首页|猪繁殖与呼吸综合征病毒MS2装甲病毒样颗粒质控品的制备及应用

猪繁殖与呼吸综合征病毒MS2装甲病毒样颗粒质控品的制备及应用

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为研制一种可以应用猪繁殖与呼吸综合征病毒(PRRSV)实时荧光定量PCR(RT-qPCR)核酸检测的阳性质控品,本研究使用MS2噬菌体装甲RNA(Armored RNA)技术制备PRRSV-1和PRRSV-2 M基因的阳性质控品.将扩增的PRRSV-1和PRRSV-2 M基因进行纯化回收,连接到内含MS2成熟酶蛋白基因与衣壳蛋白的pET28b载体,通过转化至BL21(DE3)后,经IPTG诱导表达,利用PEG6000沉淀法纯化,制备出内含PRRSV M 基因装甲RNA病毒样颗粒(AR-PRRSV).后续进行性能评估,作为PRRSV-1和PRRSV-2 M基因的阳性质控品,AR-PRRSV1M和AR-PRRSV2M使用YY/T 1652-2019标准进行计算,数据表明均匀性良好,-20、4、25 ℃能稳定保存60 d,37 ℃能稳定保存30 d.使用RT-qPCR进行初步定量后,利用数字定量PCR(ddPCR)对制备的装甲病毒样颗粒AR-PRRSV1M 和 AR-PRRSV2M 进行定值,结果 104 拷贝/μL 的 AR-PRRSV1M 和 AR-PRRSV2M ddPCR 定值均为(1.33±0.50)×104拷贝/μL.本研究结果表明,应用定值后的AR-PRRSVM,能够实现对检测全过程(核酸提取、反转录和RT-qPCR)的质量控制.
Preparation and application of PRRSV MS2 armored virus-like particles qualityas control products
In order to develop a positive quality control products for the detection of porcine repro-ductive and respiratory syndrome virus(PRRSV)nucleic acid by real-time fluorescent quantitative PCR(RT-qPCR),the positive quality control products of PRRSV-1 and PRRSV-2 M genes were prepared using armored RNA technology of MS2 phage.PRRSV-1 and PRRSV-2 M genes were amplified,purified and recovered,and ligated into pET28b vector containing MS2 mature enzyme protein gene and capsid protein.After transformed into BL21(DE3),the gene products were in-duced by IPTG and purified by PEG6000 precipitation method to prepare the armored RNA virus-like particles(AR-PRRSV)containing PRRSV M gene.Following the performance evaluation,as the positive quality control products of PRRSV-1 and PRRSV-2 M genes,AR-PRRSV1M and AR-PRRSV2M were calculated using YY/T 1652-2019 standard.Results showed that it had a good u-niformity,stable storage for the armored virus-like particles at-20,4,25 ℃ for 60 d,and 37 ℃ for 30 d.The prepared armored virus-like particles AR-PRRSV1M and AR-PRRSV2M were deter-mined by digital quantitative PCR(ddPCR)after preliminary quantification by RT-qPCR.The 104 copies/μL of AR-PRRSV1M and AR-PRRSV2M ddPCR fixation was(1.33+0.50)× 104 cop-ies/μL.The above results indicates that the AR-PRRSVM can be used as the quality control of the whole detection process(nucleic acid extraction,reverse transcription and RT-qPCR).

何嘉敏、庞旋飞、罗律、杨佳臻、张宝真、伍建敏、刘文娜、李中圣、白挨泉

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佛山科学技术学院生命工程与工程学院,广东佛山 528231

广东海大畜牧兽医研究院有限公司,广东 广州 511400

猪繁殖与呼吸综合征病毒 装甲RNA 核酸检测 质控品

2024

中国兽医学报
吉林大学

中国兽医学报

CSTPCD北大核心
影响因子:0.702
ISSN:1005-4545
年,卷(期):2024.44(11)