Literature DB >> 15558344

Efficient method for mycobacterial DNA extraction in blood cultures aids rapid PCR identification of Mycobacterium tuberculosis and Mycobacterium avium.

S M Nakatani1, M Burger, M C Assef, S R Brockelt, L L Cogo, I J T Messias-Reason.   

Abstract

The study presented here evaluated the utility of several methods of extracting mycobacterial nucleic acids from positive blood culture samples and examined the effect of each method on the performance of an in-house PCR used directly in the peripheral blood of 80 patients with AIDS to identify Mycobacterium spp. The modified Boom method for extracting DNA from blood cultures proved to be the most efficient, with subsequent PCR analysis yielding 100% positivity (7 samples positive for M. avium and 5 for M. tuberculosis). Only three of 12 patients with a positive blood culture had a PCR result positive for M. avium in peripheral blood. The identification of mycobacteria by PCR in blood culture took about 3 days, reducing the time to diagnosis by several weeks. These results demonstrate that PCR is a sensitive and quick method for identifying mycobacteria, especially when a good DNA extraction method is applied.

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Year:  2004        PMID: 15558344     DOI: 10.1007/s10096-004-1236-z

Source DB:  PubMed          Journal:  Eur J Clin Microbiol Infect Dis        ISSN: 0934-9723            Impact factor:   3.267


  14 in total

1.  Early identification of Mycobacterium tuberculosis and Mycobacterium avium using the polymerase chain reaction on samples positive by a rapid commercial culture system.

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Journal:  Eur J Clin Microbiol Infect Dis       Date:  1999-05       Impact factor: 3.267

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Review 5.  Structure, function and biogenesis of the cell envelope of mycobacteria in relation to bacterial physiology, pathogenesis and drug resistance; some thoughts and possibilities arising from recent structural information.

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6.  [Comparative study of various staining methods for mycobacteria].

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Journal:  Hansenol Int       Date:  1988-12

7.  Direct identification of Mycobacterium avium complex and Mycobacterium gordonae from MB/BacT bottles using AccuProbe.

Authors:  A P Louro; K B Waites; E Georgescu; W H Benjamin
Journal:  J Clin Microbiol       Date:  2001-02       Impact factor: 5.948

8.  Evaluation of a fluorescence in situ hybridization assay for differentiation between tuberculous and nontuberculous Mycobacterium species in smears of Lowenstein-Jensen and Mycobacteria Growth Indicator Tube cultures using peptide nucleic acid probes.

Authors:  P Hongmanee; H Stender; O F Rasmussen
Journal:  J Clin Microbiol       Date:  2001-03       Impact factor: 5.948

9.  Improved amplification of microbial DNA from blood cultures by removal of the PCR inhibitor sodium polyanetholesulfonate.

Authors:  D N Fredricks; D A Relman
Journal:  J Clin Microbiol       Date:  1998-10       Impact factor: 5.948

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Journal:  J Clin Microbiol       Date:  1995-03       Impact factor: 5.948

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  2 in total

1.  Detection of Mycobacterium tuberculosis complex by nested polymerase chain reaction in pulmonary and extrapulmonary specimens.

Authors:  Adriana Antônia da Cruz Furini; Heloisa da Silveira Paro Pedro; Jean Francisco Rodrigues; Lilian Maria Lapa Montenegro; Ricardo Luiz Dantas Machado; Célia Franco; Haiana Charifker Schindler; Ida Maria Foschiani Dias Batista; Andrea Regina Baptista Rossit
Journal:  J Bras Pneumol       Date:  2013 Nov-Dec       Impact factor: 2.624

2.  Two alternative DNA extraction methods to improve the detection of Mycobacterium-tuberculosis-complex members in cattle and red deer tissue samples.

Authors:  Shari Fell; Stephanie Bröckl; Mathias Büttner; Anna Rettinger; Pia Zimmermann; Reinhard K Straubinger
Journal:  BMC Microbiol       Date:  2016-09-15       Impact factor: 3.605

  2 in total

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