Functionality of Borrelia burgdorferi LuxS: The Lyme disease spirochete produces and responds to the pheromone autoinducer-2 and lacks a complete activated-methyl cycle

Kate von Lackum, Kelly Babb, Sean P. Riley, Rachel L. Wattier, Tomasz Bykowski, Brian Stevenson

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Borrelia burgdorferi produces Pfs and LuxS enzymes for breakdown of the toxic byproducts of methylation reactions, producing 4,5-dihydroxy-2,3-pentanedione (DPD), adenine, and homocysteine. DPD and its spontaneously rearranged derivatives constitute a class of bacterial pheromones named autoinducer-2 (AI-2). We describe that B. burgdorferi produces DPD during laboratory cultivation. Furthermore, addition of in vitro synthesized DPD to cultured B. burgdorferi resulted in altered expression levels of a specific set of bacterial proteins, among which is the outer surface lipoprotein VlsE. While a large number of bacteria utilize homocysteine, the other LuxS product, for synthesis of methionine as part of the activated-methyl cycle, B. burgdorferi was found to lack that ability. We propose that the main function of B. burgdorferi LuxS is to synthesize DPD and that the Lyme disease spirochete utilizes a form of DPD as a pheromone to control gene expression.

Original languageEnglish
Pages (from-to)92-102
Number of pages11
JournalInternational Journal of Medical Microbiology
Volume296
Issue numberSUPPL. 1
DOIs
StatePublished - May 22 2006

Bibliographical note

Funding Information:
This work was supported by National Institutes of Health Grants R01-AI53101 and 5T32-AI49795. We thank Bonnie Bassler, Michael Norgard, George Stauffer, and Xiaofeng Yang for providing bacterial strains; Tom Schwan for sharing unpublished results; Bonnie Bassler, Kenneth Cornell, Klaus Winzer, and Wolfram Zückert for helpful discussions; Sarah Wackerbarth for statistical analyses; and Sara Bair, Sarah Kearns, Natalie Mickelsen, Jennifer Miller, Ashutosh Verma, and Michael Woodman for assistance in this research.

Funding

This work was supported by National Institutes of Health Grants R01-AI53101 and 5T32-AI49795. We thank Bonnie Bassler, Michael Norgard, George Stauffer, and Xiaofeng Yang for providing bacterial strains; Tom Schwan for sharing unpublished results; Bonnie Bassler, Kenneth Cornell, Klaus Winzer, and Wolfram Zückert for helpful discussions; Sarah Wackerbarth for statistical analyses; and Sara Bair, Sarah Kearns, Natalie Mickelsen, Jennifer Miller, Ashutosh Verma, and Michael Woodman for assistance in this research.

FundersFunder number
National Institutes of Health (NIH)R01-AI53101
National Institute of Allergy and Infectious DiseasesT32AI049795

    Keywords

    • Bacterial gene regulation
    • Borrelia burgdorferi
    • Homocysteine
    • Methionine
    • Pheromone
    • Quorum sensing

    ASJC Scopus subject areas

    • Microbiology
    • Microbiology (medical)
    • Infectious Diseases

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