Base de dados : MEDLINE
Pesquisa : B04.715.435 [Categoria DeCS]
Referências encontradas : 145 [refinar]
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  1 / 145 MEDLINE  
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[PMID]:28934492
[Au] Autor:Du Z; Alekhina OM; Vassilenko KS; Simon AE
[Ad] Endereço:Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742, USA.
[Ti] Título:Concerted action of two 3' cap-independent translation enhancers increases the competitive strength of translated viral genomes.
[So] Source:Nucleic Acids Res;45(16):9558-9572, 2017 Sep 19.
[Is] ISSN:1362-4962
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Several families of plant viruses evolved cap-independent translation enhancers (3'CITE) in the 3' untranslated regions of their genomic (g)RNAs to compete with ongoing cap-dependent translation of cellular mRNAs. Umbravirus Pea enation mosaic virus (PEMV)2 is the only example where three 3'CITEs enhance translation: the eIF4E-binding Panicum mosaic virus-like translational enhancer (PTE) and ribosome-binding 3' T-shaped structure (TSS) have been found in viruses of different genera, while the ribosome-binding kl-TSS that provides a long-distance interaction with the 5' end is unique. We report that the PTE is the key translation promoting element, but inhibits translation in cis and in trans in the absence of the kl-TSS by sequestering initiation factor eIF4G. PEMV2 strongly outcompeted a cellular mRNA mimic for translation, indicating that the combination of kl-TSS and PTE is highly efficient. Transferring the 3'-5' interaction from the kl-TSS to the PTE (to fulfill its functionality as found in other viruses) supported translationin vitro, but gRNA did not accumulate to detectable levels in protoplasts in the absence of the kl-TSS. It was shown that the PTE in conjunction with the kl-TSS did not markedly affect the translation initiation rate but rather increased the number of gRNAs available for translation. A model is proposed to explain how 3'CITE-based regulation of ribosome recruitment enhances virus fitness.
[Mh] Termos MeSH primário: Elementos Facilitadores Genéticos
Genoma Viral
Luteoviridae/genética
Capuzes de RNA/genética
[Mh] Termos MeSH secundário: Arabidopsis/virologia
Códon de Iniciação
Fator de Iniciação 4G em Eucariotos/genética
Fator de Iniciação 4G em Eucariotos/metabolismo
Luteoviridae/metabolismo
Polirribossomos/metabolismo
Biossíntese de Proteínas
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Codon, Initiator); 0 (Eukaryotic Initiation Factor-4G); 0 (RNA Caps)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171024
[Lr] Data última revisão:
171024
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170922
[St] Status:MEDLINE
[do] DOI:10.1093/nar/gkx643


  2 / 145 MEDLINE  
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[PMID]:28905257
[Au] Autor:Yoo RH; Lee SW; Lim S; Zhao F; Igori D; Baek D; Hong JS; Lee SH; Moon JS
[Ad] Endereço:Food Microbiology Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Cheongju, 28159, Republic of Korea.
[Ti] Título:Complete genome analysis of a novel umbravirus-polerovirus combination isolated from Ixeridium dentatum.
[So] Source:Arch Virol;162(12):3893-3897, 2017 Dec.
[Is] ISSN:1432-8798
[Cp] País de publicação:Austria
[La] Idioma:eng
[Ab] Resumo:Two novel viruses, isolated in Bonghwa, Republic of Korea, from an Ixeridium dentatum plant with yellowing mottle symptoms, have been provisionally named Ixeridium yellow mottle-associated virus 1 (IxYMaV-1) and Ixeridium yellow mottle-associated virus 2 (IxYMaV-2). IxYMaV-1 has a genome of 6,017 nucleotides sharing a 56.4% sequence identity with that of cucurbit aphid-borne yellows virus (genus Polerovirus). The IxYMaV-2 genome of 4,196 nucleotides has a sequence identity of less than 48.3% with e other species classified within the genus Umbravirus. Genome properties and phylogenetic analysis suggested that IxYMaV-1 and -2 are representative isolates of new species classifiable within the genus Polerovirus and Umbravirus, respectively.
