Nursery plant propagation by grafting has been widely used in modern viticulture to minimize the damage caused by biotic and abiotic stresses.In grapevine(Vitis spp.),an effective way to control disease damage is to p...Nursery plant propagation by grafting has been widely used in modern viticulture to minimize the damage caused by biotic and abiotic stresses.In grapevine(Vitis spp.),an effective way to control disease damage is to provide producers and growers with pathogen-free stock plants.In this study,five grapevine rootstock varieties,‘SO4’,‘101-14’,‘5BB’,‘110R’and‘1103P’,were selected as explants to establish an in vitro culture protocol,and three species of grapevine viruses were tested by real-time RT-PCR.The results showed that MS medium supplemented with 0.2 mg/L IBA,1.0 mg/L 6-BA,0.5 mg/L KT,4.0 mg/L adenine for culture initiation,and WPM supplemented with 0.2 mg/L IBA for subculture were suitable for all five rootstock varieties,with multiplication coefficients ranging from 1.6 to 4.4.Virus testing showed that single RT-PCR was more effective for detecting the three viruses compared to double or triple RT-PCR.Only plantlets free from the aforementioned viruses were retained for subculture.Plantlets were hardened at room temperature under natural lighting in Hoagland solution for 2 weeks and transplanted to pots filled with mixed media in a greenhouse.This protocol is applicable for rapid propagation of the five grapevine rootstock varieties and can be used for commercial production of virus-free grapevine stocks.展开更多
The coronavirus disease 2019(covID-19)pandemic has progressed over 2 years since its onset causing significant health concerns all over the world and is currently curtailed by mass vaccination.mmunity acquired against...The coronavirus disease 2019(covID-19)pandemic has progressed over 2 years since its onset causing significant health concerns all over the world and is currently curtailed by mass vaccination.mmunity acquired against severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)can be following either infection or vaccination.However,one can never be sure whether the acquired immunity is adequate to protect the individual from subsequent infection because of three important factors:individual variations in humoral response dynamics,waning of protective antibodies over time,and the emergence of immune escape mutants.Therefore,a test that can accurately dfferentiate the protected from the vulnerable is the need of the hour.The plaque reduction neutralization assay is the conventional gold standard test for estimating the titers of neutralizing antibodies that confer protection.However,it has got several drawbacks,which hinder the practical application of this test for wide-scale usage.Hence,various tests have been developed to detect protective immunity against SARS-CoV-2 that directly or indirectly assess the presence of neutralizing antibodies to SARS-Cov-2 in a lower biosafety setting.In this review,the pros and cons of the currently available assays are elaborated in detail and special focus is put on the scope of the novel split nanoluciferase technology for detecting SARS-CovV-2 neutralizing antibodies.展开更多
文摘Nursery plant propagation by grafting has been widely used in modern viticulture to minimize the damage caused by biotic and abiotic stresses.In grapevine(Vitis spp.),an effective way to control disease damage is to provide producers and growers with pathogen-free stock plants.In this study,five grapevine rootstock varieties,‘SO4’,‘101-14’,‘5BB’,‘110R’and‘1103P’,were selected as explants to establish an in vitro culture protocol,and three species of grapevine viruses were tested by real-time RT-PCR.The results showed that MS medium supplemented with 0.2 mg/L IBA,1.0 mg/L 6-BA,0.5 mg/L KT,4.0 mg/L adenine for culture initiation,and WPM supplemented with 0.2 mg/L IBA for subculture were suitable for all five rootstock varieties,with multiplication coefficients ranging from 1.6 to 4.4.Virus testing showed that single RT-PCR was more effective for detecting the three viruses compared to double or triple RT-PCR.Only plantlets free from the aforementioned viruses were retained for subculture.Plantlets were hardened at room temperature under natural lighting in Hoagland solution for 2 weeks and transplanted to pots filled with mixed media in a greenhouse.This protocol is applicable for rapid propagation of the five grapevine rootstock varieties and can be used for commercial production of virus-free grapevine stocks.
基金supported by an Japan Agency for Medical Research and Development(AMED)grant(P21fk0108104)to A.R.
文摘The coronavirus disease 2019(covID-19)pandemic has progressed over 2 years since its onset causing significant health concerns all over the world and is currently curtailed by mass vaccination.mmunity acquired against severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)can be following either infection or vaccination.However,one can never be sure whether the acquired immunity is adequate to protect the individual from subsequent infection because of three important factors:individual variations in humoral response dynamics,waning of protective antibodies over time,and the emergence of immune escape mutants.Therefore,a test that can accurately dfferentiate the protected from the vulnerable is the need of the hour.The plaque reduction neutralization assay is the conventional gold standard test for estimating the titers of neutralizing antibodies that confer protection.However,it has got several drawbacks,which hinder the practical application of this test for wide-scale usage.Hence,various tests have been developed to detect protective immunity against SARS-CoV-2 that directly or indirectly assess the presence of neutralizing antibodies to SARS-Cov-2 in a lower biosafety setting.In this review,the pros and cons of the currently available assays are elaborated in detail and special focus is put on the scope of the novel split nanoluciferase technology for detecting SARS-CovV-2 neutralizing antibodies.
