Identification of medically important pathogenic fungi by reference strand-mediated conformational analysis (RSCA)

被引:6
作者
McIlhatton, BP [1 ]
Keating, C
Curran, MD
McMullin, MF
Barr, JG
Madrigal, JA
Middleton, D
机构
[1] City Hosp, No Ireland Reg Histocompatibil & Immunogenet Lab, Belfast, Antrim, North Ireland
[2] Queens Univ Belfast, Sch Med, Belfast, Antrim, North Ireland
[3] Queens Univ Belfast, Sch Biol & Biochem, Belfast BT7 1NN, Antrim, North Ireland
[4] Royal Victoria Hosp, Dept Haematol, Belfast BT12 6BA, Antrim, North Ireland
[5] Queens Univ Belfast, Dept Haematol, Belfast, Antrim, North Ireland
[6] Royal Victoria Hosp, Dept Bacteriol & Mycol, Belfast BT12 6BA, Antrim, North Ireland
[7] Royal Free Hosp, Anthony Nolan Res Inst, London NW3 2QG, England
[8] Univ Ulster, Sch Biomed Sci, Coleraine BT52 1SA, Londonderry, North Ireland
关键词
D O I
10.1099/0022-1317-51-6-468
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This report describes the application of reference strand-mediated conformational analysis (RSCA), a novel DNA typing technique, for the identification of clinically significant fungal pathogens. RSCA is a heteroduplex-based conformational method which relies on detecting differences in the DNA conformation of heteroduplexes generated in this study by the annealing of different fungal 18S rRNA amplicons to a common fluorescent-labelled reference (FLR). These heteroduplexes are then observed with laser-based instrumentation and computer software to detect differences in the DNA conformation reproducibly. This technique was shown to generate unique and reproducible profiles for the 18S rRNA gene sequences of a number of medically important fungi, distinguishing different Candida species (C. albicans, C. kefyr, C. dubliniensis, C. lusitaniae, C. guilliermondii, C. tropicalis, C. krusei, C. glabrata, C. sake and C parapsilosis), and in some cases detecting single nucleotide differences between 18S rRNA sequences. The RSCA technique was further evaluated with 50 human clinical isolates of Candida spp., previously identified by culture techniques, and was shown to identify the isolates correctly. This technique displays enormous potential as an alternative to DNA sequence determination and has the potential to become an automated technique that can be implemented in the routine setting.
引用
收藏
页码:468 / 478
页数:11
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