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仔猪对VP3或VP7外衣壳蛋白的感染免疫赋予其对携带相应抗原的强毒轮状病毒攻击的抵抗力。

Infection immunity of piglets to either VP3 or VP7 outer capsid protein confers resistance to challenge with a virulent rotavirus bearing the corresponding antigen.

作者信息

Hoshino Y, Saif L J, Sereno M M, Chanock R M, Kapikian A Z

机构信息

Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.

出版信息

J Virol. 1988 Mar;62(3):744-8. doi: 10.1128/JVI.62.3.744-748.1988.

Abstract

A single-gene substitution reassortant 11-1 was generated from two porcine rotaviruses, OSU (serotype 5) and Gottfried (serotype 4). This reassortant derived 10 genes, including gene 4 encoding VP3, from the OSU strain and only gene 9, encoding a major neutralization glycoprotein (VP7), from the Gottfried strain and was thus designated VP3:5; VP7:4. Oral administration of this reassortant to colostrum-deprived gnotobiotic newborn pigs induced a high level of neutralizing antibodies not only to Gottfried VP7 but also to OSU VP3, thus demonstrating that VP3 is as potent an immunogen as VP7 in inducing neutralizing antibodies during experimental oral infection. Gnotobiotic piglets infected previously with the reassortant were completely resistant to oral challenge with the virulent Gottfried strain (VP3:4; VP7:4), as indicated by failure of symptoms to develop and lack of virus shedding. Similarly, prior infection with the reassortant induced almost complete protection against diarrhea and significant restriction of virus replication after oral challenge with the virulent OSU strain (VP3:5; VP7:5). Thus, it appears that (i) the immune system of the piglet responds equally well to two rotavirus outer capsid proteins, VP3 and VP7, during primary enteric rotavirus infection; (ii) antibody to VP3 and antibody to VP7 are each associated with resistance to diarrhea; and (iii) infection with a reassortant rotavirus bearing VP3 and VP7 neutralization antigens derived from two viruses of different serotype induces immunity to both parental viruses. The relevance of these findings to the development of effective reassortant rotavirus vaccines is discussed.

摘要

从两种猪轮状病毒,即俄亥俄州立大学(OSU,血清型5)株和戈特弗里德(Gottfried,血清型4)株产生了单基因替换重配病毒11-1。该重配病毒从OSU株获得了10个基因,包括编码VP3的基因4,而仅从Gottfried株获得了编码主要中和糖蛋白(VP7)的基因9,因此被命名为VP3:5;VP7:4。给初乳缺乏的无菌新生仔猪口服这种重配病毒,不仅诱导产生了针对Gottfried VP7的高水平中和抗体,还诱导产生了针对OSU VP3的高水平中和抗体,从而证明在实验性口服感染期间,VP3在诱导中和抗体方面与VP7一样是有效的免疫原。如症状未出现和无病毒排出所示,先前感染过重配病毒的无菌仔猪对强毒Gottfried株(VP3:4;VP7:4)的口服攻击完全有抵抗力。同样,先前感染过重配病毒可诱导几乎完全抵抗腹泻,并在受到强毒OSU株(VP3:5;VP7:5)口服攻击后显著限制病毒复制。因此,似乎(i)在原发性肠道轮状病毒感染期间,仔猪的免疫系统对两种轮状病毒外衣壳蛋白VP3和VP7的反应同样良好;(ii)针对VP3的抗体和针对VP7的抗体均与抵抗腹泻有关;(iii)感染携带源自两种不同血清型病毒的VP3和VP7中和抗原的重配轮状病毒可诱导对两种亲本病毒的免疫。讨论了这些发现与有效重配轮状病毒疫苗开发的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c8/253627/5417285aef54/jvirol00082-0091-a.jpg

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