School of Biological Sciences, Bangor University, Memorial Building, Deiniol Road, Bangor, Gwynedd, LL57 2UW, UK.
Swedish University of Agricultural Sciences, Almas Alle 8, 750 07, Uppsala, Sweden.
Microbiome. 2018 Jan 30;6(1):21. doi: 10.1186/s40168-018-0408-5.
Britain's native oak species are currently under threat from acute oak decline (AOD), a decline-disease where stem bleeds overlying necrotic lesions in the inner bark and larval galleries of the bark-boring beetle, Agrilus biguttatus, represent the primary symptoms. It is known that complex interactions between the plant host and its microbiome, i.e. the holobiont, significantly influence the health status of the plant. In AOD, necrotic lesions are caused by a microbiome shift to a pathobiome consisting predominantly of Brenneria goodwinii, Gibbsiella quercinecans, Rahnella victoriana and potentially other bacteria. However, the specific mechanistic processes of the microbiota causing tissue necrosis, and the host response, have not been established and represent a barrier to understanding and managing this decline.
We profiled the metagenome, metatranscriptome and metaproteome of inner bark tissue from AOD symptomatic and non-symptomatic trees to characterise microbiota-host interactions. Active bacterial virulence factors such as plant cell wall-degrading enzymes, reactive oxygen species defence and flagella in AOD lesions, along with host defence responses including reactive oxygen species, cell wall modification and defence regulators were identified. B. goodwinii dominated the lesion microbiome, with significant expression of virulence factors such as the phytopathogen effector avrE. A smaller proportion of microbiome activity was attributed to G. quercinecans and R. victoriana. In addition, we describe for the first time the potential role of two previously uncharacterised Gram-positive bacteria predicted from metagenomic binning and identified as active in the AOD lesion metatranscriptome and metaproteome, implicating them in lesion formation.
This multi-omic study provides novel functional insights into microbiota-host interactions in AOD, a complex arboreal decline disease where polymicrobial-host interactions result in lesion formation on tree stems. We present the first descriptions of holobiont function in oak health and disease, specifically, the relative lesion activity of B. goodwinii, G. quercinecans, Rahnella victoriana and other bacteria. Thus, the research presented here provides evidence of some of the mechanisms used by members of the lesion microbiome and a template for future multi-omic research into holobiont characterisation, plant polymicrobial diseases and pathogen defence in trees.
英国本土的橡树物种目前正受到急性橡树衰退(AOD)的威胁,这是一种衰退性疾病,在这种疾病中,树干会流血,覆盖在内部树皮的坏死病变和树皮钻孔甲虫 Agrilus biguttatus 的幼虫画廊是主要症状。已知植物宿主与其微生物组(即整体生物)之间的复杂相互作用显著影响植物的健康状况。在 AOD 中,坏死病变是由微生物组向主要由 Brenneria goodwinii、Gibbsiella quercinecans、Rahnella victoriana 和潜在其他细菌组成的病理生物组转变引起的。然而,导致组织坏死的微生物组的具体机制过程以及宿主反应尚未确定,这是理解和管理这种衰退的障碍。
我们对 AOD 症状性和非症状性树木的内树皮组织进行了宏基因组、宏转录组和宏蛋白质组分析,以描述微生物组-宿主相互作用。在 AOD 病变中,鉴定到了活性细菌毒力因子,如植物细胞壁降解酶、活性氧物质防御和鞭毛,以及宿主防御反应,包括活性氧物质、细胞壁修饰和防御调节剂。B. goodwinii 主导病变微生物组,显著表达了毒力因子,如植物病原体效应物 avrE。微生物组活性的一小部分归因于 G. quercinecans 和 R. victoriana。此外,我们首次描述了两个以前未表征的革兰氏阳性细菌的潜在作用,这些细菌是通过宏基因组分箱预测的,并在 AOD 病变宏转录组和宏蛋白质组中被鉴定为活性,暗示它们参与了病变的形成。
这项多组学研究为 AOD 中微生物组-宿主相互作用提供了新的功能见解,AOD 是一种复杂的树木衰退疾病,其中多微生物-宿主相互作用导致树干上形成病变。我们首次描述了橡树健康和疾病中的整体生物功能,特别是 B. goodwinii、G. quercinecans、Rahnella victoriana 和其他细菌的相对病变活性。因此,本研究提供了病变微生物组成员使用的一些机制的证据,并为未来的多组学研究提供了模板,以研究整体生物特性、树木多微生物疾病和病原体防御。