Zhengkaixu , Carl S. Luciano , Susan T. Ballard , Roberte E. Rhoads , John G. Shaw
{"title":"脂质体包封多病毒RNA对烟草原生质体的侵染","authors":"Zhengkaixu , Carl S. Luciano , Susan T. Ballard , Roberte E. Rhoads , John G. Shaw","doi":"10.1016/0304-4211(84)90216-5","DOIUrl":null,"url":null,"abstract":"<div><p>The RNA of the potyvirus, tobacco vein mottling virus (TVMV), was encapsulated in reverse-phase evaporation vesicle liposomes containing phosphatidylserine and cholesterol. The liposomes were used to inoculate tobacco mesophyll protoplasts. Analysis of extracts of protoplasts, by enzyme-linked immunosorbent assay (ELISA), hybridization with labeled cDNA, electron microscopy and infectivity assays, indicated that significant multiplication of the virus had occurred after incubation of the protoplasts for 2–3 days. It was estimated that approx. 15% of the protoplasts had become infected.</p></div>","PeriodicalId":20221,"journal":{"name":"Plant Science Letters","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1984-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0304-4211(84)90216-5","citationCount":"4","resultStr":"{\"title\":\"Infection of tobacco protoplasts with liposome-encapsulated potyviral RNA\",\"authors\":\"Zhengkaixu , Carl S. Luciano , Susan T. Ballard , Roberte E. Rhoads , John G. Shaw\",\"doi\":\"10.1016/0304-4211(84)90216-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The RNA of the potyvirus, tobacco vein mottling virus (TVMV), was encapsulated in reverse-phase evaporation vesicle liposomes containing phosphatidylserine and cholesterol. The liposomes were used to inoculate tobacco mesophyll protoplasts. Analysis of extracts of protoplasts, by enzyme-linked immunosorbent assay (ELISA), hybridization with labeled cDNA, electron microscopy and infectivity assays, indicated that significant multiplication of the virus had occurred after incubation of the protoplasts for 2–3 days. It was estimated that approx. 15% of the protoplasts had become infected.</p></div>\",\"PeriodicalId\":20221,\"journal\":{\"name\":\"Plant Science Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1984-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0304-4211(84)90216-5\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Science Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0304421184902165\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Science Letters","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0304421184902165","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Infection of tobacco protoplasts with liposome-encapsulated potyviral RNA
The RNA of the potyvirus, tobacco vein mottling virus (TVMV), was encapsulated in reverse-phase evaporation vesicle liposomes containing phosphatidylserine and cholesterol. The liposomes were used to inoculate tobacco mesophyll protoplasts. Analysis of extracts of protoplasts, by enzyme-linked immunosorbent assay (ELISA), hybridization with labeled cDNA, electron microscopy and infectivity assays, indicated that significant multiplication of the virus had occurred after incubation of the protoplasts for 2–3 days. It was estimated that approx. 15% of the protoplasts had become infected.