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Antifungal profile against Candida auris clinical isolates of tyroscherin and its new analog produced by the deep-sea-derived fungal strain Scedosporium apiospermum FKJ-0499

  • Haruki Azami,
  • Yoshihiro Watanabe,
  • Kazunari Sakai,
  • Hiroki Nakahara,
  • Hiroki Kojima,
  • Toshiyuki Tokiwa,
  • Kenichi Nonaka,
  • Yoshihiko Noguchi,
  • Yuriko Nagano,
  • Tomoyasu Hirose,
  • Toshiaki Sunazuka,
  • Hidehito Matsui,
  • Naoaki Arima,
  • Kazutoyo Abe,
  • Hideaki Hanaki,
  • Masato Iwatsuki

摘要

A new antifungal compound, named N-demethyltyroscherin (1), was discovered from the static fungal cultured material of Scedosporium apiospermum FKJ-0499 isolated from a deep-sea sediment sample together with a known compound, tyroscherin (2). The structure of 1 was elucidated as a new analog of 2 by MS and NMR analyses. The absolute configuration of 1 was determined by chemical derivatization. Both compounds showed potent in vitro antifungal activity against clinically isolated Candida auris strains, with MIC values ranging from 0.0625 to 4 µg ml–1.