Kim Yong Kwan, Lim Seong-In, Cho Yoon-Young, Song Jae-Young, Kim JoonBae, An Dong-Jun
Viral Disease Division, Animal and Plant Quarantine Agency, Anyang, Gyeonggi-do, 430-757, Republic of Korea.
Median Diagnostics Inc, Chuncheon, Gangwon-do, 200-883, Republic of Korea.
J Virol Methods. 2014 Aug;204:44-8. doi: 10.1016/j.jviromet.2014.03.020. Epub 2014 Mar 31.
A novel assay, the CSFV DNAChip, was developed to clearly and rapidly discriminate three genotypes of classical swine fever virus (CSFV). Total RNA was extracted from clinical samples and then subjected to a one-step reverse-transcription polymerase chain reaction (RT-PCR) using Cy3-labeled primers from the 5' non-coding region (NCR) of CSFV. Amplicons were hybridized to the CSFV DNAChip and fluorescence scanning was performed for detection of CSFV. A cut-off fluorescence intensity value of 5000 was determined by two-graph receiver operating curve (TG-ROC) analysis. The limit of detection values for the developed DNA chip assay were 0.313ng/μL for amplicon concentration and 1TCID50/100μL for virus titer. Using the developed DNA chip, 157 field samples (91 CSFV-positive and 66 CSFV-negative) were investigated. The genotypes determined by the CSFV DNAChip agreed completely with those determined by nucleotide sequence analysis of the viral genome. The developed CSFV DNAChip will be helpful in implementing a CSFV eradication strategy, as it provides a rapid and accurate diagnostic assay that can discriminate easily among CSFV genotypes.
一种新型检测方法——猪瘟病毒DNA芯片被开发出来,用于清晰、快速地区分经典猪瘟病毒(CSFV)的三种基因型。从临床样本中提取总RNA,然后使用来自CSFV 5'非编码区(NCR)的Cy3标记引物进行一步逆转录聚合酶链反应(RT-PCR)。扩增产物与猪瘟病毒DNA芯片杂交,并进行荧光扫描以检测CSFV。通过双图接收器操作曲线(TG-ROC)分析确定了5000的截止荧光强度值。所开发的DNA芯片检测方法的检测限为扩增产物浓度0.313ng/μL,病毒滴度1TCID50/100μL。使用所开发的DNA芯片,对157份现场样本(91份CSFV阳性和66份CSFV阴性)进行了检测。猪瘟病毒DNA芯片确定的基因型与病毒基因组核苷酸序列分析确定的基因型完全一致。所开发的猪瘟病毒DNA芯片将有助于实施猪瘟病毒根除策略,因为它提供了一种快速、准确的诊断方法,可以轻松地区分猪瘟病毒基因型。