生活史特征是否影响新大陆黑鹂(黄鹂科)母系免疫因子的模式?

IF 2.2 4区 生物学 Q2 BIOLOGY
C. Fassbinder-Orth, L. Igl, D. Hahn, K. M. Watts, T. Wilcoxen, K. Ramos-Álvarez
{"title":"生活史特征是否影响新大陆黑鹂(黄鹂科)母系免疫因子的模式?","authors":"C. Fassbinder-Orth, L. Igl, D. Hahn, K. M. Watts, T. Wilcoxen, K. Ramos-Álvarez","doi":"10.1093/IOB/OBY011","DOIUrl":null,"url":null,"abstract":"\n Avian immunology developed originally by investigating domesticated poultry species (Galliformes), but in recent decades eco-immunological studies of wild bird species have revealed that avian immune systems are more diverse than initially assumed. This study compares six immunological elements in eggs of six species within the same family, the New World blackbirds (Icteridae),whose members differ most notably in two life history parameters, brood parasitism and body size. We measured the maternal immune investment of passive immune components in both yolk and albumen: lysozyme, ovotransferrin, and immunoglobulins (Igs), and LPS-specific Igs. We predicted that brood parasites would have higher levels of immune activity for both innate and adaptive immunity compared with non-brood parasites, and that increased body size could increase microbial exposure of larger animals, resulting in an increase in some adaptive immune responses, such as LPS-specific Igs. We found that brood parasites had significantly higher levels of Igs and lysozyme levels in albumen, but significantly lower levels of Igs in yolk compared with non-brood parasites. Igs in yolk scaled according to body size, with the smallest organisms (the brood parasites) having the lowest levels, and the largest organism (common grackle) having the highest. Our results confirm the findings of other studies of comparative immunity among species in a single taxon that (1) similarities in immune investment cannot be assumed among closely related species and (2) single measures of immune defense cannot be assumed to be indicators of a species’ overall immune strategy, as life history traits can differentially affect immune responses.","PeriodicalId":13666,"journal":{"name":"Integrative Organismal Biology","volume":"1 1","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2018-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/IOB/OBY011","citationCount":"4","resultStr":"{\"title\":\"Do Life History Traits Influence Patterns of Maternal Immune Elements in New World Blackbirds (Icteridae)?\",\"authors\":\"C. Fassbinder-Orth, L. Igl, D. Hahn, K. M. Watts, T. Wilcoxen, K. Ramos-Álvarez\",\"doi\":\"10.1093/IOB/OBY011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n Avian immunology developed originally by investigating domesticated poultry species (Galliformes), but in recent decades eco-immunological studies of wild bird species have revealed that avian immune systems are more diverse than initially assumed. This study compares six immunological elements in eggs of six species within the same family, the New World blackbirds (Icteridae),whose members differ most notably in two life history parameters, brood parasitism and body size. We measured the maternal immune investment of passive immune components in both yolk and albumen: lysozyme, ovotransferrin, and immunoglobulins (Igs), and LPS-specific Igs. We predicted that brood parasites would have higher levels of immune activity for both innate and adaptive immunity compared with non-brood parasites, and that increased body size could increase microbial exposure of larger animals, resulting in an increase in some adaptive immune responses, such as LPS-specific Igs. We found that brood parasites had significantly higher levels of Igs and lysozyme levels in albumen, but significantly lower levels of Igs in yolk compared with non-brood parasites. Igs in yolk scaled according to body size, with the smallest organisms (the brood parasites) having the lowest levels, and the largest organism (common grackle) having the highest. Our results confirm the findings of other studies of comparative immunity among species in a single taxon that (1) similarities in immune investment cannot be assumed among closely related species and (2) single measures of immune defense cannot be assumed to be indicators of a species’ overall immune strategy, as life history traits can differentially affect immune responses.\",\"PeriodicalId\":13666,\"journal\":{\"name\":\"Integrative Organismal Biology\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2018-12-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1093/IOB/OBY011\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Integrative Organismal Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/IOB/OBY011\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative Organismal Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/IOB/OBY011","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 4

摘要

鸟类免疫学最初是通过研究驯养的家禽物种(Galliformes)发展起来的,但近几十年来对野生鸟类的生态免疫学研究表明,鸟类的免疫系统比最初假设的更为多样。这项研究比较了新世界黑鸟科(Icteridae)同一科中六个物种的卵子中的六种免疫元素,它们的成员在两个生活史参数上的差异最为显著,即孵化寄生和体型。我们测量了卵黄和蛋白中被动免疫成分的母体免疫投入:溶菌酶、卵转铁蛋白、免疫球蛋白(Igs)和LPS特异性Igs。我们预测,与非繁殖寄生虫相比,繁殖寄生虫在先天免疫和适应性免疫方面都具有更高水平的免疫活性,体型的增加可能会增加大型动物的微生物暴露,导致一些适应性免疫反应的增加,如LPS特异性Ig。我们发现,与非孵化寄生虫相比,孵化寄生虫的蛋白中Igs和溶菌酶水平显著较高,但蛋黄中Igs水平显著较低。卵黄中的Ig根据身体大小进行缩放,最小的生物体(孵化寄生虫)水平最低,最大的生物体(普通抓虫)水平最高。我们的研究结果证实了其他关于单个分类单元中物种之间比较免疫的研究结果,即(1)不能假设密切相关物种之间免疫投资的相似性,(2)不能假设免疫防御的单一措施是一个物种整体免疫策略的指标,因为生活史特征可以不同地影响免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Do Life History Traits Influence Patterns of Maternal Immune Elements in New World Blackbirds (Icteridae)?
Avian immunology developed originally by investigating domesticated poultry species (Galliformes), but in recent decades eco-immunological studies of wild bird species have revealed that avian immune systems are more diverse than initially assumed. This study compares six immunological elements in eggs of six species within the same family, the New World blackbirds (Icteridae),whose members differ most notably in two life history parameters, brood parasitism and body size. We measured the maternal immune investment of passive immune components in both yolk and albumen: lysozyme, ovotransferrin, and immunoglobulins (Igs), and LPS-specific Igs. We predicted that brood parasites would have higher levels of immune activity for both innate and adaptive immunity compared with non-brood parasites, and that increased body size could increase microbial exposure of larger animals, resulting in an increase in some adaptive immune responses, such as LPS-specific Igs. We found that brood parasites had significantly higher levels of Igs and lysozyme levels in albumen, but significantly lower levels of Igs in yolk compared with non-brood parasites. Igs in yolk scaled according to body size, with the smallest organisms (the brood parasites) having the lowest levels, and the largest organism (common grackle) having the highest. Our results confirm the findings of other studies of comparative immunity among species in a single taxon that (1) similarities in immune investment cannot be assumed among closely related species and (2) single measures of immune defense cannot be assumed to be indicators of a species’ overall immune strategy, as life history traits can differentially affect immune responses.
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
CiteScore
3.70
自引率
6.70%
发文量
48
审稿时长
20 weeks
×
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