Analysis of the ospC Regulatory Element Controlled by the RpoN-RpoS Regulatory Pathway in Borrelia burgdorferi

ABSTRACT Outer surface lipoprotein C (OspC) is a key virulence factor of Borrelia burgdorferi. ospC is differentially regulated during borrelial transmission from ticks to rodents, and such regulation is essential for maintaining the spirochete in its natural enzootic cycle. Recently, we showed that the expression of ospC in B. burgdorferi is governed by a novel alternative sigma factor regulatory network, the RpoN-RpoS pathway. However, the precise mechanism by which the RpoN-RpoS pathway controls ospC expression has been unclear. In particular, there has been uncertainty regarding whether ospC is controlled directly by RpoS (σs) or indirectly through a transactivator (induced by RpoS). Using deletion analyses and genetic complementation in an OspC-deficient mutant of B. burgdorferi, we analyzed the cis element(s) required for the expression of ospC in its native borrelial background. Two highly conserved upstream inverted repeat elements, previously implicated in ospC regulation, were not required for ospC expression in B. burgdorferi. Using similar approaches, a minimal promoter that contained a canonical −35/−10 sequence necessary and sufficient for σs-dependent regulation of ospC was identified. Further, targeted mutagenesis of a C at position −15 within the extended −10 region of ospC, which is postulated to function like the strategic C residue important for Eσs binding in Escherichia coli, abolished ospC expression. The minimal ospC promoter also was responsive to coumermycin A1, further supporting its σs character. The combined data constitute a body of evidence that the RpoN-RpoS regulatory network controls ospC expression by direct binding of σs to a σs-dependent promoter of ospC. The implication of our findings to understanding how B. burgdorferi differentially regulates ospC and other ospC-like genes via the RpoN-RpoS regulatory pathway is discussed.

[1]  P. Stewart,et al.  The burgeoning molecular genetics of the Lyme disease spirochaete , 2005, Nature Reviews Microbiology.

[2]  Ruth R. Montgomery,et al.  TROSPA, an Ixodes scapularis Receptor for Borrelia burgdorferi , 2004, Cell.

[3]  J. Radolf,et al.  Analysis of Promoter Elements Involved in the Transcriptional Initiation of RpoS-Dependent Borrelia burgdorferi Genes , 2004, Journal of bacteriology.

[4]  T. Schwan,et al.  Outer-surface protein C of the Lyme disease spirochete: a protein induced in ticks for infection of mammals. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[5]  T. J. Templeton Borrelia Outer Membrane Surface Proteins and Transmission Through the Tick , 2004, The Journal of experimental medicine.

[6]  E. Fikrig,et al.  Essential Role for OspA/B in the Life Cycle of the Lyme Disease Spirochete , 2004, The Journal of experimental medicine.

[7]  E. Fikrig,et al.  OspC facilitates Borrelia burgdorferi invasion of Ixodes scapularis salivary glands. , 2004, The Journal of clinical investigation.

[8]  K. L. Frank,et al.  aadA Confers Streptomycin Resistance in Borrelia burgdorferi , 2003, Journal of bacteriology.

[9]  J. Bono,et al.  New Antibiotic Resistance Cassettes Suitable for Genetic Studies in Borrelia burgdorferi , 2003, Journal of Molecular Microbiology and Biotechnology.

[10]  E. Fikrig,et al.  Adaptation of Borrelia burgdorferi in the tick and the mammalian host. , 2003, FEMS microbiology reviews.

[11]  M. Norgard,et al.  Regulation of Expression of the Paralogous Mlp Family in Borrelia burgdorferi , 2003, Infection and Immunity.

[12]  M. Norgard,et al.  The response regulator Rrp2 is essential for the expression of major membrane lipoproteins in Borrelia burgdorferi , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[13]  J. A. Carroll,et al.  An enhanced GFP reporter system to monitor gene expression in Borrelia burgdorferi. , 2003, Microbiology.

[14]  D. Samuels,et al.  Transcriptional regulation of the ospAB and ospC promoters from Borrelia burgdorferi , 2003, Molecular microbiology.