[Mh] Termos MeSH primário: Asteraceae/virologia
Genoma Viral
Luteoviridae/classificação
Luteoviridae/isolamento & purificação
Tombusviridae/classificação
Tombusviridae/isolamento & purificação
[Mh] Termos MeSH secundário: Luteoviridae/genética
Filogenia
Doenças das Plantas/virologia
República da Coreia
Análise de Sequência de DNA
Homologia de Sequência
Tombusviridae/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171113
[Lr] Data última revisão:
171113
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170915
[St] Status:MEDLINE
[do] DOI:10.1007/s00705-017-3512-0


  3 / 145 MEDLINE  
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[PMID]:28352973
[Au] Autor:Cheewachaiwit S; Warin N; Phuangrat B; Rukpratanporn S; Gajanandana O; Balatero CH; Chatchawankanphanich O
[Ad] Endereço:Center for Agricultural Biotechnology, Kasetsart University, Kamphaeng Saen Campus, Nakhon Pathom, 73140, Thailand.
[Ti] Título:Incidence and molecular diversity of poleroviruses infecting cucurbit crops and weed plants in Thailand.
[So] Source:Arch Virol;162(7):2083-2090, 2017 Jul.
[Is] ISSN:1432-8798
[Cp] País de publicação:Austria
[La] Idioma:eng
[Ab] Resumo:Overall, 244 samples of cucurbit crops with yellowing symptoms and selected weed species, from 15 provinces in Thailand, were screened by RT-PCR using primers Polero-CP-F and Polero-CP-R. A total of 160 samples (~66%) were infected by poleroviruses. Analysis of a 1.4 kb region covering the 3' RNA-dependent RNA polymerase (RdRp) gene, the intergenic non-coding region (iNCR), and the coat protein (CP), showed that four poleroviruses, namely, cucurbit aphid-borne yellows virus (CABYV), luffa aphid-borne yellows virus (LABYV), melon aphid-borne yellows virus (MABYV) and suakwa aphid-borne yellows virus (SABYV) were associated with the yellowing symptoms in cucurbit crops. Further analyses indicated presence of putative recombinant viruses referred to as CABYV-R and SABYV-R. CABYV-R was derived from the recombination between MABYV and the common strain of CABYV (CABYV-C). SABYV-R was derived from the recombination of MABYV and SABYV.
[Mh] Termos MeSH primário: Cucurbita/virologia
Luteoviridae/genética
Doenças das Plantas/virologia
Plantas Daninhas/virologia
RNA Replicase/genética
[Mh] Termos MeSH secundário: Produtos Agrícolas/virologia
Genoma Viral
Luteoviridae/classificação
Luteoviridae/isolamento & purificação
Fases de Leitura Aberta
Filogenia
Análise de Sequência de DNA
Tailândia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
EC 2.7.7.48 (RNA Replicase)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170802
[Lr] Data última revisão:
170802
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170330
[St] Status:MEDLINE
[do] DOI:10.1007/s00705-017-3332-2


  4 / 145 MEDLINE  
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[PMID]:28342033
[Au] Autor:Zhou B; Wang F; Zhang X; Zhang L; Lin H
[Ad] Endereço:College of Plant Protection, Anhui Agricultural University, Hefei, 230036, Anhui, China.
[Ti] Título:Sequencing and phylogenetic analysis of tobacco virus 2, a polerovirus from Nicotiana tabacum.
[So] Source:Arch Virol;162(7):2159-2162, 2017 Jul.
