Figure 6 | Scientific Reports

Figure 6

From: Development of a viability digital PCR protocol for the selective detection and quantification of live Erwinia amylovora cells in cankers

Figure 6

Effect of the maceration buffer, SDS and PMA Enhancer for Gram negative bacteria on the suppression of E. amylovora dead cell signals by v-dPCR. Apple branch macerates prepared either with AMB (solid columns) or 0.1xAMB (dashed columns) were inoculated with E. amylovora live (106 CFU mL−1), dead (106 dead cells mL−1) or a mixture of live (103 CFU mL−1) and dead cells (106 dead cell mL−1). Total cell numbers were quantified by dPCR. The effect of SDS and PMA Enhancer on viable cell quantification was assessed comparing v-dPCR viable cell counts of samples (i) only treated with PMA (100 μM); (ii) PMA plus 0.0025% (w/v) SDS (PMA + SDS); (iii) PMA plus PMA Enhancer (PMA + E). For both, total and viable cell quantification, primers targeting a 627 bp DNA sequence were used. Columns represent mean values of three independent experiments in duplicate. Error bars show the SD. Different letters denote statistically significant differences.

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