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Shewanella oneidensis Hfq promotes exponential phase growth, stationary phase culture density, and cell survival

BACKGROUND: Hfq is an RNA chaperone protein that has been broadly implicated in sRNA function in bacteria. Here we describe the construction and characterization of a null allele of the gene that encodes the RNA chaperone Hfq in Shewanella oneidensis strain MR-1, a dissimilatory metal reducing bacte...

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Autores principales: Brennan, Christopher M, Keane, Meghan L, Hunt, Taylor M, Goulet, Matthew T, Mazzucca, Nicholas Q, Sexton, Zachary, Mezoian, Taylor, Douglas, Katherine E, Osborn, Jessica M, Pellock, Brett J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575234/
https://www.ncbi.nlm.nih.gov/pubmed/23394078
http://dx.doi.org/10.1186/1471-2180-13-33
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author Brennan, Christopher M
Keane, Meghan L
Hunt, Taylor M
Goulet, Matthew T
Mazzucca, Nicholas Q
Sexton, Zachary
Mezoian, Taylor
Douglas, Katherine E
Osborn, Jessica M
Pellock, Brett J
author_facet Brennan, Christopher M
Keane, Meghan L
Hunt, Taylor M
Goulet, Matthew T
Mazzucca, Nicholas Q
Sexton, Zachary
Mezoian, Taylor
Douglas, Katherine E
Osborn, Jessica M
Pellock, Brett J
author_sort Brennan, Christopher M
collection PubMed
description BACKGROUND: Hfq is an RNA chaperone protein that has been broadly implicated in sRNA function in bacteria. Here we describe the construction and characterization of a null allele of the gene that encodes the RNA chaperone Hfq in Shewanella oneidensis strain MR-1, a dissimilatory metal reducing bacterium. RESULTS: Loss of hfq in S. oneidensis results in a variety of mutant phenotypes, all of which are fully complemented by addition of a plasmid-borne copy of the wild type hfq gene. Aerobic cultures of the hfq∆ mutant grow more slowly through exponential phase than wild type cultures, and hfq∆ cultures reach a terminal cell density in stationary phase that is ~2/3 of that observed in wild type cultures. We have observed a similar growth phenotype when the hfq∆ mutant is cultured under anaerobic conditions with fumarate as the terminal electron acceptor, and we have found that the hfq∆ mutant is defective in Cr(VI) reduction. Finally, the hfq∆ mutant exhibits a striking loss of colony forming units in extended stationary phase and is highly sensitive to oxidative stress induced by H(2)O(2) or methyl viologen (paraquat). CONCLUSIONS: The hfq mutant in S. oneidensis exhibits pleiotropic phenotypes, including a defect in metal reduction. Our results also suggest that hfq mutant phenotypes in S. oneidensis may be at least partially due to increased sensitivity to oxidative stress.
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spelling pubmed-35752342013-02-19 Shewanella oneidensis Hfq promotes exponential phase growth, stationary phase culture density, and cell survival Brennan, Christopher M Keane, Meghan L Hunt, Taylor M Goulet, Matthew T Mazzucca, Nicholas Q Sexton, Zachary Mezoian, Taylor Douglas, Katherine E Osborn, Jessica M Pellock, Brett J BMC Microbiol Research Article BACKGROUND: Hfq is an RNA chaperone protein that has been broadly implicated in sRNA function in bacteria. Here we describe the construction and characterization of a null allele of the gene that encodes the RNA chaperone Hfq in Shewanella oneidensis strain MR-1, a dissimilatory metal reducing bacterium. RESULTS: Loss of hfq in S. oneidensis results in a variety of mutant phenotypes, all of which are fully complemented by addition of a plasmid-borne copy of the wild type hfq gene. Aerobic cultures of the hfq∆ mutant grow more slowly through exponential phase than wild type cultures, and hfq∆ cultures reach a terminal cell density in stationary phase that is ~2/3 of that observed in wild type cultures. We have observed a similar growth phenotype when the hfq∆ mutant is cultured under anaerobic conditions with fumarate as the terminal electron acceptor, and we have found that the hfq∆ mutant is defective in Cr(VI) reduction. Finally, the hfq∆ mutant exhibits a striking loss of colony forming units in extended stationary phase and is highly sensitive to oxidative stress induced by H(2)O(2) or methyl viologen (paraquat). CONCLUSIONS: The hfq mutant in S. oneidensis exhibits pleiotropic phenotypes, including a defect in metal reduction. Our results also suggest that hfq mutant phenotypes in S. oneidensis may be at least partially due to increased sensitivity to oxidative stress. BioMed Central 2013-02-08 /pmc/articles/PMC3575234/ /pubmed/23394078 http://dx.doi.org/10.1186/1471-2180-13-33 Text en Copyright ©2013 Brennan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Brennan, Christopher M
Keane, Meghan L
Hunt, Taylor M
Goulet, Matthew T
Mazzucca, Nicholas Q
Sexton, Zachary
Mezoian, Taylor
Douglas, Katherine E
Osborn, Jessica M
Pellock, Brett J
Shewanella oneidensis Hfq promotes exponential phase growth, stationary phase culture density, and cell survival
title Shewanella oneidensis Hfq promotes exponential phase growth, stationary phase culture density, and cell survival
title_full Shewanella oneidensis Hfq promotes exponential phase growth, stationary phase culture density, and cell survival
title_fullStr Shewanella oneidensis Hfq promotes exponential phase growth, stationary phase culture density, and cell survival
title_full_unstemmed Shewanella oneidensis Hfq promotes exponential phase growth, stationary phase culture density, and cell survival
title_short Shewanella oneidensis Hfq promotes exponential phase growth, stationary phase culture density, and cell survival
title_sort shewanella oneidensis hfq promotes exponential phase growth, stationary phase culture density, and cell survival
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575234/
https://www.ncbi.nlm.nih.gov/pubmed/23394078
http://dx.doi.org/10.1186/1471-2180-13-33
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