[Is] ISSN:1432-8798
[Cp] País de publicação:Austria
[La] Idioma:eng
[Ab] Resumo:The complete genome sequence of a new virus, provisionally named tobacco virus 2 (TV2), was determined and identified from leaves of tobacco (Nicotiana tabacum) exhibiting leaf mosaic, yellowing, and deformity, in Anhui Province, China. The genome sequence of TV2 comprises 5,979 nucleotides, with 87% nucleotide sequence identity to potato leafroll virus (PLRV). Its genome organization is similar to that of PLRV, containing six open reading frames (ORFs) that potentially encode proteins with putative functions in cell-to-cell movement and suppression of RNA silencing. Phylogenetic analysis of the nucleotide sequence placed TV2 alongside members of the genus Polerovirus in the family Luteoviridae. To the best our knowledge, this study is the first report of a complete genome sequence of a new polerovirus identified in tobacco.
[Mh] Termos MeSH primário: Genoma Viral
Luteoviridae/classificação
Filogenia
Doenças das Plantas/virologia
Tabaco/virologia
[Mh] Termos MeSH secundário: China
Luteoviridae/genética
Luteoviridae/isolamento & purificação
Fases de Leitura Aberta
RNA Viral/genética
Análise de Sequência de DNA
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (RNA, Viral)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170802
[Lr] Data última revisão:
170802
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170326
[St] Status:MEDLINE
[do] DOI:10.1007/s00705-017-3339-8


  5 / 145 MEDLINE  
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[PMID]:28337544
[Au] Autor:Palanga E; Martin DP; Galzi S; Zabré J; Bouda Z; Neya JB; Sawadogo M; Traore O; Peterschmitt M; Roumagnac P; Filloux D
[Ad] Endereço:Laboratoire Biosciences, Unité de Formation et de Recherche en Sciences de la Vie et de la Terre (UFR-SVT), Université Ouaga I Pr Joseph Ki-Zerbo, 03 BP 7021, Ouagadougou, Burkina Faso.
[Ti] Título:Complete genome sequences of cowpea polerovirus 1 and cowpea polerovirus 2 infecting cowpea plants in Burkina Faso.
[So] Source:Arch Virol;162(7):2149-2152, 2017 Jul.
[Is] ISSN:1432-8798
[Cp] País de publicação:Austria
[La] Idioma:eng
[Ab] Resumo:The full-length genome sequences of two novel poleroviruses found infecting cowpea plants, cowpea polerovirus 1 (CPPV1) and cowpea polerovirus 2 (CPPV2), were determined using overlapping RT-PCR and RACE-PCR. Whereas the 5845-nt CPPV1 genome was most similar to chickpea chlorotic stunt virus (73% identity), the 5945-nt CPPV2 genome was most similar to phasey bean mild yellow virus (86% identity). The CPPV1 and CPPV2 genomes both have a typical polerovirus genome organization. Phylogenetic analysis of the inferred P1-P2 and P3 amino acid sequences confirmed that CPPV1 and CPPV2 are indeed poleroviruses. Four apparently unique recombination events were detected within a dataset of 12 full polerovirus genome sequences, including two events in the CPPV2 genome. Based on the current species demarcation criteria for the family Luteoviridae, we tentatively propose that CPPV1 and CPPV2 should be considered members of novel polerovirus species.
[Mh] Termos MeSH primário: Genoma Viral
Luteoviridae/genética
Doenças das Plantas/virologia
Vigna/virologia
[Mh] Termos MeSH secundário: Burkina Faso
Luteoviridae/isolamento & purificação
Fases de Leitura Aberta
Filogenia
RNA Viral/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (RNA, Viral)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170802
[Lr] Data última revisão:
170802
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170325
[St] Status:MEDLINE
[do] DOI:10.1007/s00705-017-3327-z


  6 / 145 MEDLINE  
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[PMID]:28220324
[Au] Autor:Afouda L; Kone D; Zinsou V; Dossou L; Kenyon L; Winter S; Knierim D
[Ad] Endereço:Faculté d'Agronomie, Université de Parakou, 02 B.P., 1003, Parakou, Republic of Benin.
[Ti] Título:Virus surveys of Capsicum spp. in the Republic of Benin reveal the prevalence of pepper vein yellows virus and the identification of a previously uncharacterised polerovirus species.
