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A small molecule produced by Lactobacillus species blocks Candida albicans filamentation by inhibiting a DYRK1-family kinase

Author

Listed:
  • Jessie MacAlpine

    (University of Toronto)

  • Martin Daniel-Ivad

    (University of Toronto)

  • Zhongle Liu

    (University of Toronto)

  • Junko Yano

    (Center of Excellence in Oral and Craniofacial Biology, Louisiana State University Health Sciences Center School of Dentistry)

  • Nicole M. Revie

    (University of Toronto)

  • Robert T. Todd

    (University of Minnesota Medical School)

  • Peter J. Stogios

    (University of Toronto
    Center for Structural Genomics of Infectious Diseases (CSGID))

  • Hiram Sanchez

    (University of Wisconsin School of Medicine and Public Health
    University of Wisconsin)

  • Teresa R. O’Meara

    (University of Michigan Medical School)

  • Thomas A. Tompkins

    (Rosell Institute for Microbiome and Probiotics, 6100 Avenue Royalmount)

  • Alexei Savchenko

    (University of Toronto
    Center for Structural Genomics of Infectious Diseases (CSGID)
    University of Calgary)

  • Anna Selmecki

    (University of Minnesota Medical School)

  • Amanda O. Veri

    (University of Toronto)

  • David R. Andes

    (University of Wisconsin School of Medicine and Public Health
    University of Wisconsin)

  • Paul L. Fidel

    (Center of Excellence in Oral and Craniofacial Biology, Louisiana State University Health Sciences Center School of Dentistry)

  • Nicole Robbins

    (University of Toronto)

  • Justin Nodwell

    (University of Toronto)

  • Luke Whitesell

    (University of Toronto)

  • Leah E. Cowen

    (University of Toronto)

Abstract

The fungus Candida albicans is an opportunistic pathogen that can exploit imbalances in microbiome composition to invade its human host, causing pathologies ranging from vaginal candidiasis to fungal sepsis. Bacteria of the genus Lactobacillus are colonizers of human mucosa and can produce compounds with bioactivity against C. albicans. Here, we show that some Lactobacillus species produce a small molecule under laboratory conditions that blocks the C. albicans yeast-to-filament transition, an important virulence trait. It remains unexplored whether the compound is produced in the context of the human host. Bioassay-guided fractionation of Lactobacillus-conditioned medium linked this activity to 1-acetyl-β-carboline (1-ABC). We use genetic approaches to show that filamentation inhibition by 1-ABC requires Yak1, a DYRK1-family kinase. Additional biochemical characterization of structurally related 1-ethoxycarbonyl-β-carboline confirms that it inhibits Yak1 and blocks C. albicans biofilm formation. Thus, our findings reveal Lactobacillus-produced 1-ABC can prevent the yeast-to-filament transition in C. albicans through inhibition of Yak1.

Suggested Citation

  • Jessie MacAlpine & Martin Daniel-Ivad & Zhongle Liu & Junko Yano & Nicole M. Revie & Robert T. Todd & Peter J. Stogios & Hiram Sanchez & Teresa R. O’Meara & Thomas A. Tompkins & Alexei Savchenko & Ann, 2021. "A small molecule produced by Lactobacillus species blocks Candida albicans filamentation by inhibiting a DYRK1-family kinase," Nature Communications, Nature, vol. 12(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26390-w
    DOI: 10.1038/s41467-021-26390-w
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    References listed on IDEAS

    as
    1. Yasushi Ogawa & Yosuke Nonaka & Toshiyasu Goto & Eriko Ohnishi & Toshiyuki Hiramatsu & Isao Kii & Miyo Yoshida & Teikichi Ikura & Hiroshi Onogi & Hiroshi Shibuya & Takamitsu Hosoya & Nobutoshi Ito & M, 2010. "Development of a novel selective inhibitor of the Down syndrome-related kinase Dyrk1A," Nature Communications, Nature, vol. 1(1), pages 1-9, December.
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    Cited by:

    1. Bastian Seelbinder & Zoltan Lohinai & Ruben Vazquez-Uribe & Sascha Brunke & Xiuqiang Chen & Mohammad Mirhakkak & Silvia Lopez-Escalera & Balazs Dome & Zsolt Megyesfalvi & Judit Berta & Gabriella Galff, 2023. "Candida expansion in the gut of lung cancer patients associates with an ecological signature that supports growth under dysbiotic conditions," Nature Communications, Nature, vol. 14(1), pages 1-15, December.

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