Early cytokine and antibody responses against Coxiella burnetii in aerosol infection of BALB/c mice
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Publication year
2015Source
Diagnostic Microbiology and Infectious Diseases, 81, 4, (2015), pp. 234-9ISSN
Publication type
Article / Letter to editor
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Organization
Internal Medicine
Journal title
Diagnostic Microbiology and Infectious Diseases
Volume
vol. 81
Issue
iss. 4
Page start
p. 234
Page end
p. 9
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Radboudumc 4: lnfectious Diseases and Global Health RIMLS: Radboud Institute for Molecular Life SciencesAbstract
Coxiella burnetii, a Gram-negative intracellular bacterium, can give rise to Q fever in humans and is transmitted mainly by inhalation of infected aerosols from animal reservoirs. Serology is commonly used to diagnose Q fever, but the early cellular immune response-i.e., C. burnetii-specific interferon gamma (IFN-gamma) production in response to antigen challenge-might be an additional diagnostic. Detection of IFN-gamma responses has been used to identify past and chronic Q fever infections, but the IFN-gamma response in acute Q fever has not been described. By challenging immunocompetent BALB/c mice with aerosols containing phase I C. burnetii, the timing and extent of IFN-gamma recall responses were evaluated in an acute C. burnetii infection. Other cytokines were also measured in an effort to identify other potential diagnostic markers. The data show that after initial expansion of bacteria first in lungs and then in other tissues, the infection was cleared from day 10 onwards as reflected by the decreasing number of bacteria. The antigen-induced IFN-gamma production by splenocytes coincided with emergence of IgM phase II antibodies at day 10 postinfection and preceded appearance of IgG antibodies. This was accompanied by the production of proinflammatory cytokines including interleukin (IL) 6, keratinocyte-derived cytokine, and IFN-gamma-induced protein 10, followed by monocyte chemotactic protein 1, but not by IL-1beta and tumor necrosis factor alpha, and only very low production of the anti-inflammatory cytokine IL-10. These data suggest that analysis of antigen-specific IFN-gamma responses could be a useful tool for diagnosis of acute Q fever. Moreover, the current model of C. burnetii infection could be used to give new insights into immunological factors that predispose to development of persistent infection.
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