Brilacidin, a novel antifungal agent against Cryptococcus neoformans

Author:

Diehl Camila1ORCID,Pinzan Camila Figueiredo1,de Castro Patrícia Alves1,Delbaje Endrews1,García Carnero Laura C.1,Sánchez-León Eddy2,Bhalla Kabir2,Kronstad James W.2ORCID,Kim Dong-gyu3,Doering Tamara L.3ORCID,Alkhazraji Sondus4,Mishra Nagendra N.45ORCID,Ibrahim Ashraf S.45,Yoshimura Mami6,Vega Isuhuaylas Luis Alberto7,Pham Lien Thi Kim6,Yashiroda Yoko6,Boone Charles678,dos Reis Thaila Fernanda1,Goldman Gustavo H.19ORCID

Affiliation:

1. Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil

2. Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada

3. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA

4. Division of Infectious Diseases, The Lundquist Institute for Biomedical Innovation at Harbor-University of California Los Angeles (UCLA) Medical Center, Torrance, California, USA

5. David Geffen School of Medicine at UCLA, Los Angeles, California, USA

6. RIKEN Center for Sustainable Resource Science, Wako, Saitama, Japan

7. Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada

8. Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada

9. National Institute of Science and Technology in Human Pathogenic Fungi, São Paulo, Brazil

Abstract

ABSTRACT Cryptococcus neoformans causes cryptococcosis, one of the most prevalent fungal diseases, generally characterized by meningitis. There is a limited and not very effective number of drugs available to combat this disease. In this manuscript, we show the host defense peptide mimetic brilacidin (BRI) as a promising antifungal drug against C. neoformans . BRI can affect the organization of the cell membrane, increasing the fungal cell permeability. We also investigated the effects of BRI against the model system Saccharomyces cerevisiae by analyzing libraries of mutants grown in the presence of BRI. In S. cerevisiae , BRI also affects the cell membrane organization, but in addition the cell wall integrity pathway and calcium metabolism. In vivo experiments show BRI significantly reduces C. neoformans survival inside macrophages and partially clears C. neoformans lung infection in an immunocompetent murine model of invasive pulmonary cryptococcosis. We also observed that BRI interacts with caspofungin (CAS) and amphotericin (AmB), potentiating their mechanism of action against C. neoformans . BRI + CAS affects endocytic movement, calcineurin, and mitogen-activated protein kinases. Our results indicate that BRI is a novel antifungal drug against cryptococcosis. IMPORTANCE Invasive fungal infections have a high mortality rate causing more deaths annually than tuberculosis or malaria. Cryptococcosis, one of the most prevalent fungal diseases, is generally characterized by meningitis and is mainly caused by two closely related species of basidiomycetous yeasts, Cryptococcus neoformans and Cryptococcus gattii . There are few therapeutic options for treating cryptococcosis, and searching for new antifungal agents against this disease is very important. Here, we present brilacidin (BRI) as a potential antifungal agent against C. neoformans . BRI is a small molecule host defense peptide mimetic that has previously exhibited broad-spectrum immunomodulatory/anti-inflammatory activity against bacteria and viruses. BRI alone was shown to inhibit the growth of C. neoformans , acting as a fungicidal drug, but surprisingly also potentiated the activity of caspofungin (CAS) against this species. We investigated the mechanism of action of BRI and BRI + CAS against C. neoformans . We propose BRI as a new antifungal agent against cryptococcosis.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

American Society for Microbiology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Busting Cryptococcus with brilacidin;Nature Reviews Microbiology;2024-07-08

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