Palm Foliage as Pathways of Pathogenic Botryosphaeriaceae Fungi and Host of New Lasiodiplodia Species from Mexico

Tropical palm foliage is increasingly imported to satisfy the steady growing demand in European floristry. This palm foliage presumably carries along diverse fungi whose taxonomic and functional diversity have not been addressed so far. The present study investigated Botryosphaeriaceae fungi associated with the foliage of palm species Chamaedorea elegans, C. metallica, C. seifrizii, Dypsis lutescens and Lodoicea maldivica imported from Mexico. Five species were identified using combined morphological characterisation and multilocus phylogenetic analyses based on ITS, TEF-1α, TUB2 and RPB2. In addition to Endomelanconiopsis endophytica, Lasiodiplodia brasiliensis and L. euphorbicola, two new species, namely, L. lodoiceae sp. nov. and L. mexicanensis sp. nov, are proposed. Apart from E. endophytica, mostly known as endophyte, L. brasiliensis and L. euphorbicola are responsible for different rot diseases and the dieback of important tropical crop plants. In pathogenicity tests on the temperate pome fruits apple (Malus domestica) and pear (Pyrus communis), all six Botryosphaeriaceae species induced necrotic lesions at different degrees of severity, with highest the aggressiveness from L. euphorbicola and L. mexicanensis on apple and from L. mexicanensis on pear. The results indicate that tropical palm foliage can be a pathway of potentially pathogenic fungi that may give rise to concerns with regard to plant health in the destination countries.


Introduction
Tropical palms (Arecales, Arecaceae) naturally inhabiting warm climate regions [1] are currently distributed worldwide, mostly due to their use as ornamental plants and important accessory in interior decoration and in floristry. There is perpetual increasing demand of tropical palm foliage in Europe and thus the import from third countries [2]. Generally, the import should comply with existing phytosanitary requirements aiming at preventing the introduction and spread of harmful organisms in the EU through plant import (Regulation EU 2016/2031. If the introduction of the entire palm plants is regulated, the trade of palm foliage is going on freely. Furthermore, it has not yet been investigated which fungi are associated and which phytosanitary risk may be related to this foliage.
Tropical plants are recognized to support the highest-level diversity of endophytes and latent pathogenic fungi [3]. Numerous studies disclosed that different fungal assemblages are particularly associated with palms [4][5][6]. Hereupon, it can be ascertained that imported palms bring along considerable fungal diversity. Extensive studies on some tropical palms [4,7] found out that fungal communities potentially differ from that on temperate palms [8,9]. In this respect, tropical palms likely represent the pathway of numerous tropical fungal species exotic to Europe. Common pathogenic fungi associated to palm diseases mostly belong to the families Pestalotiopsidaceae and Glomerellaceae and have an immense

Phylogenetic Analysis and Species Identification
Fifty-eight Botryosphaeriaceae isolates obtained from palm foliage were grouped into seventeen morphospecies. The TEF-1α sequences of the representatives of morphospecies formed seven OTUs, out of which one identified as Endomelanconiopsis and six belonged to Lasiodiplodia. To identify OTUs at the species level, a concatenated ITS and TEF-1α dataset was analysed for Endomelanconiopsis. The alignment comprised 24 entries and Phyllosticta parthenocissi (CBS 111645) was added and used as an outgroup. From the 1043 characters, including gaps, 36 (3.5%) were parsimony informative. An MP analysis found 10,000 equally parsimonious trees of 248 steps with CI = 0.984, RI = 0949, RC = 0.933 and HI = 0.016). The Bayesian, ML and MP trees had identical topologies. Three highly supported clades were delimited corresponding to the currently known Endomelanconiopsis species and all isolates from palm foliage were grouped to E. endophytica (Figure 1). For the species identification of Lasiodiplodia, combined datasets of four loci, ITS, TEF-1α, TUB2 and RPB2, consisted of 83 Lasiodiplodia isolates. Diplodia seriata (CBS 112555) and D. mutila (CBS 112553) were included and used as outgroup taxa. The alignment contained 