Affiliation:
1. Department of Immunology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany
2. Institute for Immunology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Abstract
ABSTRACT
Rickettsioses are emerging febrile diseases caused by obligate intracellular bacteria belonging to the family
Rickettsiaceae. Rickettsia typhi
belongs to the typhus group (TG) of this family and is the causative agent of endemic typhus, a disease that can be fatal. In the present study, we analyzed the course of
R. typhi
infection in C57BL/6 RAG1
−/−
mice. Although these mice lack adaptive immunity, they developed only mild and temporary symptoms of disease and survived
R. typhi
infection for a long period of time. To our surprise, 3 to 4 months after infection, C57BL/6 RAG1
−/−
mice suddenly developed lethal neurological disorders. Analysis of these mice at the time of death revealed high bacterial loads, predominantly in the brain. This was accompanied by a massive expansion of microglia and by neuronal cell death. Furthermore, high numbers of infiltrating CD11b
+
macrophages were detectable in the brain. In contrast to the microglia, these cells harbored
R. typhi
and showed an inflammatory phenotype, as indicated by inducible nitric oxide synthase (iNOS) expression, which was not observed in the periphery. Having shown that
R. typhi
persists in immunocompromised mice, we finally asked whether the bacteria are also able to persist in resistant C57BL/6 and BALB/c wild-type mice. Indeed,
R. typhi
could be recultivated from lung, spleen, and brain tissues from both strains even up to 1 year after infection. This is the first report demonstrating persistence and reappearance of
R. typhi
, mainly restricted to the central nervous system in immunocompromised mice.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
22 articles.
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