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Virol.53, 163–166 (1977).","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF01314857",{"doi":396},"10.1007\u002FBF01314857",{"id":20,"text":398,"url":20,"identifiers":399},"Perry, R. P., Kelley, D. E.: Gene transcription: Actinomycin D dose response for various RNA species. J. Cell Biol.43, 103a (1969).",{},{"id":356,"text":401,"url":358,"identifiers":402},"Powell, K. L., Courtney, R. J.: Polypeptides synthesized in herpes simplex virus type 2-infected HEp-2 cells. Virology66, 217–228 (1975).",{"doi":360},{"id":356,"text":404,"url":358,"identifiers":405},"Purifoy, D. J. M.: Comparison of DNA polymerase activities induced by herpes simplex virus type 1 and 2. Intervirology6, 356–366 (1975\u002F1976).",{"doi":360},{"id":407,"text":408,"url":409,"identifiers":410},"d6b77cb1-cdc1-4f5c-a71d-9d96e3ff9848","Purifoy, D. J. M., Benyesh-Melnick, M.: DNA polymerase induction by DNA-negative temperature-sensitive mutants of herpes simplex virus type 2. Virology68, 374–386 (1975).","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F0042682275902809",{"doi":411},"10.1016\u002F0042-6822(75)90280-9",{"id":356,"text":413,"url":358,"identifiers":414},"Thouless, M. E., Skinner, G. R. B.: Differences in the properties of thymidine kinase produced in cells infected with type 1 and type 2 herpes virus. J. gen. Virol.12, 195–197 (1971).",{"doi":360},{"id":416,"createTime":417,"updateTime":418,"relativeEntities":419,"slug":420,"properties":421,"entityType":121,"verifyStatus":240,"verifyTime":430,"verifyNote":242,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":431,"fullTextUrl":20,"authors":432,"publicationType":168,"publisherRelationship":450,"citationCount":21,"citationInfo":502,"publishDate":505,"publishYear":503,"citationAnalyzeStatus":351,"lastCitationAnalyze":418,"indexDatabases":506,"openAccess":20,"references":507,"isForceReanalyzing":224},"c9417368-350c-4944-8070-d0a4a4edd29a","2024-01-05T12:27:34.481+00:00","2026-08-18T20:44:24.427+00:00",[],"The-complete-genome-sequence-of-HetPV20-an1-an-alphapartitivirus-infecting-the-conifer-pathogenic-fungus-Heterobasidion-annosum",{"abstract":422,"title":424,"gsPaper":426,"doi":428},{"EN":423},"Root rot fungi of the genus Heterobasidion are highly destructive conifer pathogens in the northern Boreal forest region. This report describes the complete genome sequence of Heterobasidion partitivirus 20 infecting a Finnish strain of Heterobasidion annosum. The bisegmented dsRNA genome of HetPV20-an1 encodes a predicted RNA-dependent RNA polymerase of 605 amino acids (aa) and a capsid protein of 536 aa. Based on sequence similarity and phylogenetic analysis, this virus is a new member of the genus Alphapartitivirus. HetPV20-an1 shares ~65% RdRP aa sequence identity with the most similar virus strain, Rosellinia necatrix partitivirus 2, whereas the CP of HetPV20-an1 is most similar to that of rose partitivirus with ~27% overall aa sequence identity. HetPV20-an1 is only distantly related to previously known partitiviruses of Heterobasidion species and shares ~29% RdRP aa sequence identity and ~16% CP aa sequence identity with Heterobasidion partitivirus 1 from H. abietinum.",{"EN":425},"The complete genome sequence of HetPV20-an1, an alphapartitivirus infecting the conifer-pathogenic fungus Heterobasidion annosum",{"VOID":427},"[\"9565311241251533639\"]",{"VOID":429},"10.1007\u002Fs00705-018-3707-z","2024-05-03T23:50:41.663+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00705-018-3707-z",[433],{"id":434,"sortIndex":21,"researcher":20,"roles":435,"affiliations":436,"properties":445,"displayName":447,"givenName":20,"familyName":20},"e9571417-654e-4c9b-aa9b-8c9dd80dedd4",[129],[437],{"id":438,"sortIndex":21,"affiliation":439,"properties":20},"cbb74b39-9b24-490e-ac53-edfda08484c1",{"id":438,"createTime":20,"updateTime":20,"relativeEntities":440,"slug":20,"properties":441,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":444,"statistic":20},[],{"title":442},{"VI":443},"Natural Resources Institute Finland, Helsinki, Finland",[],{"title":446,"gsAuthor":448},{"VI":447},"Eeva