Affiliation:
1. Departments of Microbiology & Molecular Genetics and Medicine, University of California—Irvine, Irvine, California 92697,1 and
2. Department of Microbiology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 782842
Abstract
ABSTRACT
Borrelia hermsii
, an agent of relapsing fever, undergoes antigenic variation of serotype-specifying membrane proteins during mammalian infections. When
B. hermsii
is cultivated in broth medium, one serotype, 33, eventually predominates in the population. Serotype 33 has also been found to be dominant in ticks but not in mammalian hosts. We investigated the biology and genetics of two independently derived clonal populations of serotype 33 of
B. hermsii
. Both isolates infected immunodeficient mice, but serotype 33 cells were limited in number and were only transiently present in the blood. Probes for
vsp33
, which encodes the serotype-specifying Vsp33 outer membrane protein, revealed that the gene was located on a 53-kb linear plasmid and that there was only one locus for the gene in serotype 33. The
vsp33
probe and probes for other variable membrane protein genes showed that expression of Vsp33 was determined at the level of transcription and that when the
vsp33
expression site was active, an expression site for other variable proteins was silent. The study confirmed that serotype 33 is distinct from other serotypes of
B. hermsii
in its biology and demonstrated that
B. hermsii
can change its major surface protein through switching between two expression sites.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
39 articles.
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