Affiliation:
1. Department of Infectious Diseases, Leiden University Medical Center, Leiden,1 and
2. Research Laboratory for Infectious Diseases, National Institute of Public Health and the Environment, Bilthoven,2 The Netherlands
Abstract
ABSTRACT
Immunization with whole-cell pertussis vaccines (WCV) containing heat-killed
Bordetella pertussis
cells and with acellular vaccines containing genetically or chemically detoxified pertussis toxin (PT) in combination with filamentous hemagglutinin (FHA), pertactin (Prn), or fimbriae confers protection in humans and animals against
B. pertussis
infection. In an earlier study we demonstrated that FHA is involved in the adherence of these bacteria to human bronchial epithelial cells. In the present study we investigated whether mouse antibodies directed against
B. pertussis
FHA, PTg, Prn, and fimbriae, or against two other surface molecules, lipopolysaccharide (LPS) and the 40-kDa outer membrane porin protein (OMP), that are not involved in bacterial adherence, were able to block adherence of
B. pertussis
and
B. parapertussis
to human bronchial epithelial cells. All antibodies studied inhibited the adherence of
B. pertussis
to these epithelial cells and were equally effective in this respect. Only antibodies against LPS and 40-kDa OMP affected the adherence of
B. parapertussis
to epithelial cells. We conclude that antibodies which recognize surface structures on
B. pertussis
or on
B. parapertussis
can inhibit adherence of the bacteria to bronchial epithelial cells, irrespective whether these structures play a role in adherence of the bacteria to these cells.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
31 articles.
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