J. Vainio",{"VOID":449},"[\"rX-DI-EAAAAJ\"]",{"url":431,"publisher":451,"properties":497},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":452,"slug":10,"properties":453,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":457,"manageAffiliations":466,"indexDatabases":477,"url":87,"thumbnailPath":20,"statistic":492,"gsStatistic":20,"type":100,"analyzePriority":20},[],{"issn":454,"title":455,"eissn":456},{"VOID":13},{"EN":15},{"VOID":17},[458,462],{"id":24,"createTime":20,"updateTime":20,"relativeEntities":459,"label":460,"description":461,"parentId":20,"standard":20,"scholarHubFieldId":20},[],{"EN":27},{},{"id":30,"createTime":20,"updateTime":20,"relativeEntities":463,"label":464,"description":465,"parentId":20,"standard":20,"scholarHubFieldId":20},[],{"EN":33},{},[467,472],{"id":37,"createTime":20,"updateTime":20,"relativeEntities":468,"slug":20,"properties":469,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":471,"statistic":20},[],{"title":470},{"EN":41},[43],{"id":45,"createTime":20,"updateTime":20,"relativeEntities":473,"slug":20,"properties":474,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":476,"statistic":20},[],{"title":475},{"EN":49},[43],[478,485],{"id":53,"indexDatabase":479,"url":64,"indexYears":65,"academicFieldIds":484,"indexDatabaseRanking":69},{"id":55,"createTime":20,"updateTime":20,"relativeEntities":480,"label":481,"description":482,"key":61,"publicationTags":483,"standard":20},[],{"EN":58,"VI":58},{"EN":58,"VI":60},[63],[67,68],{"id":71,"indexDatabase":486,"url":84,"indexYears":20,"academicFieldIds":491,"indexDatabaseRanking":20},{"id":73,"createTime":20,"updateTime":20,"relativeEntities":487,"label":488,"description":489,"key":80,"publicationTags":490,"standard":20},[],{"EN":76,"VI":76},{"EN":78,"VI":79},[82,83],[86],{"impactFactor":21,"impactFactorByYear":493,"i10Index":21,"i10IndexLast5Year":21,"totalPublication":90,"totalPublicationByYear":494,"totalCitation":21,"totalCitationByYear":495,"totalCitationPerPublication":21,"totalCitationPerPublicationByYear":496,"hindexLast5Year":21,"hindex":21},{},{"1978":92,"1979":93,"1981":93,"1982":93,"1983":92,"1984":92,"1985":94,"1986":94,"1987":94,"1988":94,"1989":92,"1990":92,"1992":92,"1993":93,"1994":92,"1995":92,"1996":94,"2000":92,"2001":92,"2002":92,"2003":95,"2004":94,"2005":93,"2006":92,"2007":93,"2008":93,"2009":92,"2010":96,"2011":96,"2012":94,"2013":93,"2014":97,"2015":95,"2016":96,"2017":95,"2018":96,"2019":92,"2020":96,"2021":94,"2022":93,"2023":93},{},{},{"pages":498,"volume":500},{"VOID":499},"1113-1116",{"VOID":501},"163",{"total":21,"publishYear":503,"statisticByYear":504},2018,{},"2018-01-11",[82,69],[508,511,514,517,523,529,535,538],{"id":356,"text":509,"url":358,"identifiers":510},"Garbelotto M, Gonthier P (2013) Biology, epidemiology, and control of Heterobasidion species worldwide. Annu Rev Phytopathol 51:39–59",{"doi":360},{"id":356,"text":512,"url":358,"identifiers":513},"Vainio EJ, Hantula J (2016) Taxonomy, biogeography and importance of Heterobasidion viruses. Virus Res 219:2–10",{"doi":360},{"id":356,"text":515,"url":358,"identifiers":516},"Ihrmark K (2001) Double-stranded RNA elements in the root rot fungus Heterobasidion annosum. Dissertation, Swedish University of Agricultural Sciences",{"doi":360},{"id":518,"text":519,"url":520,"identifiers":521},"485a7a81-d4c3-4078-9278-c91521cc2065","Vainio EJ, Chiba S, Ghabrial SA, Maiss E, Roossinck M, Sabanadzovic S, Suzuki N, Xie J, Nibert M, ICTV Consortium (2017) ICTV virus taxonomy profile: Partitiviridae. J Gen Virol. https:\u002F\u002Fdoi.org\u002F10.1099\u002Fjgv.0.000985","https:\u002F\u002Fwww.microbiologyresearch.org\u002Fcontent\u002Fjournal\u002Fjgv\u002F10.1099\u002Fjgv.0.000985",{"doi":522},"10.1099\u002Fjgv.0.000985",{"id":524,"text":525,"url":526,"identifiers":527},"1b1dd5c7-8f9b-42ed-af9b-1da72966000e","Hyder R, Piri T, Hantula J, Nuorteva H, Vainio EJ (2017) Distribution of viruses inhabiting Heterobasidion annosum in a pine-dominated forest plot in southern Finland. Microb Ecol. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs00248-017-1027-6","http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs00248-017-1027-6",{"doi":528},"10.1007\u002Fs00248-017-1027-6",{"id":530,"text":531,"url":532,"identifiers":533},"a1e6b6a5-387a-4d1b-b105-191b23423bac","Vainio EJ, Keriö S, Hantula J (2011) Description of a new putative virus infecting the conifer pathogenic fungus Heterobasidion parviporum with resemblance to Heterobasidion annosum P-type partitivirus. Arch Virol 156:79–86","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00705-010-0823-9",{"doi":534},"10.1007\u002Fs00705-010-0823-9",{"id":356,"text":536,"url":358,"identifiers":537},"Sasaki A, Miyanishi M, Ozaki K, Onoue M, Yoshida K (2005) Molecular characterization of a partitivirus from the plant pathogenic ascomycete Rosellinia necatrix. Arch Virol 150:1069–1083",{"doi":360},{"id":539,"text":540,"url":541,"identifiers":542},"16b1b740-77c5-45ab-b52c-0acc81c66ef6","Nibert ML, Ghabrial SA, Maiss E, Lesker T, Vainio EJ, Jiang D, Suzuki N (2014) Taxonomic reorganization of family Partitiviridae and other recent progress in partitivirus research. Virus Res 