in blood

J Mol Diagn. 2005 Oct;7(4):486-94. doi: 10.1016/S1525-1578(10)60579-X.

Abstract

Heightened concern about the dangers of bioterrorism requires that measures be developed to ensure the safety of the blood supply. Multiplex detection of such agents using a blood-screening DNA microarray is a sensitive and specific method to screen simultaneously for a number of suspected agents. We have developed and optimized a multiplex polymerase chain reaction microarray assay to screen blood for three potential bioterror bacterial pathogens and a human ribosomal RNA gene internal control. The analytical sensitivity of the assay was demonstrated to be 50 colony-forming units/ml for Bacillus anthracis, Francisella tularensis, and Yersinia pseudotuberculosis (surrogate for Yersinia pestis). The absence of any false-positives demonstrated high analytical specificity. Screening B. anthracis-infected mouse blood samples and uninfected controls demonstrated effectiveness and specificity in a preclinical application. This study represents proof of the concept of microarray technology to screen simultaneously for multiple bioterror pathogens in blood samples.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Anthrax / blood*
  • Anthrax / diagnosis*
  • Anthrax / microbiology
  • Bacillus anthracis / genetics*
  • Bacillus anthracis / isolation & purification*
  • Bioterrorism*
  • Mice
  • Oligonucleotide Array Sequence Analysis / methods*
  • Polymerase Chain Reaction*