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在口蹄疫病毒诊断中评估原代细胞和细胞系对南非领土(SAT)血清型的敏感性。

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.

作者信息

Kabelo T, Fana E, Lebani K

机构信息

Department of Biological Sciences and Biotechnology, Faculty of Science, Botswana International University of Science and Technology, Private Bag 16, Palapye, Botswana.

OIE FMD Regional Reference Laboratory for Sub-Saharan Africa, Botswana Vaccine Institute, Private Bag 0031, Gaborone, Botswana.

出版信息

Heliyon. 2020 May 7;6(5):e03905. doi: 10.1016/j.heliyon.2020.e03905. eCollection 2020 May.

Abstract

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.

摘要

病毒分离是口蹄疫病毒(FMDV)诊断程序中检测的金标准。该技术严重依赖于使用敏感细胞来快速准确地检测FMDV。为了研究原代羔羊肾细胞(RM)、幼仓鼠肾细胞(BHK-21)和猪肾细胞衍生物(IR-P1)对南非领土(SAT)血清型FMDV感染的敏感性,我们检测了在每种细胞类型上诱导细胞病变效应(CPE)所需的病毒浓度。结果表明,RM和IR-P1细胞的敏感性较高且无显著差异(<0.05)。然而,BHK-21对所用毒株表现出低敏感性。还对每种细胞类型的三批细胞进行了比较,以确定这些细胞对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本都给出了一致的结果,而RM细胞批次之间存在显著差异(>0.05)。使用半数组织培养感染剂量(TCID50/ml)来确定诱导CPE所需的病毒滴度。IR-P1细胞系被证明对所有细胞批次的TCID50/mL始终较高,而RM细胞批次的TCID50/mL值存在差异。IR-P1细胞系被认为是一种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毒株表现出相对较高且可重复的敏感性。本研究结果表明,在FMDV诊断工作中可以考虑使用IR-P1细胞系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef7e/7215193/f509eff7b72a/gr1.jpg

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