188:128–141","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0168170214001695",{"doi":543},"10.1016\u002Fj.virusres.2014.04.007",{"id":545,"createTime":546,"updateTime":547,"relativeEntities":548,"slug":549,"properties":550,"entityType":121,"verifyStatus":240,"verifyTime":561,"verifyNote":242,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":562,"fullTextUrl":20,"authors":563,"publicationType":168,"publisherRelationship":607,"citationCount":20,"citationInfo":20,"publishDate":659,"publishYear":660,"citationAnalyzeStatus":661,"lastCitationAnalyze":662,"indexDatabases":663,"openAccess":20,"references":20,"isForceReanalyzing":224},"342aa8cd-0eed-4bb9-8173-2088551e4539","2024-01-21T23:50:18.183+00:00","2026-08-18T15:13:17.599+00:00",[],"Some-characteristics-of-Mycoplasma-virus-Hr1-isolated-from-and-infectingMycoplasma-hyorhinis",{"abstract":551,"title":553,"gsPaper":555,"references":557,"doi":559},{"EN":552},"Mycoplasma virus Hr1 is a short tailed bacteriophage with a polyhedral head about 34 nm across and a tail about 14 nm long. It produces plaques on some strains ofMycoplasma hyorhinis.",{"EN":554},"Some characteristics of Mycoplasma virus Hr1, isolated from and infectingMycoplasma hyorhinis",{"VOID":556},"[]",{"VOID":558},"Gourlay, R. N.: Isolation of a virus infecting a strain ofMycoplasma laidlawii. Nature (Lond.)225, 1165 (1970).\nGourlay, R. N.: Mycoplasmatales virus-laidlawii 2, a new virus isolated fromAcholeplasma laidlawii. J. gen. Virol.12, 65–67 (1971).\nGourlay, R. N., Wyld, S. G.: Isolation of Mycoplasmatales virus-laidlawii 3, a new virus infectingAcholeplasma laidlawii. J. gen. Virol.19, 279–283 (1973).\nCole, R. M., Mitchell, W. O., Garon, C. F.:Spiroplasmavirus citri 3: propagation, purification, proteins and nuclice acid. Science198, 1262–1263 (1977).\nLiss, A., Cole, R. M.: Spiroplasmavirus Group 1: Isolation, growth and properties. Current Microbiol.5, 357–362 (1981).\nRenaudin, J., Ricard, B., Garnier, M., Bove, J. M.: Purification and partial characterization of SPV4. Abstract, Fourth Internat. Congress Internat. Org. Mycoplasmology, Tokyo, Japan, 125 (1982).\nHoward, C. J., Gourlay, R. N., Wyld, S. G.: Isolation of a virus, MVBr1, fromMycoplasma bovirhinis. FEMS Microbiol. Letters7, 163–165 (1980).\nGourlay, R. N., Wyld, S. G., Garwes, D. J.: Some properties of Mycoplasma virus Br1. Arch. Virol.15, 1–15 (1983).\nWhittlestone, P.: Porcine mycoplasmas. In: The Mycoplasmas, Vol. II: Human and Animal Mycoplasma, 133–176. New York: Academic Press 1979.\nBarile, M. F.: Mycoplasma—tissue cell interations. In: The Mycoplasmas, Vol. II: Human and Animal Mycoplasmas, 425–474. New York: Academic Press 1979.\nHoward, C. J., Gourlay, R. N., Collins, J.: Serological studies with bovine ureaplasmas (T-mycoplasmas). Internat. J. Syst. Bacteriol.28, 473–477 (1978).\nGourlay, R. N., Wyld, S. G., Garwes, D. J., Pocock, D. H.: Comparison of Mycoplasmatales virus MV-Lg-pS 2-L172 with Plasmavirus MV-L2 and the other mycoplasma viruses. Arch. Virol.61, 289–296 (1979).\nClyde, W. A.: Mycoplasma species identification based upon growth inhibition by specific antisera. J. Immunol.92, 958–965 (1964).\nRosendal, S., Black, F. T.: Direct and indirect immunoflourescence of unfixed and fixed mycoplasma colonies. Acta path. microbiol. Scand.B 80, 615–622 (1972).\nCole, R. M.: Mycoplasma and spiroplasma viruses: Ultrastructure. In: The Mycoplasmas, Vol. 1: Cell Biology, 385–410. New York: Academic Press 1979.\nGarwes, D. J., Pike, B. V., Wyld, S. G., Pocock, D. H., Gourlay, R. N.: Characterization of Mycoplasmatales virus-laidlawii 3. J. gen. Virol.29, 11–24 (1975).\nMatthews, R. E. F.: Classification and nomenclature of viruses. Intervirology17, 4–199 (1982).",{"VOID":560},"10.1007\u002FBF01314867","2024-09-04T18:16:37.234+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF01314867",[564,579,592],{"id":565,"sortIndex":21,"researcher":20,"roles":566,"affiliations":567,"properties":576,"displayName":578,"givenName":20,"familyName":20},"90d5a17a-64b7-4afa-ab6f-ab1789668318",[129],[568],{"id":569,"sortIndex":21,"affiliation":570,"properties":20},"5b3c80c6-0f74-4f85-8975-de0554bb05d0",{"id":569,"createTime":20,"updateTime":20,"relativeEntities":571,"slug":20,"properties":572,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":575,"statistic":20},[],{"title":573},{"VI":574},"Agricultural Research Council, Institute for Research on Animal Diseases, Compton, Newbury",[],{"title":577},{"VI":578},"R. N. Gourlay",{"id":580,"sortIndex":92,"researcher":20,"roles":581,"affiliations":582,"properties":589,"displayName":591,"givenName":20,"familyName":20},"22fadc8f-921c-48c7-86d6-bf6e94c58924",[129],[583],{"id":569,"sortIndex":21,"affiliation":584,"properties":20},{"id":569,"createTime":20,"updateTime":20,"relativeEntities":585,"slug":20,"properties":586,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":588,"statistic":20},[],{"title":587},{"VI":574},[],{"title":590},{"VI":591},"S. G. Wyld",{"id":593,"sortIndex":93,"researcher":20,"roles":594,"affiliations":595,"properties":604,"displayName":606,"givenName":20,"familyName":20},"03a7aa87-2fdb-40aa-ad5c-e9c7102d9607",[129],[596],{"id":597,"sortIndex":21,"affiliation":598,"properties":20},"46738f25-de97-4b02-b4ab-f0d2da94a665",{"id":597,"createTime":20,"updateTime":20,"relativeEntities":599,"slug":20,"properties":600,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":603,"statistic":20},[],{"title":601},{"VI":602},"Beecham