Diaporthe rosae Samarak. & K. D. Hyde

Fallahi, Maryam, Armand, Alireza, Al-Otibi, Fatimah, Hyde, Kevin D. & Jayawardena, Ruvishika S., 2025, Pathogenic fungi (Sordariomycetes) associated with annual and perennial crops in Northern Thailand, MycoKeys 117, pp. 191-265 : 191-265

publication ID

https://doi.org/10.3897/mycokeys.117.137112

DOI

https://doi.org/10.5281/zenodo.15374967

persistent identifier

https://treatment.plazi.org/id/06D9BCEB-235B-533B-81DA-651C54B11D80

treatment provided by

MycoKeys by Pensoft

scientific name

Diaporthe rosae Samarak. & K. D. Hyde
status

 

Diaporthe rosae Samarak. & K. D. Hyde , Fungal Diversity: 185 (2018)

Fig. 17 View Figure 17

Description.

Pathogenic to makhuea kheun ( Solanum xanthocarpum ) and causes dark brown to black stem lesions, circular to irregular necrotic leaf spots with dark margins, and water-soaked fruit lesions that enlarge over time. Sexual morph not observed. Conidiomata pycnidial, multiloculate, scattered, globose, or asymmetrical, black. Peridium consists of brown cells with angular texture on the surface. Conidiophores hyaline, smooth-walled, two-septate, branched, compactly aggregated, cylindrical, straight to sinuous, occasionally reduced to conidiogenous cells. Conidiogenous cells phialidic, subcylindrical, or ampulliform, slightly tapering towards the apex. Beta conidia aseptate, hyaline, smooth-walled, 13–23 × 0.8–1.4 μm (mean = 19 × 1.3 μm, n = 30). Gamma and alpha conidia are absent.

Culture characteristics.

Colonies on PDA reach 35–40 mm in diameter after 7 days of growth at 25 ° C in the dark, felted, white clots of mycelium arranged outward, becoming pale yellow with age. The reverse is whitish and ozonate.

Material examined.

Thailand • Chiang Rai Province, Phan District, Sai Khao , on the stem of makhuea kheun ( Solanum xanthocarpum ). February 2023, Maryam Fallahi, dried culture MF 101-1 ( MFLU 24-0245 ), living culture, MFLUCC 24-0243 .

Notes.

Based on phylogenetic analysis of combined ITS, tef 1, tub 2, cal, and his 3 sequence data, the strain MFLUCC 24-0243 clustered with the ex-type strain of Diaporthe rosae ( MFLUCC 17-2658 ) by 87 % ML bootstrap support (Fig. 16 View Figure 16 ). The base pair differences between D. rosae strains MFLUCC 24-0243 and MFLUCC 17-2658 revealed a 2.07 % (10 / 481 bp) difference in cal, and no difference in ITS and tub 2. The sequence data for tef 1 and his 3 are not available for the ex-type strain of D. rosae ( MFLUCC 17-2658 ). Diaporhe rosae ( MFLUCC 24-0243 ) and the ex-type of D. rosae ( MFLU 17-2658 ) are similar. However, D. rosae ( MFLUCC 24-0243 ) produced slightly larger beta conidia with an L / W ratio = 14.6 (19 × 1.3 μm in D. rosae ( MFLUCC 24-0243 ) vs. 17.5 × 1 μm in D. rosae ( MFLUCC 17-2658 )). Diaporthe rosae was erected by Wanasinghe et al. (2018) as a saprobic taxon that was isolated from a dead pedicel of Rosa sp. in Chiang Rai Province, Thailand. Based on the phylogenetic tree of Norphanphoun et al. (2022), D. rosae clustered in the D. sojae species complex. This study reports D. rosae ( MFLUCC 24-0243 ) from makhuea kheun ( Solanum xanthocarpum ), identifying this plant as a new host.

Kingdom

Fungi

Phylum

Ascomycota

Class

Dothideomycetes

Order

Botryosphaeriales

Family

Botryosphaeriaceae

Genus

Diaporthe

Loc

Diaporthe rosae Samarak. & K. D. Hyde

Fallahi, Maryam, Armand, Alireza, Al-Otibi, Fatimah, Hyde, Kevin D. & Jayawardena, Ruvishika S. 2025
2025
Loc

Diaporthe rosae

Samarak. & K. D. Hyde 2018: 185
2018