Reina Ramses, Grego Elena, Profiti Margherita, Glaria Idoia, Robino Patrizia, Quasso Antonio, Amorena Beatriz, Rosati Sergio
Dipartimento di Produzioni Animali, Epidemiologia ed Ecologia, Università degli Studi di Torino, Grugliasco, TO, Italy.
Vet Microbiol. 2009 Sep 18;138(3-4):251-7. doi: 10.1016/j.vetmic.2009.04.005. Epub 2009 Apr 10.
Small ruminant lentivirus (SRLV) belonging to the highly divergent genotype E has recently been identified in the Italian goat breed Roccaverano. In this report we have developed a specific serological test based on recombinant matrix/capsid antigen fusion protein. Performance has been evaluated and compared with a similar test based on genotype B antigen. Herds under study were selected according to the infectious status characterized by blood PCR and sequencing. Results clearly showed that B and E based recombinant ELISA only detected homologous infection and an apparent cross-reactivity was recorded in a herd in which co-infection was present. Three commercially available ELISAs showed different abilities in detecting genotype E infection, being the whole virus-based immunoassay the best choice. Genotype E-recombinant antigen was not detected in ELISA by three commercially available Mabs known to be cross-reactive among CAEV and MVV capsid antigens, further supporting the high divergence of the E genotype from others. Finally, a SRLV-free herd according to commercial ELISA testing, was analysed in the same area where genotype E was identified and few animals belonging to Roccaverano breed were found slightly reactive with the E antigens. Our results suggest that the prevalence of genotype E in other small ruminant populations may be conveniently estimated using a comparative assay based on a combination of genotype specific recombinant antigens and may highlight a wider space in which SRLVs evolve.
最近在意大利罗卡韦拉诺山羊品种中发现了属于高度分化的E基因型的小反刍兽疫病毒(SRLV)。在本报告中,我们基于重组基质/衣壳抗原融合蛋白开发了一种特异性血清学检测方法。对其性能进行了评估,并与基于B基因型抗原的类似检测方法进行了比较。根据血液PCR和测序所确定的感染状况选择了受研究的畜群。结果清楚地表明,基于B和E的重组酶联免疫吸附测定(ELISA)仅检测到同源感染,并且在存在共同感染的一个畜群中记录到明显的交叉反应。三种市售ELISA在检测E基因型感染方面表现出不同的能力,基于全病毒的免疫测定是最佳选择。已知在山羊关节炎脑炎病毒(CAEV)和梅迪-维斯纳病毒(MVV)衣壳抗原之间具有交叉反应性的三种市售单克隆抗体(Mab)在ELISA中未检测到E基因型重组抗原,这进一步支持了E基因型与其他基因型的高度分化。最后,在鉴定出E基因型的同一地区对一个根据市售ELISA检测无SRLV的畜群进行了分析,发现少数属于罗卡韦拉诺品种的动物与E抗原呈轻微反应。我们的结果表明,使用基于基因型特异性重组抗原组合的比较测定法可以方便地估计其他小反刍兽种群中E基因型的流行率,并且可能突出了SRLV进化的更广阔空间。