RelA regulates virulence and intracellular survival of Francisella novicida

1 Biomedical Sciences, Dstl Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2 School of Biosciences, University of Exeter, Geoffrey Pope Building, Stocker Road, Exeter EX4 4QD, UK Analysis of the genome of Francisella tularensis has revealed few regulatory systems, and how the organism adapts to condi...

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Published inMicrobiology (Society for General Microbiology) Vol. 155; no. 12; pp. 4104 - 4113
Main Authors Dean, R. E, Ireland, P. M, Jordan, J. E, Titball, R. W, Oyston, P. C. F
Format Journal Article
LanguageEnglish
Published Reading Soc General Microbiol 01.12.2009
Society for General Microbiology
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Abstract 1 Biomedical Sciences, Dstl Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2 School of Biosciences, University of Exeter, Geoffrey Pope Building, Stocker Road, Exeter EX4 4QD, UK Analysis of the genome of Francisella tularensis has revealed few regulatory systems, and how the organism adapts to conditions in different niches is poorly understood. The stringent response is a global stress response mediated by (p)ppGpp. The enzyme RelA has been shown to be involved in generation of this signal molecule in a range of bacterial species. We investigated the effect of inactivation of the relA gene in Francisella by generating a mutant in Francisella novicida . Under amino acid starvation conditions, the relA mutant was defective for (p)ppGpp production. Characterization showed the mutant to grow similarly to the wild-type, except that it entered stationary phase later than wild-type cultures, resulting in higher cell yields. The relA mutant showed increased biofilm formation, which may be linked to the delay in entering stationary phase, which in turn would result in higher cell numbers present in the biofilm and reduced resistance to in vitro stress. The mutant was attenuated in the J774A macrophage cell line and was shown to be attenuated in the mouse model of tularaemia, but was able to induce a protective immune response. Therefore, (p)ppGpp appears to be an important intracellular signal, integral to the pathogenesis of F. novicida . Correspondence R. E. Dean redean{at}dstl.gov.uk Abbreviations: CV, crystal violet; FPI, Francisella pathogenicity island; MLD, median lethal dose; SPI, Salmonella pathogenicity island
AbstractList Analysis of the genome of Francisella tularensis has revealed few regulatory systems, and how the organism adapts to conditions in different niches is poorly understood. The stringent response is a global stress response mediated by (p)ppGpp. The enzyme RelA has been shown to be involved in generation of this signal molecule in a range of bacterial species. We investigated the effect of inactivation of the relA gene in Francisella by generating a mutant in Francisella novicida. Under amino acid starvation conditions, the relA mutant was defective for (p)ppGpp production. Characterization showed the mutant to grow similarly to the wild-type, except that it entered stationary phase later than wild-type cultures, resulting in higher cell yields. The relA mutant showed increased biofilm formation, which may be linked to the delay in entering stationary phase, which in turn would result in higher cell numbers present in the biofilm and reduced resistance to in vitro stress. The mutant was attenuated in the J774A macrophage cell line and was shown to be attenuated in the mouse model of tularaemia, but was able to induce a protective immune response. Therefore, (p)ppGpp appears to be an important intracellular signal, integral to the pathogenesis of F. novicida.
Analysis of the genome of Francisella tularensis has revealed few regulatory systems, and how the organism adapts to conditions in different niches is poorly understood. The stringent response is a global stress response mediated by (p)ppGpp. The enzyme RelA has been shown to be involved in generation of this signal molecule in a range of bacterial species. We investigated the effect of inactivation of the relA gene in Francisella by generating a mutant in Francisella novicida . Under amino acid starvation conditions, the relA mutant was defective for (p)ppGpp production. Characterization showed the mutant to grow similarly to the wild-type, except that it entered stationary phase later than wild-type cultures, resulting in higher cell yields. The relA mutant showed increased biofilm formation, which may be linked to the delay in entering stationary phase, which in turn would result in higher cell numbers present in the biofilm and reduced resistance to in vitro stress. The mutant was attenuated in the J774A macrophage cell line and was shown to be attenuated in the mouse model of tularaemia, but was able to induce a protective immune response. Therefore, (p)ppGpp appears to be an important intracellular signal, integral to the pathogenesis of F. novicida .
1 Biomedical Sciences, Dstl Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2 School of Biosciences, University of Exeter, Geoffrey Pope Building, Stocker Road, Exeter EX4 4QD, UK Analysis of the genome of Francisella tularensis has revealed few regulatory systems, and how the organism adapts to conditions in different niches is poorly understood. The stringent response is a global stress response mediated by (p)ppGpp. The enzyme RelA has been shown to be involved in generation of this signal molecule in a range of bacterial species. We investigated the effect of inactivation of the relA gene in Francisella by generating a mutant in Francisella novicida . Under amino acid starvation conditions, the relA mutant was defective for (p)ppGpp production. Characterization showed the mutant to grow similarly to the wild-type, except that it entered stationary phase later than wild-type cultures, resulting in higher cell yields. The relA mutant showed increased biofilm formation, which may be linked to the delay in entering stationary phase, which in turn would result in higher cell numbers present in the biofilm and reduced resistance to in vitro stress. The mutant was attenuated in the J774A macrophage cell line and was shown to be attenuated in the mouse model of tularaemia, but was able to induce a protective immune response. Therefore, (p)ppGpp appears to be an important intracellular signal, integral to the pathogenesis of F. novicida . Correspondence R. E. Dean redean{at}dstl.gov.uk Abbreviations: CV, crystal violet; FPI, Francisella pathogenicity island; MLD, median lethal dose; SPI, Salmonella pathogenicity island
Author Titball, R. W
Dean, R. E
Ireland, P. M
Jordan, J. E
Oyston, P. C. F
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Francisella novicida
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Virulence
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Snippet 1 Biomedical Sciences, Dstl Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2 School of Biosciences, University of Exeter, Geoffrey Pope Building, Stocker Road,...
Analysis of the genome of Francisella tularensis has revealed few regulatory systems, and how the organism adapts to conditions in different niches is poorly...
Analysis of the genome of Francisella tularensis has revealed few regulatory systems, and how the organism adapts to conditions in different niches is poorly...
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StartPage 4104
SubjectTerms Animals
Bacterial Proteins - genetics
Bacterial Proteins - physiology
Bacteriology
Base Sequence
Biofilms - growth & development
Biological and medical sciences
Cell Line
DNA Primers - genetics
DNA, Bacterial - genetics
Female
Francisella - genetics
Francisella - growth & development
Francisella - pathogenicity
Francisella - physiology
Francisella novicida
Francisella tularensis
Fundamental and applied biological sciences. Psychology
Genes, Bacterial
Gram-Negative Bacterial Infections - immunology
Gram-Negative Bacterial Infections - microbiology
Guanosine Pentaphosphate - biosynthesis
Guanosine Tetraphosphate - biosynthesis
Macrophages - microbiology
Mice
Mice, Inbred BALB C
Microbiology
Mutation
Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains
Stress, Physiological
Transcription Factor RelA - genetics
Transcription Factor RelA - physiology
Virulence - genetics
Virulence - physiology
Title RelA regulates virulence and intracellular survival of Francisella novicida
URI http://mic.sgmjournals.org/cgi/content/abstract/155/12/4104
https://www.ncbi.nlm.nih.gov/pubmed/19762448
https://search.proquest.com/docview/21275012
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