Abstract

The occurrence of Cryptococcus neoformans, the human fungal pathogen that primarily infects immunocompromised individuals, has been progressing at an alarming rate. The increased incidence of infection of C. neoformans with antifungal drugs resistance has become a global concern. Potential antifungal agents with extremely low toxicity are urgently needed. Herein, the biological activities of recombinant javanicin (r-javanicin) against C. neoformans were evaluated. A time-killing assay was performed and both concentration- and time-dependent antifungal activity of r-javanicin were indicated. The inhibitory effect of the peptide was initially observed at 4 h post-treatment and ultimately eradicated within 36 to 48 h. Fungal outer surface alteration was characterized by the scanning electron microscope (SEM) whereas a negligible change with slight shrinkage of external morphology was observed in r-javanicin treated cells. Confocal laser scanning microscopic analysis implied that the target(s) of r-javanicin is conceivably resided in the cell thereby allowing the peptide to penetrate across the membrane and accumulate throughout the fungal body. Finally, cryptococcal cells coped with r-javanicin were preliminarily investigated using label-free mass spectrometry-based proteomics. Combined with microscopic and proteomics analysis, it was clearly elucidated the peptide localized in the intracellular compartment where carbohydrate metabolism and energy production associated with glycolysis pathway and mitochondrial respiration, respectively, were principally interfered. Overall, r-javanicin would be an alternative candidate for further development of antifungal agents.

Highlights

  • The number of immunocompromised individuals including patients with organ transplantations, AIDS, as well as people living with cancer and receiving chemotherapy is increasing worldwide [1]

  • The results indicated that C. neoformans adjusted 106 colony-forming units (CFU)/mL was completely killed at a peptide concentration of 25 μg/mL whereas it needed a two-fold increase (50 μg/mL) while 107 CFU/mL yeast cells prepared for proteomic analysis, were examined

  • The growth inhibition of r-javanicin antimicrobial peptide against C. neoformans was initiated at 4 h post-treatment

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Summary

Introduction

The number of immunocompromised individuals including patients with organ transplantations, AIDS, as well as people living with cancer and receiving chemotherapy is increasing worldwide [1]. These individuals are at risk of being infected with opportunistic fungal pathogens, resulting in the increase of morbidity and mortality rates [2]. Treatment of cryptococcal meningitis relies on the use of three classes of antifungal drugs, amphotericin B, flucytosine, and fluconazole [4]. These agents are limited due to their adverse effects in which are sometimes lethal to humans [5,6]. Novel antifungal agents to control cryptococcosis are urgently needed

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