Disruption of HaVipR1 confers Vip3Aa resistance in the moth crop pest Helicoverpa armigera

The global reliance on Bacillus thuringiensis (Bt) proteins for controlling lepidopteran pests in cotton, corn, and soybean crops underscores the critical need to understand resistance mechanisms. Vip3Aa, one of the most widely deployed and currently effective Bt proteins in genetically modified crops, plays a pivotal role in pest management. This study investigates the molecular basis of Vip3Aa resistance in Australian Helicoverpa armigera through genetic crosses, and integrated genomic and transcriptomic analyses. We identified a previously uncharacterized gene, LOC110373801 (designated HaVipR1), as potentially important in Vip3Aa resistance in two field-derived resistant lines. Functional validation using CRISPR/Cas9 knockout in susceptible lines confirmed the gene's role in conferring high-level resistance to Vip3Aa. Despite extensive laboratory selection of Vip3Aa-resistant colonies in Lepidoptera, the biochemical mechanisms underlying resistance have remained elusive. Our research identifies HaVipR1 as a potential contributor to resistance, adding to our understanding of how insects may develop resistance to this important Bt protein. The identification of HaVipR1 contributes to our understanding of potential resistance mechanisms and may inform future resistance management strategies. Future work should explore the biochemical pathways influenced by HaVipR1 and assess its interactions with other resistance mechanisms. The approach utilized here underscores the value of field-derived resistant lines for understanding resistance in agricultural pests and highlights the need for targeted approaches to manage resistance sustainably.

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Publication Details

Journal
PLoS Biology
Published
2025-05-29
DOI
https://doi.org/10.1371/journal.pbio.3003165
Citations
9
Primary Topic
Insect Resistance and Genetics
Type
article
Field-Weighted Citation Impact
7.25

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article

Disruption of HaVipR1 confers Vip3Aa resistance in the moth crop pest Helicoverpa armigera

Amanda Padovan, Karl Gordon, Stephen L. Pearce, Andreas Bachler et al.
9 citations
PLoS Biology
Insect Resistance and Genetics
7.25
article

Disruption of HaVipR1 confers Vip3Aa resistance in the moth crop pest Helicoverpa armigera

Amanda Padovan, Karl Gordon, Stephen L. Pearce, Andreas Bachler, Ashley E. Tessnow, Tom Walsh, Wee Tek Tay, Craig Anderson, Bill James, Sharon Downes, Gregory A. Sword, Yidong Wu, Michelle Williams, Yiyun Wei
article en
9 citations

Abstract

The global reliance on Bacillus thuringiensis (Bt) proteins for controlling lepidopteran pests in cotton, corn, and soybean crops underscores the critical need to understand resistance mechanisms. Vip3Aa, one of the most widely deployed and currently effective Bt proteins in genetically modified crops, plays a pivotal role in pest management. This study investigates the molecular basis of Vip3Aa resistance in Australian Helicoverpa armigera through genetic crosses, and integrated genomic and transcriptomic analyses. We identified a previously uncharacterized gene, LOC110373801 (designated HaVipR1), as potentially important in Vip3Aa resistance in two field-derived resistant lines. Functional validation using CRISPR/Cas9 knockout in susceptible lines confirmed the gene's role in conferring high-level resistance to Vip3Aa. Despite extensive laboratory selection of Vip3Aa-resistant colonies in Lepidoptera, the biochemical mechanisms underlying resistance have remained elusive. Our research identifies HaVipR1 as a potential contributor to resistance, adding to our understanding of how insects may develop resistance to this important Bt protein. The identification of HaVipR1 contributes to our understanding of potential resistance mechanisms and may inform future resistance management strategies. Future work should explore the biochemical pathways influenced by HaVipR1 and assess its interactions with other resistance mechanisms. The approach utilized here underscores the value of field-derived resistant lines for understanding resistance in agricultural pests and highlights the need for targeted approaches to manage resistance sustainably.

PLoS BiologyVol. 23(5)
Nanjing Agricultural University (CN), Commonwealth Scientific and Industrial Research Organisation (AU), Cotton Research and Development Corporation (AU), Institute of Genetics and Cancer (GB), Texas A&M University (US), University of Edinburgh (GB)
Cotton Incorporated, Commonwealth Scientific and Industrial Research Organisation, Cotton Research and Development Corporation
Zero hunger
Openalex Percentile: Top 3%
Insect Resistance and Genetics
7.25
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