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Phyllosticta capitalensis on Punica granatum (CPC 20252). a – c Leaf spots on host plant d – f . Vertical section through pycnidia showing developing conidia g – k . Conidia ( d , bar =20 μ m, g – k bars =10 μ m) 

Phyllosticta capitalensis on Punica granatum (CPC 20252). a – c Leaf spots on host plant d – f . Vertical section through pycnidia showing developing conidia g – k . Conidia ( d , bar =20 μ m, g – k bars =10 μ m) 

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Phyllosticta capitalensis is an endophyte and weak plant pathogen with a worldwide distribution presently known from 70 plant families. This study isolated P. capitalensis from different host plants in northern Thailand, and determined their different life modes. Thirty strains of P. capitalensis were isolated as endophytes from 20 hosts. An additi...

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... description of Phyllosticta capitalensis (Fig. 2) On Punica granatum Pycnidia epiphyllous, globose, brown or black, 120-125 μm high, 135-140 μm wide, wall 12- 15 μm thick. Conidiogenous cells lining wall of pycnidium, phialidic, cylindrical, hyaline, 2-2.2×2.2-3 μm. Conidia ellipsoidal, hyaline, 1-celled, smooth-walled, 8-11 × 5- 6 μm, surrounded by a mucilaginous sheath, bearing a ...
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... description of (Fig. ...

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... Phyllosticta species also exist as endophytes (Baayen et al. 2002, Okane et al. 2003, Wulandari et al. 2010, Wikee et al. 2013b, Asiandu et al. 2021, as well as saprobes (van der Aa & Vanev 2002, Glienke et al. 2011. One of the most common endophytes, P. capitalensis, has a ubiquitous distribution on a myriad of hosts (Wikee et al. 2013b). ...
... Phyllosticta species also exist as endophytes (Baayen et al. 2002, Okane et al. 2003, Wulandari et al. 2010, Wikee et al. 2013b, Asiandu et al. 2021, as well as saprobes (van der Aa & Vanev 2002, Glienke et al. 2011. One of the most common endophytes, P. capitalensis, has a ubiquitous distribution on a myriad of hosts (Wikee et al. 2013b). Phyllosticta capitalensis is also a weak phytopathogen causing leaf spots (Wikee et al. 2013b), suggesting that some species can switch lifestyles depending on the environment and hosts that they colonize. ...
... One of the most common endophytes, P. capitalensis, has a ubiquitous distribution on a myriad of hosts (Wikee et al. 2013b). Phyllosticta capitalensis is also a weak phytopathogen causing leaf spots (Wikee et al. 2013b), suggesting that some species can switch lifestyles depending on the environment and hosts that they colonize. Endophytic P. capitalensis also possesses potential antagonistic effects against pathogenic P. citricarpa on citrus (Tran et al. 2019). ...
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... × 9.0-11.0 μm) are longer than those of P. cryptomeriae (9 − 13.5 μm) (Petrini et al. 1991) and P. cunninghamii (2.0-3.0 μm) (Sydow 1897) and wider than those of P. cunninghamii (1.0 μm) (Sydow 1897) and P. concentrica (6.0-9.0 μm) (Wikee et al. 2013a). Therefore, Phyllosticta endophytica is proposed as a new species. ...
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... P. capitalensis is an important plant pathogen that produces leaf spots on more than 20 species of plants worldwide, including reports of P. capitalensis causing leaf spot disease on Japanese privet in Iran (Wikee et al., 2013b;Esmaeilzadeh et al., 2020;Liao et al., 2020;Jiang et al., 2022;Li et al., 2022;Sabahi et al., 2022;Zhang et al., 2022). However, to the best of our knowledge, this is the first report of leaf brown spots caused by P. capitalensis on L. japonicum in China. ...
... However, to the best of our knowledge, this is the first report of leaf brown spots caused by P. capitalensis on L. japonicum in China. P. capitalensis has also been reported as an endophyte with a wide range of hosts such as Magnoliaceae, Citrus spp., Calophyllum spp., Mangifera indica and Punica granatum (Wikee et al., 2013b). Endophytic Phyllosticta species could become pathogenic under environmental pressure (Wikee et al., 2013a;Wikee et al., 2013b). ...
