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Characterization and variation of zucchini yellow mosaic virus isolated from pumpkins in Korea : 국내 호박에서 분리한 zucchini yellow mosaic virus의 特性 및 變異究明

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Authors

권상욱

Advisor
김국형
Issue Date
2003
Publisher
서울대학교 대학원
Keywords
물집현상Zucchini yellow mosaic virus황화현상Rt-pcr기주범위Sequence analysisCucumis meloCucmis saivus
Description
Thesis (master`s)--서울대학교 대학원 :농생명공학부,2003.
Abstract
Zucchini yellow mosaic virus (ZYMV), a member of the Genus Potyvirus, is one of the most
economically important viruses of cucurbit crops. Biological variability has been observed among
ZYMV isolates, concerning host range, symptomatology and aphid transmissibility. We obtained
three ZYMV isolates from pumpkins at Andong (ZYMV-PA), Euiryung (ZYMV-PE), and Suwon (ZYMV-PS),
respectively. In order to determine biological variability of each ZYMV isolate, these isolates
were inoculated to the different host plants including cucurbit and some indicator plants. Each
ZYMV isolate displayed distinctive symptoms on cucurbit plants as well as indicator plants.
Symptoms induced by ZYMV isolates in watermelon, leaves in watermelon; ZYMV-PA isolate developed
a yellow mosaic, leaves of ZYMV-PE isolate developed a yellow mosaic and became blistered and
those of ZYMV-PS isolate developed a yellow mosaic and blistered. In cucumber, leaves of ZYMV-PA
leaves became severely blistered and malformed, leaves of ZYM-PE developed vein banding and
leaves of ZYMV-PS developed a yellow mosaic and became severely blistered, malformed. In
oriental melon, leaves of ZYMV-PA inoculated plants developed yellowing and became severly
blistered and malformed, leaves of ZYMV-PE developed yellowing, vein banding and became dwarfed
and leaves of ZYMV-PS developed yellowing, vein banding and became malformed. Only ZYMV-PS did
not infected with Gomphrena globosa, indicator plant.
Sequence of the genomic RNA of each isolate was also determined by reverse transcriptionpolymerase
chain reaction (RT-PCR) using specific oligonucleotide primers and by the 5'' and 3''
RACE. The genomic RNA was 9.5 kb in length and contained one open reading frame encoding 350 kDa
protein that is proteolytically cleaved by self-encoded proteases into functional proteins.
The base composition of three isolates, PA was 31.34% adenine, 23.59% guanine, 19.19% cytosine,
25.88% uracil, PE isolate was 31.53% adenine, 23.59% guanine, 19.10% cytosine, 25.79% uracil, PS
isolate was 31.56% adenine, 23.57% guanine, 19.11% cytosine, 25.76% uracil.
Language
English
URI
http://dcollection.snu.ac.kr:80/jsp/common/DcLoOrgPer.jsp?sItemId=000000057907

https://hdl.handle.net/10371/68523
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