Fomitiporia punicata and Phaeoacremonium minimum associated with Esca complex of grapevine in China

The Esca disease complex includes some of the most important trunk diseases of grapevines (Vitis spp.) and causes serious yield losses in grape production worldwide. However, there has been no detailed study on its presence and associated pathogens in China. During 2017–2019, a preliminary field survey was conducted in eight vineyards in Hebei and Ningxia provinces, China when unusual foliar symptoms were observed. Symptoms were distinct tiger striped leaves, which are typical of grapevine leaf stripe disease (GLSD), one of the most common diseases in the Esca complex. Tiger-stripe leaf symptoms were found in four vineyards, and incidence was cultivar dependent varying with vineyard and year. A total of 266 fungal isolates were obtained from wood tissues of grapevines with typical foliar symptoms of GLSD. Based on morphological characters and multigene-combined phylogenetic analyses, the Ascomycete Phaeoacremonium minimum, one of the pathogens associated with Esca complex was identified. The basidiomycete Fomitiporia punicata, which has never been reported infecting grapevine, was also identified and found to be associated with wood rot in grapevine. The remaining isolates included some known wood pathogens, such as Neofusicoccum species and Diaporthe species. Koch’s postulates were performed in the greenhouse, confirming that both F. punicata and P. minimum caused leaf interveinal chlorosis and necrosis that resembled the GLSD symptoms of the Esca complex observed in the field. The present study provides the first detailed report of the Esca complex in China. In addition, this is the first record of F. punicata associated with Esca complex of grapevine worldwide. The results of this study provide new insights into the knowledge of the Esca complex.


Background
Grape is one of the most important fruit crops in the world, and also the most economically important for making wine, beverages and other products. In 2018, the global grape cultivation area was 7,449,000 ha, of which China accounted for 12% and ranked in second place (OIV 2019). Grapevine trunk diseases (GTDs) have been reported in recent years in some vineyards in China, especially in mature vineyards (Yan et al. 2013). The most important grapevine trunk disease in China is Botryosphaeria dieback, which was first reported by Li et al. (2010). The main symptoms associated with Botryosphaeria dieback are fruit dropping and wood cankers (Yan et al. 2013). Botryosphaeria dieback causes a 10-20% reduction in yield and eventual death of vines in extreme environmental conditions such as long periods of high temperature or rainy seasons (Li et al. 2010). Six Botryosphaeriaceae species (Botryosphaeria dothidea, Diplodia seriata, Lasiodiplodia theobromae, Lasiodiplodia pseudotheobromae, Neofusicoccum parvum and Neofusicoccum mangiferae) associated with Botryosphaeria dieback in China (Li et al. 2010;Yan et al. 2013;Dissanayake et al. 2015bDissanayake et al. , 2015c. Another emerging grapevine trunk disease in China is Diaporthe dieback (Dissanayake et al. 2015a), and ten Diaporthe species (Diaporthe eres, D. hongkongensis, D. phaseolorum, D. sojae, D. guangxiensis, D. hubeiensis, D. viniferae, D. gulyae, D. pescicola and D. unshiuensis) associated with the disease in China (Dissanayake et al. 2015a;Manawasinghe et al. 2019). Esca disease complex was first reported in China in 2020, and P. minimum was the pathogen associated with the symptoms (Ye et al. 2020).
Esca complex, some of which show typical leaf symptoms, includes the most devastating diseases on grapevine causing serious economic losses in many grapegrowing countries and regions (Mugnai et al. 1999;Gramaje et al. 2015;Spies et al. 2018;Guerin-Dubrana et al. 2019). The average incidence of Esca increased to 32.6% in mature vineyards of Marche region, central eastern Italy from 2005 to 2007 (Romanazzi et al. 2009). The Esca complex is characterized by five different diseases based on wood symptoms, foliar symptoms, life stages of the vines and the causal agents, i.e., dark wood streaking, Petri disease, grapevine leaf stripe disease (GLSD), white rot and Esca proper (Mugnai et al. 1999;Surico 2009;Gubler et al. 2015;Mondello et al. 2018). This disease complex exhibits both external (e.g., symptomatic leaves and berries) and internal (i.e., diseased wood and branches) symptoms (Mugnai et al. 1999;Surico 2009;Gubler et al. 2015). The most characteristic foliar symptoms of the Esca complex are seen in the leaves, which develop a tiger-stripe pattern (Mugnai et al. 1999;Surico 2009;Gubler et al. 2015), and small reddish or dark purple spots on berries, which are known as "black measles" (Mugnai et al. 1999). Another common symptom in vineyards is vine apoplexy (Mugnai et al. 1999). The trunk (scion and sometimes rootstock) and main branches show several types of wood discoloration and necrosis (Mugnai et al. 1999;Surico 2009;Gubler et al. 2015). The internal symptoms in wood vary with the age of symptomatic grapevines and the pathogens involved (Mugnai et al. 1999;Fischer 2006;Cloete 2015;Mondello et al. 2018).
Esca disease was recently reported in China (Ye et al. 2020), but no detailed study has been conducted on the causal organisms or their pathogenicity. The present research was based on surveys and samples collection from Hebei and Ningxia provinces in China. Hebei Province has a long history of grape cultivation (Chu and Chen 2018). Ningxia Province is regarded as one of the best ecological zones in China for grape cultivation, mainly attributed to its suitable climate, such as adequate rain and sunshine, and large temperature difference between day and night, especially the low temperatures and less rain in autumn, and now it has developed into the largest wine grape-growing region in northwest China (Chen 2018). The objectives of this study were to (i) conduct a preliminary vineyard survey to determine the extent of Esca complex in Hebei and Ningxia provinces in China; (ii) investigate wood symptoms associated with GLSD; (iii) identify fungal pathogens associated with GLSD based on morphological characters and multigene-combined phylogenetic analyses; and (iv) evaluate the pathogenicity of some of the fungi associated with Esca symptoms.

