Corina Maurer, Alexandria Schauer, Orlando Yañez, Peter Neumann, Anna Gajda, Robert J. Paxton, Loïc Pellissier, Oliver Schweiger, Hajnalka Szentgyörgyi, Adam J. Vanbergen, Matthias Albrecht
{"title":"物种特征、景观质量以及与蜜蜂的花卉资源重叠决定了病毒在植物授粉者网络中的传播方式","authors":"Corina Maurer, Alexandria Schauer, Orlando Yañez, Peter Neumann, Anna Gajda, Robert J. Paxton, Loïc Pellissier, Oliver Schweiger, Hajnalka Szentgyörgyi, Adam J. Vanbergen, Matthias Albrecht","doi":"10.1038/s41559-024-02555-w","DOIUrl":null,"url":null,"abstract":"<p>Emerging infectious diseases pose a threat to pollinators. Virus transmission among pollinators via flowers may be reinforced by anthropogenic land-use change and concomitant alteration of plant–pollinator interactions. Here, we examine how species’ traits and roles in flower-visitation networks and landscape-scale factors drive key honeybee viruses—black queen cell virus (BQCV) and deformed wing virus—in 19 wild bee and hoverfly species, across 12 landscapes varying in pollinator-friendly (flower-rich) habitat. Viral loads were on average more than ten times higher in managed honeybees than in wild pollinators. Viral loads in wild pollinators were higher when floral resource use overlapped with honeybees, suggesting these as reservoir hosts, and increased with pollinator abundance and viral loads in honeybees. Viral prevalence decreased with the amount of pollinator-friendly habitat in a landscape, which was partly driven by reduced floral resource overlap with honeybees. Black queen cell virus loads decreased with a wild pollinator’s centrality in the network and the proportion of visited dish-shaped flowers. Our findings highlight the complex interplay of resource overlap with honeybees, species traits and roles in flower-visitation networks and flower-rich pollinator habitat shaping virus transmission.</p>","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"10 1","pages":""},"PeriodicalIF":13.9000,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Species traits, landscape quality and floral resource overlap with honeybees determine virus transmission in plant–pollinator networks\",\"authors\":\"Corina Maurer, Alexandria Schauer, Orlando Yañez, Peter Neumann, Anna Gajda, Robert J. Paxton, Loïc Pellissier, Oliver Schweiger, Hajnalka Szentgyörgyi, Adam J. Vanbergen, Matthias Albrecht\",\"doi\":\"10.1038/s41559-024-02555-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Emerging infectious diseases pose a threat to pollinators. Virus transmission among pollinators via flowers may be reinforced by anthropogenic land-use change and concomitant alteration of plant–pollinator interactions. Here, we examine how species’ traits and roles in flower-visitation networks and landscape-scale factors drive key honeybee viruses—black queen cell virus (BQCV) and deformed wing virus—in 19 wild bee and hoverfly species, across 12 landscapes varying in pollinator-friendly (flower-rich) habitat. Viral loads were on average more than ten times higher in managed honeybees than in wild pollinators. Viral loads in wild pollinators were higher when floral resource use overlapped with honeybees, suggesting these as reservoir hosts, and increased with pollinator abundance and viral loads in honeybees. Viral prevalence decreased with the amount of pollinator-friendly habitat in a landscape, which was partly driven by reduced floral resource overlap with honeybees. Black queen cell virus loads decreased with a wild pollinator’s centrality in the network and the proportion of visited dish-shaped flowers. Our findings highlight the complex interplay of resource overlap with honeybees, species traits and roles in flower-visitation networks and flower-rich pollinator habitat shaping virus transmission.</p>\",\"PeriodicalId\":18835,\"journal\":{\"name\":\"Nature ecology & evolution\",\"volume\":\"10 1\",\"pages\":\"\"},\"PeriodicalIF\":13.9000,\"publicationDate\":\"2024-10-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature ecology & evolution\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1038/s41559-024-02555-w\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature ecology & evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41559-024-02555-w","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ECOLOGY","Score":null,"Total":0}
Species traits, landscape quality and floral resource overlap with honeybees determine virus transmission in plant–pollinator networks
Emerging infectious diseases pose a threat to pollinators. Virus transmission among pollinators via flowers may be reinforced by anthropogenic land-use change and concomitant alteration of plant–pollinator interactions. Here, we examine how species’ traits and roles in flower-visitation networks and landscape-scale factors drive key honeybee viruses—black queen cell virus (BQCV) and deformed wing virus—in 19 wild bee and hoverfly species, across 12 landscapes varying in pollinator-friendly (flower-rich) habitat. Viral loads were on average more than ten times higher in managed honeybees than in wild pollinators. Viral loads in wild pollinators were higher when floral resource use overlapped with honeybees, suggesting these as reservoir hosts, and increased with pollinator abundance and viral loads in honeybees. Viral prevalence decreased with the amount of pollinator-friendly habitat in a landscape, which was partly driven by reduced floral resource overlap with honeybees. Black queen cell virus loads decreased with a wild pollinator’s centrality in the network and the proportion of visited dish-shaped flowers. Our findings highlight the complex interplay of resource overlap with honeybees, species traits and roles in flower-visitation networks and flower-rich pollinator habitat shaping virus transmission.
Nature ecology & evolutionAgricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
22.20
自引率
2.40%
发文量
282
期刊介绍:
Nature Ecology & Evolution is interested in the full spectrum of ecological and evolutionary biology, encompassing approaches at the molecular, organismal, population, community and ecosystem levels, as well as relevant parts of the social sciences. Nature Ecology & Evolution provides a place where all researchers and policymakers interested in all aspects of life's diversity can come together to learn about the most accomplished and significant advances in the field and to discuss topical issues. An online-only monthly journal, our broad scope ensures that the research published reaches the widest possible audience of scientists.