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Article

Prasiolopsis wulf-kochii (Prasiolales, Trebouxiophyceae), a New Species Occurring in Hairs of the Sloth Bradypus tridactylus

by
Tatyana Darienko
1,2 and
Thomas Pröschold
1,*
1
Research Department for Limnology, Leopold-Franzens-University of Innsbruck, A-5310 Mondsee, Austria
2
Institute for Microbiology and Genetics, Department of Applied Bioinformatics, Georg-August-University of Göttingen, D-37077 Göttingen, Germany
*
Author to whom correspondence should be addressed.
Plants 2024, 13(17), 2405; https://doi.org/10.3390/plants13172405
Submission received: 7 August 2024 / Revised: 22 August 2024 / Accepted: 26 August 2024 / Published: 28 August 2024
(This article belongs to the Section Plant Systematics, Taxonomy, Nomenclature and Classification)
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Abstract

:
The monotypic genus Prasiolopsis has been known for a long time, but is often overlooked because of difficulties in identification and the morphological variability between uniseriate filaments and cell packages forming pseudoparenchymatic thalli depending on age. We investigated a strain (SAG 84.81) originally denoted as Trichophilus welckeri, which was isolated from the hairs of the sloth Bradypus tridactylus, and compared it with other available strains of Prasiolopsis and of the sister genus Pseudomarvania. Our investigations clearly showed that this strain differed in morphology, especially of the chloroplast, from those originally described for Trichophilus. Phylogenetic analyses of the SSU and ITS rDNA sequences revealed that the strain SAG 84.81 is sister to several strains of P. ramosa within the Prasiola clade (Trebouxiophyceae). Using the ITS-2/CBC approach, we clearly demonstrated that this strain represented a new species of Prasiolopsis, which we proposed here as P. wulf-kochii. In addition, we evaluated the ITS-2/CBC approach by comparing it with the two species of Pseudomarvania. All investigated strains showed CBCs and HCBCs, which support their species delimitation. The sequencing data of Trichophilus welckeri available in GenBank were phylogenetically re-evaluated by including all representatives of the Ulotrichales (Ulvophyceae). Our analyses showed that these sequences formed their own lineage within this order.

