Colletotrichum chrysophilum W. A. S. Vieira, W. G. Lima, M. P. S. Câmara & V. P. Doyle

Gomdola, Deecksha, Jeewon, Rajesh, McKenzie, Eric H. C., Jayawardena, Ruvishika S., Al-Otibi, Fatimah, Tang, Xia, Wang, Yong, Hyde, Kevin D. & Fu, Li, 2025, Phylogenetic diversity of Colletotrichum species (Sordariomycetes, Glomerellales, Glomerellaceae) associated with plant diseases in Thailand, MycoKeys 119, pp. 137-195 : 137-195

publication ID

https://doi.org/10.3897/mycokeys.119.152323

DOI

https://doi.org/10.5281/zenodo.15801137

persistent identifier

https://treatment.plazi.org/id/745EE575-890A-56F2-AA01-321A75D10542

treatment provided by

MycoKeys by Pensoft

scientific name

Colletotrichum chrysophilum W. A. S. Vieira, W. G. Lima, M. P. S. Câmara & V. P. Doyle
status

 

Colletotrichum chrysophilum W. A. S. Vieira, W. G. Lima, M. P. S. Câmara & V. P. Doyle View in CoL , Mycologia 109 (6): 927 (2017)

Figs 2 View Figure 2 , 7 View Figure 7

Description.

Associated with leaf spots of Terminalia sp. Leaf spots irregular or oval, pale brown, surrounded with a dark brown margin. Sexual morph: Not observed. Asexual morph on substrate: Conidiomata 70–120 × 60–120 µm (x ̄ = 94.5 × 96 µm, n = 10), semi-immersed, scattered, globose to subglobose, black, sometimes erumpent. Setae not observed. Conidiomatal wall 8.5–21 µm thick (x ̄ = 14.6 µm, n = 10), consisting of 3–5 layers of thick-walled pseudoparenchymatous cells of textura angularis, outer layers dark brown, inner layer pale brown to hyaline. Asexual morph on PDA: Conidiophores hyaline, smooth-walled, aseptate, unbranched. Conidiogenous cells 16–22 × 3–4.5 µm (x ̄ = 18.9 × 3.6 µm, n = 10), hyaline, cylindrical to ampulliform, straight or flexuous, tapering towards the apex. Conidia 13–19 × 4.5–6 µm (x ̄ = 15.8 × 5.1 µm, n = 30; L / W ratio = 3.1), hyaline, cylindrical or oblong, smooth-walled, guttulate, aseptate, mostly with rounded ends. Appressoria 7–12 × 7–13 µm (x ̄ = 10.9 × 10.5 µm, n = 5), hyaline, single-celled, globose to subglobose or irregular, smooth-walled.

Culture characteristics.

Colonies on PDA reaching approximately 45 mm diam. after 7 d of incubation at 25 ° C; mycelium greyish white, elevation flat or raised, aerial and filamentous with an entire or undulate margin.

Specimen examined.

Thailand • Chiang Rai Province, around the vicinity of Central Plaza , associated with leaf spots of Terminalia sp. ( Combretaceae ), 11 Jul 2019, D. Gomdola DG 01 - SM ( MFLU 25-0005 ), living culture MFLUCC 25-0006 .

GenBank accession numbers.

ITS = PV 263293; GAPDH = PV 290899; CHS 1 = PV 274250; ACT = PV 297876; TUB 2 = PV 295619; H 3 = PV 400141; and CAM = PV 299285.

Known hosts, distributions, and lifestyles

(listed chronologically). Endophytic on Theobroma cacao and Genipa americana in Panama ( Rojas et al. 2010) and Terpsichore taxifolia in Puerto Rico ( Doyle et al. 2013).

Pathogenic; anthracnose on fruits of Musa sp. in Minas Gerais, Pernambuco, Santa Catarina, and São Paulo states in Brazil and Mexico ( Vieira et al. 2017; Fuentes-Aragón et al. 2021), leaves of Anacardium humile and A. occidentale in Brazil ( Veloso et al. 2018, 2021), fruits of Mangifera indica in Mexico ( Fuentes-Aragón et al. 2020 a), fruits of Persea americana in Mexico ( Fuentes-Aragón et al. 2020 b) and Brazil ( Soares et al. 2021), leaves of Bauhinia forficata in Brazil (de Souza Junior et al. 2021), leaves of Manihot esculenta in Brazil ( Machado et al. 2021), fruits of Carica papaya in Mexico ( Pacheco-Esteva et al. 2022), and leaves of V accinium corymbosum in Brazil ( Soares et al. 2022).

Bitter rot of Malus domestica in New York ( Khodadadi et al. 2020) and Spain ( Cabrefiga et al. 2022).

Preharvest decay of Malus domestica in Italy ( Deltedesco and Oettl 2023).

Leaf spots on Euterpe oleracea and Malus domestica in Brazil and Uruguay ( Astolfi et al. 2022; dos Santos et al. 2022; Andrello et al. 2024).

Associated with leaf spots of Terminalia sp. in Thailand (this study).

Notes.

Our isolate ( MFLUCC 25-0006 ) grouped with Colletotrichum chrysophilum ( URM 7368 , A 20 _ F 13 _ 004, PP _ 212 b, PP _ 211 a, PP _ 209 c, PP _ 208 d, PP _ 210 d, and CBS 146410 ) with 100 % ML and 1.00 PP support (Fig. 2 View Figure 2 ). Based on our phylogenetic analyses, C. chrysophilum is positioned within the C. gloeosporioides species complex (Figs 1 View Figure 1 , 2 View Figure 2 ), congruent with the findings of Vieira et al. (2017). No nucleotide difference was observed in ITS (495 bp), GAPDH (219 bp), CHS 1 (267 bp), ACT (216 bp), TUB 2 (648 bp), and CAM (656 bp) regions between our isolate ( MFLUCC 25-0006 ) and C. chrysophilum ( URM 7368 ).

MFLUCC 25-0006 is morphologically similar to the ex-type of C. chrysophilum ( URM 7368 ), producing hyaline, smooth-walled, guttulate, aseptate, and cylindrical or oblong conidia with rounded ends ( Vieira et al. 2017). The conidial L / W ratio of our isolate is similar to that of C. chrysophilum ( URM 7368 ) (L / W ratio = 3.1 vs. 3.1).

Based on phylogenetic and morphological species concepts, we identify our isolate as Colletotrichum chrysophilum . This study represents the first report of C. chrysophilum associated with leaf spots on Terminalia sp. and establishes a new geographical record in Thailand.

MFLUCC

Mae Fah Luang University Culture Collection

URM

University of the Ryukyus

CBS

Centraalbureau voor Schimmelcultures, Fungal and Yeast Collection

Kingdom

Fungi

Phylum

Ascomycota

Class

Sordariomycetes

Order

Glomerellales

Family

Glomerellaceae

Genus

Colletotrichum

Loc

Colletotrichum chrysophilum W. A. S. Vieira, W. G. Lima, M. P. S. Câmara & V. P. Doyle

Gomdola, Deecksha, Jeewon, Rajesh, McKenzie, Eric H. C., Jayawardena, Ruvishika S., Al-Otibi, Fatimah, Tang, Xia, Wang, Yong, Hyde, Kevin D. & Fu, Li 2025
2025
Loc

Colletotrichum chrysophilum W. A. S. Vieira, W. G. Lima, M. P. S. Câmara & V. P. Doyle

W. A. S. Vieira, W. G. Lima, M. P. S. Camara & V. P. Doyle 2017: 927
2017