Sarocladium formosanum K. W. Cheng & H. A. Ariyaw. 2025, sp. nov.

Sarocladium formosanum K. W. Cheng & H. A. Ariyaw. sp. nov. Fig. 26 Typification. TAIWAN • Guanshan Township, Taitung County, 23°02'17.6"N, 121°11'26.3"E, serpentine soil in rice field, 3 rd November 2022, K. W. Cheng, holotype, NTUPPMH 22-222 (Permanently preserved in a metabolically inactive state), ex-holotype NTUPPMCC 22-289. Etymology. Named after Formosa, the former name of Taiwan, where the type specimen was collected. Description. Sexual morph undetermined. Asexual morph Conidia were observed on WA. Conidiophores solitary, hyaline, straight to slightly flexuous, smooth-walled, arising from hyphal ropes or vegetative hyphae. Phialides subulate, hyaline, wide at the base, with, 13–30 µm long. Adelophialides and schizophialides not observed. Conidia unicellular, cylindrical with rounded ends, hyaline, smooth-walled, 1 - celled, few with inconspicuous 1 to 2 guttules on the end (s), sometimes aggregated in clusters forming a slimy head, 3.5–5.3 µm × 1.1–2.1 µm (x ̄ = 4.4 × 1.5 µm, L / W ratio = 3.08, n = 50). Culture characteristics. Colony exhibit slow growth, reaching 35 mm diam with flat, pale orange, wrinkled in the center, slimy, and smooth margin. The reverse side of the colony displayed similar characteristics. Notes. In the present study, Sarocladium formosanum forms a distinct clade with strong support (99 % / 1.00) based on multi-locus phylogenetic analysis (Fig. 27). Moreover, S. formosanum shows significant genetic divergence from its closest relatives, ex-type strain of S. strictum (CBS 346.70) and S. bactrocephalum (CBS 749.69) with 95.5 % identity to S. strictum (677 / 710 bp) and 93.1 % identity to S. bactrocephalum (661 / 710 bp) in the rpb 2 gene. Morphologically, S. formosanum lacks adelophialides, schizophialides, and chlamydospores, which distinguishes it from S. mali (Fig. 26; Hou et al. 2019). Several Sarocladium species have been recorded in Taiwan. S. spinificis was reported as an endophyte of the coastal grass Spinifex littoreus (Yeh and Kirschner 2014), while S. attenuatum, S. oryzae, S. sparsum, and S. spirale were isolated from rice grains and leaf sheaths (Ou et al. 2020). However, our species, S. formosanum and S. serpentinicola, were isolated from serpentine environments and formed distinct clades from these previously reported species in the phylogeny. While this study establishes S. formosanum as a distinct species, future studies should aim to recover additional isolates from similar environments to further validate its phenotypic variation and ecological distribution.

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Zenodo (CERN European Organization for Nuclear Research)
Published
2025-06-27
DOI
https://doi.org/10.5281/zenodo.15785908
Primary Topic
Plant Pathogens and Fungal Diseases
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article
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article

Sarocladium formosanum K. W. Cheng & H. A. Ariyaw. 2025, sp. nov.

Zenodo (CERN European Organization for Nuclear Research)
Plant Pathogens and Fungal Diseases
article

Sarocladium formosanum K. W. Cheng & H. A. Ariyaw. 2025, sp. nov.

article en

Abstract

Sarocladium formosanum K. W. Cheng & H. A. Ariyaw. sp. nov. Fig. 26 Typification. TAIWAN • Guanshan Township, Taitung County, 23°02'17.6"N, 121°11'26.3"E, serpentine soil in rice field, 3 rd November 2022, K. W. Cheng, holotype, NTUPPMH 22-222 (Permanently preserved in a metabolically inactive state), ex-holotype NTUPPMCC 22-289. Etymology. Named after Formosa, the former name of Taiwan, where the type specimen was collected. Description. Sexual morph undetermined. Asexual morph Conidia were observed on WA. Conidiophores solitary, hyaline, straight to slightly flexuous, smooth-walled, arising from hyphal ropes or vegetative hyphae. Phialides subulate, hyaline, wide at the base, with, 13–30 µm long. Adelophialides and schizophialides not observed. Conidia unicellular, cylindrical with rounded ends, hyaline, smooth-walled, 1 - celled, few with inconspicuous 1 to 2 guttules on the end (s), sometimes aggregated in clusters forming a slimy head, 3.5–5.3 µm × 1.1–2.1 µm (x ̄ = 4.4 × 1.5 µm, L / W ratio = 3.08, n = 50). Culture characteristics. Colony exhibit slow growth, reaching 35 mm diam with flat, pale orange, wrinkled in the center, slimy, and smooth margin. The reverse side of the colony displayed similar characteristics. Notes. In the present study, Sarocladium formosanum forms a distinct clade with strong support (99 % / 1.00) based on multi-locus phylogenetic analysis (Fig. 27). Moreover, S. formosanum shows significant genetic divergence from its closest relatives, ex-type strain of S. strictum (CBS 346.70) and S. bactrocephalum (CBS 749.69) with 95.5 % identity to S. strictum (677 / 710 bp) and 93.1 % identity to S. bactrocephalum (661 / 710 bp) in the rpb 2 gene. Morphologically, S. formosanum lacks adelophialides, schizophialides, and chlamydospores, which distinguishes it from S. mali (Fig. 26; Hou et al. 2019). Several Sarocladium species have been recorded in Taiwan. S. spinificis was reported as an endophyte of the coastal grass Spinifex littoreus (Yeh and Kirschner 2014), while S. attenuatum, S. oryzae, S. sparsum, and S. spirale were isolated from rice grains and leaf sheaths (Ou et al. 2020). However, our species, S. formosanum and S. serpentinicola, were isolated from serpentine environments and formed distinct clades from these previously reported species in the phylogeny. While this study establishes S. formosanum as a distinct species, future studies should aim to recover additional isolates from similar environments to further validate its phenotypic variation and ecological distribution.

Zenodo (CERN European Organization for Nuclear Research)
University of California, Riverside (US), Chulalongkorn University (TH), National Taiwan University (TW)
Life in Land
Openalex Percentile: Top 49%
Plant Pathogens and Fungal Diseases
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