New Disease Reports (2019) 39, 2. [http://dx.doi.org/10.5197/j.2044-0588.2019.039.002]
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First report of Chickpea chlorotic dwarf virus in watermelon (Citrullus lanatus) in Morocco

N. Radouane 1,2, S. Ezrari 1,2, G.P. Accotto 3, M. Benjelloun 2, R. Lahlali 1, A. Tahiri 1 and A.M. Vaira 3*

*annamaria.vaira@ipsp.cnr.it

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Received: 30 Oct 2018; Published: 08 Jan 2019

Keywords: Citrullus lanatus, Mastrevirus, viral plant disease, watermelon

Watermelon (Citrullus lanatus) is one of the most important cucurbit crops in the world, with a total production of c. 118 million tons (FAO, 2017). It is a popular fruit in many Mediterranean countries and is widely cultivated. In Morocco an area of 16,680 ha is grown annually with a production of 619,322 tonnes in 2017.

During 2015 watermelon plants with fruits showing cracking, yellowing and brown areas in the flesh were observed in some areas in Morocco. During 2017, similar symptoms were again observed in the regions of Marrakech, Tifelt and Zagoura. The symptoms observed (Fig. 1) were similar to those caused by Chickpea chlorotic dwarf virus (CpCDV, genus Mastrevirus, family Geminiviridae) which was recently reported affecting watermelon in Tunisia inducing "hard fruit syndrome" (Zaagueri et al., 2017a).

Seventeen samples of watermelon leaves from symptomatic plants were collected (six from Marrakech, four from Tifelt and seven from Zagoura) and were subjected to total nucleic acid extraction by the TLES buffer-based method (50 mM Tris-HCl, pH 9, 150 mM LiCl, 5 mM EDTA, and 5% SDS), according to Noris et al. (1996). CpCDV infection was detected by dot-blot hybridization, using a digoxigenin-labeled probe targeting the coat protein gene (Zaagueri et al., 2017b) and was confirmed by PCR using a novel primer pair CpCDV-SEQ2 (5'-CGACACATAAGGTTCAGGTTG-3') and CpCDV-Tu-1145-R (5'-AGGCAACCCTTGGGAGTCA-3'), amplifying a 544 bp fragment in the Rep gene. Four samples out of fifteen collected in 2017 (samples 11, 12, 14 and 15) and one sample out of two collected in 2015 (Sample 'R') were positive for CpCDV by PCR (Fig. 2, upper panel). All five infected samples were collected in the Zagoura area, south-eastern Morocco. Infection in three of five of the samples was confirmed by dot-blotting (Fig. 2, lower panel). To further confirm CpCDV detection, three positive samples collected in 2017 were amplified by PCR using the CP-targeting primer pair CpCDV-CP-F/R (Zaagueri et al., 2017b) and the 501 bp products were sequenced on both strands. The three sequences (GenBank Accession Nos. MH500777 - MH500779) were almost identical except for four mismatches. BLAST analysis identified a CpCDV isolate from squash in Egypt (KF692356) as the best match in the NCBI database.

These results constitute the first record of CpCDV infecting watermelon in Morocco and indicate that the virus has been present in the country since at least 2015. In the Mediterranean region, CpCDV has only been previously reported in Egypt (Fahmy et al., 2015) and Tunisia (Zaagueri et al., 2017b), and this report indicates that the virus may be more widely distributed than indicated by published records.

Figure1+
Figure 1: Watermelon fruit showing symptoms resembling “hard fruit syndrome” (Courtesy of Mr Faiq Mourad, Prograines, Morocco).
Figure 1: Watermelon fruit showing symptoms resembling “hard fruit syndrome” (Courtesy of Mr Faiq Mourad, Prograines, Morocco).
Figure2+
Figure 2: Upper panel: 1% agarose gel showing PCR amplification of the CpCDV-specific fragment (544bp) in watermelon samples 1 to 15 (collected in 2017) and L, R (collected in 2015); M: 100bp marker, the 500bp fragment is labelled with *; nt: no template control; +: positive control. Lower panel: dot blot assay of the same samples; H: healthy watermelon tissue; L: unspecific reaction not confirmed by PCR; +: positive control.
Figure 2: Upper panel: 1% agarose gel showing PCR amplification of the CpCDV-specific fragment (544bp) in watermelon samples 1 to 15 (collected in 2017) and L, R (collected in 2015); M: 100bp marker, the 500bp fragment is labelled with *; nt: no template control; +: positive control. Lower panel: dot blot assay of the same samples; H: healthy watermelon tissue; L: unspecific reaction not confirmed by PCR; +: positive control.

Acknowledgements

The authors would like to thank D. Marian for his excellent technical assistance.


References

  1. Fahmy IF, Taha O, El-Ashry AN, 2015. First genome analysis and molecular characterization of Chickpea chlorotic dwarf virus Egyptian isolate infecting squash. Virus Disease 26, 33-41. [http://dx.doi.org/10.1007/s13337-014-0246-4]
  2. FAO, 2017. Corporate Statistical Database, http://www.fao.org/faostat/en/#data/QC. Accessed 7 January 2019.
  3. Noris E, Accotto GP, Tavazza R, Brunetti A, Crespi S, Tavazza M, 1996. Resistance to tomato yellow leaf curl geminivirus in Nicotiana benthamiana plants transformed with a truncated viral C1 gene. Virology 224, 130-138. [http://dx.doi.org/10.1006/viro.1996.0514]
  4. Zaagueri T, Miozzi L, Mnari-Hattab M, Noris E, Accotto GP, Vaira AM, 2017a. Deep sequencing data and infectivity assays indicate that Chickpea chlorotic dwarf virus is the etiological agent of the "hard fruit syndrome" of watermelon. Viruses 9, 311. [http://dx.doi.org/10.3390/v9110311]
  5. Zaagueri T, Mnari-Hattab M, Zammouri S, Hajlaoui MR, Accotto GP, Vaira, AM, 2017b. First report of Chickpea chlorotic dwarf virus in watermelon (Citrullus lanatus) in Tunisia. Plant Disease , 392. [http://dx.doi.org/10.1094/PDIS-07-16-1028-PDN]

To cite this report: Radouane N, Ezrari S, Accotto GP, Benjelloun M, Lahlali R, Tahiri A, Vaira AM, 2019. First report of Chickpea chlorotic dwarf virus in watermelon (Citrullus lanatus) in Morocco. New Disease Reports 39, 2. [http://dx.doi.org/10.5197/j.2044-0588.2019.039.002]

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