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Original Articles

In ovo inhibition of fowlpoxvirus replication by a gall extract from Guiera senegalensis

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Pages 127-132 | Received 02 Apr 2004, Accepted 02 Jan 2004, Published online: 19 Oct 2010

Figures & data

Figure 1. Electron micrograph of FPV (arrows) stained with phosphotungstic acid (60 000× magnification). Bar=100 nm.

Figure 1. Electron micrograph of FPV (arrows) stained with phosphotungstic acid (60 000× magnification). Bar=100 nm.

Figure 2. PCR results of the FPV isolates from Burkina Faso. M, molecular markers; W, water control; P, positive control; C, cell culture control; 1, 2, 3, PCR products from FPVBKFOuaga 20021, FPVBKFOuaga 20022 and FPVBKFOuaga 20023 strains, respectively.

Figure 2. PCR results of the FPV isolates from Burkina Faso. M, molecular markers; W, water control; P, positive control; C, cell culture control; 1, 2, 3, PCR products from FPVBKFOuaga 20021, FPVBKFOuaga 20022 and FPVBKFOuaga 20023 strains, respectively.

Table 1. The toxic effects of increasing doses of a G. senegalensis extract for chicken embryos

Figure 3. Effect of G. senegalensis gall extracts on FPV growth on CAMs of 12-day-old chicken embryos. The effects of different concentrations used are indicated (arrows) at: (a) 0 μg/ml, a zone of diffuse lesions; (b) 25 μg/ml, well-formed pocks; (c) 250 μg/ml, considerably reduced number of pocks.

Figure 3. Effect of G. senegalensis gall extracts on FPV growth on CAMs of 12-day-old chicken embryos. The effects of different concentrations used are indicated (arrows) at: (a) 0 μg/ml, a zone of diffuse lesions; (b) 25 μg/ml, well-formed pocks; (c) 250 μg/ml, considerably reduced number of pocks.

Table 2. Antiviral activity of different doses of a G. senegalensis gall extract

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