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Infect Immun, February 1998, p. 432-440, Vol. 66, No. 2
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Population Structure of the Relapsing Fever
Spirochete Borrelia hermsii as Indicated by Polymorphism of
Two Multigene Families That Encode Immunogenic Outer Surface
Lipoproteins
B. Joseph
Hinnebusch,1,*
Alan G.
Barbour,2,3
Blanca I.
Restrepo,3,
and
Tom
G.
Schwan1
Laboratory of Microbial Structure and
Function, Rocky Mountain Laboratories, National Institute of
Allergy and Infectious Diseases, National Institutes of Health,
Hamilton, Montana1;
Departments of
Microbiology & Molecular Genetics and Medicine, University of
California Irvine College of Medicine, Irvine,
California2; and
Department of
Microbiology, University of Texas Health Science Center, San Antonio,
Texas3
Received 10 June 1997/Returned for modification 19 August
1997/Accepted 17 November 1997
The tick-borne relapsing fever spirochete Borrelia
hermsii evades the mammalian immune system by periodically
switching expression among members of two multigene families that
encode immunogenic, antigenically distinct outer surface proteins. The
type strain, B. hermsii HS1, has at least 40 complete genes
and pseudogenes that participate in this multiphasic
antigenic variation. Originally termed vmp (for variable
major protein) genes, they have been reclassified as vsp
(for variable small protein) and vlp (for variable
large protein) genes, based on size and amino acid sequence similarities. To date, antigenic variation in B. hermsii
has been studied only in the type strain, HS1. Nucleotide sequence
comparisons of 23 B. hermsii HS1 genes revealed five
distinct groups, the vsp gene family and four subfamilies
of vlp genes. We used PCR with family- and
subfamily-specific primers, followed by restriction fragment length polymorphism analysis, to compare the vsp
and vlp repertoires of HS1 and seven other B. hermsii isolates from Washington, Idaho, and California. This
analysis, together with pulsed-field gel electrophoresis genome
profiles, revealed that the eight isolates formed three distinct
groups, which likely represent clonal lineages. Members of the three
groups coexisted in the same geographic area, but they could
also be isolated across large geographical distances. This population
structure may result from immune selection by the host, as
has been proposed for other pathogens with polymorphic antigens.
*
Corresponding author. Mailing address: Laboratory of
Microbial Structure and Function, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of
Health, 903 S. 4th St., Hamilton, MT 59840. Phone: (406) 363-9260. Fax:
(406) 363-9204. E-mail: joe_hinnebusch{at}nih.gov.

Present address: Corporación para Investigaciones
Biológicas (CIB), Medellín, Colombia.
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