Cargando…

Implication of Lateral Genetic Transfer in the Emergence of Aeromonas hydrophila Isolates of Epidemic Outbreaks in Channel Catfish

To investigate the molecular basis of the emergence of Aeromonas hydrophila responsible for an epidemic outbreak of motile aeromonad septicemia of catfish in the Southeastern United States, we sequenced 11 A. hydrophila isolates that includes five reference and six recent epidemic isolates. Comparat...

Descripción completa

Detalles Bibliográficos
Autores principales: Hossain, Mohammad J., Waldbieser, Geoffrey C., Sun, Dawei, Capps, Nancy K., Hemstreet, William B., Carlisle, Kristen, Griffin, Matt J., Khoo, Lester, Goodwin, Andrew E., Sonstegard, Tad S., Schroeder, Steven, Hayden, Karl, Newton, Joseph C., Terhune, Jeffery S., Liles, Mark R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835674/
https://www.ncbi.nlm.nih.gov/pubmed/24278351
http://dx.doi.org/10.1371/journal.pone.0080943
_version_ 1782292191599656960
author Hossain, Mohammad J.
Waldbieser, Geoffrey C.
Sun, Dawei
Capps, Nancy K.
Hemstreet, William B.
Carlisle, Kristen
Griffin, Matt J.
Khoo, Lester
Goodwin, Andrew E.
Sonstegard, Tad S.
Schroeder, Steven
Hayden, Karl
Newton, Joseph C.
Terhune, Jeffery S.
Liles, Mark R.
author_facet Hossain, Mohammad J.
Waldbieser, Geoffrey C.
Sun, Dawei
Capps, Nancy K.
Hemstreet, William B.
Carlisle, Kristen
Griffin, Matt J.
Khoo, Lester
Goodwin, Andrew E.
Sonstegard, Tad S.
Schroeder, Steven
Hayden, Karl
Newton, Joseph C.
Terhune, Jeffery S.
Liles, Mark R.
author_sort Hossain, Mohammad J.
collection PubMed
description To investigate the molecular basis of the emergence of Aeromonas hydrophila responsible for an epidemic outbreak of motile aeromonad septicemia of catfish in the Southeastern United States, we sequenced 11 A. hydrophila isolates that includes five reference and six recent epidemic isolates. Comparative genomics revealed that recent epidemic A. hydrophila isolates are highly clonal, whereas reference isolates are greatly diverse. We identified 55 epidemic-associated genetic regions with 313 predicted genes that are present in epidemic isolates but absent from reference isolates and 35% of these regions are located within genomic islands, suggesting their acquisition through lateral gene transfer. The epidemic-associated regions encode predicted prophage elements, pathogenicity islands, metabolic islands, fitness islands and genes of unknown functions, and 34 of the genes encoded in these regions were predicted as virulence factors. We found two pilus biogenesis gene clusters encoded within predicted pathogenicity islands. A functional metabolic island that encodes a complete pathway for myo-inositol catabolism was evident by the ability of epidemic A. hydrophila isolates to use myo-inositol as a sole carbon source. Testing of A. hydrophila field isolates found a consistent correlation between myo-inositol utilization as a sole carbon source and the presence of an epidemic-specific genetic marker. All epidemic isolates and one reference isolate shared a novel O-antigen cluster. Altogether we identified four different O-antigen biosynthesis gene clusters within the 11 sequenced A. hydrophila genomes. Our study reveals new insights into the evolutionary changes that have resulted in the emergence of recent epidemic A. hydrophila strains.
format Online
Article
Text
id pubmed-3835674
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-38356742013-11-25 Implication of Lateral Genetic Transfer in the Emergence of Aeromonas hydrophila Isolates of Epidemic Outbreaks in Channel Catfish Hossain, Mohammad J. Waldbieser, Geoffrey C. Sun, Dawei Capps, Nancy K. Hemstreet, William B. Carlisle, Kristen Griffin, Matt J. Khoo, Lester Goodwin, Andrew E. Sonstegard, Tad S. Schroeder, Steven Hayden, Karl Newton, Joseph C. Terhune, Jeffery S. Liles, Mark R. PLoS One Research Article To investigate the molecular basis of the emergence of Aeromonas hydrophila responsible for an epidemic outbreak of motile aeromonad septicemia of catfish in the Southeastern United States, we sequenced 11 A. hydrophila isolates that includes five reference and six recent epidemic isolates. Comparative genomics revealed