<i>Trypanosoma cruzi</i> Letm1 is involved in mitochondrial Ca <sup>2+</sup> transport, and is essential for replication, differentiation, and host cell invasion
Guilherme Rodrigo Reis Monteiro dos Santos, Ana Catarina Rezende Leite, Noelia Lander, Miguel Ángel Chiurillo, Anı́bal E. Vercesi, Roberto Docampo
Abstract
Abstract Leucine zipper‐EF‐hand containing transmembrane protein 1 (Letm1) is a mitochondrial inner membrane protein involved in Ca 2+ and K + homeostasis in mammalian cells. Here, we demonstrate that the Letm1 orthologue of Trypanosoma cruzi , the etiologic agent of Chagas disease, is important for mitochondrial Ca 2+ uptake and release. The results show that both mitochondrial Ca 2+ influx and efflux are reduced in TcLetm1 knockdown ( TcLetm1 ‐KD) cells and increased in TcLetm1 overexpressing cells, without alterations in the mitochondrial membrane potential. Remarkably, TcLetm1 knockdown or overexpression increases or does not affect mitochondrial Ca 2+ levels in epimastigotes, respectively. TcLetm1 ‐KD epimastigotes have reduced growth, and both overexpression and knockdown of TcLetm1 cause a defect in metacyclogenesis. TcLetm1 ‐KD also affected mitochondrial bioenergetics. Invasion of host cells by TcLetm1 ‐KD trypomastigotes and their intracellular replication is greatly impaired. Taken together, our findings indicate that TcLetm1 is important for Ca 2+ homeostasis and cell viability in T cruzi .