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本文引用的文献

1
Small ruminant lentiviruses: immunopathogenesis of visna-maedi and caprine arthritis and encephalitis virus.小反刍兽瘟病毒:绵羊肺腺瘤病病毒和山羊关节炎脑炎病毒的免疫发病机制。
Comp Immunol Microbiol Infect Dis. 2012 May;35(3):259-69. doi: 10.1016/j.cimid.2011.12.003. Epub 2012 Jan 9.
2
Diagnostic performance of PCR and ELISA on blood and milk samples and serological survey for small ruminant lentiviruses in central Spain.西班牙中部地区血液和奶样中 PCR 和 ELISA 的诊断性能及小反刍兽瘟病毒血清学调查。
Vet Rec. 2011 Jan 8;168(1):20. doi: 10.1136/vr.c4951. Epub 2011 Jan 4.
3
Diagnostic performance of ELISA and PCR in identifying SRLV-infected sheep and goats using serum, plasma and milk samples and in early detection of infection in dairy flocks through bulk milk testing.ELISA 和 PCR 检测方法在血清、血浆和奶样中鉴别 SRLV 感染绵羊和山羊,以及通过牛奶混样检测在奶牛群中早期检测感染的诊断性能。
Vet Microbiol. 2010 May 19;142(3-4):193-8. doi: 10.1016/j.vetmic.2009.09.060. Epub 2009 Oct 20.
4
Mapping and characterization of visna/maedi virus cytotoxic T-lymphocyte epitopes.维斯纳/梅迪病毒细胞毒性T淋巴细胞表位的定位与特性分析
J Gen Virol. 2008 Oct;89(Pt 10):2586-2596. doi: 10.1099/vir.0.2008/002634-0.
5
Prevention strategies against small ruminant lentiviruses: an update.针对小型反刍动物慢病毒的预防策略:最新进展
Vet J. 2009 Oct;182(1):31-7. doi: 10.1016/j.tvjl.2008.05.008. Epub 2008 Aug 27.
6
Vaccination of sheep with Maedi-visna virus gag gene and protein, beneficial or harmful?用梅迪-维斯纳病毒gag基因和蛋白对绵羊进行疫苗接种,有益还是有害?
Vaccine. 2007 Sep 17;25(37-38):6713-20. doi: 10.1016/j.vaccine.2007.07.004. Epub 2007 Jul 26.
7
Evidence of proviral clearance following postpartum transmission of an ovine lentivirus.绵羊慢病毒产后传播后前病毒清除的证据。
Virology. 2007 May 25;362(1):226-34. doi: 10.1016/j.virol.2006.12.021. Epub 2007 Jan 30.
8
Effect of 17beta-estradiol and progesterone on the expression of FeLV in chronically infected cells.17β-雌二醇和孕酮对慢性感染细胞中猫白血病病毒(FeLV)表达的影响。
Vet Microbiol. 2005 Aug 30;109(3-4):191-9. doi: 10.1016/j.vetmic.2005.06.005.
9
Diagnostic tests for small ruminant lentiviruses.小型反刍动物慢病毒的诊断测试
Vet Microbiol. 2005 Apr 25;107(1-2):49-62. doi: 10.1016/j.vetmic.2005.01.012.
10
Viral expression and leukocyte adhesion after in vitro infection of goat mammary gland cells with caprine arthritis-encephalitis virus.山羊关节炎-脑炎病毒体外感染山羊乳腺细胞后的病毒表达与白细胞黏附
Vet Immunol Immunopathol. 2005 Jan 10;103(1-2):93-9. doi: 10.1016/j.vetimm.2004.08.016.

小反刍兽疫病毒感染小反刍动物后乳中特异性抗体和前病毒 DNA 的演变。

Evolution of specific antibodies and proviral DNA in milk of small ruminants infected by small ruminant lentivirus.

机构信息

Departamento Sanidad Animal, Facultad Veterinaria, Universidad Complutense, Madrid 28040, Spain.

出版信息

Viruses. 2013 Oct 22;5(10):2614-23. doi: 10.3390/v5102614.

DOI:10.3390/v5102614
PMID:24153063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3814608/
Abstract

The diagnosis of Small Ruminant Lentivirus (SRLV) is based on clinical signs, pathological lesions and laboratory testing. No standard reference test for the diagnosis of maedi visna has been validated up to the present, and it is puzzling that tests which detect antibodies against the virus and tests which detect the proviral genome may render opposite results. The aim of this study was to evaluate the presence in milk throughout a lactation period of specific antibodies by ELISA and of SRLV proviral DNA by a PCR of the highly conserved pol region. A six-month study was conducted with the milk of 28 ewes and 31 goats intensively reared. The percentage of animals with antibodies against SRLV increased throughout the study period. Seroprevalence in sheep was 28% at the beginning of the study and by the end it had increased up to 52.4%. In goats, initial seroprevalence of 5.6% increased to 16%. The percentage of PCR positive ewes was stable throughout the study period. Of the positive sheep, 21.4% were PCR-positive before antibodies could be detected and most of them became PCR-negative shortly after the first detection of antibodies. This might suggest that antibodies have a neutralizing effect. In addition, an equal percentage of sheep were always PCR-negative but either became ELISA-positive or was always ELISA-positive, which might support this hypothesis. On the other hand, the PCR results in goats did not follow any pattern and oscillated between 35.3% and 55.6% depending on the month. Most goats positive by PCR failed to develop antibodies in the 6 months tested. We may conclude that the infection and the antibody response to it follow a different trend in sheep and goats.

摘要

小反刍兽疫病毒(SRLV)的诊断基于临床症状、病理病变和实验室检测。迄今为止,尚未验证出针对绵羊肺腺瘤病(Maedi-Visna)的标准参考检测方法,令人困惑的是,检测病毒抗体的检测方法和检测前病毒基因组的检测方法可能会得出相反的结果。本研究旨在通过 ELISA 评估泌乳期内牛奶中特异性抗体的存在情况,并通过高度保守的 pol 区 PCR 检测 SRLV 前病毒 DNA。对 28 只绵羊和 31 只山羊进行了为期六个月的密集养殖试验。研究期间,动物对 SRLV 的抗体比例逐渐增加。绵羊在研究开始时的血清阳性率为 28%,到研究结束时上升至 52.4%。山羊的初始血清阳性率为 5.6%,上升至 16%。研究期间,PCR 阳性绵羊的比例保持稳定。在阳性绵羊中,有 21.4%在可检测到抗体之前即为 PCR 阳性,其中大多数在首次检测到抗体后不久即转为 PCR 阴性。这可能表明抗体具有中和作用。此外,有相同比例的绵羊始终为 PCR 阴性,但要么转为 ELISA 阳性,要么始终为 ELISA 阳性,这可能支持这一假说。另一方面,山羊的 PCR 结果没有任何规律,根据月份在 35.3%到 55.6%之间波动。大多数 PCR 阳性的山羊在 6 个月的检测中未能产生抗体。我们可以得出结论,绵羊和山羊的感染和对其的抗体反应遵循不同的趋势。