KAJIAN SEROLOGI DAN MOLEKULER CRINIVIRUS PADA TANAMAN TOMAT
Tomato chlorosis virus (ToCV) and Tomato infectious chlorosis virus (TICV) are whitefly vectors-transmitted virus, members of the family Closteroviridae, genus Crinivirus that causes yellowing which has been causing serious production problems in tomato crops, production is affected through decrease...
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Main Authors: | , |
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Format: | Theses and Dissertations NonPeerReviewed |
Published: |
[Yogyakarta] : Universitas Gadjah Mada
2014
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Subjects: | |
Online Access: | https://repository.ugm.ac.id/130868/ http://etd.ugm.ac.id/index.php?mod=penelitian_detail&sub=PenelitianDetail&act=view&typ=html&buku_id=71301 |
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Institution: | Universitas Gadjah Mada |
Summary: | Tomato chlorosis virus (ToCV) and Tomato infectious chlorosis virus
(TICV) are whitefly vectors-transmitted virus, members of the family
Closteroviridae, genus Crinivirus that causes yellowing which has been causing
serious production problems in tomato crops, production is affected through
decreased fruit size and numbers yield.
This research aimed to detect the ToCV and TICV in tomato plant by
serological and molecular detection and knowing the detection methods that
specific, accurate, fast, and simple. The sample of disease plant was collected
from Kopeng and Magelang (Central Java), Indonesia. Five methods are
serological (DTBIA, IEM, and IC-PCR) and molecular methods (SDT-RT-PCR,
and RT-PCR from commercial kit) were using specific polyclonal antibodies and
primers of TICV and ToCV.
The result of IEM methods was found two types of particles viruses which
flexuous filamentus. Particle lengths of ToCV and TICV were 810.69 nm and
872.34 nm, respectively. The positive reaction of DTBIA method indicated purple
or magenta discoloration in the phloem limited of top, bottom, side shoots, and
yellow curly symptoms on plants and healthy plants remained green, no color
change. IC-PCR, SDT-RT-PCR, and RT-PCR methods were successfully
amplified TICV DNA from Magelang isolate, 416 bp size. Blast analysis of
nucleotide and amino acid sequences to make sure that Crinivirus species is
TICV.
The ToCV species was detected with IEM and DTBIA methods, where as
the TICV species by the IEM, DTBIA, IC-PCR, SDT-RT-PCR, and RT-PCR. The
fifth method is specific detection tool, the IC-PCR have higher accuracy, the
DTBIA more practical and cheper, the IEM have faster but expensive. The SDTRT-
PCR methods are simpler, faster, and cheper than RT-PCR to gain the total
RNA. Based from the nucleotide sequencing and amino acid gene CPd, the
Magelang isolate that infected in tomatoes was detected as TICV that include in
the GenusCrinivirus, Family Closteroviridae.
Key words: Yellowing diseases, Tomatoes, TICV, ToCV, Serological detection,
Molecular detection |
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