Heat Stress Drives Rapid Viral and Antiviral Innate Immunity Activation in Hexacorallia.

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ton Sharoni, Adrian Jaimes-Becerra, Magda Lewandowska, Reuven Aharoni, Christian R Voolstra, Maoz Fine, Yehu Moran
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引用次数: 0

Abstract

The class Hexacorallia, encompassing stony corals and sea anemones, plays a critical role in marine ecosystems. Coral bleaching, the disruption of the symbiosis between stony corals and zooxanthellate algae, is driven by seawater warming and further exacerbated by pathogenic microbes. However, how pathogens, especially viruses, contribute to accelerated bleaching remains poorly understood. Here the model sea anemone Nematostella vectensis is used to explore these dynamics by creating a transgenic line with a reporter gene regulated by sequences from two RIG-I-like receptor genes involved in antiviral responses. Under heat stress, the reporter genes showed significant upregulation. Further, transcriptomes from N. vectensis, Exaiptasia diaphana and the stony coral Stylophora pistillata were analysed to reveal stress-induced activation of a set of bona fide immune-related genes conserved between the three species. Population-specific differences in stress-induced transcriptional responses of immune-related genes were evident in both Nematostella and Stylophora, depending on geographic origin. In Exaiptasia, the presence of zooxanthellae also influenced stress-induced immune gene expression. To test whether the viruses themselves contribute to this immune response under stress, we subjected N. vectensis to heat stress and measured the transcription dynamics of resident viruses as well as selected antiviral genes. While the antiviral genes responded within hours of heat stress, viral gene expression was already upregulated within 30 min, suggesting that their increase might be contributing to the elevated immune response under stress, and consequentially, the further demise of organismal homeostasis. These findings highlight the interplay between environmental stress, viruses, immune responses and symbiotic states in Hexacorallia.

热应激驱动hexacorellia病毒和抗病毒先天免疫的快速激活。
六爪纲包括石珊瑚和海葵,在海洋生态系统中起着至关重要的作用。珊瑚白化,即石珊瑚与虫黄藻共生关系的破坏,是由海水变暖驱动的,并由致病微生物进一步加剧。然而,病原体,尤其是病毒,是如何加速白化的,人们知之甚少。本研究利用海葵模型vectensis Nematostella来探索这些动态,方法是创建一个带有报告基因的转基因系,该报告基因由参与抗病毒反应的两个rig - i样受体基因序列调控。在热胁迫下,报告基因表现出显著的上调。此外,研究人员还分析了N. vectensis、Exaiptasia diaphana和石质珊瑚Stylophora pistilllata的转录组,以揭示三种珊瑚之间保守的一组真正的免疫相关基因在应激诱导下的激活。在线虫属和茎柱属中,应激诱导的免疫相关基因转录反应的种群特异性差异是明显的,这取决于地理起源。在绦虫中,虫黄藻的存在也影响应激诱导的免疫基因表达。为了测试病毒本身是否在应激条件下对这种免疫反应有贡献,我们将黑僵菌置于热应激条件下,并测量了驻留病毒的转录动力学以及选择的抗病毒基因。虽然抗病毒基因在热应激的几个小时内起反应,但病毒基因表达在30分钟内就已经上调,这表明它们的增加可能导致应激下免疫反应的升高,从而导致机体内稳态的进一步破坏。这些发现强调了环境压力、病毒、免疫反应和hexacorellia共生状态之间的相互作用。
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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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