Published June 16, 2026 | Version v1

Neocosmospora bostrycoides Sandoval-Denis, L. Lombard and Crous

  • 1. Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biology and Food Engineering, Qujing Normal University, Qujing 655099, China & Key Laboratory of Yunnan Provincial Department of Education of the Deep-Time Evolution on Biodiversity from the Origin of the Pearl River, Qujing Normal University, Qujing, Yunnan Province, 655011, China & School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand & Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand
  • 2. Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biology and Food Engineering, Qujing Normal University, Qujing 655099, China & Key Laboratory of Yunnan Provincial Department of Education of the Deep-Time Evolution on Biodiversity from the Origin of the Pearl River, Qujing Normal University, Qujing, Yunnan Province, 655011, China
  • 3. Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand
  • 4. Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand & Department Microbial Drugs, Helmholtz Centre for Infection Research (HZI), Inhoffenstrasse 7, 38124, Braunschweig, Germany
  • 5. CEFE, Univ Montpellier, CNRS, EPHE, IRD, Laboratory of Botany, Phytochemistry and Mycology, Faculty of Pharmacy, Montpellier, France
  • 6. Department of Biological Sciences, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia
  • 7. College of Agronomy and Biological Science, Yuxi Normal University, Yuxi, Yunnan 653100, China
  • 8. School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand & Microbial Products and Innovations Research Group, Mae Fah Luang University, Chiang Rai, 57100, Thailand & Advanced Microbial Metabolites and Phytochemical Technology, Mae Fah Luang University, Chiang Rai 57100 Thailand

Description

Neocosmospora bostrycoides (Wollenw. & Reinking) Sandoval-Denis, L. Lombard and Crous, Persoonia 43: 115 (2019)

Fig. 9

Description.

Associated with contaminated rubber latex. Sexual morph: Undetermined. Asexual morph on PDA: Conidiophores abundant on aerial and substrate mycelium, erect and simple, straight or flexuous, smooth- and thin-walled, bearing terminal or lateral, forming monophialides on the apices. Phialides (11 –) 15 × 30 (– 35) × 2.5–5 μm (x – = 22 × 4 μm, n = 30), subcylindrical to subulate, monophialidic, smooth- and thin-walled with a short flared apical collarette. Aerial conidia 5–11 × 2.5–5 μm (x – = 6.8 × 3.6 μm, n = 50), obovoidal, broadly ellipsoidal to ellipsoidal, straight or rarely curved, 0 (– 1) - septate, hyaline, smooth- and thin-walled, clustering abundantly in false heads at the tip of monophialides. Sporodochial conidiophores sparingly verticillately branched, bearing terminal whorls of 2–3 - monophialides. Sporodochial phialides 11–20 × 3–4 μm (x – = 15 × 3.4 μm, n = 30), flask-shaped, subcylindrical to short subulate, smooth- and thin-walled, conidiogenous loci with inconspicuous periclinal thickening and collarette. Sporodochial conidia 22–38 × 4–6 μm (x – = 31 × 4.6 μm, n = 50), moderately to distinctly dorsiventrally curved narrowing gently toward base, dorsal line usually almost straight; apical cell often equal in length to adjacent cell, blunt and rounded with curved apex; basal cell often distinctly notched, 1–4 - septate, hyaline, smooth- and thick-walled. Chlamydospores 6–10 μm diam., abundantly formed, globose to subglobose, smooth- and thick-walled, terminal or intercalary in hyphae or conidia, solitary, in chains or in clusters.

Culture characteristics.

Colonies on PDA at room temperature (20–25 ° C) covered the entire 6 cm Petri dish within three days, white to pale yellow, with abundant aerial mycelium; reverse white to pale yellow. Sporulation was observed after prolonged incubation on PDA at room temperature.

Material examined.

China, • Yunnan Province, Lincang City, contaminated rubber latex, 28 July 2022, Rui-Fang Xu, L-12 A (GMB-W 1263), living culture GMBCC 2519.

Notes.

Phylogenetic analysis placed strain GMBCC 2519 within the Neocosmospora bostrycoides lineage, supported by 100 % ML and 1.00 BYPP values (Fig. 6). Morphologically, GMB-W 1263 closely resembles the reference strain Neocosmospora bostrycoides (CBS 130391). It aligns with the species description but is characterized by shorter sporodochial conidia (22–38 μm vs. 40.5–51.5 μm) (Sandoval-Denis et al. 2019). Nucleotide comparisons revealed differences of 5 bp in ITS (2 gaps), 3 bp in LSU (0 gaps), and 6 bp in rpb 2 (0 gaps) between GMBCC 2519 and Neocosmospora bostrycoides (CBS 144.25). Neocosmospora bostrycoides was collected from contaminated old rubber latex in a container near a rubber tree. In the present study, this species showed measurable surface-associated changes on natural rubber under laboratory incubation conditions.

Notes

Published as part of Xu, Rui-Fang, Karunarathna, Samantha C., Hyde, Kevin D., Phukhamsakda, Chayanard, Rapior, Sylvie, Dai, Dong-Qin, Wang, Mei-Mei, Ali, Sajad, Yang, Jing-Ya, Kakumyan, Pattana & Tibpromma, Saowaluck, 2026, Screening and identification of fungal species associated with early-stage deterioration of natural rubber, pp. 119-156 in MycoKeys 134 on pages 119-156, DOI: 10.3897/mycokeys.134.195079

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Linked records

Additional details

Biodiversity

Collection code
GMBCC
Material sample ID
GMB-W 1263, GMBCC 2519
Event date
2022-07-28
Verbatim event date
2022-07-28
Scientific name authorship
Sandoval-Denis, L. Lombard and Crous
Kingdom
Fungi
Phylum
Ascomycota
Order
Hypocreales
Family
Nectriaceae
Genus
Neocosmospora
Species
bostrycoides
Taxon rank
species

References