Incidence, Molecular Detection, and Partial Nucleotide Sequencing of Some Viruses Causing Fig Mosaic Disease (FMD) on Fig Plants in Egypt

Figure 4

(a) RT-PCR amplification of fig mosaic virus (FMV) in fig samples as demonstrated by gel electrophoresis analysis. M: DNA marker ladder weight 100 bp, lanes (1–15): different symptomatic fig samples, lane 16: positive control, and lane 17: healthy fig sample used as a negative control. (b) Gel electrophoresis demonstrating RT-PCR amplification of fig leaf mottle-associated virus 1 (FLMaV-1) in fig samples. M: DNA marker ladder weight 100 bp, lanes (1–14): different symptomatic fig samples, lane 15: positive control, and lane 16: healthy fig sample used as a negative control. (c) Gel electrophoresis demonstrating RT-PCR amplification of fig leaf mottle-associated virus 2 (FLMaV-2) in fig samples. M: DNA marker ladder weight 100 bp, lanes (1–14): different symptomatic fig samples, lane 15: positive control, and lane 16: healthy fig sample used as a negative control.

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