that recent epidemic A. hydrophila isolates are highly clonal, whereas reference isolates are greatly diverse. We identified 55 epidemic-associated genetic regions with 313 predicted genes that are present in epidemic isolates but absent from reference isolates and 35% of these regions are located within genomic islands, suggesting their acquisition through lateral gene transfer. The epidemic-associated regions encode predicted prophage elements, pathogenicity islands, metabolic islands, fitness islands and genes of unknown functions, and 34 of the genes encoded in these regions were predicted as virulence factors. We found two pilus biogenesis gene clusters encoded within predicted pathogenicity islands. A functional metabolic island that encodes a complete pathway for myo-inositol catabolism was evident by the ability of epidemic A. hydrophila isolates to use myo-inositol as a sole carbon source. Testing of A. hydrophila field isolates found a consistent correlation between myo-inositol utilization as a sole carbon source and the presence of an epidemic-specific genetic marker. All epidemic isolates and one reference isolate shared a novel O-antigen cluster. Altogether we identified four different O-antigen biosynthesis gene clusters within the 11 sequenced A. hydrophila genomes. Our study reveals new insights into the evolutionary changes that have resulted in the emergence of recent epidemic A. hydrophila strains. Public Library of Science 2013-11-20 /pmc/articles/PMC3835674/ /pubmed/24278351 http://dx.doi.org/10.1371/journal.pone.0080943 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Hossain, Mohammad J.
Waldbieser, Geoffrey C.
Sun, Dawei
Capps, Nancy K.
Hemstreet, William B.
Carlisle, Kristen
Griffin, Matt J.
Khoo, Lester
Goodwin, Andrew E.
Sonstegard, Tad S.
Schroeder, Steven
Hayden, Karl
Newton, Joseph C.
Terhune, Jeffery S.
Liles, Mark R.
Implication of Lateral Genetic Transfer in the Emergence of Aeromonas hydrophila Isolates of Epidemic Outbreaks in Channel Catfish
title Implication of Lateral Genetic Transfer in the Emergence of Aeromonas hydrophila Isolates of Epidemic Outbreaks in Channel Catfish
title_full Implication of Lateral Genetic Transfer in the Emergence of Aeromonas hydrophila Isolates of Epidemic Outbreaks in Channel Catfish
title_fullStr Implication of Lateral Genetic Transfer in the Emergence of Aeromonas hydrophila Isolates of Epidemic Outbreaks in Channel Catfish
title_full_unstemmed Implication of Lateral Genetic Transfer in the Emergence of Aeromonas hydrophila Isolates of Epidemic Outbreaks in Channel Catfish
title_short Implication of Lateral Genetic Transfer in the Emergence of Aeromonas hydrophila Isolates of Epidemic Outbreaks in Channel Catfish
title_sort implication of lateral genetic transfer in the emergence of aeromonas hydrophila isolates of epidemic outbreaks in channel catfish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835674/
https://www.ncbi.nlm.nih.gov/pubmed/24278351
http://dx.doi.org/10.1371/journal.pone.0080943
work_keys_str_mv AT hossainmohammadj implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT waldbiesergeoffreyc implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT sundawei implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT cappsnancyk implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT hemstreetwilliamb implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT carlislekristen implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT griffinmattj implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT khoolester implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT goodwinandrewe implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT sonstegardtads implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT schroedersteven implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT haydenkarl implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT newtonjosephc implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT terhunejefferys implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish
AT lilesmarkr implicationoflateralgenetictransferintheemergenceofaeromonashydrophilaisolatesofepidemicoutbreaksinchannelcatfish