Fungalpedia – Note 251, Thyrostroma

 

Thyrostroma Höhn.

Citation when using this entry: Aumentado et al. 2024 (in prep) – Fungalpedia, plant pathogens. 

Index FungorumFacesoffungiMycoBankGenBank, Fig. 1

Classification: Botryosphaeriaceae, Botryosphaeriales, Incertae sedis, Dothideomycetes, Pezizomycotina, Ascomycota, Fungi

Thyrostroma was established by Höhnel (1911) and typified with T. compactum. This genus belongs to the Dothidotthiaceae family of the order Pleosporales within the Dothideomycetes class of Ascomycota (Hongsanan et al. 2020). Thyrostroma has previously been considered synonymous with several other genera, including Coryneum, Stegonsporium, Stigmina, Thyrococcum, Thyrostromella, and Wilsonomyces (Höhnel 1911, Morgan-Jones 1971, Sutton & Pascoe 1989). Previously, Thyrostroma was considered to be the asexual form of Dothidotthia owing to its hyphomycete state in culture (Phillips et al. 2008), but there has been no phylogenetic validation to support this connection. The incorporation of new morphological insights and phylogenetic examinations established that Thyrostroma and Dothidotthia species are not congeneric and should be retained as separate genera (Crous et al. 2016, Marin-Felix et al. 2017, Senwanna et al. 2019).

Thyrostroma is identified by its sporodochial conidiomata, which are punctiform and dark brown or black. The stroma are immersed to superficial, and brown. The conidiophores are brown, with a finely roughened surface, and are cylindrical to subcylindrical, with 1–3 septa. The conidiogenous cells are brown, sub-cylindrical, and finely roughened. Conidiogenous cells proliferate percurrently at the apex. The conidia are cylindrical, clavate, ellipsoid, or fusoid, pale to medium brown and have a smooth wall. Conidia have (1–) 4 transverse septa and can have 0 to 3 oblique or longitudinal septa. The conidial apex is rounded, whereas the base is truncated (Crous et al. 2016, Marin-Felix et al. 2017).

The taxonomy of Thyrostroma previously relied more on morphological characteristics when there were still no phylogenetic studies involved. Consequently, Thyrostroma grouped in a well-supported clade within the Dothidotthiaceae using LSU sequence data (Marin-Felix et al. 2017, Crous et al. 2019). To accurately identify genera and species, along with determining their taxonomic position, phylogenetic examinations using LSU, SSU, ITS, and tef1-α genetic markers were employed (Senwanna et al. 2019). Although a combined approach of LSU, SSU, ITS, and tef1-α genes sufficiently resolves species differentiation, a comparison of ITS and tef1-α gene regions indicates that most Thyrostroma species are not markedly distinct from each other. In light of this, Senwanna et al. (2019) proposed that rpb2 and tub2 genes are reliable markers for discerning species within Thyrostroma. Similarly, Jayawardena et al. (2020) reconstructed the phylogeny employing similar genetic markers and validated thirteen species, supporting the findings of Marin-Felix et al. (2017), Senwanna et al. (2019), and Hyde et al. (2020).

Thyrostroma species are pathogens, saprobes, or endophytes. As a pathogen, Thyrostroma is associated with canker, dieback, and leaf spots in terrestrial habitats (Yuan & Old 1990, Marin-Felix et al. 2017, Senwanna et al. 2019). Species of Thyrostroma have been recorded from various symptomatic plants viz., Cornus officinalis (Crous et al. 2016), Sambucus caerulea, Styphnolobium japonicum, Tilia spp. (Marin-Felix et al. 2017), and Ulmus spp. (Ellis 1971). Pathogenicity tests were conducted on Prunus spp., which produced circular to irregular lesions (Tovar-Pedraza et al. 2013, Nabi et al. 2018). A cross-infectivity study by Rasool et al. (2020) on Prunus spp. revealed that Thyrostroma isolates originating from cherries demonstrated the capability to infect apricots, but the isolates sourced from apricots and almonds did not exhibit cross-infectivity when subjected to other stone fruit hosts. Nevertheless, further studies are needed to underpin the host-specificity and pathogenic breadth of Thyrostroma.

