Affiliation:
1. Bacterial Pathogenesis Program, Seattle Biomedical Research Institute, Seattle, Washington 98109
2. Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan 48109-0244
Abstract
ABSTRACT
Haemophilus influenzae
is subject to phase variation mediated by changes in the length of simple sequence repeat regions within several genes, most of which encode either surface proteins or enzymes involved in the synthesis of lipopolysaccharides (LPS). The translational repeat regions that have been described thus far all consist of tandemly repeated tetranucleotides. We describe an octanucleotide repeat region within a putative LPS biosynthetic gene,
losA
. Approximately 20 percent of nontypeable
H. influenzae
strains contain copies of
losA
and
losB
in a genetic locus flanked by
infA
and
ksgA
. Of 30 strains containing
losA
at this site, 24 contained 2 tandem copies of the octanucleotide CGAGCATA, allowing full-length translation of
losA
(on), and 6 strains contained 3, 4, 6, or 10 tandem copies (
losA
off). For a serum-sensitive strain, R3063, with
losA
off (10 repeat units), selection for serum-resistant variants yielded a heterogeneous population in which colonies with increased serum resistance had
losA
on (2, 8, or 11 repeat units), and colonies with unchanged sensitivity to serum had 10 repeats. Inactivation of
losA
in strains R3063 and R2846 (strain 12) by insertion of the
cat
gene decreased the serum resistance of these strains compared to
losA
-on variants and altered the electrophoretic mobility of LPS. We conclude that expression of
losA
, a gene that contributes to LPS structure and affects serum resistance, is determined by octanucleotide repeat variation.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
23 articles.
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