4.6 Article

Bt Cry1Ac resistance in Trichoplusia ni is conferred by multi-gene mutations

Journal

INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY
Volume 140, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ibmb.2021.103678

Keywords

Trichoplusia ni; Bacillus thuringiensis; Bt resistance; Cry1Ac; ABCC2 gene; APN genes

Funding

  1. USDA AFRI Foundational Program Competitive Grants [2016-67013-24754, 2019-67013-29349]
  2. NIFA [2016-67013-24754, 810759] Funding Source: Federal RePORTER

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The study identified a 4 bp frameshift insertion in the ABCC2 gene as the specific mutation conferring Cry1Ac resistance in Trichoplusia ni through whole genome resequencing, and confirmed the importance of ABCC2 in the resistance process. Additionally, another gene mutation was found to be responsible for altered expression of APN1 and APN6. Furthermore, the study suggested the presence of additional Cry1Ac resistance-conferring mutation(s) in the resistant strain, which have yet to be identified.
The three-domain Cry toxin Cry1Ac from Bacillus thuringiensis (Bt) is an important insecticidal toxin in Bt sprays and has been used in transgenic Bt-crops to confer insect resistance. The cabbage looper, Trichoplusia ni, has developed resistance to Bt sprays in commercial greenhouses, and the resistance to Cry1Ac has been previously identified to be associated with altered expression of the APN1 and APN6 genes and be genetically linked to a locus on chromosome 15. In this study, the Cry1Ac resistance locus in T. ni was further finely mapped, and the specific Cry1Ac resistance-conferring mutation in the resistance locus was identified to be a 4 bp frameshift insertion in the ABCC2 gene by whole genome resequencing, midgut transcriptome analysis, candidate gene cDNA sequencing and mutation site genomic DNA sequencing. By CRISPR/Cas9 mutagenesis, a series of ABCC2 and ABCC3 mutant T. ni strains were generated, and the role of ABCC2 in the toxicity of Cry1Ac in T. ni was confirmed. The results from this study also showed that knockout of ABCC2 in T. ni conferred resistance to Cry1Ac at a level lower than that in the greenhouse-derived resistant T. ni strain and that the Cry1Ac resistanceassociated alteration of APN1 and APN6 expression was independent of ABCC2 gene mutations, indicating that the altered expression of APN1 and APN6 was controlled by another gene mutation in Cry1Ac resistant T. ni. Furthermore, T. ni larval bioassays showed that the level of Cry1Ac resistance in F1 families from reciprocal crosses of the Cry1Ac resistant strain with an ABCC2 knockout CRISPR strain was significantly higher than that in ABCC2 knockout strain, indicating the presence of additional Cry1Ac resistance-conferring mutation(s) in the Cry1Ac resistant strain. Therefore, the resistance to Cry1Ac in T. ni is conferred by a mutation in ABCC2 and an additional mutation (or mutations) which leads to altered expression of APN1 and APN6. The additional Cry1Ac resistance mutation or mutations remain to be identified.

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