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Published on: March 16, 2018
Interactions of antimicrobial peptides with Leishmania and trypanosomes and their functional role in host parasitism
Bradford S McGwire1, Manjusha M Kulkarni
1Center for Microbial Interface Biology, Department of Internal Medicine, The Ohio State University, Columbus, Ohio, USA. brad.mcgwire@osumc.edu
Abstract:
Antimicrobial peptides (AMPs) are multifunctional components of the innate systems of both insect and mammalian hosts of the pathogenic trypanosomatids Leishmania and Trypanosoma species. Structurally diverse AMPs from a wide range of organisms have in vitro activity against these parasites acting mainly to disrupt surface-membranes. In some cases AMPs also localize intracellularly to affect calcium levels, mitochondrial function and induce autophagy, necrosis and apoptosis. In this review we discuss the work done in the area of AMP interactions with trypanosomatid protozoa, propose potential targets of AMP activity at the cellular level and discuss how AMPs might influence parasite growth and differentiation in their hosts to determine the outcome of natural infection.
Insights
Antimicrobial peptides (AMPs) disrupt trypanosomatid protozoa membranes and affect intracellular functions. This review explores AMPs
Area of Science:
- Parasitology
- Immunology
- Biochemistry
Background:
- Antimicrobial peptides (AMPs) are key innate immune components in hosts of trypanosomatids.
- Pathogenic trypanosomatids, including Leishmania and Trypanosoma species, are targeted by AMPs.
Purpose of the Study:
- To review AMP interactions with trypanosomatid protozoa.
- To identify potential cellular targets of AMP activity.
- To explore AMPs' influence on parasite growth, differentiation, and infection outcomes.
Main Methods:
- Literature review of existing research on AMPs and trypanosomatids.
- Analysis of in vitro studies demonstrating AMP activity.
- Discussion of proposed intracellular mechanisms and host-parasite interactions.
Main Results:
- AMPs exhibit in vitro activity against trypanosomatids, primarily by disrupting parasite membranes.
- AMPs can localize intracellularly, affecting host cell calcium, mitochondria, and inducing cell death pathways (autophagy, necrosis, apoptosis).
Conclusions:
- AMPs represent a promising therapeutic avenue against trypanosomatid infections.
- Further research into AMP mechanisms and host interactions is crucial for understanding infection outcomes.
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