Cytospora Ehrenb., Sylv. mycol. berol.: 28 (1818)
Cytospora was introduced by Ehrenberg (1818) as the type genus of the family Cytosporaceae in Diaporthales (Wehmeyer 1975; Barr 1978; Eriksson 2001; Castlebury et al. 2002). The genus is an important pathogenic fungus, causing canker and dieback on branches of a wide range of hosts with a wide distribution (Adams et al. 2005, 2006; Hyde et al. 2017, 2018; Norphanphoun et al. 2017, 2018).
Classification –Sordariomycetes, Diaporthomycetidae, Diaporthales, Valsaceae
Type species – Cytospora chrysosperma (Pers.) Fr. 1823
Distribution – Worldwide
Disease symptoms – Canker and dieback disease on branches
Hosts – Species of Abies, Acer, Berberis, Betula, Ceratonia, Cornus, Cotinus, Crataegus, Elaeagnus, Eriobotrya, Eucalyptus, Juniperus, Lumnitzera, Malus, Picea, Pinus, Platanus, Platycladus, Populus, Prunus, Pyrus, Quercus, Rosa, Salix, Sequoia, Sibiraea, Sorbaronia, Sorbus, Spiraea, Styphnolobium, Syringa, Syzygium, Tibouchina, Ulmus, Vitis and Xylocarpus (Norphanphoun et al. 2018).
Morphological based identification and diversity
Cytospora is characterized by multi-loculate conidiomata with ostiolar necks and unicellular, elongate-allantoid to subcylindrical, hyaline conidia (Fan et al. 2015a, b; Norphanphoun et al. 2017, 2018; Fig. 7). The genus which was reported as causing canker diseases in many woody plants was established in 1818 and studied in detail by taxonomists (Fries 1823; Saccardo 1884). Valsa Fr. was reported as the sexual stage of this genus and therefore, Valsa was treated as a synonym of Cytospora (1818) based on the International Code of Nomenclature for Algae, Fungi, and Plants (ICN, McNeill et al. 2012), with Cytospora being the oldest and most widely used name (Adams et al. 2005; Fotouhifar et al. 2010; Fan et al. 2014; Rossman et al. 2015). Previously, the conventional identification of species in Cytospora was based on their host association, often with vague morphological descriptions. Mycologists began to elucidate the relationships between Cytospora species and their hosts, with morphological observations combined with phylogenetic analyses using internal transcribed spacer (ITS) regions as an effective fungal DNA barcode (Adams et al. 2005, 2006; Fotouhifar et al. 2010; Schoch et al. 2012). The establishment of multi-gene analyses using ITS, LSU, ACT, RPB2, TUB2 has proved comprehensive for the species level (Fan et al. 2015a, b, 2020; Liu et al. 2015; Yang et al. 2015; Hyde et al. 2016; Li et al. 2016; Norphanphoun 2017, 2018; Phookamsak et al. 2019).