Pharmaceuticals, Animal Health Research Centre, Tadworth, United Kingdom",[],{"title":605},{"VI":606},"M. E. Poulton",{"url":562,"publisher":608,"properties":654},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":609,"slug":10,"properties":610,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":614,"manageAffiliations":623,"indexDatabases":634,"url":87,"thumbnailPath":20,"statistic":649,"gsStatistic":20,"type":100,"analyzePriority":20},[],{"issn":611,"title":612,"eissn":613},{"VOID":13},{"EN":15},{"VOID":17},[615,619],{"id":24,"createTime":20,"updateTime":20,"relativeEntities":616,"label":617,"description":618,"parentId":20,"standard":20,"scholarHubFieldId":20},[],{"EN":27},{},{"id":30,"createTime":20,"updateTime":20,"relativeEntities":620,"label":621,"description":622,"parentId":20,"standard":20,"scholarHubFieldId":20},[],{"EN":33},{},[624,629],{"id":37,"createTime":20,"updateTime":20,"relativeEntities":625,"slug":20,"properties":626,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":628,"statistic":20},[],{"title":627},{"EN":41},[43],{"id":45,"createTime":20,"updateTime":20,"relativeEntities":630,"slug":20,"properties":631,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":633,"statistic":20},[],{"title":632},{"EN":49},[43],[635,642],{"id":53,"indexDatabase":636,"url":64,"indexYears":65,"academicFieldIds":641,"indexDatabaseRanking":69},{"id":55,"createTime":20,"updateTime":20,"relativeEntities":637,"label":638,"description":639,"key":61,"publicationTags":640,"standard":20},[],{"EN":58,"VI":58},{"EN":58,"VI":60},[63],[67,68],{"id":71,"indexDatabase":643,"url":84,"indexYears":20,"academicFieldIds":648,"indexDatabaseRanking":20},{"id":73,"createTime":20,"updateTime":20,"relativeEntities":644,"label":645,"description":646,"key":80,"publicationTags":647,"standard":20},[],{"EN":76,"VI":76},{"EN":78,"VI":79},[82,83],[86],{"impactFactor":21,"impactFactorByYear":650,"i10Index":21,"i10IndexLast5Year":21,"totalPublication":90,"totalPublicationByYear":651,"totalCitation":21,"totalCitationByYear":652,"totalCitationPerPublication":21,"totalCitationPerPublicationByYear":653,"hindexLast5Year":21,"hindex":21},{},{"1978":92,"1979":93,"1981":93,"1982":93,"1983":92,"1984":92,"1985":94,"1986":94,"1987":94,"1988":94,"1989":92,"1990":92,"1992":92,"1993":93,"1994":92,"1995":92,"1996":94,"2000":92,"2001":92,"2002":92,"2003":95,"2004":94,"2005":93,"2006":92,"2007":93,"2008":93,"2009":92,"2010":96,"2011":96,"2012":94,"2013":93,"2014":97,"2015":95,"2016":96,"2017":95,"2018":96,"2019":92,"2020":96,"2021":94,"2022":93,"2023":93},{},{},{"pages":655,"volume":657},{"VOID":656},"81-85",{"VOID":658},"77","1983-03-01",1983,"ERROR_IN_GET_PLATFORM_ID","2026-08-18T15:13:17.598+00:00",[82,69],{"id":665,"createTime":666,"updateTime":667,"relativeEntities":668,"slug":669,"properties":670,"entityType":121,"verifyStatus":240,"verifyTime":681,"verifyNote":242,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":682,"fullTextUrl":20,"authors":683,"publicationType":168,"publisherRelationship":712,"citationCount":764,"citationInfo":765,"publishDate":768,"publishYear":766,"citationAnalyzeStatus":351,"lastCitationAnalyze":769,"indexDatabases":770,"openAccess":20,"references":20,"isForceReanalyzing":224},"a6107441-2716-4554-810e-4214a341612a","2023-12-29T20:21:26.239+00:00","2026-08-17T14:30:41.445+00:00",[],"Reovirus-cytotoxicity-Some-properties-of-the-UV-irradiated-reovirus-and-its-capsid-proteins",{"abstract":671,"title":673,"gsPaper":675,"references":677,"doi":679},{"EN":672},"Ultraviolet light (UV) inactivation of infectious reovirus type 2 for 2 to 10 minutes resulted in the acquisition of cytotoxic (CT) property by the virus. The CT property was maximum after 10 mins irradiation and could not be associated with any detectable changes in the physical, chemical and biological properties of the irradiated virus. In contrast, prolonged irradiation (60 minutes) resulted in a loss of CT property which was associated with severe alterations in a number of viral properties. Furthermore, the loss of CT-induction was apparently not due to a lack of adsorption of the irradiated particles to the cell. Experiments with reovirus “empties” and urea-degraded virus indicated that the protein components of the outer capsid structure were in a manner yet to be defined involved with the CT phenomenon. The UV-irradiated reovirus exhibited transcriptase activity without prior activation by either brief heating or chymotrypsin treatments.",{"EN":674},"Reovirus cytotoxicity: Some properties of the UV-irradiated reovirus and its capsid proteins",{"VOID":676},"[\"7478958734910054437\"]",{"VOID":678},"Banerjee, A. K., andA. J. Shatkin: Transcription in vitro by reovirus-associated ribonucleic acid-dependent polymerase. J. Virol.17, 503–510 (1970).