Apparent role for Borrelia burgdorferi LuxS during mammalian infection.

Abstract:

:The Lyme disease spirochete, Borrelia burgdorferi, controls protein expression patterns during its tick-mammal infection cycle. Earlier studies demonstrated that B. burgdorferi synthesizes 4,5-dihydroxy-2,3-pentanedione (autoinducer-2 [AI-2]) and responds to AI-2 by measurably changing production of several infection-associated proteins. luxS mutants, which are unable to produce AI-2, exhibit altered production of several proteins. B. burgdorferi cannot utilize the other product of LuxS, homocysteine, indicating that phenotypes of luxS mutants are not due to the absence of that molecule. Although a previous study found that a luxS mutant was capable of infecting mice, a critical caveat to those results is that bacterial loads were not quantified. To more precisely determine whether LuxS serves a role in mammalian infection, mice were simultaneously inoculated with congenic wild-type and luxS strains, and bacterial numbers were assessed using quantitative PCR. The wild-type bacteria substantially outcompeted the mutants, suggesting that LuxS performs a significant function during mammalian infection. These data also provide further evidence that nonquantitative infection studies do not necessarily provide conclusive results and that regulatory factors may not make all-or-none, black-or-white contributions to infectivity.

journal_name

Infect Immun

journal_title

Infection and immunity

authors

Arnold WK,Savage CR,Antonicello AD,Stevenson B

doi

10.1128/IAI.00032-15

subject

Has Abstract

pub_date

2015-04-01 00:00:00

pages

1347-53

issue

4

eissn

0019-9567

issn

1098-5522

pii

IAI.00032-15

journal_volume

83

pub_type

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