1687 characters including gaps, out of which 400 (23.7%) were parsimony informative. An MP analysis resulted in 11,921 equally parsimonious trees of 1170 steps with CI = 0.576, RI = 0.850, RC = 0.490 and HI = 0.424. The best-fit model TrN+I+G was selected for the combined data and used in the Bayesian analysis. The Bayesian and ML trees had identical topologies, the same as that of the 50% majority rule consensus of the MP trees. The RAxML tree is shown in Figure 2. RAxML trees resulting from the analysis of individual loci are shown in Figures S1-S4. The multigene tree was consistent with the recently revised global phylogeny of Lasiodiplodia [37]. The nine representatives of Lasiodiplodia isolates from palm foliage grouped in four subclades were well supported by all analyses. Two isolates were resolved in a clade including the ex-type of L. euphorbicola (CMM3652), two isolates clustered with L. brasiliensis (ex-type CMM 4015) and two isolates grouped with Lasiodiplodia sp. LACAM1 forming a clade closely related to L. parva. The remaining three isolates formed a distinct lineage sister to the ex-type of L. pontae (CMM1277). This lineage and the clade of Lasiodiplodia sp. LACAM1 are proposed to represent new species. Phylogenetic trees from individual loci greatly varied in topology. Excepting some basal nodes that were strictly resolved and constant among trees, the upper nodes differed among loci. The TEF-1α phylogeny had a better resolution, displaying roughly the same groupings as resolved with the four loci phylogeny. The two new Lasiodiplodia lineages were both resolved, albeit the isolate LACAM1 did not clearly group to the second lineage. The ITS and RPB2 phylogenies (Figures S1 and S4) further supported these lineages as representing new Lasiodiplodia species. Additionally, the support for new species was provided by base-pairs sequence comparison with the ex-type of the closely related species.  Colour shading indicate well-delimited phylogenetic species. The tree is rooted to Diplodia mutila (CMW7060) and Diplodia seriata (CBS 112555). Isolates from palm foliage are in bold characters and ex-type isolates are marked with T .

Pathogenicity of Botryosphaeriaceae Species on Apple and Pear
Pathogenicity tests were primarily conducted on fruits, but there is a prospect to carry on later further inoculation trials using seedlings. All isolates of the six Botryosphaeriaceae species tested on apple (Malus domestica) and pear (P. communis) fruits produced round necrotic lesions that progressed inside as rots. Sites on the fruit inoculated with sterile PDA as controls had restricted halos attributed to wound reactions. The pathogenicity was evaluated based on the size of the lesions developed from the inoculation point compared to the control. Confirmation was obtained with the fulfilment of Koch's postulates by the successful re-isolation of the inoculated isolates. Isolates of same species produced different lesion lengths with a very wide difference among isolates of L. mexicanensis on apple. The severity of the isolates varied within fruit type ( Figure 3). The highest aggressiveness recorded on apple was caused by L. euphorbicola followed by L. mexicanensis, which produced the largest necrotic lesions (mean up to 70 mm after 8 d). Moderate aggressiveness on apple was observed with L. brasiliensis and E. endophytica. On pear, the most aggressive species was L. mexicanensis followed by L. lodoiceae and L. brasiliensis. Moderate aggressiveness on pear was caused by E. endophytica. The lowest aggressiveness was caused by L. lodoiceae on apple and L. euphorbicola on pear. During infection on apple, mycelium of all species was mostly embedded in the necrotic area. Contrarily, three species L. brasiliensis, L. mexicanensis and L. lodoiceae externally produced a mycelial mass on pear.
Cultural characteristics: colonies on PDA at 25 • C ( Figure 4A1) early white, uniformly producing flattened dense mycelial mat, later greyish to brownish at the margin and grey greenish to dark grey in the centre, entire edge, margin flat, cottony, and centre slightly to strongly fluffy, grey to grey greenish. Growth reaching a maximal of 29.7 mm day −1 . Colonies at 35 • C early sparse, flat, grey to dark grey, becoming grey-green at the centre, edge rough to irregular. Growth slower with maximum 22.3 mm day −1 .
