Host body size, not host population size, predicts genome-wide effective population size of parasites.

IF 3.4 1区 生物学 Q2 EVOLUTIONARY BIOLOGY Evolution Letters Pub Date : 2023-08-01 DOI:10.1093/evlett/qrad026
Jorge Doña, Kevin P Johnson
{"title":"Host body size, not host population size, predicts genome-wide effective population size of parasites.","authors":"Jorge Doña,&nbsp;Kevin P Johnson","doi":"10.1093/evlett/qrad026","DOIUrl":null,"url":null,"abstract":"<p><p>The effective population size (<i>N</i><sub><i>e</i></sub>) of an organism is expected to be generally proportional to the total number of individuals in a population. In parasites, we might expect the effective population size to be proportional to host population size and host body size, because both are expected to increase the number of parasite individuals. However, among other factors, parasite populations are sometimes so extremely subdivided that high levels of inbreeding may distort these predicted relationships. Here, we used whole-genome sequence data from dove parasites (71 feather louse species of the genus <i>Columbicola</i>) and phylogenetic comparative methods to study the relationship between parasite effective population size and host population size and body size. We found that parasite effective population size is largely explained by host body size but not host population size. These results suggest the potential local population size (infrapopulation or deme size) is more predictive of the long-term effective population size of parasites than is the total number of potential parasite infrapopulations (i.e., host individuals).</p>","PeriodicalId":48629,"journal":{"name":"Evolution Letters","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355176/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolution Letters","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/evlett/qrad026","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The effective population size (Ne) of an organism is expected to be generally proportional to the total number of individuals in a population. In parasites, we might expect the effective population size to be proportional to host population size and host body size, because both are expected to increase the number of parasite individuals. However, among other factors, parasite populations are sometimes so extremely subdivided that high levels of inbreeding may distort these predicted relationships. Here, we used whole-genome sequence data from dove parasites (71 feather louse species of the genus Columbicola) and phylogenetic comparative methods to study the relationship between parasite effective population size and host population size and body size. We found that parasite effective population size is largely explained by host body size but not host population size. These results suggest the potential local population size (infrapopulation or deme size) is more predictive of the long-term effective population size of parasites than is the total number of potential parasite infrapopulations (i.e., host individuals).

Abstract Image

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
宿主体大小,而不是宿主种群大小,预测全基因组范围内寄生虫的有效种群大小。
一个生物的有效种群大小(Ne)通常与种群中的个体总数成正比。在寄生虫中,我们可以预期有效种群大小与宿主种群大小和宿主体型成正比,因为两者都有望增加寄生虫个体的数量。然而,在其他因素中,寄生虫种群有时如此细分,以至于高水平的近亲繁殖可能会扭曲这些预测的关系。本文利用鸽子寄生虫(71种属羽虱)的全基因组序列数据和系统发育比较方法,研究了寄主种群大小和体大小与寄生虫有效种群大小的关系。我们发现寄生虫的有效种群大小在很大程度上与宿主体型有关,而与宿主种群大小无关。这些结果表明,潜在的当地种群大小(种群内或群落内大小)比潜在的寄生虫种群内总数(即寄主个体)更能预测寄生虫的长期有效种群大小。
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
Evolution Letters
Evolution Letters EVOLUTIONARY BIOLOGY-
CiteScore
13.00
自引率
2.00%
发文量
35
审稿时长
10 weeks
期刊介绍: Evolution Letters publishes cutting-edge new research in all areas of Evolutionary Biology. Available exclusively online, and entirely open access, Evolution Letters consists of Letters - original pieces of research which form the bulk of papers - and Comments and Opinion - a forum for highlighting timely new research ideas for the evolutionary community.
期刊最新文献
Assessing the role of mitonuclear interactions on mitochondrial function and organismal fitness in natural Drosophila populations Genomic patterns in the dwarf kingfishers of northern Melanesia reveal a mechanistic framework explaining the paradox of the great speciators Unraveling mate choice evolution through indirect genetic effects Insular environment-dependent introgression from an arid-grassland orchid to a wetland orchid on an oceanic island Coordination of care reduces conflict and predation risk in a cooperatively breeding bird
×
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