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Antibacterial gene transfer across the tree of life
Though horizontal gene transfer (HGT) is widespread, genes and taxa experience biased rates of transferability. Curiously, independent transmission of homologous DNA to archaea, bacteria, eukaryotes, and viruses is extremely rare and often defies ecological and functional explanations. Here, we demo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241558/ https://www.ncbi.nlm.nih.gov/pubmed/25422936 http://dx.doi.org/10.7554/eLife.04266 |
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author | Metcalf, Jason A Funkhouser-Jones, Lisa J Brileya, Kristen Reysenbach, Anna-Louise Bordenstein, Seth R |
author_facet | Metcalf, Jason A Funkhouser-Jones, Lisa J Brileya, Kristen Reysenbach, Anna-Louise Bordenstein, Seth R |
author_sort | Metcalf, Jason A |
collection | PubMed |
description | Though horizontal gene transfer (HGT) is widespread, genes and taxa experience biased rates of transferability. Curiously, independent transmission of homologous DNA to archaea, bacteria, eukaryotes, and viruses is extremely rare and often defies ecological and functional explanations. Here, we demonstrate that a bacterial lysozyme family integrated independently in all domains of life across diverse environments, generating the only glycosyl hydrolase 25 muramidases in plants and archaea. During coculture of a hydrothermal vent archaeon with a bacterial competitor, muramidase transcription is upregulated. Moreover, recombinant lysozyme exhibits broad-spectrum antibacterial action in a dose-dependent manner. Similar to bacterial transfer of antibiotic resistance genes, transfer of a potent antibacterial gene across the universal tree seemingly bestows a niche-transcending adaptation that trumps the barriers against parallel HGT to all domains. The discoveries also comprise the first characterization of an antibacterial gene in archaea and support the pursuit of antibiotics in this underexplored group. DOI: http://dx.doi.org/10.7554/eLife.04266.001 |
format | Online Article Text |
id | pubmed-4241558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42415582015-01-29 Antibacterial gene transfer across the tree of life Metcalf, Jason A Funkhouser-Jones, Lisa J Brileya, Kristen Reysenbach, Anna-Louise Bordenstein, Seth R eLife Genomics and Evolutionary Biology Though horizontal gene transfer (HGT) is widespread, genes and taxa experience biased rates of transferability. Curiously, independent transmission of homologous DNA to archaea, bacteria, eukaryotes, and viruses is extremely rare and often defies ecological and functional explanations. Here, we demonstrate that a bacterial lysozyme family integrated independently in all domains of life across diverse environments, generating the only glycosyl hydrolase 25 muramidases in plants and archaea. During coculture of a hydrothermal vent archaeon with a bacterial competitor, muramidase transcription is upregulated. Moreover, recombinant lysozyme exhibits broad-spectrum antibacterial action in a dose-dependent manner. Similar to bacterial transfer of antibiotic resistance genes, transfer of a potent antibacterial gene across the universal tree seemingly bestows a niche-transcending adaptation that trumps the barriers against parallel HGT to all domains. The discoveries also comprise the first characterization of an antibacterial gene in archaea and support the pursuit of antibiotics in this underexplored group. DOI: http://dx.doi.org/10.7554/eLife.04266.001 eLife Sciences Publications, Ltd 2014-11-25 /pmc/articles/PMC4241558/ /pubmed/25422936 http://dx.doi.org/10.7554/eLife.04266 Text en Copyright © 2014, Metcalf et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genomics and Evolutionary Biology Metcalf, Jason A Funkhouser-Jones, Lisa J Brileya, Kristen Reysenbach, Anna-Louise Bordenstein, Seth R Antibacterial gene transfer across the tree of life |
title | Antibacterial gene transfer across the tree of life |
title_full | Antibacterial gene transfer across the tree of life |
title_fullStr | Antibacterial gene transfer across the tree of life |
title_full_unstemmed | Antibacterial gene transfer across the tree of life |
title_short | Antibacterial gene transfer across the tree of life |
title_sort | antibacterial gene transfer across the tree of life |
topic | Genomics and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241558/ https://www.ncbi.nlm.nih.gov/pubmed/25422936 http://dx.doi.org/10.7554/eLife.04266 |
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