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Simultaneous Detection and Identification of Candida Aspergillus and Cryptococcus Species by Reverse Line Blot Hybridization

机译:反向印迹杂交技术同时检测和鉴定念珠菌曲霉和隐球菌

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摘要

We report on a reverse line blot (RLB) assay, utilizing fungal species-specific oligonucleotide probes to hybridize with internal transcribed spacer 2 region sequences amplified using a nested panfungal PCR. Reference and clinical strains of 16 Candida species (116 strains), Cryptococcus neoformans (five strains of Cryptococcus neoformans var. neoformans, five strains of Cryptococcus neoformans var. grubii, and six strains of Cryptococcus gatti), and five Aspergillus species (68 strains) were all correctly identified by the RLB assay. Additional fungal species (16 species and 26 strains) not represented on the assay did not exhibit cross-hybridization with the oligonucleotide probes. In simulated clinical specimens, the sensitivity of the assay for Candida spp. and Aspergillus spp. was 100.5 cells/ml and 102 conidia/ml, respectively. This assay allows sensitive and specific simultaneous detection and identification of a broad range of fungal pathogens.
机译:我们报告了反向线印迹(RLB)测定法,利用真菌物种特异性寡核苷酸探针与使用巢式Panfungal PCR扩增的内部转录间隔区2区序列杂交。参考和临床菌株16种念珠菌(116株),新隐球菌(5株新隐球菌,新福尔摩斯变种,5株新隐球菌,格鲁比变种和6株隐球菌加蒂)和5种曲霉菌(68株)通过RLB分析正确鉴定。试验中未显示的其他真菌种类(16种和26个菌株)未显示与寡核苷酸探针的交叉杂交。在模拟的临床标本中,测定对假丝酵母属的敏感性。和曲霉属。分别是10 0.5 细胞/ ml和10 2 分生孢子/ ml。该测定法可以同时灵敏,特异地检测和鉴定各种真菌病原体。

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