Multi-Gene Phylogenetic Analyses Revealed Five New Species and Two New Records of Distoseptisporales from China

Abstract

Eight hyphomycetes were collected as part of an investigation into the diversity of hyphomycetous fungi in China. Based on morphology and multi-loci (LSU, ITS, tef1α, and rpb2) phylogenetic analyses, five new taxa, including a new Aquapteridospora species A. hyalina and four novel Distoseptispora species, viz D. aquisubtropica, D. septata, D. tropica, and D. wuzhishanensis were introduced in Distoseptisporales (Sordariomycetes). Two new habitat records, viz Distoseptispora pachyconidia and D. xishuangbannaensis were firstly reported. Also provided in this study are detailed descriptions of eight new collections and a revised phylogenetic tree for the Distoseptisporales.

1. Introduction

The two genera, Distoseptispora (Distoseptisporaceae) and Aquapteridospora (Aquapteridosporaceae) were recently introduced to Distoseptisporales (Diaporthomycetidae) [1,2,3]. Yang et al. [4] established Aquapteridospora (Diaporthomycetidae) as a monotypic genus, with A. lignicola as the type species. In later research, Hyde et al. [1] introduced Aquapteridosporaceae to accommodate Aquapteridospora and placed this family in the order Distoseptisporales based on divergence estimates, morphological characteristics, and phylogenetic analysis. This was followed in the “Outline of Fungi and fungus-like taxa” by Wijayawardene et al. [5]. Currently, Aquapteridospora consists of five species, most of which were collected from freshwater habitats. Only, A. bambusinum was discovered on dead bamboo culms [6]. The genus is distinguished by its macronematous, mononematous, solitary, unbranched, cylindrical conidiophores; its polyblastic, pale brown conidiogenous cells; and its fusiform, euseptate, guttulate conidia [1,4]. According to phylogenetic analyses, Aquapteridospora formed a distinct sister clade to all Distoseptispora species [4,7]. Morphologically, Aquapteridospora has macronematous, mononematous and unbranched conidiophores, monoblastic conidiogenous cells, and solitary conidia, similar to Distoseptispora. However, Aquapteridospora differs from Distoseptispora in its terminal conidiogenous cells, longer conidiophores, and fusiform euseptate conidia [2,3,4,8].

The type species of Distoseptispora was designated as D. fluminicola by Su et al. [9]. In recent years, a number of Distoseptispora (Distoseptisporaceae, Distoseptisporales) species have been accepted. Currently, 55 species including 41 freshwater species and 14 terrestrial species have been accepted in Distoseptispora [2,10,11,12,13,14,15,16]. Most Distoseptispora species are located in Asia, primarily in China and Thailand, with 26 species in the former and 27 in the latter [3,17,18,19,20,21], while two species viz D. adscendens and D. leonensis [22,23] were found in Hungary and Malaysia, respectively. Most Distoseptispora species are saprobic on palms, Pandanus, Tectona, bamboo, Clematidis, and Carex including unidentified submerged wood [9,24,25,26,27,28], and only D. caricis has been reported as an endophytic species [29]. In addition, D. hyalina is the only one species known to have a sexual morph [7].

During a survey of hyphomycetes in China, eight hyphomycetous taxa were collected from Hainan and Guizhou Provinces. Based on morphological evidence and phylogenetic analyses of sequence combinations of LSU, ITS, tef1α, and rpb2, five new species in genera Aquapteridospora and Distoseptispora, namely A. hyalina, D. aquisubtropica, D. septata, D. tropica, and D. wuzhishanensis, and two new habitat records of D. pachyconidia and D. xishuangbannaensis, were identified, and their full descriptions and illustrations are provided in the present report.

2. Materials and Methods

2.1. Sample Collection, Specimen Examination, and Isolation

Fresh specimens of decaying wood were randomly collected from freshwater and terrestrial habitats in Hainan and Guizhou Province, China (Figure 1). Samples were brought back to the laboratory in plastic bags with the collection details including localities and dates. Samples were incubated at room temperature in ziplock bags or sterile moist plastic boxes for about two weeks. Colonies on decaying wood surface were examined, observed, and photographed for their appearance with stereomicroscopes (SMZ 745 and SMZ 800N, Nikon, Tokyo, Japan) from low (0.75 times) to high (5 times) magnification. Fresh colonies were picked with sterile needles at a stereomicroscope magnification of 5 times and placed on a slide with a small amount of distilled water, and then placed under a Nikon EOS 90D digital camera attached to ECLIPSE Ni compound microscope (Nikon, Tokyo, Japan) for microscopic morphological characteristics. The dimensions of conidiophores, conidiogenous cells, and conidia were measured using Tarosoft (R) Image Frame Workprogram. In the species descriptions, arithmetic means as “$\overline{x}$”, and “n” stand for the number of measured elements. Photoplates were processed with Adobe PhotoShop CC 2019 (Adobe Systems, San Jose, CA, USA).

Single spore isolations were performed on water agar (WA) and germinated conidia were aseptically transferred to fresh potato dextrose agar (PDA) following the method of Senanayake et al. [30]. Cultures were grown on PDA and incubated in an incubator at 25 °C for 5 weeks and morphological characters, including color, shape, and size were recorded. The dried specimens were deposited at the Herbarium of Kunming Institute of Botany, Chinese Academy of Sciences (HKAS), Kunming, China, and the Herbarium of Guizhou Academy of Agriculture Sciences (GZAAS), Guiyang, China. Cultures were deposited in Guizhou Culture Collection, China (GZCC). Index Fungorum and Faces of Fungi numbers were acquired by the guideline in Jayasiri et al. [31] and Index Fungorum (2022) [32].

