Literature DB >> 17510263

Species identification and strain differentiation of clinical Candida isolates using the DiversiLab system of automated repetitive sequence-based PCR.

Mark G Wise1, Mimi Healy1, Kristy Reece1, Rebecca Smith2, Dobbie Walton1, Wendy Dutch1, Alex Renwick1, Joe Huong1, Steve Young2, Jeffrey Tarrand3, Dimitrios P Kontoyiannis4.   

Abstract

The DiversiLab system, which uses repetitive sequence-based PCR (rep-PCR) to genotype micro-organisms, was evaluated as a molecular typing tool for members of the genus Candida. Initially, 41 clinical Candida spp. (7 Candida krusei, 10 Candida parapsilosis, 7 Candida albicans, 10 Candida tropicalis and 7 Candida glabrata), previously identified at the species level by morphological and biochemical analysis, were analysed with the DiversiLab system. Species identification was confirmed by DNA sequence analysis of the contiguous internal transcribed spacer (ITS) region (ITS1-5.8S-ITS2). On the basis of an 80 % similarity threshold, rep-PCR consistently clustered like species and this set of isolates, along with five ATCC reference strains, was used to create a DNA fingerprint library with the DiversiLab software. Subsequently, an additional set of 115 clinical Candida isolates, identified biochemically as C. albicans (n=94), C. glabrata (n=8), C. parapsilosis (n=5), C. tropicalis (n=3), C. krusei (n=3) and Candida lusitaniae (n=2), isolated at a regional reference laboratory, were typed using DiversiLab. One hundred and six of these isolates clustered with members of the Candida library at >80 % similarity and thus could be assigned species identification, and initial calculations showed that identification via rep-PCR fingerprinting was 95 % concordant (101/106) with the biochemical/morphological identification. However, ITS region sequencing of the five discrepant samples, as well as the nine isolates that were <80 % similar to the database samples, showed that nine were misidentified with traditional biochemical/morphological methods. For the misidentified isolates, the sequence-based identification was in agreement with the DiversiLab clustering, yielding an actual correlation of >99 %. As traditional techniques can take several days to provide information about Candida at the genus/species level, genotyping with the DiversiLab system holds promise for more-rapid speciation of members of this genus. This system may also be useful for epidemiological studies such as source tracking that require Candida subspecies discrimination.

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Year:  2007        PMID: 17510263     DOI: 10.1099/jmm.0.47106-0

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  10 in total

1.  Comparison of typing results obtained for methicillin-resistant Staphylococcus aureus isolates with the DiversiLab system and pulsed-field gel electrophoresis.

Authors:  Fred C Tenover; Emily A Gay; Stacie Frye; Samantha J Eells; Mimi Healy; John E McGowan
Journal:  J Clin Microbiol       Date:  2009-06-24       Impact factor: 5.948

Review 2.  The role of the laboratory in the diagnosis of invasive candidiasis.

Authors:  Maria Teresa Montagna; Giuseppina Caggiano; Elisa Borghi; Giulia Morace
Journal:  Drugs       Date:  2009       Impact factor: 9.546

3.  Microsatellite genotyping clarified conspicuous accumulation of Candida parapsilosis at a cardiothoracic surgery intensive care unit.

Authors:  Magda Diab-Elschahawi; Christina Forstner; Ferry Hagen; Jacques F Meis; Andrea M Lassnig; Elisabeth Presterl; Corné H W Klaassen
Journal:  J Clin Microbiol       Date:  2012-08-08       Impact factor: 5.948

4.  Conventional Morphology Versus PCR Sequencing, rep-PCR, and MALDI-TOF-MS for Identification of Clinical Aspergillus Isolates Collected Over a 2-Year Period in a University Hospital at Kayseri, Turkey.

Authors:  Altay Atalay; Ayse Nedret Koc; Ahmet Suel; Hafize Sav; Gonca Demir; Ferhan Elmali; Nuri Cakir; Seyedmojtaba Seyedmousavi
Journal:  J Clin Lab Anal       Date:  2016-03-01       Impact factor: 2.352

5.  Long-Term Rasamsonia argillacea Complex Species Colonization Revealed by PCR Amplification of Repetitive DNA Sequences in Cystic Fibrosis Patients.

Authors:  Abdelmounaim Mouhajir; Olivier Matray; Sandrine Giraud; Laurent Mély; Christophe Marguet; Isabelle Sermet-Gaudelus; Solène Le Gal; Franck Labbé; Christine Person; Françoise Troussier; Jean-Jacques Ballet; Gilles Gargala; Rachid Zouhair; Marie-Elisabeth Bougnoux; Jean-Philippe Bouchara; Loïc Favennec
Journal:  J Clin Microbiol       Date:  2016-09-07       Impact factor: 5.948

6.  Molecular epidemiology of Cryptococcus neoformans and Cryptococcus gattii in China between 2007 and 2013 using multilocus sequence typing and the DiversiLab system.

Authors:  H-T Dou; Y-C Xu; H-Z Wang; T-S Li
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2014-12-04       Impact factor: 3.267

7.  High-throughput identification and quantification of Candida species using high resolution derivative melt analysis of panfungal amplicons.

Authors:  Tasneem Mandviwala; Rupali Shinde; Apoorv Kalra; Jack D Sobel; Robert A Akins
Journal:  J Mol Diagn       Date:  2009-12-10       Impact factor: 5.568

8.  Reliability of Pseudomonas aeruginosa semi-automated rep-PCR genotyping in various epidemiological situations.

Authors:  A Doléans-Jordheim; B Cournoyer; E Bergeron; J Croizé; H Salord; J André; M-A Mazoyer; F N R Renaud; J Freney
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2009-05-16       Impact factor: 3.267

9.  Host factors and clinical outcomes of Candida colonization in critically ill patients.

Authors:  David M Jacobs; Nicholas D Beyda; Orarik Asuphon; M Jahangir Alam; Kevin W Garey
Journal:  Mycopathologia       Date:  2014-08-31       Impact factor: 2.574

Review 10.  Molecular methods for pathogen and microbial community detection and characterization: current and potential application in diagnostic microbiology.

Authors:  Christopher D Sibley; Gisele Peirano; Deirdre L Church
Journal:  Infect Genet Evol       Date:  2012-02-09       Impact factor: 3.342

  10 in total

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