Francisella tularensis is the causative agent of the zoonotic disease tularemia. We investigated a pathogenic factor of F. tularensis subsp. novicida (F. novicida). Accordingly, we established a novel infection model using HeLa cells. F. novicida usually infects macrophage lineage cells and less frequently epithelial cells. We successfully infected HeLa cells expressing the Fc receptor (HeLa–FcγRII cells) using F. novicida supplemented with mouse serum containing F. novicida antibodies. A total of 2, 232 transposon mutants of F. novicida were screened to determine the relatively fewer cytotoxic strains of the HeLa–FcγRII cells, and 13 strains were thus isolated. Sequencing analysis of transposon insertion sites identified 13 genes, including FTN₀096. We focused on FTN₀096. Although the F. novicida wild-type strain proliferated in HeLa–FcγRII and THP-1 cells, the number of intracellular FTN₀096 mutant decreased. FTN₀096 mutant cannot escape from phagolysosomes in the initial phases of infection. Moreover, FTN₀096 mutant was detected in the mitochondria and Golgi complex. These findings indicate the importance of FTN₀096 of F. novicida for intracellular replication in the cells.
Wardhana et al. (Fri,) studied this question.