2.2. DNA Extraction, PCR Amplification, and Sequencing

Fresh fungal mycelia were scraped with sterilized toothpicks and transferred to 1.5 mL microcentrifuge tubes. Genomic DNA was extracted using the Biospin Fungus Genomic DNA Extraction Kit (BioFlux, Shanghai, China), following the manufacturer’s protocol. The primer pairs of LR0R/LR5, ITS5/ITS4, 983F/2218R, and frpb2-5f/frpb2-7cr were used to amplify the large subunit ribosomal DNA (LSU) [33], the internal transcribed spacer (ITS) [34], the translation elongation factor 1 alpha (tef1α) [35] and the RNA polymerase II second largest subunit (rpb2) gene regions [36], respectively. The amplification reactions were completed in a 50 μL reaction volume, including 2 μL DNA template, 2 μL of each forward and reverse primers, and 44 μL of 1.1 × T3 Supper PCR Mix (Qingke Biotech, Chongqing, China). Amplification reactions were carried out as follows (

Table 1. PCR protocols.

Locus	Primer	Initial Denaturation	Denaturation	Annealing	Elongation	Final Extension	Hold
LSU	ITS5/ITS4	94 °C/3 min	94 °C/45 s	56 °C/50 s	72 °C/1 min	72 °C/10 min	4 °C
			40 cycles
ITS	LR0R/LR5	94 °C/3 min	94 °C/45 s	56 °C/50 s	72 °C/1 min	72 °C/10 min
			40 cycles
tef1α	983F/2218R	94 °C/3 min	94 °C/30 s	56 °C/50 s	72 °C/1 min	72 °C/10 min
			30 cycles
rpb2	frpb2-5f/frpb2-7cr	95 °C/5 min	95 °C/15 s	56 °C/50 s	72 °C/1 min	72 °C/10 min
			35 cycles

).

The quality of PCR amplification products was verified on 1% agarose electrophoresis gels stained with ethidium bromide. Purification and sequencing of PCR products were completed at Beijing Tsingke Biological Engineering Technology and Services Co., Ltd. (Beijing, China).

2.3. Phylogenetic Analyses

Original sequences were checked using BioEdit v 7.0.5.3 [37]. Forward and reverse sequences were assembled using SeqMan v. 7.0.0 (DNASTAR, Madison, WI, USA). The taxa used in this study were selected based on the closest matches from BLASTn search results (https://blast.ncbi.nlm.nih.gov/Blast.cgi, accessed on 15 October 2022), and from previous studies (

Table 2. Taxa used in this study and the GenBank accession numbers of DNA sequences.

