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Bacterial symbiont sharing in <I>Megalomyrmex</I> social parasites and their fungus-growing ant hosts

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dc.contributor.author Liberti, Joanito en
dc.contributor.author Sapountzis, Panagiotis en
dc.contributor.author Hansen, Lars H. en
dc.contributor.author Sørensen, Søren J. en
dc.contributor.author Adams, Rachelle M. M. en
dc.contributor.author Boomsma, Jacobus J. en
dc.date.accessioned 2015-05-15T12:50:31Z
dc.date.available 2015-05-15T12:50:31Z
dc.date.issued 2015
dc.identifier.citation Liberti, Joanito, Sapountzis, Panagiotis, Hansen, Lars H., Sørensen, Søren J., Adams, Rachelle M. M., and Boomsma, Jacobus J. 2015. "Bacterial symbiont sharing in Megalomyrmex social parasites and their fungus-growing ant hosts." <em>Molecular ecology</em>. 24 (12):3151&ndash;3169. <a href="https://doi.org/10.1111/mec.13216">https://doi.org/10.1111/mec.13216</a> en
dc.identifier.issn 0962-1083
dc.identifier.uri http://hdl.handle.net/10088/26231
dc.description.abstract Bacterial symbionts are important fitness determinants of insects. Some hosts have independently acquired taxonomically related microbes to meet similar challenges, but whether distantly related hosts that live in tight symbiosis can maintain similar microbial communities has not been investigated. Varying degrees of nest-sharing between Megalomyrmex social parasites (Solenopsidini) and their fungus-growing ant hosts (Attini) from the genera Cyphomyrmex, Trachymyrmex and Sericomyrmex allowed us to address this question, as both ant lineages rely on the same fungal diet, interact in varying intensities, and are distantly related. We used tag-encoded FLX 454 pyrosequencing and diagnostic PCR to map bacterial symbiont diversity across the Megalomyrmex phylogenetic tree, which also contains free-living generalist predators. We show that social parasites and hosts share a subset of bacterial symbionts, primarily consisting of Entomoplasmatales, Bartonellaceae, Acinetobacter, Wolbachia and Pseudonocardia and that Entomoplasmatales and Bartonellaceae can co-infect specifically associated combinations of hosts and social parasites with identical 16S rRNA genotypes. We reconstructed in more detail the population-level infection dynamics for Entomoplasmatales and Bartonellaceae in M. symmetochus guest ants and their Sericomyrmex amabilis hosts. We further assessed the stability of the bacterial communities through a diet-manipulation experiment and evaluated possible transmission modes in shared nests such as consumption of the same fungus garden food, eating of host brood by social parasites, trophallaxis and grooming interactions between the ants, or parallel acquisition from the same nest environment. Our results imply that cohabiting ant social parasites and hosts may obtain functional benefits of bacterial symbiont transfer even when they are not closely related. This article is protected by copyright. All rights reserved. en
dc.relation.ispartof Molecular ecology en
dc.title Bacterial symbiont sharing in <I>Megalomyrmex</I> social parasites and their fungus-growing ant hosts en
dc.type Journal Article en
dc.identifier.srbnumber 135886
dc.identifier.doi 10.1111/mec.13216
rft.jtitle Molecular ecology
rft.volume 24
rft.issue 12
rft.spage 3151
rft.epage 3169
dc.description.SIUnit NH-Entomology en
dc.description.SIUnit NMNH en
dc.description.SIUnit Peer-reviewed en
dc.citation.spage 3151
dc.citation.epage 3169


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