Diaporthe thailandica Louangphan, Phukhams., K. D. Hyde & Bhunjun 2025, sp. nov.

Diaporthe thailandica Louangphan, Phukhams., K. D. Hyde & Bhunjun sp. nov. Figs 3, 4 Etymology. The name refers to the country where the holotype was collected. Holotype. MFLU 23–0473. Description. Saprobic on decaying dicot, visible as black necks immerging through the host surface. Sexual morph: Ascomata 328–495 × 303–371 µm (x ̄ = 400 × 343 µm, n = 10), immersed in the host epidermis, globose to sub-globose, solitary or occur in clusters, black, ostiolate, papillate. Ostiole neck 220 × 86 µm, long, filled with periphysate. Peridium 20–50 µm wide, composed of several layers of cells of textura angularis, outer layers dark brown and inner layers hyaline to brown, thin-walled. Paraphyses 3.2–6.6 µm (n = 20), thin-walled, 2–4 - septate, hyaline, wide at base, tapering towards the apex. Asci 45–58.9 × 8.6–12.7 µm (x ̄ = 51.5 × 10.5 µm, n = 40), unitunicate, 8 - spored, clavate to subclavate, straight to slightly curved, sessile, with a J-, apical ring. Ascospores 11–15.5 × 3.9–5.6 µm (x ̄ = 13.5 × 4.7 µm, n = 40) L / W = 2.8, overlapping uniseriate to biseriate, 1 - septate, constricted at the septum, ellipsoidal, smooth-walled, 2–4 - guttulate, straight, hyaline, without appendages or a mucilaginous sheath. Asexual morph on PDA: Conidiomata 500–700 × 300–600 µm (x ̄ = 580 × 480 µm, n = 10), pycnidial, scattered or aggregated, globose or variable in shape, ostiolate with prominent neck, dark brown to black, pycnidal wall brown, consisting of thick-walled cells of textura angularis, conidial mass globose, initially hyaline to yellowish, becoming white to cream, conidial droplets exuding from central ostioles. Conidiophores 10–29.5 × 1.3–2.5 μm (x ̄ = 16.9 × 1.9 µm, n = 40), ampulliform to subcylindrical, filiform, branched to unbranched, 1–3 - septate, hyaline, smooth, straight or slightly curved, wider at base, tapering towards the apex. Conidiogenous cells 2.1–8.1 × 1–2.3 μm (x ̄ = 4.2 × 1.5 µm, n = 40), subcylindrical, filiform, straight to curved, tapering towards the apex, collarette not flared, hyaline. Alpha conidia 5.3–8.8 × 2.3–3.5 μm (x ̄ = 7.3 × 2.9 μm, n = 40), ellipsoid, apex bluntly rounded, base obtuse to subtruncate, smooth, hyaline, bi- to multi-guttulate. Beta conidia 8.5–18.5 × 1.2–2 μm (x ̄ = 13.3 × 1.7 μm, n = 40), filiform, flexible to slightly curved, hyaline, base subtruncate, and aseptate. Gamma conidia not observed. Culture characteristics. Colonies on PDA, reaching 40 mm diam., after 2 weeks at 25 ° C, initially white, turning pale brown after 7–10 days, radiating to the edge, margin undulate, medium dense, flat or umbonate; reverse, cream, radiating white outwardly with grey patches. Material examined. Thailand, Chiang Rai Province, Muang District, on a dead unidentified dicot, 16 January 2023, J. Louangphan, CR 1-09 (MFLU 23–0473, holotype); ex-type MFLUCC 24–0523 = MFLUCC 23–0299. Host. Unidentified branch (this study). Distribution. Thailand (this study). Notes. Diaporthe thailandica (MFLUCC 23-0299 and MFLUCC 24–0523) formed a sister clade with isolates of D. raonikayaporum (CBS 133182, MFLUCC 14–1133, and MFLUCC 14–1136) with 100 % ML / 1.00 BPP support (Fig. 1). Diaporthe thailandica differs from D. raonikayaporum in its conidiomata (500–700 × 300–600 µm vs. 110–200 × 50–130 μm), conidiophores (10–29.5 × 1.3–2.5 μm vs. 16–26 × 2–3 μm), conidiogenous cells (2.1–8.1 × 1–2.3 μm vs. 5–10 × 2–3 μm), and beta conidia (8.5–18.5 vs. 7–13 μm) (Gomes et al. 2013). Diaporthe thailandica differs from D. raonikayaporum (= D. neoraonikayaporum MFLUCC 14–1133) in its conidiomata (500–700 × 300–600 µm vs. 690–1190 × 805–1285 μm), conidiophores (10–29.5 μm vs. 15–23 μm), alpha conidia (5.3–8.8 × 2.3–3.5 μm vs. 4–6 × 2–3 μm), and beta conidia (8.5–18.5 μm vs. 13–21 μm) (Doilom et al. 2017). Gamma conidia was observed in D. raonikayaporum (= D. neoraonikayaporum) but not in D. thailandica (Doilom et al. 2017). Diaporthe thailandica further differs from D. raonikayaporum, which has only been reported as an asexual morph (Gomes et al. 2013; Doilom et al. 2017). Our strain differs significantly (> 2.5 %) compared to the sequence data of D. raonikayaporum (Table 3). However, our isolate does not have cal sequence data, while his 3 sequence data is not available for D. raonikayaporum (MFLUCC 14–1133 and MFLUCC 14–1136). A pairwise homoplasy index showed Φw = 1.0 when a genealogical correlation model was applied between Diaporthe thailandica and D. raonikayaporum (Fig. 5). Thus, Diaporthe thailandica is reported as a new species based on morphology and molecular evidence. - Data not available.

