BRC-BIO - Expanding the ‘community’ in Community Genetics: Infracommunity genomics of duck symbionts to determine the eco-evolutionary factors underpinning holobiont evolution.
BRC-BIO - Expanding the ‘community’ in Community Genetics: Infracommunity genomics of duck symbionts to determine the eco-evolutionary factors underpinning holobiont evolution.
批准号:
2218190
负责人:
Erika Ebbs
金额:
$49.12万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-08-15 至 2025-07-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
How host-parasite interactions are maintained over ecological time and evolutionary time (i.e. many generations) is a significant biological question, with real-world applications in medicine, public health, and conservation. It is often overlooked, though, that a single host can contain a diverse community (i.e. infracommunity) of parasites.. The proposed research focuses on duck hosts and seeks to understand their parasite infracommunity structure and predictability. Ducks transmit several diseases of human importance, including Avian Influenza Virus (AIV) and Human Cercarial Dermatitis (HCD). As a group, ducks can be divided based on ecological traits (habitat selection, feeding behaviors) into two groupings, dabbling and diving ducks. Prior studies have suggested that dabbling ducks may support a higher rate of transmission of AIV and HCD. This work will characterize infracommunities of four dabbling and four diving duck species within the Eastern USA, to determine if infracommunities are specific to host species and/or ecological group. We will look deeply into the genetics of recovered parasite populations to determine if host species and/or ecological group help explain critical public health parameters, such has higher rates of transmission. Human-induced environmental change has resulted in significant changes to duck populations, such that some species are thriving in altered habitats, and others are in decline. There is thus an urgency to understand the ecology and evolution of duck parasite infracommunities to better model diseases such as AIV and HCD in a changing world. Within an individual host, a community of symbionts (infracommunity) assembles in response to both ecological and evolutionary processes. Does the shared host environment act in a concerted way to shape the structure, assembly, and microevolution of infracommunities? The proposed research takes a community genetics approach to provide robust insights into the evolutionary processes within and across species of a shared host environment. This work will investigate the helminth (parasitic worms) and viral communities of eight duck species, which can be divided into two distinct ecological groups (dabbling vs. diving species) based on host-traits. The proposed research will use long-read Oxford Nanopore Sequencing to 1) characterize infracommunity structure across hosts and ecological groups and 2) compare population genetic structure and diversity of recovered core taxa (i.e. 70% prevalence). Merging community ecology and population genetics will help uncover the ecological determinants of infracommunity assembly, microevolution and ultimately provide insights into the evolution of the hologenome. Prior work with both helminths (Trematoda: Trichobilharzia) and Avian Influenza Virus (AIV) have shown higher prevalence, genetic diversity, and larger effective sizes are associated with dabblers, suggesting host-traits shape infracommunity assembly and within-host microevolutionary patterns. Understanding the predictability and taxonomic scalability of infracommunity assembly, and identifying what ecological factors support transmission, could improve our ability to model zoonotic waterborne diseases associated with waterfowl.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
国内基金
海外基金
登录
查看更多内容
NGQDs/BiO2-x/PANI新型复合光催化剂的构筑及其可见光催化还原Cr(VI)的性能与机制研究
-
批准号:2026JJ80226
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:唐新德
-
依托单位:
骨胶原(Bio-Oss Collagen)联合龈下喷砂+骨皮质切开术治疗
根分叉病变的临床疗效研究
-
批准号:2024JJ9542
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2024
-
负责人:潘涛华
-
依托单位:
基于通用型 M13-Bio 噬菌体信号放大的动态
光散射免疫传感检测平台的建立及机制研究
-
批准号:Q24C200014
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2024
-
负责人:湛胜楠
-
依托单位:
智能双栅调控InSe Bio-FET可控构筑与原位细胞传感机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2024
-
负责人:
-
依托单位:
2D/2D BiO2-x/graphyne异质结光热活化过硫酸盐降解水体中抗生素的机理研究
-
批准号:LY23E080003
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:李必胜
-
依托单位:
过渡金属掺杂与原位外延生长Z型异质结协同增强BiO2-x的宽光谱光催化活化分子氧去除水中难降解微塑料的机理研究
-
批准号:--
-
项目类别:--
-
资助金额:60万元
-
批准年份:2021
-
负责人:张高科
-
依托单位:
BIO促进脂肪来源干细胞修复急性心肌梗死的作用及机制
-
批准号:32071365
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2020
-
负责人:杨向群
-
依托单位:
Z型异质结“(金属氧化物MOx@薄层碳TC)/BiO1-xCl”的可控构筑及其光催化性能的研究
-
批准号:22005126
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2020
-
负责人:孙立鸣
-
依托单位:
6-BIO 抗肝脏衰老的作用与作用机制研究
-
批准号:19ZR1438800
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2019
-
负责人:苗雅
-
依托单位:
基于MOFs热解构建薄层碳包覆的BiO1-xX基Z型异质结及其光催化水氧化苯制苯酚反应的研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2019
-
负责人:
-
依托单位: