Establishment of a Cas12a-Based Visual Detection Method Involving PMNT for the Colletotrichum gloeosporioides Species Complex
文献类型： 外文期刊
作者： Zheng, Liu 1 ; Jiang, Wei 3 ; Zou, Xiaohua 1 ; Song, Lili 4 ; Xu, Xiaofeng 2 ; Han, Yongchao 5 ; Lian, Hongli 6 ; Wu, Xiao 3 ; Fang, Xianping 1 ; Zhang, Liqing 1 ;
作者机构： 1.Shanghai Acad Agr Sci, Forestry & Fruit Tree Res Inst, Shanghai Key Lab Protected Hort Technol, Shanghai, Peoples R China
2.Shanghai Normal Univ, Coll Life Sci, Shanghai 200234, Peoples R China
3.Shanghai Acad Agr Sci, Biotechnol Res Inst, Shanghai Key Lab Agr Genet & Breeding, Shanghai 201106, Peoples R China
4.Peoples Govt Nanping Town, Pingliang 744600, Peoples R China
5.Hubei Acad Agr Sci, Inst Ind Crops, Hubei Key Lab Vegetable Germplasm Enhancement & Ge, Wuhan 430064, Peoples R China
6.Shanghai Jiao Tong Univ, Sch Agr & Biol, Shanghai 212400, Peoples R China
关键词： anthracnose; CRISPR-Cas12a; field diagnosis; PMNT; visual method
期刊名称：PLANT DISEASE （ 影响因子：4.4； 五年影响因子：4.8 ）
ISSN： 0191-2917
年卷期： 2025 年 109 卷 3 期
页码：
收录情况： SCI
摘要： Strawberry anthracnose, caused by Colletotrichum spp., is a devastating disease that significantly reduces strawberry yield and quality. This study aimed to develop a simple diagnostic method to detect infection by the Colletotrichum gloeosporioides species complex (CGSC), the most predominant and virulent Colletotrichum species complex causing strawberry anthracnose in China. In this study, a Cas12aVIP diagnostic method was developed for the rapid detection of the CGSC in strawberry seedlings. This method targets the beta-tubulin gene and combines recombinase polymerase amplification (RPA), the CRISPR/Cas12a system, and a cationic-conjugated polythiophene derivative [poly(3-(3 '-N,N,N-triethylamino-1 '-propyloxy)-4-methyl-2,5-thiophene hydrochloride) (PMNT)] mixed with single-stranded DNA. This method shows high sensitivity (10 copies per reaction) and no cross-reactivity against related pathogens. The entire procedure, from sample to result, can be completed within 50 min, including simplified DNA extraction (15 min), RPA reaction (37 degrees C for 20 min), CRISPR/Cas12a detection (37 degrees C for 10 min), and visual detection by the naked eye (1 to 2 min). Furthermore, the Cas12aVIP assay successfully detected the CGSC in naturally infected strawberry seedling samples in field conditions. Asymptomatic infected plants and plant residues have been identified as primary inoculum sources for the CGSC. This method enables visible detection without the need for expensive equipment or specialized technical skills, thereby offering an efficient and straightforward approach for detecting the CGSC in strawberries. The newly developed detection method can be used to promote healthier strawberry production.
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