[15]  S. Norris,et al.  A plasmid‐encoded nicotinamidase (PncA) is essential for infectivity of Borrelia burgdorferi in a mammalian host , 2003, Molecular microbiology.

[16]  A. Kolb,et al.  DNA supercoiling contributes to disconnect σS accumulation from σS‐dependent transcription in Escherichia coli , 2003, Molecular microbiology.

[17]  O. Morozova,et al.  Novel antibiotic-resistance markers in pGK12-derived vectors for Borrelia burgdorferi. , 2003, Gene.

[18]  R. Hengge-aronis,et al.  Stationary phase gene regulation: what makes an Escherichia coli promoter sigmaS-selective? , 2002, Current opinion in microbiology.

[19]  S. Rauser,et al.  Dynamics of Dissemination and Outer Surface Protein Expression of Different European Borrelia burgdorferi Sensu Lato Strains in Artificially Infected Ixodes ricinus Nymphs , 2002, Journal of Clinical Microbiology.

[20]  J. Radolf,et al.  Identification of loci critical for replication and compatibility of a Borrelia burgdorferi cp32 plasmid and use of a cp32‐based shuttle vector for the expression of fluorescent reporters in the Lyme disease spirochaete , 2002, Molecular microbiology.

[21]  R. Burgess,et al.  Promoter recognition and discrimination by EσS RNA polymerase , 2001, Molecular microbiology.

[22]  F. Cabello,et al.  Expression of Borrelia burgdorferi OspC and DbpA is controlled by a RpoN–RpoS regulatory pathway , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[23]  E. Dobrikova,et al.  Genetic manipulation of spirochetes--light at the end of the tunnel. , 2001, Trends in microbiology.

[24]  R. Hengge-aronis,et al.  What makes an Escherichia coli promoter σS dependent? Role of the −13/−14 nucleotide promoter positions and region 2.5 of σS , 2001 .

[25]  T. Schwan Temporal regulation of outer surface proteins of the Lyme-disease spirochaete Borrelia burgdorferi. , 2001, Biochemical Society transactions.

[26]  J. Bono,et al.  Isolation of a circular plasmid region sufficient for autonomous replication and transformation of infectious Borrelia burgdorferi , 2001, Molecular microbiology.

[27]  J. Ohnishi,et al.  Antigenic and genetic heterogeneity of Borrelia burgdorferi populations transmitted by ticks. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[28]  Maria Labandeira-Rey,et al.  Decreased Infectivity in Borrelia burgdorferi Strain B31 Is Associated with Loss of Linear Plasmid 25 or 28-1 , 2001, Infection and Immunity.

[29]  S. Norris,et al.  Correlation between plasmid content and infectivity in Borrelia burgdorferi. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[30]  J. Bono,et al.  DNA exchange and insertional inactivation in spirochetes. , 2000, Journal of molecular microbiology and biotechnology.

[31]  S. Wikel,et al.  Interdependence of environmental factors influencing reciprocal patterns of gene expression in virulent Borrelia burgdorferi , 2000, Molecular microbiology.

[32]  Ruth R. Montgomery,et al.  Attachment of Borrelia burgdorferi within Ixodes scapularis mediated by outer surface protein A. , 2000, The Journal of clinical investigation.

[33]  D. Haake Spirochaetal lipoproteins and pathogenesis. , 2000, Microbiology.

[34]  J. Bono,et al.  Efficient Targeted Mutagenesis inBorrelia burgdorferi , 2000, Journal of bacteriology.

[35]  E. Dobrikova,et al.  Development of an extrachromosomal cloning vector system for use in Borrelia burgdorferi. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[36]  O. White,et al.  A bacterial genome in flux: the twelve linear and nine circular extrachromosomal DNAs in an infectious isolate of the Lyme disease spirochete Borrelia burgdorferi , 2000, Molecular microbiology.

[37]  T. Schwan,et al.  Temporal Changes in Outer Surface Proteins A and C of the Lyme Disease-Associated Spirochete, Borrelia burgdorferi, during the Chain of Infection in Ticks and Mice , 2000, Journal of Clinical Microbiology.