Field surveys
A field survey was conducted in eight vineyards in Hebei and Ningxia provinces in China (Table 1). The presence of foliar symptoms was recorded during the growing season, and the internal wood symptoms of the symptomatic vines were observed in late summer ( Fig. 1a-f). Tiger-stripe foliar symptoms, the typical symptoms of GLSD, were observed in four (Hb-1, Nx-1, Nx-4 and Nx-5) of eight surveyed vineyards, while no obvious symptoms were found in the other four vineyards (Hb-2, Hb-3, Nx-2 and Nx-3) (Table 1). Among the 7670 plants examined, 95 plants showed tiger-stripe foliar symptoms, and no apoplectic symptom was found during the survey. The incidence of tiger stripe-like foliar symptoms was quite variable from year-to-year, and also varied a lot between cultivars, both of which are well-known characteristics of this disease. For example, the incidence of the tiger-stripe foliar symptoms at Hb-1 was low in 2017 (1.0%) but much higher in 2018 (5.6%); the incidence of the disease between cultivars in the same year and vineyard were obviously different (0.7% on Merlot, 5.0% on Cabernet Franc, 0.3% on Marselan, 16.7% on Petit Verdot in 2018). Internal necrosis and decay in wood were randomly analysed in some vines with typical foliar symptoms of GLSD in vineyards Hb-1, Nx-1 and Nx-4, and the main wood symptoms detected in 12 vines are shown in Additional file 1: Table S1.

