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Construction and Application of Newcastle Disease Virus P Gene Pseudovirus
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Haiming WANG1, 2, Tong GUO2, 3, Yu DING2, Yang LI2, Zhenxing GONG1, Jingjing WANG2, Hualei LIU2
Acta Veterinaria et Zootechnica Sinica | 2026, 57(3) : 1605 - 1612
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Acta Veterinaria et Zootechnica Sinica | 2026, 57(3): 1605-1612
• PREVENTIVE VETERINARY MEDICINE •
Construction and Application of Newcastle Disease Virus P Gene Pseudovirus
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Haiming WANG1, 2, Tong GUO2, 3, Yu DING2, Yang LI2, Zhenxing GONG1, Jingjing WANG2, Hualei LIU2
Affiliations
  • 1.College of Animal Science and Technology,Ningxia University,Yinchuan 750021,China
  • 2.Avian Disease Surveillance Room,China Animal Health and Epidemiology Center,Qingdao 266032,China
  • 3.College of Veterinary Medicine,Qingdao Agricultural University,Qingdao 266109,China
Published: 2026-03-23 doi: 10.11843/j.issn.0366-6964.2026.03.036
Outline
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This study aimed to construct a safe and effective Newcastle disease virus (NDV) pseudovirus for the quality control of NDV nucleic acid detection. The P gene of NDV was amplified by RT-PCR and linked to the lentiviral expression vector PLV-Puro to construct Puro-NDV/P. Puro-NDV/P plasmids and two helper plasmids were extracted, and a total of 293T cells were transfected, and pseudovirus particles containing NDV P genes were successfully constructed. The constructed pseudovirus particles were properly diluted and lyophilized to prepare RNA-positive quality controls, and calibrated, uniformity and stability tested. A Taqman fluorescence quantitative PCR detection method was established by successfully constructing NDV P gene pseudovirus. The results showed that 15 positive quality control products were randomly selected for fluorescence RT-PCR detection, and the Ct value coefficient of variation (CV) was 0.90%, which was good uniformity. The copy number of the prepared positive quality control products was 6.58×102 copies·μL-1. The quality controls were stored at 4 ℃, 25 ℃ for short-term storage (1 week), and -20 ℃ for a long time (6 months), and the Ct value was detected by fluorescence RT-PCR without significant change, and the stability was good. A real-time fluorescence RT-PCR detection method based on NDV P gene pseudovirus was established. The NDV pseudovirus prepared in this test has the advantages of good uniformity and stability, and can be used for the research and development, evaluation and quality control of NDV nucleic acid detection kits, providing a reliable tool for the standardized detection of NDV.

Newcastle disease virus  /  pseudovirus  /  positive control  /  fluorescent quantitative RT- PCR
王海鸣, 郭通, 丁雨, 李阳, 龚振兴, 王静静, 刘华雷. 新城疫病毒P基因假病毒的构建与初步应用. 畜牧兽医学报, 2026 , 57 (3) : 1605 -1612 . DOI: 10.11843/j.issn.0366-6964.2026.03.036
Haiming WANG, Tong GUO, Yu DING, Yang LI, Zhenxing GONG, Jingjing WANG, Hualei LIU. Construction and Application of Newcastle Disease Virus P Gene Pseudovirus[J]. Acta Veterinaria et Zootechnica Sinica, 2026 , 57 (3) : 1605 -1612 . DOI: 10.11843/j.issn.0366-6964.2026.03.036
Year 2026 volume 57 Issue 3
143
67
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Article Info
doi: 10.11843/j.issn.0366-6964.2026.03.036
  • Receive Date:2025-06-10
  • Online Date:2026-09-16
  • Published:2026-03-23
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History
  • Received:2025-06-10
Funding
Affiliations
    1.College of Animal Science and Technology,Ningxia University,Yinchuan 750021,China
    2.Avian Disease Surveillance Room,China Animal Health and Epidemiology Center,Qingdao 266032,China
    3.College of Veterinary Medicine,Qingdao Agricultural University,Qingdao 266109,China

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WANG Jingjing, E-mail:
LIU Hualei, E-mail:
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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