1. Introduction

The genus Prasiolopsis was described by Vischer [1] as an alga, which was known for a long time as Pleurococcus vulgaris [2,3]. It is characterized by uniseriate filaments at young stages, and cell packages forming pseudoparenchymatic thalli when they become older. The presence of an asteroid chloroplast with a central pyrenoid demonstrated that this genus belongs to the order Prasiolales. Originally, this order was established by Schaffner [4], containing only the genus Prasiola (C. Agardh) Meneghini. Knebel [5] provided the first monograph on the Prasiolales and added the genus Gayella Rosenvinge, which was later renamed by Silva [6] to Rosenvingiella, in this order. In addition to Prasiolopsis, Vischer [1] described the genus Prasiococcus, which was found on calcified stones. The species of Prasiola and Rosenvingiella are morphologically characterized by the formation of blade-like pseudoparenchymatic thalli, which are derived from cell packages and sexual reproduction by oogamy [7,8,9,10]. They occur in marine and freshwater habitats. The monotypic genera Prasiococcus and Prasiolopsis were found in terrestrial habitats and had a sarcinoid organization. The latter genus formed irregularly branched filaments with age [1,10,11].
Ultrastructural studies have revealed that the Prasiolales have a counterclockwise orientation in the flagellar basal bodies of motile cells [12], which are typical for Trebouxiophyceae. Phylogenetic studies confirmed that all these genera belong to the so-called Prasiola clade of the Trebouxiophyceae [13,14,15]. Heesch et al. [16] established three new genera among the Prasiolales: Prasionema Heesch, Pazoutova & Rindi, Prasionella Heesch, Pazoutova & Rindi and Rosenvingiellopsis Heesch, Pazoutova & Rindi. All these representatives belong to the family Prasiolaceae Blackman & Tansley and formed a monophyletic lineage (Prasiola clade) within the Trebouxiophyceae, with the surprise that other genera with different morphologies (coccoid or rod-like short filaments or sarcinoid) also belonged to this group [11,17,18]. The following genera are members of the Prasiola clade (= Prasiolales emend.) besides the taxa already mentioned above: Raphidonema Lagerheim, Pseudochlorella J.W.G.Lund, Edaphochlorella Darienko & Pröschold, Pseudomarvania Elias & Neustupa, Stichococcus Nägeli, Desmococcus F.Brand, Diplosphaera Bialosuknia, Pseudostichococcus L.Moewus, Protostichococcus Pröschold & Darienko, Deuterostichococcus Pröschold & Darienko, Tritostichococcus Pröschold & Darienko and Tetratostichococcus Pröschold & Darienko.
Interestingly, Karsten et al. [14] sequenced the SSU rDNA of a strain (SAG 84.81) originally assigned as Trichophilus welckeri, which was closely related to the authentic strain of Prasiolopsis ramosa Vischer (SAG 26.83). The phylogenetic position of SAG 84.81 was later confirmed by plastome data [19]. Trichophilus welckeri was originally described by Weber-van-Bosse [20] as an alga that grew on and in the hairs of the sloth Bradypus tridactylus. This alga formed prostrate, irregularly branched, uniseriate to partly multiseriate filaments with uninucleate cells, each with a parietal chloroplast without a pyrenoid. Trichophilus reproduces using two types of motile cells, large quadri- and small biflagellated zoospores. Suutari et al. [21] investigated 71 hair samples of six sloth species (Bradypus variegatus, B. tridactylus, B. torquatus, B. pygmaeus, Choloepus hoffmanni and C. didactylus) collected in French Guiana, Panama, Costa Rica and Brazil. The sequencing results of these samples revealed that the different sloth species hosted a number of green algae as well as other pro- and eukaryotic microorganisms. However, one alga was frequently found and often abundant on sloth fur, which they concluded to be Trichophilus welckeri based on a morphological comparison with the original description. In contrast to the phylogenetic position of SAG 84.81, this alga did not belong to the Trebouxiophyceae; it represented a lineage within the Ulvophyceae.
The aim of this study is to compare the morphology and SSU/ITS rDNA sequences of SAG 84.81 with other strains of Prasiolopsis ramosa using the integrative approach used for Stichococcus and its relatives by Pröschold and Darienko [11]. In addition, we re-analyzed the SSU data designated as Trichophilus welckeri by Suutari et al. [21] to find out the correct phylogenetic position among the Ulvophyceae.

2. Results

2.1. Molecular Phylogeny of Prasiolopsis and Its Relatives

The phylogenetic analyses of the concatenated data set of SSU and ITS rDNA sequences revealed that the investigated strains formed two lineages within the Prasiola clade of the Trebouxiophyceae (Figure 1). Both the genera Prasiolopsis and Pseudomarvania (highlighted in yellow and blue in the Figure 1, respectively) are sisters to a clade consisting of the genera Stichococcus and Desmococcus. All of the genera were highly supported in all of the Bayesian and bootstrap analyses. The four strains of Prasiolopsis differed in 99 bases in the SSU/ITS sequences in total. The strains SAG 26.83 and SAG 2495 were completely identical and strain PR-1 only differed by one base from the other two of Prasiolopsis ramosa. In contrast, the strain SAG 84.81, which was originally assigned as Trichophilus welckeri, showed 98 base differences. 229 base differences could be observed between the two strains of Pseudomarvania representing two species (P. ampulliformis and P. aerophytica). All of the newly investigated strains had a group I intron at position 1506 with length variations of 447 bases in SAG 2047 up to 508 bases in SAG 84.81. Interestingly, the strain SAG 2148 had an additional intron at position 943 with an exceptional length of 1762 bases. The BLASTn search [22] for this intron did not find any similarity in GenBank.
The phylogenetic tree presented in Figure 1 did not contain any sequences of Prasiola and its related taxa because no SSU and ITS rDNA sequences are available. To find out the phylogenetic relationship between these taxa and our investigated strains (marked in a white box in Figure 1), we analyzed them with SSU rDNA sequences of representative taxa belonging to the Prasiolaceae. The phylogenetic analyses revealed that the genera Prasiola, Rosenvingiella, Prasinococcus and Prasiolopsis were sisters to the genus Pseudomarvania (Figure 2). Interestingly, Prasiola and Rosenvingiella seemed to be polyphyletic. However, the SSU sequences among both genera showed a low variability (~2%). The sarcinoid Prasinococcus is phylogenetically similar among different blade-forming Prasiola and Rosenvingiella.
The genetic differences within the strains belonging to Prasiolopsis and Pseudomarvania varied as mentioned above (99 versus 229) among the SSU and ITS rDNA sequences. Both Pseudomarvania strains represented species, which raised the question of whether the differences among the Prasiolopsis strains were also differences between species. To figure out if that is the case, we compared the secondary structures of ITS-1 and ITS-2 of both genera.
The strains of Prasiolopsis ramosa (SAG 26.83, SAG 2495 and PR-1) had identical ITS-1 and ITS-2 secondary structures, but the strain SAG 84.81 differed in both ITS-1 and ITS-2, which indicated that this strain represents another species (Figure 3). The ITS-1 secondary structures of both species showed differences, especially at the end of each of the four helices. These four helix structures are typical for green algae, as presented (see Coleman and Mai [23]). The ITS-2 secondary structure also showed four helices (see Mai and Coleman [24]). Compared with ITS-1, the differences among the helices of ITS-2 were distributed across Helix I, II and IV. The ITS-2/CBC approach used for Stichococcus-like organisms presented in Pröschold and Darienko [11] revealed that both species differed from each other due to 12 changes (one CBC; two HCBCs; and nine deleted, single or unpaired bases). These findings supported that SAG 84.81 represents a new species, which will be described below.
The ITS-1 and ITS-2 secondary structures of both Pseudomarvania species had the same four helix structures as shown for Prasiolopsis. However, both strains differed in more regions. Mainly, only the bases of each helix were almost constant between them. The ITS-2/CBC approach demonstrated that the recognition of two separate species is confirmed by eight CBCs, four HCBCs and thirty deleted, single or unpaired bases (Figure 4).