Type species: Thyrostroma compactum (Sacc.) Höhn. 1911

Other species: (Species Fungorum – search Thyrostroma)

 

Figure 1– Thyrostroma tiliae (a-c) and Thyrostroma cornicola (d-e). a Canker symptoms. b Sporodochia on host surface. c Vertical section of sporodochium. d Conidiogenous cells and attachment of conidia. e. Conidia. Scale bars: c = 200 µm; d,e = 10 μm. Redrawn from Crous et al. (2016) and Senwanna et al. (2019).

 

References

Crous PW, Wingfield MJ, Richardson DM, Leroux JJ, Strasberg D et al. 2016 – Fungal Planet description sheets: 400–468. Persoonia-Molecular Phylogeny and Evolution of Fungi, 36(1), 316–458.

Crous PW, Schumache RK, Akulov A, Thangavel R et al. 2019 – New and interesting fungi. 2. Fungal Syst Evol, 3, 57–134.

Ellis MB. 1971 – Dematiaceous hyphomycetes. Commonwealth Mycological Institute, Kew.

Höhnel FXR von. 1911 – Fragmente zur mykologie. XIII Mitteilung (Nr. 642 bis 718). Sitzungsberichte der Kaiserlichen Akademie der Wissenschaften in Wien Mathematisch-Naturwissenschaftliche Classe, Abt., 1 120, 379–484.

Hongsanan S, Hyde KD, Phookamsak R, Wanasinghe DN, McKenzie EH et al. 2020 – Refined families of Dothideomycetes: Orders and families incertae sedis in Dothideomycetes. Fungal Diversity,105, 17–318.

Hyde KD, Norphanphoun C, Maharachchikumbura SS, Bhat DJ et al. 2020 – Refined families of Sordariomycetes. Mycosphere 11, 305–1059.

Jayawardena RS, Hyde KD, Chen YJ, Papp V et al. 2020 – One stop shop IV: taxonomic update with molecular phylogeny for important phytopathogenic genera: 76–100 (2020). Fungal Diversity, 103, 87–218.

Marin-Felix Y, Groenewald JZ, Cai L, Chen Q et al. 2017 – Genera of phytopathogenic fungi: GOPHY 1. Studies in Mycology, 86, 99–216.

Morgan-Jones G. 1971 – Sciniatosporium Kalchbr., and its synonyms Marcosia Syd., Stigmina Sacc, Thyrostroma Höhnel, and Thyrostromella Syd., non Höhnel. Can J Bot. 49(6), 993–1009.

Nabi A, Shah MU, Padder BA, Dar MS et al. 2018 – Morpho-cultural, pathological and molecular variability in Thyrostroma carpophilum causing shot hole of stone fruits in India. European Journal of Plant Pathology, 151, 613–627.

Phillips AJL, Alves A, Pennycook SR, Johnston PR et al. 2008 – Resolving the phylogenetic and taxonomic status of dark-spored teleomorph genera in the Botryosphaeriaceae. Persoonia, 21, 29–55.

Rasool RS, Wani AA, Masoodi KZ, Bhat ZA et al. 2020 – Study on Cross Infectivity of Different Isolates of Thyrostroma carpophilum on Stone Fruits in Kashmir Valley. Int. J. Curr. Microbiol. App. Sci. 9(3), 616–23.

Senwanna C, Wanasinghe DN, Bulgakov TS, Wang Y et al. 2019 – Towards a natural classification of Dothidotthia and Thyrostroma in Dothidotthiaceae (Pleosporineae, Pleosporales). Mycosphere, 10(1), 701.

Sutton BC, Pascoe IG. 1989 – Reassessment of Peltosoma, Stigmina and Batcheloromyces and description of Hyphothyrium gen. nov. Mycological Research, 92(2), 210–22.

Tovar-Pedraza JM, Ayala-Escobar V, Segura-León OL. 2013 – Thyrostroma carpophilum causing apricot shot-hole in Mexico. Australasian Plant Disease Notes, 8, 31–3. 

Yuan ZQ, Old KM. 1990 – A new species of Thyrostroma from Australia. Mycol Res, 94, 573–576.

 

Entry by

Herbert Dustin R. Aumentado, Center of Excellence in Fungal Research and School of Science, Mae Fah Luang University, Chiang Rai, Thailand 

 

(Edited by Ruvishika S. Jayawardena & Kevin D. Hyde, Samaneh Chaharmiri-Dokhaharani, & Achala R. Rathnayaka)

 

Published online 20 May 2024