欧洲蝴蝶沃尔巴克氏体寄主转移和繁殖操纵基因座的广泛发生。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Eric Toro-Delgado, Dominik R Laetsch, Alex Hayward, Gerard Talavera, Konrad Lohse, Roger Vila
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引用次数: 0

摘要

沃尔巴克氏体是节肢动物和线虫中最常见的细菌内共生体。虽然沃尔巴克氏体主要是通过卵细胞质从亲代向后代垂直传播,但在进化时间尺度上,沃尔巴克氏体的水平传播被认为是常见的。然而,在密切相关的物种中,每种传播机制的相对频率尚未得到系统的研究。此外,虽然沃尔巴克氏体通常被认为是繁殖操纵者,但尚不清楚共生体诱导这种影响的频率。在本研究中,我们对18对欧洲蝴蝶姐妹种的沃尔巴克氏体菌株的全基因组序列数据进行了研究,分析了它们之间的存在、表型和系统发育关系。我们发现姐妹物种共享沃尔巴克氏菌菌株比随机物种对更频繁,并且菌株共享的可能性在年轻的寄主物种对中更高,特别是那些范围重叠较大的寄主物种。我们还发现,感染同一姊妹种对的沃尔巴克氏菌菌株之间的分裂时间通常早于宿主分化,排除了有利于水平转移的共分化。然而,有些菌株比宿主的线粒体分裂时间更年轻,因此在某些情况下不能排除渗透转移的可能性。此外,所有新组装的沃尔巴克氏体基因组都含有与细胞质不相容和雄性杀伤相关的假定同源基因。这支持了感染欧洲蝴蝶的沃尔巴克氏体菌株的生殖操纵的可能性,到目前为止,这只是从线粒体多样性模式推断出来的。我们的研究结果表明,即使在最近形成的宿主类群之间,沃尔巴克氏体的水平和渐进式转移也很频繁,这表明共生体的周转率比以前从远亲宿主的调查中推断的要高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Wolbachia Host Shifts and Widespread Occurrence of Reproductive Manipulation Loci in European Butterflies.

Wolbachia is the most frequent bacterial endosymbiont of arthropods and nematodes. Although it is mostly vertically transmitted, from parent to offspring through the egg cytoplasm, horizontal transfer of Wolbachia is thought to be common over evolutionary timescales. However, the relative frequency of each transmission mechanism has not been studied systematically in closely related species. Additionally, while Wolbachia is generally regarded as a reproductive manipulator, it is unclear how frequently the symbiont induces such effects. In this study, we investigated the presence, phenotypes and phylogenetic relationships among Wolbachia strains in whole genome sequence data for 18 European butterfly sister-species pairs. We find that sister-species share Wolbachia strains more often than random species pairs and that the probability of strain sharing is higher for younger pairs of host species, especially those with greater range overlap. We also find that split times between Wolbachia strains that infect the same sister-species pair generally pre-date host divergence, ruling out co-divergence in favour of horizontal transfer. However, some strains are younger than the mitochondrial split times of their hosts, so introgressive transfer cannot be ruled out in some cases. In addition, all newly assembled Wolbachia genomes contained putative homologues of genes associated with cytoplasmic incompatibility and male killing. This supports the potential for reproductive manipulation in Wolbachia strains infecting European butterflies, which until now was only inferred from mitochondrial diversity patterns. Our results show that horizontal and introgressive transfer of Wolbachia are frequent even between recently speciated host taxa, suggesting the symbiont's turnover rate is higher than had been inferred previously from surveys of distantly related hosts.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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