Kaushik Sarshti, Maan Sushila, Batra Kanisht, Sindhu Swati, Kadian Vijay, Kumar Aman
Lala Lajpat Rai University of Veterinary and Animal Sciences (LUVAS), Hisar, Haryana, India.
PLoS One. 2025 Jul 2;20(7):e0326700. doi: 10.1371/journal.pone.0326700. eCollection 2025.
Porcine enterovirus G (PEV-G) presents a considerable threat to the swine industry, causing a range of diseases that include diarrhea, encephalomyelitis, reproductive disorders, and respiratory infections. Conventional diagnostic approaches, such as virus isolation and RT-PCR, are frequently labor-intensive and reliant on specialized equipments. Therefore, there is an immediate need for isothermal nucleic acid amplification techniques-specifically, Recombinase Polymerase Amplification (RPA) and Polymerase Spiral Reaction (PSR) that offer rapid, sensitive, and field-deployable detection of PEV-G. In this study, we successfully developed and optimized two isothermal nucleic acid amplification assays namely RPA/RT-RPA and PSR/RT-PSR to detect PEV-G in swine populations in Haryana. Primers were specifically designed to target the polyprotein region of PEV-G for both assays. Optimal conditions regarding temperature, incubation time, primer concentration, and magnesium ion concentration were established. The RPA assay demonstrated a sensitivity of 1.417 × 10⁴ copies with a detection time of just 20 minutes. The PSR assay exhibited a lower sensitivity of 2.3 x 105 copies in comparison to RPA assay in gel based detection system and required 2.5 hours for detection. Both assays showed exceptional specificity for PEV-G, with no observable cross-reactivity with other related porcine viruses. Additionally, visual detection using Picogreen dye provided a practical solution for field use, with limits of detection of 14 copies for RPA and 2.3 copies for PSR. Validation on 100 archived field samples showed that isothermal assays have comparable sensitivity to conventional PCR. This study underscores the potential of RPA and PSR as effective and cost-efficient diagnostic tools, enabling timely and precise detection of PEV-G in both laboratory and field contexts. Such advancements are vital for improving disease management strategies and reducing economic losses within the swine industry.
猪肠道病毒G(PEV-G)对养猪业构成了相当大的威胁,可引发一系列疾病,包括腹泻、脑脊髓炎、繁殖障碍和呼吸道感染。传统的诊断方法,如病毒分离和逆转录聚合酶链反应(RT-PCR),通常劳动强度大且依赖专业设备。因此,迫切需要等温核酸扩增技术,特别是重组酶聚合酶扩增(RPA)和聚合酶螺旋反应(PSR),以实现对PEV-G的快速、灵敏且可现场部署的检测。在本研究中,我们成功开发并优化了两种等温核酸扩增检测方法,即RPA/RT-RPA和PSR/RT-PSR,用于检测哈里亚纳邦猪群中的PEV-G。两种检测方法的引物均专门设计用于靶向PEV-G的多聚蛋白区域。确定了温度、孵育时间、引物浓度和镁离子浓度的最佳条件。RPA检测方法的灵敏度为1.417×10⁴拷贝,检测时间仅为20分钟。在基于凝胶的检测系统中,PSR检测方法的灵敏度低于RPA检测方法,为2.3×10⁵拷贝,检测需要2.5小时。两种检测方法对PEV-G均表现出极高的特异性,与其他相关猪病毒未观察到交叉反应。此外,使用Picogreen染料进行视觉检测为现场使用提供了一种实用的解决方案,RPA的检测限为14拷贝,PSR的检测限为2.3拷贝。对100份存档现场样本的验证表明,等温检测方法与传统PCR具有相当的灵敏度。本研究强调了RPA和PSR作为有效且经济高效的诊断工具的潜力,能够在实验室和现场环境中及时、精确地检测PEV-G。这些进展对于改善疾病管理策略和减少养猪业的经济损失至关重要。