， a global-distributed biological warfare agent， is the causative agent of Q fever. Correct diagnosis of Q fever is challenging and developing a fast， simple， and reliable detection method is necessary. In this study， recombinase polymerase amplification (RPA) assay combined with lateral flow (LF) test was developed targeting 23S rRNA gene of Xinqiao strain. Primers and probe were designed and synthesized， with one set with high amplification efficiency screened for establishment of the method. Reaction conditions were optimized. Sensitivity， specificity， and accuracy were evaluated. The established RPA-LF reaction could be completed in 30 minutes by combining RPA at 37°C with LF at room temperature， with visually judged results. The method showed good specificity without recognizing other bacteria evaluated. It detected positive plasmid and genomic DNA at levels of 10 copies/reaction and 7 copies/reaction， respectively， levels comparable to that of real-time quantitative PCR (RT-qPCR) targeting 23S rRNA gene established previously. Both RPA-LF and RT-qPCR were used to detect -infected mouse samples and the results were fully consistent. The method showed superior detection performance and will provide technical support against in resources-limited areas.