Material examined. Mexico, on leaves lesion of Lodoicea maldivica (Arecaceae), isolated 11 July 2017, Douanla-Meli (AGMy0002 Holotype, dried on pine needles; ex-type culture: DSM 112340. Additional material: Mexico, on leaves lesion of Lodoicea maldivica, isolated 20 July 2017, Douanla-Meli DSM 112341, AGQMy0005).  Notes: The four loci phylogeny resolved L. lodoiceae as a sister taxon of L. pontae. Both species can be, however, morphologically distinguished based on conidia characteristics. Conidia of L. lodoiceae showed septation at the immature stage and are at maturity smaller compared to the longer and larger conidia (16.4-26.4 × 9.6-15 µm) of L. pontae. Furthermore, the bi-gutulate character can distinguish the conidia of L. lodoiceae from those of L. pontae. The conidiogenous shape and size of L. lodoiceae differ from those of L. pontae. In addition, the production of reddish pigment at 35 • C characterizing L. pontae was not observed with L. lodoiceae. In base-pairs sequence comparison and nucleotide similarity (NS) between the ex-type culture of L. pontae (CMM1277) and the ex-type culture of L. lodoiceae (DSM 112340) based on alignable lenght, L. lodoiceae differs on ITS with one base pair (472/473; 99.8% NS) from L. pontae and both formed in ML tree ( Figure S1), a group also including L. gravistriata, L. subglobosa and L. macroscopora. On TEF-1α, L. lodoiceae differs with 11 base pairs (265/276; 96% NS) and the ML analysis ( Figure S2) placed it as a distinct lineage closely related to L. pontae. On TUB2, it differs from L. pontae with five base pairs and one indel (400/405; 98.8% NS) and the ML tree ( Figure S3) placed both species as closely related. The RPB2 sequence of L. pontae (CMM1277) was not available and the ML tree ( Figure S4) placed L. lodoiceae as a distinct lineage with sister L. plurivora.
Lasiodiplodia mexicanensis C. Douanla-Meli, sp. nov. Figure 4B, MB 841285. Etymology: the epithet refers to the country, Mexico, from where material of the host plant is originated.
Sexual form: not observed. Asexual form: no mature conidiomata developed on pine needle on PDA, MEA, Water Agar and SNA, even after six months under 12 h photoperiod and at various temperatures. The few conidiomatal primordia formed ( Figure 4B3) did not further develop and mature. Meanwhile, under the 12 h photoperiod, thickened dark and frequently divided rhyzomorphic mycelium abundantly developed on agar and also invaded the pine needle ( Figure 4B4,5). These mycelial cords were very brittle and composed of aggregated brown to dark brown hyphae. Individual hyphae were dichotomously branched, regularly septate, 4-9 µm diameter on the long trunk, with branches arising at acute angles and continuing as slender stalks of 2-3 µm diameter ( Figure 4B6,7).
Cultural characteristics: colonies on PDA at 25 • C early white, producing uniformly flattened dense mycelial mat, later becoming greyish to brownish at the margin and grey greenish to dark grey in the centre, entire edge, margin flat and cottony and centre slightly to strongly fluffy, brownish to reddish pigment diffusing in agar ( Figure 4A1). Growth faster, reaching 8 mm after 24 h, maximal growth rate of 30.4 mm day −1 . Colonies at 35 • C early sparse, flat, grey to dark grey, becoming grey reddish to red after three days as the heavy production of pigment starts, characteristically zonate, edge rough to irregular. Pigment red to dark red, diffusing in agar and colouring the mycelium ( Figure 4B2). Growth slower with maximum 23.5 mm day −1 .
