在非洲-欧亚飞行路线上,地域范围更广的鸟类血液寄生虫多样性更高,但流行率却不高

IF 3.7 2区 医学 Q1 PARASITOLOGY
Mary La Chapelle, Marcello Ruta, Jenny C. Dunn
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引用次数: 0

摘要

据预测,随着全球气温的变化以及宿主和病媒范围的转移,疟原虫属、血丝虫属和白细胞虫属的禽类血液寄生虫将改变其分布范围和流行程度。研究表明,即使是轻微的寄生虫血症也可能导致快速死亡,尤其是在幼稚的种群中。因此,了解鸟类疟疾和类疟疾寄生虫的流行和多样性的大规模模式非常重要,因为我们对它们在野外的影响还不完全了解。我们进行了系统发育控制分析,以检验非洲-欧亚飞行路线上的留鸟和迁徙鸟种之间血吸虫感染(疟原虫、血吸虫和白细胞虫)的流行率和品系多样性的差异。为了检验迁徙策略或迁徙范围的大小是否会导致留居物种和迁徙物种之间寄生虫感染率和多样性的差异,我们将留居物种分为三类:我们利用 MalAvi 数据库中包含 27,861 只鸟类个体的子集数据,对三类留鸟进行了研究:仅欧亚留鸟(36 种)、仅非洲留鸟(41 种)、两洲留鸟(17 种)以及洲际迁徙鸟(64 种)。我们发现,居住在两大洲的物种的寄生虫总体多样性高于所有其他类别。欧亚大陆居民的疟原虫多样性低于所有其他群体,而迁徙者和居住在两大洲的物种的血吸虫多样性均高于非洲和欧亚大陆居民。白细胞虫的多样性在不同群体之间没有差异。流行模式不太明显,不同属之间存在明显差异。居住在两大洲的物种和非洲居民中的疟原虫和白细胞虫流行率均高于移民和欧亚居民。欧亚居民中血吸虫的流行率低于居住在两大洲的物种。尽管我们发现寄生虫多样性与寄生虫流行率的模式截然不同,但我们的发现与之前在南北美洲航道上的发现形成了鲜明对比,在南北美洲航道上,长途迁徙者的寄生虫多样性高于居民和短途迁徙者。重要的是,我们的研究结果表明,在非洲-南极航道沿线的物种中,地理范围可能比迁徙策略对寄生虫多样性的影响更大。我们的分析结果在三个寄生虫属之间存在差异,这表明病媒生态学可能是决定这些大规模模式的重要因素。我们的研究结果加深了我们对寄生虫多样性和丰度的全球模式的理解,并强调需要更好地理解病媒生态学的影响,以了解感染风险的驱动因素并预测对环境变化的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bird species with wider geographical ranges have higher blood parasite diversity but not prevalence across the African-Eurasian flyway

Bird species with wider geographical ranges have higher blood parasite diversity but not prevalence across the African-Eurasian flyway

Bird species with wider geographical ranges have higher blood parasite diversity but not prevalence across the African-Eurasian flyway

Avian blood parasites, from the genera Plasmodium, Haemoproteus and Leucocytozoon, are predicted to alter their range and prevalence as global temperatures change, and host and vector ranges shift. Understanding large-scale patterns in the prevalence and diversity of avian malaria and malaria-like parasites is important due to an incomplete understanding of their effects in the wild, where studies suggest even light parasitaemia can potentially cause rapid mortality, especially in naïve populations. We conducted phylogenetically controlled analyses to test for differences in prevalence and lineage diversity of haemoparasite infection (for Plasmodium, Haemoproteus and Leucocytozoon) in and between resident and migratory species along the African-Eurasian flyway. To test whether migratory strategy or range size drives differences in parasite prevalence and diversity between resident and migrant species, we included three categories of resident species: Eurasian only (n = 36 species), African only (n = 41), and species resident on both continents (n = 17), alongside intercontinental migrants (n = 64), using a subset of data from the MalAvi database comprising 27,861 individual birds. We found that species resident on both continents had a higher overall parasite diversity than all other categories. Eurasian residents had lower Plasmodium diversity than all other groups, and both migrants and species resident on both continents had higher Haemoproteus diversity than both African and Eurasian residents. Leucocytozoon diversity did not differ between groups. Prevalence patterns were less clear, with marked differences between genera. Both Plasmodium and Leucocytozoon prevalence was higher in species resident on both continents and African residents than in migrants and Eurasian residents. Haemoproteus prevalence was lower in Eurasian residents than species resident on both continents. Our findings contrast with previous findings in the North-South American flyway, where long-distance migrants had higher parasite diversity than residents and short-distance migrants, although we found contrasting patterns for parasite diversity to those seen for parasite prevalence. Crucially, our results suggest that geographic range may be more important than migratory strategy in driving parasite diversity within species along the African-Palaearctic flyway. Our findings differ between the three parasite genera included in our analysis, suggesting that vector ecology may be important in determining these large-scale patterns. Our results add to our understanding of global patterns in parasite diversity and abundance, and highlight the need to better understand the influence of vector ecology to understand the drivers of infection risk and predict responses to environmental change.

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来源期刊
CiteScore
8.40
自引率
2.50%
发文量
76
审稿时长
23 days
期刊介绍: International Journal for Parasitology offers authors the option to sponsor nonsubscriber access to their articles on Elsevier electronic publishing platforms. For more information please view our Sponsored Articles page. The International Journal for Parasitology publishes the results of original research in all aspects of basic and applied parasitology, including all the fields covered by its Specialist Editors, and ranging from parasites and host-parasite relationships of intrinsic biological interest to those of social and economic importance in human and veterinary medicine and agriculture.
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