Affiliation:
1. Department of Microbiology and Immunology, University of California at Los Angeles School of Medicine, Los Angeles, California 90095-1747
Abstract
ABSTRACT
We describe here a side-by-side comparison of murine respiratory infection by
Bordetella pertussis
and
Bordetella bronchiseptica
strains whose genomes are currently being sequenced (Tohama I and RB50, respectively).
B. pertussis
and
B. bronchiseptica
are most appropriately classified as subspecies. Their high degree of genotypic and phenotypic relatedness facilitates comparative studies of pathogenesis. RB50 and Tohama I differ in their abilities to grow in the nose, trachea, and lungs of BALB/c mice and to induce apoptosis, lung pathology, and an antibody response. To focus on the interactions between the bacteria and particular aspects of the host immune response, we used mice with specific immune defects. Mice lacking B cells and T cells were highly susceptible to
B. bronchiseptica
and were killed by intranasal inoculation with doses as low as 500 CFU. These mice were not killed by
B. pertussis
, even when doses as high as 10
5
CFU were delivered to the lungs.
B. bronchiseptica
, which was highly resistant to naive serum in vitro, caused bacteremia in these immunodeficient mice, while
B. pertussis
, which was highly sensitive to naive serum, did not cause bacteremia.
B. bronchiseptica
was, however, killed by immune serum in vitro, and adoptive transfer of anti-
Bordetella
antibodies protected SCID-beige mice from
B. bronchiseptica
lethal infection. Neutropenic mice were similarly killed by
B. bronchiseptica
but not
B. pertussis
infection, suggesting neutrophils are critical to the early inflammatory response to the former but not the latter.
B. bronchiseptica
was dramatically more active than
B. pertussis
in mediating the lysis of J774 cells in vitro and in inducing apoptosis of inflammatory cells in mouse lungs. This side-by-side comparison describes phenotypic differences that may be correlated with genetic differences in the comparative analysis of the genomes of these two highly related organisms.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
87 articles.
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