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Potential mechanisms of attenuation for rifampicin-passaged strains of Flavobacterium psychrophilum

BACKGROUND: Flavobacterium psychrophilum is the etiologic agent of bacterial coldwater disease in salmonids. Earlier research showed that a rifampicin-passaged strain of F. psychrophilum (CSF 259-93B.17) caused no disease in rainbow trout (Oncorhynchus mykiss, Walbaum) while inducing a protective im...

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Autores principales: Gliniewicz, Karol, Wildung, Mark, Orfe, Lisa H., Wiens, Gregory D., Cain, Kenneth D., Lahmers, Kevin K., Snekvik, Kevin R., Call, Douglas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571129/
https://www.ncbi.nlm.nih.gov/pubmed/26377311
http://dx.doi.org/10.1186/s12866-015-0518-1
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author Gliniewicz, Karol
Wildung, Mark
Orfe, Lisa H.
Wiens, Gregory D.
Cain, Kenneth D.
Lahmers, Kevin K.
Snekvik, Kevin R.
Call, Douglas R.
author_facet Gliniewicz, Karol
Wildung, Mark
Orfe, Lisa H.
Wiens, Gregory D.
Cain, Kenneth D.
Lahmers, Kevin K.
Snekvik, Kevin R.
Call, Douglas R.
author_sort Gliniewicz, Karol
collection PubMed
description BACKGROUND: Flavobacterium psychrophilum is the etiologic agent of bacterial coldwater disease in salmonids. Earlier research showed that a rifampicin-passaged strain of F. psychrophilum (CSF 259-93B.17) caused no disease in rainbow trout (Oncorhynchus mykiss, Walbaum) while inducing a protective immune response against challenge with the virulent CSF 259–93 strain. We hypothesized that rifampicin passage leads to an accumulation of genomic mutations that, by chance, reduce virulence. To assess the pattern of phenotypic and genotypic changes associated with passage, we examined proteomic, LPS and single-nucleotide polymorphism (SNP) differences for two F. psychrophilum strains (CSF 259–93 and THC 02–90) that were passaged with and without rifampicin selection. RESULTS: Rifampicin resistance was conveyed by expected mutations in rpoB, although affecting different DNA bases depending on the strain. One rifampicin-passaged CSF 259–93 strain (CR) was attenuated (4 % mortality) in challenged fish, but only accumulated eight nonsynonymous SNPs compared to the parent strain. A CSF 259–93 strain passaged without rifampicin (CN) accumulated five nonsynonymous SNPs and was partially attenuated (28 % mortality) compared to the parent strain (54.5 % mortality). In contrast, there were no significant change in fish mortalities among THC 02–90 wild-type and passaged strains, despite numerous SNPs accumulated during passage with (n = 174) and without rifampicin (n = 126). While only three missense SNPs were associated with attenuation, a Ser492Phe rpoB mutation in the CR strain may contribute to further attenuation. All strains except CR retained a gliding motility phenotype. Few proteomic differences were observed by 2D SDS-PAGE and there were no apparent changes in LPS between strains. Comparative methylome analysis of two strains (CR and TR) identified no shared methylation motifs for these two strains. CONCLUSION: Multiple genomic changes arose during passage experiments with rifampicin selection pressure. Consistent with our hypothesis, unique strain-specific mutations were detected for the fully attenuated (CR), partially attenuated (CN) and another fully attenuated strain (B17). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-015-0518-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-45711292015-09-17 Potential mechanisms of attenuation for rifampicin-passaged strains of Flavobacterium psychrophilum Gliniewicz, Karol Wildung, Mark Orfe, Lisa H. Wiens, Gregory D. Cain, Kenneth D. Lahmers, Kevin K. Snekvik, Kevin R. Call, Douglas R. BMC Microbiol Research Article BACKGROUND: Flavobacterium psychrophilum is the etiologic agent of bacterial coldwater disease in salmonids. Earlier research showed that a rifampicin-passaged strain of F. psychrophilum (CSF 259-93B.17) caused no disease in rainbow trout (Oncorhynchus mykiss, Walbaum) while inducing a protective immune response against challenge with the virulent CSF 259–93 strain. We hypothesized that rifampicin passage leads to an accumulation of genomic mutations that, by chance, reduce virulence. To assess the pattern of phenotypic and genotypic changes associated with passage, we examined proteomic, LPS and single-nucleotide polymorphism (SNP) differences for two F. psychrophilum strains (CSF 259–93 and THC 02–90) that were passaged with and without rifampicin selection. RESULTS: Rifampicin resistance was conveyed by expected mutations in rpoB, although affecting different DNA bases depending on the strain. One rifampicin-passaged CSF 259–93 strain (CR) was attenuated (4 % mortality) in challenged fish, but only accumulated eight nonsynonymous SNPs compared to the parent strain. A CSF 259–93 strain passaged without rifampicin (CN) accumulated five nonsynonymous SNPs and was partially attenuated (28 % mortality) compared to the parent strain (54.5 % mortality). In contrast, there were no significant change in fish mortalities among THC 02–90 wild-type and passaged strains, despite numerous SNPs accumulated during passage with (n = 174) and without rifampicin (n = 126). While only three missense SNPs were associated with attenuation, a Ser492Phe rpoB mutation in the CR strain may contribute to further attenuation. All strains except CR retained a gliding motility phenotype. Few proteomic differences were observed by 2D SDS-PAGE and there were no apparent changes in LPS between strains. Comparative methylome analysis of two strains (CR and TR) identified no shared methylation motifs for these two strains. CONCLUSION: Multiple genomic changes arose during passage experiments with rifampicin selection pressure. Consistent with our hypothesis, unique strain-specific mutations were detected for the fully attenuated (CR), partially attenuated (CN) and another fully attenuated strain (B17). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-015-0518-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-16 /pmc/articles/PMC4571129/ /pubmed/26377311 http://dx.doi.org/10.1186/s12866-015-0518-1 Text en © Gliniewicz et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gliniewicz, Karol
Wildung, Mark
Orfe, Lisa H.
Wiens, Gregory D.
Cain, Kenneth D.
Lahmers, Kevin K.
Snekvik, Kevin R.
Call, Douglas R.
Potential mechanisms of attenuation for rifampicin-passaged strains of Flavobacterium psychrophilum
title Potential mechanisms of attenuation for rifampicin-passaged strains of Flavobacterium psychrophilum
title_full Potential mechanisms of attenuation for rifampicin-passaged strains of Flavobacterium psychrophilum
title_fullStr Potential mechanisms of attenuation for rifampicin-passaged strains of Flavobacterium psychrophilum
title_full_unstemmed Potential mechanisms of attenuation for rifampicin-passaged strains of Flavobacterium psychrophilum
title_short Potential mechanisms of attenuation for rifampicin-passaged strains of Flavobacterium psychrophilum
title_sort potential mechanisms of attenuation for rifampicin-passaged strains of flavobacterium psychrophilum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571129/
https://www.ncbi.nlm.nih.gov/pubmed/26377311
http://dx.doi.org/10.1186/s12866-015-0518-1
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