Comparative Proteomics of Resistant and Susceptible Strains of Frankliniella occidentalis to Abamectin

IF 2.5 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS ELECTROPHORESIS Pub Date : 2025-01-09 DOI:10.1002/elps.202400171
Zahra Gholami, Foad Fatehi, Fatemeh Habibpour Mehraban, Paul A. Haynes, Khalil Talebi Jahromi, Vahid Hosseininaveh, Hadi Mosallanejad, Pär K. Ingvarsson, Naser Farrokhi
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Abstract

Western flower thrips, Frankliniella occidentalis (Thysanoptera: Thripidae) is an invasive agricultural pest with developed resistance to abamectin in some strains due to frequent treatment with the pesticide. In this study, we examined differentially expressed proteins (DEPs) between abamectin-resistant (AbaR; under abamectin selective pressure) and susceptible strains (AbaS; without abamectin selective pressure) of F. occidentalis. Proteins were isolated from second instar larvae of both strains and separated via two-dimensional polyacrylamide gel electrophoresis. Nano-flow liquid chromatography–tandem mass spectrometry identified selected protein spot features. From 70 DEPs, 43 spot features were identified: A total of 23 showed an increase in abundance, and 20 were down-regulated in response to abamectin pressure. The enzymatic and structural proteins were classified into the functional groups of macromolecular metabolisms, signaling and cellular processes, immune system, genetic information processing, and exoskeleton-related proteins. The up-regulation of exoskeleton-related proteins may contribute to forming a thicker cuticle, potentially hindering abamectin penetration, which is an interesting finding that needs further investigation. Two novel proteins, triacylglycerol lipase and cuticle protein CPF 2, were only expressed in AbaR. This work provides insights into abamectin resistance mechanisms in F. occidentalis, which will provide important information for developing insecticide resistance management approaches for this pest.

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西方富兰克林菌对阿维菌素耐药和敏感菌株的蛋白质组学比较。
西方花蓟马,Frankliniella occidentalis(蓟翅目:蓟科)是一种入侵性农业害虫,由于频繁使用阿维菌素,部分品种已产生抗药性。在这项研究中,我们检测了阿巴菌素耐药(AbaR;在阿维菌素选择压力下)和敏感菌株(AbaS;无阿维菌素选择压力)。从两种菌株的二龄幼虫中分离蛋白质,并通过双向聚丙烯酰胺凝胶电泳进行分离。纳米流液相色谱-串联质谱法鉴定了选定的蛋白质斑点特征。从70个dep中鉴定出43个斑点特征:共有23个表现出丰度增加,20个表现出对阿维菌素压力的下调。酶和结构蛋白被划分为大分子代谢、信号和细胞过程、免疫系统、遗传信息处理和外骨骼相关蛋白的功能群。外骨骼相关蛋白的上调可能有助于形成更厚的角质层,潜在地阻碍阿维菌素的渗透,这是一个有趣的发现,需要进一步研究。三酰基甘油脂肪酶和角质层蛋白cpf2仅在AbaR中表达。本研究为了解西方白僵菌对阿维菌素的抗性机制提供了新的思路,为开发该害虫的抗药性管理方法提供了重要的信息。
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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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