2.2. Morphology and Phenotypic Plasticity of the Investigated Prasiolopsis Strains

The strains SAG 26.83, SAG 2495 and PR-1 showed an identical morphology, which was also described by Vischer [1] and documented by Kornmann and Sahling [10] for Prasiolopsis ramosa. The young thallus formed uniseriate short filaments, which can branch. The old thalli became multiseriate forming cell packages that are arranged into pseudoparenchyms. The chloroplasts were asteroid with a central pyrenoid. Cells were cylindrical with a cell length of 15–25 µm and a cell width of 7–9 µm (Figure 5). In contrast, the strain SAG 84.81 had smaller cell sizes and different cell shapes. The detailed description of the morphology is given in the following description of the new species of Prasiolopsis.
Prasiolopsis wulf-kochii sp. nov. (Figure 6)
Description: Young thalli consist of short-branched filaments. Later cells divide longitudinally and latitudinally, which lead to formation of bi-serial filaments or cubical cell packages and become pseudoparenchymatic. The cells in filaments are short, cylindrical, quadratic, sometimes almost spherical and constricted. The end cells of filaments are ovoid, sometimes pointed, or slightly curved. The cell size of cylindrical cells varies from 6.8 × 7.7 to 7.9 × 17.6 µm. Cells in packages are spherical and compressed from sites. Isodiametric cells are 6.8 × 7.5 to 10.2 × 14.9 µm. Compressed cells are 4.3 × 7.2 to 6.2 × 13.9 µm. Young cells have relatively thin cell walls of 0.5 µm, which become thicker with age up to 1.0 µm. Vegetative cells possess asteroid chloroplasts with a pyrenoid surrounded by many starch grains. Asexual reproduction occurs by vegetative division and aplanospore formation. No motile stages were observed.
Diagnosis: Differs from P. ramosa by having a smaller cell size and ecological distribution as well as its SSU+ITS sequences (GenBank: PQ108893) and ITS-2 Barcode: PR-2 in Figure 2.
Holotype (designated here): The strain SAG 84.81 has been permanently cryopreserved in a metabolically inactive state at the Culture Collection of Algae (SAG), University of Göttingen, Germany.
Etymology: The species is named in honor of Dr. Wulf Koch who was the curator of the Culture Collection of Algae (SAG) at the University of Göttingen (1954–1979). He isolated this strain in 1977 from the hairs of the sloth Bradypus tridactylus.