Notes: Four loci phylogenetic analyses grouped isolates of L. mexicanensis with the isolate LACAM1 on a well-supported clade (100% BPP, 88% MLB and 71% MPB). Closely related species to L. mexicanensis were L. parva, L. citricola and L. euphorbicola, respectively. In cultural characteristics, L. mexicanensis differs from all above related species by the production of reddish brown to red pigment and even at both 25 and 35 • C. In addition, the development in culture of rhizomorph-like structures characterizes L. mexicanensis. The conidial characters of isolates from C. seifrizii were not observed as they did not form mature conidiomata in culture. However, the description of the asexual form of the isolate LACAM1 is available in [25]. Phylogenetically, the relationship between L. mexicanensis and L. parva was poorly supported. L. citricola was resolved basal to the clade of L. mexicanensis and L. parva and L. euphorbicola was distantly resolved sister to the clade of L. mexicanensis, L. parva and L. citricola. In base-pairs sequence comparison and nucleotide similarity between the ex-type culture of L. parva (CBS 456.78) and ex-type culture of L. mexicanensis (DSM 112342), there were five base differences on ITS (525/530; 99.4% NS) and the ML analysis ( Figure S1) placed it as a distinct lineage with 92% support ( Figure S1). On TEF-1α, L. mexicanensis differs with three base pairs (301/304; 99% NS) from P. parva and in the ML tree ( Figure S2) L. mexicanensis grouped to P. parva in an unresolved clade. On TUB2 and RPB2, L. mexicanensis is identical to L. parva. The ML trees (Figures S3 and S4)

Discussion
Despite the fact that sampling was restricted to Mexico, this study is the first targeting on Botryosphaeriaceae fungi from various palms species and their pathogenic potential. Mexico, as an important hotspot of tropical palm species [38,39], was the unique supplier of palm foliage to German market during the sampling period. The foliage of four out of the five palms species hosted a diversity of five Botryosphaeriaceae species. Accurate species identification using multilocus sequence analysis and including RPB2 region [40] endorsed two novelties among the four delimited Lasiodiplodia species. The two novelties are warranted and clearly circumscribed in the current Lasiodiplodia phylogeny [37].
The genus Lasiodiplodia, similarly to the whole family of Botryosphaeriaceae, is characterised by a higher level of cryptic species [37,41,42] and species boundary delimitation of cryptic taxa is difficult to resolve [37]. The first new species described in this study, L. lodoiceae isolated from Lodoicea maldivica, was resolved as sibling to L. pontae. This species was described associated with a necrotic canker on Anacardium occidentale and Spondias purpurea in Brazil and phylogenetically placed with sister species L. crassispora [28]. However, there has been no further record of L. pontae until a very recent study showed its strong phylogenetic affinity with the Venezuelan isolate CBS 117454 from Eucalyptus urophylla [37]. L. pontae also has always formed a monospecific clade [32,37,42]. In our four loci analysis, L. plurivora was a sister species to the clade of L. pontae and L. lodoiceae. Isolates of L. lodoiceae, even though clustering to L. pontae, formed a clade highly supported by posterior probability (99%) in the analysis of combined four loci. As noted with other phylogenies of Lasiodiplodia, Bayesian analysis provided better clade support than maximum parsimony and likelihood [28,37,42]. Low bootstrap support of Lasiodiplodia clades has been partly ascribed to missing data [40], as many Lasiodiplodia species lack sequences of TUB2 and mostly RPB2 loci.
