CRISPR/Cas9 mediated validation of spermatogenesis‐related gene, tssk2 as a component of genetic pest management of fall armyworm, Spodoptera frugiperda (J. E. Smith) (Lepidoptera: Noctuidae)

生物 夜蛾 清脆的 粘虫 病虫害综合治理 生物技术 昆虫不育技术 Cas9 夜蛾科 甜菜 有害生物分析 遗传学 生态学 植物 基因 重组DNA
作者
Cholenahalli Narayanappa Anu,K. R. Ashok,Chikmagalur Nagaraja Bhargava,Yogi Dhawane,Maligeppagol Manamohan,Girish Kumar Jha,Ramasamy Asokan
出处
期刊:Archives of Insect Biochemistry and Physiology [Wiley]
卷期号:116 (1): e22121-e22121 被引量:7
标识
DOI:10.1002/arch.22121
摘要

Abstract Invasive insect pests, currently, pose a serious economic threat to several staple crops all over the world, one such being the fall armyworm, Spodoptera frugiperda. It was first observed in Africa since 2016, outside of its natural habitat in the Americas. Subsequently, it invaded several countries in South and South East Asia and also very recently in Australia. In all the newly invaded regions, maize is the principal crop attacked causing a serious economic concern to the poor farmers, particularly in the developing countries. Owing to the innate genetic ability, it defies many of the management options that include insecticides, Bt transgenics, and so forth. This is due to its high mobility, polyphagy and ability for quick development of resistance to several classes of insecticides. At this critical juncture, CRISPR/Cas9 mediated genome editing has shown a lot of promise in developing a novel area‐wide pest management strategy called precision‐guided sterile insect technique (pgSIT). pgSIT was initially demonstrated in Drosophila melanogaster which holds a greater promise for the environmentally friendly management of several globally significant agricultural pests such as S. frugiperda. Therefore, before developing both sgRNA and Cas9 transgenic lines, we have validated the target gene such as tssk2 through a non‐transgenic approach by microinjecting ribo nucleo protein complex (Cas9 protein and tssk2 sgRNA) into G0 eggs of S. frugiperda. In the current investigation, we have obtained five edited males with distinct mutations which were further used for crossing studies to ascertain the effect of tssk2 editing affecting egg hatchability.

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