\nBorsa, J., andA. F. Graham: RNA polymerase activity in purified virions. Biochem. biophys. Res. Commun.33, 895–901 (1968).\nBrenner, S., andR. W. Horne: A negative staining method for high resolution electron microscopy of viruses. Biochim. biophys. Acta (Amst.)34, 103–110 (1959).\nGomatos, P. J., I. Tamm, S. Dales, andR. M. Franklin: Reovirus type 3: Physical characteristics and interactions with L cells. Virology17, 441–454 (1962).\nHuang, A. S., andR. R. Wagner: Inhibition of cellular RNA synthesis by nonreplicating vesicular stomatitis virus. Proc. nat. Acad. Sci. (Wash.)54, 1574–1584 (1965).\nJacobson, K. B.: Ribonucleotides of RNA: Separation by chromatography on sheets of diethylaminoethylcellulose. Science138, 515–516 (1962).\nKapular, A. M., N. Mendelsohn, H. Klett, andG. Acs: Four base specific nucleoside 5′-triphosphates in the subviral care of reovirus. Nature (Lond.)225, 1209–1213 (1970).\nLevine, A. J., andH. S. Ginsberg: Role of adenovirus structural proteins in cessation of host cell biosynthetic functions. J. Virol.2, 430–439 (1968).\nLoh, P. C., H. R. Hohl, andM. Soergel: Fine structure of reovirus type 2. J. Bact.89, 1140–1144 (1965).\nLoh, P. C., andH. K. Oie: Role of lysine in the replication of reovirus. I. Synthesis of complete and empty virions. J. Virol.4, 890–895 (1969).\nLoh, P. C., andH. K. Oie: Growth characteristics of reovirus type 2: Ultraviolet light inactivated virion preparations and cell death. Arch. ges. Virusforsch.26, 197–208 (1969).\nLoh, P. C., H. K. Oie, andK. P. Camyre: Role of lysine in the replication of reovirus. II. Characterization of empties and effect on macromolecular synthesis. Arch. ges. Virusforsch.35, 114–125 (1972).\nLoh, P. C., H. K. Oie, andR. M. T. Ratnayake: Accelerated cytopathology in HeLa cells induced by reovirus and cycloheximide. Infect. Immunol.2, 705–712 (1970).\nLoh, P. C., andA. J. Shatkin: Structural proteins of reovirus. J. Virol.2, 1353–1359 (1968).\nPayne, F. E., H. Kurtz, andW. W. Ackermann: Initial stages of the interaction of HeLa cells with poliovirus. Arch. ges. Virusforsch.8, 1–15 (1958).\nPereira, H. G.: The cytopathic effect of animal viruses. Advanc. Virus Res.8, 245–285 (1961).\nRosen, L.: Serologic grouping of reoviruses by hemagglutination inhibition. Amer. J. Hyg.71, 242–249 (1960).\nScherrer, K., andJ. E. Darnell: Sedimentation characteristics of rapidly labelled RNA from HeLa cells. Biochem. biophys. Res. Commun.7, 486–489 (1962).\nShatkin, A. J., andJ. D. Sipe: RNA polymerase activity in purified reoviruses. Proc. nat. Acad. Sci. (Wash.)61, 1462–1469 (1968).\nShatkin, A. J., J. D. Sipe, andP. C. Loh: Separation of ten reovirus segments by polyacrylamide gel electrophoresis. J. Virol.2, 986–991 (1968).\nSmith, K. D., andP. C. Hanawalt: Molecular Photobiology. New York: Academic Press, Inc., 1969.\nSmith, R. E., H. J. Zweerink, andW. K. Joklik: Polypeptide components of virions, top components and cores of reovirus type 3. Virology39, 791–810 (1969).\nSpendlove, R. S., E. H. Lennette, C. O. Knight, andJ. N. Chin: Development of viral antigen and infectious virus in HeLa cells infected with reovirus. J. Immunol.90, 548–553 (1963).\nVasquez, C., andP. Tournier: The morphology of reovirus. 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Their usefulness as group-specific identification probes was also determined. The viral nucleic acid was extracted from the infected cells and the purified dsRNA genome segments were fractionated by polyacrylamide gel electrophoresis, transferred to a nylon membrane and hybridized to the32P labeled DNA probes. The three probes recognized all the samples tested. Genome segment 7, that code for the mayor inner capsid protein VP7, showed the most variation in the hybridization signal with the US proto-serotypes and all the Israeli samples studied. The genome segments 9 and 10 that code for the minor inner capsid protein VP6 and the nonstructural protein NS3, respectively, were highly conserved in all the samples tested despite their distant geographical regions of origin. The last two mentioned clones showed to be good group-specific probes for the identification of BLU samples from Israel and United States. 