| Literature DB >> 19786560 |
K E Russell-Lodrigue1, M Andoh, M W J Poels, H R Shive, B R Weeks, G Q Zhang, C Tersteeg, T Masegi, A Hotta, T Yamaguchi, H Fukushi, K Hirai, D N McMurray, J E Samuel.
Abstract
Q fever is a zoonotic disease of worldwide significance caused by the obligate intracellular bacterium Coxiella burnetii. Humans with Q fever may experience an acute flu-like illness and pneumonia and/or chronic hepatitis or endocarditis. Various markers demonstrate significant phylogenetic separation between and clustering among isolates from acute and chronic human disease. The clinical and pathological responses to infection with phase I C. burnetii isolates from the following four genomic groups were evaluated in immunocompetent and immunocompromised mice and in guinea pig infection models: group I (Nine Mile, African, and Ohio), group IV (Priscilla and P), group V (G and S), and group VI (Dugway). Isolates from all of the groups produced disease in the SCID mouse model, and genogroup-consistent trends were noted in cytokine production in response to infection in the immunocompetent-mouse model. Guinea pigs developed severe acute disease when aerosol challenged with group I isolates, mild to moderate acute disease in response to group V isolates, and no acute disease when infected with group IV and VI isolates. C. burnetii isolates have a range of disease potentials; isolates within the same genomic group cause similar pathological responses, and there is a clear distinction in strain virulence between these genomic groups.Entities:
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Year: 2009 PMID: 19786560 PMCID: PMC2786457 DOI: 10.1128/IAI.00851-09
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441