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Zenodo (CERN European Organization for Nuclear Research)
Published
2025-03-17
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https://doi.org/10.5281/zenodo.15041746
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Plant Pathogens and Fungal Diseases
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article

Diaporthe thailandica Louangphan, Phukhams., K. D. Hyde & Bhunjun 2025, sp. nov.

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

Diaporthe thailandica Louangphan, Phukhams., K. D. Hyde & Bhunjun 2025, sp. nov.

article en

Abstract

Diaporthe thailandica Louangphan, Phukhams., K. D. Hyde & Bhunjun sp. nov. Figs 3, 4 Etymology. The name refers to the country where the holotype was collected. Holotype. MFLU 23–0473. Description. Saprobic on decaying dicot, visible as black necks immerging through the host surface. Sexual morph: Ascomata 328–495 × 303–371 µm (x ̄ = 400 × 343 µm, n = 10), immersed in the host epidermis, globose to sub-globose, solitary or occur in clusters, black, ostiolate, papillate. Ostiole neck 220 × 86 µm, long, filled with periphysate. Peridium 20–50 µm wide, composed of several layers of cells of textura angularis, outer layers dark brown and inner layers hyaline to brown, thin-walled. Paraphyses 3.2–6.6 µm (n = 20), thin-walled, 2–4 - septate, hyaline, wide at base, tapering towards the apex. Asci 45–58.9 × 8.6–12.7 µm (x ̄ = 51.5 × 10.5 µm, n = 40), unitunicate, 8 - spored, clavate to subclavate, straight to slightly curved, sessile, with a J-, apical ring. Ascospores 11–15.5 × 3.9–5.6 µm (x ̄ = 13.5 × 4.7 µm, n = 40) L / W = 2.8, overlapping uniseriate to biseriate, 1 - septate, constricted at the septum, ellipsoidal, smooth-walled, 2–4 - guttulate, straight, hyaline, without appendages or a mucilaginous sheath. Asexual morph on PDA: Conidiomata 500–700 × 300–600 µm (x ̄ = 580 × 480 µm, n = 10), pycnidial, scattered or aggregated, globose or variable in shape, ostiolate with prominent neck, dark brown to black, pycnidal wall brown, consisting of thick-walled cells of textura angularis, conidial mass globose, initially hyaline to yellowish, becoming white to cream, conidial droplets exuding from central ostioles. Conidiophores 10–29.5 × 1.3–2.5 μm (x ̄ = 16.9 × 1.9 µm, n = 40), ampulliform to subcylindrical, filiform, branched to unbranched, 1–3 - septate, hyaline, smooth, straight or slightly curved, wider at base, tapering towards the apex. Conidiogenous cells 2.1–8.1 × 1–2.3 μm (x ̄ = 4.2 × 1.5 µm, n = 40), subcylindrical, filiform, straight to curved, tapering towards the apex, collarette not flared, hyaline. Alpha conidia 5.3–8.8 × 2.3–3.5 μm (x ̄ = 7.3 × 2.9 μm, n = 40), ellipsoid, apex bluntly rounded, base