3. Discussion

3.1. Systematics, Ecology and Geographical Distribution of the Genus Prasiolopsis

In our study, the genus Prasiolopsis was found to contain two species: P. ramosa and the newly described P. wulf-kochii. As demonstrated, both species differed in terms of their morphology and molecular signatures, such as secondary structures of ITS-1 and ITS-2 and ITS-2 barcode with CBCs and HCBCs (Figure 1, Figure 2, Figure 3, Figure 5 and Figure 6). In addition, the strains SAG 26.83 and SAG 84.81 also showed differences in two plastid-coding genes, rbcL and tufA, which are available in GenBank [15,16,18]. Both strains differed in three amino acids in rbcL (22 base differences between EF203015 for SAG 26.83 to KM462862 for SAG 83.81) and two in tufA (21 base differences between LN877828 and KM462862), which supported the separation into two species. P. wulf-kochii was originally denoted as Trichophilus welckeri, a species occurring in or on the hairs of sloths. However, the presence of an asteroid chloroplast with a central pyrenoid and the absence of zoospores (typical for Prasiolopsis) contradicted this identification. Trichophilus had parietal chloroplasts without pyrenoid and formed two types of zoospores [20]. Both Prasiolopsis species have different ecological preferences. P. ramosa have been found on barks of trees [1,2,3], supralittoral of coast lines [18], marble monuments [25], granite outcrops [26] and granite walls, whereas P. wulf-kochii is only known from hairs of sloths (this study). Despite these few records, Prasiolopsis seemed to have a worldwide distribution, however, its recognition is probably caused by difficulties of identification based solely on morphology, as already mentioned by Vischer [1]. Das [27] reported Prasiolopsis ramosa from a sub-alpine waterfall of the Eastern Himalaya (India), but the provided micrographs in their study were of poor quality. Therefore, the identification is questionable because no morphological features were clearly visible. By checking the records in the GBIF database (https://www.gbif.org; accessed on 5 August 2024), 50 entries of Prasiolopsis have been reported from around the world (Europe, Australia, USA, Greenland and Antarctica). Unfortunately, these records cannot be assigned at the species level because these metabarcoding studies focused on topics other than Prasiolales and its relatives and there are only a few sequencing reads assigned as Prasiolopsis that cannot be proven because the sequencing data are not accessible. Further studies are necessary to decide if Prasiolopsis is a rare genus or merely overlooked by environmental studies.
Interestingly, Pseudomarvania—a genus with different morphology and reproduction—belongs to the family Prasiolaceae with the genera Prasiola, Rosenvingiella, Prasiococcus and Prasiolopsis. The two species of Pseudomarvania had a coccoid-to-rod-like morphology, and consisted of single, parietal, cup-shaped chloroplasts. Both taxa reproduce by budding, which is unique among all specimens belonging to the Prasiola clade [28,29,30].

3.2. The Mystery of Trichophilus Welckeri—A New View on an Old Story

As mentioned above, the strain SAG 84.81 was originally assigned as Trichophilus welckeri. Our study clearly revealed that this strain represents a new species of Prasiolopsis. This raises the question: What is Trichophilus? Two species of this genus have been described: T. welckeri Weber-van-Bosse [20] and T. neniae Lagerheim [31]. Both are epizoic on or in the hairs of different species of sloths and the shells of the freshwater snail Nenia, respectively. Since that time, epizoic algae have been the subject of different studies. Parasitic, symbiotic, and mutualistic interactions between vertebrates-algae are summarized in several recent reviews [32,33,34,35]. The algae–sloth interaction was of special interest. Pauli et al. [35] and Kaup et al. [33] referred to this as “mobile ecosystems”. Suutari et al. [21] studied the biomes on several sloth species using molecular methods. They discovered that many different eukaryotic algae lived in or on the hairs of the six investigated sloth species. These findings were confirmed by Kaup et al. [33]. Interestingly, both studies found one lineage, which they identified as Trichophilus welckeri. Phylogenetic analyses revealed that it belonged to the Ulvophyceae. Unfortunately, no cultured material of this species is available, and the morphological comparison presented in Suutari et al. [21] with the original description by Weber-van-Bosse [20] did not clearly demonstrate the identity of Trichophilus. For clarification of the taxonomic status of Trichophilus, it is necessary to isolate clonal cultures from the hairs of sloths, which then need to be investigated by the integrative approach used in this study. Despite the uncertain status of Trichophilus, the phylogenetic analyses of Suutari et al. [21] revealed that the so-called Trichophilus belonged to the Ulvophyceae without clear affiliation because of lack of data at that time. To find out if the three clades A, B and C belong to another described genus of the Ulotrichales or represent their own lineage within this order, we reanalyzed the SSU rDNA of these clades together with all representatives of this order.
Interestingly, the phylogenetic analyses clearly revealed that the sequences of Suutari et al. [21] represented their own lineage within the Ulotrichales, which is highly supported in all Bayesian and bootstrap analyses (Figure 7). Unfortunately, no ITS rDNA sequences of the three clades are available in GenBank. Therefore, it cannot be determined if these clades represent a species within this genus. It is also necessary to isolate cultures to determine which kind of interaction this green algal lineage has with the different species of sloths.

