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In Vivo Infection with Leishmania amazonensis to Evaluate Parasite Virulence in Mice
Published on: February 20, 2020
L-arginine metabolism and its impact on host immunity against Leishmania infection
1Department of Microbiology, Institute for Human Infections and Immunity, Center for Biodefense and Emerging Infections, Sealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555-1070, USA.
Abstract:
Leishmaniasis is a vector-borne disease found in many countries worldwide. The causative agent of the disease, Leishmania spp., lives as an obligate intracellular parasite within mammalian hosts. Since tissue macrophages are major target cells for parasite replication, the outcome of infection depends largely on the activation status of these cells. L-arginine is a crucial amino acid required for both nitric oxide (NO)-mediated parasite killing and polyamine-mediated parasite replication. This review highlights the significance of L-arginine as a factor determining the outcomes of Leishmania infection in vitro and its influences on host immune responses in vivo. Various therapeutic approaches targeting L-arginine metabolic pathways during infections with Leishmania are also discussed.
Insights
L-arginine metabolism critically impacts Leishmania infection outcomes. Understanding its role in host immune responses and parasite replication is key for developing new therapies against this vector-borne disease.
Area of Science:
- Immunology
- Parasitology
- Molecular Biology
Background:
- Leishmaniasis is a global vector-borne disease caused by Leishmania parasites.
- Parasites infect mammalian macrophages, making their activation status crucial for infection outcome.
- L-arginine is vital for both parasite killing (via nitric oxide) and replication (via polyamines).
Purpose of the Study:
- To review the role of L-arginine in Leishmania infection.
- To explore L-arginine's influence on host immune responses in vitro and in vivo.
- To discuss therapeutic strategies targeting L-arginine metabolism.
Main Methods:
- Literature review of studies on Leishmania infection and L-arginine metabolism.
- Analysis of in vitro and in vivo experimental data.
- Synthesis of information on therapeutic approaches.
Main Results:
- L-arginine availability dictates Leishmania parasite fate within macrophages.
- Nitric oxide production, dependent on L-arginine, is essential for parasite clearance.
- Polyamines, also derived from L-arginine, support parasite replication.
Conclusions:
- L-arginine is a central metabolic factor influencing Leishmania infection dynamics.
- Targeting L-arginine pathways offers potential therapeutic avenues for leishmaniasis.
- Further research into L-arginine metabolism is crucial for effective disease control.
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