Affiliation:
1. Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, Texas, USA
Abstract
ABSTRACT
Borrelia burgdorferi
survives in nature through a complex tick-mammalian life cycle. During its transit between ticks and mammalian hosts,
B. burgdorferi
must dramatically alter its outer surface profile in order to interact with and adapt to these two diverse niches. It has been established that the regulator BosR (BB0647) in
B. burgdorferi
plays important roles in modulating borrelial host adaptation. However, to date, how
bosR
expression itself is controlled in
B. burgdorferi
remains largely unknown. Previously, it has been shown that DNA sequences upstream of BosR harbor multiple sites for the binding of recombinant BosR, suggesting that BosR may influence its own expression in
B. burgdorferi
. However, direct experimental evidence supporting this putative autoregulation of BosR has been lacking. Here, we investigated the expression of
bosR
throughout the tick-mammal life cycle of
B. burgdorferi
via quantitative reverse transcription (RT)-PCR analyses. Our data indicated that
bosR
is expressed not only during mouse infection, but also during the tick acquisition, intermolt, and transmission phases. Further investigation revealed that
bosR
expression in
B. burgdorferi
is influenced by environmental stimuli, such as temperature shift and pH change. By employing luciferase reporter assays, we also identified two promoters potentially driving
bosR
transcription. Our study offers strong support for the long-postulated function of BosR as an autoregulator in
B. burgdorferi
.
Funder
HHS | National Institutes of Health
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
10 articles.
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