Literature DB >> 9854084

Rapid identification of up to three Candida species in a single reaction tube by a 5' exonuclease assay using fluorescent DNA probes.

J H Shin1, F S Nolte, B P Holloway, C J Morrison.   

Abstract

We used fungus-specific PCR primers and species-specific DNA probes to detect up to three Candida species in a single reaction tube by exploiting the 5' to 3' exonuclease activity of Taq DNA polymerase. Probes to the internal transcribed spacer region of the rRNA gene were labeled at the 5' end with one of three fluorescent reporter dyes, 6-carboxy-fluorescein (FAM), tetrachloro-6-carboxy-fluorescein (TET), or hexachloro-6-carboxy-fluorescein (HEX), and at the 3' end with a quencher dye, 6-carboxy-tetramethyl-rhodamine. During PCR amplification, each reporter dye emits a characteristic wavelength as it is cleaved from its specific target DNA and from the quencher dye. Therefore, signals from up to three probes can be detected simultaneously during the PCR assay. Six probes were designed for use in this study: CA-FAM, CT-TET, and CP-HEX were added to one tube to simultaneously detect the typically fluconazole-sensitive species C. albicans, C. tropicalis, and C. parapsilosis, respectively. CG-FAM and CK-TET were added to a second tube to simultaneously detect the typically more innately fluconazole-resistant species C. glabrata and C. krusei, respectively. All-CAN-TET, a Candida genus probe, was added to a third tube to detect DNAs from all Candida species tested. DNAs recovered from 61 blood culture bottles, including 23 positive for C. albicans, 18 positive for C. glabrata, 6 positive for C. tropicalis, 6 positive for C. krusei, 5 positive for C. parapsilosis, and 3 positive for mixed fungemias, were tested. Control samples included those from blood culture bottles with no growth (n = 10) or from patients with confirmed bacteremia (n = 10). Probes detected and correctly identified the organisms in 58 of 61 specimens (95.1%) and gave no false-positive results. This method is simple and rapid and does not require post-PCR hybridization and incubation steps. It is sensitive and specific for the detection and identification of Candida species from blood culture bottles, including those containing mixtures of Candida species, and should facilitate an earlier specific diagnosis, leading to more appropriately targeted antifungal drug therapy.

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Year:  1999        PMID: 9854084      PMCID: PMC84197     

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


  27 in total

1.  National surveillance of nosocomial blood stream infection due to species of Candida other than Candida albicans: frequency of occurrence and antifungal susceptibility in the SCOPE Program. SCOPE Participant Group. Surveillance and Control of Pathogens of Epidemiologic.

Authors:  M A Pfaller; R N Jones; S A Messer; M B Edmond; R P Wenzel
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Journal:  Clin Infect Dis       Date:  1996-05       Impact factor: 9.079

3.  Comparison of antigen detection and PCR assay using bronchoalveolar lavage fluid for diagnosing invasive pulmonary aspergillosis in patients receiving treatment for hematological malignancies.

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Journal:  J Clin Microbiol       Date:  1995-12       Impact factor: 5.948

4.  Detection of surgical pathogens by in vitro DNA amplification. Part I. Rapid identification of Candida albicans by in vitro amplification of a fungus-specific gene.

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Journal:  Surgery       Date:  1990-08       Impact factor: 3.982

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Journal:  Am J Med       Date:  1991-09-16       Impact factor: 4.965

6.  Antifungal susceptibility testing of isolates from a randomized, multicenter trial of fluconazole versus amphotericin B as treatment of nonneutropenic patients with candidemia. NIAID Mycoses Study Group and the Candidemia Study Group.

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Journal:  Antimicrob Agents Chemother       Date:  1995-01       Impact factor: 5.191

Review 7.  Importance of Candida species other than C. albicans as pathogens in oncology patients.

Authors:  J R Wingard
Journal:  Clin Infect Dis       Date:  1995-01       Impact factor: 9.079

8.  Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase.

Authors:  P M Holland; R D Abramson; R Watson; D H Gelfand
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-15       Impact factor: 11.205

9.  Microtitration plate enzyme immunoassay to detect PCR-amplified DNA from Candida species in blood.

Authors:  S Fujita; B A Lasker; T J Lott; E Reiss; C J Morrison
Journal:  J Clin Microbiol       Date:  1995-04       Impact factor: 5.948

10.  PCR identification of four medically important Candida species by using a single primer pair.

Authors:  J A Jordan
Journal:  J Clin Microbiol       Date:  1994-12       Impact factor: 5.948

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  22 in total

1.  Multiplex PCR using internal transcribed spacer 1 and 2 regions for rapid detection and identification of yeast strains.

Authors:  S I Fujita; Y Senda; S Nakaguchi; T Hashimoto
Journal:  J Clin Microbiol       Date:  2001-10       Impact factor: 5.948

2.  Early detection and identification of commonly encountered Candida species from simulated blood cultures by using a real-time PCR-based assay.

Authors:  Younes Maaroufi; Jean-Marc De Bruyne; Valérie Duchateau; Aspasia Georgala; Françoise Crokaert
Journal:  J Mol Diagn       Date:  2004-05       Impact factor: 5.568

3.  Rapid identification of candida species by TaqMan PCR.

Authors:  M Guiver; K Levi; B A Oppenheim
Journal:  J Clin Pathol       Date:  2001-05       Impact factor: 3.411

4.  Development of novel real-time PCR assays for detection and differentiation of eleven medically important Aspergillus and Candida species in clinical specimens.

Authors:  Claudia Schabereiter-Gurtner; Brigitte Selitsch; Manfred L Rotter; Alexander M Hirschl; Birgit Willinger
Journal:  J Clin Microbiol       Date:  2007-01-24       Impact factor: 5.948

5.  Identification of Aspergillus species using internal transcribed spacer regions 1 and 2.

Authors:  T Henry; P C Iwen; S H Hinrichs
Journal:  J Clin Microbiol       Date:  2000-04       Impact factor: 5.948

6.  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

7.  Rapid detection of Candida albicans in clinical blood samples by using a TaqMan-based PCR assay.

Authors:  Younes Maaroufi; Corine Heymans; Jean-Marc De Bruyne; Valerie Duchateau; Hector Rodriguez-Villalobos; Michel Aoun; Françoise Crokaert
Journal:  J Clin Microbiol       Date:  2003-07       Impact factor: 5.948

8.  Comparison of different methods of isolation of DNA of commonly encountered Candida species and its quantitation by using a real-time PCR-based assay.

Authors:  Younes Maaroufi; Naïma Ahariz; Mireille Husson; Françoise Crokaert
Journal:  J Clin Microbiol       Date:  2004-07       Impact factor: 5.948

9.  Rapid differentiation of Aspergillus species from other medically important opportunistic molds and yeasts by PCR-enzyme immunoassay.

Authors:  Liliana de Aguirre; Steven F Hurst; Jong Soo Choi; Jong Hee Shin; Hans Peter Hinrikson; Christine J Morrison
Journal:  J Clin Microbiol       Date:  2004-08       Impact factor: 5.948

10.  Rapid identification of commonly encountered Candida species directly from blood culture bottles.

Authors:  Rangaraj Selvarangan; Uyen Bui; Ajit P Limaye; Brad T Cookson
Journal:  J Clin Microbiol       Date:  2003-12       Impact factor: 5.948

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