4. Materials and Methods

4.1. Cultures and Light Microscopy

All investigated strains, except for strain PR-1, originated from the Culture Collection of Algae (SAG) at the University of Göttingen, Germany (http://sagdb.uni-goettingen.de). Origins of the strains are listed as follows:
  • SAG 26.83: Switzerland, Basel, bark of a fruit tree (47°28′52″ N, 7°51′7″ E); authentic strain of Prasiolopsis ramosa [1].
  • SAG 2495: Germany, Hamburg, surface of a marble monument (53°33′43″ N, 9°59′27″ E); assigned as Prasiolopsis sp. [25].
  • SAG 84.81: Brazil, Amazonia, from hairs of the sloth Bradypus tridactylus; assigned as Trichophilus welckeri.
  • Strain PR-1: Austria, Vienna, Türkenschanzpark, wall near Dänenstrasse (48°14′8″ N, 16°20′2″ E); assigned as Prasiolopsis ramosa.
  • For comparison, two strains of the sister genus Pseudomarvania were investigated:
  • SAG 2047: Japan, Hiroshima Prefecture, Taishaku-kyo Gorge, bark on Cephalotaxus harringtonia (34°51′0″ N, 133°14′1″ E), authentic strain of Pseudomarvania ampulliformis [28,29].
  • SAG 2148: Malaysia, Peninsular Malaysia, Hulu Kelantan, lowland rainforest, bark on Pandanus sp. (5°13′10″ N, 101°48′00″ E), authentic strain of Pseudomarvania aerophytica [29,30].
All strains were cultivated at 18 °C, with 50 μmol photons/m2s provided by daylight fluorescent tubes (Osram L36 W/954 Lumilux de lux daylight, Munich, Germany), and a light–dark cycle of 16:8 hrs on agarized modified Bold’s Basal Medium (3N-BBM+V; medium 26a in Schlösser [36]). The light microscopic investigations were conducted using an Olympus BX-60 microscope (Olympus, Tokyo, Japan), and the micrographs were taken with a ProgRes C14plus camera using the ProgRes CapturePro imaging system ((version 2.9.0.1), both from Jenoptik, Jena, Germany).

4.2. DNA Extraction, PCR, Sequencing and Phylogenetic Analyses

The genomic DNA of the strains was extracted using the DNeasy Plant Mini Kit (Qiagen, Hilden, Germany) and following the instructions provided by the manufacturer. The SSU and ITS rDNA were amplified in PCR reactions using the Taq PCR MasterMix Kit (Qiagen, Hilden, Germany) with two primer combinations EAF3/G800R and G500F/ITS055R [37]. All PCR products were purified and sequenced as described by Darienko et al. [37]. The sequences are available in the EMBL, GenBank and DDBJ sequence databases under the accession numbers given in Figure 1.
The SSU rDNA sequences of all strains were aligned according to their secondary structures. The ITS-1 and ITS- 2 sequences of all strains were folded according to the protocol described in detail in Pröschold and Darienko [11]. The alignment was included in a data set of 25 SSU and ITS rDNA sequences of Prasiola clade (2671 bp).
We used the Automated Model Selection tool implemented in PAUP* version 4.0a (build 169; [38]) for the decision about which evolutionary model best fit the data set. The settings of the best model are given in the legend of Figure 1. EMBL/GenBank accession numbers of published sequences and strain designations are provided in both of these figures. Phylogenetic trees were constructed using distance, parsimony and maximum likelihood criteria using PAUP [38], and the robustness of the tree topologies was proven with different Bayesian and bootstrap analyses (1000 replicates). In addition, the programs RAxML version 8.2.12 [39], MrBayes version 3.2.7a [40] and PHASE package 2.0 [41,42,43,44,45] were used.
The secondary structures of ITS-1 and ITS-2 sequences were folded using the computer programs mfold [46] and visualized using the web-based program PseudoViewer3 (http://pseudoviewer.inha.ac.kr; [47]).

