匈牙利火山爆发后热液喷口动物及其共生体对种群下降的基因组响应对比

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Corinna Breusing, Michelle A Hauer, Ian V Hughes, Johann S Becker, David Casagrande, Brennan T Phillips, Peter R Girguis, Roxanne A Beinart
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引用次数: 0

摘要

遗传瓶颈是减少自然种群有效规模和多样性的进化事件,通常限制了种群适应环境变化的能力。鉴于人类对全球生态系统的影响正在加速,了解种群在遗传瓶颈后如何进化对物种保护变得越来越重要。2022年西南太平洋Hunga火山喷发的火山灰沉积物导致该地区与热液喷口相关的动物共生急剧减少,从而使人们能够深入了解深海人口瓶颈的影响。本研究采用宏基因组测序技术对劳盆地软体动物-微生物共生的爆发前后样本进行分析,以研究其遗传变异模式和有效种群大小。我们的数据表明,动物宿主种群目前在全基因组多样性方面只显示出很小的变化,但在大多数情况下,有效规模的长期下降可能因火山影响而加剧。相比之下,宿主相关的共生体种群表现出显著的基因组变异减少,包括某些栖息地特定菌株的潜在损失。然而,对类似软体动物共生体的环境序列的检测表明,失去的与宿主相关的共生体多样性可能从自由生活的共生体池中恢复。宿主和共生体种群之间的差异可能与它们不同的遗传结构和先前存在的连通性水平有关,尽管宿主动物种群瓶颈的全部程度可能只有在几代之后才能识别出来。这些结果增加了我们对自然干扰后动物微生物种群进化动力学的理解,并有助于评估它们对自然和人为影响的恢复能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contrasting Genomic Responses of Hydrothermal Vent Animals and Their Symbionts to Population Decline After the Hunga Volcanic Eruption.

Genetic bottlenecks are evolutionary events that reduce the effective size and diversity of natural populations, often limiting a population's ability to adapt to environmental change. Given the accelerating human impact on ecosystems worldwide, understanding how populations evolve after a genetic bottleneck is becoming increasingly important for species conservation. Ash deposits from the 2022 Hunga volcanic eruption in the Southwest Pacific led to a drastic decline of animal symbioses associated with hydrothermal vents in this region, allowing insights into the effects of population bottlenecks in the deep sea. Here, we applied metagenomic sequencing to pre- and post-eruption samples of mollusc-microbial symbioses from the Lau Basin to investigate patterns of genetic variation and effective population size. Our data indicate that animal host populations currently show only small changes in genome-wide diversity but in most cases experienced a long-term decline in effective size that was likely intensified by the volcanic impact. By contrast, host-associated symbiont populations exhibited a notable decrease in genomic variation, including potential loss of certain habitat-specific strains. However, detection of environmental sequences resembling mollusc symbionts suggests that lost host-associated symbiont diversity might be recovered from the free-living symbiont pool. The differences between host and symbiont populations might be related to their contrasting genetic structures and pre-existing levels of connectivity, although the full extent of population bottlenecks in the host animals might only be recognisable after a few generations. These results add to our understanding of the evolutionary dynamics of animal-microbe populations following a natural disturbance and help assess their resilience to both natural and anthropogenic impacts.

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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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