{"title":"Innovative antigens for more accurate diagnosis of Q fever","authors":"Katarína Palkovicová , Gabriela Flores-Ramírez , Marco Quevedo-Diaz , Frantisek Csicsay , Ludovít Skultety","doi":"10.1016/j.mimet.2025.107106","DOIUrl":null,"url":null,"abstract":"<div><div><em>Coxiella burnetii</em>, the causative agent of Q fever, poses a significant public health concern worldwide. Diagnosis primarily relies on serological tests. Traditional antigen production methods, typically involving embryonated hen eggs, are labor-intensive, costly, and require biosafety level 3 facilities. In this study, we tested inactivated whole-cell antigens (SAP9 and NMII/AP9) from <em>C. burnetii</em> strains grown in axenic media, offering a safer and more efficient alternative to egg-based production. These antigens were validated using an <em>in-house</em> ELISA method against human patient sera, demonstrating high sensitivity and specificity comparable to ELISA and to the Gold Standard, IFA commercial kits. Notably SAP9 and NMII/AP9 antigens showed no cross-reactivity with intracellular pathogens that cause illness with similar symptoms. This approach represents significant advancement in diagnostic antigen production for Q fever, facilitating cost-effective epidemiological studies and enhancing laboratory safety.</div></div>","PeriodicalId":16409,"journal":{"name":"Journal of microbiological methods","volume":"232 ","pages":"Article 107106"},"PeriodicalIF":1.7000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of microbiological methods","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167701225000223","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Coxiella burnetii, the causative agent of Q fever, poses a significant public health concern worldwide. Diagnosis primarily relies on serological tests. Traditional antigen production methods, typically involving embryonated hen eggs, are labor-intensive, costly, and require biosafety level 3 facilities. In this study, we tested inactivated whole-cell antigens (SAP9 and NMII/AP9) from C. burnetii strains grown in axenic media, offering a safer and more efficient alternative to egg-based production. These antigens were validated using an in-house ELISA method against human patient sera, demonstrating high sensitivity and specificity comparable to ELISA and to the Gold Standard, IFA commercial kits. Notably SAP9 and NMII/AP9 antigens showed no cross-reactivity with intracellular pathogens that cause illness with similar symptoms. This approach represents significant advancement in diagnostic antigen production for Q fever, facilitating cost-effective epidemiological studies and enhancing laboratory safety.
期刊介绍:
The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach.
All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.