Taxon	Strain	GenBank Accessions				Reference
		LSU	ITS	tef1α	rpb2
Aquapteridospora fusiformis	MFLU 18-1601T	MK849798	MK828652	MN194056	–	Luo et al. (2019)
A. aquatica	MFLUCC 17-2371T	MW287767	MW286493	–	–	Dong et al. (2021)
A. bambusinum	MFLUCC 12-0850T	KU863149	KU940161	KU940213		Dai et al. (2016)
A. bambusinum	MFLUCC 21-0027	MZ412526	MZ412514	MZ442688	–	Bao et al. (2021)
A. hyalina	GZCC 22-0072T	ON527945	ON527937	ON533681	ON533689	This study
A. hyalina	GZCC 22-0073	ON527948	ON527940	ON533684	ON533691	This study
A. jiangxiensis	JAUCC 3008T	MZ871501	MZ871502	MZ855767	MZ855768	Peng et al. (2022)
A. lignicola	MFLU 15-1172T	KU221018	MZ868774	MZ892980	MZ892986	Yang et al. (2015)
Distoseptispora adscendens	HKUCC 10820	DQ408561	–	–	DQ435092	Shenoy et al. (2006)
D. amniculi	MFLU 21-0138T	MZ868761	MZ868770	–	MZ892982	Yang et al. (2021)
D. appendiculata	MFLUCC 18-0259T	MN163023	MN163009	MN174866	–	Luo et al. (2019)
D. aqualignicola	KUNCC 21-10729T	ON400845	OK341186	OP413480	OP413474	Zhang et al. (2022)
D. aquamyces	KUNCC 21-10731T	OK341199	OK341187	OP413482	OP413476	Zhang et al. (2022)
D. aquatica	MFLUCC 15-0374T	KU376268	MF077552	–	–	Su et al. (2016)
D. aquatica	MFLUCC 18-0646	MK849793	MK828648	–	–	Luo et al. (2019)
D. aquisubtropica	GZCC 22-0075T	ON527941	ON527933	ON533677	ON533685	This study
D. atroviridis	HKAS 112616T	MZ868763	MZ868772	MZ892978	MZ892984	Yang et al. (2021)
D. bambusae	MFLUCC 20-0091T	MT232718	MT232713	MT232880	MT232881	Sun et al. (2020)
D. bambusae	MFLUCC 14-0583	MT232717	MT232712	–	MT232882	Sun et al. (2020)
D. bambusicola	GZCC 21-0667T	MZ474872	MZ474873	–	–
D. bangkokensis	MFLU 21-0110T	MZ518206	MZ518205	–	–	Shen et al. (2021)
D. cangshanensis	MFLUCC 16-0970T	MG979761	MG979754	MG988419	–	Luo et al. (2018)
D. caricis	CPC 36498T	MN567632	MN562124	–	MN556805	Crous et al. (2019)
D. caricis	CPC 36442	–	MN562125	–	MN556806	Crous et al. (2019)
D. chinensis	GZCC 21-0665T	MZ474867	MZ474871	MZ501609	–	Hyde et al. (2021)
D. clematidis	MFLUCC 17-2145T	MT214617	MT310661	–	MT394721	Phukhamsakda et al. (2020)
D. crassispora	KUMCC 21-10726T	OK341196	OK310698	OP413479	OP413473	Zhang et al. (2022)
D. curvularia	KUMCC 21-10725T	OK341195	OK310697	OP413478	OP413472	Zhang et al. (2022)
D. cylindricospora	HKAS 115796T	OK513523	OK491122	OK524220	–	Phukhamsakda et al. (2022)
D. dehongensis	KUMCC 18-0090T	MK079662	MK085061	MK087659	–	Hyde et al. (2019)
D. effusa	GZCC 19-0532T	MZ227224	MW133916	–	–	Yang et al. (2021)
D. eusptata	MFUCC 20-0154T	MW081544	MW081539	–	MW151860	Li et al. (2021)
D. eusptata	MFLU 20-0568	MW081545	MW081540	MW084994	MW084996	Li et al. (2021)
D. fasciculata	KUMCC 19-0081T	MW287775	MW286501	MW396656	–	Dong et al. (2021)
D. fluminicola	MFLUCC 15-0417T	KU376270	MF077553	–	–	Su et al. (2016)
D. fusiformis	HKAS 112617T	MZ868764	MZ868773	MZ892979	MZ892985	Yang et al. (2021)
D. guizhouensis	GZCC 21-0666T	MZ474869	MZ474868	MZ501610	MZ501611	Hyde et al. (2021)
D. guttulata	MFLUCC 16-0183T	MF077554	MF077543	MF135651	–	Yang et al. (2018)
D. guttulata	DLUCC B43	MN163016	MN163011	–	–	Luo et al. (2019)
D. hyalina	MFLU 21-0137T	MZ868760	MZ868769	MZ892976	MZ892981	Yang et al. (2021)
D. hydei	MFLUCC 20-0481T	MT742830	MT734661	–	MT767128	Monkai et al. (2020)
D. lancangjiangensis	KUN-HKAS 112712T	MW879522	MW723055	–	MW882260	Shen et al. (2021)
D. leonensis	HKUCC 10822	DQ408566	–	–	DQ435089	Shenoy et al. (2006)
D. lignicola	MFLUCC 18-0198T	MK849797	MK828651	–	–	Luo et al. (2019)
D. longispora	HFJAU 0705T	MH555357	MH555359	–	–	Yang et al. (2021)
D. martinii	CGMCC 318651T	KX033566	KU999975	–	–	Xia et al. (2017)
D. meilingensis	JAUCC 4727T	OK562396	OK562390	OK562408	–	Zhai et al. (2022)
D. multiseptata	MFLUCC 16-1044	MF077555	MF077544	MF135652	MF135644	Yang et al. (2018)
D. multiseptata	MFLUCC 15-0609T	KX710140	KX710145	MF135659	–	Hyde et al. (2016)
D. neorostrata	MFLUCC 18-0376T	MN163017	MN163008	–	–	Luo et al. (2019)
D. nonrostrata	KUNCC 21-10730T	OK341198	OK310699	OP413481	OP413475	Zhang et al. (2022)
D. obclavata	MFLUCC 18-0329T	MN163010	MN163012	–	–	Luo et al. (2019)
D. obpyriformis	MFLUCC 17-01694T	MG979764	–	MG988422	MG988415	Luo et al. (2018)
D. obpyriformis	DLUCC 0867	MG979765	MG979757	MG988423	MG988416	Luo et al. (2018)
D. pachyconidia	KUMCC 21-10724T	OK341194	OK310696	OP413477	OP413471	Zhang et al. (2022)
D. pachyconidia	GZCC 22-0074	ON527942	ON527934	ON533678	ON533686	This study
D. palmarum	MFLUCC 18-1446T	MK079663	MK085062	MK087660	MK087670	Hyde et al. (2019)
D. phangngaensis	MFLUCC 16-0857T	MF077556	MF077545	MF135653	–	Yang et al. (2018)
D. rayongensis	MFLUCC 18-0415T	MH457137	MH457172	MH463253	MH463255	Hyde et al. (2020)
D. rayongensis	MFLUCC 18-0417	MH457138	MH457173	MH463254	MH463256	Hyde et al. (2020)
D. rostrata	MFLUCC 16-0969T	MG979766	MG979758	MG988424	MG988417	Luo et al. (2018)
D. rostrata	DLUCC 0885	MG979767	MG979759	MG988425	–	Luo et al. (2018)
D. saprophytica	MFLUCC 18-1238T	MW287780	MW286506	MW396651	MW504069	Dong et al. (2021)
D. septata	GZCC 22-0078T	ON527947	ON527939	ON533683	ON533690	This study
D. songkhlaensis	MFLUCC 18-1234T	MW287755	MW286482	MW396642	–	Dong et al. (2021)
D. submersa	MFLUCC 16-0946T	MG979768	MG979760	MG988426	MG988418	Luo et al. (2018)
D. suoluoensis	MFLUCC 17-0224T	MF077557	MF077546	MF135654	–	Yang et al. (2018)
D. suoluoensis	MFLUCC 17-1305	MF077558	MF077547	–	–	Yang et al. (2018)
D. tectonae	MFLUCC 12-0291T	KX751713	KX751711	KX751710	KX751708	Hyde et al. (2016)
D. tectonae	MFLU 20-0262	MT232719	MT232714	–	–	Sun et al. (2020)
D. tectonae	MFLUCC 15-0981	MW287763	MW286489	MW396641	–	Dong et al. (2021)
D. tectonigena	MFLUCC 12-0292T	KX751714	KX751712	–	KX751709	Hyde et al. (2016)
D. thailandica	MFLUCC 16-0270T	MH260292	MH275060	MH412767	–	Tibpromma et al. (2018)
D. thysanolaenae	KUMCC 18-0182T	MK064091	MK045851	MK086031	–	Phukhamsak et al. (2019)
D. tropica	GZCC 22-0076T	ON527943	ON527935	ON533679	ON533687	This study
D. verrucosa	HKAS 112652T	MZ868762	MZ868771	MZ892977	MZ892983	Yang et al. (2021)
D. wuzhishanensis	GZCC 22-0077T	ON527946	ON527938	ON533682	–	This study
D. xishuangbannaensis	KUMCC 17-0290T	MH260293	MH275061	MH412768	MH412754	Tibpromma et al. (2018)
D. xishuangbannaensis	GZCC 22-0079	ON527944	ON527936	ON533680	ON533688	This study
D. yongxiuensis	JAUCC 4725T	OK562394	OK562388	OK562406	–	Zhai et al. (2022)
D. yunjushanensis	JAUCC 4723T	OK562398	OK562392	OK562410	–	Zhai et al. (2022)
D. yunnanensis	MFLUCC 20-0153T	MW081546	MW081541	MW084995	MW151861	Li et al. (2021)
Myrmecridium aquaticum	MFLUCC 15-0366T	MK849804	–	–	–	Luo et al. (2019)
M. aquaticum	S 1158	MK849803	MK828656	MN194061	MN124540	Luo et al. (2019)
M. banksiae	CBS 132536T	JX069855	JX069871	–	–	Crous et al. (2012)
M. montsegurinum	JF 13180T	KT991664	KT991674	–	KT991654	Réblová et al. (2016)
M. schulzeri	CBS 100.54	EU041826	EU041769	–	–	Arzanlou et al. (2007)
Pseudostanjehughesia aquitropica	MFLUCC 16-0569T	MF077559	MF077548	MF135655	–	Yang et al. (2018)
Ps. lignicola	MFLUCC 15-0352T	MK849787	MK828643	MN194047	MN124534	Luo et al. (2019)
Sporidesmium bambusicola	HKUCC 3578T	DQ408562	–	–	–	Shenoy et al. (2006)
S. dulongense	MFLUCC 17-0116T	MH795817	MH795812	MH801191	MH801190	Luo et al. (2019)
S. lageniforme	DLUCC 0880T	MK849782	MK828640	MN194044	MN124533	Luo et al. (2019)
S. pyriformatum	MFLUCC 15-0620T	KX710141	KX710146	MF135662	MF135649	Hyde et al. (2016)
S. thailandense	MFLUCC 15-0617	MF077561	MF077550	MF135657	–	Yang et al. (2018)
S. thailandense	MFLUCC 15-0964T	MF374370	MF374361	MF370957	MF370955	Zhang et al. (2017)

