Fig. 2

Disruption of pgm1 and growth assays. A Schematic representation of disruption of pgm1 using CRISPR-Cas9 gene-editing system for nonhomologous insertion of the hxgprt selectable marker cassette. The dotted line represents the region in the first exon of pgm1 targeted by the small guide RNA (sgPGM1). B Image of DNA gel electrophoresis of PCR1-3 performed using DNA from wildtype (WT) and mutant (Δpgm1) to demonstrate integration of the hxgprt expression cassette at the pgm1 locus. The expected product for PCR1 (212 bp) was obtained only for WT while products for PCR2 (813 bp) and PCR3 (1185 bp) were amplified only with Δpgm1 DNA. C Intracellular growth. HFFs were infected with 1.2 × 10⁵ WT or Δpgm1 parasites for 24 h in cDMEM. Monolayers were fixed and stained with antibodies raised against SAG1 (tachyzoite surface marker) and GRA7 (PV marker). Intracellular parasites were enumerated in at least 20 vacuoles/strain/experiment, N = 3 independent experiments; error bars = standard error of the mean; p-value was determined by Chi-square test. D Total numbers of plaques counted 10 days after infection of HFFs with 250 WT or Δpgm1 parasites. E Plaque areas were determined for 85 WT and 109 Δpgm1 plaques using Fiji/ImageJ in pixels², N = 3 replicates/strain in a single experiment, error bar = standard deviation; ns: p-value > 0.05 by nonparametric Mann–Whitney test