Anti-leishmanial compounds from microbial metabolites: a promising source.

Bioactive compounds Leishmaniasis Microbial metabolites Scientific database Secondary metabolites

Journal

Applied microbiology and biotechnology
ISSN: 1432-0614
Titre abrégé: Appl Microbiol Biotechnol
Pays: Germany
ID NLM: 8406612

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 13 07 2021
accepted: 20 09 2021
revised: 18 09 2021
pubmed: 10 10 2021
medline: 3 11 2021
entrez: 9 10 2021
Statut: ppublish

Résumé

Leishmania is a complex disease caused by the protozoan parasites and transmitted by female phlebotomine sandfly. The disease affects some of the poorest people on earth with an estimated 700,000 to 1 million new cases annually. The current treatment for leishmaniasis is toxic, long, and limited, in view of the high resistance rate presented by the parasite, necessitating new perspectives for treatment. The discovery of new compounds with different targets can be a hope to make the treatment more efficient. Microbial metabolites and their structural analogues with enormous scaffold diversity and structural complexity have historically played a key role in drug discovery. We found thirty-nine research articles published between 1999 and 2021 in the scientific database (PubMed, Science Direct) describing microbes and their metabolites with activity against leishmanial parasites which is the focus of this review. KEY POINTS: • Leishmania affects the poorest regions of the globe • Current treatments for leishmaniasis are toxic and of limited efficacy • Microbial metabolites are potential sources of antileishmania drugs.

Identifiants

pubmed: 34625819
doi: 10.1007/s00253-021-11610-6
pii: 10.1007/s00253-021-11610-6
doi:

Substances chimiques

Antiprotozoal Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

8227-8240

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Ana F S da Cunha (AFS)

Industrial Biotechnology Post-Graduation Program, University of Tiradentes, Aracaju, Sergipe, Brazil.

Yvanna L Di C Oliveira (YL)

Pharmaceutical Sciences Post-Graduation Program, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil.

Silvio S Dolabella (SS)

Pharmaceutical Sciences Post-Graduation Program, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil.

Ricardo Scher (R)

Laboratory of Cancer and Leishmania Biology and Immunology, Department of Morphology, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil.

Eliana B Souto (EB)

CEB - Centre of Biological Engineering, University of Minho, Campus de Gualtar, Braga, Portugal. eliana.souto@ceb.uminho.pt.

Jorge A Lopez (JA)

Industrial Biotechnology Post-Graduation Program, University of Tiradentes, Aracaju, Sergipe, Brazil.

Sona Jain (S)

Industrial Biotechnology Post-Graduation Program, University of Tiradentes, Aracaju, Sergipe, Brazil. sonajain24@yahoo.com.

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