Literature DB >> 18824041

Evaluation of five commercial nucleic acid extraction kits for their ability to inactivate Bacillus anthracis spores and comparison of DNA yields from spores and spiked environmental samples.

Leslie A Dauphin1, Benjamin D Moser, Michael D Bowen.   

Abstract

This study evaluated five commercial extraction kits for their ability to recover DNA from Bacillus anthracis spores and spiked environmental samples. The kits evaluated represent the major types of methodologies which are commercially available for DNA or total nucleic acid extraction, and included the ChargeSwitch gDNA Mini Bacteria Kit, NucliSens Isolation Kit, Puregene Genomic DNA Purification Kit, QIAamp DNA Blood Mini Kit, and the UltraClean Microbial DNA Isolation Kit. Extraction methods were performed using the spores of eight virulent strains of B. anthracis. Viability testing of nucleic acid extracts showed that the UltraClean kit was the most efficient at depleting samples of live B. anthracis spores. TaqMan real-time PCR analysis revealed that the NucliSens, QIAamp and UltraClean kits yielded the best level of detection from spore suspensions. Comparisons of processed samples from spiked swabs and three powder types indicated that DNA extraction using the UltraClean kit resulted in the most consistently positive results and the lowest limit of detection. This study demonstrated that different nucleic extraction methodologies, represented here by various commercial extraction kits, differ in their ability to inactivate live B. anthracis spores as well as DNA yield and purity. In addition, the extraction method used can influence the sensitivity of real-time PCR assays for B. anthracis.

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Year:  2008        PMID: 18824041     DOI: 10.1016/j.mimet.2008.09.004

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  18 in total

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2.  Viability of Mycobacterium tuberculosis after processing with commercial nucleic acid extraction kits.

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Journal:  Appl Environ Microbiol       Date:  2011-12-30       Impact factor: 4.792

4.  Real-time polymerase chain reaction assay for rapid and sensitive detection of anthrax spores in spiked soil and talcum powder.

Authors:  Neha Jain; S Merwyn; G P Rai; G S Agarwal
Journal:  Folia Microbiol (Praha)       Date:  2012-04-17       Impact factor: 2.099

5.  Evaluation of automated and manual commercial DNA extraction methods for recovery of Brucella DNA from suspensions and spiked swabs.

Authors:  Leslie A Dauphin; Rebecca J Hutchins; Liberty A Bost; Michael D Bowen
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6.  Comparison of eight methods for the extraction of Bacillus atrophaeus spore DNA from eleven common interferents and a common swab.

Authors:  Helen L Rose; Caroline A Dewey; Morgan S Ely; Sarah L Willoughby; Tanya M Parsons; Victoria Cox; Phillippa M Spencer; Simon A Weller
Journal:  PLoS One       Date:  2011-07-26       Impact factor: 3.240

7.  Comparison of the sensitivity of culture, PCR and quantitative real-time PCR for the detection of Pseudomonas aeruginosa in sputum of cystic fibrosis patients.

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Journal:  BMC Microbiol       Date:  2009-11-29       Impact factor: 3.605

8.  Comparison of DNA extraction kits for detection of Burkholderia pseudomallei in spiked human whole blood using real-time PCR.

Authors:  Nicole L Podnecky; Mindy G Elrod; Bruce R Newton; Leslie A Dauphin; Jianrong Shi; Sutthinan Chawalchitiporn; Henry C Baggett; Alex R Hoffmaster; Jay E Gee
Journal:  PLoS One       Date:  2013-02-27       Impact factor: 3.240

9.  DNA extract characterization process for microbial detection methods development and validation.

Authors:  Nathan D Olson; Jayne B Morrow
Journal:  BMC Res Notes       Date:  2012-12-03

10.  PCR amplification of a triple-repeat genetic target directly from whole blood in 15 minutes as a proof-of-principle PCR study for direct sample analysis for a clinically relevant target.

Authors:  Christopher M Connelly; Laura R Porter; Joel R TerMaat
Journal:  BMC Med Genet       Date:  2014-12-12       Impact factor: 2.103

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