[So] Source:Arch Virol;162(6):1599-1607, 2017 Jun.
[Is] ISSN:1432-8798
[Cp] País de publicação:Austria
[La] Idioma:eng
[Ab] Resumo:Surveys were conducted in 2014 and 2015 in Southern and Northern Benin, respectively, to identify the viruses infecting peppers (Capsicum spp.). The samples were screened by ELISA for cucumber mosaic virus (CMV), pepper veinal mottle virus (PVMV), potato virus Y (PVY) and tomato yellow leaf curl virus (TYLCV). A generic reverse transcription PCR (RT-PCR) was used to test for the presence of poleroviruses. ELISA tests confirmed the prevalence of all viruses, while the RT-PCR detected pepper vein yellows virus (PeVYV) which is reported for the first time in Benin. A further, divergent polerovirus isolate was detected from a single pepper sample originating from southern Benin. Screening of samples collected from solanaceous plants during virus surveys in Mali (conducted in 2009) also detected this divergent polerovirus isolate in two samples from African eggplants. The complete genome sequence was obtained from the Mali isolate using transcriptome sequencing and by conventional Sanger sequencing of overlapping RT-PCR products. Based on the sequence characteristics of this isolate we propose a new polerovirus species, African eggplant yellowing virus (AeYV).
[Mh] Termos MeSH primário: Capsicum/virologia
Luteoviridae/genética
Luteoviridae/isolamento & purificação
Doenças das Plantas/virologia
[Mh] Termos MeSH secundário: Benin
Cucumovirus/genética
Ensaio de Imunoadsorção Enzimática/métodos
Genoma Viral
Filogenia
Reação em Cadeia da Polimerase
Potyvirus/genética
RNA Viral
Análise de Sequência de DNA
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (RNA, Viral)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170720
[Lr] Data última revisão:
170720
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170222
[St] Status:MEDLINE
[do] DOI:10.1007/s00705-017-3274-8


  7 / 145 MEDLINE  
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[PMID]:28035870
[Au] Autor:Agrofoglio YC; Delfosse VC; Casse MF; Hopp HE; Kresic IB; Distéfano AJ
[Ad] Endereço:First author: INTA-CICVyA, CONICET, Instituto de Biotecnología, 1686 Buenos Aires; second author: INTA-CICVyA, CONICET, Instituto de Biotecnología and School of Science and Technology, UNSAM, 1653 Buenos Aires; third and fifth authors: EEA Sáenz Peña, INTA, 3700 Chaco, Argentina; and fourth and sixt
[Ti] Título:Identification of a New Cotton Disease Caused by an Atypical Cotton Leafroll Dwarf Virus in Argentina.
[So] Source:Phytopathology;107(3):369-376, 2017 03.
[Is] ISSN:0031-949X
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:An outbreak of a new disease occurred in cotton (Gossypium hirsutum) fields in northwest Argentina starting in the 2009-10 growing season and is still spreading steadily. The characteristic symptoms of the disease included slight leaf rolling and a bushy phenotype in the upper part of the plant. In this study, we determined the complete nucleotide sequences of two independent virus genomes isolated from cotton blue disease (CBD)-resistant and -susceptible cotton varieties. This virus genome comprised 5,866 nucleotides with an organization similar to that of the genus Polerovirus and was closely related to cotton leafroll dwarf virus, with protein identity ranging from 88 to 98%. The virus was subsequently transmitted to a CBD-resistant cotton variety using Aphis gossypii and symptoms were successfully reproduced. To study the persistence of the virus, we analyzed symptomatic plants from CBD-resistant varieties from different cotton-growing fields between 2013 and 2015 and showed the presence of the same virus strain. In addition, a constructed full-length infectious cDNA clone from the virus caused disease symptoms in systemic leaves of CBD-resistant cotton plants. Altogether, the new leafroll disease in CBD-resistant cotton plants is caused by an atypical cotton leafroll dwarf virus.