Author Contributions

Conceptualization, methodology, validation, formal analysis, investigation, resources, data curation, writing—original draft preparation, writing—review and editing, visualization, project administration, funding acquisition, T.D. and T.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded in whole or in part by the Austrian Science Fund (FWF), grant number P 34416-B [Grant-DOI 10.55776/P34416] to T.D. and T.P. For open access purposes, the author has applied a CC BY public copyright license to any author accepted manuscript version arising from this submission.

Data Availability Statement

Data are contained within the article.

Acknowledgments

We would like to thank the staff of SAG for supporting and maintaining the investigated strains. We are very grateful for the critical comments made by both anonymous reviewers.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Molecular phylogeny of the Prasiola clade (Trebouxiophyceae) based on SSU and ITS rDNA sequence comparisons. The phylogenetic tree shown was created using the maximum likelihood method based on a data set of 2671 aligned positions of 25 taxa using PAUP 4.0a build169. For the analysis, the GTR+I+G (base frequencies: A 0.22644, C 0.29080, G 0.27799, U 0.20477; rate matrix A-C 1.7066, A-G 1.7909, A-U 1.1175, C-G 1.1230, C-U 4.3140, G-U 1.0000) with the proportion of invariable sites (I = 0.6004) and gamma-shaped parameters (G = 0.4542) was chosen, which was calculated as the best model by an automated model selection tool implemented in PAUP. The branches in bold are highly supported in all analyses (Bayesian values >0.95 calculated with PHASE and MrBayes; bootstrap values >70% calculated with PAUP using maximum likelihood, neighbor-joining, maximum parsimony and RAxML using maximum likelihood). The sister genera Raphidonema, Pseudochlorella and Edaphochlorella were chosen as an outgroup. The newly sequenced strains are highlighted in bold.
Figure 1. Molecular phylogeny of the Prasiola clade (Trebouxiophyceae) based on SSU and ITS rDNA sequence comparisons. The phylogenetic tree shown was created using the maximum likelihood method based on a data set of 2671 aligned positions of 25 taxa using PAUP 4.0a build169. For the analysis, the GTR+I+G (base frequencies: A 0.22644, C 0.29080, G 0.27799, U 0.20477; rate matrix A-C 1.7066, A-G 1.7909, A-U 1.1175, C-G 1.1230, C-U 4.3140, G-U 1.0000) with the proportion of invariable sites (I = 0.6004) and gamma-shaped parameters (G = 0.4542) was chosen, which was calculated as the best model by an automated model selection tool implemented in PAUP. The branches in bold are highly supported in all analyses (Bayesian values >0.95 calculated with PHASE and MrBayes; bootstrap values >70% calculated with PAUP using maximum likelihood, neighbor-joining, maximum parsimony and RAxML using maximum likelihood). The sister genera Raphidonema, Pseudochlorella and Edaphochlorella were chosen as an outgroup. The newly sequenced strains are highlighted in bold.
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Figure 2. Molecular phylogeny of the Prasiolaceae within the Prasiola clade (Trebouxiophyceae) based on SSU rDNA sequence comparisons. The phylogenetic tree shown was created using the maximum likelihood method based on a data set of 1781 aligned positions of 19 taxa using PAUP 4.0a build169. For the analysis, the TIM+I+G (base frequencies: A 0.25323, C 0.21503, G 0.27496, U 0.25678; rate matrix A-C 1.0000, A-G 1.6233, A-U 0.5636, C-G 0.5636, C-U 6.2596, G-U 1.0000) with the highest proportion of invariable sites (I = 0.8541) and gamma-shaped parameters (G = 0.9731) was chosen, which was calculated as the best model by automated model selection tool implemented in PAUP. The branches in bold are highly supported in all analyses (Bayesian values >0.95 calculated with PHASE and MrBayes; bootstrap values >70% calculated with PAUP using maximum likelihood, neighbor-joining, maximum parsimony and RAxML using maximum likelihood). The sister genera Stichococcus and Desmococcus were chosen as an outgroup (marked in green). The newly sequenced strains are highlighted in bold.
