[结合 DNA 聚合酶和实时 PCR 仪器检测未经授权转基因木瓜方法的验证研究]。

IF 0.2 4区 农林科学 Q4 FOOD SCIENCE & TECHNOLOGY
Chie Taguchi, Keisuke Soga, Yohei Sugano, Aoi Hosokawa, Miyu Sugino, Jumpei Narushima, Satoko Yoshiba, Reiko Adachi, Norihito Shibata
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引用次数: 0

摘要

在日本官方对未经授权的转基因木瓜的检测方法中,主要使用两种含 DNA 聚合酶的实时 PCR 试剂(TaqMan Gene Master Mix [TaqMan Gene] 或 FastGene QPCR Probe Mastermix w/ROX [FastGene])中的一种进行测量。2022 年,我们对未经授权的转基因木瓜品系 PRSV-YK 进行了实验室性能研究,结果发现,使用 TaqMan 基因与 7500 Fast & 7500 Real-Time PCR 系统 (ABI7500) 和 QuantStudio 12K Flex (QS12K) 进行 PRSV-YK 检测测试时,阈值周期 (Cq) 值很高,这表明可能会出现假阴性。需要对所有未经授权的转基因木瓜品系检测测试是否可能存在类似问题进行评估。在本研究中,我们对未经授权的转基因木瓜品系(PRSV-YK、PRSV-SC 和 PRSV-HN)、花椰菜花叶病毒 35S 启动子(CaM)和木瓜阳性对照(Chy)进行了检测测试、并研究了两种类型的 DNA 聚合酶(TaqMan Gene 和 FastGene)和三种类型的实时 PCR 仪器(ABI7500、QS12K 和 LightCycler 480 Instrument II [LC480])对每种检测方法的检测限(LOD)的影响。在使用 ABI7500 和 QS12K 进行的 PRSV-YK 和 PRSV-SC 检测试验中,使用 TaqMan Gene 进行的测量显示出比 FastGene 更高的 LOD。在这种情况下,扩增图上的指数扩增曲线得到了证实;但是,扩增曲线没有越过ΔRn阈值线,在阈值线=0.2的情况下,没有得到正确的Cq值。其他检测(使用 ABI7500 和 QS12K 进行的 PRSV-HN、CaM 和 Chy 检测,以及使用 LC480 进行的所有检测)显示,使用任一种 DNA 聚合酶进行的各项检测的 LOD 均无明显差异。因此,在使用ABI7500或QS12K进行PRSV-YK和PRSV-SC检测测试时,应使用FastGene,以避免在低混合水平下对含有转基因木瓜品系PRSV-YK和PRSV-SC的食品进行假阴性检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Verification Study of the Detection Method for Unauthorized Genetically Modified Papaya by Combining DNA Polymerases and Real-time PCR Instruments].

In the Japanese official detection method for unauthorized genetically modified (GM) papayas, one of two types of real-time PCR reagents with DNA polymerase (TaqMan Gene Master Mix [TaqMan Gene] or FastGene QPCR Probe Mastermix w/ROX [FastGene]) is primarily used for measurement. In 2022, we conducted a laboratory performance study on the unauthorized GM papaya line PRSV-YK, and the results revealed that high threshold cycle (Cq) values for the PRSV-YK detection test were obtained using TaqMan Gene with the 7500 Fast & 7500 Real-Time PCR System (ABI7500) and QuantStudio 12K Flex (QS12K), indicating the possibility of false negatives. The possibility of similar problems with all unauthorized GM papaya lines detection tests needs to be evaluated. In this study, we performed detection tests on unauthorized GM papaya lines (PRSV-YK, PRSV-SC, and PRSV-HN), the cauliflower mosaic virus 35S promotor (CaM), and a papaya positive control (Chy), and examined how the limits of detection (LOD) for each test are affected by two types of DNA polymerases (TaqMan Gene and FastGene) and three types of real-time PCR instruments (ABI7500, QS12K, and LightCycler 480 Instrument II [LC480]). In the PRSV-YK and PRSV-SC detection tests using ABI7500 and QS12K, measurement with TaqMan Gene showed a higher LOD than FastGene. In this case, an exponential amplification curve was confirmed on the amplification plot; however, the amplification curve did not cross the ΔRn threshold line and the correct Cq value was not obtained with a threshold line=0.2. The other tests (PRSV-HN, CaM, and Chy with ABI7500 and QS12K, and all detection tests with LC480) showed no important differences in the LOD for each test using either DNA polymerase. Therefore, when performing PRSV-YK and PRSV-SC detection tests with the ABI7500 or QS12K, FastGene should be used to avoid false negatives for foods containing GM papaya lines PRSV-YK and PRSV-SC at low mixing levels.

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来源期刊
Food Hygiene and Safety Science
Food Hygiene and Safety Science Medicine-Public Health, Environmental and Occupational Health
CiteScore
0.70
自引率
0.00%
发文量
28
审稿时长
18-36 weeks
期刊介绍: Information not localized
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