Multiple diptericins of the black soldier fly (Hermetia illucens) differentially respond to bacterial challenges.

IF 3.6 3区 生物学 Q1 ZOOLOGY Journal of invertebrate pathology Pub Date : 2024-11-13 DOI:10.1016/j.jip.2024.108234
Yoo Bin Yoon, Ji Won Woo, Beom Jun Park, Kihwan Park, Sangwook Kang, David Chung, Dong Ho Lee, Yuno Do, Soon Cheol Park, Sung-Jin Cho
{"title":"Multiple diptericins of the black soldier fly (Hermetia illucens) differentially respond to bacterial challenges.","authors":"Yoo Bin Yoon, Ji Won Woo, Beom Jun Park, Kihwan Park, Sangwook Kang, David Chung, Dong Ho Lee, Yuno Do, Soon Cheol Park, Sung-Jin Cho","doi":"10.1016/j.jip.2024.108234","DOIUrl":null,"url":null,"abstract":"<p><p>Due to its significant bioconversion potential, the black soldier fly (BSF), Hermetia illucens, shows great promise as a cost-effective alternative for recycling biological waste. BSF larvae (BSFL) are constantly exposed high levels of pathogenic microorganisms, including bacteria and fungi, which endows BSFL with a robust immune system. Diptericin, a type of glycine-rich antimicrobial peptide (AMP) that exhibits activity against gram-negative bacteria, contains proline-rich domains (P-domains) and glycine-rich domains (G-domains); these domains are separated by a furin cleavage site. Although the presence and expression patterns of BSFL diptericins have been documented, their basic molecular properties remain unclear. To the best of our knowledge, in the present study, we report, for the first time, the molecular characteristics of seven full-length cDNA sequences of H. illucens diptericins and their expression patterns following challenges with gram-positive or gram-negative bacteria. Seven diptericin paralogs are located in tandem on chromosome 2, spanning a total length of 38.6 kb, with an average intergenic distance of approximately 5.5 kb. Sequence analysis revealed that three diptericins (HipDptA/B/C) are pseudogenized due to premature stop codons. In contrast, the other diptericins (HiDpt1/2/3/4) possess mature-sized G-domains rich in glycine at the C-terminus, which are essential for AMP activity, along with proline-rich domain (P-domain) in the N-terminal and either two (HiDpt1/2/3) or one (HiDpt4) putative furin cleavage sites (R-X-R/K-R) between these domains. These furin cleavage sites possibly produce a glycine-rich AMP and one or two additional peptides with unknown functions. Similar to other diptericins, the expression of HiDpt1/2/3/4 mRNAs is predominantly induced by gram-negative bacteria, increasing typically by ≥ 1,000-fold (up to 5,000-fold). Additionally, HiDpt1/3/4 show significant responses to gram-positive bacteria such as Micrococcus luteus, though not as strongly as to gram-negative bacteria. These findings suggest that HiDpts function as a rapid, effective, and broad-spectrum first-line defense mechanism in the BSFL immune system.</p>","PeriodicalId":16296,"journal":{"name":"Journal of invertebrate pathology","volume":" ","pages":"108234"},"PeriodicalIF":3.6000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of invertebrate pathology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.jip.2024.108234","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Due to its significant bioconversion potential, the black soldier fly (BSF), Hermetia illucens, shows great promise as a cost-effective alternative for recycling biological waste. BSF larvae (BSFL) are constantly exposed high levels of pathogenic microorganisms, including bacteria and fungi, which endows BSFL with a robust immune system. Diptericin, a type of glycine-rich antimicrobial peptide (AMP) that exhibits activity against gram-negative bacteria, contains proline-rich domains (P-domains) and glycine-rich domains (G-domains); these domains are separated by a furin cleavage