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Global evolutionary genetics of Aedes aegypti, the dengue and yellow fever mosquito.

机译:埃及伊蚊,登革热和黄热病蚊子的全球进化遗传学。

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The mosquito species Aedes aegypti is the principal vector of dengue and yellow fever viruses across the tropics and subtropics worldwide. Dengue fever is on the rise, affecting approximately 50 million people every year, with 40% of the global human population at risk for infection. Populations of the mosquito display an impressive range of phenotypic and genetic variation. The evolutionary history of this species has been profoundly shaped by humans, and most populations across the globe are highly associated with human habitats. However, it has long been hypothesized that the species originated in Africa as a sylvan form breeding in natural water containers (e.g. treeholes) and feeding primarily on non-human animals. Many ecologically similar populations still exist across sub-Saharan Africa, and are known as the subspecies Aedes aegypti formosus. The more common, highly human-associated subspecies, Aedes aegypti aegypti, is thought to have evolved from such ancestral forest forms through adaptations to human habitats, and spread with human movement across the global tropics. In recent years, an increasing number of human-associated Ae. aegypti populations have been identified in Africa, where the true domestic form, Ae. ae. aegypti was believed absent. This raised the question as to whether these populations represent independent incursions of Ae. ae. formosus into human habitats, or are evolutionarily related to domestic populations (Ae. ae. aegypti) from other areas of the world.;In this dissertation work, I used presumed neutral genetic markers (microsatellites, sequenced nuclear loci, and SNPs) to 1) examine genetic structure in the species and test whether geographically, ecologically, and temporally distinct populations of Ae. aegypti are also genetically distinct, and 2) determine the evolutionary history of the species, including the emergence of ecological phenotypes and domesticity. Results of population genetic analyses showed the two subspecies of Ae. aegypti to be genetically distinct, and though populations of Ae. ae. formosus across Africa did not show much structuring, high levels of genetic structure were found between populations within the pantropical domestic subspecies Ae. ae. aegypti (Chapters 1 and 4). Because of this, I was able to clearly assign individual pantropical mosquitoes back to their population of origin, an ability that was used in Chapter 2 to determine that a recent introduction of Ae. aegypti in the Netherlands originated from a tire shipment out of Miami, Florida. In contrast, genetic structuring was largely absent across temporally distinct populations: those collected several years apart from the same location. However, this pattern varied by collection site (Chapter 3).;Phylogenetic and population genetic analyses of global Ae. aegypti populations support the hypothesis that the species originated in Africa as a form similar to Ae. ae. formosus, from which the domestic subspecies evolved and spread to the New World, followed by the Asia-Pacific region (Chapters 1 and 4). Two patterns strongly support this conclusion: (a) sub-Saharan African samples show considerably greater genetic variation, especially with regard to the number of alleles present and (b) phylogenetic analyses indicate the African populations are basal, i.e., are subtended by the deepest branches in the overall tree. However, human-associated populations in Africa appear to be the result of independent incursions of the species into human habitats, as they are genetically identified as Ae. ae. formosus, and evolutionarily distinct from the domestic subspecies Ae. ae. aegypti. This suggests that the species has the propensity to continue invading human habitats across the African landscape, leading to increased opportunities for epidemic disease spread. Overall, the studies performed during the course of my dissertation research indicate that humans have profoundly affected genetic diversity in Ae. aegypti and have shaped the evolutionary history of the species. These evolutionary patterns may be relevant in other disease vector systems, as well as in a multitude of invasive species with close ecological interactions with humans.
机译:埃及伊蚊(Aedes aegypti)是全世界热带和亚热带地区登革热和黄热病病毒的主要媒介。登革热正在上升,每年影响约5000万人,全球40%的人口有感染的危险。蚊子的表型和遗传变异范围广。该物种的进化史已被人类深深地塑造,全球大多数人口与人类栖息地高度相关。然而,长期以来一直假设该物种起源于非洲,是一种在自然水容器(例如树洞)中繁殖的西尔万形式,主要以非人类动物为食。整个撒哈拉以南非洲地区仍然存在许多生态相似的种群,被称为埃及伊蚊亚种。人们认为,更常见的,与人类有高度联系的亚种埃及伊蚊(Aedes aegypti aegypti)已从这种祖先的森林形式演变成对人类栖息地的适应,并随着人类在全球热带地区的活动而传播。近年来,与人类相关的Ae越来越多。在非洲,已经发现埃及的埃及人种群,那里是真正的家禽。 e人们认为埃及埃及人不在。这就提出了一个问题,即这些人口是否代表独立入侵的Ae。 e进入人类栖息地,或在进化上与来自世界其他地区的家庭种群(埃及伊蚊)有关;在本论文中,我使用了假定的中性遗传标记(微卫星,测序的核基因座和SNP)至1 )检查物种的遗传结构,并测试Ae的地理,生态和时间上是否不同。埃及也有遗传差异,并且2)确定该物种的进化历史,包括生态表型和驯养性的出现。群体遗传分析的结果显示了Ae的两个亚种。埃及人在遗传上是不同的,尽管是埃及人的种群。 e整个非洲的山毛榉没有显示出太多的结构,在泛热带家养亚种Ae的种群之间发现了高水平的遗传结构。 e埃及(第1章和第4章)。因此,我能够将各个泛热带蚊子明确地分配给它们的起源种群,这一能力在第二章中用于确定最近引入的Ae。荷兰的aegypti源自佛罗里达州迈阿密的轮胎装运。相反,在时间上截然不同的群体中,基因结构基本上不存在:那些在同一地点以外数年收集的。但是,这种模式因采集地点而异(第3章)。全球Ae的系统发育和种群遗传分析。埃及种群支持以下假设:该物种起源于非洲,其形式类似于Ae。 e形态,国内亚种从此形成并传播到新世界,其次是亚太地区(第1章和第4章)。有两种模式有力地支持了这一结论:(a)撒哈拉以南非洲样本显示出相当大的遗传变异,尤其是在存在的等位基因数量方面;(b)系统发育分析表明,非洲种群是基础种群,即被最深的种群所包围整体树中的树枝。但是,非洲的人类相​​关种群似乎是该物种独立侵入人类栖息地的结果,因为它们在基因上被确定为Ae。 e具孔性,在进化上与家养亚种不同。 e埃及。这表明该物种有可能继续侵入整个非洲景观的人类栖息地,从而导致流行病传播的机会增加。总体而言,在我的论文研究过程中进行的研究表明,人类已对Ae的遗传多样性产生了深远的影响。埃及和已经塑造了该物种的进化历史。这些进化模式可能与其他疾病媒介系统以及与人类有着密切生态相互作用的多种入侵物种有关。

著录项

  • 作者

    Brown, Julia Elizabeth.;

  • 作者单位

    Yale University.;

  • 授予单位 Yale University.;
  • 学科 Biology Evolution and Development.;Biology Ecology.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 158 p.
  • 总页数 158
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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