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. 2020 Nov 13;10:559915. doi: 10.3389/fcimb.2020.559915

Figure 2.

Figure 2

The ankF::Tn mutant has no replication defect in axenic culture. (A) Scheme of the genomic region of wild-type C. burnetii and C. burnetii-ankF::Tn at the ankF locus. The transposable element is inserted between bp 507 and 508 of the ankF coding sequence and contains a GFP reporter under the control of the C. burnetii promotor P311 and a chloramphenicol resistance cassette under the control of the C. burnetii promotor P1169. (B) Agarose gel of PCR products from wild-type C. burnetii and ankF::Tn generated with primers specific for the ankF coding sequence (shown as halved arrows in A). (C) Wild-type C. burnetii and ankF::Tn were inoculated at an OD600 of 0.01 in ACCM-2 medium and incubated at 37°C, 2.5% O2 and 5% CO2. OD600 was determined by spectrophotometric analysis at the indicated time-points post-inoculation. Error bars represent the mean standard deviation of three independent experiments.