Biological properties, transmission, serological characterization and varietal susceptibility of an isolate of Papaya leaf curl virus affecting papaya crops in Eastern Uttar Pradesh, India

2015 ◽  
Vol 48 (7) ◽  
pp. 611-621 ◽  
Author(s):  
Durgesh Dubey ◽  
Naveen Pandey ◽  
Ajay Kumar Tiwari ◽  
Parmatma Prasad Upadhyaya
Plant Disease ◽  
2020 ◽  
Vol 104 (11) ◽  
pp. 3089
Author(s):  
Aamir Lal ◽  
Eui-Joon Kil ◽  
Kainat Rauf ◽  
Muhammad Ali ◽  
Sukchan Lee

2020 ◽  
Vol 165 (8) ◽  
pp. 1877-1881
Author(s):  
Afzal Akram ◽  
Aqsa Hafeez Khan ◽  
Ghulam Rasool ◽  
Shahid Mansoor ◽  
Peter Moffett ◽  
...  

Plant Disease ◽  
2021 ◽  
Author(s):  
Minor R Maliano ◽  
Tomas Melgarejo ◽  
Maria J. Rojas ◽  
Natalia Barboza ◽  
Robert Gilbertson

Since the early 1990s, squash production in Costa Rica has been affected by a whitefly-transmitted disease characterized by stunting and yellow mottling of leaves. The squash yellow mottle disease (SYMoD) was shown to be associated with a bipartite begomovirus, originally named squash yellow mild mottle virus (SYMMoV). It was subsequently established that SYMMoV is a strain of melon chlorotic leaf curl virus (MCLCuV), a bipartite begomovirus that causes a chlorotic leaf curl disease of melons in Guatemala. In the present study, the complete sequences of the DNA-A and DNA-B components of a new isolate of the strain MCLCuV-Costa Rica (MCLCuV-CR) were determined. Comparisons of full-length DNA-A sequences revealed 97% identity with a previously characterized isolate of MCLCuV-CR, and identities of 90 to 91% with those of isolates of the strain MCLCuV-Guatemala (MCLCuV-GT), which is below or at the current begomovirus species demarcation threshold of 91%. A more extensive analysis of the MCLCuV-CR and -GT sequences revealed substantial divergence in both components and different histories of recombination for the DNA-A components. The cloned full-length DNA-A and DNA-B components of this new MCLCuV-CR isolate were infectious and induced SYMoD in a range of squashes and in pumpkin, thereby fulfilling Koch’s postulates for this disease. However, in contrast to MCLCuV-GT, MCLCuV-CR induced mild symptoms in watermelon and no symptoms in melon and cucumber. Taken together, our results indicate that MCLCuV-CR and -GT have substantially diverged, genetically and biologically, and have evolved to cause distinct diseases of different cucurbit crops. Taxonomically, these viruses are at the strain/species boundary, but retain the designation as strains of Melon chlorotic leaf curl virus under current ICTV guidelines.


2010 ◽  
pp. 241-246 ◽  
Author(s):  
N. Srivastava ◽  
R. Chandra ◽  
S. Saxena ◽  
A. Bajpai

Plant Disease ◽  
2003 ◽  
Vol 87 (2) ◽  
pp. 204-204 ◽  
Author(s):  
L.-S. Chang ◽  
Y.-S. Lee ◽  
H.-J. Su ◽  
T.-H. Hung

Papaya leaf curl disease was first reported in India in 1939 (1). Caused by begomovirus, Papaya leaf curl virus (PaLCV) (2), this disease was discovered in the papaya orchards of southern Taiwan in 2002. Infected papaya developed symptoms such as downward curling of leaves, twisted petioles, vein enation, and stunting. Diseased plants produced small and distorted fruits that tend to fall prematurely. Typical twin virion was observed in the diseased papaya cells by electron microscopy. In addition, our whitefly-transmission test demonstrated that the sweet potato whitefly (Bemisia tabaci) could transmit this virus. For further molecular identification, two opposing primers were selected for the polymerase chain reaction (PCR) detection of PaLCV from the published nucleotide sequences of PaLCV (Genbank Accession No. NC004147) (3). The primer pair, composed of the forward primer 5′ -GCT AGA AAT TAT GTC GAA GCG-3′ and the reverse primer 5′-TCA ACT ACA ACC TGA GGA AAG C-3′, was designed to amplify a PaLCV-specific 1,031-bp fragment containing 774 bp of the coat protein gene open reading frame (CP-ORF) using PCR. Five diseased papaya samples with typical leaf-curl symptoms tested positive in the PCR-based assay with this specific primer pair, whereas five healthy papaya samples tested negative. However, the sequencing results of the PCR product from five PaLCV-infected papayas indicated the CP-ORF of PaLCV in Taiwan (PaLCV-Tw) was somewhat different from PaLCV in India (PaLCV-Id). The DNA sequences (Genbank Accession No. AY183472) of CP-ORF of PaLCV-Tw were 80% identical to those of PaLCV-Id, and their translated amino acid sequences were 77% identical. This indicates that PaLCV-Tw and PaLCV-Id are two different species or strains. References: (1) K. M. Thomas and C. S. Krishnaswamy. Curr. Sci. 8:316,1939. (2) S. Saxena et al. Plant Dis. 82:126, 1998. (3) S. Saxena et al. Biochem. Mol. Biol. Int. 45:101, 1998.


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