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使用生物合成肽疫苗保护牛和猪免受口蹄疫侵害。

Protection of cattle and swine against foot-and-mouth disease, using biosynthetic peptide vaccines.

作者信息

Morgan D O, Moore D M

机构信息

USDA, Agricultural Research Services, Plum Island Animal Disease Center, Greenport, NY 11944.

出版信息

Am J Vet Res. 1990 Jan;51(1):40-5.

PMID:2154148
Abstract

A single dose of foot-and-mouth disease (FMD) virus protein 1 (VP1) peptide, expressed in Escherichia coli as a fusion protein with 190 amino acids (AA) of the LE' protein of the tryptophan operon of E coli, elicited an immune response in steers sufficient to withstand the challenge of exposure to animals with acute FMD. The 58-micrograms dose of viral peptide, composed of a segment of the VP1 from the A12 strain (A12) of FMD virus (FMDV; A12-32dimer) in a tandem repeat configuration of AA137 through 168 and emulsified with oil adjuvant, elicited a serologic response in cattle equivalent to that obtained using conventional whole virus vaccines. Two groups of swine were vaccinated, 1 with the A12-32dimer as used in cattle and 1 with AA131 through 157 from VP1 of the A24 strain (A24) of FMDV (A24-peptide), expressed in the same system as A12-32dimer, but as a single copy per molecule. In swine, the 58-micrograms dose of the A12-32dimer repeated at 28 days was an effective immunogen; all swine were protected against A12 and, in addition, the vaccine protected 50% of the swine against A24. The 29-micrograms dose of A24-peptide, administered according to the same schedule, elicited protection against A24 in 50% of the vaccinates and, in addition, protected 25% of those vaccinates against A12. The serologic response elicited by A12-32dimer against A24 virus was considerably greater than the response elicited by A24-peptide against A12 virus. The evidence of multiple immunogenic epitopes between AA131 and AA168 was evaluated.

摘要

单剂量口蹄疫(FMD)病毒蛋白1(VP1)肽在大肠杆菌中表达为与大肠杆菌色氨酸操纵子LE'蛋白的190个氨基酸(AA)的融合蛋白,在公牛中引发了足以抵御急性口蹄疫动物暴露挑战的免疫反应。58微克剂量的病毒肽由口蹄疫病毒(FMDV;A12)A12株的VP1片段(A12 - 32二聚体)组成,呈AA137至168的串联重复构型,并与油佐剂乳化,在牛中引发的血清学反应与使用传统全病毒疫苗获得的反应相当。两组猪进行了疫苗接种,一组接种牛使用的A12 - 32二聚体,另一组接种在与A12 - 32二聚体相同系统中表达但每个分子为单拷贝的FMDV A24株VP1的AA131至157(A24 - 肽)。在猪中,58微克剂量的A12 - 32二聚体于28天时重复接种是一种有效的免疫原;所有猪均对A12具有抵抗力,此外,该疫苗还使50%的猪对A24具有抵抗力。按照相同方案接种的29微克剂量的A24 - 肽,使50%的接种猪对A24具有抵抗力,此外,还使25%的接种猪对A12具有抵抗力。A12 - 32二聚体针对A24病毒引发的血清学反应明显大于A24 - 肽针对A12病毒引发的反应。评估了AA131和AA168之间多个免疫原性表位的证据。

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