Fungal isolation, phylogenetic analyses and taxonomy
Fungi were isolated from discoloured grapevine wood tissues and initially grouped on the basis of their morphological characteristics. From different types of symptomatic wood tissues, 266 fungal isolates were obtained. The fungal species associated with the main internal wood symptoms were determined (Additional file 1: Table S2). In a 19-year-old grapevine showing wood rot in vineyard Hb-1, the most abundant types of fungi according to morphological characters were Fomitiporia-like and Phaeoacremonium-like. The remaining isolates were grouped as Botryosphaeriaceae species and Diaporthaceae species. A high percentage of Fomitiporia species were found from rotten wood in vineyard Hb-1. Phaeoacremonium isolates were obtained from black streaks, symptomatic pith tissues and asymptomatic wood tissues at the base of trunk and rootstock in two vines in vineyards Nx-1 and Hb-1. Botryosphaeriaceae species were isolated from wood tissues with symptoms of white rot, black streaks and brown necrosis in vineyards Hb-1 and Nx-1. Diaporthaceae species were isolated from brown necrotic tissues in vineyard Hb-1. Most of these fungi were isolated from the same diseased vines, confirming that several different pathogens often occur in the same grapevine at the same time in the field, as is well known for GTDs.
Major characteristics of the two species, F. punicata and P. minimum, are as follows: The morphological characteristics of Fomitiporia-like isolates (cottony to woolly vegetative mycelium, with yellowish to brownish aerial hyphae, clamp connections present in hyphae, no conidia) were identical on PDA, thus two isolates (JZB3350001 and JZB3350002) were selected for molecular analysis. To identify the isolates at the species level, phylogenetic analyses were conducted based on LSU, ITS and tef1 sequences. The combined dataset of Fomitiporia species consisted of two isolates (JZB3350001 and JZB3350002) obtained in this study and sequences of 78 taxa retrieved from GenBank (Groenewald et al. 2001;Chen and Cui 2017) (Table 2). Phellinus uncisetus MUCL 46231 and P. uncisetus MUCL 47061 were used as outgroup taxa. The dataset consisted of 2477 total characters of which 1575 were constant and 208 were parsimony-uninformative. A heuristic search of the remaining 609 parsimonyinformative characters produced 1000 most parsimonious trees with a length of 1796 steps (CI = 0.547, RI = 0.774, RCI = 0.423 and HI = 0.453). Topology of the maximum likelihood tree was similar to the maximum parsimony tree. The best scoring RAxML tree with a final likelihood value of −15,647.433442 is presented in Fig. 2. In the phylogenetic analysis, JZB3350001 and JZB3350002 clustered together with F. punicata, with 94% (ML) and 95% (MP) bootstrap values, respectively.
Pathogenic on trunk and rootstock of Vitis vinifera. Asexual morph: no spores were produced on PDA or malt extract agar (MEA) cultures incubated at 25°C in the dark for more than 3 months. Sexual morph: undetermined.
Culture characteristics: Colonies on PDA reached 38.8 ± 7.5 mm diameter after 10 days of incubation at 25°C, yellowish, with cottony to wooly vegetative mycelium, with yellowish to brownish aerial hyphae, clamp connections, no conidia (Fig. 3c, d).
Culture characteristics: Colonies on PDA reached 39.5 ± 1.9 mm diameter after 21 days of incubation at 25°C, with rare aerial mycelia and produced a yellow pigment on PDA (Fig. 3a, b). Mycelium texture was mostly verrucose.
Material examined: China, Hebei Province, Huailai County and Ningxia Province, Yinchuan, on trunk and root of V. vinifera, 10 August 2018, Qingtong Ye and Fig. 1 The training systems in the surveyed vineyards and symptoms on 19-year-old 'Cabernet' grapevines. a-c Foliar symptoms of GLSD-like (Esca complex) disease, initially appeared as chlorotic spots and subsequently coalesced, turned dark red, and finally became necrotic. d-f Internal symptoms of the same vine with foliar symptoms: discolored wood showing white rot and brown necrosis. g, h The mini "J" and vertical training systems in the surveyed vineyards in Hebei and Ningxia provinces, China

Pathogenicity of F. punicata
Sixty days after inoculation, 5 of the 20 plants inoculated with F. punicata showed chlorotic leaf spots that gradually coalesced. Three months post-inoculation, in control plants, there were neither leaf symptoms nor any significant discoloration in the wood (Fig. 5a-e). While in the vines inoculated with F. punicata, the interveinal discolorations on leaves turned dark red and finally became necrotic, and internal wood discolorations were also observed: brown discoloured lesions spread up and down from the inoculation sites in the trunk (Fig. 5f-j), but no white rot symptoms were found in the wood. F. punicata induced wood discolorations with a mean length of 8.2 ± 1.1 mm. The inoculated fungus was reisolated and confirmed as F. punicata, with an 80% isolation ratio. No fungal pathogens were isolated from control plants.

