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Development and evaluation of an up-converting phosphor technology-based lateral flow assay for rapid and quantitative detection of Coxiella burnetii phase I strains.
Zhang, Pingping; Jiao, Jun; Zhao, Yong; Fu, Mengjiao; Wang, Jin; Song, Yajun; Zhou, Dongsheng; Wang, Yongqiang; Wen, Bohai; Yang, Ruifu; Xiong, Xiaolu.
Afiliación
  • Zhang P; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, P. R. China.
  • Jiao J; Beijing Key Laboratory of POCT for Bio-emergency and Clinic (No.BZ0329), Beijing, P. R. China.
  • Zhao Y; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, P. R. China.
  • Fu M; Beijing Key Laboratory of POCT for Bio-emergency and Clinic (No.BZ0329), Beijing, P. R. China.
  • Wang J; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, P. R. China.
  • Song Y; Beijing Key Laboratory of POCT for Bio-emergency and Clinic (No.BZ0329), Beijing, P. R. China.
  • Zhou D; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, P. R. China.
  • Wang Y; Beijing Key Laboratory of POCT for Bio-emergency and Clinic (No.BZ0329), Beijing, P. R. China.
  • Wen B; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, P. R. China.
  • Yang R; Beijing Key Laboratory of POCT for Bio-emergency and Clinic (No.BZ0329), Beijing, P. R. China.
  • Xiong X; State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, P. R. China.
BMC Microbiol ; 20(1): 251, 2020 08 12.
Article en En | MEDLINE | ID: mdl-32787788
ABSTRACT

BACKGROUND:

Coxiella burnetii is an obligate intracellular Gram-negative bacterium that causes a zoonotic disease commonly called Q fever globally. In this study, an up-converting phosphor technology-based lateral flow (UPT-LF) assay was established for the rapid and specific detection of phase I strains of C. burnetii.

RESULTS:

Specific monoclonal antibodies (10B5 and 10G7) against C. burnetii phase I strains were prepared and selected for use in the UPT-LF assay by the double-antibody-sandwich method. The detection sensitivity of the Coxiella-UPT-LF was 5 × 104 GE/ml for a purified C. burnetii phase I strain and 10 ng/ml for LPS of C. burnetii Nine Mile phase I (NMI). Good linearity was observed for C. burnetii phase I and NMI LPS quantification (R2 ≥ 0.989). The UPT-LF assay also exhibited a high specificity to C. burnetii, without false-positive results even at 108 GE/ml of non-specific bacteria, and good inclusivity for detecting different phase I strains of C. burnetii. Moreover, the performance of the Coxiella-UPT-LF assay was further confirmed using experimentally and naturally infected samples.

CONCLUSIONS:

Our results indicate that Coxiella-UPT-LF is a sensitive and reliable method for rapid screening of C. burnetii, suitable for on-site detection in the field.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fiebre Q / Técnicas Biosensibles / Coxiella burnetii / Anticuerpos Monoclonales Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: BMC Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fiebre Q / Técnicas Biosensibles / Coxiella burnetii / Anticuerpos Monoclonales Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: BMC Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2020 Tipo del documento: Article