@article{mbs:/content/journal/micro/10.1099/mic.0.043513-0, author = "Deringer, James R. and Chen, Chen and Samuel, James E. and Brown, Wendy C.", title = "Immunoreactive Coxiella burnetii Nine Mile proteins separated by 2D electrophoresis and identified by tandem mass spectrometry", journal= "Microbiology", year = "2011", volume = "157", number = "2", pages = "526-542", doi = "https://doi.org/10.1099/mic.0.043513-0", url = "https://www.microbiologyresearch.org/content/journal/micro/10.1099/mic.0.043513-0", publisher = "Microbiology Society", issn = "1465-2080", type = "Journal Article", keywords = "IFA, incomplete Freund's adjuvant", keywords = "IPG, immobilized pH gradient", keywords = "WCV, whole-cell vaccine", keywords = "ACN, acetonitrile", keywords = "CMRV, chloroform, methanol residue vaccine", keywords = "LC-MS/MS, liquid chromatography-tandem MS", keywords = "WCKI, whole-cell killed vaccine", abstract = " Coxiella burnetii is a Gram-negative obligate intracellular pathogen and the causative agent of Q fever in humans. Q fever causes acute flu-like symptoms and may develop into a chronic disease leading to endocarditis. Its potential as a bioweapon has led to its classification as a category B select agent. An effective inactivated whole-cell vaccine (WCV) currently exists but causes severe granulomatous/necrotizing reactions in individuals with prior exposure, and is not licensed for use in most countries. Current efforts to reduce or eliminate the deleterious reactions associated with WCVs have focused on identifying potential subunit vaccine candidates. Both humoral and T cell-mediated responses are required for protection in animal models. In this study, nine novel immunogenic C. burnetii proteins were identified in extracted whole-cell lysates using 2D electrophoresis, immunoblotting with immune guinea pig sera, and tandem MS. The immunogenic C. burnetii proteins elicited antigen-specific IgG in guinea pigs vaccinated with whole-cell killed Nine Mile phase I vaccine, suggesting a T cell-dependent response. Eleven additional proteins previously shown to react with immune human sera were also antigenic in guinea pigs, showing the relevance of the guinea pig immunization model for antigen discovery. The antigens described here warrant further investigation to validate their potential use as subunit vaccine candidates.", }