Literature DB >> 20486192

Evaluation of the alkaline wash/lysis procedure for the molecular diagnosis of a positive bacterial blood culture in clinical routine practice.

Sheng-Chuan Hsi1, Jun-Ren Sun, Tzong-Shi Chiueh.   

Abstract

Blood culture is commonly used to detect microorganisms in patients with a suspected blood infection. This study evaluated the alkaline wash/lysis procedure to extract DNA of microorganisms in a clinical blood culture. A multiplex polymerase chain reaction (PCR) targeting the 16S rDNA (ribosomal DNA) gene and the fungal ITS (internal transcribed spacer) gene was used as a reliable indicator for the presence of microorganism DNA in the extracts. A total of 535 BacT/ALERT positive blood culture bottles were evaluated. Multiplex PCR showed positive results in 530 DNA extracts, but 5 DNA extracts gave negative results. We conclude that the alkaline wash/lysis procedure in combination with the multiplex PCR is a simple and sensitive method, which can be used in a standard diagnostic laboratory to detect microorganisms in blood culture material. (c) 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20486192      PMCID: PMC6647685          DOI: 10.1002/jcla.20396

Source DB:  PubMed          Journal:  J Clin Lab Anal        ISSN: 0887-8013            Impact factor:   2.352


  30 in total

1.  Polymorphic internal transcribed spacer region 1 DNA sequences identify medically important yeasts.

Authors:  Y C Chen; J D Eisner; M M Kattar; S L Rassoulian-Barrett; K Lafe; U Bui; A P Limaye; B T Cookson
Journal:  J Clin Microbiol       Date:  2001-11       Impact factor: 5.948

2.  Detection of bacteria in platelet concentrates: comparison of broad-range real-time 16S rDNA polymerase chain reaction and automated culturing.

Authors:  Tamimount Mohammadi; Ruby N I Pietersz; Christina M J E Vandenbroucke-Grauls; Paul H M Savelkoul; Henk W Reesink
Journal:  Transfusion       Date:  2005-05       Impact factor: 3.157

Review 3.  Real-time PCR in clinical microbiology: applications for routine laboratory testing.

Authors:  M J Espy; J R Uhl; L M Sloan; S P Buckwalter; M F Jones; E A Vetter; J D C Yao; N L Wengenack; J E Rosenblatt; F R Cockerill; T F Smith
Journal:  Clin Microbiol Rev       Date:  2006-01       Impact factor: 26.132

4.  Relevance of routine use of the anaerobic blood culture bottle.

Authors:  Patrick Grohs; Jean-Luc Mainardi; Isabelle Podglajen; Xavier Hanras; C Eckert; A Buu-Hoï; E Varon; Laurent Gutmann
Journal:  J Clin Microbiol       Date:  2007-06-20       Impact factor: 5.948

5.  Identification and characterization of immunoglobulin G in blood as a major inhibitor of diagnostic PCR.

Authors:  W A Al-Soud; L J Jönsson; P Râdström
Journal:  J Clin Microbiol       Date:  2000-01       Impact factor: 5.948

6.  A potent inhibitor of Taq polymerase copurifies with human genomic DNA.

Authors:  R de Franchis; N C Cross; N S Foulkes; T M Cox
Journal:  Nucleic Acids Res       Date:  1988-11-11       Impact factor: 16.971

7.  Preparation of mycobacterial DNA from blood culture fluids by simple alkali wash and heat lysis method for PCR detection.

Authors:  J K Kulski; T Pryce
Journal:  J Clin Microbiol       Date:  1996-08       Impact factor: 5.948

8.  Two novel real-time reverse transcriptase PCR assays for rapid detection of bacterial contamination in platelet concentrates.

Authors:  Jens Dreier; Melanie Störmer; Knut Kleesiek
Journal:  J Clin Microbiol       Date:  2004-10       Impact factor: 5.948

9.  Experience with the MicroSeq D2 large-subunit ribosomal DNA sequencing kit for identification of commonly encountered, clinically important yeast species.

Authors:  Leslie Hall; Sherri Wohlfiel; Glenn D Roberts
Journal:  J Clin Microbiol       Date:  2003-11       Impact factor: 5.948

10.  Rapid detection of methicillin-susceptible and methicillin-resistant Staphylococcus aureus directly from positive BacT/Alert blood culture bottles using real-time polymerase chain reaction: evaluation and comparison of 4 DNA extraction methods.

Authors:  Graham Michael Hogg; James Patrick McKenna; Grace Ong
Journal:  Diagn Microbiol Infect Dis       Date:  2008-05-22       Impact factor: 2.803

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  2 in total

1.  Rapid detection of blaKPC carbapenemase genes by internally controlled real-time PCR assay using bactec blood culture bottles.

Authors:  Musa Hindiyeh; Gill Smollan; Zehava Grossman; Daniela Ram; Jana Robinov; Natasha Belausov; Debbie Ben-David; Ilana Tal; Yehudit Davidson; Ari Shamiss; Ella Mendelson; Nathan Keller
Journal:  J Clin Microbiol       Date:  2011-05-11       Impact factor: 5.948

2.  16S rRNA gene sequencing is a non-culture method of defining the specific bacterial etiology of ventilator-associated pneumonia.

Authors:  Li-Ping Xia; Long-Yan Bian; Min Xu; Ying Liu; Ai-Ling Tang; Wen-Qin Ye
Journal:  Int J Clin Exp Med       Date:  2015-10-15
  2 in total

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