site. Although the presence and expression patterns of BSFL diptericins have been documented, their basic molecular properties remain unclear. To the best of our knowledge, in the present study, we report, for the first time, the molecular characteristics of seven full-length cDNA sequences of H. illucens diptericins and their expression patterns following challenges with gram-positive or gram-negative bacteria. Seven diptericin paralogs are located in tandem on chromosome 2, spanning a total length of 38.6 kb, with an average intergenic distance of approximately 5.5 kb. Sequence analysis revealed that three diptericins (HipDptA/B/C) are pseudogenized due to premature stop codons. In contrast, the other diptericins (HiDpt1/2/3/4) possess mature-sized G-domains rich in glycine at the C-terminus, which are essential for AMP activity, along with proline-rich domain (P-domain) in the N-terminal and either two (HiDpt1/2/3) or one (HiDpt4) putative furin cleavage sites (R-X-R/K-R) between these domains. These furin cleavage sites possibly produce a glycine-rich AMP and one or two additional peptides with unknown functions. Similar to other diptericins, the expression of HiDpt1/2/3/4 mRNAs is predominantly induced by gram-negative bacteria, increasing typically by ≥ 1,000-fold (up to 5,000-fold). Additionally, HiDpt1/3/4 show significant responses to gram-positive bacteria such as Micrococcus luteus, though not as strongly as to gram-negative bacteria. These findings suggest that HiDpts function as a rapid, effective, and broad-spectrum first-line defense mechanism in the BSFL immune system.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
黑兵蝇(Hermetia illucens)的多种双鞭毛虫毒素对细菌挑战的不同反应。
由于具有巨大的生物转化潜力,黑兵蝇(Hermetia illucens)有望成为一种具有成本效益的生物废物循环利用替代品。BSF 幼虫(BSFL)经常接触大量病原微生物,包括细菌和真菌,这赋予了 BSFL 强大的免疫系统。双黄连是一种富含甘氨酸的抗菌肽(AMP),对革兰氏阴性细菌具有活性,它含有富脯氨酸结构域(P-domains)和富含甘氨酸结构域(G-domains);这些结构域之间有一个呋喃裂解位点。虽然 BSFL 双鞭毛虫毒素的存在和表达模式已被记录在案,但它们的基本分子特性仍不清楚。据我们所知,在本研究中,我们首次报告了七种全长 cDNA 序列的 H. illucens 双黄连蛋白的分子特征及其在革兰氏阳性或革兰氏阴性细菌挑战下的表达模式。7 个双鞭毛虫素同源物串联在 2 号染色体上,总长度为 38.6 kb,基因间的平均距离约为 5.5 kb。序列分析表明,由于过早终止密码子,三种双鞭毛虫蛋白(HipDptA/B/C)被假基因化。与此相反,其他双鞭毛虫毒素(HiDpt1/2/3/4)在 C 端具有成熟大小的富含甘氨酸的 G-结构域(这对 AMP 活性至关重要),在 N 端具有富含脯氨酸的结构域(P-结构域),在这些结构域之间有两个(HiDpt1/2/3)或一个(HiDpt4)假定的呋喃裂解位点(R-X-R/K-R)。这些呋喃裂解位点可能会产生一个富含甘氨酸的 AMP 和一到两个功能未知的附加肽。与其他双鞭毛虫毒素类似,HiDpt1/2/3/4 mRNA 的表达主要由革兰氏阴性细菌诱导,通常会增加≥ 1,000 倍(最高达 5,000 倍)。此外,HiDpt1/3/4 对革兰氏阳性细菌(如黄体微球菌)的反应也很明显,但不如对革兰氏阴性细菌的反应强烈。这些发现表明,HiDpts 是 BSFL 免疫系统中快速、有效和广谱的一线防御机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
6.10
自引率
5.90%
发文量
94
审稿时长
1 months
期刊介绍: The Journal of Invertebrate Pathology presents original research articles and notes on the induction and pathogenesis of diseases of invertebrates, including the suppression of diseases in beneficial species, and the use of diseases in controlling undesirable species. In addition, the journal publishes the results of physiological, morphological, genetic, immunological and ecological studies as related to the etiologic agents of diseases of invertebrates. The Journal of Invertebrate Pathology is the adopted journal of the Society for Invertebrate Pathology, and is available to SIP members at a special reduced price.
期刊最新文献
Bombyx mori PAT4 gene inhibits BmNPV infection and replication through autophagy. A histopathological guide for the social spider Stegodyphus dumicola. Inheritance of Cry2Ab2 resistance in two Helicoverpa zea(Lepidoptera: Noctuidae) populations resistant to single- and dual-Bacillus thuringiensis proteins. Multiple diptericins of the black soldier fly (Hermetia illucens) differentially respond to bacterial challenges. Identification of Albopleistophora grylli n. gen. n. sp. (Microsporidia) and its impact on crickets (Gryllus spp.) in food-and-feed culture systems.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1