{"title":"Harnessing plant-mediated RNAi for effective management of Phthorimaea absoluta by targeting AChE1 and SEC23 genes","authors":"Muneeb Hassan Hashmi , Haneef Tariq , Faisal Saeed , Ufuk Demirel , Ayhan Gökçe , Hans Merzendorfer , Emre Aksoy , Allah Bakhsh","doi":"10.1016/j.stress.2024.100569","DOIUrl":null,"url":null,"abstract":"<div><p>Tomato production on a global scale is under persistent pressure due to the devastating impact of <em>Phthorimaea absoluta</em> Meyrick (Lepidoptera: Gelechiidae), the South American tomato leaf miner. To combat this devastating pest, we explored the potential of plant-mediated RNA interference (RNAi) as a novel strategy for its management. Using transgenic techniques, we developed RNAi constructs (<em>p35S::dsAChE1, p35S::dsSEC23</em>) targeting crucial genes, <em>AChE1</em> and <em>SEC23</em>, in <em>P. absoluta</em>. These genes play pivotal roles in insect physiology and development. The transformation of tomato cultivar Rio Grande was carried out with these RNAi constructs using <em>Agrobacterium tumefaciens</em>. The results demonstrated a significant reduction in transcript levels of both <em>AChE1</em> and <em>SEC23</em> in <em>P. absoluta</em>. Silencing <em>AChE1</em> resulted in substantial mortality rates, reduced larval weight gain, and deformities, highlighting its pivotal role in insect survival. <em>SEC23</em> gene silencing also induced mortality and influenced insect physiology. Furthermore, we explored the susceptibility of <em>AChE1</em> to organophosphate insecticides, revealing its relevance in insecticide susceptibility. These findings support the potential of <em>AChE1</em> and <em>SEC23</em> as valuable targets for RNAi-based control of <em>P. absoluta</em> for the first time, providing multifaceted insights into insect physiology and insecticide susceptibility, thereby offering valuable insights for the development of effective strategies to mitigate the impact of this destructive pest.</p></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"14 ","pages":"Article 100569"},"PeriodicalIF":6.8000,"publicationDate":"2024-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667064X24002227/pdfft?md5=727cbfc704ab4ac5a7cd9f6da139bc1b&pid=1-s2.0-S2667064X24002227-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X24002227","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Tomato production on a global scale is under persistent pressure due to the devastating impact of Phthorimaea absoluta Meyrick (Lepidoptera: Gelechiidae), the South American tomato leaf miner. To combat this devastating pest, we explored the potential of plant-mediated RNA interference (RNAi) as a novel strategy for its management. Using transgenic techniques, we developed RNAi constructs (p35S::dsAChE1, p35S::dsSEC23) targeting crucial genes, AChE1 and SEC23, in P. absoluta. These genes play pivotal roles in insect physiology and development. The transformation of tomato cultivar Rio Grande was carried out with these RNAi constructs using Agrobacterium tumefaciens. The results demonstrated a significant reduction in transcript levels of both AChE1 and SEC23 in P. absoluta. Silencing AChE1 resulted in substantial mortality rates, reduced larval weight gain, and deformities, highlighting its pivotal role in insect survival. SEC23 gene silencing also induced mortality and influenced insect physiology. Furthermore, we explored the susceptibility of AChE1 to organophosphate insecticides, revealing its relevance in insecticide susceptibility. These findings support the potential of AChE1 and SEC23 as valuable targets for RNAi-based control of P. absoluta for the first time, providing multifaceted insights into insect physiology and insecticide susceptibility, thereby offering valuable insights for the development of effective strategies to mitigate the impact of this destructive pest.
期刊介绍:
The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues.
Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and:
Lack of water (drought) and excess (flooding),
Salinity stress,
Elevated temperature and/or low temperature (chilling and freezing),
Hypoxia and/or anoxia,
Mineral nutrient excess and/or deficiency,
Heavy metals and/or metalloids,
Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection,
Viral, phytoplasma, bacterial and fungal plant-pathogen interactions.
The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.