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Infect. Immun., Apr 1997, 1165-1171, Vol 65, No. 4
KJ Indest, R Ramamoorthy, M Sole, RD Gilmore, BJ Johnson and MT Philipp
Previously, we had identified non-OspA-OspB surface proteins of Borrelia
burgdorferi that are targeted by the antibody-dependent complement-mediated
killing mechanism. Here we demonstrate by Western blotting that one of
these proteins, P35, is upregulated at the onset of stationary phase in
vitro. Northern analysis revealed that the upregulation of P35 is at the
level of transcription. In addition, the expression of an open reading
frame (ORF) located downstream of the p35 gene was found to be regulated in
the same fashion as that of P35. This ORF encodes a 7.5-kDa lipoprotein.
The transcriptional start sites for both of these genes were determined, to
aid in the identification of the putative promoter regions. Additional
sequencing of the 5' flanking region of the p35 gene revealed a region of
dyad symmetry 52 bp upstream of the transcription start site. Southern
analysis demonstrated that the expression of these genes was not due to a
cell- density-dependent rearrangement in the genome of B. burgdorferi.
These findings provide an in vitro model for studying mechanisms of gene
regulation in B. burgdorferi.
Copyright © 1997, American Society for Microbiology
Cell-density-dependent expression of Borrelia burgdorferi lipoproteins in vitro
Department of Parasitology, Tulane Regional Primate Research Center, Tulane University Medical Center, Covington, Louisiana, USA.
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