obtuse to subtruncate, smooth, hyaline, bi- to multi-guttulate. Beta conidia 8.5–18.5 × 1.2–2 μm (x ̄ = 13.3 × 1.7 μm, n = 40), filiform, flexible to slightly curved, hyaline, base subtruncate, and aseptate. Gamma conidia not observed. Culture characteristics. Colonies on PDA, reaching 40 mm diam., after 2 weeks at 25 ° C, initially white, turning pale brown after 7–10 days, radiating to the edge, margin undulate, medium dense, flat or umbonate; reverse, cream, radiating white outwardly with grey patches. Material examined. Thailand, Chiang Rai Province, Muang District, on a dead unidentified dicot, 16 January 2023, J. Louangphan, CR 1-09 (MFLU 23–0473, holotype); ex-type MFLUCC 24–0523 = MFLUCC 23–0299. Host. Unidentified branch (this study). Distribution. Thailand (this study). Notes. Diaporthe thailandica (MFLUCC 23-0299 and MFLUCC 24–0523) formed a sister clade with isolates of D. raonikayaporum (CBS 133182, MFLUCC 14–1133, and MFLUCC 14–1136) with 100 % ML / 1.00 BPP support (Fig. 1). Diaporthe thailandica differs from D. raonikayaporum in its conidiomata (500–700 × 300–600 µm vs. 110–200 × 50–130 μm), conidiophores (10–29.5 × 1.3–2.5 μm vs. 16–26 × 2–3 μm), conidiogenous cells (2.1–8.1 × 1–2.3 μm vs. 5–10 × 2–3 μm), and beta conidia (8.5–18.5 vs. 7–13 μm) (Gomes et al. 2013). Diaporthe thailandica differs from D. raonikayaporum (= D. neoraonikayaporum MFLUCC 14–1133) in its conidiomata (500–700 × 300–600 µm vs. 690–1190 × 805–1285 μm), conidiophores (10–29.5 μm vs. 15–23 μm), alpha conidia (5.3–8.8 × 2.3–3.5 μm vs. 4–6 × 2–3 μm), and beta conidia (8.5–18.5 μm vs. 13–21 μm) (Doilom et al. 2017). Gamma conidia was observed in D. raonikayaporum (= D. neoraonikayaporum) but not in D. thailandica (Doilom et al. 2017). Diaporthe thailandica further differs from D. raonikayaporum, which has only been reported as an asexual morph (Gomes et al. 2013; Doilom et al. 2017). Our strain differs significantly (> 2.5 %) compared to the sequence data of D. raonikayaporum (Table 3). However, our isolate does not have cal sequence data, while his 3 sequence data is not available for D. raonikayaporum (MFLUCC 14–1133 and MFLUCC 14–1136). A pairwise homoplasy index showed Φw = 1.0 when a genealogical correlation model was applied between Diaporthe thailandica and D. raonikayaporum (Fig. 5). Thus, Diaporthe thailandica is reported as a new species based on morphology and molecular evidence. - Data not available.

Zenodo (CERN European Organization for Nuclear Research)
Kunming Institute of Botany (CN), King Saud University (SA), Mae Fah Luang University (TH), Chiang Mai University (TH)
Life in Land
Openalex Percentile: Top 47%
Plant Pathogens and Fungal Diseases
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