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家禽新城疫病毒的逆转录重组酶辅助扩增检测法

Reverse Transcription Recombinase-Aided Amplification Assay for Newcastle Disease Virus in Poultry.

作者信息

Yehia Nahed, Abd El Wahed Ahmed, Mohamed Ahmed Abd Elhalem, Arafa Abdelsattar, Said Dalia, Shalaby Mohamed A, Ceruti Arianna, Truyen Uwe, Kobialka Rea Maja

机构信息

Reference Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Agriculture Research Center, Dokki, Giza 12618, Egypt.

Institute of Animal Hygiene and Veterinary Public Health, Leipzig University, 04109 Leipzig, Germany.

出版信息

Pathogens. 2025 Sep 1;14(9):867. doi: 10.3390/pathogens14090867.

Abstract

Newcastle disease (ND) is a highly contagious and economically significant viral infection that affects poultry globally, with recurrent outbreaks occurring even among vaccinated flocks in Egypt. Caused by the Newcastle disease virus (NDV), the disease results in substantial losses due to high mortality rates, decreased productivity, and the imposition of trade restrictions. This study aimed to develop a rapid, sensitive, and field-deployable diagnostic assay based on real-time reverse transcription recombinase-aided amplification (RT-RAA) for the detection of all NDV genotypes in clinical avian specimens. Primers and an exo-probe were designed based on the most conserved region of the NDV matrix gene. After testing ten primer combinations, the pair NDV RAA-F1 and RAA-R5 demonstrated the highest sensitivity, detecting as low as 6.89 EID/mL (95% CI). The RT-RAA assay showed excellent clinical sensitivity and specificity, with no cross-reactivity to other common respiratory pathogens such as avian influenza virus, infectious bronchitis virus, or infectious laryngotracheitis virus. All 25 field samples that were tested positive by real-time RT-PCR, including those with high CT values (~35), were detected by RT-RAA in 2-11 min, indicating superior sensitivity and speed. The assay requires only basic equipment and can be performed under isothermal conditions, making it highly suitable for on-site detection in resource-limited or rural settings. The successful implementation of RT-RAA can improve NDV outbreak response, support timely vaccination strategies, and enhance disease control efforts. Overall, the assay presents a promising alternative to conventional diagnostic methods, contributing to the sustainability and productivity of the poultry sector in endemic regions.

摘要

新城疫(ND)是一种具有高度传染性且在经济上具有重要意义的病毒感染,影响着全球的家禽,即使在埃及接种过疫苗的鸡群中也会反复爆发。该疾病由新城疫病毒(NDV)引起,由于高死亡率、生产力下降以及贸易限制的实施,导致了巨大的损失。本研究旨在开发一种基于实时逆转录重组酶辅助扩增(RT-RAA)的快速、灵敏且可在现场部署的诊断检测方法,用于检测临床禽类样本中的所有NDV基因型。根据NDV基质基因最保守的区域设计了引物和外切探针。在测试了十种引物组合后,NDV RAA-F1和RAA-R5这一对引物表现出最高的灵敏度,可检测低至6.89 EID/mL(95%置信区间)。RT-RAA检测方法显示出优异的临床灵敏度和特异性,与其他常见呼吸道病原体如禽流感病毒、传染性支气管炎病毒或传染性喉气管炎病毒无交叉反应。所有25份经实时RT-PCR检测呈阳性的现场样本,包括那些CT值较高(约35)的样本,均在2 - 11分钟内被RT-RAA检测到,表明其具有更高的灵敏度和速度。该检测方法仅需基本设备,且可在等温条件下进行,非常适合在资源有限或农村地区进行现场检测。RT-RAA的成功应用可改善新城疫疫情应对,支持及时的疫苗接种策略,并加强疾病防控工作。总体而言,该检测方法为传统诊断方法提供了一种有前景的替代方案,有助于流行地区家禽业的可持续发展和生产力提升。

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