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Development of a TaqMan MGB RT-PCR assay for the detection of type A and subtype H10 avian influenza viruses

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Abstract

H10 subtype avian influenza viruses have caused several epidemics in poultry and mammals, and specific, rapid and sensitive methods for detection are urgently needed. Herein, TaqMan minor groove binder (MGB) probes and multiplex real-time RT-PCR primers were designed based on gene regions encoding conserved domains of the nucleoprotein and H10 hemagglutinin. The developed multiplex real-time RT-PCR assay displayed high specificity, repeatability, and a detection limit of 10 copies per reaction. This diagnostic method could prove valuable for the rapid detection of H10 subtype AIVs in China.

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Funding

This study was funded by Grants from the National Science Foundation of the People’s Republic of China (81502852) and the Independent Task of State Key Laboratory for Diagnosis and Treatment of Infectious Diseases (Nos. 2017ZZ10 and 2018ZZ06).

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Correspondence to Haibo Wu.

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The authors declare that they have no conflict of interest.

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Handling Editor: William G. Dundon.

Electronic supplementary material

Below is the link to the electronic supplementary material.

705_2018_3889_MOESM1_ESM.pdf

Primers and probes used in the multiplex real-time RT-PCR assays. Regions targeted by primer pairs and probes for NA (A) and H10 (B) sequences are boxed. (PDF 1094 kb)

Supplementary material 2 (DOCX 23 kb)

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Yang, F., Chen, B., Liu, F. et al. Development of a TaqMan MGB RT-PCR assay for the detection of type A and subtype H10 avian influenza viruses. Arch Virol 163, 2497–2501 (2018). https://doi.org/10.1007/s00705-018-3889-4

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  • DOI: https://doi.org/10.1007/s00705-018-3889-4

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