Figure 2. Molecular phylogeny of the Prasiolaceae within the Prasiola clade (Trebouxiophyceae) based on SSU rDNA sequence comparisons. The phylogenetic tree shown was created using the maximum likelihood method based on a data set of 1781 aligned positions of 19 taxa using PAUP 4.0a build169. For the analysis, the TIM+I+G (base frequencies: A 0.25323, C 0.21503, G 0.27496, U 0.25678; rate matrix A-C 1.0000, A-G 1.6233, A-U 0.5636, C-G 0.5636, C-U 6.2596, G-U 1.0000) with the highest proportion of invariable sites (I = 0.8541) and gamma-shaped parameters (G = 0.9731) was chosen, which was calculated as the best model by automated model selection tool implemented in PAUP. The branches in bold are highly supported in all analyses (Bayesian values >0.95 calculated with PHASE and MrBayes; bootstrap values >70% calculated with PAUP using maximum likelihood, neighbor-joining, maximum parsimony and RAxML using maximum likelihood). The sister genera Stichococcus and Desmococcus were chosen as an outgroup (marked in green). The newly sequenced strains are highlighted in bold.
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Figure 3. ITS-1 and ITS-2 secondary structures of the Prasiolopsis strains investigated in this study. The line structures have been drawn with PseudoViewer (http://pseudoviewer.inha.ac.kr). The helices were folded with mfold (http://www.unafold.org/RNA_form.php). The white boxes indicate the differences between both species. The conserved region of ITS-2 was used as barcode using the ITS-2/CBC approach as demonstrated in Pröschold and Darienko [11]. The ITS-2 Barcode is given as a number code (1 = A–U; 2 = U–A; 3 = G-C; 4 = C–G; 5 = G•U; 6 = U•G; 7 = mismatch; 8 = deletion, single or unpaired bases). The species are highlighted in the different colors.
Figure 3. ITS-1 and ITS-2 secondary structures of the Prasiolopsis strains investigated in this study. The line structures have been drawn with PseudoViewer (http://pseudoviewer.inha.ac.kr). The helices were folded with mfold (http://www.unafold.org/RNA_form.php). The white boxes indicate the differences between both species. The conserved region of ITS-2 was used as barcode using the ITS-2/CBC approach as demonstrated in Pröschold and Darienko [11]. The ITS-2 Barcode is given as a number code (1 = A–U; 2 = U–A; 3 = G-C; 4 = C–G; 5 = G•U; 6 = U•G; 7 = mismatch; 8 = deletion, single or unpaired bases). The species are highlighted in the different colors.
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Figure 4. ITS-1 and ITS-2 secondary structures of the Pseudomarvania strains investigated in this study. The line structures have been drawn with PseudoViewer (http://pseudoviewer.inha.ac.kr). The helices were folded with mfold (http://www.unafold.org/RNA_form.php). The white boxes indicate the differences between both species. The conserved region of ITS-2 was used as barcode using the ITS-2/CBC approach as demonstrated in Pröschold and Darienko [11]. The ITS-2 Barcode is given as number code (1 = A–U; 2 = U–A; 3 = G-C; 4 = C–G; 5 = G•U; 6 = U•G; 7 = mismatch; 8 = deletion, single or unpaired bases). The species are highlighted in the different colors.
Figure 4. ITS-1 and ITS-2 secondary structures of the Pseudomarvania strains investigated in this study. The line structures have been drawn with PseudoViewer (http://pseudoviewer.inha.ac.kr). The helices were folded with mfold (http://www.unafold.org/RNA_form.php). The white boxes indicate the differences between both species. The conserved region of ITS-2 was used as barcode using the ITS-2/CBC approach as demonstrated in Pröschold and Darienko [11]. The ITS-2 Barcode is given as number code (1 = A–U; 2 = U–A; 3 = G-C; 4 = C–G; 5 = G•U; 6 = U•G; 7 = mismatch; 8 = deletion, single or unpaired bases). The species are highlighted in the different colors.
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Figure 5. Morphology and phenotypic plasticity of Prasiolopsis ramosa ((A–C) SAG 2495 and (D–I) SAG 26.83) on 3N-BBM+V medium. (A,B). Young uniseriate branched filaments; (C). Filaments with cells becoming spherical; (D). Filaments becoming multiseriate; (E–I). Filaments forming cell packages. Scale bar = 30 μm.
