RCA

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Molecular Characterization of Watermelon Chlorotic Stunt Virus (WmCSV) from Palestine

Journal Title, Volume, Page: 
Viruses 2014, 6(6), 2444-2462; doi:10.3390/v6062444
Year of Publication: 
2014
Authors: 
Mohammed S. Ali-Shtayeh
Biodiversity and Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus 970, Palestine
Current Affiliation: 
Department of Biology and Biotechnology, Faculty of Science, An-Najah National University, Nablus, Palestine
Rana M. Jamous
Biodiversity and Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus 970, Palestine
Omar B. Mallah
Biodiversity and Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus 970, Palestine
Salam Y. Abu-Zeitoun
Biodiversity and Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus 970, Palestine
Preferred Abstract (Original): 

The incidence of watermelon chlorotic stunt disease and molecular characterization of the Palestinian isolate of Watermelon chlorotic stunt virus (WmCSV-[PAL]) are described in this study. Symptomatic leaf samples obtained from watermelon Citrullus lanatus (Thunb.), and cucumber (Cucumis sativus L.) plants were tested for WmCSV-[PAL] infection by polymerase chain reaction (PCR) and Rolling Circle Amplification (RCA). Disease incidence ranged between 25%–98% in watermelon fields in the studied area, 77% of leaf samples collected from Jenin were found to be mixed infected with WmCSV-[PAL] and SLCV. The full-length DNA-A and DNA-B genomes of WmCSV-[PAL] were amplified and sequenced, and the sequences were deposited in the GenBank. Sequence analysis of virus genomes showed that DNA-A and DNA-B had 97.6%–99.42% and 93.16%–98.26% nucleotide identity with other virus isolates in the region, respectively. Sequence analysis also revealed that the Palestinian isolate of WmCSV shared the highest nucleotide identity with an isolate from Israel suggesting that the virus was introduced to Palestine from Israel.  

MSShtayeh's picture

Squash Leaf Curl Virus (SLCV): A Serious Disease Threatening Cucurbits Production in Palestine

Journal Title, Volume, Page: 
Virus Genes November 2013
Year of Publication: 
2013
Authors: 
M S Ali-Shtayeh
Biodiversity & Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus, Palestine
Current Affiliation: 
Department of Biology and Biotechnology, Faculty of Science, An-Najah National University, Nablus, Palestine
R M Jamous
Biodiversity & Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus, Palestine
E Y Hussein
Biodiversity & Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus, Palestine
O B Mallah
Biodiversity & Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus, Palestine
S Y Abu-Zeitoun
Biodiversity & Biotechnology Research Unit, Biodiversity and Environmental Research Center-BERC, Til, Nablus, Palestine
Preferred Abstract (Original): 

The incidence of squash leaf curl disease and molecular characterization of the Palestinian isolate of Squash leaf curl virus [SLCV-(PAL)] are described in this study. Symptomatic leaf samples obtained from squash (Cucurbita pepo), watermelon [Citrullus lanatus (Thunb.)], and cucumber (Cucumis sativus L.) plants were tested for SLCV-[PAL] infection by PCR and RCA. SLCV was also found to occur naturally in Chenopodium murale, Convolvulus sp, and Prosporis farcta which showed yellowing. The disease incidence was 85 % in samples collected from Nablus in summer season, while it was 98 % in samples collected from Qalqilia in autumn. On the other hand, SLCV incidence did not exceed 25 % in winter season. The full-length DNA-A and DNA-B genomes of SLCV-[PAL] were amplified and sequenced, and the sequences were deposited in the GenBank. Sequence analysis reveals that SLCV-[PAL] is closely related to other isolates from Lebanon (SLCV-LB2), Jordan (SLCV-JO), Israel (SLCV-IL), and Egypt (SLCV-EG). DNA-A of SLCV-[PAL] showed the highest nucleotide identity (99.4 %) with SLCV-JO, and SLCV-LB2, while DNA-B had the highest nucleotide identity (99.3 %) with SLCV-IL. However, following genome sequencing, it was found that due to two separate point mutations, two viral open reading frames (ORF) were altered in some SLCV Palestinian isolates. The AC2 ORF was extended by 141 nucleotides, while the AC4 ORF was extended by 36 nucleotides.

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