scholarly journals A pathogenicity determinant maps to the N-terminal coat protein region of thePepino mosaic virusgenome

2014 ◽  
Vol 16 (3) ◽  
pp. 308-315 ◽  
Author(s):  
Celia R. A. Duff-Farrier ◽  
Andy M. Bailey ◽  
Neil Boonham ◽  
Gary D. Foster
Keyword(s):  
Coat Protein ◽  
Coat Protein Region ◽  
Pathogenicity Determinant

scholarly journals Molecular analyses of the coat protein region of different viruses on Poaceae belonging to the Potyviridae

Agronomie ◽  
1995 ◽  
Vol 15 (7-8) ◽  
pp. 491-494 ◽  
Author(s):  
R. Götz ◽  
W. Huth ◽  
E. Maiss
Keyword(s):  
Coat Protein ◽  
Molecular Analyses ◽  
Coat Protein Region

A unique nucleotide sequence variant in the coat protein region of the genome of aMaize dwarf mosaic virusisolate

2011 ◽  
Vol 46 (1) ◽  
pp. 11-15
Author(s):  
Gyöngyvér Gell ◽  
Kathrin Petrik ◽  
E. Balázs
Keyword(s):  
Nucleotide Sequence ◽  
Coat Protein ◽  
Sequence Variant ◽  
Coat Protein Region

EXPRESSION OF THE PLUM POX VIRUS COAT PROTEIN REGION IN ESCHERICHIA COLI

1989 ◽  
pp. 131-132
Author(s):  
D. Mattanovich ◽  
G. Himmler ◽  
M. Laimer ◽  
A. da Camara Machado ◽  
V. Hanzer ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Coat Protein ◽  
Plum Pox Virus ◽  
Coat Protein Region ◽  
Virus Coat Protein ◽  
Virus Coat

Identification a coat protein region of cucumber mosaic virus (CMV) essential for long-distance movement in cucumber

2011 ◽  
Vol 156 (12) ◽  
pp. 2279-2283 ◽  
Author(s):  
Katalin Salánki ◽  
László Kiss ◽  
Ákos Gellért ◽  
Ervin Balázs
Keyword(s):  
Coat Protein ◽  
Cucumber Mosaic Virus ◽  
Mosaic Virus ◽  
Long Distance ◽  
Coat Protein Region ◽  
Long Distance Movement

scholarly journals Cloning and Partial Characterization of Cotton Leaf Curl Burewala Virus From Khanewal

2021 ◽  
Vol 3 (1) ◽  
pp. 28-34
Author(s):  
Fizza Akhter ◽  
Muhammad Tahir
Keyword(s):  
Coat Protein ◽  
Complete Characterization ◽  
Universal Primers ◽  
Ammonium Bromide ◽  
Cotton Leaf ◽  
Cotton Production ◽  
Leaf Sample ◽  
Coat Protein Region ◽  
Leaf Curl

Begomoviruses are a serious threat to cotton production throughout the world. In Pakistan, enormous crop losses occur as a result of cotton leaf curl disease (CLCuD) caused by begomoviruses. Molecular characterization of begomoviruses has made possible the identification and analysis of begomoviruses prevalent in a host plant. Infected cotton leaf sample (C-59) was obtained from area around Khanewal during 2011. The total DNA was isolated from the infected sample by Cetyl trimethyl ammonium bromide (CTAB) method. An expected size band of approximately 1100bp, covering coat protein region of the virus, was amplified using universal primers. The amplified product was T/A cloned and sequenced to its entirety. DNA sequence showed 99% nucleotide sequence identity to each of Cotton leaf curl Burewala virus ((CLCuBuV; Accession No HF549Begomoviruses are a serious threat to cotton production throughout the world. In Pakistan, enormous crop losses occur as a result of cotton leaf curl disease (CLCuD) caused by begomoviruses. Molecular characterization of begomoviruses has made possible the identification and analysis of begomoviruses prevalent in a host plant. Infected cotton leaf sample (C-59) was obtained from area around Khanewal during 2011. The total DNA was isolated from the infected sample by Cetyl trimethyl ammonium bromide (CTAB) method. An expected size band of approximately 1100bp, covering coat protein region of the virus, was amplified using universal primers. The amplified product was T/A cloned and sequenced to its entirety. DNA sequence showed 99% nucleotide sequence identity to each of Cotton leaf curl Burewala virus ((CLCuBuV; Accession No HF549184)) and Cotton leaf curl Kokhran virus (CLCuKV; Accession No AJ002449)). Since CLCuBuV is a recombinant of CLCuKV and Cotton leaf curl Multan virus and the coat protein region of CLCuBuV was derived from CLCuKV that is most probable reason that the available sequence showed identity with CLCuBuV as well as CLCuKV. A complete characterization of full length virus will determine whether isolate C-59 is CLCuBuV or CLCuKV. Literature indicates that there is no existence of CLCuKV within the region and CLCuBuV is dominating within Indo-Pak184)) and Cotton leaf curl Kokhran virus (CLCuKV; Accession No AJ002449)). Since CLCuBuV is a recombinant of CLCuKV and Cotton leaf curl Multan virus and the coat protein region of CLCuBuV was derived from CLCuKV that is most probable reason that the available sequence showed identity with CLCuBuV as well as CLCuKV. A complete characterization of full length virus will determine whether isolate C-59 is CLCuBuV or CLCuKV. Literature indicates that there is no existence of CLCuKV within the region and CLCuBuV is dominating within Indo-Pak

