Literature DB >> 15071024

Significance of amplified fragment length polymorphism in identification and epidemiological examination of Candida species colonization in children undergoing allogeneic stem cell transplantation.

L M Ball1, M A Bes, B Theelen, T Boekhout, R M Egeler, E J Kuijper.   

Abstract

Candida albicans and non-C. albicans Candida species are increasingly being isolated from patients in high-risk categories, most notably, those who have undergone stem cell transplantation (SCT). Identification of the presence of non-C. albicans Candida species early in the course of the transplant procedure is important, as these species exhibit different sensitivities to the available antifungal treatments and cause mortality at rates that vary from those for C. albicans. Amplified fragment length polymorphism (AFLP) analysis has been shown to be a reliable method of reproducibly identifying medically important Candida species. We investigated the use of serial AFLP analysis of 54 routine surveillance cultures for the identification and epidemiological examination of Candida sp. colonization in five consecutive children undergoing allogeneic SCT. One child became colonized with a C. albicans strain and remained colonized with this strain during the whole admission period. Another child had persistent colonization with a C. albicans strain with striking variations in its AFLP patterns over time, which was considered indicative of microevolution. Candida dubliniensis, Candida lusitaniae, and Saccharomyces cerevisiae were identified in the three remaining patients, with two children being simultaneously and transiently colonized with different species. These findings show that colonization with yeasts during transplantation is a complex and dynamic interaction between the host and the organism(s). In our study three strains from eight separate time points were incorrectly identified as C. albicans by a rapid enzyme test. AFLP analysis of surveillance cultures allowed more accurate and informative epidemiological evaluations of pathogenic yeasts in children during transplantation.

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Year:  2004        PMID: 15071024      PMCID: PMC387556          DOI: 10.1128/JCM.42.4.1673-1679.2004

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


  38 in total

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Journal:  J Clin Microbiol       Date:  1999-10       Impact factor: 5.948

Review 2.  Towards a targeted, risk-based, antifungal strategy in neutropenic patients.

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Journal:  Br J Haematol       Date:  2000-08       Impact factor: 6.998

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Journal:  J Gen Microbiol       Date:  1991-09

Review 4.  Candida infections: an overview.

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Journal:  Crit Rev Microbiol       Date:  1987       Impact factor: 7.624

5.  Retrospective analysis of yeast colonization and infections in paediatric bone marrow transplant recipients.

Authors:  J E Hoppe; M Klausner; T Klingebiel; D Niethammer
Journal:  Mycoses       Date:  1997 Jan-Feb       Impact factor: 4.377

6.  In vitro susceptibility testing and DNA typing of Saccharomyces cerevisiae clinical isolates.

Authors:  L Zerva; R J Hollis; M A Pfaller
Journal:  J Clin Microbiol       Date:  1996-12       Impact factor: 5.948

7.  Selective decontamination with nystatin for control of a Candida outbreak in a neonatal intensive care unit.

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Journal:  J Hosp Infect       Date:  1993-08       Impact factor: 3.926

8.  Candida dubliniensis candidemia in patients with chemotherapy-induced neutropenia and bone marrow transplantation.

Authors:  J F Meis; M Ruhnke; B E De Pauw; F C Odds; W Siegert; P E Verweij
Journal:  Emerg Infect Dis       Date:  1999 Jan-Feb       Impact factor: 6.883

9.  Non-albicans Candida is the most common cause of candidemia in pediatric cancer patients.

Authors:  C A Mullen; H Abd El-Baki; H Samir; J J Tarrand; K V Rolston
Journal:  Support Care Cancer       Date:  2003-03-11       Impact factor: 3.603

10.  Colonizing populations of Candida albicans are clonal in origin but undergo microevolution through C1 fragment reorganization as demonstrated by DNA fingerprinting and C1 sequencing.

Authors:  S R Lockhart; J J Fritch; A S Meier; K Schröppel; T Srikantha; R Galask; D R Soll
Journal:  J Clin Microbiol       Date:  1995-06       Impact factor: 5.948

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  7 in total

1.  Multilocus sequence typing for analyses of clonality of Candida albicans strains in Taiwan.

Authors:  Kuo-Wei Chen; Yee-Chun Chen; Hsiu-Jung Lo; Frank C Odds; Tzu-Hui Wang; Chi-Yang Lin; Shu-Ying Li
Journal:  J Clin Microbiol       Date:  2006-06       Impact factor: 5.948

Review 2.  Multilocus sequence typing of pathogenic Candida species.

Authors:  Frank C Odds; Mette D Jacobsen
Journal:  Eukaryot Cell       Date:  2008-05-02

3.  Genotyping of Candida orthopsilosis clinical isolates by amplification fragment length polymorphism reveals genetic diversity among independent isolates and strain maintenance within patients.

Authors:  Arianna Tavanti; Lambert A M Hensgens; Emilia Ghelardi; Mario Campa; Sonia Senesi
Journal:  J Clin Microbiol       Date:  2007-02-28       Impact factor: 5.948

4.  Oral candidiasis and oral yeast carriage among institutionalised South African paediatric HIV/AIDS patients.

Authors:  Elaine Blignaut
Journal:  Mycopathologia       Date:  2007-02-12       Impact factor: 2.574

5.  Molecular epidemiology of Fonsecaea species.

Authors:  Mohammad Javad Najafzadeh; Jiufeng Sun; Vania A Vicente; Corne H W Klaassen; Alexandro Bonifaz; A H G Gerrits van den Ende; Steph B J Menken; G Sybren de Hoog
Journal:  Emerg Infect Dis       Date:  2011-03       Impact factor: 6.883

6.  An interlaboratory comparison of ITS2-PCR for the identification of yeasts, using the ABI Prism 310 and CEQ8000 capillary electrophoresis systems.

Authors:  Thierry De Baere; Anne Van Keerberghen; Peter Van Hauwe; Hans De Beenhouwer; An Boel; Gerda Verschraegen; Geert Claeys; Mario Vaneechoutte
Journal:  BMC Microbiol       Date:  2005-03-18       Impact factor: 3.605

7.  PCR melting profile (PCR MP)--a new tool for differentiation of Candida albicans strains.

Authors:  Beata Krawczyk; Justyna Leibner-Ciszak; Anna Mielech; Magdalena Nowak; Józef Kur
Journal:  BMC Infect Dis       Date:  2009-11-11       Impact factor: 3.090

  7 in total

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