Pathogenicity of P. minimum
At 108 days post-inoculation (dpi), leaves of three out of ten vine cuttings inoculated with the P. minimum isolate JZB3190002 displayed necrotic lesions starting from the edge of the leaf blade, which initially appeared as chlorotic spots subsequently coalesced along the veins. At 208 dpi, no discolouration or necrosis was recorded in the control vines ( Fig. 6a-f), while three inoculated vines showed a clear interveinal discoloration and necrosis on leaves, which resembled the tiger-like symptom. Analysis of the internal wood symptoms revealed the development of brown necrosis in the stem starting from the base (Fig. 6g-l) of the three symptomatic inoculated vines. The pathogen was re-isolated and confirmed as P. mimimum, with 60% isolation ratio. No fungal species were isolated from control plants.

Discussion
GLSD, one of the diseases within the Esca complex was observed in our surveys. The most prevalent external symptoms of the disease were tiger stripe pattern on leaves. All the symptomatic vines (with typical foliar  symptoms) that were checked for internal wood symptoms showed discoloration and necrosis in wood tissues. The white rot wood symptom was found at the base of trunk and rootstock of only one adult grapevine (19year-old), which was consistent with previous studies that white rot symptom were frequently found in old vineyards (Mugnai et al. 1999;Mondello et al. 2018). No signs of black measles and apoplexy were found during the survey. The disease incidence of Esca complex varied with cultivar, vineyard and year, confirming the symptoms fluctuation as a typical phenomenon in this disease (Surico et al. 2006). This fluctuation is also known to be affected by the vineyard age, amount of rainfall in the rainy seasons (Surico et al. 2000) together with other environmental factors (Surico et al. 2006). During the surveys, we discovered the reason why there have been no reports of Esca complex in China up to now. Usually, the grape growers do not realize that the tiger-striped foliar symptoms are caused by biotic agents and they treat them as if they were a nutrient deficiency. To our knowledge, it is possible for the vascular pathogens to be introduced with infected propagation materials from abroad, whereas the decay causing agents usually do not move with propagation materials, but instead they contaminate the pruning wounds on vines. The wood decay agents reported here have never been recorded outside China before. In our study, morphological characterization combined with multigene-combined phylogenetic analyses demonstrated that the prevalent isolates that are associated with wood symptoms are F. punicata and P. minimum. P. minimum was found in both Hebei and Ningxia provinces, while F. punicata was detected only in Hebei Province. Pathogenicity tests confirmed that both of these two fungal species were able to cause tiger stripe symptoms on leaves.
Fomitiporia species associated with Esca complex were found to vary with geographic location (Cloete 2015). Fomitiporia mediterranea has been reported mainly in European and Mediterranean grape-growing regions (Larignon and Dubos 1997;Fischer 2002;Luque et al. 2009;Akgul et al. 2015;Baranek et al. 2018), F. polymorpha in North America (Fischer 2006), F. australiensis in Australia (Fischer 2006) and F. capensis in South Africa (Cloete et al. 2014). Fomitiporia punicata was first reported on Punica granatum (Punicaceae) by Dai et al.  2008), and this is the first report of F. punicata infecting grapevines and causing Esca complex disease. In China, the fruiting bodies of F. punicata were found on living trees of Punica granatum in Shanxi Province (Dai et al. 2008). Although we isolated this fungus from diseased grapevines in this study, we did not find any fruiting bodies. It was also indicated in previous study that the fruiting bodies of basidiomycete species associated with Esca complex are rarely formed and observed on grapevines (Cloete et al. 2014).
Several genera of vascular pathogens, like Phaeoacremonium, Phaeomoniella and Cadophora, and  6 Pathogenicity test of Phaeoacremonium minimum in the greenhouse. a-f Control plant. g-l The Plant inoculated with P. minimum showed interveinal discolorations and necrosis on leaves, and black necrosis within rootstock at 208 dpi basidiomycete species belonging to the genera Inocutis, Inonotus, Fomitiporella, Fomitiporia, Phellinus and Stereum, have been reported on grapevine worldwide (Fischer 2006;Cloete 2015). Of these, P. minimum is one of the most frequently reported species while Phaeomoniella chlamydospora is the most virulent species (Gramaje et al. 2018). Phaeoacremonium minimum has been reported on a wide range of woody hosts, primarily on Vitis species (Gramaje et al. 2015;da Silva et al. 2017;Spies et al. 2018). It also has a wide distribution and has been reported in Algeria, Argentina, Australia, Brazil, California, Chile, China, France, Iran, Italy, South Africa, Spain, Uruguay, Turkey and the USA (Crous et al. 1996;Larignon and Dubos 1997;Scheck et al. 1998;Gatica et al. 2001;Groenewald et al. 2001;Edwards and Pascoe 2004;Gimenez-Jaime et al. 2006;Mostert et al. 2006;Abreo et al. 2011;Berraf-Tebbal et al. 2011;Úrbez-Torres et al. 2012;Correia et al. 2013;Mohammadi et al. 2013;Ye et al. 2020).
Other fungi causing Esca complex include species in the genera Neofusicoccum and Diaporthe. Neofusicoccum and Diaporthe species are also the causal organisms of GTDs (Yan et al. 2013;Dissanayake et al. 2015a). Diplodia seriata and Eutypa lata have been isolated from Esca-affected vines in Europe (Mugnai et al. 1999). Therefore, it is possible to isolate the pathogens causing Esca complex and Botryosphaeria dieback from the same grapevine during the growing season in China. The results also provide evidence that in China GTDs are associated with a wide range of fungal taxa.
As shown in the present study, the Esca complex symptoms in China are also associated with rootstock infection, thus removing the whole infected plants is a very critical control measure currently available to inhibit the spread of this disease. Moreover, frequent and extensive pruning or large rejuvenation cuttings are known to be favourable for the development of Esca disease (Mugnai et al. 1999). Extensive wounds are normally created in summer and winter trimming; thus, protection of pruning wounds is an essential measure to prevent the spread of the disease in the vineyards. Further intensive field surveys are required in all grapegrowing regions in China to understand the extent and severity of these diseases.

