Abstract

Simple SummaryMonitoring of resistance alleles is critical to the sustainability of transgenic crops producing insecticidal Cry proteins. Highly sensitive and cost-effective DNA-based methods are needed to improve current bioassay-based resistance screening. Our goal was to evaluate the use of targeted sequencing in detecting known and novel candidate resistance alleles to Cry proteins. As a model, we used field-collected fall armyworm (Spodoptera frugiperda) from Puerto Rico, the first location reporting continued practical field-evolved S. frugiperda resistance to corn producing the Cry1F insecticidal protein, and sequenced the SfABCC2 gene previously identified as critical to Cry1F toxicity. Targeted sequencing of SfABCC2 detected a previously reported Cry1F resistance allele and mutations originally identified in populations from Brazil. Importantly, targeted sequencing also identified nonsynonymous and frameshift mutations as novel candidate resistance alleles. These results advocate for the use of targeted sequencing in screening for resistance alleles to Cry proteins and support potential gene flow, including resistance alleles, between S. frugiperda from Brazil and the Caribbean. Evolution of practical resistance is the main threat to the sustainability of transgenic crops producing insecticidal proteins from Bacillus thuringiensis (Bt crops). Monitoring of resistance to Cry and Vip3A proteins produced by Bt crops is critical to mitigate the development of resistance. Currently, Cry/Vip3A resistance allele monitoring is based on bioassays with larvae from inbreeding field-collected moths. As an alternative, DNA-based monitoring tools should increase sensitivity and reduce overall costs compared to bioassay-based screening methods. Here, we evaluated targeted sequencing as a method allowing detection of known and novel candidate resistance alleles to Cry proteins. As a model, we sequenced a Cry1F receptor gene (SfABCC2) in fall armyworm (Spodoptera frugiperda) moths from Puerto Rico, a location reporting continued practical field resistance to Cry1F-producing corn. Targeted sequencing detected a previously reported Cry1F resistance allele (SfABCC2mut), in addition to a resistance allele originally described in S. frugiperda populations from Brazil. Moreover, targeted sequencing detected mutations in SfABCC2 as novel candidate resistance alleles. These results support further development of targeted sequencing for monitoring resistance to Bt crops and provide unexpected evidence for common resistance alleles in S. frugiperda from Brazil and Puerto Rico.

Highlights

  • IntroductionEffective control of S. frugiperda in the Western hemisphere in addition to pesticides, has been provided by genetically modified corn and cotton producing insecticidal proteins from the bacterium Bacillus thuringiensis (Bt), namely Cry1F, Cry1Ab, Cry1A.105, Cry2Ab and Vip3Aa. In the past decade, resistance to Cry1F, Cry1Ab and Cry1A.105 was reported for S. frugiperda populations in Puerto Rico and the continental US (Florida and North Carolina) [4,5], Brazil [6] and Argentina [7]

  • We focused our analysis on S. frugiperda samples from Puerto Rico, as both SfABCC2mut and Cry1F resistance are highly frequent at this location [8,18]

  • We provide proof of concept for the use of targeted sequencing in the monitoring of known mutations and the discovery of candidate resistance alleles to Cry1F in S. frugiperda

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Summary

Introduction

Effective control of S. frugiperda in the Western hemisphere in addition to pesticides, has been provided by genetically modified corn and cotton producing insecticidal proteins from the bacterium Bacillus thuringiensis (Bt), namely Cry1F, Cry1Ab, Cry1A.105, Cry2Ab and Vip3Aa. In the past decade, resistance to Cry1F, Cry1Ab and Cry1A.105 was reported for S. frugiperda populations in Puerto Rico and the continental US (Florida and North Carolina) [4,5], Brazil [6] and Argentina [7]. Fall armyworm resistance to these Cry proteins is recessive and genetically linked to mutations in an ABC transporter superfamily C2 gene (SfABCC2) [8,9,10]. Genetic knockout of SfABCC2 leads to resistance against Cry1F [12,13] further supporting that truncation of SfABCC2 is predictive of a Cry1F-resistant phenotype

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