Localization of the divisome protein FtsL in Francisella tularensis LVS.

• DOI: 10.55632/pwvas.v97i2.1139
• Publication Date: 2025-04-08T15:25:00Z
• Authors: Abigale Riggle; Stuart Cantlay

Francisella tularensis is a gram-negative bacterium categorized as a tier 1 select agent. Fatal disease can be caused by very low doses, leading to the potential of F. tularensis being used as a bioterror agent. Understanding cell division in F. tularensis could yield important insights for the development of a vaccine or antimicrobial treatments. Understanding how F. tularensis divides may also shed light on how the bacterium is able to enter a Viable-but-not-Culturable (VBNC) state. This VBNC state could be a contributing factor to survival in the environment and during phagocytosis into host cells. Known divisome proteins of Escherichia coli include FtsZ, FtsA, and ZipA, which are involved in the assembly of the cytokinetic proto-ring. Divisome proteins, such as the FtsQLBWI complex and FtsN are recruited to the proto-ring, directing the formation of the division septum. Currently, very little is known about the F. tularensis divisome. Ftl_1540 is predicted to encode the FtsL homolog in F. tularensis Live Vaccine Strain (LVS). To learn more about the function of FtsL, we aim to generate an FtsL-EMGFP fluorescence fusion protein by cloning Ftl_1540 into two EMGFP reporter plasmids, pSC18, which contains a strong promoter, and pSC13 which is promoterless. We expect that ftsL cloned into pSC18 will result in robust production of FtsL-EMGFP allowing its localization in bacterial cells and the promoterless construct will serve as a negative control. (This work was supported by NIH Grant P20GM103434 to the West Virginia IDeA Network for Biomedical Research Excellence).