The second new species, L. mexicanensis, isolated from C. seifrizii grouped with the Peruvian isolate LACAM1, which was recovered from necrotized branch of Mango indica and determined as hybrid of L. citricola and L. parva [25]. Our combined analysis resolved L. parva and L. mexicanensis as distinct species forming a clade and L. citricola was a sister species to this clade. This result therefore put in question the hybrid character of the isolate LACAM1 that was backed by the shared polymorphism with both L. citricola and L. parva, solely based on ITS and TEF-1α [25]. The first previous study suggesting hybridisation in Lasiodiplodia proposed four hybrid species, L. laeliocattleyae, L. brasiliense, L. missouriana and L. viticola based on the analysis of five genes ITS, TEF-1α, TUB2, RPB2 and cmdA [40]. Nevertheless, if L. missouriana has been synonymized to one of its purported parents, L. gilanensis [37], the other three hybrid species are further on consistently resolved as distinct species [25,37,42]. Higher genetic similarity characterizing Lasiodiplodia species may affect many genes [37,39], thus distinct and distant species as resolved in multilocus analysis, may be essentially different by few nucleotides on a single gene [37]. This seems to be the case for L. mexicanensis differing from closely related species L. parva, L. citricola and L. euphorbicola by few nucleotides on ITS, TEF-1α, TUB2 and RPB2 genes. However, the two genes, ITS and TEF-1α are well-suited for the distinction between L. mexicanensis and L. parva. Isolate LACAM1 was not available to generate the RPB2, but its grouping to L. mexicanensis was equally supported in the three loci (ITS, TEF-1α, TUB2) tree (not shown). Isolates from C. seifrizii did not form any morph to be used for accurate morphological comparison. It is not common, but some Lasiodiplodia isolates may not sporulate under culture conditions [26]. Despite this lack of morphological traits, multiple loci analysis confidently pleaded that these isolates belong together with LACAM1 to a distinct phylogenetic species.
Botryosphaeriaceae isolates were mostly (approx. 80%) obtained from necrotic lesions close to blight disease. Except for L. mexicanensis recovered from asymptomatic leaves, all other species were isolated from lesions, but from which were also isolated further fungi such as Colletotrichum, Pestalotiopsis, Fusarium, Alternaria usually causing blight disease [10][11][12]43]. Determining fungi causing these blight symptoms was not part of the focus of this study. However, at least L. brasiliensis, isolated in this study, is implicated in leaf blight disease in palms. It causes, together with other Lasiodiplodia species, the blight disease of Cocos nucifera [44,45] and is also involved in the postharvest stem-end rot, considerably damaging fruits of this host [17,44,45]. Furthermore, L. brasiliensis first described associated with papaya stem-end rot in Brazil [22] is now plurivorous and geographically widespread, causing cankers, dieback and blights on diverse woody and crop plants [18,23,25,[46][47][48]. L. euphorbicola hitherto not reported on palm is equally plurivorous, widespread in Brazil causing dieback, collar and root rot, gummosis, cladode brown spot on crop plants [20,21,23,24,49]. Its geographical distribution includes West Africa and further countries such as Botswana, Madagascar, Namibia and Zimbabwe where it affects Adansonia digitata [39]. Surprisingly, despite the host diversity examined, the most common L. theobromae colonising plants, including many Arecaceae, in the warm regions [19,50] was not recovered. Instead, the predominantly endophytic E. endophytica was the most frequent species. It has shown weak aggressiveness on young Terminalia mantaly and T. catappa [51].
In light of this knowledge on the recorded Botryosphaeriaceae species as plant pathogens, trials were conducted and suggested a potential risk on apple and pear, two important temperate pome fruit species. All six Botryosphaeriaceae fungi were able to cause rot damage on both fruits under the experimental conditions. Hence, it can be expected that, if all these species are able to successfully establish in Europe, they may be regarded as a potential threat at least inducing fruit rot disease on apple and pear. The geographical range of L. theobromae, the northernmost distributed fruit-rotting Lasiodiplodia already includes Europe [52][53][54]. It is the most common Lasiodiplodia species associated with preand postharvest fruit diseases, with the most common being the stem-end rot [55,56]. L. theobromae belongs to the Botryosphaeriaceae fungi complex causing the severe fruit rot of grapevines with great adaptation to Northern Hemisphere [54]. Therefore, there is a likelihood that Botryosphaeriaceae fungi associated with palm foliage can also establish and spread in Europe. Furthermore, increasing temperature as an immediate consequence of the ongoing climate change may be a critical factor in determining the successful settling [57][58][59].
