Detection and molecular characterization of phytoplasma associated with chickpea phyllody disease in south India
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作者:
M. S. Pallavi
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机构:University of Agricultural Sciences,Department of Plant Pathology
M. S. Pallavi
H. K. Ramappa
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机构:University of Agricultural Sciences,Department of Plant Pathology
H. K. Ramappa
K. S. Shankarappa
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机构:University of Agricultural Sciences,Department of Plant Pathology
K. S. Shankarappa
K. T. Rangaswamy
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机构:University of Agricultural Sciences,Department of Plant Pathology
K. T. Rangaswamy
W. A. R. T. Wickramaarachchi
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机构:University of Agricultural Sciences,Department of Plant Pathology
W. A. R. T. Wickramaarachchi
M. N. Maruthi
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机构:University of Agricultural Sciences,Department of Plant Pathology
M. N. Maruthi
机构:
[1] University of Agricultural Sciences,Department of Plant Pathology
[2] GKVK,AICRP on Pigeonpea, Zonal Agricultural Research Station
[3] University of Agricultural Sciences,Department of Horticultural Plant Pathology, K.R.C. College of Horticulture, Arabhavi
[4] University of Horticultural Sciences,591 310
[5] University of Greenwich,Natural Resources Institute
来源:
Phytoparasitica
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2012年
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40卷
关键词:
Nested-PCR;
Polymerase chain reaction;
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学科分类号:
摘要:
Chickpea (Cicer arietinum L.) plants showing typical symptoms of infection by a phytoplasma that causes phyllody disease have been commonly observed in recent years in parts of south India. The symptoms included pale green leaves, bushy appearance due to excessive stunting of shoots, reduced internodal length and excessive axillary proliferation. The causal agent of the phyllody disease was identified based on symptoms, amplification of 16S rDNA of the phytoplasma by polymerase chain reaction (PCR) from infected samples, as well as by sequencing and phylogenetic analysis. First round PCR and nested-PCR protocols were standardized for improved efficiency and reliability of the diagnostic protocols. Using the primers P1/P7 and R16F2n/R16R2, 1,800 bp and 1,200 bp size products were amplified in first round PCR and nested-PCR protocols, respectively. The PCR product was cloned and sequenced and compared with the reference phytoplasma sequences from the database (NCBI). The Indian chickpea phyllody phytoplasma 16S rDNA sequences shared the highest nucleotide identity (>98%) with the 16S rII group phytoplasma candidates, also infecting chickpea from Australia and Pakistan. This is the first report of a phytoplasma of the 16SrII-group infecting chickpea from India. The genetic similarities and the potential threat of this new disease to chickpea cultivation in India are discussed.
机构:
KSCSTE Kerala Forest Res Inst, Forest Pathol Dept, Div Forest Hlth, Trichur, Kerala, India
Bot Survey India, Andaman & Nicobar Reg Ctr, Port Blair 744102, IndiaKSCSTE Kerala Forest Res Inst, Forest Pathol Dept, Div Forest Hlth, Trichur, Kerala, India
Mahadevakumar, S.
Sarma, P. V. S. R. N.
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机构:
Univ Hyderabad, Sch Life Sci, Dept Plant Sci, Hyderabad, Telangana, IndiaKSCSTE Kerala Forest Res Inst, Forest Pathol Dept, Div Forest Hlth, Trichur, Kerala, India
Sarma, P. V. S. R. N.
Danteswari, C.
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机构:
Univ Hyderabad, Sch Life Sci, Dept Plant Sci, Hyderabad, Telangana, IndiaKSCSTE Kerala Forest Res Inst, Forest Pathol Dept, Div Forest Hlth, Trichur, Kerala, India
Danteswari, C.
Joy, Josna
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机构:
Univ Mysore, Dept Studies Microbiol, Mysuru, Karnataka, IndiaKSCSTE Kerala Forest Res Inst, Forest Pathol Dept, Div Forest Hlth, Trichur, Kerala, India
Joy, Josna
Chandranayaka, S.
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机构:
Univ Mysore, Dept Studies Biotechnol, Millets Pathol Lab, Mysuru 570006, Karnataka, IndiaKSCSTE Kerala Forest Res Inst, Forest Pathol Dept, Div Forest Hlth, Trichur, Kerala, India
Chandranayaka, S.
Patro, T. S. S. K.
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机构:
Acharya NG Ranga Agr Univ, Dept Plant Pathol, Agr Res Stn, Vizianagaram 535001, Andhra Pradesh, IndiaKSCSTE Kerala Forest Res Inst, Forest Pathol Dept, Div Forest Hlth, Trichur, Kerala, India