Fd. Menozzi et al., SURFACE-ASSOCIATED FILAMENTOUS HEMAGGLUTININ INDUCES AUTOAGGLUTINATION OF BORDETELLA-PERTUSSIS, Infection and immunity, 62(10), 1994, pp. 4261-4269
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.