【Animal modeling】-Establishment of multiplex detection method of serological liquid chip technology for common infectious diseases in transgenic mice

  OBJECTIVE: To prepare mouse MHV, LCM, ECT and HANT liquid-phase chips, and to establish an xMAP multiplex detection method for infectious disease antibodies in transgenic mice.

  Methods: The fluorescent microspheres were coupled with mouse MHV, LCM, ECT and HANT proteins respectively, and the optimal protein coupling amount, optimal working concentration of detection antibody and optimal working concentration of Streptavidin-PE were optimized. Mouse MHV, LCM, ECT and HANT liquid-phase chips were used for multiplex detection of xMAP on 56 transgenic mouse serum samples, negative serum, positive serum and quality control serum. And the traditional ELISA method was used to verify the detection results of xMAP.

  Results: 1) The optimal coupling amounts of mouse MHV, LCM, ECT and HANT proteins were 20 μg, 20 μg, 40 μg and 20 μg, respectively, and the optimal concentrations of detection antibodies were 2 μg/mL and 2 μg/mL, respectively. , 2 μg/mL and 4 μg/mL; the optimal concentration of Streptavidin-PE antibody was 2 μg/mL; (2) xMAP test results showed that the serum MHV MFI of No. 14, No. 23, No. 55 and No. 56 transgenic mice The MFI value and index value of the serum of the other mice were lower than those of the quality control serum, indicating that the transgenic mice No. 14, No. 23, No. 55 and No. 56 were positive for MHV antibodies, and the rest of the mice were positive for MHV antibodies. MHV, LCM, ECT and HANT antibodies were negative; (3) ELISA test results showed that the MHV A450 value and index value of transgenic mice No. 14, No. 23, No. 55 and No. 56 were higher than those of the quality control serum, and the serum levels of the other mice were higher than those of the control serum. The A450 value and index value were both lower than those of the quality control serum, indicating that the transgenic mice No. 14, No. 23, No. 55 and No. 56 were positive for MHV antibodies, and the other mice were negative for MHV, LCM, ECT and HANT antibodies. The ELISA test results were consistent with xMAP The test results are consistent.

  Conclusion: The established xMAP multiplex detection technology can be applied to the detection of infectious diseases in transgenic mice.