شماره مدرك :
4069
شماره راهنما :
3847
پديد آورنده :
شاه پسندي، مهدي
عنوان :

رديابي و تعيين برخي خصوصيات ملكولي پلروويروس هاي آلوده كننده چغندرقند در استان هاي اصفهان و چهارمحال بختياري

مقطع تحصيلي :
كارشناسي ارشد
گرايش تحصيلي :
بيماري شناسي گياهي
محل تحصيل :
اصفهان: دانشگاه صنعتي اصفهان، دانشكده كشاورزي
سال دفاع :
1386
صفحه شمار :
يازده، 85، [II] ص.: مصور، جدول، نمودار
يادداشت :
ص. ع. به فارسي و انگليسي
استاد راهنما :
امير مساح، علي آهون منش
توصيفگر ها :
ويروس زردي , داس اليزا , تاس اليزا
تاريخ نمايه سازي :
05/05/87
استاد داور :
مسعود بهار، پرويز احسان زاده
تاريخ ورود اطلاعات :
1396/03/08
كتابنامه :
كتابنامه
رشته تحصيلي :
كشاورزي
دانشكده :
مهندسي كشاورزي
كد ايرانداك :
ID3847
چكيده فارسي :
به فارسي و انگليسي: قابل رؤيت در نسخه ديجيتال
چكيده انگليسي :
AbstractMembers of the genus Polerovirus Luteoviridae that cause yellowing in sugar beetconsist of three species Beet mild yellowing virus BMYV Beet western yellows virus BWYV and Beet chlorosis virus BChV For detection and determination of certainmolecular properties of poleroviruses infecting sugar beet during 1385 1386 571 leafsamples of sugar beet with yellowing and thickening symptoms in older leaves werecollected from sugar beet fields at Isfahan and Charmahal o bakhtiary provinces Samples were tested using a polyclonal BWYV antibody in DAS ELISA technique None of samples in Chahar mahal o bakhtiary province were infected to polerovirusesof infecting sugar beet Of the 290 Isfahan samples tested 5 samples recognizedinfected to polerovirus by DAS ELISA RT PCR was conducted on the ELISA positivesamples using specific primers of beet poleroviruses The primer used to amplify ORF3 Coat protein gen of beet poleroviruses was CP and CP Three sets of primers wereused to amplify ORF0 of beet poleroviruses consisting of MpxBM and MpxBM MpxBW and MpxBW and MpxBC and MpxBC for specific detection of BMYV BWYV and BChV respectively Expected sizes of 563 bp and 441 bp were amplifiedusing CP and CP and MpxBM and MpxBM primers respectively These specificamplifications represent presence of BMYV in infected sugar beet samples The PCRproducts of an isolate named BMYV Lav were cloned and sequenced Multiplealignment of deduced amino acid sequence of ORF0 gene of BMYV Lav and those ofother poleroviruses infecting beet and rape revealed the highest similarity with BMYV 1 isolate 98 whereas analysis of amino acid CP gene showed the highest similaritywith a BWYV isolate 97 9 with Brassica yellow virus GB In phylogenetic analysisbased on amino acid sequence of ORF0 gene a gene at 5 end of genome BMYV Lavwas placed in BMYV isolates group whereas alignment of Coat protein CP gene agene at 3 end of genome of BMYV Lav showed that BMYV Lav isolate was closer toBWYV isolates than BMYV isolates These results suggested taking place ofrecombination in BMYV Lav
استاد راهنما :
امير مساح، علي آهون منش
استاد داور :
مسعود بهار، پرويز احسان زاده
لينک به اين مدرک :

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