构建和开发携带增强型绿色荧光蛋白的新型狂犬病毒载体

Seyed Hamidreza Naghi Mousavi, Alireza Gholami, Mojtaba Jafarinia, Mehdi Ajorloo
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摘要

目的:狂犬病是最致命的病毒性疾病之一。本研究在 PV 株的基础上开发了表达 EGFP 蛋白的重组狂犬病毒 PVEGFP,并将其应用于病毒中和抗体(VNA)滴定方法中。方法:在之前讨论过的重组病毒 PVMCS 株系中插入 EGFP 基因。将重组病毒应用于快速荧光聚焦抑制试验(RFFIT)VNA滴定法,并对六名接种者进行了验证研究。研究结果重组狂犬病毒株的繁殖特性与其祖先毒株 PVMCS 相似。它还能用 RFFIT 方法测得 VNA 滴度,与使用 CVS-11 病毒测得的滴度没有显著差异。结论在 RFFIT 方法中使用 PVEGFP 毒株可获得快速、可靠且经济实惠的结果。
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Construction and development of new rabies virus vectors carrying enhanced green fluorescent protein
Aim: Rabies is one of the most lethal viral diseases. This study developed a recombinant rabies virus, PVEGFP, expressing an EGFP protein based on PV strain to be applied in virus-neutralizing antibody (VNA) titration methods. Methods: The EGFP gene was inserted into the PVMCS strain, a previously discussed recombinant virus. The recombinant virus was applied in the rapid fluorescent focus inhibition test (RFFIT) VNA titration method, and six vaccinated persons were studied for validation. Results: The recombinant rabies strain showed similar propagation properties to its ancestry strain, PVMCS. It could also measure VNA titers in the RFFIT method not significantly different from those acquired using the CVS-11 virus. Conclusion: Utilizing the PVEGFP strain in the RFFIT method can produce rapid, reliable and affordable results.
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