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In: Hames BD, Higgins SJ (eds) Nucleic acid hybridization, a practical approach. IRL Press, Oxford, pp 73–111",{"doi":360},{"id":20,"text":1433,"url":20,"identifiers":1434},"Barzilai E (1982) Bluetongue antibodies in camels sera in Israel. Refuah Vet 39: 90–93",{},{"id":356,"text":1436,"url":358,"identifiers":1437},"Barzilai E, Shimshony A (1985) Bluetongue: virological and epidemiological observations in Israel. In: Barber TL, Jochin MM (eds) Progress in clinical and biological research, vol 178, bluetongue and related orbiviruses. AR Liss, New York, pp 545–553",{"doi":360},{"id":20,"text":1439,"url":20,"identifiers":1440},"Barzilai E, Tadmor A, Shimshony A (1971) Natural bluetongue infection in mountain gazelle (Gazella gazella). Refuah Vet 28: 93–97",{},{"id":356,"text":1442,"url":358,"identifiers":1443},"Birboin HC, Doly J (1979) A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res 7: 1513–1523",{"doi":360},{"id":356,"text":1445,"url":358,"identifiers":1446},"Clarke IN, McCrae MA (1981) A rapid and sensitive method for analysing the genome profiles of field isolations of rotavirus. J Virol Methods 2: 203–209",{"doi":360},{"id":356,"text":1448,"url":358,"identifiers":1449},"Colman A, Byers MJ, Primrose SB, Lyons A (1978) Rapid purification of plasmids DNAs by hydroxiapatite chromatography. Eur J Biochem 91: 303–310",{"doi":360},{"id":356,"text":1451,"url":358,"identifiers":1452},"de Mattos CA, de Mattos CC, Osburn BI (1989) Recombinant cDNA probe from bluetongue virus genome segment 10 for identification of bluetongue virus. J Vet Diag Invest 1: 237–241",{"doi":360},{"id":356,"text":1454,"url":358,"identifiers":1455},"de Mattos CC, de Mattos CA, Osburn BI, Ianconescu M, Kaufman R (1991) Evidence of genome segment 5 reassortment in bluetongue virus field isolates. Am J Vet Res (in press)",{"doi":360},{"id":356,"text":1457,"url":358,"identifiers":1458},"de Mattos CC, de Mattos CA, Osburn BI, Dangler CA, Chuang RY, Doi RH (1989) Recombinant DNA probe for serotype-specific identification of bluetongue virus 17. Am J Vet Res 50: 536–541",{"doi":360},{"id":356,"text":1460,"url":358,"identifiers":1461},"Dunn SJ, Oberst RD, Stott JL, Osburn BI (1989) Molecular cloning of serogroup and serotype-specific genome segments from bluetongue virus serotype 11. Am J Vet Res 50: 1684–1689",{"doi":360},{"id":356,"text":1463,"url":358,"identifiers":1464},"Dunn SJ, Stott JL (1989) Identification of genetic variation between strains of bluetongue virus serotype 11 using cDNA probes. Virology 170: 579–582",{"doi":360},{"id":356,"text":1466,"url":358,"identifiers":1467},"Fukuso A, Yu Y, Yamaguchi S, Roy P (1989) Completion of the sequence of bluetongue virus serotype 10 by the characterization of a structural protein VP6, and a nonstructural protein, NS2. J Gen Virol 70: 1677–1689",{"doi":360},{"id":20,"text":1469,"url":20,"identifiers":1470},"Goor S (1950) A disease similar to bluetongue in Israel. Refuah Vet 7: 165",{},{"id":20,"text":1472,"url":20,"identifiers":1473},"Gould AR (1988 a) The use of recombinant DNA probes to group and type orbivurs: a comparison of Australian and South Africa isolates. Arch Virol 99: 205–220",{},{"id":356,"text":1475,"url":358,"identifiers":1476},"Gould AR (1988 b) Nucleotide sequence of the Australian bluetongue virus serotype 1 RNA segment 10. J Gen Virol 69: 945–949",{"doi":360},{"id":20,"text":1478,"url":20,"identifiers":1479},"Hattori M, Sakaki Y (1986) Dideoxy method using denature plasmid templates. Anal Biochem 152: 232–238",{},{"id":1481,"text":1482,"url":1483,"identifiers":1484},"1af8b208-d7e9-4e10-9534-6183ae70ad40","Huismans H, Cloete M, Le Roux A (1987) The genetic relatedness of a number of individual cognate genes of viruses in the bluetongue and closely related serogroups. Virology 161: 421–428","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F0042682287901358",{"doi":1485},"10.1016\u002F0042-6822(87)90135-8",{"id":20,"text":1487,"url":20,"identifiers":1488},"Komarov A, Goldsmit L (1951) A disease similar to bluetongue in cattle and sheep in Israel. Refuah Vet 8: 96–100",{},{"id":20,"text":1490,"url":20,"identifiers":1491},"Komarov A, Haig DA (1952) Identification of a strain of bluetongue virus isolated in Israel. J South African Vet Med Assoc 23: 153–156",{},{"id":20,"text":1493,"url":20,"identifiers":1494},"Kowalik TF, Li JKK (1989) Sequence analyses and structural predictions of dsRNA segments S1 and VP7 from United States bluetongue virus 13 and 10. Virology 172: 189–195",{},{"id":356,"text":1496,"url":358,"identifiers":1497},"Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 277: 680–685",{"doi":360},{"id":356,"text":1499,"url":358,"identifiers":1500},"Lee JW, Roy P (1986) Nucleotide sequence of cDNA clone of RNA segment 10 of bluetongue virus (serotype 10). J Gen Virol 67: 2833–2837",{"doi":360},{"id":356,"text":1502,"url":358,"identifiers":1503},"Oberst RD, Squire KRE, Stott JL, Chuang RY, Osburn BI (1985) The coexistence of multiple bluetongue virus electropherotypes in individual cattle during natural infection. J Gen Virol 66: 1901–1909",{"doi":360},{"id":1505,"text":1506,"url":1507,"identifiers":1508},"2859f0ce-73be-4e95-b1d1-13f945ed1ef0","Rigby PWJ, Dieckmann M, Rhodes C, Berg P (1977) Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase. J