Abstract

Fungi interact closely with bacteria, both on the surfaces of the hyphae and within their living tissues (i.e. endohyphal bacteria, EHB). These EHB can be obligate or facultative symbionts and can mediate diverse phenotypic traits in their hosts. Although EHB have been observed in many lineages of fungi, it remains unclear how widespread and general these associations are, and whether there are unifying ecological and genomic features can be found across EHB strains as a whole. We cultured 11 bacterial strains after they emerged from the hyphae of diverse Ascomycota that were isolated as foliar endophytes of cupressaceous trees, and generated nearly complete genome sequences for all. Unlike the genomes of largely obligate EHB, the genomes of these facultative EHB resembled those of closely related strains isolated from environmental sources. Although all analysed genomes encoded structures that could be used to interact with eukaryotic hosts, pathways previously implicated in maintenance and establishment of EHB symbiosis were not universally present across all strains. Independent isolation of two nearly identical pairs of strains from different classes of fungi, coupled with recent experimental evidence, suggests horizontal transfer of EHB across endophytic hosts. Given the potential for EHB to influence fungal phenotypes, these genomes could shed light on the mechanisms of plant growth promotion or stress mitigation by fungal endophytes during the symbiotic phase, as well as degradation of plant material during the saprotrophic phase. As such, these findings contribute to the illumination of a new dimension of functional biodiversity in fungi.

Highlights

  • All eukaryotes have evolved in the presence of bacteria, with diverse bacteria adopting an endosymbiotic and intracellular habitat across the eukaryotic tree of life [1, 2]

  • Whole-genome sequences can provide a broader picture of evolutionary relationships among bacterial strains than phylogenies built from single loci [39]

  • Our data demonstrated that the Burkholderia sp. 9120 strain whose genome is reported here is phylogenetically distinct from the previously characterized endohyphal bacteria (EHB) B. rhizoxinica (Fig. 2) and Burkholderia terrae, which forms a close relationship with fungi from soil [40, 41]

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Summary

Introduction

All eukaryotes have evolved in the presence of bacteria, with diverse bacteria adopting an endosymbiotic and intracellular habitat across the eukaryotic tree of life [1, 2]. Much like the diverse Metazoa that host rich bacterial microbiomes, fungi interact closely with bacteria both on the surfaces of hyphae and within their living hyphae (i.e. endofungal or endohyphal bacteria, EHB) [3,4,5,6,7]. These EHB can be either obligate or facultative symbionts and can mediate diverse phenotypic traits in their hosts. Data statement: All supporting data, code and protocols have been provided within the article or through supplementary data files

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