Conclusions
Here we provide the first detailed study of the presence of Esca complex of grapevine in China. We also present the first record of F. punicata associated with Esca complex of grapevine worldwide and confirm the presence of P. minimum in the same vines infected with F. punicata. Further studies need to be carried out to understand the impact of this disease complex in China.

Vineyard surveys and sample collection
Hebei and Ningxia provinces are two major wine and table grape-growing regions in China (Chen 2018). The climate of Hebei and Ningxia provinces is temperate monsoon climate (Yan et al. 2013). The soil type in surveyed vineyards of Hebei Province is mainly sandy soils (Wang 2012), and gravel calcareous soils in Ningxia Province (Wang 2018). The average altitude of vineyards we investigated in Hebei and Ningxia provinces is about 1300-1600 and 1000-1500 m.a.s.l., respectively. The annual rainfall in Ningxia Province does not exceed 200 mm. The sunshine, soil, moisture, altitude and latitude at the Helan Mountain's East Foothill are conducive to grape cultivation.
Surveys of Esca complex symptoms were carried out in Hebei (36°01′-42°37′N, 113°04′-119°53′E) and Ningxia provinces (35°14-39°23′N, 104°17-107°39′E) from 2017 to 2019. At least one cultivar was investigated in each vineyard. Disease incidence was calculated by counting the plants in a block of grapevines in each vineyard that showed foliar symptoms among the total number of standing vines surveyed. The surveyed vineyards varied from 5 to 20-year-old. The training system applied in the surveyed vineyards were mini "J" and, in some vineyards in the two provinces of China were vertical training system (Fig. 1g, h). Based on the information obtained from the winegrowers, the original propagation materials in vineyards Hb-1, Hb-2, Hb-3 and Nx-1 were bought from France. The surveyed grape cultivars are Marselan, Chardonnay, Merlot, Petit Verdot, Cabernet Franc, and there were some unknown varieties as well. Some grapevines were grafted but the rootstock is unknown, and some were self-rooted.
GLSD foliar symptoms (Esca complex) were recorded by the grape growers in some vineyards, which are included in Table 1. The yearly variation in incidence of GLSD foliar symptoms in different regions and cultivars was recorded. Characteristic symptoms, such as tiger striped leaves and wood discoloration, were recorded and photographed. Samples from symptomatic trunk and rootstock of 12 plants were collected and taken to the laboratory for further study.