... P. capitalensis has also been reported as an endophyte with a wide range of hosts such as Magnoliaceae, Citrus spp., Calophyllum spp., Mangifera indica and Punica granatum (Wikee et al., 2013b). Endophytic Phyllosticta species could become pathogenic under environmental pressure (Wikee et al., 2013a;Wikee et al., 2013b). Therefore, P. capitalensis is expected to pose a serious threat to the production of ornamental plants in this area. ...
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... Apart from P. citricarpa, seven other species of Phyllosticta have been linked to citrus, such as P. capitalensis, which is commonly reported as an endophyte or weak pathogen with a broad host range and distribution across different regions [13][14][15] P. citriasiana causes Citrus Tan Spot disease specifically in C. maxima in Asia [16], while P. citribraziliensis is associated with Citrus species in Brazil [14]. P. citrichinaensis causes freckle spot in China [17], P. citrimaxima causes Citrus Tan Spot on the fruit of C. maxima in Thailand [18], P. paracapitalensis is found in Italy, Spain, and New Zealand [2], and P. paracitricarpa is present in China and Greece [2,17]. ...
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... Phyllosticta citricarpa is considered as a quarantine pest in Europe and the USA, thereby jeopardizing international trade (Baayen et Glienke et al. 2011). One of the most common endophytes, P. capitalensis, has a ubiquitous distribution on a myriad of hosts (Wikee et al. 2013b). Phyllosticta capitalensis is also a weak phytopathogen causing leaf spots (Wikee et al. 2013b), suggesting that some species can switch lifestyles depending on the environment and hosts that they colonize. ...
... One of the most common endophytes, P. capitalensis, has a ubiquitous distribution on a myriad of hosts (Wikee et al. 2013b). Phyllosticta capitalensis is also a weak phytopathogen causing leaf spots (Wikee et al. 2013b), suggesting that some species can switch lifestyles depending on the environment and hosts that they colonize. Endophytic P. capitalensis also possesses potential antagonistic effects against pathogenic P. citricarpa on citrus (Tran et al. 2019). ...
... However, no conidia or other morphological characters were observed. Nonetheless, culture characteristics of our isolates are consistent with those described by Wikee et al. (2013b), also shown herein (Fig. 6). ...
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... As pathogens, Phyllosticta species cause spots on the leaves or fruits of many economical plants (e.g., Musa spp., Citrus spp. and Vitis spp.), leading to substantial economic losses Wong et al. 2012;Wikee et al. 2013b;Tran et al. 2017). As endophytes, some species were found associated with leaf spots but did not cause any symptom in pathogenicity tests, e.g., P. oblongifoliae was isolated from leaf spots of Garcinia oblongifolia, P. pterospermi was isolated from leaf spots of Pterospermum heterophyllum, and P. capitalensis was isolated from leaf spots of Citrus spp. ...
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Phyllosticta (Phyllostictaceae, Botryosphaeriales) includes plant pathogens, endophytes and saprobes, occurring on various hosts worldwide. During the present study, isolates associated with leaf spots were obtained from the hosts Quercus aliena and Viburnum odoratissimum, and identified based on morphological features and phylogenetic inference from the analyses of five loci (ITS, LSU, tef1, act and gapdh). Results supported the introduction of two novel species, namely Phyllosticta anhuiensis and P. guangdongensis. Phylogenetically, P. anhuiensis and P. guangdongensis formed two well-separated lineages in the P. concentri-ca and P. capitalensis species complexes, distinguishing from all presently accepted species in this genus by DNA sequence data. Morphologically, P. anhuiensis and P. guangdongensis have the typical structure of the genus Phyllosticta, and differed from their closely related species by the length of the conidial appendage.
