Chang Yen-Chen, Kao Chi-Fei, Chang Chia-Yu, Jeng Chian-Ren, Tsai Pei-Shiue, Pang Victor Fei, Chiou Hue-Ying, Peng Ju-Yi, Cheng Ivan-Chen, Chang Hui-Wen
Graduate Institute of Molecular and Comparative Pathobiology, School of Veterinary Medicine, National Taiwan University, No. 1, Section 4, Roosevelt Rd., Taipei 10617, Taiwan.
School of Veterinary Medicine, National Taiwan University, No. 1, Section 4, Roosevelt Rd., Taipei 10617, Taiwan.
Viruses. 2017 May 19;9(5):121. doi: 10.3390/v9050121.
A genogroup 2b (G2b) porcine epidemic diarrhea virus (PEDV) Taiwan Pintung 52 (PEDVPT) strain was isolated in 2014. The pathogenicity and host antibody responses elicited by low-passage (passage 5; PEDVPT-P5) and high-passage (passage 96; PEDVPT-P96) PEDVPT strains were compared in post-weaning PEDV-seronegative pigs by oral inoculation. PEDVPT-P5-inoculation induced typical diarrhea during 1-9 days post inoculation with fecal viral shedding persisting for 26 days. Compared to PEDVPT-P5, PEDVPT-P96 inoculation induced none-to-mild diarrhea and lower, delayed fecal viral shedding. Although PEDVPT-P96 elicited slightly lower neutralizing antibodies and PEDV-specific immunoglobulin G (IgG) and immunoglobulin A (IgA) titers, a reduction in pathogenicity and viral shedding of the subsequent challenge with PEDVPT-P5 were noted in both PEDVPT-P5- and PEDVPT-P96-inoculated pigs. Alignment and comparison of full-length sequences of PEDVPT-P5 and PEDVPT-P96 revealed 23 nucleotide changes and resultant 19 amino acid substitutions in non-structure proteins 2, 3, 4, 9, 14, 15, spike, open reading frame 3 (ORF3), and membrane proteins with no detectable deletion or insertion. The present study confirmed the pathogenicity of the PEDVPT isolate in conventional post-weaning pigs. Moreover, data regarding viral attenuation and potency of induced antibodies against PEDVPT-P5 identified PEDVPT-P96 as a potential live-attenuated vaccine candidate.
2014年分离出一株基因群2b(G2b)型猪流行性腹泻病毒(PEDV)台湾屏东52(PEDVPT)毒株。通过口服接种,在断奶后PEDV血清阴性猪中比较了低代次(第5代;PEDVPT-P5)和高代次(第96代;PEDVPT-P96)PEDVPT毒株引发的致病性和宿主抗体反应。接种PEDVPT-P5后1至9天引发典型腹泻,粪便病毒排出持续26天。与PEDVPT-P5相比,接种PEDVPT-P96引发无至轻度腹泻以及更低、更延迟的粪便病毒排出。尽管PEDVPT-P96引发的中和抗体以及PEDV特异性免疫球蛋白G(IgG)和免疫球蛋白A(IgA)滴度略低,但在接种PEDVPT-P5和PEDVPT-P96的猪中,均观察到用PEDVPT-P5进行后续攻毒时致病性和病毒排出的降低。PEDVPT-P5和PEDVPT-P96全长序列的比对和比较揭示了非结构蛋白2、3、4、9、14、15、刺突、开放阅读框3(ORF3)和膜蛋白中有23个核苷酸变化以及由此产生的19个氨基酸替换,未检测到缺失或插入。本研究证实了PEDVPT分离株在常规断奶后猪中的致病性。此外,关于PEDVPT-P96的病毒减毒和诱导抗体效力的数据确定PEDVPT-P96为一种潜在的减毒活疫苗候选物。