Identification of Multifunctional Putative Bioactive Peptides in the Insect Model Red Palm Weevil (Rhynchophorus ferrugineus).

IF 4.8 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Biomolecules Pub Date : 2024-10-19 DOI:10.3390/biom14101332
Carmen Scieuzo, Roberta Rinaldi, Fabiana Giglio, Rosanna Salvia, Mohammed Ali AlSaleh, Jernej Jakše, Arnab Pain, Binu Antony, Patrizia Falabella
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Abstract

Innate immunity, the body's initial defense against bacteria, fungi, and viruses, heavily depends on antimicrobial peptides (AMPs), which are small molecules produced by all living organisms. Insects, with their vast biodiversity, are one of the most abundant and innovative sources of AMPs. In this study, AMPs from the red palm weevil (RPW) Rhynchophorus ferrugineus (Coleoptera: Curculionidae), a known invasive pest of palm species, were examined. The AMPs were identified in the transcriptomes from different body parts of male and female adults, under different experimental conditions, including specimens collected from the field and those reared in the laboratory. The RPW transcriptomes were examined to predict antimicrobial activity, and all sequences putatively encoding AMPs were analyzed using several machine learning algorithms available in the CAMPR3 database. Additionally, anticancer, antiviral, and antifungal activity of the peptides were predicted using iACP, AVPpred, and Antifp server tools, respectively. Physicochemical parameters were assessed using the Antimicrobial Peptide Database Calculator and Predictor. From these analyses, 198 putatively active peptides were identified, which can be tested in future studies to validate the in silico predictions. Genome-wide analysis revealed that several AMPs have predominantly emerged through gene duplication. Noticeably, we detect a newly originated defensin allele from an ancestral defensin via the deletion of two amino acids following gene duplication in RPW, which may confer an enhanced resilience to microbial infection. Our study shed light on AMP gene families and shows that high duplication and deletion rates are essential to achieve a diversity of antimicrobial mechanisms; hence, we propose the RPW AMPs as a model for exploring gene duplication and functional variations against microbial infection.

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鉴定昆虫模型红掌象鼻虫(Rhynchophorus ferrugineus)体内的多功能假定生物活性肽。
先天性免疫是人体抵御细菌、真菌和病毒的最初防御手段,它在很大程度上依赖于抗菌肽(AMPs),而抗菌肽是由所有生物体产生的小分子。昆虫具有丰富的生物多样性,是抗菌肽最丰富、最具创新性的来源之一。本研究对已知入侵棕榈物种的害虫红掌象鼻虫(RPW)Rhynchophorus ferrugineus(鞘翅目:Curculionidae)的 AMPs 进行了研究。在不同的实验条件下,包括从野外采集的标本和在实验室饲养的标本,从雌雄成虫的不同身体部位的转录组中鉴定了 AMPs。通过研究 RPW 转录组来预测抗菌活性,并使用 CAMPR3 数据库中的几种机器学习算法对所有可能编码 AMPs 的序列进行分析。此外,还使用 iACP、AVPpred 和 Antifp 服务器工具分别预测了多肽的抗癌、抗病毒和抗真菌活性。使用抗菌肽数据库计算器和预测器对理化参数进行了评估。通过这些分析,确定了 198 种可能具有活性的肽,可在今后的研究中对这些肽进行测试,以验证硅预测结果。全基因组分析表明,几种 AMP 主要是通过基因复制出现的。值得注意的是,我们在 RPW 基因复制后,通过缺失两个氨基酸从祖先防御素中检测到了一个新起源的防御素等位基因,这可能会增强对微生物感染的抵抗力。我们的研究揭示了AMP基因家族,并表明高复制率和高缺失率是实现抗微生物机制多样性的必要条件;因此,我们建议将RPW AMPs作为探索基因复制和抗微生物感染功能变异的模型。
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来源期刊
Biomolecules
Biomolecules Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
3.60%
发文量
1640
审稿时长
18.28 days
期刊介绍: Biomolecules (ISSN 2218-273X) is an international, peer-reviewed open access journal focusing on biogenic substances and their biological functions, structures, interactions with other molecules, and their microenvironment as well as biological systems. Biomolecules publishes reviews, regular research papers and short communications.  Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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