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J. Bacteriol., Apr 1997, 2289-2299, Vol 179, No. 7
Y Ge, IG Old, I Saint Girons and NW Charon
A large motility operon, referred to as the flgB operon, was identified,
characterized, and mapped at 310 to 320 kb on the linear chromosome of the
spirochete Borrelia burgdorferi. This is the first report that a
sigma70-like promoter rather than a sigma28-like promoter is involved in
the transcription of a major motility operon in bacteria. From these
results in conjunction with results from a previous study (Y. Ge and N. W.
Charon, Gene, in press), we have identified 26 genes in this operon that
are relevant to motility and flagellar synthesis. With few exceptions, the
gene order and deduced gene products were most similar to those of other
spirochetes and Bacillus subtilis. Primer extension analysis indicated that
transcription initiated from a conserved sigma70-like promoter immediately
upstream of flgB; this promoter mapped within the heat- shock-induced
protease gene hslU. Reverse transcriptase PCR analysis indicated that a
single transcript of 21 kb initiated at this promoter and extended through
flgE and (with our previous results) onto the putative motility gene flbE.
The flgB promoter element had strong activity in both Escherichia coli and
Salmonella typhimurium. As expected, a mutant of S. typhimurium with an
inactivated flagellum- specific sigma28 factor did not affect the function
of this promoter. Western blot analysis indicated that B. burgdorferi
recombinant FliG and FliI were antigenically similar to those of E. coli
and other spirochetes. Although complementation of E. coli or S.
typhimurium fliG or fliI mutants with the B. burgdorferi genes was
unsuccessful, B. burgdorferi recombinant FliI completely inhibited
flagellar synthesis and motility of wild-type E. coli and S. typhimurium.
These results show that spirochete motility genes can influence flagellar
synthesis in other species of bacteria. Finally, Western blot analysis with
sera from infected humans and animals indicated a weak or nondetectable
response to recombinant FliG and FliI. These results indicate that these
antigens are not favorable candidate reagents to be used in the diagnosis
of Lyme disease.
Copyright © 1997, American Society for Microbiology
Molecular characterization of a large Borrelia burgdorferi motility operon which is initiated by a consensus sigma70 promoter
Department of Microbiology and Immunology, West Virginia University, Robert C. Byrd Health Sciences Center, Morgantown 26506-9177, USA.
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