Development of a TaqMan probe-based multiplex real-time PCR for the simultaneous detection of four clinically important filamentous fungi

被引:0
|
作者
Wei, Yutong [1 ,2 ]
Lin, Yangxuan [1 ,2 ]
Zhao, Jingya [2 ]
Li, Dingchen [2 ]
Yang, Zhankui [2 ,3 ]
Chen, Fangyan [2 ]
Han, Li [1 ,2 ]
机构
[1] Anhui Med Univ, Sch Publ Hlth, Hefei, Anhui, Peoples R China
[2] Chinese PLA Ctr Dis Control & Prevent, Dept Disinfect & Infect Control, Beijing, Peoples R China
[3] Zhengzhou Univ, Zhengzhou, Peoples R China
来源
MICROBIOLOGY SPECTRUM | 2024年 / 12卷 / 09期
基金
中国国家自然科学基金;
关键词
fungal infection; multiplex real-time qPCR; Aspergillus fumigatus; Mucorales; Histoplasma capsulatum; Fusarium spp; POLYMERASE-CHAIN-REACTION; HISTOPLASMA-CAPSULATUM; ASSAY; IDENTIFICATION; DIAGNOSIS; QPCR;
D O I
10.1128/spectrum.00634-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Filamentous fungi present significant health hazards to immunocompromised individuals globally; however, the prompt and precise identification of them during infection remains challenging. In this study, a TaqMan probe-based multiplex real-time PCR (M-qPCR) assay was developed to detect simultaneously the target genes of four important pathogenic filamentous fungi: ANXC4 gene of Aspergillus fumigatus, EF1-alpha gene of Fusarium spp., mitochondrial rnl gene of Mucorales, and hcp100 gene of Histoplasma capsulatum. In this M-qPCR assay, the limit of detection (LoD) to all four kinds of fungi was 100 copies and the correlation coefficients (R-2) were above 0.99. The specificity of this assay is 100%, and the minimum detection limit is 100 copies/reaction. In conclusion, an M-qPCR detection assay was well established with high specificity and sensitivity for rapid and simultaneous detection on four important filamentous fungi in the clinic.
引用
收藏
页数:15
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