Evolutionarily diverse fungal zoospores show contrasting swimming patterns specific to ultrastructure

Curr Biol. 2024 Oct 7;34(19):4567-4576.e3. doi: 10.1016/j.cub.2024.08.016. Epub 2024 Sep 11.

Abstract

Zoosporic fungi, also called chytrids, produce single-celled motile spores with flagellar swimming tails (zoospores).1,2 These fungi are key components of aquatic food webs, acting as pathogens, saprotrophs, and prey.3,4,5,6,7,8 Little is known about the swimming behavior of fungal zoospores, a crucial factor governing dispersal, biogeographical range, ecological function, and infection dynamics.6,9 Here, we track the swimming patterns of zoospores from 12 evolutionarily divergent species of zoosporic fungi from across seven orders of the Chytridiomycota and the Blastocladiomycota. We report two major swimming patterns that correlate with the cytoskeletal ultrastructure of these zoospores. Specifically, we show that species without major cytoplasmic tubulin components swim in a circular fashion, while species with prominent cytoplasmic tubulin structures swim in a pattern akin to a random walk (move-stop-redirect-move). We confirm cytoskeletal architecture by performing fluorescence confocal microscopy across all 12 species. We then treat representative species with variant swimming behaviors and cytoplasmic-cytoskeletal arrangements with tubulin-stabilizing (Taxol) and depolymerizing (nocodazole) pharmacological compounds. We observed that when treating the "random walk" species with nocodazole, their swimming behavior changed to a circular-swimming pattern. Confocal imaging of the nocodazole-treated zoospores demonstrates that these cells maintain flagellum tubulin structures but lack their characteristic cytoplasmic tubulin structures. Our data demonstrate that the capability of zoospores to perform "complex" random-walk movement is linked to the presence of prominent cytoplasmic tubulin structures and suggest a link between cytology, sensory systems, and swimming behavior in a diversity of zoosporic fungi.

Keywords: chytrid; fungi; light-sensing; motility; phototaxis; tubulin; ultrastructure; zoospores.

MeSH terms

  • Biological Evolution*
  • Blastocladiomycota / physiology
  • Cytoskeleton / physiology
  • Flagella / physiology
  • Flagella / ultrastructure
  • Spores, Fungal* / physiology
  • Spores, Fungal* / ultrastructure
  • Tubulin / metabolism

Substances

  • Tubulin