Direct parental CRISPR gene editing in the predatory bug Orius strigicollis, a biocontrol agent against small arthropods

Abstract

AbstractBACKGROUNDThe predatory flower bug Orius strigicollis serves as a valuable biocontrol agent against small arthropods; however, its effectiveness can vary, especially when population establishment fails due to low prey/pest densities. A promising approach to improve the efficacy of O. strigicollis as a biocontrol agent is through gene editing. However, as females lay their eggs in plant tissue, the conventional embryo injection approach is challenging in this species.RESULTSIn this study, we aimed to develop an efficient and practical gene editing technique for O. strigicollis using direct parental CRISPR (DIPA‐CRISPR). Female bugs at various postemergence stages received Cas9 ribonucleoprotein injections, with subsequent genotyping of their offspring (G0) using PCR and a heteroduplex mobility assay. We targeted the kynurenine 3‐monooxygenase gene (cinnabar), pivotal for insect ommochrome pigment biosynthesis. Through experimental optimization, we achieved a peak gene editing efficiency of 52%, i.e., 52% of G0 progeny carried gene‐edited alleles when injecting 1 day postemergence. Notably, some gene‐edited G0 adults exhibited a red‐eye mosaic phenotype, in contrast to the black‐eyed wild type. Crossing experiments confirmed the heritability of the introduced mutations in the subsequent generation (G1), enabling the establishment of a cinnabar‐knockout line with bright red eyes.CONCLUSIONWe demonstrate that our DIPA‐CRISPR gene editing method tailored for O. strigicollis is efficient and practical. Our findings highlight the potency of DIPA‐CRISPR as a tool for O. strigicollis genetic engineering and suggest broader applications for enhancing other biocontrol agents. © 2024 Society of Chemical Industry.