This study unveiled the potential of tropical palm foliage as source of crop plant pathogenic Botryosphaeriaceae fungi and as pathways facilitating their movement. These Botryosphaeriaceae fungi represent a tiny part of the fungal community in palm foliage. Combined culture method and analysis of metagenomic data also recovered fungi of the families Pestalotiopsidaceae, Glomerellaceae, Nectriaceae comprising notorious plant pathogens with many species exotic to Europe (data not published). It is to be noted that the movement of plant material, even in compliance with strict requirements, can always create undesirable effects. Indeed, it is not possible within the scope of border control to carry out inclusive investigation for all harmful organisms (fungi, bacteria, viruses and insects). Further undertakings on the overall biological community of palm foliage are required and will enable researchers to comprehensively size up the phytosanitary risks.

Sampling and Fungal Isolation
Palm foliage sampling was conducted between June 2017 and February 2018 and consisted of taking thee bunches of foliage from each of the 12 consignments, for a total of 36 foliage bunches, all originating from Mexico. Samples often presented diverse disease symptoms and included five palm species: Chamaedorea elegans, C. metallica, C. seifrizii, Dypsis lutescens and Lodoicea maldivica. Sampled tissues were surface sterilized in 70% ethanol for 1 min, in 1.5% sodium hypochlorite for 5 min, in 70% ethanol for 30 s and finally rinsed twice (5 min each) in sterile distilled water. In total 648 pieces of approximately 5 mm were cut from both asymptomatic and symptomatic (when present) tissues and placed (5 pieces) on each MEA plate amended with 1% tetracycline. Plates were incubated at 25 • C with a 12 h photoperiod for 4 days. Growing colonies were transferred onto new MEA plate. Isolates with cottony and grey, greyish-green to black tones resembling those of Botryosphaeriaceae fungi were subcultured on 2% water agar (WA) or SNA medium amended with sterilized pine needles and incubated (4-5 weeks) at 25 • C under near-ultraviolet light with 12 h photoperiod. From sporulating colonies, single-spore cultures were obtained on potato dextrose agar (PDA) according to [60]. Nonsporulating isolates underwent ITS sequencing for confirming the assignment to Botryosphaeriaceae. Representative isolates of all species were deposited in the culture collection of the Federal Research Centre for Cultivated Plants (JKI), Braunschweig, Germany, and the ex-type living cultures of the new species were additionally deposited at the Leibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig.

Morphocultural Characterization of Isolates
Isolates were further grouped into morphotypes based on growth rate and characters of conidia. Representative isolates of morphotypes were used for morphocultural characterization carried out on 9-cm-diameter PDA plates and incubated for 10 d at 25 • C and 35 • C with a 12 h photoperiod. Colony radius was measured daily from the 3rd to the 10th day in 2 perpendicular directions and was used to calculate the mycelial growth rate (mm d −1 ). Three replicates for each isolate were used and the assay was repeated twice. Conidiomata were formed between 2-4 wk. Photographs of cultures were made with a Canon EOS 60D. Microscopic characters were observed and measured in lactic acid using differential interference contrast (DIC) illumination on a Leica DM 5500 B microscope, and the images were captured using a Leica DFC 550 digital camera (400×) coupled to the microscope. Average measure of each microscopic structure was calculated from 50 measurements.