Mol Biol 113: 237","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F0022283677900523",{"doi":1509},"10.1016\u002F0022-2836(77)90052-3",{"id":1511,"text":1512,"url":1513,"identifiers":1514},"d32c4e10-080d-4713-9a82-da19038ac84b","Ritter GC, Roy P (1988) Genetic relationships of bluetongue virus serotypes isolated from different parts of the world. Virus Res 11: 33–47","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002F0168170288900652",{"doi":1515},"10.1016\u002F0168-1702(88)90065-2",{"id":20,"text":1517,"url":20,"identifiers":1518},"Roy P (1989) Bluetongue virus genetics and genome structure. Review article. Virus Res 13: 179–296",{},{"id":356,"text":1520,"url":358,"identifiers":1521},"Roy P, Adachi A, Urakawa T, Booth TF, Thomas CP (1990) Identification of bluetongue virus VP6 protein as nucleic acid-binding protein and the localization of VP6 in virus-infected vertebrate cells. J Virol 64: 1–8",{"doi":360},{"id":356,"text":1523,"url":358,"identifiers":1524},"Samal BSK, El-Hussein A, Holbrook FR, Beaty BJ, Ramig RF (1987) Mixed infection ofCulicoides variipennis with bluetongue virus serotypes 10 and 17: evidence for high frequency reassortement in the vector. J Gen Virol 68: 2319–2329",{"doi":360},{"id":1526,"text":1527,"url":1528,"identifiers":1529},"e90bf99b-9410-42e8-9f2e-85484320e3c4","Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74: 5463–5467","https:\u002F\u002Fpnas.org\u002Fdoi\u002Ffull\u002F10.1073\u002Fpnas.74.12.5463",{"doi":1530},"10.1073\u002Fpnas.74.12.5463",{"id":20,"text":1532,"url":20,"identifiers":1533},"Shimshony A, Goldsmit L, Barzilai E (1980) Bluetongue in Israel. Bull Off Int Epizool 92: 525–534",{},{"id":1535,"text":1536,"url":1537,"identifiers":1538},"1f747713-ad8a-4063-99eb-2763e55e2887","Smith TF, Waterman MS (1981) Identification of common molecular subsequences. J Mol Biol 147: 195–197","https:\u002F\u002Flinkinghub.elsevier.com\u002Fretrieve\u002Fpii\u002F0022283681900875",{"doi":1539},"10.1016\u002F0022-2836(81)90087-5",{"id":356,"text":1541,"url":358,"identifiers":1542},"Squire KRE, Chuang RY, Dunn SJ, Dangler CA, Falbo MT, Chuang LF, Osburn BI (1986) Multiple bluetongue virus cloned genetic probes: application to diagnostics and bluetongue genetic relationships. Am J Vet Res 47: 1785–1788",{"doi":360},{"id":356,"text":1544,"url":358,"identifiers":1545},"Squire KRE, Osburn BI, Chuang RY, Doi RH (1983) A survey of electropherotype relationships of bluetongue virus isolates from the Western United States. J Gen Virol 64: 2103–2115",{"doi":360},{"id":356,"text":1547,"url":358,"identifiers":1548},"Stott JL, Oberst RD, Channell MB (1987) Genome segment reassortment between two serotypes of bluetongue virus in a natural host. J Virol 61: 2670–2674",{"doi":360},{"id":356,"text":1550,"url":358,"identifiers":1551},"Sugiyama K, Bishop DHL, Roy P (1981) Analysis of the genomes of bluetongue virus recovered in the United States I. Oligonucleotide fingerprint studies that indicate the existence of naturally occurring reassortant bluetongue isolates. Virology 114: 210–217",{"doi":360},{"id":20,"text":1553,"url":20,"identifiers":1554},"Sugiyama K, Bishop DHL, Roy P (1982) Analyses of the genomes of bluetongue viruses recovered from different states of the United States and at different times. Am J Epidemiol 115: 332–347",{},{"id":20,"text":1556,"url":20,"identifiers":1557},"Waldvogel AS (1987) Comparison of virulence of two strains of bluetongue virus serotype 11 in newborn mice and fetal calves. PhD dissertation, University of California, Davis",{},{"id":356,"text":1559,"url":358,"identifiers":1560},"Waldvogel AS, Anderson CA, Higgins RJ, Osburn BI (1987) Neurovirulence of UC2 and UC8 strains of bluetongue virus serotype 11 in newborn mice. Vet Pathol 24: 404–410",{"doi":360},{"id":356,"text":1562,"url":358,"identifiers":1563},"Waldvogel AS, Stott JL, Squire KRE, Osburn BI (1986) Strain-dependent virulence characteristics of bluetongue serotype 11. J Gen Virol 67: 765–769",{"doi":360},{"id":356,"text":1565,"url":358,"identifiers":1566},"Yu Y, Fukuso A, Ritter DG, Roy P (1988) Complete nucleotide sequence of the group reactive antigen VP7 genome of bluetongue virus. Nucleic Acids Res 16: 1620",{"doi":360},{"id":1568,"createTime":1569,"updateTime":1570,"relativeEntities":1571,"slug":1572,"properties":1573,"entityType":121,"verifyStatus":240,"verifyTime":1583,"verifyNote":242,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":1584,"fullTextUrl":20,"authors":1585,"publicationType":168,"publisherRelationship":1716,"citationCount":20,"citationInfo":20,"publishDate":1767,"publishYear":1768,"citationAnalyzeStatus":661,"lastCitationAnalyze":1570,"indexDatabases":1769,"openAccess":20,"references":20,"isForceReanalyzing":224},"f66d1724-543b-49ff-8171-bb1f158c937f","2023-12-13T16:25:32.676+00:00","2026-08-15T22:17:48.479+00:00",[],"Complete-genome-sequence-of-a-distinct-calla-lily-chlorotic-spot-virus-isolated-in-mainland-China",{"abstract":1574,"title":1576,"gsPaper":1578,"references":1579,"doi":1581},{"EN":1575},"The