SURFACE-ASSOCIATED FILAMENTOUS HEMAGGLUTININ INDUCES AUTOAGGLUTINATION OF BORDETELLA-PERTUSSIS

Citation
Fd. Menozzi et al., SURFACE-ASSOCIATED FILAMENTOUS HEMAGGLUTININ INDUCES AUTOAGGLUTINATION OF BORDETELLA-PERTUSSIS, Infection and immunity, 62(10), 1994, pp. 4261-4269
Citations number
49
Categorie Soggetti
Immunology,"Infectious Diseases
Journal title
ISSN journal
00199567
Volume
62
Issue
10
Year of publication
1994
Pages
4261 - 4269
Database
ISI
SICI code
0019-9567(1994)62:10<4261:SFHIA>2.0.ZU;2-L
Abstract
Filamentous hemagglutinin (FHA) is a major adhesin produced by Bordete lla pertussis, the etiologic agent of whooping cough. FHA has been sho wn to be surface associated but is also secreted by virulent bacteria. Microscopic observations of lungs of mice infected with B. pertussis showed that the bacteria grow as clusters within the alveolar lumen. W hen B. pertussis was cultivated in vitro with chemically defined mediu m, bacteria grew as aggregates, mimicking growth observed in vivo. Thi s aggregation was abolished by the addition of cyclodextrin (CDX) to t he growth medium and depended on the production of FHA, because a muta nt lacking the FHA structural gene failed to form aggregates in a CDX- free medium. Western blot (immunoblot) analyses revealed that, in the absence of CDX, FHA was attached to the bacterial surface and was not efficiently released into the growth medium. Hydrophobic chromatograph y of FHA showed that CDX drastically reduced the hydrophobicity of FHA , suggesting a direct binding of CDX to FHA, which was further support ed by the partial protection of FHA from trypsin digestion in the pres ence of CDX. In addition, free FHA can interact in a CDX-inhibitable m anner with solid phase-immobilized FHA. It can therefore be postulated that the B. pertussis aggregates are most likely due to direct FHA-FH A interaction.