期刊
PLANTS-BASEL
卷 12, 期 4, 页码 -出版社
MDPI
DOI: 10.3390/plants12040894
关键词
RT-qPCR; qELISA; bioassay; local lesion; Nicotiana spp; TaqMan; disinfection
After the entry of a regulated pathogen, it is important to destroy infected plants and disinfect the cultivated area. The selection of an effective disinfectant is crucial. This study investigated the application of quantitative ELISA, RT-qPCR, and bioassays for evaluating disinfectant efficacy. The results showed that bioassays were the only method capable of quantifying the differences in virus titer on different germ carriers and virus-infected plant sap.
After entry of a quarantine/regulated pathogen, infected plants shall be destroyed, and the cultivated area (e.g., greenhouse) shall be disinfected. Therefore, the selection of an effective disinfectant plays an important role. With the availability of different methods for virus quantification, we investigated the application of quantitative ELISA (qELISA), RT-qPCR (reverse transcription-quantitative polymerase chain reaction), and bioassays for the quantification of disinfectant efficacy. Therefore, we estimated the titer reduction in tomato brown rugose fruit virus (ToBRFV), a regulated pathogen, in plant sap and on germ carriers after treatment with MENNO Florades 4% for 16 h. The virus load before and after the treatment was measured with the mentioned methods. The RT-qPCR and qELISA methods showed very low efficacy in the presence of the disinfectant. Although bioassays are time-consuming, need purified particles for establishing the quantification models, and are less sensitive than RT-qPCR, they were able to quantify the differences in virus titer in the presence/absence of disinfectant. Interestingly, the bioassays reached at least the lower limit sensitivity of a qELISA. By being less sensitive to the presence of the disinfectant, bioassays proved to be the only technique for the determination of the disinfectant efficacy against ToBRFV on different germ carriers as well as on virus-infected plant sap.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据