新西兰石龙子和壁虎的辐射与独特的病毒体有关。

IF 2.3 Q2 ECOLOGY BMC ecology and evolution Pub Date : 2024-06-13 DOI:10.1186/s12862-024-02269-4
Stephanie J Waller, Richelle G Butcher, Lauren Lim, Kate McInnes, Edward C Holmes, Jemma L Geoghegan
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摘要

背景:新西兰拥有 120 多种本地特有的石龙子和壁虎物种,这些物种是在过去 2000 万至 4000 万年间繁衍出来的,很可能是受中新世期间形成的多种栖息地的开发利用所驱动。动物宿主最近的辐射可能会促进病毒的跨物种传播,这可能反映了它们之间密切的遗传关系,因此病毒在新宿主身上出现的障碍相对较低。相反,随着动物宿主适应新的生态位,甚至在特定的地理位置内,它们的病毒也能适应新的生态位。因此,那些在辐射后实现了生态位特化的动物可能会携带基因上与众不同的病毒。通过对新西兰的八个本地石龙子和壁虎物种以及唯一引进的蜥蜴物种彩虹石龙子(Lampropholis delicata)进行元转录本组分析,我们旨在揭示这些宿主体内病毒的多样性,并确定新西兰石龙子和壁虎的辐射是否以及如何影响病毒的多样性和进化:结果:我们在 9 个采样物种中的 7 个物种中发现了 15 种新型爬行动物病毒,涵盖 11 个不同的病毒科。值得注意的是,我们在所分析的本地动物中没有发现病毒宿主转换现象,甚至在同一地理位置采样的动物之间也没有发现病毒宿主转换现象。这与宿主物种分化可能导致病毒种群孤立、受生态位限制,从而阻止跨物种传播的观点相吻合。利用基于蛋白质结构相似性的方法,我们进一步发现了一种高度分化的布尼亚类病毒,它有可能在布尼亚病毒科中形成一个新的家族:这项研究拓宽了我们对新西兰爬行动物病毒的了解,并说明了生态位适应如何限制病毒与宿主的相互作用。
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The radiation of New Zealand's skinks and geckos is associated with distinct viromes.

Background: New Zealand is home to over 120 native endemic species of skinks and geckos that radiated over the last 20-40 million years, likely driven by the exploitation of diverse habitats formed during the Miocene. The recent radiation of animal hosts may facilitate cross-species virus transmission, likely reflecting their close genetic relationships and therefore relatively low barriers for viruses to emerge in new hosts. Conversely, as animal hosts adapt to new niches, even within specific geographic locations, so too could their viruses. Consequently, animals that have niche-specialised following radiations may be expected to harbour genetically distinct viruses. Through a metatranscriptomic analysis of eight of New Zealand's native skink and gecko species, as well as the only introduced lizard species, the rainbow skink (Lampropholis delicata), we aimed to reveal the diversity of viruses in these hosts and determine whether and how the radiation of skinks and geckos in New Zealand has impacted virus diversity and evolution.

Results: We identified a total of 15 novel reptilian viruses spanning 11 different viral families, across seven of the nine species sampled. Notably, we detected no viral host-switching among the native animals analysed, even between those sampled from the same geographic location. This is compatible with the idea that host speciation has likely resulted in isolated, niche-constrained viral populations that have prevented cross-species transmission. Using a protein structural similarity-based approach, we further identified a highly divergent bunya-like virus that potentially formed a new family within the Bunyavirales.

Conclusions: This study has broadened our understanding of reptilian viruses within New Zealand and illustrates how niche adaptation may limit viral-host interactions.

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