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dc.contributor.authorLivieratos, I.C.
dc.contributor.authorCoutts, Robert H.A.
dc.contributor.authorAvgelis, A.D.
dc.date.accessioned2013-10-01T11:30:16Z
dc.date.available2013-10-01T11:30:16Z
dc.date.issued1999
dc.identifier.citationLivieratos , I C , Coutts , R H A & Avgelis , A D 1999 , ' Molecular characterization of the cucurbit yellow stunting disorder virus coat protein gene ' , Phytopathology , vol. 89 , no. 11 , pp. 1050-1055 .
dc.identifier.issn0031-949X
dc.identifier.otherPURE: 1954491
dc.identifier.otherPURE UUID: 4dd26003-4bb2-4b65-bfcb-1a1e219898aa
dc.identifier.otherScopus: 0032697414
dc.identifier.urihttp://hdl.handle.net/2299/11696
dc.description.abstractCucurbit yellow stunting disorder virus (CYSDV) is a partially characterized bipartite closterovirus transmitted by the tobacco whitefly (Bemisia tabaci). CYSDV has emerged as a serious pathogen in southeastern Spain and the Mediterranean Region, causing yellowing disease of cucumber and melon crops. Using a modified reverse-transcription polymerase chain reaction protocol with gel-extracted dsRNA templates, fragments of CYSDV RNA2 were amplified and cloned. Sequence analysis of the cloned fragments revealed open reading frames encoding the heat shock protein 70 homolog, two proteins of unknown function (p58 and p9), and the coat protein (CP) of the virus in a contiguous gene arrangement similar to that of lettuce infectious yellows virus (LIYV) RNA2. The complete CYSDV CP gene is 756 nt long and encodes a protein with a molecular mass of 28.5 kDa. A comparison of the amino acid sequence of the CYSDV CP gene with those of other closteroviruses revealed significant levels of similarity with sweet potato chlorotic stunt virus and LIYV (36 and 27%, respectively), both of which are members of the recently proposed Crinivirus genus of closteroviruses. The complete CYSDV CP gene was cloned into a bacterial expression vector, and the resulting fusion protein was purified and used to produce antiserum. Purified immunoglobulins specifically detected CYSDV in infected plant extracts, both in immunoblot and indirect enzyme-linked immunosorbent assays with a titer exceeding 2,000 times for both assays.en
dc.format.extent6
dc.language.isoeng
dc.relation.ispartofPhytopathology
dc.titleMolecular characterization of the cucurbit yellow stunting disorder virus coat protein geneen
dc.contributor.institutionGeography, Environment and Agriculture
dc.contributor.institutionCrop and Environmental Protection
dc.contributor.institutionAgriculture, Veterinary and Food Sciences
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.contributor.institutionDepartment of Human and Environmental Sciences
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=0032697414&partnerID=8YFLogxK
dc.relation.schoolSchool of Life and Medical Sciences
dcterms.dateAccepted1999
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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