El-Tholoth Mohamed, Bai Huiwen, Mauk Michael G, Anis Eman, Bau Haim H
Department of Virology, Faculty of Veterinary Medicine, Mansoura University, Mansoura 35516, Egypt.
Department of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, PA 19104, USA.
Animals (Basel). 2021 Nov 9;11(11):3203. doi: 10.3390/ani11113203.
Infectious laryngotracheitis (ILT) is a viral disease of chickens' respiratory system that imposes considerable financial burdens on the chicken industry. Rapid, simple, and specific detection of this virus is crucial to enable proper control measures. Polymerase chain reaction (PCR)-based molecular tests require relatively expensive instruments and skilled personnel, confining their application to centralized laboratories. To enable chicken farms to take timely action and contain the spread of infection, we describe a rapid, simple, semi-quantitative benchtop isothermal amplification (LAMP) assay, and a field-deployable microfluidic device for the diagnosis of ILTV infection in chickens. Our assay performance was compared and favorably agreed with quantitative PCR (qPCR). The sensitivity of our real-time LAMP test is 250 genomic copies/reaction. Clinical performance of our microfluidic device using samples from diseased chickens showed 100% specificity and 100% sensitivity in comparison with benchtop LAMP assay and the gold-standard qPCR. Our method facilitates simple, specific, and rapid molecular ILTV detection in low-resource veterinary diagnostic laboratories and can be used for field molecular diagnosis of suspected ILT cases.
传染性喉气管炎(ILT)是一种鸡呼吸系统的病毒性疾病,给养鸡业带来了相当大的经济负担。快速、简单且特异的该病毒检测对于采取适当的控制措施至关重要。基于聚合酶链反应(PCR)的分子检测需要相对昂贵的仪器和技术人员,限制了其仅能应用于集中化实验室。为使养鸡场能够及时采取行动并遏制感染传播,我们描述了一种快速、简单的半定量台式等温扩增(LAMP)检测方法,以及一种可用于现场的微流控装置,用于诊断鸡的传染性喉气管炎病毒(ILTV)感染。我们将检测性能与定量PCR(qPCR)进行了比较,结果令人满意。我们实时LAMP检测的灵敏度为250个基因组拷贝/反应。使用病鸡样本对我们微流控装置进行的临床性能评估显示,与台式LAMP检测和金标准qPCR相比,其特异性和灵敏度均为100%。我们的方法便于在资源有限的兽医诊断实验室进行简单、特异且快速的分子ILTV检测,可用于疑似ILT病例的现场分子诊断。