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)

Author:

Anu Cholenahalli Narayanappa12ORCID,Ashok Karuppannasamy134ORCID,Bhargava Chikmagalur Nagaraja12ORCID,Dhawane Yogi1ORCID,Manamohan Maligeppagol1ORCID,Jha Grish Kumar5,Asokan Ramasamy1ORCID

Affiliation:

1. Division of Basic Sciences ICAR‐Indian Institute of Horticultural Research Bengaluru Karnataka India

2. Department of Agricultural Entomology University of Agricultural Sciences Bengaluru Karnataka India

3. Department of Agricultural Entomology Tamil Nadu Agricultural University Coimbatore Tamil Nadu India

4. Tata Institute for Genetics and Society Bengaluru Karnataka India

5. Division of Bioinformatics ICAR‐Indian Agricultural Statistics Research Institute New Delhi India

Abstract

AbstractInvasive 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.

Publisher

Wiley

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