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Infection and Immunity, December 2000, p. 7152-7155, Vol. 68, No. 12
Department of Molecular Genetics,
Biochemistry, and Microbiology, University of Cincinnati,
Cincinnati, Ohio 45267-0524,1 and
Departments of Medicine and Pharmacology, University of
Virginia School of Medicine, Charlottesville, Virginia
229082
Received 22 May 2000/Returned for modification 15 August
2000/Accepted 9 September 2000
A previous study showed that opsonization with human immune serum
could either promote or antagonize phagocytosis of Bordetella pertussis by human neutrophils depending on whether the bacteria expressed adenylate cyclase toxin. Opsonization of the wild-type strain
inhibited phagocytosis relative to unopsonized controls. In contrast,
mutants lacking adenylate cyclase toxin were efficiently phagocytosed
when opsonized with human immune serum. In this study, we examined
opsonization in the presence or absence of monoclonal antibodies to
adenylate cyclase toxin. Addition of neutralizing monoclonal antibodies
to adenylate cyclase toxin converted a serum that previously inhibited
both attachment and phagocytosis of the wild-type strain to one that
increased both attachment and phagocytosis compared to the no-serum
control. Monoclonal antibodies that recognize the adenylate cyclase
toxin but fail to neutralize activity were without effect. These
results suggest that adenylate cyclase toxin inhibits both Fc
receptor-mediated attachment and phagocytosis of B. pertussis by neutrophils.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Neutralizing Antibodies to Adenylate Cyclase Toxin
Promote Phagocytosis of Bordetella pertussis by Human
Neutrophils

*
Corresponding author. Mailing address: Department of
Molecular Genetics, Biochemistry, and Microbiology, University of
Cincinnati, 231 Bethesda Ave., Cincinnati, OH 45267-0524. Phone: (513)
558-2820. Fax: (513) 558-8474. E-mail:
alison.weiss{at}uc.edu.
Present address: Department of Microbiology, Cornell University,
Ithaca, NY 14853.
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