Subtle microbiome manipulation using probiotics reduces antibiotic-associated mortality in fish

dc.contributor.author Schmidt, Victor T.
dc.contributor.author Gomez-Chiarri, Marta
dc.contributor.author Roy, Chelsea
dc.contributor.author Smith, Katherine F.
dc.contributor.author Amaral-Zettler, Linda A.
dc.date.accessioned 2018-01-16T21:14:37Z
dc.date.available 2018-01-16T21:14:37Z
dc.date.issued 2017-11-07
dc.description © The Author(s), 2017. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in mSystems 2 (2017): e00133-17, doi:10.1128/mSystems.00133-17. en_US
dc.description.abstract Prophylactic antibiotics in the aquaculture and ornamental fish industry are intended to prevent the negative impacts of disease outbreaks. Research in mice and humans suggests that antibiotics may disturb microbiome communities and decrease microbiome-mediated disease resistance, also known as “colonization resistance.” If antibiotics impact fish as they do mice and humans, prophylactic administrations on aquaculture farms may increase downstream disease susceptibility in target hosts, despite short-term pathogen control benefits. We tested the effects of antibiotics on mortality after a pathogen challenge in the Poecilia sphenops black molly and subsequently tested if probiotic inoculations could reverse any antibiotic-induced losses of disease resistance. We found that antibiotic treatment significantly increased fish mortality. We further found that our two candidate probiotic bacterial species, Phaeobacter inhibens S4Sm and Bacillus pumilus RI06-95Sm, were able to colonize black molly microbiomes and reverse the negative impacts of antibiotics. Despite the positive impact on survival, probiotic treatment did not influence overall microbiome community structure or diversity. Our results suggest that subtle manipulations of microbiome composition can have dramatic impacts on host phenotype. The results of this study have implications for how antibiotic-treated microbiomes can be restored and suggest that small-scale additions may be as effective as wholesale transplants. en_US
dc.description.sponsorship L.A.-Z., V.S., and K.S. acknowledge support from National Science Foundation Doctoral Dissertation Improvement Grant no. 1402051 for V.S. en_US
dc.identifier.citation mSystems 2 (2017): e00133-17 en_US
dc.identifier.doi 10.1128/mSystems.00133-17
dc.identifier.uri https://hdl.handle.net/1912/9485
dc.language.iso en_US en_US
dc.publisher American Society for Microbiology en_US
dc.relation.uri https://doi.org/10.1128/mSystems.00133-17
dc.rights Attribution 4.0 International *
dc.rights.uri http://creativecommons.org/licenses/by/4.0/ *
dc.subject Antibiotics en_US
dc.subject Aquaculture en_US
dc.subject Bacillus en_US
dc.subject Colonization resistance en_US
dc.subject Microbial ecology en_US
dc.subject Microbiome en_US
dc.subject Phaeobacter en_US
dc.subject Probiotics en_US
dc.subject Vibrio en_US
dc.title Subtle microbiome manipulation using probiotics reduces antibiotic-associated mortality in fish en_US
dc.type Article en_US
dspace.entity.type Publication
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relation.isAuthorOfPublication.latestForDiscovery 31a97761-4103-494a-a2c3-fdaa083a1e02
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