[38]  J. Piesman,et al.  Inhibition of Borrelia burgdorferi Migration from the Midgut to the Salivary Glands following Feeding by Ticks on OspC-Immunized Mice , 2000, Infection and Immunity.

[39]  J. Radolf,et al.  Identification, Characterization, and Expression of Three New Members of the Borrelia burgdorferi Mlp (2.9) Lipoprotein Gene Family , 1999, Infection and Immunity.

[40]  S. Salzberg,et al.  Genomic sequence of a Lyme disease spirochaete, Borrelia burgdorferi , 1997, Nature.

[41]  A. Barbour,et al.  Analysis of promoters in Borrelia burgdorferi by use of a transiently expressed reporter gene , 1997, Journal of bacteriology.

[42]  J. Bono,et al.  The Borrelia burgdorferi circular plasmid cp26: conservation of plasmid structure and targeted inactivation of the ospC gene , 1997, Molecular microbiology.

[43]  R. C. Johnson,et al.  Correlation of plasmids with infectivity of Borrelia burgdorferi sensu stricto type strain B31 , 1996, Infection and immunity.

[44]  R. Hengge-aronis,et al.  Back to log phase: σS as a global regulator in the osmotic control of gene expression in Escherichia coli , 1996, Molecular microbiology.

[45]  N. Fujita,et al.  Promoter selectivity of Escherichia coli RNA polymerase E sigma 70 and E sigma 38 holoenzymes. Effect of DNA supercoiling. , 1996, The Journal of biological chemistry.

[46]  Ruth R. Montgomery,et al.  Direct demonstration of antigenic substitution of Borrelia burgdorferi ex vivo: exploration of the paradox of the early immune response to outer surface proteins A and C in Lyme disease , 1996, The Journal of experimental medicine.

[47]  E. Fikrig,et al.  Borrelia burgdorferi OspA is an arthropod-specific transmission- blocking Lyme disease vaccine , 1996, The Journal of experimental medicine.

[48]  T. Schwan,et al.  Induction of an outer surface protein on Borrelia burgdorferi during tick feeding. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[49]  T. Schwan,et al.  Homology between Borrelia burgdorferi OspC and members of the family of Borrelia hermsii variable major proteins. , 1994, Gene.

[50]  A. Sampieri,et al.  Molecular characterization and expression of p23 (OspC) from a North American strain of Borrelia burgdorferi , 1993, Infection and immunity.

[51]  R. Pollack,et al.  Standardization of medium for culturing Lyme disease spirochetes , 1993, Journal of clinical microbiology.

[52]  P. Rosa,et al.  Regulation of expression of major outer surface proteins in Borrelia burgdorferi , 1993, Infection and immunity.

[53]  A. Steere Current understanding of Lyme disease. , 1993, Hospital practice.

[54]  R. Marconi,et al.  Transcriptional analyses and mapping of the ospC gene in Lyme disease spirochetes , 1993, Journal of bacteriology.

[55]  C. Garon,et al.  Coumermycin A1 inhibits growth and induces relaxation of supercoiled plasmids in Borrelia burgdorferi, the Lyme disease agent , 1993, Antimicrobial Agents and Chemotherapy.

[56]  F. Lottspeich,et al.  Molecular analysis and expression of a Borrelia burgdorferi gene encoding a 22kDa protein (pC) in Escherichia coli , 1992, Molecular microbiology.

[57]  Jean Côté,et al.  Lyme Disease , 1991, International journal of dermatology.

[58]  A. Barbour,et al.  Plasmid analysis of Borrelia burgdorferi, the Lyme disease agent , 1988, Journal of clinical microbiology.

[59]  P. Stewart,et al.  The plasmids of Borrelia burgdorferi: essential genetic elements of a pathogen. , 2005, Plasmid.

[60]  A. Ishihama,et al.  Promoter selectivity of Escherichia coli RNA polymerase , 2004, Molecular and General Genetics MGG.

[61]  D. Samuels,et al.  Electrotransformation of the spirochete Borrelia burgdorferi. , 1995, Methods in molecular biology.

[62]  H. Coller,et al.  Poisson statistical analysis of repetitive subcloning by the limiting dilution technique as a way of assessing hybridoma monoclonality. , 1986, Methods in enzymology.