Genetic Characterisation of the Bacterial Microbiota Associating With a Strain of Epichloë Fungal Endophyte of Perennial Ryegrass and the Interaction With Its Paenibacillus Members

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Daniel A. Bastías, Linda J. Johnson, Sandeep Kumar, Ruy Jáuregui, Emma R. Applegate, Stuart D. Card
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Abstract

Plant-associated fungi can host unique bacterial microbiota to provide multiple benefits to their fungal hosts. Here it was characterised the bacterial microbiota associated with an Epichloë fungal endophyte (strain AR135) isolated from perennial ryegrass (Lolium perenne) via both 16S rRNA gene sequencing and direct microbial isolation and investigated the microbe-microbe interactions between these bacteria and the fungus. The bacterial microbiota of AR135 was dominated by members within the genus Paenibacillus, with 99% of abundance (on average); although bacteria within genera Delftia and Bradyrhizobium were also present. Paenibacillus cells were located on the surface of hyphae of AR135 fungus in vitro on synthetic media and in planta within perennial ryegrass leaves. Two bacterial strains, E100 and E300, identified as Paenibacillus, were isolated from the AR135 mycelium. E300 drastically altered the abundance of both the whole bacterial microbiota (increased by 63%) and E100 (reduced to 0%). None of the variations observed in the abundance of total bacterial microbiota and E100 and E300 were associated with changes in the fungal biomass of Epichloë. The findings show that Epichloë fungal endophytes can host bacterial communities, the structure of which was regulated by key members of the bacterial community.

多年生黑麦草Epichloë真菌内生菌相关菌群的遗传特征及其与芽孢杆菌成员的相互作用
植物相关真菌可以宿主独特的细菌微生物群,为它们的真菌宿主提供多种好处。本文通过16S rRNA基因测序和直接微生物分离,对从多年生黑麦草(Lolium perenne)中分离的Epichloë真菌内生菌(菌株AR135)进行了细菌微生物群的表征,并研究了这些细菌与真菌之间的微生物相互作用。AR135菌群以芽孢杆菌属成员为主,平均丰度为99%;尽管代尔夫特属和缓生根瘤菌属的细菌也存在。体外合成培养基上的AR135真菌菌丝表面和多年生黑麦草叶片内的植物中均有芽孢杆菌细胞。从AR135菌丝体中分离到2株芽孢杆菌E100和E300。E300极大地改变了整个细菌微生物群的丰度(增加了63%)和E100(减少到0%)。观察到的总细菌微生物群丰度和E100和E300的变化与Epichloë真菌生物量的变化无关。研究结果表明,Epichloë真菌内生菌可以宿主细菌群落,其结构受细菌群落关键成员的调节。
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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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