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建立一种直接 PCR 检测方法,用于同时检测粗组织样品中的非洲猪瘟和古典猪瘟。

Establishment of a Direct PCR Assay for Simultaneous Differential Diagnosis of African Swine Fever and Classical Swine Fever Using Crude Tissue Samples.

机构信息

Exotic Disease Research Station, National Institute of Animal Health, National Agriculture and Food Research Organization, 6-20-1 Josui-honcho, Kodaira 187-0022, Tokyo, Japan.

Takara Bio Inc., Nojihigashi 7-4-38, Kusatsu 525-0058, Shiga, Japan.

出版信息

Viruses. 2022 Feb 28;14(3):498. doi: 10.3390/v14030498.

DOI:10.3390/v14030498
PMID:35336904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8948687/
Abstract

African swine fever (ASF) and classical swine fever (CSF) are contagious swine diseases that are clinically indistinguishable from each other; hence, reliable test methods for accurate diagnosis and differentiation are highly demanded. By employing a buffer system suitable for crude extraction of nucleic acids together with an impurity-tolerant enzyme, we established a multiplex assay of real-time reverse-transcription polymerase chain reaction (rRT-PCR) for simultaneous detection of ASF virus (ASFV), CSF virus (CSFV) and swine internal control derived genes in a sample without the need for prior purification of viral nucleic acids. We applied this method to test serum and tissue samples of infected pigs and wild boars and compared the statistical sensitivities and specificities with those of standard molecular diagnostic methods. When a serum was used as a test material, the newly established assay showed 94.4% sensitivity for both and 97.9 and 91.9% specificity for ASFV and CSFV detection, respectively. In contrast, the results were 100% identical with those obtained by the standard methods when a crude tissue homogenate was used as a test material. The present data indicate that this new assay offers a practical, quick, and reliable technique for differential diagnosis of ASF and CSF where geographical occurrences are increasingly overlapping.

摘要

非洲猪瘟 (ASF) 和古典猪瘟 (CSF) 是具有传染性的猪病,在临床上彼此难以区分;因此,非常需要可靠的测试方法来进行准确的诊断和区分。我们采用了一种适合粗提核酸的缓冲系统和一种耐受杂质的酶,建立了一种用于实时逆转录聚合酶链反应 (rRT-PCR) 的多重检测方法,可在无需预先纯化病毒核酸的情况下,同时检测样品中的 ASF 病毒 (ASFV)、CSFV 和猪内参基因。我们将该方法应用于感染猪和野猪的血清和组织样本的检测,并将其与标准分子诊断方法的统计灵敏度和特异性进行了比较。当使用血清作为检测材料时,新建立的检测方法对两者的灵敏度均为 94.4%,对 ASFV 和 CSF 的特异性分别为 97.9%和 91.9%。相比之下,当使用粗制组织匀浆作为检测材料时,其结果与标准方法完全一致。这些数据表明,这种新的检测方法为 ASF 和 CSF 的鉴别诊断提供了一种实用、快速和可靠的技术,因为它们在地理上的重叠越来越多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/c1568356de89/viruses-14-00498-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/a7ef1f711ccf/viruses-14-00498-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/0c3abe07469d/viruses-14-00498-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/39e1a59c39d6/viruses-14-00498-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/ed3eb204027c/viruses-14-00498-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/c1568356de89/viruses-14-00498-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/a7ef1f711ccf/viruses-14-00498-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/0c3abe07469d/viruses-14-00498-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/39e1a59c39d6/viruses-14-00498-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/ed3eb204027c/viruses-14-00498-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1645/8948687/c1568356de89/viruses-14-00498-g005.jpg

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