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International Journal of Clinical & Medical Microbiology Volume 1 (2016), Article ID 1:IJCMM-111, 5 pages
https://doi.org/10.15344/2456-4028/2016/111
Research Article
In Vitro Antifungal Activity of Cysteine Derivatives and their Combinations with Antifungal Agents Against Clinically Relevant Scedosporium species

László Galgóczy1,2*, Mónika Homa1, Tamás Papp1, Palanisamy Manikandan3,4 and Csaba Vágvölgyi1

1University of Szeged, Faculty of Science and Informatics, Department of Microbiology, Közép fasor 52, H-6726 Szeged, Hungary
2Medical University of Innsbruck, Biocenter, Division of Molecular Biology, Innrain 80-82, A-6020, Innsbruck, Austria
3Department of Microbiology and Molecular Biology, Aravind Eye Hospital and Postgraduate Institute of Ophthalmology, Coimbatore-641014, Tamilnadu, India
4College of Applied Medical Sciences, Majmaah University, Majmaah 11952, Kingdom of Saudi Arabia
Dr. László Galgóczy, Faculty of Science and Informatics, Department of Microbiology, Közép fasor 52, H-6726 Szeged, Hungary, Tel: +36 62 544005; E-mail: galgoczi@gmail.com
25 June 2016; 09 August 2016; 11 August 2016
Galgóczy L, Homa M, Papp T, Manikandan P, Vágvölgyi C (2016) In Vitro Antifungal Activity of Cysteine Derivatives and their Combinations with Antifungal Agents Against Clinically Relevant Scedosporium species. Int J Clin Med Microbiol 1: 111. doi: https://doi.org/10.15344/2456-4028/2016/111
The study was supported by the European Union co-financed by the European Social Fund (TÁMOP-4.2.2.B-15/1/KONV-2015-0006). This work was also funded by the grant LP2016-8/2016.

Abstract

Background: Members of the genus Scedosporium are emerging human pathogens, causing a wide range of infections. Their treatment means a challenge for clinicians, mostly because of the low susceptibility of these causative agents to conventional antifungal drugs. New alternative therapeutic approaches are required for better clinical outcomes. Cysteine and its derivatives alone or in combinations with antifungal drugs might have improved antifungal effects against Scedosporium species.

Methods: The in vitro antifungal effects of two cysteine forms and three of their derivatives (i.e., D-cysteine, L-cysteine, L-cysteine-methyl ester hydrochloride, N-isobutyryl-D-cysteine, and N-isobutyryl-L-cysteine) were determined using the CLSI M38-A2 broth microdilution method. The in vitro drug interactions between the most effective cysteine derivatives and some conventional antifungal drugs were also investigated using checkerboard assays in case of four clinical isolates.

Results: L-cysteine-methyl ester hydrochloride proved to be the most effective among the investigated compounds. N-isobutyryl-L-cysteine exhibited antifungal activity against one Scedosporium aurantiacum strain only. D-cysteine, L-cysteine and N-isobutyryl-D-cysteine proved to be ineffective against Scedosporium spp. in the investigated concentration range. No significant differences were found in the susceptibilities between environmental and clinical isolates. L-cysteine-methyl ester hydrochloride could interact synergistically with amphotericin B, caspofungin, terbinafine and voriconazole. Antagonistic interactions were not observed between the investigated compounds.

Conclusions: The present study provides an evidence for the in vitro antifungal activity of L-cysteinemethyl ester hydrochloride and the synergistic interactions between this cysteine derivative and conventional antifungal agents. Based on our results, L-cysteine-methyl ester hydrochloride in combination with antifungal drugs could be applicable in the treatment of human Scedosporium infections in the future. However, further studies are required to clarify the antifungal mechanism of L-cysteine-methyl ester hydrochloride and to investigate its activity in vivo.