McRAPD as a new approach to rapid and accurate identification of pathogenic yeasts.

Despite advances in antifungal prophylaxis and therapy, morbidity and mortality incurred by yeasts remain a significant burden. As pathogenic yeast species vary in their susceptibilities to antifungal agents, clinical microbiology laboratories face an important challenge to identify them rapidly and accurately. Although a vast array of phenotyping and genotyping methods has been developed, these are either unable to cover the whole spectrum of potential yeast pathogens or can do this only in a rather costly or laborious way. Random amplified polymorphic DNA (RAPD) fingerprinting was repeatedly demonstrated to be a convenient tool for species identification in pathogenic yeasts. However, its wider acceptance has been limited mainly due to special expertise and software needed for analysis and comparison of the resulting banding patterns. Based on a pilot study, we demonstrate here that a simple and rapid melting curve analysis of RAPD products can provide data for identification of five of the most medically important Candida species. We have termed this new approach melting curve of random amplified polymorphic DNA (McRAPD) to emphasize its rapidity and potential for automation, highly desirable features for a routine laboratory test.

[1]  L. Villa-Tanaca,et al.  Identification of Candida spp. by Randomly Amplified Polymorphic DNA Analysis and Differentiation between Candida albicans and Candida dubliniensis by Direct PCR Methods , 2003, Journal of Clinical Microbiology.

[2]  J. SantaLucia,et al.  Improved nearest-neighbor parameters for predicting DNA duplex stability. , 1996, Biochemistry.

[3]  G. Coombs,et al.  Rapid identification of fungi by sequencing the ITS1 and ITS2 regions using an automated capillary electrophoresis system. , 2003, Medical mycology.

[4]  T. G. Mitchell,et al.  Rapid identification of Candida species by DNA fingerprinting with PCR , 1996, Journal of clinical microbiology.

[5]  F. Dromer,et al.  Antifungal drug resistance in pathogenic fungi. , 1998, Medical mycology.

[6]  Di Lin,et al.  Genotypic identification and characterization of species and strains within the genus Candida by using random amplified polymorphic DNA , 1992, Journal of clinical microbiology.

[7]  R. Charrel,et al.  Variations in DNA concentrations significantly affect the reproducibility of RAPD fingerprint patterns. , 1995, Research in microbiology.

[8]  W. Powderly,et al.  A prospective observational study of candidemia: epidemiology, therapy, and influences on mortality in hospitalized adult and pediatric patients. , 2003, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[9]  S. Jones,et al.  Genetic speciation of Candida isolates by arbitrarily primed polymerase chain reaction. , 1996, FEMS microbiology letters.

[10]  G. Scoles,et al.  Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. , 1993, PCR methods and applications.

[11]  A. S. Melo,et al.  Evolutionary distances and identification of Candida species in clinical isolates by Randomly Amplified Polymorphic DNA (RAPD) , 2004, Mycopathologia.

[12]  T. Clark,et al.  Recent trends in the epidemiology of invasive mycoses , 2002, Current opinion in infectious diseases.

[13]  P. Grimont,et al.  Factors affecting reproducibility of random amplified polymorphic DNA fingerprinting. , 1993, Research in microbiology.

[14]  A. Limaye,et al.  Identification of Medically Important Yeasts Using PCR-Based Detection of DNA Sequence Polymorphisms in the Internal Transcribed Spacer 2 Region of the rRNA Genes , 2000, Journal of Clinical Microbiology.

[15]  R. Hobson,et al.  The global epidemiology of invasive Candida infections--is the tide turning? , 2003, The Journal of hospital infection.

[16]  P. Chan,et al.  Rapid identification of medically important Candida to species level by polymerase chain reaction and single-strand conformational polymorphism. , 2000, Diagnostic microbiology and infectious disease.

[17]  H. Einsele,et al.  Identification of medically important fungi by the PyrosequencingTM technology , 2004, Mycoses.

[18]  M. Brandt,et al.  Resolution of Discrepant Results for Candida Species Identification by Using DNA Probes , 2004, Journal of Clinical Microbiology.

[19]  A. Freydiere,et al.  Yeast identification in the clinical microbiology laboratory: phenotypical methods. , 2001, Medical mycology.

[20]  Teun Boekhout,et al.  The yeasts : a taxonomic study , 1972 .

[21]  J. Welsh,et al.  Fingerprinting genomes using PCR with arbitrary primers. , 1990, Nucleic acids research.

[22]  J. Ellis,et al.  Heteroduplex molecules formed between allelic sequences cause nonparental RAPD bands. , 1994, Nucleic acids research.

[23]  K. Livak,et al.  DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. , 1990, Nucleic acids research.

[24]  F. Odds Resistance of yeasts to azole-derivative antifungals. , 1993, The Journal of antimicrobial chemotherapy.

[25]  T. Kanbe,et al.  PCR‐based identification of pathogenic Candida species using primer mixes specific to Candida DNA topoisomerase II genes , 2002, Yeast.

[26]  Dongsheng Xu,et al.  Rapid and accurate detection of monoclonal immunoglobulin heavy chain gene rearrangement by DNA melting curve analysis in the LightCycler System. , 2002, The Journal of molecular diagnostics : JMD.

[27]  J. Michálek,et al.  PCR-RFLP detection and species identification of fungal pathogens in patients with febrile neutropenia. , 2003, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

[28]  J. Sobel,et al.  Identification of Candida species by randomly amplified polymorphic DNA fingerprinting of colony lysates , 1997, Journal of clinical microbiology.

[29]  R. Wartell,et al.  Influence of nearest neighbor sequence on the stability of base pair mismatches in long DNA; determination by temperature-gradient gel electrophoresis. , 1993, Nucleic acids research.