Evidence of phylosymbiosis in Formica ants

Insects share intimate relationships with microbes that play important roles in their biology. Yet our understanding of how host-bound microbial communities assemble and perpetuate over evolutionary time is limited. Ants host a wide range of microbes with diverse functions and are an emerging model...

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Veröffentlicht in:Frontiers in microbiology 2023-05, Vol.14, p.1044286-1044286
Hauptverfasser: Jackson, Raphaella, Patapiou, Patapios A, Golding, Gemma, Helanterä, Heikki, Economou, Chloe K, Chapuisat, Michel, Henry, Lee M
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Sprache:eng
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Zusammenfassung:Insects share intimate relationships with microbes that play important roles in their biology. Yet our understanding of how host-bound microbial communities assemble and perpetuate over evolutionary time is limited. Ants host a wide range of microbes with diverse functions and are an emerging model for studying the evolution of insect microbiomes. Here, we ask whether phylogenetically related ant species have formed distinct and stable microbiomes. To answer this question, we investigated the microbial communities associated with queens of 14 species from five clades, using deep coverage 16S rRNA amplicon sequencing. We reveal that species and clades harbor highly defined microbial communities that are dominated by four bacteria genera: , , and . Our analysis reveals that the composition of microbiomes mirrors the phylogeny of the host, i.e., phylosymbiosis, in that related hosts harbor more similar microbial communities. In addition, we find there are significant correlations between microbe co-occurrences. Our results demonstrate ants carry microbial communities that recapitulate the phylogeny of their hosts. Our data suggests that the co-occurrence of different bacteria genera may at least in part be due to synergistic and antagonistic interactions between microbes. Additional factors potentially contributing to the phylosymbiotic signal are discussed, including host phylogenetic relatedness, host-microbe genetic compatibility, modes of transmission, and similarities in host ecologies (e.g., diets). Overall, our results support the growing body of evidence that microbial community composition closely depends on the phylogeny of their hosts, despite bacteria having diverse modes of transmission and localization within the host.
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2023.1044286