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多种毒素和一种蛋白酶有助于荧光假单胞菌 PpR24 杀死蚜虫。

Multiple toxins and a protease contribute to the aphid-killing ability of Pseudomonas fluorescens PpR24.

机构信息

School of Biological Sciences, University of Reading, Reading, UK.

School of Life Sciences, University of Warwick, Coventry, UK.

出版信息

Environ Microbiol. 2024 Apr;26(4):e16604. doi: 10.1111/1462-2920.16604.

DOI:10.1111/1462-2920.16604
PMID:38561900
Abstract

Aphids are globally important pests causing damage to a broad range of crops. Due to insecticide resistance, there is an urgent need to develop alternative control strategies. In our previous work, we found Pseudomonas fluorescens PpR24 can orally infect and kill the insecticide-resistant green-peach aphid (Myzus persicae). However, the genetic basis of the insecticidal capability of PpR24 remains unclear. Genome sequencing of PpR24 confirmed the presence of various insecticidal toxins such as Tc (toxin complexes), Rhs (rearrangement hotspot) elements, and other insect-killing proteases. Upon aphids infection with PpR24, RNA-Seq analysis revealed 193 aphid genes were differentially expressed with down-regulation of 16 detoxification genes. In addition, 1325 PpR24 genes (542 were upregulated and 783 downregulated) were subject to differential expression, including genes responsible for secondary metabolite biosynthesis, the iron-restriction response, oxidative stress resistance, and virulence factors. Single and double deletion of candidate virulence genes encoding a secreted protease (AprX) and four toxin components (two TcA-like; one TcB-like; one TcC-like insecticidal toxins) showed that all five genes contribute significantly to aphid killing, particularly AprX. This comprehensive host-pathogen transcriptomic analysis provides novel insight into the molecular basis of bacteria-mediated aphid mortality and the potential of PpR24 as an effective biocontrol agent.

摘要

蚜虫是全球重要的害虫,对广泛的作物造成损害。由于抗药性,迫切需要开发替代控制策略。在我们之前的工作中,我们发现荧光假单胞菌 PpR24 可以通过口服感染并杀死抗药性的绿桃蚜(桃蚜)。然而,PpR24 的杀虫能力的遗传基础尚不清楚。PpR24 的基因组测序证实了存在各种杀虫毒素,如 Tc(毒素复合物)、Rhs(重排热点)元件和其他杀虫蛋白酶。在 PpR24 感染蚜虫后,RNA-Seq 分析显示 193 个蚜虫基因表达差异,其中 16 个解毒基因下调。此外,1325 个 PpR24 基因(542 个上调,783 个下调)受到差异表达的影响,包括负责次生代谢物生物合成、铁限制反应、氧化应激抗性和毒力因子的基因。候选毒力基因(编码分泌蛋白酶 AprX 和四种毒素成分(两种 TcA 样;一种 TcB 样;一种 TcC 样杀虫毒素)的单基因和双基因缺失显示,这五个基因都对蚜虫的致死有重要贡献,尤其是 AprX。这项全面的宿主-病原体转录组分析为细菌介导的蚜虫死亡率的分子基础以及 PpR24 作为有效生物防治剂的潜力提供了新的见解。

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