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Infection and Immunity, October 1999, p. 5500-5507, Vol. 67, No. 10
Max von Pettenkofer Institute for Hygiene and
Medical Microbiology, Ludwig Maximilians University Munich, 80336 Munich, Germany
Received 10 May 1999/Returned for modification 5 July 1999/Accepted 21 July 1999
Three different Yersinia enterocolitica serotype O8
strains harboring mutations in virulence-associated genes coding for
Yersinia adhesin A (YadA), Mn-cofactored superoxide
dismutase (SodA), and high-molecular-weight protein 1 were analyzed for
their ability to colonize and persist in tissues after orogastric
immunization of C57BL/6 mice. We demonstrated that all three
Yersinia mutant strains were markedly impaired in their
ability to disseminate into the spleens and livers of immunized mice
but were able to colonize the Peyer's patches for at least 12 days,
resulting in the induction of significant antibody titers against
Yersinia outer proteins (Yops) and in the priming of
Yersinia antigen-specific CD4+ Th1 cells
isolated from spleens. The high level of attenuation did not diminish
the immunogenic properties of the mutant strains. In fact, mice
immunized with a single oral dose of any of the mutant strains were
protected against a lethal oral-challenge infection with wild-type
Y. enterocolitica. Moreover, adoptive transfer of
Yersinia-specific antibodies from sera of mice immunized with the mutant WAP-314 sodA revealed that this protection
could be mediated by Yersinia-specific immunoglobulins.
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Rational Live Oral Carrier Vaccine Design by
Mutating Virulence-Associated Genes of Yersinia
enterocolitica
*
Corresponding author. Mailing address: Max von
Pettenkofer Institute for Hygiene and Medical Microbiology, Ludwig
Maximilians University Munich, Pettenkoferstr. 9a, 80336 Munich,
Germany. Phone: 49-89-51605200. Fax: 49-89-51605202. E-mail:
ruessmann{at}m3401.mpk.med.uni-muenchen.de.
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