Berguido Francisco J, Settypalli Tirumala Bharani Kumar, Mbuyi Curé Georges Tshilenge, Bakhom Mame Thierno, van Vuren Petrus Jansen, Pawęska Janusz T, Cattoli Giovanni, Grabherr Reingard, Lamien Charles Euloge
Animal Production and Health Laboratory, Joint FAO/IAEA Centre of Nuclear Techniques in Food and Agriculture, Department of Nuclear Sciences and Applications, International Atomic Energy Agency, Vienna, Austria.
Institute of Biotechnology, University of Natural Resources and Life Sciences (BOKU), Muthgasse18, 1190, Vienna, Austria.
Virol J. 2024 Dec 27;21(1):335. doi: 10.1186/s12985-024-02602-9.
The three members of the genus capripoxvirus (CaPV), lumpy skin disease virus (LSDV), sheeppox virus (SPPV), and goatpox virus (GTPV) have common hosts and areas of overlapping geographical distribution with Rift Valley fever virus (RVFV). Hence, to ensure more cost-effective disease surveillance we developed and evaluated a Luminex assay for the simultaneous detection of antibodies against CaPV and RVFV in domestic ruminants. In cattle, the assay had a sensitivity (Se) of 98.7% and a specificity (Sp) of 98.3% in detecting anti-LSDV antibodies; both diagnostic parameters were 100% for the detection of anti-RVFV antibodies in this species. In sheep and goats, Se and Sp were 100% for the detection of anti-SPPV and anti-GTPV antibodies while they were 100% and 98.9%, respectively for the detection of anti-RVFV antibody. The assay did not cross react with anti-parapoxvirus antibodies of cattle, sheep, and goats. This multiplex serological assay offers a practical tool for accurate detection and monitoring of the immunological status of domestic ruminant populations against veterinary and socio-economically important capripox- and phleboviral infections, thus has the potential to aid in the strategic application of vaccination programmes.
山羊痘病毒属(CaPV)的三个成员,即结节性皮肤病病毒(LSDV)、绵羊痘病毒(SPPV)和山羊痘病毒(GTPV),与裂谷热病毒(RVFV)有共同的宿主且地理分布区域重叠。因此,为确保更具成本效益的疾病监测,我们开发并评估了一种用于同时检测家养反刍动物中抗CaPV和RVFV抗体的Luminex检测方法。在牛中,该检测方法检测抗LSDV抗体的灵敏度(Se)为98.7%,特异性(Sp)为98.3%;在检测该物种中的抗RVFV抗体时,这两个诊断参数均为100%。在绵羊和山羊中,检测抗SPPV和抗GTPV抗体的Se和Sp均为100%,而检测抗RVFV抗体时,Se和Sp分别为100%和98.9%。该检测方法与牛、绵羊和山羊的抗副痘病毒抗体无交叉反应。这种多重血清学检测方法为准确检测和监测家养反刍动物群体针对兽医和社会经济上重要的痘病毒和白蛉病毒感染的免疫状态提供了一种实用工具,因此有可能有助于疫苗接种计划的战略应用。