Phylogenetic Analyses
The ITS and TEF-1α genes of representative isolates of morphotypes were initially sequenced. TEF-1α sequences were assembled into contigs with 98% similarity using Sequencher 5.0. and representative OTUs used for BLAST searches in NCBI GenBank (accessed 15.04.2021). TEF-1α dataset including sequences of ex-type isolates were analysed to reveal primary placement of isolates within Botryosphaeriaceae genera. Based on these results, TUB2 and RPB2 sequences were then generated for morphotype representatives for multilocus analysis. Genes were concatenated for constructing two multigene phylogenies using ITS and TEF-1α genes for Endomelanconiopsis and ITS, TEF-1α, TUB2, RPB2 genes for Lasiodiplodia. Sequences were aligned in MAFFT v. 7 online version [66] and manually optimized with MEGA v. 7. Phylogenetic trees were constructed using the maximum parsimony (MP), maximum likelihood (ML) and Bayesian inference (BI) methods. MP analysis conducted in PAUP v. 4.0b10 [67] used heuristic searches with Tree Bisection-Reconnection (TBR), MAXTREES set to autoincrease, saving 10 trees per replicate and clade stability assessed with 1000 bootstrap replicates. ML analyses were performed using RAxML-HPC Blackbox version 8.2.10 [68] as implemented on the CIPRES Science Gateway [69] with estimate proportion of invariable sites GTRGAMMA+I and branch support evaluated by 1000 bootstrap replicates. Bayesian inference was carried out in MrBayes v. 3.2 [70]. The best substitution model for tree reconstruction was estimated by both the Akaike information criterion and the Bayesian information criterion in jModelTest 2.0 [71]. Four Markov Chain Monte Carlo chains were run simultaneously starting from random trees for 5,000,000 generations and sampling every 100th generation. After discarding the first 25% of trees as burn-in phase, a consensus Bayesian tree and Bayesian posterior probabilities (BPP) were determined based on all remaining trees. A BPP above 0.90 was considered as significant value. The individual phylogenies were constructed using ML analyses as described above. Number of sequences aligned varied among genes due to many missing data in TUB2 and mostly RPB2. Trees were visualized and further edited in TreeGraph 2 [72]. New sequences generated in this study were deposited in GenBank (www.ncbi.nlm.nih.gov) and accession numbers are shown in Table S1 together with those retrieved from GenBank. Resulting alignments and trees have been deposited in TreeBASE (https://www.treebase.org/treebase, Submission: 28655).

Pathogenicity Test
Botryosphaeriaceae species are associated worldwide with postharvest disease and mostly fruit stem-end rot. Therefore, pathogenicity trials were conducted on fruits of Malus domestica (apple) and Pyrus communis (European pear). Both are two important pome fruits already affected by different rots and postharvest disorders during storage [73]. We selected pear variety "Comtesse de Paris" and apple variety "Goldparmäne" and fruits without visible signs of disease and fungicide treatment. Two isolates of each identified Botryosphaeriaceae fungi were used to inoculate the fruits. Fruits were first washed and surface sterilized with 1.2% sodium hypochlorite for 5 min, rinsed twice with sterile distilled water and left dry on paper filter prior to inoculation. Fruits were wounded to a 3-mm depth at two sites towards both ends. On the upper wound was placed a 3-mm diameter PDA agar plug containing 5-days-old mycelium of the isolate to be tested. Similarly, on the below wound was placed a sterile non-colonised 3-mm PDA agar plug as control. Inoculated fruits were placed each on one 90 × 14.5 mm petridish round and arranged in plastic trays equipped with lid and the bottom covered with layers of moistened sterile kitchen roll. Incubation was carried out in a thermostatically controlled incubator at 25 • C with a 12 h photoperiod. Plastic trays were first kept closed for 2 days and subsequently open for further 6 days.
After the third day of incubation, length of lesion appearing on each fruit was measured daily in two perpendicular directions until the eighth day and data used for calculating the lesion size (mm) and growth rate (mm day −1 ). The experiment was conducted in randomized design with two fruits per replicate, and there were three replicates per isolate. At the end of each replicate, Koch's postulate was verified by fungal re-isolation from necrotic tissue from each lesion. Mean values of lesions were analysed using One-way analysis of variance (ANOVA) followed by t-Test at a = 0.05 in Microsoft Excel 2010.  Table S1: Culture accession numbers, location, host and GenBank accession numbers of Botryosphaeriaceae isolates included in this study.   (Table S1). Datasets and phylogenetic trees are available in TreeBase (Submission: 28655).