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. Author manuscript; available in PMC: 2019 Jun 19.
Published in final edited form as: Can J Microbiol. 2017 Aug 17;63(10):857–863. doi: 10.1139/cjm-2017-0350

Figure 1.

Figure 1.

Liquid killing assays. C. elegans was allowed to feed for 16 hours on B. cenocepacia K56–2, E. coli OP50 (non-pathogenic control), or the B. cenocepacia CGetf mutant (ETF) in the presence of 0.2% rhamnose to mimic WT levels of etf expression. Twenty to 30 worms were added to 96-wells plates containing 100 μl of liquid killing medium with (A) or without (B) the presence of 0.2% rhamnose. Four wells were inoculated per condition. The number of worms was counted every 24 hours for 7 days and plotted as survival curves using GraphPad Prism. K56–2 carrying the plasmid pSCrhaB2, which confers resistant to trimethoprim, was included as a control.