Note: T denote ex-type strain. Newly generated sequences are indicated in bold. “–”means no data available in GenBank.

) [7,12,28]. Sequence alignments for each locus were performed using the online multiple alignment program MAFFT version 7 (https://mafft.cbrc.jp/alignment/server/, accessed on 20 October 2022) [37,38], and auto-adjusted by trimAl tool [39]. A phylogenetic tree, which infers a phylogenetic relationship, was reconstructed based on a concatenated LSU, ITS, tef1α, and rpb2 dataset using the online CIPRES Science Gateway (https://www.phylo.org/portal2/home.action, accessed on 29 October 2022) and analyzed using Maximum Likelihood (ML), Maximum Parsimony (MP) and Bayesian Inference (BI).

The “ALTER” (http://www.sing-group.org/ALTER/, accessed on 29 October 2022) website was used to convert the aligned fasta file to the phylip format for ML analyses [40]. ML analyses were performed through the CIPRES science Gateway V. 3.3 (https://www.phylo.org/portal2/home.action, accessed on 29 October 2022) [41]. The ML analysis was carried out using the RAxML-HPC v.8 on XSEDE (8.2.12) tool using a GTRGAMMA approximation with rapid bootstrap analysis followed by 1000 bootstrap replicates [42]. Maximum Parsimony (MP) analysis was carried out by using PAUP on XSEDE (4.a168) online website [43]. The 1000 random taxa were added for a heuristic search to infer MP trees. The value of MaxTrees, which collapsed branches of zero length and saved all multiple parsimonious trees, was set to 5000. Parsimony score values of tree length (TL), consistency index (CI), retention index (RI), and homoplasy index (HI) were calculated for trees generated under different optimum criteria. Clade stability was estimated using a bootstrap analysis with 1000 replicates, and the taxa was added for the random stepwise of each with 10 replicates [44].

The aligned fasta file was converted to the nexus format file for BI analysis by using AliView v. 1.27 [40]. Bayesian Inference (BI) analyses were performed by using MrBayes on XSEDE (3.2.7a) via CIPRES [42]. The best-fit evolutionary model for the individual and combined datasets was determined using MrModeltest v. 2.3. 10 [45]. GTR + G + I substitution model was selected for LSU, ITS, tef1α, and rpb2. The posterior probabilities (PP) were determined based on Bayesian Markov chain Monte Carlo (BMCMC) sampling [46]. Four simultaneous Markov chains were run for 10,000,000 generations, and trees were sampled every 1000th generation (resulting in 10,000 trees). The first 2500 trees, which represented the burn-in phase of the analysis, were discarded. The posterior probabilities (PP) in the majority rule consensus tree were calculated by the remaining 7500 trees.

Phylogenetic trees were visualized with FigTree v. 1.4.4. Adobe PhotoShop CC 2019 (Adobe Systems, San Jose, CA, USA) and Adobe Illustrator CC 2019v. 23.1.0 (Adobe Systems, San Jose, CA, USA) were used to edit trees and figures layout. Sequences generated in this study were deposited in GenBank (Table 2).

3. Phylogenetic Results

Using partial nucleotide sequences from four genes, the phylogenetic placements of our new collections were determined. The concatenated sequence matrix comprised LSU (1–855 bp), ITS (856–1448 bp), tef1α (1449–2367 bp), and rpb2 (2368–3420 bp) with a total of 3420 characters for 93 taxa and two outgroups (Pseudostanjehughesia aquitropica MFLUCC 16-0569 and Ps. lignicola MFLUCC 15-0352) [7,12,16,47,48,49,50]. Four gene analyses were conducted to compare the respective topologies and clade stabilities. There were 1733 distinct alignment patterns in the matrix, along with 31.09% undetermined characters or gaps. The ML, MP, and BI analyses of the concatenated LSU, ITS, tef1α, and rpb2 dataset yielded similar tree topologies, and Figure 2 depicts the final likelihood value of the ML analysis.

