首页> 外文期刊>Journal of Virological Methods >Evaluation of Fast Technology Analysis (FTA) cards as an improved method for specimen collection and shipment targeting viruses associated with Bovine Respiratory Disease Complex.
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Evaluation of Fast Technology Analysis (FTA) cards as an improved method for specimen collection and shipment targeting viruses associated with Bovine Respiratory Disease Complex.

机译:快速技术分析(FTA)卡的评估是一种针对与牛呼吸系统疾病相关的病毒进行标本收集和运输的改进方法。

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In order to improve the analytic quality of respiratory specimens collected from cattle for nucleic acid-based diagnosis, a study was undertaken to verify realtime PCR efficiency of specimens collected and stabilized on FTA CardsTM, filter paper which is treated chemically. Nucleic acids collected using FTA Cards without the need for a cold-chain or special liquid media handling provided realtime PCR results consistent (96.8% agreement, kappa 0.923 [95% CI=0.89-0.96]) with the same specimens collected using traditional viral transport media and shipped on ice using the U.S. Department of Transportation mandated liquid handling requirements. Nucleic acid stabilization on FTA Cards was evaluated over a temperature range (-27 degrees C to +46 degrees C) for up to 14 days to mimic environmental conditions for diagnostic sample handling between collection and processing in a routine veterinary laboratory. No significant difference (P>=0.05) was observed in realtime PCR cycle threshold values over the temperature range and time storage conditions for Bovine Viral Diarrhea virus, Bovine Respiratory Syncytial virus, Bovine Coronavirus, and Bovine Herpesvirus I. The four viruses evaluated in the study are associated with Bovine Respiratory Disease Complex where improvements in ease and reliability of specimen collection and shipping would enhance the diagnostic quality of specimens collected in the field, and ultimately improve diagnostic efficiency.
机译:为了提高从牛收集的呼吸道样本的分析质量,以进行基于核酸的诊断,进行了一项研究,以验证通过FTA Cards TM 滤纸收集并稳定的样本的实时PCR效率。经过化学处理。使用FTA卡收集的核酸不需要冷链或特殊的液体介质处理,提供的实时PCR结果与使用传统病毒转运收集的相同样本的实时PCR结果一致(96.8%一致,kappa 0.923 [95%CI = 0.89-0.96])介质,并使用美国运输部规定的液体处理要求在冰上运输。在温度范围(-27摄氏度至+46摄氏度)下,对FTA卡上的核酸稳定度进行了长达14天的评估,以模拟环境条件,以便在常规兽医实验室中收集和处理之间进行诊断性样品处理。在牛病毒性腹泻病毒,牛呼吸道合胞病毒,牛冠状病毒和牛疱疹病毒I的温度范围和时间存储条件下,实时PCR循环阈值未观察到显着差异(P> = 0.05)。这项研究与牛呼吸系统疾病综合症有关,在此方面,标本收集和运输的便利性和可靠性的提高将提高野外采集标本的诊断质量,并最终提高诊断效率。

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