宿主范围扩展和共种形成在宿主-寄生虫关联中与大山雀物种复合体分化的作用。

IF 2.3 2区 生物学 Q2 ECOLOGY
Xi Huang, Vincenzo A. Ellis, Yangyang Peng, Farah Ishtiaq, Haitao Wang, Wei Liang, Qiang Wu, Staffan Bensch, Lu Dong
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引用次数: 0

摘要

在寄生虫的进化过程中,共种形成和寄主范围扩大被认为在与寄主建立联系中起作用,而分选事件可能导致这些联系的解散。为了解决这些过程的作用,我们重点研究了感染大山雀物种复合体宿主的禽血红孢子虫寄生虫。我们估计了在物种复合体中检测到的谱系的系统地理学,并量化了它们在宿主之间的过渡概率。在不同寄主种中检测到的谱系具有很强的地理信号,但没有形成单系类群。然而,谱系的分布并不仅仅是它们传播限制的结果,因为许多只感染一种焦点物种的谱系可以在与其他焦点物种共生的鸟类中发现。此外,感染同一宿主物种的近亲谱系的感染率比偶然预期的要高得多。最后,感染P. major(最近分散的物种)的嗜血杆菌和白细胞原虫谱系比其他寄生虫更普遍,这与通才寄生虫通过感染新遇到的宿主物种来扩大其宿主范围的模式一致。我们的研究结果表明,该系统中的宿主-寄生虫关联主要是寄生虫分选事件和宿主范围扩大的结果,而不是共种形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Role of Host-Range Expansion and Co-Speciation in Host–Parasite Associations With the Divergence of the Great Tit Species Complex

The Role of Host-Range Expansion and Co-Speciation in Host–Parasite Associations With the Divergence of the Great Tit Species Complex

During the evolution of parasites, co-speciation and host-range expansion are thought to play roles in establishing associations with hosts, while sorting events can lead to dissolution of those associations. To address the roles of these processes, we focus on avian haemosporidian parasites infecting hosts of the intensively studied great tit species complex. We estimated the phylogeography of lineages detected in the species complex, and quantified their transition probabilities among hosts. Lineages detected in different host species presented a strong geographical signal but did not form monophyletic groups. Yet, distributions of lineages are not merely the result of their dispersal limitations, as many lineages that infect only one focal species can be found in birds sympatric with other focal species. Besides, closely related lineages that infect the same host species reach more similar rates of infection than expected by chance. Finally, Haemoproteus and Leucocytozoon lineages infecting P. major, the most recently dispersed species, were more generalized than others, consistent with a pattern of generalist parasites expanding their host ranges by infecting newly encountered host species. Our results suggest that host–parasite associations in this system are mainly the result of sorting events and host-range expansion of parasites, rather than co-speciation.

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来源期刊
CiteScore
4.40
自引率
3.80%
发文量
1027
审稿时长
3-6 weeks
期刊介绍: Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment. Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.
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