清脆的
生物
核酸
镰刀菌
放大器
聚合酶链反应
DNA
真菌毒素
遗传学
分子生物学
计算生物学
基因
生物技术
作者
Keqing Mu,Xiaojun Ren,Hao Yang,Ting Zhang,Weiyi Yan,Fengping Yuan,Jianhui Wu,Zhensheng Kang,Dejun Han,Ruijie Deng,Qingdong Zeng
标识
DOI:10.1021/acs.jafc.1c08391
摘要
Fusarium head blight (FHB) of wheat, mainly caused by Fusarium graminearum (F. graminearum) infection, reduces crop yield and contaminates grain with mycotoxins. We report a clustered regularly interspaced short palindromic repeats (CRISPR)-Cas12a-based nucleic acid assay for an early and rapid diagnosis of wheat FHB. Guide RNA (gRNA) was screened for highly specific recognition of polymerase chain reaction (PCR) amplicon of the internal transcribed spacer (ITS) region and the transcription elongation factor 1α (EF1α) of F. graminearum. The trans-activation of Cas12a protein cleaves the single-stranded DNA probes with the terminal fluorophore and quencher groups, thus allowing us to report the presence of ITS and EF1α of F. graminearum. Owing to the dual recognition process through PCR primers and gRNA hybridization, the approach realized specific discrimination of F. graminearum from other pathogenic fungi. It also allowed us to detect as low as 1 fg/μL total DNA from F. graminearum, which is sufficient to diagnose a 4 day F. graminearum infection. CRISPR-Cas12a-based nucleic acid assay promises the molecular diagnosis of crop diseases and broadens the application of CRISPR tools.
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