Discovery of ectosymbiotic Endomicrobium lineages associated with protists in the gut of stolotermitid termites

Summary The genus Endomicrobium is a dominant bacterial group in the gut of lower termites, and most phylotypes are intracellular symbionts of gut protists. Here we report the discovery of Endomicrobium ectosymbionts of termite gut protists. We found that bristle‐like Endomicrobium cells attached to...

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Published inEnvironmental microbiology reports Vol. 9; no. 4; pp. 411 - 418
Main Authors Izawa, Kazuki, Kuwahara, Hirokazu, Sugaya, Kaito, Lo, Nathan, Ohkuma, Moriya, Hongoh, Yuichi
Format Journal Article
LanguageEnglish
Published United States John Wiley & Sons, Inc 01.08.2017
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ISSN1758-2229
1758-2229
DOI10.1111/1758-2229.12549

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Summary:Summary The genus Endomicrobium is a dominant bacterial group in the gut of lower termites, and most phylotypes are intracellular symbionts of gut protists. Here we report the discovery of Endomicrobium ectosymbionts of termite gut protists. We found that bristle‐like Endomicrobium cells attached to the surface of spirotrichosomid protist cells inhabiting the termite Stolotermes victoriensis. Transmission electron microscopy revealed that a putative Endomicrobium cell likely attached to the protist surface via a protrusion from the tip of the bacterium. A phylotype, sharing 98.9% 16S rRNA sequence identity with the Endomicrobium ectosymbionts of the spirotrichosomid protists, was also found on the cell surface of the protist Trichonympha magna in the gut of the termite Porotermes adamsoni. We propose the novel species ‘Candidatus Endomicrobium superficiale’ for these bacteria. T. magna simultaneously harboured another Endomicrobium ectosymbiont that shared 93.5–94.2% 16S rRNA sequence identities with ‘Ca. Endomicrobium superficiale’. Furthermore, Spirotrichonympha‐like protists in P. adamsoni guts were associated with an Endomicrobium phylotype that possibly attached to the host flagella. A phylogenetic analysis suggested that these ectosymbiotic lineages have evolved multiple times from free‐living Endomicrobium lineages and are relatively distant from the endosymbionts. Our results provide novel insights into the ecology and evolution of the Endomicrobium.
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ISSN:1758-2229
1758-2229
DOI:10.1111/1758-2229.12549