Evaluation of novel synthetic peptides of avian hepatitis E virus ORF2 as vaccine candidate in chickens

IF 2.5 4区 医学 Q3 VIROLOGY
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引用次数: 0

Abstract

Avian hepatitis E virus (HEV) has resulted in significant economic losses in the poultry industry. There is currently no commercial vaccination available to prevent avian HEV infection. Previously, a novel epitope (601TFPS604) was discovered in the ORF2 protein of avian HEV. In this study, peptides were synthesized and assessed for their ability to provide immunoprotecting against avian HEV infection in poultry. Twenty-five Hy-Line Variety Brown laying hens were randomly divided into five groups; groups 1 to 3 respectively immunized with RLLDRLSRTFPS, PETRRLLDRLSR (irrelevant peptide control), or truncated avian HEV ORF2 protein (aa 339–606), while group 4 (negative control) was mock-immunized with PBS and group 5 (normal control) was not immunized or challenged. After the challenge, all hens in groups 2 and 4 showed seroconversion, fecal virus shedding, viremia, alanine aminotransferase (ALT) level increasing, liver lesions and HEV antigen in the liver. There were no pathogenic effects in other groups. Collectively, all of these findings showed that hens were completely protected against avian HEV infection when they were immunized with the peptide containing TFPS of the avian HEV ORF2 protein.

将禽戊型肝炎病毒 ORF2 的新型合成肽作为候选疫苗对鸡进行评估。
禽戊型肝炎病毒(HEV)给家禽业造成了巨大的经济损失。目前还没有商业疫苗可用于预防禽 HEV 感染。此前,在禽 HEV 的 ORF2 蛋白中发现了一个新的表位(601TFPS604)。本研究合成了多肽,并评估了它们对家禽感染禽 HEV 提供免疫保护的能力。将 25 只海系变种褐壳蛋鸡随机分为 5 组,第 1 组至第 3 组分别免疫 RLLDRLSRTFPS、PETRRLLDRLSR(无关肽对照)或截短的禽 HEV ORF2 蛋白(aa 339-606),第 4 组(阴性对照)用 PBS 进行模拟免疫,第 5 组(正常对照)不免疫也不接受挑战。挑战后,第 2 组和第 4 组的所有母鸡均出现血清转换、粪便病毒脱落、病毒血症、丙氨酸氨基转移酶(ALT)水平升高、肝脏病变和肝脏中的 HEV 抗原。其他组别则无致病影响。所有这些结果表明,用含有禽 HEV ORF2 蛋白 TFPS 的肽免疫母鸡后,可完全防止禽 HEV 感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virus research
Virus research 医学-病毒学
CiteScore
9.50
自引率
2.00%
发文量
239
审稿时长
43 days
期刊介绍: Virus Research provides a means of fast publication for original papers on fundamental research in virology. Contributions on new developments concerning virus structure, replication, pathogenesis and evolution are encouraged. These include reports describing virus morphology, the function and antigenic analysis of virus structural components, virus genome structure and expression, analysis on virus replication processes, virus evolution in connection with antiviral interventions, effects of viruses on their host cells, particularly on the immune system, and the pathogenesis of virus infections, including oncogene activation and transduction.
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