Asp‐2078‐Gly mutation in ACCase confers quizalofop‐ p ‐ethyl resistance in Eleusine indica and establishment of a LAMP – CRISPR /Cas12a visual genotyping assay for the target mutation

作者：Guanglei Jin, Haotong Li, Hou–Yong Yu, Zumin Gu, Hailan Cui, Jingchao Chen, Xiangju Li · 发表于：Pest Management Science · 年份：2026 · DOI：10.1002/ps.70468 · 被引用次数：2 · 研究领域：Weed Control and Herbicide Applications、Insect-Plant Interactions and Control、CRISPR and Genetic Engineering

BACKGROUND: Eleusine indica is a widespread, competitive weed causing yield losses in major crops. Repeated use of acetyl-CoA carboxylase (ACCase)-inhibiting herbicides in cotton fields has led to the evolution of resistant populations, posing a growing threat to cotton production in China. This study aimed to elucidate the target-site resistance mechanism of E. indica to quizalofop-p-ethyl and establish a rapid visual detection method based on the identified mutation. RESULTS: The NJC-R population showed resistance to quizalofop-p-ethyl (resistance index = 5.5). Gene sequencing revealed that an Asp-2078-Gly mutation in ACCase was one of the mechanisms underlying resistance. Loop-mediated isothermal amplification (LAMP) combined with the CRISPR/Cas12a system was developed to detect this mutation in E. indica. This method not only enabled genotype discrimination (wild-type, heterozygous, homozygous mutant), but also provided visual results within 70 min, exhibiting superior performance compared with the derived cleaved amplified polymorphic sequences assay. In addition, this method eliminated false positives from nonspecific LAMP amplification, was ~100-fold more sensitive than a polymerase chain reaction, and the assay results were 100% concordant with Sanger sequencing for the 50 samples tested. CONCLUSION: This study confirmed that the Asp-2078-Gly mutation confers quizalofop-p-ethyl resistance in E. indica from the cotton field in China, and LAMP-CRISPR/Cas12a was first ap...