万年青中几丁质结合蛋白的鉴定、功能分析及其单核苷酸多态性与副溶血性弧菌抗性的关联。

IF 4.1 2区 农林科学 Q1 FISHERIES
Shuang-Shuang Luo , Xiu-Li Chen , Ai-Jin Wang , Qing-Yun Liu , Min Peng , Chun-Ling Yang , Di-Gang Zeng , Yong-Zhen Zhao , Huan-Ling Wang
{"title":"万年青中几丁质结合蛋白的鉴定、功能分析及其单核苷酸多态性与副溶血性弧菌抗性的关联。","authors":"Shuang-Shuang Luo ,&nbsp;Xiu-Li Chen ,&nbsp;Ai-Jin Wang ,&nbsp;Qing-Yun Liu ,&nbsp;Min Peng ,&nbsp;Chun-Ling Yang ,&nbsp;Di-Gang Zeng ,&nbsp;Yong-Zhen Zhao ,&nbsp;Huan-Ling Wang","doi":"10.1016/j.fsi.2024.109966","DOIUrl":null,"url":null,"abstract":"<div><div>Chitin-binding proteins (CBPs) play pivotal roles in numerous biological processes in arthropods, including growth, molting, reproduction, and immune defense. However, their function in the antibacterial immune defense of crustaceans remains relatively underexplored. In this study, twenty CBPs were identified and characterized in <em>Penaeus vannamei</em>. Expression profiling highlighted that the majority of CBPs were highly expressed in the intestine and hepatopancreas and responded to challenge by <em>Vibrio parahaemolyticus.</em> To explore the role of these CBPs in innate immunity, six CBPs (<em>PvPrg4</em>, <em>PvKrtap16</em>, <em>PvPT-1a</em>, <em>PvPT-1b</em>, <em>PvExtensin</em> and <em>PvCP-AM1159</em>) were selected for RNAi experiments. Silencing of only <em>PvPrg4</em> and <em>PvKrtap16</em> significantly decreased the cumulative mortality of <em>V. parahaemolyticus</em>-infected shrimp. Further studies demonstrated that inhibition of <em>PvPrg4</em> and <em>PvKrtap16</em> resulted in a marked upregulation of genes associated with the NF-κB and JAK-STAT signaling pathways, as well as antimicrobial peptides (AMPs), in both the intestine and hepatopancreas. These results collectively suggested that <em>PvPrg4</em> and <em>PvKrtap16</em> potentially promote <em>V. parahaemolyticus</em> invasion by negatively regulating the JAK-STAT and NF-κB pathways, thereby inhibiting the expression of AMPs. In addition, SNP analysis identified three SNPs in the exons of <em>PvPrg4</em> that were significantly associated with tolerance to <em>V. parahaemolyticus</em>. Taken together, these findings are expected to assist in the molecular marker-assisted breeding of <em>P. vannamei</em> associated with anti-<em>V. parahaemolyticus</em> traits, as well as expand our understanding of CBP functions within the immune regulatory system of crustaceans.</div></div>","PeriodicalId":12127,"journal":{"name":"Fish & shellfish immunology","volume":"154 ","pages":"Article 109966"},"PeriodicalIF":4.1000,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Identification, functional analysis of chitin-binding proteins and the association of its single nucleotide polymorphisms with Vibrio parahaemolyticus resistance in Penaeus vannamei\",\"authors\":\"Shuang-Shuang Luo ,&nbsp;Xiu-Li Chen ,&nbsp;Ai-Jin Wang ,&nbsp;Qing-Yun Liu ,&nbsp;Min Peng ,&nbsp;Chun-Ling Yang ,&nbsp;Di-Gang Zeng ,&nbsp;Yong-Zhen Zhao ,&nbsp;Huan-Ling Wang\",\"doi\":\"10.1016/j.fsi.2024.109966\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Chitin-binding proteins (CBPs) play pivotal roles in numerous biological processes in arthropods, including growth, molting, reproduction, and immune defense. However, their function in the antibacterial immune defense of crustaceans remains relatively underexplored. In this study, twenty CBPs were identified and characterized in <em>Penaeus vannamei</em>. Expression profiling highlighted that the majority of CBPs were highly expressed in the intestine and hepatopancreas and responded to challenge by <em>Vibrio parahaemolyticus.</em> To explore the role of these CBPs in innate immunity, six CBPs (<em>PvPrg4</em>, <em>PvKrtap16</em>, <em>PvPT-1a</em>, <em>PvPT-1b</em>, <em>PvExtensin</em> and <em>PvCP-AM1159</em>) were selected for RNAi experiments. Silencing of only <em>PvPrg4</em> and <em>PvKrtap16</em> significantly decreased the cumulative mortality of <em>V. parahaemolyticus</em>-infected shrimp. Further studies demonstrated that inhibition of <em>PvPrg4</em> and <em>PvKrtap16</em> resulted in a marked upregulation of genes associated with the NF-κB and JAK-STAT signaling pathways, as well as antimicrobial peptides (AMPs), in both the intestine and hepatopancreas. These results collectively suggested that <em>PvPrg4</em> and <em>PvKrtap16</em> potentially promote <em>V. parahaemolyticus</em> invasion by negatively regulating the JAK-STAT and NF-κB pathways, thereby inhibiting the expression of AMPs. In addition, SNP analysis identified three SNPs in the exons of <em>PvPrg4</em> that were significantly associated with tolerance to <em>V. parahaemolyticus</em>. Taken together, these findings are expected to assist in the molecular marker-assisted breeding of <em>P. vannamei</em> associated with anti-<em>V. parahaemolyticus</em> traits, as well as expand our understanding of CBP functions within the immune regulatory system of crustaceans.</div></div>\",\"PeriodicalId\":12127,\"journal\":{\"name\":\"Fish & shellfish immunology\",\"volume\":\"154 \",\"pages\":\"Article 109966\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-10-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fish & shellfish immunology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1050464824006119\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"FISHERIES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fish & shellfish immunology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1050464824006119","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0