Fungal isolation and morphological characterization
Portions of scion trunks and rootstocks were put in zip-lock bags and kept at 4°C for further studies. Samples were analysed and different types of wood symptoms and discolorations were detected, which included white rot, brown necrosis, brown to black streaks appearing as black spots in cross-section, black line bordering the decayed wood, decayed pith, pith margin, asymptomatic scion trunk base and rootstock and asymptomatic tissues (no discoloration or decay). Pathogens were isolated by dissecting small wood pieces (< 5 mm 2 ) after taking off the bark. Wood chips were taken from symptomatic woods with discoloured, necrotic or decayed symptoms, disinfected in 1.5% sodium hypochlorite for 3 min, in 70% ethanol for 30 s, and then rinsed three times with sterile distilled water, dried and finally placed on potato dextrose agar (PDA) amended with ampicillin (100 mg/L). The plates were incubated at 25°C in the dark. The wood pieces without any hyphal development were transferred onto new PDA plates to avoid contamination by fast-growing fungi from the closely placed wood pieces (Hofstetter et al. 2012). Hyphal tips from actively growing margins of the colony were transferred onto new PDA plates. From morphologically identical colonies, a few strains were selected for further analysis. To obtained pure cultures, single spore isolations were made on PDA plates. Conidia were diluted with sterile distilled water and spread on 1.5% water agar (WA), and incubated at 25°C and germinating single conidia were transferred to PDA plates. For those isolates that did not produce conidia, hyphal tip isolation was performed to obtain pure cultures. Cultures were examined periodically for the development of conidiomata. Colony diameters after 5-7 days of incubation were measured. The shapes, sizes, and colour of at least 50 conidia were observed and recorded using ZENPRO 2012 software (Carl Zeiss Microscopy). All the cultures obtained in this study were deposited in the culture collection of Institute of Plant and Environment Protection, Beijing Academy of Agriculture and Forestry Sciences (JZB), Beijing, China.

DNA extraction, PCR amplification and sequence assembly
All isolates were initially identified by morphological characteristics, including colony morphology and conidial characters. At least two isolates were selected from each morphologically similar group for molecular identification. In the present study, colony characters of all the Basidiomycete isolates were similar on PDA, therefore only two isolates (JZB3350001 and JZB3350002) were selected for the phylogenetic analyses. Colonies of the Phaeoacremonium isolates differed on PDA at 25°C in dark, so eight isolates (JZB3190002, JZB3190004, JZB3190006, JZB3190007, JZB3190009 JZB31900010, JZB31900011, JZB31900012) representing different colony morphological groups were selected. Total genomic DNA was extracted from 50 to 100 mg of mycelia, scraped from 7-day-old colonies on PDA, by the CTAB method (Guo et al. 2000). For preliminary species identification, the internal transcribed spacer (ITS) region was amplified with the primer pair ITS1/ITS4 (White et al. 1990). The sequences obtained were used to search Gen-Bank with the BLASTn tool (https://blast.ncbi.nlm.nih. gov/Blast.cgi). Based on BLAST results, additional gene fragments of β-tubulin (tub2) and actin (act) were amplified and sequenced for Phaeoacremonium isolates with primer pairs T1/ Bt2b (Glass and Donaldson 1995;O'Donnell and Cigelnik 1997) and ACT-512F/ACT-783R (Carbone and Kohn 1999), respectively. For the basidiomycete isolates, nuclear large subunit ribosomal RNA gene regions (nLSU) and elongation factor-1α (tef1) gene fragments were amplified and sequenced with two primer pairs LROR/ LR7 (http://www.biology.duke. edu/fungi/mycolab/primers.htm) and EF-983F/ EF-1567R (http://ocid.NACSE.ORG/research/deephyphae/ EF1primer.pdf), respectively. The PCR mixture consisted of 1 μL of genomic DNA, 2 mM MgCl 2 , 10 μM of each deoxyribonucleotide triphosphates (dNTPs), 1 μL of each 10 μM primer and 0.3 U of Taq Silver star DNA polymerase in a 1× reaction buffer. The PCR conditions were as follows: for tub2 and tef1 amplification, initial denaturation for 3 min at 94°C, 34 cycles of denaturation at 94°C for 30 s, annealing for 30 s at 56°C, and extension for 30 s at 72°C, and a final extension for 7 min at 72°C; for act and ITS, the same as for tub2 except for annealing at 54°C; for nLSU, the same as for tub2 except for extension for 90 s at 72°C. PCR products were separated on 1% agarose gels and visualized under UV light in a Gel DocTM XR Molecular Imager (Bio-Rad, USA). Sequencing was carried out by Tsingke Company, Beijing, China. Sequence quality was confirmed by checking chromatograms with BioEdit v.5 (Hall 1999). For sequences obtained from forward and reverse primers, consensus sequences were generated with Seq-Man 3.1 (DNASTAR, Inc.). New sequences obtained in the present study were deposited in GenBank database (Table 2).

