Affiliation:
1. Department of Medical Microbiology and Immunology, University of Toledo Health Science Campus, 3055 Arlington Avenue, Toledo, Ohio 43614
2. Department of Infectious Diseases, University of Georgia College of Veterinary Medicine, Athens, Georgia 30602
Abstract
ABSTRACT
Two-partner secretion (TPS) systems are a family of proteins being rapidly identified and characterized in a growing number of gram-negative bacteria. TPS systems mediate the secretion of proteins, many involved in virulence traits such as hemolysis, adherence to epithelial cells, inhibition of bacterial growth, and immunomodulation of the host. A TPS system typically consists of a transporter located in the bacterial outer membrane (OM) which is responsible for the recognition and secretion of at least one large exoprotein. Two of the better-characterized TPS systems specify the
Bordetella pertussis
FHA and
Haemophilus influenzae
HMW1/HMW2 proteins. We identified three gene products of
Moraxella catarrhalis
strain O35E that resemble TPS proteins and designated them MhaC (transporter), MhaB1 (exoprotein), and MhaB2 (exoprotein). Western blot analysis using anti-MhaC, or antibodies reacting to both MhaB1 and MhaB2 (MhaB-reactive), revealed that these antigens are expressed in the OM of 63% of isolates tested. Mutations in the
mhaC
gene specifying the putative transporter of the
M. catarrhalis
wild-type strains O35E, O12E, and McGHS1 resulted in the absence of MhaB1/MhaB2 in the OM of mutants. These results are therefore consistent with the Mha proteins functioning as a TPS system. Furthermore, we discovered that these
mhaC
mutants exhibit markedly decreased binding to human epithelial cells relevant to pathogenesis by
M. catarrhalis
(Chang, HEp2, A549, and/or 16HBE14o
−
). Expression of O12E MhaC and MhaB1 in a nonadherent strain of
Escherichia coli
was found to increase the adherence of recombinant bacteria to HEp2 monolayers by sevenfold, thereby demonstrating that this
M. catarrhalis
TPS system directly mediates binding to human epithelial cells. The construction of isogenic mutants in the
mhaB1
and
mhaB2
genes of strain O35E also suggests that the MhaB proteins play distinct roles in
M. catarrhalis
adherence.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
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