MICU1 and MICU2 Play an Essential Role in Mitochondrial Ca2+ Uptake, Growth, and Infectivity of the Human Pathogen Trypanosoma cruzi

Author(s)

Bertolini, Mayara S. ^{[1, 2, 3]} ; Chiurillo, Miguel A. ^{[1, 2, 3]} ; Lander, Noelia ^{[1, 2, 3]} ; Vercesi, Anibal E. ^[1] ; Docampo, Roberto ^{[1, 2, 3]}

Affiliation

^[1] Univ Estadual Campinas, Fac Ciencias Med, Dept Patol Clin, Campinas, SP - Brazil

^[2] Univ Georgia, Ctr Trop & Emerging Global Dis, Athens, GA 30602 - USA

^[3] Univ Georgia, Dept Cellular Biol, Athens, GA 30602 - USA

• Document type: Journal article
• Source: MBIO; v. 10, n. 3 MAY-JUN 2019.
• Web of Science Citations: 1

Abstract

The mitochondrial Ca2+ uptake in trypanosomatids, which belong to the eukaryotic supergroup Excavata, shares biochemical characteristics with that of animals, which, together with fungi, belong to the supergroup Opisthokonta. However, the composition of the mitochondrial calcium uniporter (MCU) complex in trypanosomatids is quite peculiar, suggesting lineage-specific adaptations. In this work, we used Trypanosoma cruzi to study the role of orthologs for mitochondrial calcium uptake 1 (MICU1) and MICU2 in mitochondrial Ca2+ uptake. T. cruzi MICU1 (TcMICU1) and TcMICU2 have mitochondrial targeting signals, two canonical EF-hand calcium-binding domains, and localize to the mitochondria. Using the CRISPR/Cas9 system (i. e., clustered regularly interspaced short palindromic repeats with Cas9), we generated TcMICU1 and TcMICU2 knockout (-KO) cell lines. Ablation of either TcMICU1 or TcMICU2 showed a significantly reduced mitochondrial Ca2+ uptake in permeabilized epimastigotes without dissipation of the mitochondrial membrane potential or effects on the AMP/ATP ratio or citrate synthase activity. However, none of these proteins had a gatekeeper function at low cytosolic Ca2+ concentrations ({[}Ca2+](cyt)), as occurs with their mammalian orthologs. TcMICU1-KO and TcMICU2-KO epimastigotes had a lower growth rate and impaired oxidative metabolism, while infective trypomastigotes have a reduced capacity to invade host cells and to replicate within them as amastigotes. The findings of this work, which is the first to study the role of MICU1 and MICU2 in organisms evolutionarily distant from animals, suggest that, although these components were probably present in the last eukaryotic common ancestor (LECA), they developed different roles during evolution of different eukaryotic supergroups. The work also provides new insights into the adaptations of trypanosomatids to their particular life styles. IMPORTANCE Trypanosoma cruzi is the etiologic agent of Chagas disease and belongs to the early-branching eukaryotic supergroup Excavata. Its mitochondrial calcium uniporter (MCU) subunit shares similarity with the animal ortholog that was important to discover its encoding gene. In animal cells, the MICU1 and MICU2 proteins act as Ca2+ sensors and gatekeepers of the MCU, preventing Ca2+ uptake under resting conditions and favoring it at high cytosolic Ca2+ concentrations ({[}Ca2+] cyt). Using the CRISPR/Cas9 technique, we generated TcMICU1 and TcMICU2 knockout cell lines and showed that MICU1 and -2 do not act as gatekeepers at low {[}Ca2+] cyt but are essential for normal growth, host cell invasion, and intracellular replication, revealing lineage-specific adaptations. (AU)

• FAPESP's process: 14/08995-4 - Calcium signaling in trypanosomatids
• Grantee: Noelia Marina Lander Manfredi
• Support Opportunities: Scholarships in Brazil - Post-Doctoral
• FAPESP's process: 14/13148-9 - Calcium signaling in trypanosomatids
• Grantee: Miguel Angel Chiurillo Siervo
• Support Opportunities: Scholarships in Brazil - Post-Doctoral
• FAPESP's process: 15/25709-8 - Functional study of MICU1 and MICU2 proteins involved in Trypanosoma cruzi calcium signaling
• Grantee: Mayara Santos Bertolini
• Support Opportunities: Scholarships in Brazil - Master
• FAPESP's process: 13/50624-0 - Calcium signaling in trypanosomatids
• Grantee: Roberto Docampo
• Support Opportunities: Research Projects - SPEC Program