Phylogenetic analyses
Reference sequences of Fomitiporia and Phaeoacremonium reference species and related taxa were obtained from GenBank (Groenewald et al. 2001;Chen and Cui 2017;Spies et al. 2018), which were aligned with the sequences obtained in the present study using MAFFT (Kuraku et al. 2013;Katoh et al. 2019). The alignments were edited manually with BioEdit v7.0.9 (Hall 1999) where necessary. Phylogenetic relationships were inferred by maximum parsimony (MP) implemented in PAUP (v4.0) (Swofford 2002), and maximum likelihood (ML) in RAxML (Silvestro and Michalak 2012). In maximum parsimony, heuristic searches with tree-bisectionreconnection (TBR), as the branch-swapping algorithm and 1000 bootstrap replications were used with random sequence addition. All characters were unordered and carried equal weight, gaps were treated as missing data, Steepest descent option not in effect and MulTrees option in effect. Descriptive tree statistics including Tree length (TL), Consistency index (CI), Retention index (RI), Relative consistency index (RCI) and Homoplasy index (HI) were calculated. Resulting trees were assessed by the Kishino-Hasegawa tests to determine whether they were significantly different or not (Kishino and Hasegawa 1989). The ML analysis was performed with RAxML-HPC2 on XSEDE (8.2.8) (Stamatakis 2014) in the CIPRES Science Gateway Platform (Miller et al. 2010). For each phylogenetic tree, 1000 nonparametric bootstrapping iterations were used. Phylogenetic trees were visualized with FigTree v1.4.4 (Rambaut 2018) and edited with Microsoft PowerPoint 2016.

Pathogenicity tests
Pathogenicity test for F. punicata Young, healthy, two-year-old 'Cabernet Franc' rooted cuttings in pots were used for the pathogenicity tests. The grapevines stems were first surface sterilized with 70% ethanol, then 5-mm-diameter wounds were made on the stem using a sterilized blade. One wound was made on each plant. Mycelial plugs (5-mm-diameter) taken from actively growing colony margins of F. punicata (JZB3350001 and JZB3350002 obtained in this study) were placed on the wounds. Wounds were covered with Vaseline (petroleum jelly) and sealed with parafilm to prevent water evaporation. Control plants were inoculated with non-colonized PDA plugs. For each isolate, the experiment was replicated on 10 plants. Inoculated plants were grown under greenhouse conditions (24-25°C, 60% RH) for more than three months until they showed symptoms. When tiger stripe symptoms appeared on the leaves, inoculated and control young vines were analysed for development of wood symptoms. To confirm Koch's postulate, the target pathogen was reisolated from the inoculated vines.