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Borrelia burgdorferi SpoVG DNA- and RNA-binding protein modulates the physiology of the Lyme disease spirochete

  • Christina R. Savage
  • , Brandon L. Jutras
  • , Aaron Bestor
  • , Kit Tilly
  • , Patricia A. Rosa
  • , Yvonne Tourand
  • , Philip E. Stewart
  • , Catherine A. Brissette
  • , Brian Stevensona

Producción científica: Articlerevisión exhaustiva

23 Citas (Scopus)

Resumen

The SpoVG protein of Borrelia burgdorferi, the Lyme disease spirochete, binds to specific sites of DNA and RNA. The bacterium regulates transcription of spoVG during the natural tick-mammal infectious cycle and in response to some changes in culture conditions. Bacterial levels of spoVG mRNA and SpoVG protein did not necessarily correlate, suggesting that posttranscriptional mechanisms also control protein levels. Consistent with this, SpoVG binds to its own mRNA, adjacent to the ribosome-binding site. SpoVG also binds to two DNA sites in the glpFKD operon and to two RNA sites in glpFKD mRNA; that operon encodes genes necessary for glycerol catabolism and is important for colonization in ticks. In addition, spirochetes engineered to dysregulate spoVG exhibited physiological alterations.

Idioma originalEnglish
Número de artículoe00033.18
PublicaciónJournal of Bacteriology
Volumen200
N.º12
DOI
EstadoPublished - jun 1 2018

Nota bibliográfica

Publisher Copyright:
© 2018 American Society for Microbiology.

Financiación

This work was supported by a grant from the National Research Fund for Tick-Borne Diseases to B.S., National Institutes of Health grant P20GM113123 to C.A.B., and funds from the Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health to P.A.R. This work was supported by a grant from the National Research Fund for Tick-Borne Diseases to B.S., National Institutes of Health grant P20GM113123 to C.A.B., and funds from the Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health to P.A.R. The funders had no role in study design, data collection and analysis, the decision to publish, or preparation of the manuscript. We thank Will Arnold and Kathryn Lethbridge for helpful discussions during these studies

FinanciadoresNúmero del financiador
Division of Intramural Research
National Research Fund for Tick Borne Diseases Inc
National Institutes of Health (NIH)
National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical SciencesP20GM113123
National Institute of Allergy and Infectious Diseases
Division of Intramural Research, National Institute of Allergy and Infectious Diseases

    ASJC Scopus subject areas

    • Microbiology
    • Molecular Biology

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