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. 2024 Sep 14;24(1):119.
doi: 10.1186/s12862-024-02307-1.

Multicellularity and increasing Reynolds number impact on the evolutionary shift in flash-induced ciliary response in Volvocales

Affiliations

Multicellularity and increasing Reynolds number impact on the evolutionary shift in flash-induced ciliary response in Volvocales

Noriko Ueki et al. BMC Ecol Evol. .

Abstract

Background: Volvocales in green algae have evolved by multicellularity of Chlamydomonas-like unicellular ancestor. Those with various cell numbers exist, such as unicellular Chlamydomonas, four-celled Tetrabaena, and Volvox species with different cell numbers (~1,000, ~5,000, and ~10,000). Each cell of these organisms shares two cilia and an eyespot, which are used for swimming and photosensing. They are all freshwater microalgae but inhabit different fluid environments: unicellular species live in low Reynolds-number (Re) environments where viscous forces dominate, whereas multicellular species live in relatively higher Re where inertial forces become non-negligible. Despite significant changes in the physical environment, during the evolution of multicellularity, they maintained photobehaviors (i.e., photoshock and phototactic responses), which allows them to survive under changing light conditions.

Results: In this study, we utilized high-speed imaging to observe flash-induced changes in the ciliary beating manner of 27 Volvocales strains. We classified flash-induced ciliary responses in Volvocales into four patterns: "1: temporal waveform conversion", "2: no obvious response", "3: pause in ciliary beating", and "4: temporal changes in ciliary beating directions". We found that which species exhibit which pattern depends on Re, which is associated with the individual size of each species rather than phylogenetic relationships.

Conclusions: These results suggest that only organisms that acquired different patterns of ciliary responses survived the evolutionary transition to multicellularity with a greater number of cells while maintaining photobehaviors. This study highlights the significance of the Re as a selection pressure in evolution and offers insights for designing propulsion systems in biomimetic micromachines.

Keywords: Cilia; Flagella; Multicellularity; Reynolds number; Volvocales.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Volvocales species/strains used in this study. A Schematic illustration of representative genera in Volvocales. B Phylogenetic relationships among the Volvocalean species examined in this study (Table 1). The cladogram was constructed based on the recent phylotranscriptomics/phylogenomics [8, 9] and the chloroplast multigene phylogeny [10] of homothallic V. africanus and V. zeikusii. Note that Volvox ferrisii includes V. sp. Sagami [11]. C Bright-field images of species/strains in Volvocales used in this study. Note the difference in scale bars. For species other than Volvox, only generic names are shown. For Volvox, abbreviated generic names and specific names are shown. See Table 1 for details
Fig. 2
Fig. 2
Representative ciliary movements and photobehaviors in a unicellular and a multicellular species in Volvocales. A Ciliary and individual movement in Chlamydomonas and Volvox. Left: one stroke of an asymmetric waveform of cilia. Effective stroke (solid lines) and recovery stroke (broken lines) are shown. Modified by [6, 18]. Middle: Relationship between a cell and the direction of ciliary beating. Right: direction of the individual’s forward swimming and rotation. Black arrows: direction of ciliary beating in the asymmetric waveform. Dark gray arrows: individual’s swimming direction. Light gray arrows: direction of rotation. A, anterior pole; P, posterior pole. B Models of ciliary responses for photobehaviors in Chlamydomonas reinhardtii and Volvox ferrisii modified from [19]. The ciliary responses in magenta are focused on in this study
Fig. 3
Fig. 3
Four patterns of flash-induced ciliary response. AD Upper rows: sequential images at equal intervals covering > 1 stroke of the asymmetrical waveform before flash illumination. Bottom rows: sequential images after flashlight application in the same time interval as the upper rows. Time points from flash illumination are shown. White arrowheads indicate bends of asymmetric waveforms. A Temporal waveform conversion (Pattern 1) in Chlamydomonas reinhardtii. B No obvious response (Pattern 2) in Vitreochlamys ordinata. C A pause in ciliary beating (Pattern 3) in Eudorina elegans. D Temporal changes in ciliary beating directions (Pattern 4) in Volvox ferrisii. Scale bars: 10 μm. E Four patterns of flash-induced ciliary response. Volvocales species exhibiting each pattern are shown. An asterisk indicates species exhibiting both Patterns 3 and 4. Species with a citation ([#]) have already been reported on the pattern of ciliary responses similar to those observed in this study
Fig. 4
Fig. 4
Relationships among maximum cell number of individuals, maximum length along the anterior-posterior axis of an individual, and the patterns of photo-induced ciliary response in each species. A black triangle indicates Pattern 1, crosses indicate Pattern 2, white circles indicate Pattern 3, and gray and black circles indicate Pattern 4. Gray circles indicate species that exhibit Patterns 3 and 4. Data on Tetrabaena is derived from [19]. Species are denoted by the first letter of the genus name and the first 1 or 2 letters of the specific name. Vsp: Volvox sp. Sagami; Vau1: V. aureus NIES-891; Vau2: V. aureus 3-1 NU5. See also Table 1
Fig. 5
Fig. 5
Reynolds numbers of 27 strains in Volvocales for each pattern. Strains exhibiting Patterns 1 to 4 are listed from the top in order of decreasing Re within each pattern. Each dot derives from an individual

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