Infection and Immunity, December 2002, p. 7033-7041, Vol. 70, No. 12
0019-9567/02/$04.00+0 DOI: 10.1128/IAI.70.12.7033-7041.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Environmental Regulation and Differential Production of Members of the Bdr Protein Family of Borrelia burgdorferi
David M. Roberts,1 Melissa Caimano,2,3 John McDowell,1 Michael Theisen,4 Arne Holm,5 Edward Orff,6 David Nelson,6 Stephen Wikel,2,3 Justin Radolf,2,7,8 and Richard T. Marconi1*
Department of Microbiology and Immunology, Medical College of Virginia at Virginia Commonwealth University, Richmond, Virginia 23298-0678,1
Center for Microbial Pathogenesis,2
Department of Pathology,3
Department of Medicine,7
Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, Connecticut 06030,8
Statens Serum Institut,4
Peptide Group, Chemistry Department, KVL, Copenhagen, Denmark,5
Department of Cell and Molecular Biology, University of Rhode Island, Kingston, Rhode Island 028816
Received 18 April 2002/
Returned for modification 13 June 2002/
Accepted 25 July 2002
Borrelia burgdorferi B31MI carries 18 plasmid-carried genes that form the bdr gene family. The bdr genes of B. burgdorferi encode proteins that form three distinct subfamilies, the BdrD, BdrE, and BdrF subfamilies. bdr orthologs have been demonstrated to be carried by all Borrelia species analyzed, and their widespread distribution suggests that they play an important genus-wide functional role. The biological rationale for maintaining 18 bdr alleles has not been defined. It is our hypothesis that specific paralogs function in different environments and are differentially expressed in response to environmental conditions. As a first step in testing this hypothesis, the production patterns of the Bdr proteins in spirochetes grown under a variety of conditions were assessed through immunoblot analyses. The influence of temperature, serum deprivation, tick feeding, and the mammalian environment on Bdr production was evaluated. These analyses revealed that the synthesis of some Bdr paralogs is environmentally regulated. The production of BdrF2, BdrF1, BdrE4, and BdrE5 were upregulated in host-adapted bacteria, while the production levels of other Bdr paralogs were influenced by temperature and serum starvation. These observations suggest that different Bdr paralogs function in different biological environments and provide insight into the biological basis for maintaining multiple members of this gene family.
* Corresponding author. Mailing address: Department of Microbiology and Immunology, Medical College of Virginia at Virginia Commonwealth University, Sanger Hall, P.O. Box 980678, 1101 East Marshall St., Richmond, VA 23298-0678. Phone: (804) 828-3779. Fax: (804) 828-9946. E-mail: rmarconi{at}hsc.vcuedu.
Editor: V. J. DiRita
Infection and Immunity, December 2002, p. 7033-7041, Vol. 70, No. 12
0019-9567/02/$04.00+0 DOI: 10.1128/IAI.70.12.7033-7041.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
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Copyright © 2002 by the American Society for Microbiology. All rights reserved.