Development of a Novel PmpD-N ELISA for Chlamydia psittaci Infection

LIU Shan Shan CHU Jun ZHANG Qiang SUN Wei ZHANG Tian Yuan HE Cheng

LIU Shan Shan, CHU Jun, ZHANG Qiang, SUN Wei, ZHANG Tian Yuan, HE Cheng. Development of a Novel PmpD-N ELISA for Chlamydia psittaci Infection[J]. Biomedical and Environmental Sciences, 2016, 29(5): 315-322. doi: 10.3967/bes2016.041
Citation: LIU Shan Shan, CHU Jun, ZHANG Qiang, SUN Wei, ZHANG Tian Yuan, HE Cheng. Development of a Novel PmpD-N ELISA for Chlamydia psittaci Infection[J]. Biomedical and Environmental Sciences, 2016, 29(5): 315-322. doi: 10.3967/bes2016.041

doi: 10.3967/bes2016.041
基金项目: the National Natural Science Foundation of China under Grant No.31272542%Ministry of Science and Technology (MoST) grant 2012AA101302

Development of a Novel PmpD-N ELISA for Chlamydia psittaci Infection

Funds: the National Natural Science Foundation of China under Grant No.31272542%Ministry of Science and Technology (MoST) grant 2012AA101302
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  • 刊出日期:  2016-05-20

Development of a Novel PmpD-N ELISA for Chlamydia psittaci Infection

doi: 10.3967/bes2016.041
    基金项目:  the National Natural Science Foundation of China under Grant No.31272542%Ministry of Science and Technology (MoST) grant 2012AA101302

摘要: ObjectiveChlamydia psittaci is an avian respiratory pathogen and zoonotic agent.The wide prevalence ofC. psittaci poses a threat to the poultry industry and its employees. However, few commercial kits are available for detecting avian antibodies excluding the in-house ELISA kit. In this study, we developed a novel ELISA kit for detecting antibodies againstC. psittaci based on the N-terminal fragment of polymorphic outer membrane protein D (PmpD-N) as the coating antigen.
Methods The antigen concentrations, primary antibody, and cut-off value were determined and optimized. The ELISA, designated PmpD-N ELISA, was assessed for sensitivity, specificity, and concordance using sera samples from 48 experimentally infected and 168 uninfected SPF chickens.
Results The sensitivity and specificity of PmpD-N ELISA were 97.9%, 100%, respectively, while the concordance was 98.1% as compared to that of MOMP-ELISA. No cross-reaction with positive sera for other avian pathogens was found. Using PmpD-N ELISA, 799/836 clinical samples were positive, including 93.0% and 98.1% positivity in layers and broilers, respectively.
Conclusion These data indicate that indirect ELISA with PmpD-N as the antigen candidate is a promising approach for the surveillance ofC. psittaci infection.

English Abstract

LIU Shan Shan, CHU Jun, ZHANG Qiang, SUN Wei, ZHANG Tian Yuan, HE Cheng. Development of a Novel PmpD-N ELISA for Chlamydia psittaci Infection[J]. Biomedical and Environmental Sciences, 2016, 29(5): 315-322. doi: 10.3967/bes2016.041
Citation: LIU Shan Shan, CHU Jun, ZHANG Qiang, SUN Wei, ZHANG Tian Yuan, HE Cheng. Development of a Novel PmpD-N ELISA for Chlamydia psittaci Infection[J]. Biomedical and Environmental Sciences, 2016, 29(5): 315-322. doi: 10.3967/bes2016.041

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