The phylogenetic tree (Figure 2) demonstrates that our eight collections represent seven species within Distoseptisporales. Two isolates (GZCC 22-0072 and GZCC 22-0073) represent the new species Aquapteridospora hyalina which forms a distinct clade from other taxa of Aquapteridospora with strong support. Distoseptispora aquisubtropica and D. martinii are distinguished by their distinct conidial characteristics. Distoseptispora septata forms a sister lineage to D. guizhouensis with well support (96% ML/90% MP/1 PP). Distoseptispora tropica (GZCC 22-0076) is a significantly distinct lineage from other taxa (Figure 2). Distoseptispora wuzhishanensis forms a sister lineage to D. fasciculata with well support (97% ML/1 PP). Our isolate GZCC 22-0079 is recognized as D. xishuangbannaensis and GZCC 22-0074 as D. pachyconidia, and their molecular data are provided, respectively.

4. Taxonomy

Aquapteridospora hyalina J. Ma and Y.Z. Lu., sp. nov., Figure 3.

Index Fungorum number: IF559932; Facesoffungi number: FoF11002.

Etymology: The epithet ‘hyalina’ referring to the colourless conidia.

Holotype: HKAS 123764.

Saprobic on decaying wood in a freshwater habitat. Sexual morph: Undetermined. Asexual morph: Colonies on the natural substrate, effuse, solitary, hyaline. Mycelium mostly superficial, consisting of branched, septate, smooth, pale brown to brown hyphae. Conidiophores 68–130 × 4.5–6.5 μm ($\overline{x}$ = 91 × 5.5 μm, n = 30), macronematous, mononematous, solitary, erect, simple, straight, or slightly flexuous, unbranched, smooth, cylindrical, 3–7-septate, thick-walled, smooth-walled, brown at the base, subhyaline to pale brown towards apex. Conidiogenous cells 25–62 × 4–6.5 μm ($\overline{x}$ = 44 × 5 μm, n = 30), polyblastic, monoblastic, smooth-walled, terminal, sub-cylindrical or gradually tapering towards tip, sub-hyaline to pale brown, forming conidia sympodially on conspicuous denticles, bearing tiny, protuberant, circular scars. Conidia 17–28 × 4–6 μm ($\overline{x}$ = 20 × 5.5 μm, n = 50) acropleurogenous, solitary, fusiform, 1–3-septate, truncate obtuse at septum, hyaline when young, sub-hyaline to pale brown when mature, tapering and pointed at both ends, smooth-walled, often with single guttulate in each cell when young.

Culture characteristics: Conidia were germinated on water agar and produced germ tubes within 10 h. Colonies grown on PDA, circular, flat, reaching 18 mm diam. after 25 days of incubation at 25 °C, lightly gray at the entire margin, brown in the center, reverse-side pale brown or brown at the entire margin, pale grey in the center.

Material examined: China, Hainan Province, Baoting County, Sandao Town, Yanoda Rainforest cultural tourism area, 18°46′ N, 109°65′ E, on rotting wood in a freshwater stream, 23 October 2021, Jian Ma, Y6 (HKAS 123764, holotype; GZAAS 22-0077, isotype), ex-type living culture GZCC 22-0072; idem, Y10-1 (HKAS 123763), living culture GZCC 22-0073.

Notes: The proposed new species Aquapteridospora hyalina shares similar characteristics with other species of the genus Aquapteridospora in having macronematous, mononematous, unbranched, polyblastic conidiophores, sympodial proliferations conidiogenous cells, and fusiform and acropleurogenous conidia [4]. However, A. hyalina differs from all species of Aquapteridospora in having hyaline to pale brown conidia with distinguished guttulae in each cell when young. The phylogenetic analyses confirmed that the two strains (GZCC 22-0072 and GZCC 22-0073) of A. hyalina form a distinct clade sister to A. fusiformis within Aquapteridosporaceae (Figure 2). Therefore, based on the morphological evidence with multi-gene phylogenetic results, a new species A. hyalina is introduced.

Distoseptispora aquisubtropica J. Ma and Y.Z. Lu, sp. nov., Figure 4.

Index Fungorum number: IF559686; Facesoffungi number: FoF11334.

Etymology: ‘aquisubtropica’ is derived from subtropical, which means climate type and ‘aqui’ refers to its presence in aquatic habitat.

Holotype: HKAS 124023.

Saprobic on decaying wood submerged in a freshwater habitat. Sexual morph: Undetermined. Asexual morph: hyphomycetous. Colonies on natural substrate superficial, effuse, gregarious, smooth, septate, hairy, brown, or dark brown. Mycelium mostly immersed, composed of branched, septate, smooth, pale brown to brown hyphae. Conidiophores 16–83 × 5–11 μm ($\overline{x}$= 51 × 8 μm, n = 25), macronematous, mononematous, cylindrical, erect, simple, straight, or slightly flexuous, unbranched, smooth, thick-walled, solitary, brown at the base, pale brown or sub-hyaline towards the apex, 2–5-septate. Conidiogenous cells 3–11 × 3–7 μm ($\overline{x}$ = 6 × 5.5 μm, n = 25), holoblastic, monoblastic, terminal, integrated, cylindrical, pale brown or brown, smooth. Conidia 43–278 × 11–19 μm ($\overline{x}$= 141 × 14.5 μm, n = 38), acrogenous, solitary, multi-distoseptate, obclavate or lanceolate, rostrate, straight or slightly curved, verrucose, guttulate, thick-walled, smooth-walled, pale brown or dark brown, olivaceous, 16–31-distoseptate, usually paler towards apex, sometimes have conspicuous hyphae attached to the conidium, rounded at apex, with a truncate base.

Culture characteristics: Conidia were germinated on water agar and produced germ tubes within 10 h. Colonies grown on PDA, circular, flat, dense, dark gray, fluffy, reaching 34 mm diam. after 25 days of incubation at 25 °C, break in the center, from below olivaceous to brown at the center, pale yellow at the entire margin.

