|Cook, Kimberly - Kim|
Submitted to: Journal of Microbiological Methods
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 12/21/2006
Publication Date: 12/30/2006
Citation: Cook, K.L., Britt, J. 2006. Optimization of Methods for Obtaining, Extracting and Detecting Mycobacterium avium subsp. paratuberculosis in Environmental Samples using Quantitative, Real-Time PCR. Journal of Microbiological Methods. V29:154-160
Interpretive Summary: The goal of this study was to optimize methodologies for obtaining, extracting and evaluating the concentration of Mycobacterium avium subsp. paratuberculosis (M. paratuberculosis) in environmental samples using a quantitative, real-time PCR (QRT-PCR) based analysis. PCR-based methods are highly specific, sensitive and high-throughput making them well suited for detection of M. paratuberculosis in environmental samples in which concentrations of the target organism may be low while levels of non-target organisms are high. However, the reliability of the methods depend on overcoming specific shortcomings that nucleic acid-based methods have, namely cell lysis efficiency, DNA absorption to surfaces and PCR inhibition from co-extracted compounds present in environmental samples. Results from this study show that pooling 10 samples from the soil or manure and extracting the DNA without cell extraction using Qbiogene’s Fast® DNA Spin kit for soil give the highest yield of DNA and the highest copy number of the targeted M. paratuberculosis IS900 sequence. Results from this study suggest that DNA extraction method, sample makeup and PCR conditions each critically influence the outcome and validity of nucleic acid-based detection techniques. Detection of M. paratuberculosis IS900 sequence in pasture samples for more than 200 days following removal of a M. paratuberculosis culture positive dairy cow illustrate the importance of environmental sources of the organism.
Technical Abstract: Detection of Johne’s disease, an enteric infection of cattle caused by Mycobacterium avium subsp. paratuberculosis (M. paratuberculosis), has been impeded by the lack of rapid, reliable detection methods. The goal of this study was to optimize methodologies for obtaining, extracting and evaluating the concentration of M. paratuberculosis in manure from an infected dairy cow or in contaminated soil samples using a quantitative, real-time PCR (QRT-PCR) based analysis. Three different nucleic acid extraction techniques, the efficiency of direct versus indirect sample extraction, and sample pooling were assessed. The limit of detection was investigated by adding dilutions of M. paratuberculosis to soil. Results show that the highest yield of DNA (117 +/- 14 ng µl-1) and the highest copy number of the targeted M. paratuberculosis IS900 sequence (1.3 +/- 0.2 X 10^8 copies g-1) were obtained with DNA extracted from manure using the Fast® DNA Spin kit for soil. Pooling ten samples of M. paratuberculosis-contaminated soil improved the limit of detection ten fold. The limit of detection was between 20 and 115 M. paratuberculosis cells g-1 soil and detection was between 65% and 95% higher when samples were extracted directly using bead-beating than when using pre-treatment with cell extraction buffers. The final soil-sampling and extraction regime was applied for detection of M. paratuberculosis in pasture soil after the removal of a M. paratuberculosis culture positive dairy cow. M. paratuberculosis remained in the pasture soil for more than 200 days. Results from these studies suggest that DNA extraction method, sampling protocol and PCR conditions each critically influence the outcome and validity of the QRT-PCR analysis of M. paratuberculosis concentrations is environmental samples.