感染的地点和时间导致穴居鸟类中血吸虫感染率的性别偏差。

IF 2.1 3区 医学 Q2 PARASITOLOGY
Parasitology Pub Date : 2024-07-01 Epub Date: 2024-10-21 DOI:10.1017/S0031182024001021
William Jones, P Navaneeth Krishna Menon, Anna Qvarnström
{"title":"感染的地点和时间导致穴居鸟类中血吸虫感染率的性别偏差。","authors":"William Jones, P Navaneeth Krishna Menon, Anna Qvarnström","doi":"10.1017/S0031182024001021","DOIUrl":null,"url":null,"abstract":"<p><p>Sex biases in prevalence of disease are often attributed to intrinsic factors, such as physiological differences while a proximate role of extrinsic factors such as behavioural or ecological differences may be more difficult to establish. We combined large-scale screening for the presence and lineage identity of avian malaria (haemosporidian) parasites, in 1234 collared flycatchers (<i>Ficedula albicollis</i>) with life-history information from each bird to establish the location and timing of infection. We found an overall infection rate of 36.2% ± 0.03 (95% CI) with 25 distinct malaria lineages. Interestingly, first-year breeding males and females had similar infection prevalence while females accrued a significantly higher infection rate than males later in life. The sex difference in infection rate was driven by the most abundant <i>Haemoproteus,</i> lineage, hPHSIB1, while the infection rate of <i>Plasmodium</i> lineages was similar in males and females. Furthermore, when infections were assigned to an apparent transmission location, we found that the sex difference in infection rate trend was driven by lineages transmitted in Europe, more specifically by one lineage (the hPHSIB1), while no similar pattern was found in African lineages. We deduce that the observed infection patterns are likely to be caused by differences in breeding behaviour, with incubating females (and nestling individuals of both sexes) being easy targets for the biting insects that are the vectors of avian malaria parasites. Overall, our results are most consistent with ecological factors rather than intrinsic factors underlying the observed sex-biased infection rate of avian malaria in collared flycatchers.</p>","PeriodicalId":19967,"journal":{"name":"Parasitology","volume":" ","pages":"875-883"},"PeriodicalIF":2.1000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578888/pdf/","citationCount":"0","resultStr":"{\"title\":\"Location and timing of infection drives a sex-bias in <i>Haemoproteus</i> prevalence in a hole-nesting bird.\",\"authors\":\"William Jones, P Navaneeth Krishna Menon, Anna Qvarnström\",\"doi\":\"10.1017/S0031182024001021\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Sex biases in prevalence of disease are often attributed to intrinsic factors, such as physiological differences while a proximate role of extrinsic factors such as behavioural or ecological differences may be more difficult to establish. We combined large-scale screening for the presence and lineage identity of avian malaria (haemosporidian) parasites, in 1234 collared flycatchers (<i>Ficedula albicollis</i>) with life-history information from each bird to establish the location and timing of infection. We found an overall infection rate of 36.2% ± 0.03 (95% CI) with 25 distinct malaria lineages. Interestingly, first-year breeding males and females had similar infection prevalence while females accrued a significantly higher infection rate than males later in life. The sex difference in infection rate was driven by the most abundant <i>Haemoproteus,</i> lineage, hPHSIB1, while the infection rate of <i>Plasmodium</i> lineages was similar in males and females. Furthermore, when infections were assigned to an apparent transmission location, we found that the sex difference in infection rate trend was driven by lineages transmitted in Europe, more specifically by one lineage (the hPHSIB1), while no similar pattern was found in African lineages. We deduce that the observed infection patterns are likely to be caused by differences in breeding behaviour, with incubating females (and nestling individuals of both sexes) being easy targets for the biting insects that are the vectors of avian malaria parasites. Overall, our results are most consistent with ecological factors rather than intrinsic factors underlying the observed sex-biased infection rate of avian malaria in collared flycatchers.</p>\",\"PeriodicalId\":19967,\"journal\":{\"name\":\"Parasitology\",\"volume\":\" \",\"pages\":\"875-883\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578888/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Parasitology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1017/S0031182024001021\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/10/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Parasitology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1017/S0031182024001021","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/21 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PARASITOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

疾病流行的性别偏差通常归因于生理差异等内在因素,而行为或生态差异等外在因素的近似作用可能更难确定。我们对 1234 只领蝇雀(Ficedula albicollis)进行了大规模的鸟类疟疾(血孢子虫)寄生虫的存在和品系鉴定筛查,并结合每只鸟的生活史信息来确定感染的地点和时间。我们发现总体感染率为 36.2% ± 0.03(95% CI),有 25 个不同的疟疾系。有趣的是,第一年繁殖的雄鸟和雌鸟的感染率相似,而雌鸟的感染率明显高于雄鸟。感染率的性别差异主要是由数量最多的血吸虫(hPHSIB1)引起的,而疟原虫的感染率在雄性和雌性中相似。此外,当把感染归因于明显的传播地点时,我们发现感染率的性别差异趋势是由在欧洲传播的疟原虫系,更具体地说是由一个疟原虫系(hPHSIB1)驱动的,而在非洲的疟原虫系中没有发现类似的模式。我们推断,观察到的感染模式可能是由繁殖行为的差异造成的,孵化中的雌鸟(以及雏鸟的雌雄个体)很容易成为叮咬昆虫的目标,而叮咬昆虫正是禽类疟疾寄生虫的传播媒介。总体而言,我们的研究结果与生态因素最为一致,而非领蝇鸻鸟类疟疾性别差异感染率的内在因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Location and timing of infection drives a sex-bias in Haemoproteus prevalence in a hole-nesting bird.

Sex biases in prevalence of disease are often attributed to intrinsic factors, such as physiological differences while a proximate role of extrinsic factors such as behavioural or ecological differences may be more difficult to establish. We combined large-scale screening for the presence and lineage identity of avian malaria (haemosporidian) parasites, in 1234 collared flycatchers (Ficedula albicollis) with life-history information from each bird to establish the location and timing of infection. We found an overall infection rate of 36.2% ± 0.03 (95% CI) with 25 distinct malaria lineages. Interestingly, first-year breeding males and females had similar infection prevalence while females accrued a significantly higher infection rate than males later in life. The sex difference in infection rate was driven by the most abundant Haemoproteus, lineage, hPHSIB1, while the infection rate of Plasmodium lineages was similar in males and females. Furthermore, when infections were assigned to an apparent transmission location, we found that the sex difference in infection rate trend was driven by lineages transmitted in Europe, more specifically by one lineage (the hPHSIB1), while no similar pattern was found in African lineages. We deduce that the observed infection patterns are likely to be caused by differences in breeding behaviour, with incubating females (and nestling individuals of both sexes) being easy targets for the biting insects that are the vectors of avian malaria parasites. Overall, our results are most consistent with ecological factors rather than intrinsic factors underlying the observed sex-biased infection rate of avian malaria in collared flycatchers.

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
Parasitology
Parasitology 医学-寄生虫学
CiteScore
4.80
自引率
4.20%
发文量
280
审稿时长
3-8 weeks
期刊介绍: Parasitology is an important specialist journal covering the latest advances in the subject. It publishes original research and review papers on all aspects of parasitology and host-parasite relationships, including the latest discoveries in parasite biochemistry, molecular biology and genetics, ecology and epidemiology in the context of the biological, medical and veterinary sciences. Included in the subscription price are two special issues which contain reviews of current hot topics, one of which is the proceedings of the annual Symposia of the British Society for Parasitology, while the second, covering areas of significant topical interest, is commissioned by the editors and the editorial board.
×
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