昆虫系统共感染时,资源调节发育变化而非感染耐受。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nora K E Schulz, Danial Asgari, Siqin Liu, Stephanie S L Birnbaum, Alissa M Williams, Arun Prakash, Ann T Tate
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引用次数: 0

摘要

生物体内的能量资源既促进了寄生虫的生长,也促进了对它们的免疫反应,但目前尚不清楚能量分配是否足以解释在多种寄生虫威胁下感染结果的变化。我们对感染了两种天然寄生虫的粉甲虫(Tribolium confusum)进行了饮食调节,并利用转录组学和表型分析相结合的方法研究了资源在单次和联合感染后代谢和免疫反应的变化中所起的作用。我们的研究结果表明,相对良性的单细胞真核格林寄生虫以饮食依赖的方式改变宿主内的能量环境,进而改变幼虫的发育时间。虽然它们不会影响宿主对急性细菌感染的抵抗力,但mRNA-seq结果显示,它们会刺激另一组免疫基因的表达,并促进肠道损伤,最终导致生存率降低,无论饮食如何。因此,能量分配不足以解释免疫对合并感染结果的贡献,强调了预测跨生物组织水平合并感染影响的机制洞察力的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resources Modulate Developmental Shifts but Not Infection Tolerance Upon Co-Infection in an Insect System.

Energetic resources within organisms fuel both parasite growth and immune responses against them, but it is unclear whether energy allocation is sufficient to explain changes in infection outcomes under the threat of multiple parasites. We manipulated diet in flour beetles (Tribolium confusum) infected with two natural parasites and used a combination of transcriptomic and phenotypic assays to investigate the role of resources in shifting metabolic and immune responses after single and co-infection. Our results suggest that relatively benign, single-celled, eukaryotic gregarine parasites alter the within-host energetic environment and, by extension, juvenile development time, in a diet-dependent manner. While they do not affect host resistance to acute bacterial infection, the mRNA-seq results reveal that they stimulate the expression of an alternative set of immune genes and promote damage to the gut, ultimately contributing to reduced survival regardless of diet. Thus, energy allocation is not sufficient to explain the immunological contribution to co-infection outcomes, emphasising the importance of mechanistic insight for predicting the impact of co-infection across levels of biological organisation.

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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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