Downregulation of a transcription factor associated with resistance to Bt toxin Vip3Aa in the invasive fall armyworm

Author:

Jin Minghui12,Shan Yinxue1,Peng Yan13,Wang Wenhui2,Zhang Huihui4,Liu Kaiyu4,Heckel David G.5ORCID,Wu Kongming2ORCID,Tabashnik Bruce E.6ORCID,Xiao Yutao1ORCID

Affiliation:

1. Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Key Laboratory of Gene Editing Technologies (Hainan), Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518116, China

2. The State Key Laboratory for Biology of Plant Disease and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China

3. College of Plant Science and Technology, Huazhong Agricultural University, Wuhan 430070, China

4. Institute of Entomology, School of Life Sciences, Central China Normal University, Wuhan 430079, China

5. Department of Entomology, Max Planck Institute for Chemical Ecology, Jena D-07745, Germany

6. Department of Entomology, University of Arizona, Tucson, AZ 85721

Abstract

Transgenic crops producing insecticidal proteins from Bacillus thuringiensis (Bt) have revolutionized control of some major pests. However, more than 25 cases of field-evolved practical resistance have reduced the efficacy of transgenic crops producing crystalline (Cry) Bt proteins, spurring adoption of alternatives including crops producing the Bt vegetative insecticidal protein Vip3Aa. Although practical resistance to Vip3Aa has not been reported yet, better understanding of the genetic basis of resistance to Vip3Aa is urgently needed to proactively monitor, delay, and counter pest resistance. This is especially important for fall armyworm ( Spodoptera frugiperda ), which has evolved practical resistance to Cry proteins and is one of the world’s most damaging pests. Here, we report the identification of an association between downregulation of the transcription factor gene SfMyb and resistance to Vip3Aa in S. frugiperda . Results from a genome-wide association study, fine-scale mapping, and RNA-Seq identified this gene as a compelling candidate for contributing to the 206-fold resistance to Vip3Aa in a laboratory-selected strain. Experimental reduction of SfMyb expression in a susceptible strain using RNA interference (RNAi) or CRISPR/Cas9 gene editing decreased susceptibility to Vip3Aa, confirming that reduced expression of this gene can cause resistance to Vip3Aa. Relative to the wild-type promoter for SfMyb , the promoter in the resistant strain has deletions and lower activity. Data from yeast one-hybrid assays, genomics, RNA-Seq, RNAi, and proteomics identified genes that are strong candidates for mediating the effects of SfMyb on Vip3Aa resistance. The results reported here may facilitate progress in understanding and managing pest resistance to Vip3Aa.

Funder

the Sci-Tech Innovation 2030 Agenda

MOST | National Natural Science Foundation of China

CAAS | Agricultural Science and Technology Innovation Program

Science, Technology and Innovation Commission of Shenzhen Municipality

USDA National Institute for Food and Agriculture

Innovation Program of Chinese Academy of Agricultural Science

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference84 articles.

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