Figure 5. Morphology and phenotypic plasticity of Prasiolopsis ramosa ((A–C) SAG 2495 and (D–I) SAG 26.83) on 3N-BBM+V medium. (A,B). Young uniseriate branched filaments; (C). Filaments with cells becoming spherical; (D). Filaments becoming multiseriate; (E–I). Filaments forming cell packages. Scale bar = 30 μm.
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Figure 6. Morphology and phenotypic plasticity of Prasiolopsis wulf-kochii (SAG 84.81) on 3N-BBM+V medium. (A) Young uniseriate branched filaments; (B) filaments with cells becoming spherical; (C) filaments becoming multiseriate; (D–H) filaments forming cell packages. Scale bar = 30 μm.
Figure 6. Morphology and phenotypic plasticity of Prasiolopsis wulf-kochii (SAG 84.81) on 3N-BBM+V medium. (A) Young uniseriate branched filaments; (B) filaments with cells becoming spherical; (C) filaments becoming multiseriate; (D–H) filaments forming cell packages. Scale bar = 30 μm.
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Figure 7. Molecular phylogeny of the Ulotrichales (Ulvophyceae) based on SSU rDNA sequence comparisons. The phylogenetic tree shown was created using the maximum likelihood method based on a data set of 1772 aligned positions of 36 taxa using PAUP 4.0a build169. For the analysis, the TVM+I+G (base frequencies: A 0.24566, C 0.21777, G 0.27468, U 0.26189; rate matrix A-C 0.6147, A-G 4.0595, A-U 0.7746, C-G 0.4119, C-U 4.0595, G-U 1.0000) with the proportion of invariable sites (I = 0.7737) and gamma shape parameter (G = 0.7167) was chosen, which was calculated as the best model by automated model selection tool implemented in PAUP. The branches in bold are highly supported in all analyses (Bayesian values >0.95 calculated with PHASE and MrBayes; bootstrap values >70% calculated with PAUP using maximum likelihood, neighbor-joining, maximum parsimony and RAxML using maximum likelihood). The sister order with Acrosiphonia was chosen as an outgroup.
Figure 7. Molecular phylogeny of the Ulotrichales (Ulvophyceae) based on SSU rDNA sequence comparisons. The phylogenetic tree shown was created using the maximum likelihood method based on a data set of 1772 aligned positions of 36 taxa using PAUP 4.0a build169. For the analysis, the TVM+I+G (base frequencies: A 0.24566, C 0.21777, G 0.27468, U 0.26189; rate matrix A-C 0.6147, A-G 4.0595, A-U 0.7746, C-G 0.4119, C-U 4.0595, G-U 1.0000) with the proportion of invariable sites (I = 0.7737) and gamma shape parameter (G = 0.7167) was chosen, which was calculated as the best model by automated model selection tool implemented in PAUP. The branches in bold are highly supported in all analyses (Bayesian values >0.95 calculated with PHASE and MrBayes; bootstrap values >70% calculated with PAUP using maximum likelihood, neighbor-joining, maximum parsimony and RAxML using maximum likelihood). The sister order with Acrosiphonia was chosen as an outgroup.
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MDPI and ACS Style

Darienko, T.; Pröschold, T. Prasiolopsis wulf-kochii (Prasiolales, Trebouxiophyceae), a New Species Occurring in Hairs of the Sloth Bradypus tridactylus. Plants 2024, 13, 2405. https://doi.org/10.3390/plants13172405

AMA Style

Darienko T, Pröschold T. Prasiolopsis wulf-kochii (Prasiolales, Trebouxiophyceae), a New Species Occurring in Hairs of the Sloth Bradypus tridactylus. Plants. 2024; 13(17):2405. https://doi.org/10.3390/plants13172405

Chicago/Turabian Style

Darienko, Tatyana, and Thomas Pröschold. 2024. "Prasiolopsis wulf-kochii (Prasiolales, Trebouxiophyceae), a New Species Occurring in Hairs of the Sloth Bradypus tridactylus" Plants 13, no. 17: 2405. https://doi.org/10.3390/plants13172405

APA Style

Darienko, T., & Pröschold, T. (2024). Prasiolopsis wulf-kochii (Prasiolales, Trebouxiophyceae), a New Species Occurring in Hairs of the Sloth Bradypus tridactylus. Plants, 13(17), 2405. https://doi.org/10.3390/plants13172405

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