Related Experiment Video
Updated: Jun 23, 2026

Application of Long-term cultured Interferon-γ Enzyme-linked Immunospot Assay for Assessing Effector and Memory T Cell Responses in Cattle
Published on: July 11, 2015
Rapid serological detection of smooth Brucella strain antibodies in bovine and sheep using a dynamic flow
Kaiyutai Zhou1,2, Chenye You2, Fucheng Wang2
1State Key Laboratory of Dairy Biotechnology, Shanghai Engineering Research Center of Dairy Biotechnology, Dairy Research Institute, Bright Dairy & Food Co., Ltd, Shanghai, China.
Abstract:
Brucellosis, a severe zoonotic disease with over 2,000,000 annual human cases, poses a major threat to the livestock industry and public health. Early and accurate diagnosis in animals is crucial for control, but current methods are often time-consuming, equipment-dependent, or prone to cross-reactivity. This study developed a cost-efficient dynamic flow immunochromatography (DFICT) technique for the accurate diagnosis of bovine and sheep Smooth brucellosis. The assay utilizes a test strip with Smooth lipopolysaccharide and Streptococcus protein G (SPG) immobilized as the Test (T) and Control (C) lines, employing gold nanoparticle-SPG conjugates as the tracer. To perform the DFICT, 100 μL of the liquid conjugate is applied to the reagent well, followed by 5 μL of serum to the sample well. The results were observable within 10 min by the naked eye. The DFICT demonstrated high sensitivity, detecting antibodies in sera diluted up to 1:64, and exceptional specificity with no cross-reactivity to other common pathogens. The DFICT can be stored for 12 months at 4 °C with no loss of sensitivity or specificity. Clinical validation with 80 bovine and 161 sheep field sera showed strong agreement with standard methods (ELISA, RBT), achieving sensitivities of 94.6% (bovine) and 98.2% (sheep), and specificities of 100% and 84.0%, respectively. It's simple, equipment-free operation and reliability make the established DFICT a vital and necessary tool for large-scale, on-site screening, significantly enhancing Smooth brucellosis surveillance and control capabilities.
More Related Videos
Related Concept Videos
Western Blotting
The technique begins with separating proteins from the sample using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by protein transfer, immunoblotting, and finally, protein detection.
Enzyme-Linked Immunosorbent Assay
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen. Enzyme-substrate reaction allows the antigen to be visualized or quantified.