first complete genome sequence of calla lily chlorotic spot virus (CCSV) from Lijiang in northwestern Yunnan Province was obtained using RT-PCR with designed primers. The genome of CCSV isolate LJ-1-Yunnan is tripartite. The small (S) RNA is 3182 nucleotides (nt) in length and encodes a nonstructural protein (NSs, 1383 nt) and a nuclear nucleocapsid (N, 834 nt), separated by an 836-nt intergenic region (IGR). The medium (M) RNA is 4749 nt in length and encodes a nonstructural movement protein (NSm, 930 nt) and a glycoprotein (GnGc, 3,372 nt), also separated by a 349-nt IGR. The large (L) RNA is 8912 nt in length and encodes a predicted RNA-dependent RNA polymerase (RdRp, 8652 nt). The nucleotide sequences of the three viral RNA segments are 92-94 % identical to the published CCSV genome sequence, and the amino acid sequences of the encoded proteins are 96-98 % identical. However, the IGRs of the S and M RNAs are less similar, with 86 and 72 % identity, respectively. Genome sequence comparisons and phylogenetic analysis indicate that the Lijiang CCSV isolate is a unique tospovirus isolate that differs from CCSV isolates in other geographic regions.",{"EN":1577},"Complete genome sequence of a distinct calla lily chlorotic spot virus isolated in mainland China",{"VOID":556},{"VOID":1580},"Chen C, Chen T, Lin Y, Yeh S, Hsu H (2005) A chlorotic spot disease on calla lilies (Zantedeschia spp.) is caused by a tospovirus serologically but distantly related to Watermelon silver mottle virus. Plant Dis 89:440–445\nChen T, Li J, Lin Y, Yeh Y, Kang Y, Huang L, Yeh S (2012) Genomic characterization of Calla lily chlorotic spot virus and design of broad-spectrum primers for detection of tospoviruses. Plant Pathol 61:183–194\nCheng Y, Zheng Y, Tai C, Yen J, Chen Y, Jan F (2014) Identification, characterisation and detection of a new tospovirus on sweet pepper. Ann Appl Biol 164:107–115\nChu F, Chao C, Peng Y, Lin S, Chen C, Yeh S (2001) Serological and molecular characterization of Peanut chlorotic fan-spot virus, a new species of the genus Tospovirus. Phytopathology 91:856–863\nCortez I, Saaijer J, Wongjkaew K, Pereira A, Goldbach R, Peters D, Kormelink R (2001) Identification and characterization of a novel tospovirus species using a new RT-PCR approach. Arch Virol 146:265–278\nDe Avila A, De Haan P, Kormelink R, Resende RdO, Goldbach R, Peters D (1993) Classification of tospoviruses based on phylogeny of nucleoprotein gene sequences. J Gen Virol 74:153\nDe Oliveira AS, Melo FL, Inoue-Nagata AK, Nagata T, Kitajima EW, Resende RO (2012) Characterization of Bean necrotic mosaic virus: a member of a novel evolutionary lineage within the genus Tospovirus. PLoS One 7:e38634\nDong J, Yin Y, Fang Q, McBeath J, Zhang Z (2013) A new tospovirus causing chlorotic ringspot on Hippeastrum sp. in China. Virus Genes 46:567–570\nLin Y, Chen T, Hsu H, Liu F, Chu F, Chen C, Lin Y, Yeh S (2005) Serological comparison and molecular characterization for verification of Calla lily chlorotic spot virus as a new tospovirus species belonging to Watermelon silver mottle virus serogroup. Phytopathology 95:1482–1488\nLiu Y, Lu X, Zhi L, Zheng Y, Chen X, Xu Y, Wu F, Li Y (2012) Calla lily chlorotic spot virus from Spider Lily (Hymenocallis litteralis) and Tobacco (Nicotiana tabacum) in the South-west of China. J Phytopathol 160:201–205\nMoyer J (1999) Tospoviruses (Bunyaviridae). Encyclopedia of virology. Academic Press, New York, pp 1803–1807\nSeepiban C, Gajanandana O, Attathom T, Attathom S (2011) Tomato necrotic ringspot virus, a new tospovirus isolated in Thailand. Arch Virol 156:263–274\nShimomoto Y, Kobayashi K, Okuda M (2014) Identification and characterization of Lisianthus necrotic ringspot virus, a novel distinct tospovirus species causing necrotic disease of lisianthus (Eustoma grandiflorum). J Gen Plant Pathol 80:169–175\nTamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28:2731–2739\nTorres R, Larenas J, Fribourg C, Romero J (2012) Pepper necrotic spot virus, a new tospovirus infecting solanaceous crops in Peru. Arch Virol 157:609–615\nWhitfield AE, Ullman DE, German TL (2005) Tospovirus-thrips interactions. Annu Rev Phytopathol 43:459–489\nXu Y, Lou S, Li X, Zheng Y, Wang W, Liu Y (2013) The complete S RNA and M RNA nucleotide sequences of a hippeastrum chlorotic ringspot virus (HCRV) isolate from Hymenocallis littoralis (Jacq.) Salisb in China. Arch Virol 158:2597–2601\nYin Y, Zheng K, Dong J, Fang Q, Wu S, Wang L, Zhang Z (2014) Identification of a new tospovirus causing necrotic ringspot on tomato in China. 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