burnetii Xinqiao was isolated from ticks in China and its phase I phenotype was demonstrated in a previous study

[13]. In this current study, C. burnetii Xinqiao was used to infect BALB/c mice and a large amount of C. burnetii was found in the spleens and livers of the infected mice by qPCR analysis. The Coxiella load in spleens was significantly higher compared with that in the other organs of the infected mice, indicating that the mouse spleen is the most important organ for C. burnetii propagation and its Coxiella load may reflect the severity of C. burnetii infection. The highest Stattic in vivo level of Coxiella in spleens of the infected mice was found on day 7 pi and then gradually decreased, indicating that the see more infected mice recovered gradually from the severe infection. These results also indicate that the combination of the sublethal challenge mouse model and the qPCR assay may be a useful and sensitive way to evaluate severity of the infection caused by check details different C. burnetii strains and evaluate efficiency of drugs or vaccines against this pathogen. In order to identify the seroreactive proteins of C. burnetii Xinqiao, the whole cell lysates of the organism was separated

by 2-D electrophoresis. Immunoblot analysis using the sera of mice obtained at days 14, 21, and 28 pi, indentified 4, 9, and 14 of the separated proteins, respectively. This indicated that the specific immune responses to C. burnetii developed progressively in the infected mice with additional antigens of C. burentii recognized as the immune response grew further. In addition, 15 of the proteins were recognized by sera from two patients with acute Q fever. Among these seroreactive proteins, 9 proteins were recognized by both the mouse and human sera, indicating that these proteins are able to elicit similar humoral immune responses to C. burnetii infection in both species.

A total of 20 seroreactive proteins were recognized by the positive mouse or human sera by mass spectra of MALDI-TOF-MS. GroEL, a conserved heat shock protein (HspB) [14], has been reported as a major immunodominant antigen of C. burnetii [15]. YbgF, a tol-pal system protein that involved in bacterial outer membrane stability [16], was found in both RANTES phases of C. burnetii [12]. GroEL and YbgF were both recognized by the sera of C. burnetii-infected mice and the Q fever patient sera in this study and have been previously documented as seroreactive antigens using a proteomic approach [7–9]. While Com1, Mip, and OmpH were recognized by the sera of C. burnetii-infected mice but were not recognized by Q fever patient sera. This difference might be due to the fact that mouse and human sera were from different infection stages or there were differences in humoral immune responses to C. burnetii infection between mice and humans.