Extracellular Vesicles Released by Leishmania (Leishmania) amazonensis Promastigotes with Distinct Virulence Profile Differently Modulate the Macrophage Functions

Author:

Zauli Rogéria Cristina1,de Souza Perez Isabelle Carlos2,de Morais Aline Correia Costa1ORCID,Ciaccio Ana Carolina2,Vidal Andrey Sladkevicius1,Soares Rodrigo Pedro3ORCID,Torrecilhas Ana Claudia4,Batista Wagner Luiz4ORCID,Xander Patricia145

Affiliation:

1. Programa de Pós-Graduação Biologia-Química, Instituto de Ciências Ambientais Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema 04021-001, SP, Brazil

2. Curso de Ciências Biológicas, Instituto de Ciências Ambientais Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema 04021-001, SP, Brazil

3. Biotecnologia Aplicada a Patógenos (BAP), Instituto René Rachou, Fundação Oswaldo Cruz (FIOCRUZ), Belo Horizonte 30190-002, MG, Brazil

4. Departamento de Ciências Farmacêuticas, Instituto de Ciências Ambientais Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema 04021-001, SP, Brazil

5. Laboratório de Imunologia Celular e Bioquímica de Fungos e Protozoários, Unidade José Alencar, Universidade Federal de São Paulo campus Diadema, 4° andar, Rua São Nicolau, 210, Centro, Diadema 09913-030, SP, Brazil

Abstract

Leishmania spp. is the aetiologic agent of leishmaniasis, a disease endemic in several developing countries. The parasite expresses and secretes several virulence factors that subvert the macrophage function and immune response. Extracellular vesicles (EVs) can carry molecules of the parasites that show immunomodulatory effects on macrophage activation and disease progression. In the present work, we detected a significantly higher expression of lpg3 and gp63 genes in Leishmania amazonensis promastigotes recovered after successive experimental infections (IVD-P) compared to those cultured for a long period (LT-P). In addition, we observed a significantly higher percentage of infection and internalized parasites in groups of macrophages infected with IVD-P. Macrophages previously treated with EVs from LT-P showed higher percentages of infection and production of inflammatory cytokines after the parasite challenge compared to the untreated ones. However, macrophages infected with parasites and treated with EVs did not reduce the parasite load. In addition, no synergistic effects were observed in the infected macrophages treated with EVs and reference drugs. In conclusion, parasites cultured for a long period in vitro and recovered from animals’ infections, differently affected the macrophage response. Furthermore, EVs produced by these parasites affected the macrophage response in the early infection of these cells.

Funder

FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO

CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO

COORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

Reference45 articles.

1. (2023, October 30). World Health Organization (WHO), Control of the Leishmaniases. Available online: https://www.who.int/health-topics/leishmaniasis.

2. Leishmaniasis;Burza;Lancet,2018

3. Kamhawi, S. (2017). The yin and yang of leishmaniasis control. PLoS Negl. Trop. Dis., 11.

4. Anti-trypanosomatid drug discovery: Progress and challenges;Wyllie;Nat. Rev. Microbiol.,2023

5. Advancement in leishmaniasis diagnosis and therapeutics: An update;Kumari;Eur. J. Pharmacol.,2021

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