Literature DB >> 15770442

Electrophoretic karyotypes of C. neoformans serotype A recovered from Thai patients with AIDS.

Puriya Ngamwongsatit1, Samaniya Sukroongreung, Churairatana Nilakul, Virapong Prachayasittikul, Srisurang Tantimavanich.   

Abstract

Thirty-seven clinical isolates of C. neoformans were recovered from AIDS patients and all were serotype A according to standard typing tests. They were further analyzed using RAPD, PCR fingerprinting, and PFGE along with 2 additional reference isolates ATCC 34871 (serotype A) and RV 45981 (serotype D). Using 2 different RAPD primers, all of the clinical isolates and the reference serotype A (ATCC 34871) gave similar RAPD patterns while serotype D (RV 45981) gave distinctive pattern. Corresponding result was also obtained upon PCR by using a primer for microsatellite (GACA)4. However, using a primer specific to minisatellite M13+1, all PCR fingerprinting gave similar gel patterns (M1) for 35/37 of the clinical isolates and the reference serotype A while two clinical isolates generated different patterns called M2 and M3. The reference serotype D gave distinctive pattern called M4. PFGE gave 17 different karyotypes that could be categorized into 4 groups named EKA (1-6), EKB (1-5), EKC (1- 5) and EKD (1). The reference serotype A fell into group EKA as EKA6 while the reference serotype D fell into group EKC as EKC5. Among the clinical isolates, EKA group (20/37 isolates) and type EKA1 (16/20) dominated with only one isolate each for types EKA2 to EKA5. The next most prevalent was group EKB (12/37 isolates) which dominately fell in type EKB1 (8/12) and only one isolate each for types EKB2 to EKB5. Group EKC (4/37 isolates) and group EKD (1/37) had only one isolate for each type (EKC1 to EKC 4 and EKD1). The 2 predominant karyotypes (EKA1, 16/37 and EKB1, 8/37) may represent two originally common clones of C. neoformans expose among the patients. The high discriminatory power of PFGE infers the benefit of subtyping which lead to better understanding on the epidemiology and pathogenic potential of C. neoformans subtypes. Moreover, PCR fingerprinting and RAPD infer the feasibility of detail analysis between serotypes A and D for unencapsulated C. neoformans.

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Year:  2005        PMID: 15770442     DOI: 10.1007/s11046-004-6671-y

Source DB:  PubMed          Journal:  Mycopathologia        ISSN: 0301-486X            Impact factor:   2.574


  27 in total

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Review 2.  The evolutionary biology and population genetics underlying fungal strain typing.

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3.  Molecular typing of global isolates of Cryptococcus neoformans var. neoformans by polymerase chain reaction fingerprinting and randomly amplified polymorphic DNA-a pilot study to standardize techniques on which to base a detailed epidemiological survey.

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Journal:  Electrophoresis       Date:  1999-06       Impact factor: 3.535

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Authors:  B L Wickes; T D Moore; K J Kwon-Chung
Journal:  Microbiology       Date:  1994-03       Impact factor: 2.777

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Journal:  J Clin Microbiol       Date:  1994-05       Impact factor: 5.948

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Journal:  J Clin Microbiol       Date:  1995-07       Impact factor: 5.948

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8.  Variation in electrophoretic karyotype and antifungal susceptibility of clinical isolates of Cryptococcus neoformans at a university-affiliated teaching hospital from 1987 to 1994.

Authors:  M E Klepser; M A Pfaller
Journal:  J Clin Microbiol       Date:  1998-12       Impact factor: 5.948

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Authors:  B C Fries; F Chen; B P Currie; A Casadevall
Journal:  J Clin Microbiol       Date:  1996-06       Impact factor: 5.948

10.  Phenotypic and genotypic differentiation of several human and avian isolates of Cryptococcus neoformans.

Authors:  H Hotzel; P Kielstein; R Blaschke-Hellmessen; J Wendisch; W Bär
Journal:  Mycoses       Date:  1998-11       Impact factor: 4.377

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  2 in total

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Journal:  PLoS Negl Trop Dis       Date:  2013-07-04

Review 2.  Global Molecular Epidemiology of Cryptococcus neoformans and Cryptococcus gattii: An Atlas of the Molecular Types.

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Journal:  Scientifica (Cairo)       Date:  2013-01-09
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