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Immunological parameters in goats experimentally infected with SRLV genotype E, strain Roccaverano

机译:实验性感染SRLV基因型E的Roccaverano山羊的免疫学参数

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摘要

Genotype E of small ruminant lentivirus has been recently described in goats from different breeds in Italy. Genotype E infection may differ from known genotypes since deletions of dUTPase and VPR proteins have been confirmed in different independent areas and goat breed, and play a key role on virus replication and pathogenesis. In particular, genotype E Roccaverano strain has been described as low pathogenic since does not lead to clinical symptoms in goats. In contrast, classical CAEV infected goats of the same area and breed presented arthritis. In this study, we have used intratracheal and intra-bone marrow routes to establish genotype E persistent infections. Humoral and cellular immune responses elicited in the host against genotype E and genotype B derived antigens were evaluated until 200 days post-inoculation. Compared to genotype B antigen, seroconversion against genotype E GAG P16-25 antigen was detected at 2-3 weeks after inoculation, significantly earlier and at higher titres. Interestingly, antibody avidity did not increase in the course of the experiment neither against P16-25 nor against SU5, both derived from genotype E.T cell proliferation against P25-GST fusion protein antigens derived from genotype E was firstly detected at 15 days post-inoculation and was maintained throughout time until week 20 post-infection, while T cell proliferation against the genotype B P25 was not produced by the end of the experiment at 20 weeks post-inoculation. The strength of reaction was also higher when using P25 E as stimulator antigen.In contrast with antibody and T cell proliferation, cytotoxic-T-lymphocyte (CTL) activity in the circulating lymphocytes (effector cells) using blood-derived macrophages (BDM) as target cells, was not strain specific being surprisingly higher against genotype B infected antigen presenting cells (APCs).This is the first study reporting experimentally induced immunological changes in SRLV genotype E infection and indicates that CTL activity may be the adaptive immune response able to induce protection against heterologous infection. © 2010 Elsevier B.V.
机译:最近在意大利不同品种的山羊中描述了小反刍动物慢病毒的基因型E。 E基因型感染可能与已知基因型不同,因为已在不同的独立区域和山羊品种中确认了dUTPase和VPR蛋白的缺失,并且在病毒复制和发病机理中起着关键作用。特别地,基因型Roccaverano菌株被描述为低致病性的,因为它不会在山羊中引起临床症状。相比之下,同一地区和同一品种的经典CAEV感染山羊表现出关节炎。在这项研究中,我们使用气管内和骨髓内途径建立E型基因型持续感染。评估宿主中针对基因型E和基因型B衍生的抗原引起的体液和细胞免疫应答,直至接种后200天。与基因型B抗原相比,在接种后2-3周,显着更早和更高的滴度下检测到针对基因型E GAG P16-25抗原的血清转化。有趣的是,在实验过程中,既没有针对P16-25也没有针对SU5的抗体亲和力都没有增加,这两者均源于基因型ET细胞,并且在接种后15天首次检测到针对源于基因型E的P25-GST融合蛋白抗原。在感染后第20周的整个过程中,均应维持该病毒的水平,而在接种后20周实验结束时,尚未产生针对基因型B P25的T细胞增殖。当使用P25 E作为刺激物抗原时,反应强度也更高。与抗体和T细胞增殖相反,使用血源巨噬细胞(BDM)作为循环淋巴细胞(效应细胞)的细胞毒性T淋巴细胞(CTL)活性。靶标细胞对B型感染的抗原呈递细胞(APC)的耐药性并不高。这是第一项报道实验性诱导SRLL基因型E感染发生免疫学变化的研究,表明CTL活性可能是能够诱导的适应性免疫应答保护免受异源感染。 ©2010 Elsevier B.V.

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