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Assessment of the sensitivity of primary cells and cell lines to the Southern African Territories (SAT) serotypes in the diagnosis of foot-and-mouth disease virus

机译:评估原代细胞和细胞系对口蹄疫病毒诊断中南部非洲地区(SAT)血清型的敏感性

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摘要

Virus isolation is the gold standard for foot-and-mouth disease virus (FMDV) detection in diagnostic procedures. This technique is heavily reliant on the use of sensitive cells for rapid and accurate detection of FMDV. To investigate the sensitivity of RM (primary lamb kidney cells), BHK-21 (baby hamster kidney cells) and IR-P1 (a derivative of female pig kidney cells) to infection with FMDV of the Southern African Territories (SAT) serotypes, we examined the virus concentration required to induce cytopathic effect (CPE) on each cell type. The results suggested that sensitivity of RM and IR-P1 cells was high and not significantly different ( < 0.05). BHK-21 however, exhibited low sensitivity to the strains used. Comparisons of three batches of each cell type were also done to establish the consistency of the sensitivity of these cells to FMDV infection. IR-P1 and BHK-21 cell batches gave consistent results for all samples used whereas RM cells showed significant differences ( > 0.05) between batches. TCID 50/ml was used to determine the viral titre required to induce CPE. IR-P1 cell line proved to have consistently higher TCID50/mL for all cell batches while RM cell batches displayed a difference in TCID50/mL values. The IR-P1 cell line was concluded to be a good cell culture system for virus isolation as it showed relatively high and reproducible sensitivity to all the FMDV strains used. The findings of this study indicate that the use of IR-P1 cell line could be considered for FMDV diagnostic work.
机译:病毒隔离是诊断程序中口蹄疫病毒(FMDV)检测的金标准。该技术在很大程度上依赖于使用敏感细胞来快速准确地检测FMDV。为了研究RM(初级羊肾细胞),BHK-21(婴儿仓鼠肾细胞)和IR-P1(雌性猪肾细胞的衍生物)对南部非洲地区(SAT)血清型FMDV感染的敏感性,我们检查了诱导每种细胞类型的细胞病变效应(CPE)所需的病毒浓度。结果表明,RM和IR-P1细胞的敏感性很高,并且没有显着差异(<0.05)。然而,BHK-21对所用菌株表现出低敏感性。还对每种细胞类型的三批进行了比较,以建立这些细胞对FMDV感染敏感性的一致性。 IR-P1和BHK-21细胞批次对所有使用的样品给出一致的结果,而RM细胞在批次之间显示出显着差异(> 0.05)。 TCID 50 / ml用于确定诱导CPE所需的病毒滴度。事实证明,IR-P1细胞系所有批次的TCID50 / mL始终较高,而RM细胞批次的TCID50 / mL值却有所不同。结论IR-P1细胞系是用于病毒分离的良好细胞培养系统,因为它对所有使用的FMDV菌株显示出相对较高且可重现的敏感性。这项研究的结果表明,可以考虑将IR-P1细胞系用于FMDV诊断工作。

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