The role of the coat protein region in symptom formation on Physalis floridana varies between PVY strains

2007 ◽  
Vol 127 (1) ◽  
pp. 122-125 ◽  
Author(s):  
Ágnes Bukovinszki ◽  
Reinhard Götz ◽  
Elisabeth Johansen ◽  
Edgar Maiss ◽  
Ervin Balázs
Keyword(s):  
Coat Protein ◽  
Coat Protein Region ◽  
Symptom Formation

scholarly journals First Report of Turnip mosaic virus on Watercress in Brazil

Plant Disease ◽  
2010 ◽  
Vol 94 (8) ◽  
pp. 1066-1066 ◽  
Author(s):  
H. Costa ◽  
J. A. Ventura ◽  
A. S. Jadão ◽  
J. A. M. Rezende ◽  
A. P. O. A. Mello
Keyword(s):  
Coat Protein ◽  
Mosaic Virus ◽  
Leaf Size ◽  
Turnip Mosaic Virus ◽  
Polyclonal Antiserum ◽  
Cauliflower Mosaic Virus ◽  
Mechanical Transmission ◽  
Rt Pcr ◽  
First Report ◽  
Coat Protein Region

Watercress (Nasturtium officinale L.), a member of the family Brassicaceae, is consumed mainly as salad. Medicinal properties have also been attributed to this species. In Brazil, watercress is grown mainly by very small farmers. The crop is primarily seed propagated and growers can harvest several times per year in an established planting. Very few diseases have been reported in this crop worldwide. In Brazil, watercress infection by Cauliflower mosaic virus (CaMV) (3), Cucumber mosaic virus (CMV) (1), and an unidentified potyvirus (2) were previously reported. In January 2009, 80% of watercress plants, cv. Gigante Redondo, exhibiting severe mosaic, leaf size reduction, and plant stunting were observed in a crop in Marechal Floriano Municipality, State of Espírito Santo, Brazil. Preliminary leaf dip analysis by transmission electron microscopy revealed the presence of potyvirus-like particles. Sap from five infected plants reacted in plate-trapped antigen (PTA)-ELISA with polyclonal antiserum against Turnip mosaic virus (TuMV), but not with antiserum against CMV. Both antisera were produced in the Plant Virology Laboratory, ESALQ/USP. Mechanically inoculated watercress plants developed similar systemic mosaic symptoms. The virus was also transmitted to Nicotiana benthamiana, which exhibited severe mosaic and stunting. The presence of TuMV on these inoculated plants was confirmed by PTA-ELISA and reverse transcription (RT)-PCR. Total RNA extracted from infected and healthy watercress and infected N. benthamiana was analyzed by RT-PCR using specific pairs of primers flanking the coat protein gene of TuMV. Degenerated anti-sense (5′-t/caacccctt/gaacgcca/cagt/ca-3′) and sense (5′-gcaggtgaa/gacg/acttgat/ca/gc-3′) primers were designed after analysis to an alignment of the nucleotide sequences for five isolates of TuMV available in the GenBank (Accession Nos. NC_002509, D10927, EU680574, AB362513, and D88614). One fragment of 838 bp was amplified from samples in the infected plants, but not in the healthy controls. Two amplicons were purified and directly sequenced in both directions. Comparisons of the 731-bp consensus nucleotide sequence (Accession No. HM008961) to several other isolates of TuMV revealed 94 to 95% identity in the coat protein region. To our knowledge, this is the first report of TuMV in watercress in Brazil. Management of the disease should include propagation by seeds instead of vegetative parts of the plants and rouging of diseased plants to prevent mechanical transmission during successive harvestings. References: (1) A. J. Boari et al. Fitopatol. Bras. 25:438, 2000. (2) A. J. Boari et al. Fitopatol. Bras. 27:S200, 2002. (3) M. L. R. Z. C. Lima et al. Fitopatol. Bras. 9:403, 1984.

Expression of the plum pox virus coat protein region in Escherichia coli

Virus Genes ◽  
1989 ◽  
Vol 2 (2) ◽  
pp. 119-127 ◽  
Author(s):  
Diethard Mattanovich ◽  
Gottfried Himmler ◽  
Margit Laimer ◽  
Edgar Maiss ◽  
Ferdinand Regner ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Coat Protein ◽  
Plum Pox Virus ◽  
Coat Protein Region ◽  
Virus Coat Protein ◽  
Virus Coat

Alpha coat protein COPA (HEP-COP): presence of an Alu repeat in cDNA and identity of the amino terminus to xenin

1997 ◽  
Vol 61 (4) ◽  
pp. 369-373 ◽  
Author(s):  
V. T. K. CHOW ◽  
H. H. QUEK
Keyword(s):  
Coat Protein ◽  
Amino Terminus ◽  
Alu Repeat

Successful in silico discovery of natural inhibitors for human rhinovirus coat protein

Planta Medica ◽  
2007 ◽  
Vol 73 (09) ◽  
Author(s):  
JM Rollinger ◽  
TM Steindl ◽  
K Anrain ◽  
EP Ellmerer ◽  
M Schmidtke ◽  
...  
Keyword(s):  
Coat Protein ◽  
In Silico ◽  
Human Rhinovirus ◽  
Natural Inhibitors
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