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Methylation Warfare: Interaction of Pneumococcal Bacteriophages with Their Host.
Furi, Leonardo; Crawford, Liam A; Rangel-Pineros, Guillermo; Manso, Ana S; De Ste Croix, Megan; Haigh, Richard D; Kwun, Min J; Engelsen Fjelland, Kristine; Gilfillan, Gregor D; Bentley, Stephen D; Croucher, Nicholas J; Clokie, Martha R; Oggioni, Marco R.
Afiliação
  • Furi L; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom.
  • Crawford LA; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom.
  • Rangel-Pineros G; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom.
  • Manso AS; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom.
  • De Ste Croix M; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom.
  • Haigh RD; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom.
  • Kwun MJ; MRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom.
  • Engelsen Fjelland K; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
  • Gilfillan GD; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
  • Bentley SD; Parasites and Microbes, Wellcome Trust Sanger Institute, Hinxton, United Kingdom.
  • Croucher NJ; MRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom.
  • Clokie MR; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom.
  • Oggioni MR; Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom mro5@leicester.ac.uk.
J Bacteriol ; 201(19)2019 10 01.
Article em En | MEDLINE | ID: mdl-31285240
ABSTRACT
Virus-host interactions are regulated by complex coevolutionary dynamics. In Streptococcus pneumoniae, phase-variable type I restriction-modification (R-M) systems are part of the core genome. We hypothesized that the ability of the R-M systems to switch between six target DNA specificities also has a key role in preventing the spread of bacteriophages. Using the streptococcal temperate bacteriophage SpSL1, we show that the variants of both the SpnIII and SpnIV R-M systems are able to restrict invading bacteriophage with an efficiency approximately proportional to the number of target sites in the bacteriophage genome. In addition to restriction of lytic replication, SpnIII also led to abortive infection in the majority of host cells. During lytic infection, transcriptional analysis found evidence of phage-host interaction through the strong upregulation of the nrdR nucleotide biosynthesis regulon. During lysogeny, the phage had less of an effect on host gene regulation. This research demonstrates a novel combined bacteriophage restriction and abortive infection mechanism, highlighting the importance that the phase-variable type I R-M systems have in the multifunctional defense against bacteriophage infection in the respiratory pathogen S. pneumoniaeIMPORTANCE With antimicrobial drug resistance becoming an increasing burden on human health, much attention has been focused on the potential use of bacteriophages and their enzymes as therapeutics. However, the investigations into the physiology of the complex interactions of bacteriophages with their hosts have attracted far less attention, in comparison. This work describes the molecular characterization of the infectious cycle of a bacteriophage in the important human pathogen Streptococcus pneumoniae and explores the intricate relationship between phase-variable host defense mechanisms and the virus. This is the first report showing how a phase-variable type I restriction-modification system is involved in bacteriophage restriction while it also provides an additional level of infection control through abortive infection.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Streptococcus pneumoniae / Proteínas de Bactérias / Bacteriófagos / Proteínas Virais / Metilação de DNA Limite: Humans Idioma: En Revista: J Bacteriol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Streptococcus pneumoniae / Proteínas de Bactérias / Bacteriófagos / Proteínas Virais / Metilação de DNA Limite: Humans Idioma: En Revista: J Bacteriol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido