Ministry of Education Key Laboratory for Animal Pathogens and Biosafety, College of Veterinary Medicine, Henan Agricultural University, Zhengdong New District Longzi Lake 15#, Zhengzhou 450046, People's Republic of China.
Ministry of Education Key Laboratory for Animal Pathogens and Biosafety, College of Veterinary Medicine, Henan Agricultural University, Zhengdong New District Longzi Lake 15#, Zhengzhou 450046, People's Republic of China; Department of Life Science, Zhengzhou Normal University, Zhengzhou 450044, Henan Province, People's Republic of China.
Comp Immunol Microbiol Infect Dis. 2023 Oct;101:102054. doi: 10.1016/j.cimid.2023.102054. Epub 2023 Aug 27.
Porcine circovirus type 2 (PCV2) plays a key role in the etiology of PCV2-associated disease (PCVAD), and its predominant strain is PCV2d which is not completely controlled by most commercially available vaccines against PCV2a strains. Pseudorabies (PR) caused by pseudorabies virus (PRV) variants re-emerged in Bartha-K61 vaccine-immunized swine herds in late 2011, which brought considerable losses to the global pig husbandry. Therefore, it is significantly important to develop a safe and effective vaccine against both PCV2d and PRV infection. In the present study, the PCV2d ORF2 gene was amplified by PCR, and cloned into the BamHI site of PRV transfer plasmid pG vector to obtain the recombinant transfer plasmid pG-PCV2dCap-EGFP. Subsequently, it was transfected into ST cells infected with the three gene deleted PRV variant strain NY-gE/gI/TK to generate a recombinant virus rPRV NY-gE/gI/TK/PCV2dCap/EGFP, and then the EGFP gene was knocked out to harvest the rPRV NY-gE/gI/TK/PCV2dCap using gene-editing technology termed CRISPR/Cas9 system. The recombinant virus rPRV NY-gE/gI/TK/PCV2dCap had similar genetic stability and proliferation characteristics to the parental PRV as indicated by PCR and one-step growth curve test, and the expression of Cap was validated by Western blot. In animal experiment, higher PCV2-specific ELISA antibodies and detectable PCV2-specific neutralizing antibodies could be elicited in mice immunized with rPRV NY-gE/gI/TK/PCV2dCap compared to commercial PCV2 inactivated vaccine. Moreover, the recombinant virus rPRV NY-gE/gI/TK/PCV2dCap significantly reduced the viral loads in the hearts, livers, spleens, lungs, and kidneys in mice following a virulent PCV2d challenge. Mice immunized with rPRV NY-gE/gI/TK/PCV2dCap developed comparable PRV-specific humoral immune responses and provided complete protection against a lethal PRV challenge. Together, the rPRV NY-gE/gI/TK/PCV2dCap recombinant strain has strong immunogenicity.
猪圆环病毒 2 型(PCV2)在 PCV2 相关疾病(PCVAD)的病因学中起关键作用,其主要毒株是 PCV2d,而大多数市售的针对 PCV2a 株的疫苗并不能完全控制它。2011 年底,在使用巴氏-κ61 疫苗免疫的猪群中,由猪伪狂犬病病毒(PRV)变异株引起的伪狂犬病(PR)再次出现,给全球养猪业带来了巨大损失。因此,开发针对 PCV2d 和 PRV 感染的安全有效的疫苗具有重要意义。本研究通过 PCR 扩增 PCV2d ORF2 基因,将其克隆到 PRV 转移质粒 pG 载体的 BamHI 位点,获得重组转移质粒 pG-PCV2dCap-EGFP。随后,将其转染到感染了三个基因缺失的 PRV 变异株 NY-gE/gI/TK 的 ST 细胞中,生成重组病毒 rPRV NY-gE/gI/TK/PCV2dCap/EGFP,然后利用基因编辑技术 CRISPR/Cas9 系统敲除 EGFP 基因,收获 rPRV NY-gE/gI/TK/PCV2dCap。重组病毒 rPRV NY-gE/gI/TK/PCV2dCap 的遗传稳定性和增殖特性与亲本 PRV 相似,这通过 PCR 和一步生长曲线试验得到证实,Cap 的表达也通过 Western blot 得到验证。在动物实验中,与商品化的 PCV2 灭活疫苗相比,rPRV NY-gE/gI/TK/PCV2dCap 免疫的小鼠能够产生更高的 PCV2 特异性 ELISA 抗体和可检测的 PCV2 特异性中和抗体。此外,重组病毒 rPRV NY-gE/gI/TK/PCV2dCap 能显著降低 PCV2d 攻毒后小鼠心脏、肝脏、脾脏、肺脏和肾脏中的病毒载量。rPRV NY-gE/gI/TK/PCV2dCap 免疫的小鼠产生了相似的 PRV 特异性体液免疫应答,并能完全抵抗致死性 PRV 攻毒。总之,rPRV NY-gE/gI/TK/PCV2dCap 重组株具有较强的免疫原性。