The Secretome of Adult Murine Hookworms Is Shaped by Host Expression of STAT6.

IF 1.4 4区 医学 Q4 IMMUNOLOGY Parasite Immunology Pub Date : 2024-07-01 DOI:10.1111/pim.13056
Annabel A Ferguson, Heather L Rossi, De'Broski R Herbert
{"title":"The Secretome of Adult Murine Hookworms Is Shaped by Host Expression of STAT6.","authors":"Annabel A Ferguson, Heather L Rossi, De'Broski R Herbert","doi":"10.1111/pim.13056","DOIUrl":null,"url":null,"abstract":"<p><p>Co-evolutionary adaptation of hookworms with their mammalian hosts has been selected for immunoregulatory excretory/secretory (E/S) products. However, it is not known whether, or if so, how host immunological status impacts the secreted profile of hematophagous adult worms. This study interrogated the impact of host Signal transducer and activator of transcription 6 (STAT6) expression during the experimental evolution of hookworms through the sequential passage of the life cycle in either STAT6 deficient or WT C57BL/6 mice. Proteomic analysis of E/S products by LC-MS showed increased abundance of 15 proteins, including myosin-3, related to muscle function, and aconitate hydratase, related to iron homeostasis. However, most E/S proteins (174 of 337 unique identities) were decreased, including those in the Ancylostoma-secreted protein (ASP) category, and metallopeptidases. Several identified proteins are established immune-modulators such as fatty acid-binding protein homologue, cystatin, and acetylcholinesterase. Enrichment analysis of InterPro functional categories showed down-regulation of Cysteine-rich secretory proteins, Antigen 5, and Pathogenesis-related 1 proteins (CAP), Astacin-like metallopeptidase, Glycoside hydrolase, and Transthyretin-like protein groups in STAT6 KO-adapted worms. Taken together, these data indicate that in an environment lacking Type 2 immunity, hookworms alter their secretome by reducing immune evasion proteins- and increasing locomotor- and feeding-associated proteins.</p>","PeriodicalId":19931,"journal":{"name":"Parasite Immunology","volume":"46 7","pages":"e13056"},"PeriodicalIF":1.4000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11331508/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Parasite Immunology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/pim.13056","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Co-evolutionary adaptation of hookworms with their mammalian hosts has been selected for immunoregulatory excretory/secretory (E/S) products. However, it is not known whether, or if so, how host immunological status impacts the secreted profile of hematophagous adult worms. This study interrogated the impact of host Signal transducer and activator of transcription 6 (STAT6) expression during the experimental evolution of hookworms through the sequential passage of the life cycle in either STAT6 deficient or WT C57BL/6 mice. Proteomic analysis of E/S products by LC-MS showed increased abundance of 15 proteins, including myosin-3, related to muscle function, and aconitate hydratase, related to iron homeostasis. However, most E/S proteins (174 of 337 unique identities) were decreased, including those in the Ancylostoma-secreted protein (ASP) category, and metallopeptidases. Several identified proteins are established immune-modulators such as fatty acid-binding protein homologue, cystatin, and acetylcholinesterase. Enrichment analysis of InterPro functional categories showed down-regulation of Cysteine-rich secretory proteins, Antigen 5, and Pathogenesis-related 1 proteins (CAP), Astacin-like metallopeptidase, Glycoside hydrolase, and Transthyretin-like protein groups in STAT6 KO-adapted worms. Taken together, these data indicate that in an environment lacking Type 2 immunity, hookworms alter their secretome by reducing immune evasion proteins- and increasing locomotor- and feeding-associated proteins.

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
成年小鼠钩虫的分泌组受宿主表达 STAT6 的影响
钩虫在与哺乳动物宿主共同进化的过程中,选择了具有免疫调节作用的排泄/分泌(E/S)产物。然而,宿主的免疫状态是否会影响食血成虫的分泌物特征,或者如果会,又是如何影响的,目前尚不清楚。本研究探讨了宿主信号转导和转录激活因子 6(STAT6)表达在钩虫实验性进化过程中对 STAT6 缺陷或 WT C57BL/6 小鼠生命周期序列的影响。通过 LC-MS 对 E/S 产物进行的蛋白质组分析表明,15 种蛋白质的丰度有所增加,其中包括与肌肉功能有关的肌球蛋白-3 和与铁稳态有关的乌头水合酶。然而,大多数 E/S 蛋白质(337 个唯一标识中的 174 个)都减少了,其中包括那些属于扁桃体瘤分泌蛋白(ASP)类别的蛋白质和金属肽酶。一些被鉴定的蛋白质是已确定的免疫调节剂,如脂肪酸结合蛋白同源物、胱抑素和乙酰胆碱酯酶。InterPro 功能类别的富集分析表明,在 STAT6 KO 适应的蠕虫中,富半胱氨酸分泌蛋白、抗原 5 和致病相关 1 蛋白 (CAP)、Astacin 样金属肽酶、糖苷水解酶和 Transthyretin 样蛋白组出现了下调。总之,这些数据表明,在缺乏第二类免疫的环境中,钩虫会通过减少免疫逃避蛋白、增加运动和摄食相关蛋白来改变其分泌组。
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
Parasite Immunology
Parasite Immunology 医学-寄生虫学
CiteScore
4.70
自引率
4.50%
发文量
61
审稿时长
6-12 weeks
期刊介绍: Parasite Immunology is an international journal devoted to research on all aspects of parasite immunology in human and animal hosts. Emphasis has been placed on how hosts control parasites, and the immunopathological reactions which take place in the course of parasitic infections. The Journal welcomes original work on all parasites, particularly human parasitology, helminths, protozoa and ectoparasites.
期刊最新文献
T. Muris Infection Dynamics of a Fresh, Wild Isolate: Is the Established E Isolate Still Relevant? Schistosomicidal Effects of Moringa oleifera Seed Oil Extract on Schistosoma mansoni-Infected Mice. Immune Response in Cattle Trypanosomosis and Trypanotolerance: Main Findings and Gaps. Safety and Immunogenicity of an FhSAMS Vaccine Against Fasciola hepatica in Dairy Cattle. Toxoplasma gondii Infection of BALB/c Mice Perturbs Host Neurochemistry.
×
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