摘要

几丁质结合蛋白(CBPs)在节肢动物的许多生物过程中发挥着关键作用,包括生长、蜕皮、繁殖和免疫防御。然而,它们在甲壳类动物抗菌免疫防御中的功能仍未得到充分探索。本研究在凡纳滨对20种CBPs进行了鉴定和表征。表达谱分析显示,大多数 CBPs 在肠道和肝胰腺中高度表达,并对副溶血性弧菌的挑战做出反应。为了探索这些 CBPs 在先天性免疫中的作用,我们选择了六个 CBPs(PvPrg4、PvKrtap16、PvPT-1a、PvPT-1b、PvExtensin 和 PvCP-AM1159)进行 RNAi 实验。仅抑制 PvPrg4 和 PvKrtap16 能显著降低副溶血性弧菌感染虾的累积死亡率。进一步的研究表明,抑制 PvPrg4 和 PvKrtap16 会导致肠道和肝胰腺中与 NF-κB 和 JAK-STAT 信号通路相关的基因以及抗菌肽(AMPs)明显上调。这些结果共同表明,PvPrg4 和 PvKrtap16 可通过负向调节 JAK-STAT 和 NF-κB 通路,从而抑制 AMPs 的表达,潜在地促进副溶血性弧菌的入侵。此外,SNP 分析发现 PvPrg4 外显子中的三个 SNP 与副溶血性弧菌耐受性显著相关。综上所述,这些发现有望帮助分子标记辅助培育具有抗副溶血病毒特性的凡纳米贝,并扩大我们对 CBP 在甲壳类免疫调节系统中功能的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification, functional analysis of chitin-binding proteins and the association of its single nucleotide polymorphisms with Vibrio parahaemolyticus resistance in Penaeus vannamei
Chitin-binding proteins (CBPs) play pivotal roles in numerous biological processes in arthropods, including growth, molting, reproduction, and immune defense. However, their function in the antibacterial immune defense of crustaceans remains relatively underexplored. In this study, twenty CBPs were identified and characterized in Penaeus vannamei. Expression profiling highlighted that the majority of CBPs were highly expressed in the intestine and hepatopancreas and responded to challenge by Vibrio parahaemolyticus. To explore the role of these CBPs in innate immunity, six CBPs (PvPrg4, PvKrtap16, PvPT-1a, PvPT-1b, PvExtensin and PvCP-AM1159) were selected for RNAi experiments. Silencing of only PvPrg4 and PvKrtap16 significantly decreased the cumulative mortality of V. parahaemolyticus-infected shrimp. Further studies demonstrated that inhibition of PvPrg4 and PvKrtap16 resulted in a marked upregulation of genes associated with the NF-κB and JAK-STAT signaling pathways, as well as antimicrobial peptides (AMPs), in both the intestine and hepatopancreas. These results collectively suggested that PvPrg4 and PvKrtap16 potentially promote V. parahaemolyticus invasion by negatively regulating the JAK-STAT and NF-κB pathways, thereby inhibiting the expression of AMPs. In addition, SNP analysis identified three SNPs in the exons of PvPrg4 that were significantly associated with tolerance to V. parahaemolyticus. Taken together, these findings are expected to assist in the molecular marker-assisted breeding of P. vannamei associated with anti-V. parahaemolyticus traits, as well as expand our understanding of CBP functions within the immune regulatory system of crustaceans.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Fish & shellfish immunology
Fish & shellfish immunology 农林科学-海洋与淡水生物学
CiteScore
7.50
自引率
19.10%
发文量
750
审稿时长
68 days
期刊介绍: Fish and Shellfish Immunology rapidly publishes high-quality, peer-refereed contributions in the expanding fields of fish and shellfish immunology. It presents studies on the basic mechanisms of both the specific and non-specific defense systems, the cells, tissues, and humoral factors involved, their dependence on environmental and intrinsic factors, response to pathogens, response to vaccination, and applied studies on the development of specific vaccines for use in the aquaculture industry.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信