» Articles » PMID: 33806654

Microorganisms As a Potential Source of Molecules to Control Trypanosomatid Diseases

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2021 Apr 3
PMID 33806654
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Trypanosomatids are the causative agents of leishmaniasis and trypanosomiasis, which affect about 20 million people in the world's poorest countries, leading to 95,000 deaths per year. They are often associated with malnutrition, weak immune systems, low quality housing, and population migration. They are generally recognized as neglected tropical diseases. New drugs against these parasitic protozoa are urgently needed to counteract drug resistance, toxicity, and the high cost of commercially available drugs. Microbial bioprospecting for new molecules may play a crucial role in developing a new generation of antiparasitic drugs. This article reviews the current state of the available literature on chemically defined metabolites of microbial origin that have demonstrated antitrypanosomatid activity. In this review, bacterial and fungal metabolites are presented; they originate from a range of microorganisms, including cyanobacteria, heterotrophic bacteria, and filamentous fungi. We hope to provide a useful overview for future research to identify hits that may become the lead compounds needed to accelerate the discovery of new drugs against trypanosomatids.

Citing Articles

Saturated Iso-Type Fatty Acids from the Marine Bacterium with Anti-Trypanosomal Potential.

Santos Ferreira D, de Castro Levatti E, Santa Cruz L, Costa A, Migotto A, Yamada A Pharmaceuticals (Basel). 2024; 17(4).

PMID: 38675459 PMC: 11053438. DOI: 10.3390/ph17040499.


Plant Terpenoids as Hit Compounds against Trypanosomiasis.

Durao R, Ramalhete C, Madureira A, Mendes E, Duarte N Pharmaceuticals (Basel). 2022; 15(3).

PMID: 35337138 PMC: 8951850. DOI: 10.3390/ph15030340.

References
1.
Moyersoen J, Choe J, Fan E, Hol W, Michels P . Biogenesis of peroxisomes and glycosomes: trypanosomatid glycosome assembly is a promising new drug target. FEMS Microbiol Rev. 2004; 28(5):603-43. DOI: 10.1016/j.femsre.2004.06.004. View

2.
Suganuma K, Sarwono A, Mitsuhashi S, Jakalski M, Okada T, Nthatisi M . Mycophenolic Acid and Its Derivatives as Potential Chemotherapeutic Agents Targeting Inosine Monophosphate Dehydrogenase in Trypanosoma congolense. Antimicrob Agents Chemother. 2016; 60(7):4391-3. PMC: 4914658. DOI: 10.1128/AAC.02816-15. View

3.
Pimentel-Elardo S, Kozytska S, Bugni T, Ireland C, Moll H, Hentschel U . Anti-parasitic compounds from Streptomyces sp. strains isolated from Mediterranean sponges. Mar Drugs. 2010; 8(2):373-80. PMC: 2852844. DOI: 10.3390/md8020373. View

4.
Garcia Linares G, Ravaschino E, Rodriguez J . Progresses in the field of drug design to combat tropical protozoan parasitic diseases. Curr Med Chem. 2006; 13(3):335-60. DOI: 10.2174/092986706775476043. View

5.
Da Costa J, Rodrigues A, Farias L, Frade P, Da Silva B, do Nascimento J . Biological effects of kojic acid on human monocytes in vitro. Biomed Pharmacother. 2018; 101:100-106. DOI: 10.1016/j.biopha.2018.02.036. View