Role of mitochondrial complex I genes in host plant expansion of Bactrocera tau (Tephritidae: Diptera) by CRISPR/Cas9 system.

IF 2.9 1区 农林科学 Q1 ENTOMOLOGY Insect Science Pub Date : 2025-01-19 DOI:10.1111/1744-7917.13495
Wei Shi, Linsheng He, Ruixiang Li, Jun Cao
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Abstract

Host expansion facilitates tephritid flies to expand their ranges. Unraveling the mechanisms of host expansion will help to efficiently control these pests. Our previous works showed mitochondrial complex I genes Ndufs1, Ndufs3, and Ndufa7 being upregulated during host expansion of Bactrocera tau (Walker), one of the highly hazardous species of tephritids. However, their roles in the host expansion of B. tau remain unknown. Here, using clustered regularly interspaced short palindromic repeats (CRISPR) / CRISPR-associated nuclease 9 (Cas9) editing system for the first time, a stable homozygous Ndufa7 strain (Btndufa7-/-), heterozygous Ndufs1 (Btndufs1+/-), and Ndufs3 strains (Btndufs3+/-) were obtained from F3 generation of B. tau, after gene knockout. Reduced sizes of larvae and pupae of the Ndufa7 knockout strain were first observed. Notably, the mean values of fitness estimation (pupal numbers, single-pupal weight and emergence rate) and Ndufa7 gene expression in the Ndufa7 knockout strain were slightly reduced on 2 native hosts (summer squash and cucumber), while it sharply decreased on the novel host banana and the potential host pitaya, compared with those of the wild-type strain. Furthermore, the Ndufa7 knockout strain did not survive on the novel host guava. These results suggested that Ndufa7 disturbs the survival on native hosts, expansion to novel hosts, and further expansion to potential hosts of B. tau. Homozygous lethality occurred after the knockout of Ndufs1 or Ndufs3, suggesting that these 2 genes play a role in the early development of B. tau. This study revealed that Ndufa7 is a target gene for the management of tephritids and opens a new avenue for pest control research.

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利用CRISPR/Cas9系统研究线粒体复合体I基因在双翅目小实蝇宿主植物扩增中的作用
寄主的扩大有助于绦虫蝇扩大其活动范围。揭示寄主扩展的机制将有助于有效地控制这些害虫。我们之前的研究表明,线粒体复合体I基因Ndufs1、Ndufs3和Ndufa7在小实蝇(Bactrocera tau, Walker)宿主扩增过程中表达上调。然而,它们在B. tau宿主扩张中的作用尚不清楚。本文首次利用簇状规则间隔短重复序列(CRISPR) / CRISPR相关核酸酶9 (Cas9)编辑系统,在基因敲除后,从B. tau的F3代中获得了稳定的纯合子Ndufa7菌株(Btndufa7-/-)、杂合子Ndufs1菌株(Btndufs1+/-)和Ndufs3菌株(Btndufs3+/-)。首先观察到Ndufa7基因敲除菌株的幼虫和蛹缩小。值得注意的是,与野生型菌株相比,Ndufa7敲除菌株的适合度估计(蛹数、单蛹重和羽化率)和Ndufa7基因表达量的平均值在2个本地寄主(南瓜和黄瓜)上略有降低,而在新寄主香蕉和潜在寄主火龙果上则急剧降低。此外,Ndufa7敲除菌株在新宿主番石榴上无法存活。这些结果表明,Ndufa7干扰了B. tau在原生宿主上的生存、向新宿主的扩展以及向潜在宿主的进一步扩展。敲除Ndufs1或Ndufs3后发生纯合致死,提示这两个基因在B. tau的早期发育中起作用。本研究揭示了Ndufa7是防治该病的靶基因,为防治该病开辟了新的途径。
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来源期刊
Insect Science
Insect Science 生物-昆虫学
CiteScore
7.80
自引率
5.00%
发文量
1379
审稿时长
6.0 months
期刊介绍: Insect Science is an English-language journal, which publishes original research articles dealing with all fields of research in into insects and other terrestrial arthropods. Papers in any of the following fields will be considered: ecology, behavior, biogeography, physiology, biochemistry, sociobiology, phylogeny, pest management, and exotic incursions. The emphasis of the journal is on the adaptation and evolutionary biology of insects from the molecular to the ecosystem level. Reviews, mini reviews and letters to the editor, book reviews, and information about academic activities of the society are also published.
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