Mejía Luis C, Herre Edward A, Sparks Jed P, Winter Klaus, García Milton N, Van Bael Sunshine A, Stitt Joseph, Shi Zi, Zhang Yufan, Guiltinan Mark J, Maximova Siela N
Smithsonian Tropical Research Institute Unit 9100, USA ; Department of Plant Science and The Huck Institutes of the Life Sciences, The Pennsylvania State University University Park, PA, USA.
Smithsonian Tropical Research Institute Unit 9100, USA.
Front Microbiol. 2014 Sep 12;5:479. doi: 10.3389/fmicb.2014.00479. eCollection 2014.
It is increasingly recognized that macro-organisms (corals, insects, plants, vertebrates) consist of both host tissues and multiple microbial symbionts that play essential roles in their host's ecological and evolutionary success. Consequently, identifying benefits and costs of symbioses, as well as mechanisms underlying them are research priorities. All plants surveyed under natural conditions harbor foliar endophytic fungi (FEF) in their leaf tissues, often at high densities. Despite producing no visible effects on their hosts, experiments have nonetheless shown that FEF reduce pathogen and herbivore damage. Here, combining results from three genomic, and two physiological experiments, we demonstrate pervasive genetic and phenotypic effects of the apparently asymptomatic endophytes on their hosts. Specifically, inoculation of endophyte-free (E-) Theobroma cacao leaves with Colletotrichum tropicale (E+), the dominant FEF species in healthy T. cacao, induces consistent changes in the expression of hundreds of host genes, including many with known defensive functions. Further, E+ plants exhibited increased lignin and cellulose content, reduced maximum rates of photosynthesis (Amax), and enrichment of nitrogen-15 and carbon-13 isotopes. These phenotypic changes observed in E+ plants correspond to changes in expression of specific functional genes in related pathways. Moreover, a cacao gene (Tc00g04254) highly up-regulated by C. tropicale also confers resistance to pathogen damage in the absence of endophytes or their products in host tissues. Thus, the benefits of increased pathogen resistance in E+ plants are derived in part from up-regulation of intrinsic host defense responses, and appear to be offset by potential costs including reduced photosynthesis, altered host nitrogen metabolism, and endophyte heterotrophy of host tissues. Similar effects are likely in most plant-endophyte interactions, and should be recognized in the design and interpretation of genetic and phenotypic studies of plants.
人们越来越认识到,大型生物(珊瑚、昆虫、植物、脊椎动物)由宿主组织和多种微生物共生体组成,这些共生体在宿主的生态和进化成功中发挥着重要作用。因此,确定共生关系的益处和成本以及其潜在机制是研究的重点。在自然条件下调查的所有植物的叶片组织中都含有叶内生真菌(FEF),且密度通常很高。尽管对宿主没有产生明显影响,但实验表明,FEF可减少病原体和食草动物造成的损害。在这里,结合三个基因组实验和两个生理实验的结果,我们证明了看似无症状的内生菌对其宿主具有普遍的遗传和表型影响。具体而言,用健康可可树中占主导地位的FEF物种热带炭疽菌(E+)接种无菌(E-)可可树叶片,可诱导数百个宿主基因的表达发生一致变化,其中许多基因具有已知的防御功能。此外,E+植株的木质素和纤维素含量增加,最大光合速率(Amax)降低,氮-15和碳-13同位素富集。在E+植株中观察到的这些表型变化与相关途径中特定功能基因的表达变化相对应。此外,一个被热带炭疽菌高度上调的可可基因(Tc00g04254)在宿主组织中不存在内生菌或其产物的情况下也能赋予对病原体损害的抗性。因此,E+植株中病原体抗性增加的益处部分源于宿主内在防御反应的上调,并且似乎被包括光合作用降低、宿主氮代谢改变以及宿主组织的内生菌异养等潜在成本所抵消。大多数植物与内生菌的相互作用可能都有类似的影响,并且在植物的遗传和表型研究的设计和解释中应该予以考虑。