Sadlova, J.; Vojtkova, B.; Becvar, T.; Dobramysl, U.; Moeri, S.; Alagoez, C.; Wheeler, R. J.; Volf, P.; Gluenz, E.; Albuquerque-Wendt, A.

Leishmania amastigotes ingested by female phlebotomine sand flies are exposed to a harsh and dynamic environment, markedly different from that of their mammalian host. Within the sand fly s alimentary tract, these parasite forms encounter shifts in temperature, pH and nutrient availability, which trigger significant morphological and physiological adaptations. Membrane transporter proteins, channels and pumps play a crucial role in facilitating the movement of solutes across eukaryotic membranes. Previously, a systematic loss-of-function screen of the L. mexicana transportome identified forty transporter deletion mutants that caused significant loss of fitness in macrophage and mouse infections. Here, using an independently generated library of over 300 barcoded gene deletion mutants, we monitored their growth fitness for seven days in vitro and tested which transporters are required for Leishmania promastigotes to successfully colonise Lutzomyia longipalpis sand flies for nine days. Overall, fitness scores correlated between promastigotes from long-term in vitro culture and in vivo sand fly infections. More importantly, for 34 mutants, a significant loss of fitness was observed exclusively in vivo. Moreover, deletion of the vacuolar H+ ATPase (V-ATPase) proved detrimental for parasite persistence and promastigote differentiation in the sand fly, uncovering a key role for the V-ATPase at different stages throughout the Leishmania life cycle.