Hyperbranched rolling circle amplification as a rapid and sensitive method for species identification within the Cryptococcus species complex

被引:57
作者
Kaocharoen, Sirada [2 ]
Wang, Bin [3 ]
Tsui, Kin Ming
Trilles, Luciana [4 ]
Kong, Fanrong [5 ]
Meyer, Wieland [1 ,6 ]
机构
[1] Westmead Hosp, ICPMR, Westmead Millennium Inst, Mol Mycol Res Lab,CIDM, Westmead, NSW 2145, Australia
[2] Chulalongkorn Univ, Grad Sch, Inter Dept Med Microbiol, Bangkok, Thailand
[3] Univ Sydney, Westmead Millennium Inst, Ctr Virus Res, Retroviral Genet Lab, Sydney, NSW 2006, Australia
[4] Fundacao Oswaldo Cruz, Inst Pesquisa Clin Evandro Chargas, Lab Micol, Rio De Janeiro, Brazil
[5] Westmead Hosp, Inst Clin Pathol & Med Res, Ctr Infect Dis & Microbiol Publ Hlth, Westmead, NSW 2145, Australia
[6] Univ Sydney, Westmead Hosp, Fac Med, Western Clin Sch, Sydney, NSW 2006, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Cryptococcus neoformans; Cryptococcus gattii; hyperbranched rolling circle amplification; internal transcribed spacer; species identification;
D O I
10.1002/elps.200700903
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Cryptococcus species complex contains two closely related basidiomycetous yeasts: Cryptococcus neoformans and C. gattii, which cause cryptococcosis in humans and other animals. The species and varieties are characterized, by different clinical, epidemiological, biochemical and molecular features. The currently used identification methods are either time-consuming or not anymore commercially available. However, a rapid, sensitive and robust assay for the detection of these pathogens is vital for early diagnosis and appropriate treatment decisions. To overcome those limitations, four padlock probes targeting species-specific single nucleotide polymorphisms at the internal transcribed spacers (ITSs) of the RNA gene locus were developed and applied during isothermal hyperbranched rolling circle amplification (HRCA). The probes were tested against 99 samples, including 94 clinical cryptococcal cultures, three closely related Cryptococcus species, and two clinical specimens. The use of the padlock probes and the combination of probe signal amplification by HRCA provided a quick and sensitive assay for the accurate identification of C. neoformans var. grubii, C. neoformans var. neoformans and C. gattii. HRCA was also useful to detect hybrids, when they were heterozygous at the ITS locus. The H RCA results were in agreement with previous genotyping data based on PCR fingerprinting, amplified fragment length polymorphism. and ITS sequencing.
引用
收藏
页码:3183 / 3191
页数:9
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