Literature DB >> 11724865

Rapid identification of Mycobacteria to the species level using INNO-LiPA Mycobacteria, a reverse hybridization assay.

P N Suffys1, A da Silva Rocha, M de Oliveira, C E Campos, A M Barreto, F Portaels, L Rigouts, G Wouters, G Jannes, G van Reybroeck, W Mijs, B Vanderborght.   

Abstract

INNO-LiPA Mycobacteria (LiPA; Innogenetics, Zwijnaarde, Belgium) is a kit for the simultaneous detection and identification of Mycobacterium species in culture and identifies the Mycobacterium tuberculosis complex, the M. avium complex (MAC), and the following Mycobacterium species: M. kansasii, M. avium, M. intracellulare, M. scrofulaceum, M. gordonae, M. xenopi, and the M. chelonae-M. abscessus complex. The assay, which targets the 16S-23S rRNA spacer region, was evaluated on 157 mycobacterial strains that had been identified by conventional techniques and PCR-restriction enzyme analysis of the hsp65 gene (PRA). Forty-seven reference strains consisting of 37 different species and 110 human clinical isolates were submitted to the test, and all were hybridized with the Mycobacterium genus probe (MYC) on the LiPA strip (100% sensitivity). Ninety-four isolates hybridized to their corresponding species- or complex-specific probes; only one isolate phenotypically identified as M. gordonae did not react with its specific probe (99.4% accuracy). Thirty-seven MAC strains were phenotypically identified to the complex level and to the species level by LiPA as M. avium (n = 18) or M. intracellulare (n = 7) or as belonging to the M. avium-M. intracellulare-M. scrofulaceum complex (n = 12). Of the last 12 strains, 10 had M. avium PRA patterns and 2 had M. intracellulare PRA patterns. Three isolates that had been identified as a single species by conventional identification were proven to be mixed cultures by the LiPA assay. The whole procedure can be performed in 1 working day, starting with the supernatant of a small amount of bacterial mass that had been treated by freezing and then boiling.

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Year:  2001        PMID: 11724865      PMCID: PMC88569          DOI: 10.1128/JCM.39.12.4477-4482.2001

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  23 in total

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4.  PCR-restriction enzyme analysis of a bone marrow isolate from a human immunodeficiency virus-positive patient discloses polyclonal infection with two Mycobacterium avium strains.

Authors:  R S Oliveira; M P Sircili; S Y Ueki; M A Telles; B Schnabel; M R Briones; S C Leão
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5.  Genotypic characterization of five subspecies of Mycobacterium kansasii.

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6.  Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis.

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  32 in total

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2.  Evaluation of INNO-LiPA MYCOBACTERIA v2: improved reverse hybridization multiple DNA probe assay for mycobacterial identification.

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3.  Evaluation of genotype and LiPA MYCOBACTERIA assays for identification of Finnish mycobacterial isolates.

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Journal:  J Clin Microbiol       Date:  2002-09       Impact factor: 5.948

4.  Identification of mycobacteria by using INNO LiPA.

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5.  Identification of clinically relevant viridans group streptococci by sequence analysis of the 16S-23S ribosomal DNA spacer region.

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6.  Prospective evaluation of the GenoType assay for routine identification of mycobacteria.

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7.  Rapid identification of mycobacterial whole cells in solid and liquid culture media by matrix-assisted laser desorption ionization-time of flight mass spectrometry.

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9.  Array-based identification of species of the genera Abiotrophia, Enterococcus, Granulicatella, and Streptococcus.

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10.  Commercial DNA probes for mycobacteria incorrectly identify a number of less frequently encountered species.

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Journal:  J Clin Microbiol       Date:  2009-11-11       Impact factor: 5.948

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