... The genus Phyllosticta was established by Persoon (1818) and as a monophyletic genus in Phyllostictaceae (Botryosphaeriales) (Wijayawardene et al. 2020). Currently, there are 183 species grouped in six species complexes in Phyllosticta, and members include plant pathogens, endophytes and saprobes on various host plants (Wulandari et al. 2009, Wikee et al. 2013a, Norphanphoun et al. 2020, Hattori et al. 2020, Bhunjun et al. 2021, Crous et al. 2021, Nguyen et al. 2022, Tan & Shivas 2022, Zhang et al. 2022. Morphologically, species of Phyllosticta are characterised by globose pycnidial conidiomata, subcylindrical to ampulliform conidiogenous cells, and hyaline, 1-celled, globose, subglobose, ellipsoidal to ovoid conidia, usually enclosed in a mucoid layer, bearing a single apical mucoid appendage (van der Aa & Vanev 2002), which are the main features in distinguishing Phyllosticta from other genera. ...
... Phyllosticta contains many plant pathogenic and endophytic species, commonly occurring worldwide on a broad range of host plants (Wikee et al. 2013a). Generally, Phyllosticta species cause disease symptoms on leaves, including necrotic lesions often containing many black, globose or subglobose, and semi-immersed pycnidia (Wikee et al. 2011). ...
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... Wikee et al. [3] reinstated Phyllostictaceae as a separate family in Botryosphaeriales to accommodate Phyllosticta, which consists of Phyllosticta and Pseudofusicoccum [34]. Phyllosticta species are mostly endophytes, but several are plant pathogens that cause leaf spots in a broad range of hosts worldwide [38][39][40][41][42]. Barr [43] introduced Planistromellaceae, which currently comprises two genera, namely, Kellermania and Umthunziomyces [33]. ...
... Hyaline to pigmented and septate to aseptate conidia occur among taxa in Botryosphaeriaceae. Most of the conidia in Phyllostictaceae are hyaline and aseptate, while few are pigmented and septate [3,39,41,96]. Phyllosticta philoprina and Pseudofusicoccum artocarpi have pigmented conidia and among them, P. artocarpi has septate conidia (Table S1). Both Pseudofusicoccum ardesiacum and P. kimberleyensis have hyaline, septate conidia [19,97]. ...
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Botryosphaeriales (Dothideomycetes, Ascomycota) occur in a wide range of habitats as endo-phytes, saprobes, and pathogens. The order Botryosphaeriales has not been subjected to evaluation since 2019 by Phillips and co-authors using phylogenetic and evolutionary analyses. Subsequently, many studies introduced novel taxa into the order and revised several families separately. In addition , no ancestral character studies have been conducted for this order. Therefore, in this study, we re-evaluated the character evolution and taxonomic placements of Botryosphaeriales species based on ancestral character evolution, divergence time estimation, and phylogenetic relationships, including all the novel taxa that have been introduced so far. Maximum likelihood, maximum parsimony, and Bayesian inference analyses were conducted on a combined LSU and ITS sequence alignment. Ancestral state reconstruction was carried out for conidial colour, septation, and nutritional mode. Divergence times estimates revealed that Botryosphaeriales originated around 109 Mya in the early epoch of the Cretaceous period. All six families in Botryosphaeriales evolved in the late epoch of the Cretaceous period (66-100 Mya), during which Angiosperms also appeared, rapidly diversified and became dominant on land. Families of Botryosphaeriales diversified during the Paleogene and Neogene periods in the Cenozoic era. The order comprises the families Aplosporellaceae, Botryosphaeriaceae, Melanopsaceae, Phyllostictaceae, Planistromellaceae and Saccharataceae. Furthermore, current study assessed two hypotheses; the first one being "All Botryosphaeriales species originated as endophytes and then switched into saprobes when their hosts died or into pathogens when their hosts were under stress"; the second hypothesis states that "There is a link between the conidial colour and nutritional mode in botryosphaerialean taxa". Ancestral state reconstruction and nutritional mode analyses revealed a pathogenic/saprobic nutritional mode as the ancestral character. However, we could not provide strong evidence for the first hypothesis mainly due to the significantly low number of studies reporting the endophytic botryosphaerialean taxa. Results also showed that hyaline and aseptate conidia were ancestral characters in Botryosphaeriales and supported the relationship between conidial pigmentation and the pathogenicity of Botryosphaeriales species.