Parasite manipulation of host phenotypes inferred from transcriptional analyses in a trematode-amphipod system

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
David M. Rand, Joaquin C. B. Nunez, Shawn Williams, Stephen Rong, John T. Burley, Kimberly B. Neil, Adam N. Spierer, Wilson McKerrow, David S. Johnson, Yevgeniy Raynes, Thomas J. Fayton, Nicholas Skvir, David A. Ferranti, Maya Greenhill Zeff, Amanda Lyons, Naima Okami, David M. Morgan, Kealohanuiopuna Kinney, Bianca R. P. Brown, Anne E. Giblin, Zoe G. Cardon
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引用次数: 0

Abstract

Manipulation of host phenotypes by parasites is hypothesized to be an adaptive strategy enhancing parasite transmission across hosts and generations. Characterizing the molecular mechanisms of manipulation is important to advance our understanding of host–parasite coevolution. The trematode (Levinseniella byrdi) is known to alter the colour and behaviour of its amphipod host (Orchestia grillus) presumably increasing predation of amphipods which enhances trematode transmission through its life cycle. We sampled 24 infected and 24 uninfected amphipods from a salt marsh in Massachusetts to perform differential gene expression analysis. In addition, we constructed novel genomic tools for O. grillus including a de novo genome and transcriptome. We discovered that trematode infection results in upregulation of amphipod transcripts associated with pigmentation and detection of external stimuli, and downregulation of multiple amphipod transcripts implicated in invertebrate immune responses, such as vacuolar ATPase genes. We hypothesize that suppression of immune genes and the altered expression of genes associated with coloration and behaviour may allow the trematode to persist in the amphipod and engage in further biochemical manipulation that promotes transmission. The genomic tools and transcriptomic analyses reported provide new opportunities to discover how parasites alter diverse pathways underlying host phenotypic changes in natural populations.

从吸虫-片足类动物系统的转录分析推断,寄生虫操纵宿主表型
寄生虫对宿主表型的操纵被假设为一种适应性策略,增强了寄生虫在宿主和代之间的传播。表征操纵的分子机制对促进我们对宿主-寄生虫共同进化的理解很重要。已知吸虫(Levinseniella byrdi)会改变其片脚类寄主(Orchestia grillus)的颜色和行为,可能会增加片脚类的捕食,从而增强吸虫在其生命周期中的传播。我们从马萨诸塞州的盐沼中取样了24只感染和24只未感染的片脚类动物进行差异基因表达分析。此外,我们构建了新的基因组工具,包括一个新的基因组和转录组。我们发现吸虫感染导致与色素沉着和外部刺激检测相关的片足类转录物上调,以及与无脊椎动物免疫反应相关的多种片足类转录物下调,如液泡atp酶基因。我们推测,免疫基因的抑制和与颜色和行为相关的基因表达的改变可能允许吸虫在片足类动物中持续存在,并参与进一步的生化操作,促进传播。所报道的基因组工具和转录组学分析为发现寄生虫如何改变自然种群中宿主表型变化的多种途径提供了新的机会。
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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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