Department of Biology, University of Miami, Coral Gables, FL, USA.
Department of Ecology and Evolutionary Biology, University of Toronto, Toronto, ON, Canada.
Mol Ecol. 2018 Apr;27(8):1860-1873. doi: 10.1111/mec.14550. Epub 2018 Apr 11.
A mechanistic understanding of community ecology requires tackling the nonadditive effects of multispecies interactions, a challenge that necessitates integration of ecological and molecular complexity-namely moving beyond pairwise ecological interaction studies and the "gene at a time" approach to mechanism. Here, we investigate the consequences of multispecies mutualisms for the structure and function of genomewide differential coexpression networks for the first time, using the tractable and ecologically important interaction between legume Medicago truncatula, rhizobia and mycorrhizal fungi. First, we found that genes whose expression is affected nonadditively by multiple mutualists are more highly connected in gene networks than expected by chance and had 94% greater network centrality than genes showing additive effects, suggesting that nonadditive genes may be key players in the widespread transcriptomic responses to multispecies symbioses. Second, multispecies mutualisms substantially changed coexpression network structure of 18 modules of host plant genes and 22 modules of the fungal symbionts' genes, indicating that third-party mutualists can cause significant rewiring of plant and fungal molecular networks. Third, we found that 60% of the coexpressed gene sets that explained variation in plant performance had coexpression structures that were altered by interactive effects of rhizobia and fungi. Finally, an "across-symbiosis" approach identified sets of plant and mycorrhizal genes whose coexpression structure was unique to the multiple mutualist context and suggested coupled responses across the plant-mycorrhizal interaction to rhizobial mutualists. Taken together, these results show multispecies mutualisms have substantial effects on the molecular interactions in host plants, microbes and across symbiotic boundaries.
为了深入理解群落生态学,我们需要解决多物种相互作用的非加和效应,这一挑战需要整合生态学和分子复杂性,即超越种间相互作用的研究和“一次一个基因”的机制研究方法。在这里,我们首次调查了多物种互利共生对全基因组差异共表达网络结构和功能的影响,使用豆科植物苜蓿、根瘤菌和菌根真菌之间可控制和重要的相互作用。首先,我们发现,多个互利共生者的非加和作用影响其表达的基因在基因网络中的连接度高于预期的随机水平,且网络中心性比表现出加和效应的基因高出 94%,这表明非加和基因可能是广泛的转录组对多物种共生反应的关键参与者。其次,多物种互利共生极大地改变了宿主植物基因的 18 个模块和真菌共生体基因的 22 个模块的共表达网络结构,表明第三方互利共生者可以导致植物和真菌分子网络的显著重构。第三,我们发现,解释植物性能变化的 60%共表达基因集的共表达结构受到根瘤菌和真菌相互作用的影响。最后,一种“跨共生体”的方法鉴定了一组植物和菌根基因,其共表达结构在多互利共生体的情况下是独特的,并表明植物-菌根相互作用对根瘤菌互利共生者的耦合反应。总之,这些结果表明多物种互利共生对宿主植物、微生物和跨共生体边界的分子相互作用有显著影响。