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Development and application of a high-sensitivity immunochromatographic test strip for detecting pseudorabies virus.
Yin, Jiajia; Liu, Huimin; Chen, Yumei; Zhou, Jingming; Liu, Yankai; Liang, Zhenglun; Zhu, Xifang; Liu, Hongliang; Ding, Peiyang; Liu, Enping; Zhang, Ying; Wu, Sixuan; Wang, Aiping.
Afiliación
  • Yin J; Longhu Laboratory, Zhengzhou, China.
  • Liu H; School of Life Sciences, Zhengzhou University, Zhengzhou, China.
  • Chen Y; Longhu Laboratory, Zhengzhou, China.
  • Zhou J; College of Basic Science, Zhengzhou University of Technology, Zhengzhou, Henan, China.
  • Liu Y; Longhu Laboratory, Zhengzhou, China.
  • Liang Z; School of Life Sciences, Zhengzhou University, Zhengzhou, China.
  • Zhu X; Henan Provincial Key Laboratory of Immunobiology, Zhengzhou, China.
  • Liu H; Longhu Laboratory, Zhengzhou, China.
  • Ding P; School of Life Sciences, Zhengzhou University, Zhengzhou, China.
  • Liu E; Henan Provincial Key Laboratory of Immunobiology, Zhengzhou, China.
  • Zhang Y; Longhu Laboratory, Zhengzhou, China.
  • Wu S; School of Life Sciences, Zhengzhou University, Zhengzhou, China.
  • Wang A; Henan Provincial Key Laboratory of Immunobiology, Zhengzhou, China.
Front Microbiol ; 15: 1399123, 2024.
Article en En | MEDLINE | ID: mdl-38765685
ABSTRACT

Introduction:

Pseudorabies (PR) is a multi-animal comorbid disease caused by pseudorabies virus (PRV), which are naturally found in pigs. At the end of 2011, the emergence of PRV variant strains in many provinces in China had caused huge economic losses to pig farms. Rapid detection diagnosis of pigs infected with the PRV variant helps prevent outbreaks of PR. The immunochromatography test strip with colloidal gold nanoparticles is often used in clinical testing due to its low cost and high throughput.

Methods:

This study was designed to produce monoclonal antibodies targeting PRV through immunization of mice using the eukaryotic system to express the gE glycoprotein. Subsequently, paired monoclonal antibodies were screened based on their sensitivity and specificity for use in the preparation of test strips. Results and

discussion:

The strip prepared in this study was highly specific, only PRV was detected, and there was no cross-reactivity with glycoprotein gB, glycoprotein gC, glycoprotein gD, and glycoprotein gE of herpes simplex virus and varicellazoster virus, porcine epidemic diarrhea virus, Senecavirus A, classical swine fever virus, porcine reproductive and respiratory syndrome virus, and porcine parvovirus. Moreover, it demonstrated high sensitivity with a detection limit of 1.336 × 103 copies/µL (the number of viral genome copies per microliter); the coincidence rate with the RT-PCR detection method was 96.4%. The strip developed by our laboratory provides an effective method for monitoring PRV infection and controlling of PR vaccine quality.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Microbiol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Microbiol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza