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Issue 1063 coverRickettsioses: From Genome to Proteome, Pathobiology, and Rickettsiae as an International Threat Volume 1063 published December 2005
Ann. N.Y. Acad. Sci. 1063: 171–175 (2005). doi: 10.1196/annals.1355.027
Copyright © 2005 by the New York Academy of Sciences
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Balb/c Mouse Model and Real-Time Quantitative Polymerase Chain Reaction for Evaluation of the Immunoprotectivity against Q Fever

JINGBO ZHANG, BOHAI WEN, MEILING CHEN, JUN ZHANG AND DONGSHENG NIU

Beijing Institute of Microbiology and Epidemiology and State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China

Address for correspondence: Bohai Wen, Beijing Institute of Microbiology and Epidemiology and State Key Laboratory of Pathogen and Biosecurity, 20 Dong-Da-Jie Street, Fengtai, Beijing 100071, China. Voice: +86-10-63820718; fax: +86-10-63815259. wenbohai{at}yahoo.com

The Balb/c mice were infected with Coxiella burnetii and samples of blood and major organs from the infected mice were collected on days 1 to 14 after infection. The DNAs extracted from the samples were detected by a developed real-time quantitative PCR specific for C. burnetii and high loads of C. burnetii were found in spleens, livers, and lungs, particularly in spleens. The Balb/c mice were immunized with whole cell antigen (WCA) of C. burnetii and coxiella loads in spleens of mice were assessed by the real-time quantitative PCR on day 7 after challenge with C. burnetii. The analysis suggested that phase I whole cells were excellent immunogen that elicited complete protection against coxiella infection by two-booster but not one-booster immunization. The results suggest that the combination of Balb/c model and the real-time quantitative PCR assay is a reliable and sensitive way to evaluate the efficiency of vaccines against Q fever.

Key Words: Coxiella burnetii • BALB/c mice • real-time PCR • immunization






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