Evolution and ecology of parasitism and symbiosis in insects

共生是塑造地球上生命的最重要力量之一。生物学最近的一个重大发展是认识到所有多细胞生物体都有共生微生物。长期以来，这些都是令人难以置信的困难研究；然而，分子和计算生物学的进步已经彻底改变了我们对微生物共生的理解。例如，我们刚刚开始解开生活在人类肠道中的数万亿种微生物的功能，以及它们在新陈代谢、免疫和发育中的重要作用。事实上，有人认为，如果不包括微生物区系，就不能考虑一个有机体的生态和进化，而不把这个有机体视为一个‘全息组’(即宿主的核、细胞器和共生体基因组的总和)。*我的研究目的是了解昆虫共生的生态和进化后果。几乎所有昆虫都感染了遗传的细菌共生体，这些共生体是从母亲传给后代的，通常是在卵细胞质中，类似于线粒体(它们本身是古代共生的后代)。在母体传播中，宿主和共生体的适合度是紧密相连的。事实上，许多昆虫遗传的共生体已经进化出来，以提高宿主的适应性，例如通过保护它们免受天敌的攻击。然而，一些遗传的共生体通过操纵宿主繁殖来增加雌性的频率，例如通过将雄性宿主转变为雌性，然后雌性可以传播更多的共生体。这些共生体被称为“生殖寄生虫”，突出了共生体和宿主之间在传播问题上发生冲突的可能性。这项提议的一个主要目的是研究这种冲突的后果，例如，通过询问遗传共生体在男性宿主中是否表现出功能减弱(因为男性是进化的死胡同)。遗传共生体和线粒体之间的联系更加紧密，这一提议的另一个主要目的是了解共生体和线粒体如何相互作用和影响，以及它们之间是否存在共同适应。最后，我将研究其他扭曲性别比例的自私遗传因素对共生体和线粒体的影响。*我建议研究两个昆虫模型系统。第一种是食用菌果蝇，它含有一种螺旋体细菌共生体，可以保护它免受致命的寄生线虫的侵袭。由于这种强大的保护作用，螺旋体正在整个北美迅速传播。第二种是书虱Liposcelis bostrychophila(寄生虱子的近亲)，它是多态的，因为母亲遗传的性别比扭曲，大多数女性只生女儿。此外，扭曲雌性的线粒体基因组有30%的差异，并且具有与正常雌性完全不同的基因顺序和基因组结构。

Symbiosis is one of the most important forces shaping life on our planet. A major recent development in biology is the realization that all multicellular organisms harbour symbiotic microbes. These have long been incredibly difficult to study; however, advances in molecular and computational biology have revolutionized our understanding of microbial symbiosis. For example, we are just beginning to disentangle the function of the trillions of microbes that live in the human gut, and their important roles in metabolism, immunity, and development. Indeed, it has been argued that one cannot consider the ecology and evolution of an organism without including its microbiota, viewing the organism as a `hologenome' (i.e. the host's nuclear, organellar, and symbiont genomes combined).***My research aims to understand the ecological and evolutionary consequences of symbiosis in insects. Virtually all insects are infected with inherited bacterial symbionts that are transmitted from mothers to their offspring, often in the egg cytoplasm, similar to mitochondria (themselves the descendants of an ancient symbiosis). In maternal transmission, host and symbiont fitness are tightly linked. Indeed, many insect inherited symbionts have evolved to increase the fitness of their hosts, for example by defending them against natural enemies. However, some inherited symbionts manipulate host reproduction to increase the frequency of females, for example by transforming male hosts into females that can then transmit more symbionts. These symbionts, termed `reproductive parasites', highlight the potential for conflicts between symbionts and hosts over transmission. A major aim of this proposal is to examine the consequences of this conflict, for example by asking whether inherited symbionts show reduced function in male hosts (since males are an evolutionary dead end). Tighter still is the link between inherited symbionts and mitochondria, and another major aim of this proposal is to understand how symbionts and mitochondria interact and affect one another, and whether there is co-adaptation between them. Finally, I will examine the effect that other selfish genetic elements that distort sex ratios have on symbionts and mitochondria.***I propose to study two insect model systems. The first, the mushroom-feeding fly Drosophila neotestacea, harbours a Spiroplasma bacterial symbiont that protects it against a virulent parasitic nematode. Due to this strong protective benefit, Spiroplasma is spreading rapidly across N. America. The second, the booklouse Liposcelis bostrychophila (a relative of parasitic lice), is polymorphic for an extraordinary maternally inherited sex-ratio distortion, with most females producing only daughters. Also, the mitochondrial genomes of distorting females are ~30% divergent and have a completely different gene order and genome structure than their `normal' counterparts.********