Material examined: China, Guizhou Province, Zhenyuan County, 27°05′ N, 108°41′ E, on decaying wood submerged from a freshwater stream, 1 May 2021, Jian Ma, XXJ11-3 (HKAS 124023, holotype; GZAAS 22-0080, isotype), ex-type living culture GZCC 22-0075.

Notes: According to a BLASTn search on NCBI GenBank, the ITS and LSU sequences of the new isolate (Distoseptispora aquisubtropica) share 92.95% similarity across 85% of the query sequence coverage and 99.6% similarity across 86% of the query sequence coverage with D. martini, respectively. The phylogenetic results indicate that D. aquisubtropica forms a sister clade to D. martinii with well-supported values (100% ML/75% MP/1 PP). The morphological features of D. aquisubtropica are compatible with the Distoseptispora generic concept, while D. martini resembles Acrodictys rather than Distoseptospora [13]. Distoseptospora aquisubtropica can be distinguished from D. martini by its obclavate or lanceolate conidia, while the latter is oblate or subglobose [13]. Based on a pairwise comparison of ITS and LSU nucleotides, D. aquisubtropica differs from D. martinii in 24/453 bp (5.3%) for ITS and 5/515 bp (0.97%) for LSU, respectively. Therefore, we identified D. aquisubtropica as a novel species, according to the species delimitation guidelines proposed by Chethana et al. and Maharachchikumbura et al. [51,52].

Distoseptispora pachyconidia R. Zhu and H. Zhang. Journal of Fungi 30: 22 (2022). Figure 5.

Index Fungorum Number: IF559924; Facesoffungi number: FoF12581.

Saprobic on decaying wood in terrestrial habitats. Sexual morph: Undetermined. Asexual morph: Colonies effuse, gregarious, brown, or dark brown, hairy. Mycelium immersed and partly superficial, consisting of branched, septate, smooth, pale brown to brown hyphae. Conidiophores 14–44 × 4–7 μm ($\overline{x}$ = 26 × 5 μm, n = 20), macronematous, mononematous, brown to dark brown, solitary, 2–4-septate, erect, straight, or flexuous, unbranched, smooth, cylindrical, singly or in groups, truncate at the apex, slightly constricted at septa. Conidiogenous cells 4–9 × 4–5.5 μm ($\overline{x}$ = 6 × 4.5 μm, n = 20), holoblastic, monoblastic, integrated, terminal, determinate, pale brown to brown, smooth, cylindrical. Conidia 50–242 × 11–20 μm ($\overline{x}$ = 111 × 13 μm, n = 30) acrogenous, solitary, obclavate, rostrate, smooth-walled, straight or slightly curved, up to 38-distoseptate, guttulate, olivaceous to dark brown, mostly slightly constricted at septa, tapering towards the rounded apex, truncate at the base.

Culture characteristics: Conidia were germinated on water agar and produced germ tubes within 10 h. Colonies grown on PDA, circular, mycelium flat, dense, reaching 40 mm diam. after 30 days of incubation at 25 °C, gray or brown, reverse-side dark brown.

Material examined: China, Hainan Province, Haikou City, Xiuying District, Ecological leisure trail, on decaying wood on the ground, 20°01′ N, 110°25′ E, 10 August 2021, Jian Ma, HK2 (HKAS 123754), living culture GZCC 22-0074.

Notes: Zhang et al. [16] introduced Distoseptispora pachyconidia from decaying wood in Yunnan Province, China. Analyses of multi-gene revealed that the new isolate GZCC 22-0074 clustered with D. pachyconidia. The morphological characteristics of this isolate are similar to the protologue of D. pachyconidia. However, GZCC 22-0074 differs from D. pachyconidia in having different colors of conidia (olivaceous to dark brown vs. pale-brown with a green tinge) and the number of conidial septa (up to 38 vs. 8–21-distoseptate) [16]. According to a pairwise nucleotide comparison of ITS, LSU, tef1α and rpb2, our isolate differs from the type strain of D. pachyconidia (HKAS 122179) in 1/520 bp (0.2%) for ITS, 1/852 bp (0.1%) for LSU, 1/913 bp (0.1%) for tef1α and 0/1052 bp (0%) for rpb2, respectively. Thus, the phylogenetic evidence did not show significant differences between them (Figure 2). We therefore identified the new isolate as D. pachyconidia.

Distoseptispora septata J. Ma and Y.Z. Lu, sp. nov., Figure 6.

Index Fungorum number: IF559688; Facesoffungi number: FoF11337.

Etymology: ‘septata’ referring to ‘septate’ conidia.

Holotype: HKAS 123759.

Saprobic on decaying wood submerged in a freshwater habitat. Sexual morph: Undetermined. Asexual morph: hyphomycetous. Colonies on natural substrate superficial, effuse, gregarious, smooth, septate, hairy, brown, or dark brown. Mycelium mostly immersed, composed of branched, septate, smooth, pale brown to brown hyphae. Conidiophores 23–86 × 3–7 μm ($\overline{x}$ = 44 × 5.5 μm, n = 30), macronematous, mononematous, cylindrical, erect, simple, mostly flexuous, unbranched, smooth, thick-walled, solitary, brown, 1–6-septate. Conidiogenous cells 5–18 × 4–6 μm ($\overline{x}$ = 9 × 5 μm, n = 30), holoblastic, monoblastic, terminal, integrated, cylindrical, pale brown or brown, smooth. Conidia 22–179 × 10–16 μm ($\overline{x}$ = 89 × 13 μm, n = 35), acrogenous, solitary, multi-distoseptate and up to 25-septate, obclavate, rostrate, straight or slightly curved, verrucose, guttulate, thick-walled, smooth-walled, pale brown or dark brown, olivaceous-green, usually paler towards apex, rounded at apex, with a truncate base.

Culture characteristics: Conidia were germinated on water agar and produced germ tubes within 10 h. Colonies grown on PDA, circular, flat, dense, fluffy, reaching 35 mm diam. after 25 days of incubation at 25 °C, olivaceous-green, paler brown and dark brown, reverse-side dark brown.

