A Minisonicator To Rapidly Disrupt Bacterial Spores for DNA Analysis

Phillip Belgrader,* Derek Hansford, Gregory T. A. Kovacs, Kodumudi Venkateswaran, Raymond Mariella, Jr., Fred Milanovich, Shanavaz Nasarabadi, Margaret Okuzumi, Farzad Pourahmadi, and M. Allen Northrup
Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94551, and Cepheid, 1190 Borregas Avenue, Sunnyvale, California 94089
Anal. Chem., 1999, 71 (19), pp 4232–4236
DOI: 10.1021/ac990347o
Publication Date (Web): August 31, 1999
Copyright © 1999 American Chemical Society
*

 Address correspondence to this author at:  Cepheid, 1190 Borregas Ave., Sunnyvale, CA 94089. (tel) 408-541-4191; (fax) 408-541-4192; (e-mail) belgrader@ cepheid.com.

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 Lawrence Livermore National Laboratory.

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 Cepheid.

Abstract

Concerns about the use of anthrax spores as a weapon of mass destruction have motivated the development of portable instruments capable of detecting and monitoring a suspected release of the agent. Optimal detection of bacterial spores by PCR requires that the spores be disrupted to make the endogenous DNA available for amplification. The entire process of spore lysis, PCR, and detection can take several hours using conventional methods and instruments. In this report, a minisonicator and prototype spore lysis cartridge were built to disrupt Bacillus spores in 30 s for rapid, real-time PCR analysis. Utilization of the minisonicator improved PCR analysis by decreasing the limit of detection, reducing the time of detection, and increasing the signal amplitude. Total time of spore disruption and detection using the minisonicator and a microchip PCR instrument was less than 15 min.

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History

  • Published In Issue October 01, 1999
  • Received for review April 6, 1999. Accepted July 21, 1999.

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