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重叠聚合酶链反应和同源重组技术产生的缺失 gI/gE 的重组伪狂犬病病毒诱导抗 PRV 变异株 PRV-GD2013 的保护。

Recombinant pseudorabies virus with gI/gE deletion generated by overlapping polymerase chain reaction and homologous recombination technology induces protection against the PRV variant PRV-GD2013.

机构信息

College of Veterinary Medicine, South China Agricultural University, 483 Wu Shan Road, Tianhe District, Guangzhou, 510642, Guangdong Province, China.

Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou, China.

出版信息

BMC Vet Res. 2021 Apr 14;17(1):164. doi: 10.1186/s12917-021-02861-6.

Abstract

BACKGROUND

Since 2011, numerous highly virulent and antigenic variant viral strains have been reported in pigs that were vaccinated against the swine pseudorabies virus. These infections have led to substantial economic losses in the Chinese swine industry.

RESULTS

This study, constructed a novel recombinant vaccine strain with gI/gE deletion (PRV-GD2013-ΔgI/gE) by overlapping PCR and homologous recombination technology. The growth curves and plaque morphology of the recombinant virus were similar to those of the parental strain. However, PRV-GD2013-ΔgI/gE infection was significantly attenuated in mice compared with that of PRV-GD2013. Two-week-old piglets had normal rectal temperatures and displayed no clinical symptoms after being inoculated with 10 TCID PRV-GD2013-ΔgI/gE, indicating that the recombinant virus was avirulent in piglets. Piglets were immunized with different doses of PRV-GD2013-ΔgI/gE, or a single dose of Bartha-K61 or DMEM, and infected with PRV-GD2013 at 14 days post-vaccination. Piglets given high doses of PRV-GD2013-ΔgI/gE showed no obvious clinical symptoms, and their antibody levels were higher than those of other groups, indicating that the piglets were completely protected from PRV-GD2013.

CONCLUSIONS

The PRV-GD2013-ΔgI/gE vaccine strain could be effective for immunizing Chinese swine herds against the pseudorabies virus (PRV) strain.

摘要

背景

自 2011 年以来,在中国的猪群中已报道了许多针对猪伪狂犬病病毒(PRV)接种疫苗的高毒力和高抗原变体病毒株。这些感染导致中国养猪业遭受了巨大的经济损失。

结果

本研究通过重叠 PCR 和同源重组技术构建了一种新的 gI/gE 缺失(PRV-GD2013-ΔgI/gE)重组疫苗株。重组病毒的生长曲线和蚀斑形态与亲本株相似。然而,与 PRV-GD2013 相比,PRV-GD2013-ΔgI/gE 感染在小鼠中显著减弱。2 周龄仔猪接种 10 TCID PRV-GD2013-ΔgI/gE 后直肠温度正常,无临床症状,表明重组病毒在仔猪中无毒力。仔猪分别接种不同剂量的 PRV-GD2013-ΔgI/gE 或单次剂量的 Bartha-K61 或 DMEM,于接种后 14 天用 PRV-GD2013 攻毒。给予高剂量 PRV-GD2013-ΔgI/gE 的仔猪无明显临床症状,其抗体水平高于其他组,表明仔猪完全免受 PRV-GD2013 的侵害。

结论

PRV-GD2013-ΔgI/gE 疫苗株可有效免疫中国猪群抵抗伪狂犬病病毒(PRV)株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1137/8048318/a5cd528c1f6a/12917_2021_2861_Fig1_HTML.jpg

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