Material examined: China, Hainan Province, Wuzhishan City, Shui Man Town, Wuzhishan National Nature Reserve, 18°92′ N, 109°63′ E, on dead wood in a freshwater stream, 26 December 2021, Xia Tang, W17 (HKAS 123759, holotype; GZAAS 22-0083, isotype), ex-type living culture GZCC 22-0078.

Notes: Distoseptispora septata shares a sister relationship to D. guizhouensis with strong support (96% ML/90% MP/1 PP). However, D. septata differs from D. guizhouensis in having smaller conidia (22–179 × 10–16 μm vs. 90–273 × 15–21 μm). Particularly, D. guizhouensis is distinguished from D. septata by distinctly flexuous conidiophores. Based on a pairwise comparison of ITS nucleotides, D. septata differs from D. guizhouensis by 13/535 bp (2.4%). Following the guidelines for defining species boundaries of Chethana et al. and Pem et al. [51,53], we therefore introduce GZCC 22-0078 as a new species.

Distoseptispora tropica J. Ma and Y.Z. Lu, sp. nov., Figure 7.

Index Fungorum number: IF559689; Facesoffungi number: FoF11335.

Etymology: ‘tropica’ derived from the climate in which the species was discovered.

Holotype: HKAS 123761.

Saprobic on dead wood, in terrestrial habitat. Sexual morph: Undetermined. Asexual morph: hyphomycetous. Colonies on dead wood, effuse, scattered or in small groups, gregarious, hairy, smooth, brown, or dark brown. Mycelium mostly immersed, composed of branched, septate, smooth, brown to dark brown. Conidiophores 60–151 × 3.5–7 μm ($\overline{x}$ = 94 × 5 μm, n = 20), macronematous, mononematous, cylindrical, erect, straight, or slightly flexuous, unbranched, smooth, thick-walled, dark brown, solitary or caespitose, dark brown and rounded at the apex, paler brown at the upper part, 5–7 septate. Conidiogenous cells 10–21 × 3.5–6 μm ($\overline{x}$ = 159 × 5 μm, n = 20), holoblastic, monoblastic, terminal, integrated, cylindrical, pale brown or brown, smooth. Conidia 39–75 × 7.5–10.5 μm ($\overline{x}$ = 47 × 8 μm, n = 30), acrogenous, verrucose, solitary, multi-distoseptate, obclavate, rostrate, upper part tapering towards the apex, guttulate, thick-walled, smooth, olivaceous brown or dark brown, 5–7 distoseptate, with conspicuous hyphae attachment conidium, with a truncate base.

Culture characteristics: Conidia were germinated on water agar and produced germ tubes within 10 h. Colonies grown on PDA, circular, flat, dense, fluffy, reaching 40 mm diam. after 40 days of incubation at 25 °C, grayish brown mycelium on the surface, reverse-side dark brown.

Material examined: China, Hainan Province, Haikou City, Xiuying District, Ecological leisure trail, 20°01′ N, 110°25′ E, on decaying wood in terrestrial habitat, 10 August 2021, Jian Ma, HK9 (HKAS 123761, holotype; GZAAS 22-0081, isotype), ex-type living culture GZCC 22-0076.

Notes: Distoseptispora tropica shares an extremely similar morphology with the species of Distoseptispora, Ellisembia, and Sporidesmium [7,9,54]. However, phylogenetic analysis (Figure 2) indicates that D. tropica belongs to Distoseptispora. Distoseptispora tropica forms a distinct lineage basal to Clade 1 with strong support (100% ML/100% MP/1 PP). However, D. tropica differs from other taxa in Clade 1 in having longer conidiophores and smaller conidia.

Distoseptispora wuzhishanensis J. Ma and Y.Z. Lu, sp. nov., Figure 8.

Index Fungorum number: IF559706; Facesoffungi number: FoF11336.

Etymology: ‘wuzhishanensis’ derived from the city where the species was discovered.

Holotype: HKAS 123762.

Saprobic on decaying wood in a freshwater habitat. Sexual morph: Undetermined. Asexual morph: hyphomycetous. Colonies on substrate superficial, effuse, solitary, smooth, septate, hairy, brown, or dark brown. Mycelium mostly immersed, composed of branched, septate, smooth, pale brown to brown hyphae. Conidiophores 16–56 × 5–7 μm ($\overline{x}$ = 35 × 6 μm, n = 25), macronematous, mononematous, cylindrical, erect, scattered or in small groups, straight or slightly flexuous, unbranched, smooth, thick-walled, brown at the base, pale brown towards the apex, 1–4 septate. Conidiogenous cells 6.5–10.5 × 4.5–6 μm ($\overline{x}$ = 8 × 5 μm, n = 25), holoblastic, monoblastic, terminal, integrated, cylindrical, pale brown or brown, smooth. Conidia 76–143 × 11–17 μm ($\overline{x}$ = 108 × 13.5 μm, n = 40), acrogenous, solitary, multi-distoseptate, obclavate, rostrate, straight, or slightly curved, verrucose, guttulate, thick-walled, smooth-walled, pale brown or dark brown, olivaceous-green and yellow, usually up to 22-distoseptate, strongly constricted at septa, usually paler towards apex, rounded at apex, with a truncate base.

Culture characteristics: Conidia were germinated on water agar and produced germ tubes within 10 h. Colonies grown on PDA, circular, flat, dense, fluffy, reaching 24 mm diam. after 25 days of incubation at 25 °C, olivaceous-green or brown mycelium on the surface, reverse side partly paler brown to dark brown.

Material examined: China, Hainan Province, Wuzhishan City, Shui Man Town, Wuzhishan National Nature Reserve, 18°92′ N, 109°63′ E, on dead wood in a freshwater stream, 26 December 2021, Xia Tang, W21 (HKAS 123762, holotype; GZAAS 22-0082, isotype), ex-type living culture GZCC 22-0077.