[Mh] Termos MeSH primário: Afídeos/virologia
Genoma Viral/genética
Gossypium/virologia
Luteoviridae/classificação
Doenças das Plantas/virologia
[Mh] Termos MeSH secundário: Animais
Luteoviridae/genética
Luteoviridae/isolamento & purificação
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170720
[Lr] Data última revisão:
170720
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161231
[St] Status:MEDLINE
[do] DOI:10.1094/PHYTO-09-16-0349-R


  8 / 145 MEDLINE  
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[PMID]:27932519
[Au] Autor:Pinheiro PV; Ghanim M; Alexander M; Rebelo AR; Santos RS; Orsburn BC; Gray S; Cilia M
[Ad] Endereço:From the ‡Department of Entomology, Cornell University, Ithaca, New York 14853.
[Ti] Título:Host Plants Indirectly Influence Plant Virus Transmission by Altering Gut Cysteine Protease Activity of Aphid Vectors.
[So] Source:Mol Cell Proteomics;16(4 suppl 1):S230-S243, 2017 Apr.
[Is] ISSN:1535-9484
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The green peach aphid, , is a vector of the (PLRV, Luteoviridae), transmitted exclusively by aphids in a circulative manner. PLRV transmission efficiency was significantly reduced when a clonal lineage of was reared on turnip as compared with the weed physalis, and this was a transient effect caused by a host-switch response. A trend of higher PLRV titer in physalis-reared aphids as compared with turnip-reared aphids was observed at 24 h and 72 h after virus acquisition. The major difference in the proteomes of these aphids was the up-regulation of predicted lysosomal enzymes, in particular the cysteine protease cathepsin B (cathB), in aphids reared on turnip. The aphid midgut is the site of PLRV acquisition, and cathB and PLRV localization were starkly different in midguts of the aphids reared on the two host plants. In viruliferous aphids that were reared on turnip, there was near complete colocalization of cathB and PLRV at the cell membranes, which was not observed in physalis-reared aphids. Chemical inhibition of cathB restored the ability of aphids reared on turnip to transmit PLRV in a dose-dependent manner, showing that the increased activity of cathB and other cysteine proteases at the cell membrane indirectly decreased virus transmission by aphids. Understanding how the host plant influences virus transmission by aphids is critical for growers to manage the spread of virus among field crops.
[Mh] Termos MeSH primário: Afídeos/virologia
Brassica napus/parasitologia
Catepsina B/metabolismo
Luteoviridae/fisiologia
Physalis/parasitologia
[Mh] Termos MeSH secundário: Animais
Afídeos/enzimologia
Afídeos/fisiologia
Trato Gastrointestinal/enzimologia
Trato Gastrointestinal/virologia
Interações Hospedeiro-Parasita
Proteínas de Insetos/metabolismo
Insetos Vetores/enzimologia
Insetos Vetores/fisiologia
Insetos Vetores/virologia
Doenças das Plantas/virologia
Vírus de Plantas/fisiologia
Proteômica/métodos
Regulação para Cima
Carga Viral
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Insect Proteins); EC 3.4.22.1 (Cathepsin B)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170726
[Lr] Data última revisão:
170726
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161210
[St] Status:MEDLINE
[do] DOI:10.1074/mcp.M116.063495


  9 / 145 MEDLINE  
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[PMID]:27915037
[Au] Autor:Doumayrou J; Sheber M; Bonning BC; Miller WA
[Ad] Endereço:Department of Plant Pathology & Microbiology, Iowa State University, Ames, IA 50011, USA. Electronic address: juliette.doumayrou@gmail.com.
[Ti] Título:Quantification of Pea enation mosaic virus 1 and 2 during infection of Pisum sativum by one step real-time RT-PCR.
[So] Source:J Virol Methods;240:63-68, 2017 Feb.