Notes: According to phylogenetic tree (Figure 2), Distoseptispora wuzhishanensis forms a close lineage to D. fasciculata with high bootstrap support (99% ML/0.99 PP). The morphological characteristics of the new taxon match well with the species concept of Distoseptispora in conidiophores and conidia. However, D. wuzhishanensis differs from D. fasciculata in having longer conidiophores (16–56 × 5–7 μm vs. 12–16 × 5–6 μm) [3].

Distoseptispora xishuangbannaensis Tibpromma and K.D. Hyde. Fungal Diversity 93: 82 (2018). Figure 9.

Index Fungorum Number: IF554554; Facesoffungi number: FoF04563.

Saprobic on decaying wood, submerged in freshwater habitats. Sexual morph: Undetermined. Asexual morph: hyphomycetous. Colonies effuse, hairy, gregarious, olivaceous, or brown. Mycelium mostly immersed, composed of branched, smooth, septate, pale brown to brown hyphae. Conidiophores 19–52 × 5–7 μm ($\overline{x}$ = 29 × 6 μm, n = 20), macronematous, mononematous, unbranched, solitary, straight or slightly flexuous, brown at the base, pale brown towards the apex, slightly tapering distally, truncate at the apex, 1–4 septate. Conidiogenous cells 2–8.5 × 4.0–7 μm ($\overline{x}$= 6 × 5 μm, n = 20), blastic, holoblastic, monoblastic, terminal, integrated, cylindrical, pale brown. Conidia 88–269 × 11–15 μm ($\overline{x}$ = 165 × 13 μm, n = 30), solitary, acrogenous, cylindric-obclavate, rostrate, straight, or slightly curved, guttulate, thick-walled, smooth-walled, green-brown or brown, up to 42-distoseptate, usually paler olivaceous towards apex, rounded at apex, with a truncate base.

Culture characteristics: Conidia were germinated on water agar and produced germ tubes within 10 h. Colonies grown on PDA, circular, fluffy, reaching 36 mm diam. after 28 days of incubation at 25 °C, lightly grey in the center, olivaceous at the entire margin, reverse side pale brown and brown mycelium.

Material examined: China, Hainan Province, Lingshui Lizu Autonomous County, Diaoluoshan National Nature Reserve, 18°43′ N, 109°43′ E, on rotting wood in a freshwater habitat, 24 August 2021, Jian Ma, DL40 (HKAS 123760), living culture GZCC 22-0079.

Notes: Tibpromma et al. [20] introduced Distoseptispora xishuangbannaensis from dead leaf sheaths of Pandanus utilis in China. Analyses of multiple genes revealed that our new isolate (GZCC 22-0079) is closely related to D. xishuangbannaensis. Distoseptispora xishuangbannaensis possesses macronematous, straight or slightly flexuous conidiophores, holoblastic, monoblastic, brown conidiogenous cells, and acrogenous, cylindrical-obclavate conidia. The morphological characteristics of our isolate share similar characters with the holotype of D. xishuangbannaensis (HKAS 101809), but our isolate has longer and wider conidiophores (19–52 × 5–7 μm vs. 12–17 × 2–5 μm) and smaller conidia (88–269 × 11–15 μm vs. 160–305 × 8–15 μm) [20]. According to a pairwise nucleotide comparison of ITS, tef1α and rpb2, our new isolate differs from D. xishuangbannaensis in 5/498 bp (1%) for ITS, 3/898 bp (0.3%) for tef1α and 2/1052 bp (0.2%) for rpb2, respectively, and the phylogenetic result did not show significant differences between the new isolate and D. xishuangbannaensis (Figure 2). We therefore identified the new isolate as D. xishuangbannaensis.

5. Discussion

In recent years, studies on the number of saprotrophic fungi have received extensive attention [55,56]. For example, freshwater fungi occur in streams and other aquatic bodies [2,57], Calabon et al. [51] listed 3870 species, and numerous taxa are still being discovered [1]. Calabon et al. [51] listed 22 Distoseptispora species from freshwater and this study brings the total to 40 species. Analyses of morphological characteristics and molecular data indicate that eight collections, including five new species, namely A. hyalina, D. aquisubtropica, D. septata, D. tropica, and D. wuzhishanensis are introduced. Five Aquapteridospora epithets (A. lignicola, A. fusiformis, A. bambusinum, A. jiangxiensis, and A. aquatica) are listed in Index Fungorum [32,58]. Morphologically, A. hyalina corresponds well with the generic concept of Aquapteridospora [4,6,58]. However, the new isolate differs from other new species of genus Aquapteridospora by having conidia that have a truncate obtuse at their septum. Multi-gene analyses indicated that A. hyalina, a species phylogenetically distinct in the genus Aquapteridospora, was most closely related to A. fusiformis with weak support.

Morphologically, the asexual morph of Distoseptispora resembles Sporidesmium taxa [9]. Yang et al. [7] reported the existence of the sexual morph of Distoseptispora. Combining the morphological characteristics and the phylogenetic evidence of all species in genus Distoseptispora, we found that some Distoseptispora species form sister clades in phylogeny but have different morphologies. For example, D. martini and D. aquisubtropica have a close phylogenetic relationship. However, D. martini has distinctive oblate or subglobose conidia, while D. aquisubtropica has obclavate or lanceolate conidia. In addition, there are some species with similar morphologies but are genetically unrelated. For example, D. tropica and D. verrocosa have an identical morphology of conidiophores and conidia, but the two species have a distant phylogenetic relationship. Considering this phenomenon, additional molecular data and morphological characteristics are required for verification and expansion.

Previous studies of Distoseptispora have primarily been conducted in China (Guizhou, Yunnan, Sichuan, and Jiangxi Provinces) and in Thailand, which are subtropical and tropical regions. In this paper, eight collections were discovered in freshwater and terrestrial habitats in the Provinces of Hainan and Guizhou, China. Thus, it is unclear whether it has a close relationship with the climate. It may be a result of the limited geographical regions sampled.