[Is] ISSN:1879-0984
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Pea enation mosaic virus 1 (PEMV1) and Pea enation mosaic virus 2 (PEMV2) are two viruses in an obligate symbiosis that cause pea enation mosaic disease mainly in plants in the Fabaceae family. This virus system is a valuable model to investigate plant virus replication, movement and vector transmission. Thus, here we describe growth conditions, virus detection methods, and virus accumulation behavior. To measure the accumulation and movement of PEMV1 and PEMV2 in plants during the course of infection, we developed a quantitative real-time one-step reverse transcription PCR procedure using the SYBR-green technology. Viral primers were designed that anneal to conserved but distinct regions in the RNA-dependent RNA polymerase gene of each virus. Moreover, the normalization of viral accumulation was performed to correct for sample-to-sample variation by designing primers to two different Pisum sativum housekeeping genes: actin and ß-tubulin. Transcript levels for these housekeeping genes did not change significantly in response to PEMV infection. Conditions were established for maximum PCR efficiency for each gene, and quantification using QuBit technology. Both viruses reached maximum accumulation around 21days post-inoculation of pea plants. These results provide valuable tools and knowledge to allow reproducible studies of this emerging model virus system virus complex.
[Mh] Termos MeSH primário: Luteoviridae/isolamento & purificação
Ervilhas/virologia
Reação em Cadeia da Polimerase em Tempo Real
Reação em Cadeia da Polimerase Via Transcriptase Reversa
Tombusviridae/isolamento & purificação
[Mh] Termos MeSH secundário: Primers do DNA
Genes Essenciais
Luteoviridae/classificação
Luteoviridae/genética
Luteoviridae/fisiologia
RNA Viral/genética
Tombusviridae/classificação
Tombusviridae/genética
Tombusviridae/fisiologia
Replicação Viral
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (DNA Primers); 0 (RNA, Viral)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171013
[Lr] Data última revisão:
171013
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161205
[St] Status:MEDLINE


  10 / 145 MEDLINE  
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[PMID]:27848014
[Au] Autor:Nakazono-Nagaoka E; Fujikawa T; Iwanami T
[Ad] Endereço:NARO Institute of Fruit Tree and Tea Science, National Agriculture and Food Research Organization (NARO), Fujimoto 2-1, Tsukuba, Ibaraki, 305-8605, Japan.
[Ti] Título:Nucleotide sequences of Japanese isolates of citrus vein enation virus.
[So] Source:Arch Virol;162(3):879-883, 2017 Mar.
[Is] ISSN:1432-8798
[Cp] País de publicação:Austria
[La] Idioma:eng
[Ab] Resumo:The genomic sequences of five Japanese isolates of citrus vein enation virus (CVEV) isolates that induce vein enation were determined and compared with that of the Spanish isolate VE-1. The nucleotide sequences of all Japanese isolates were 5,983 nt in length. The genomic RNA of Japanese isolates had five potential open reading frames (ORF 0, ORF 1, ORF 2, ORF 3, and ORF 5) in the positive-sense strand. The nucleotide sequence identity among the Japanese isolates and Spanish isolate VE-1 ranged from 98.0% to 99.8%. Comparison of the partial amino acid sequences of ten Japanese isolates and three Spanish isolates suggested that four amino acid residues, at positions of 83, 104, and 113 in ORF 2 and position 41 in ORF 5, might be unique to some Japanese isolates.
[Mh] Termos MeSH primário: Citrus/virologia
Luteoviridae/isolamento & purificação
Doenças das Plantas/virologia
[Mh] Termos MeSH secundário: Sequência de Aminoácidos
Genoma Viral
Japão
Luteoviridae/química
Luteoviridae/classificação
Luteoviridae/genética
Dados de Sequência Molecular
Fases de Leitura Aberta
Filogenia
Homologia de Sequência de Aminoácidos
Proteínas Virais/química
Proteínas Virais/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Viral Proteins)
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170321
[Lr] Data última revisão:
170321
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161117
[St] Status:MEDLINE
[do] DOI:10.1007/s00705-016-3139-6



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