New Records of Canker-Causing Pathogens of Acacia spp. and Pithecellobium dulce in Southern Italy
by
, , , and
Giuseppa Rosaria Leonardi
1
,
Laura Vecchio
1,
Giorgio Gusella
1,*,
Dalia Aiello
1,
Hermann Voglmayr
2 and
Giancarlo Polizzi
1 1
Dipartimento di Agricoltura, Alimentazione e Ambiente (Di3A), Università degli Studi di Catania, Via S. Sofia 100, 95123 Catania, Italy
2
Department of Botany and Biodiversity Research, University of Vienna, Rennweg 14, 1030 Vienna, Austria
*
Author to whom correspondence should be addressed.
J. Fungi 2025, 11(12), 874; https://doi.org/10.3390/jof11120874 (registering DOI)
Submission received: 19 November 2025
/
Revised: 5 December 2025
/
Accepted: 8 December 2025
/
Published: 10 December 2025
(This article belongs to the Section Fungal Pathogenesis and Disease Control)
Abstract
Surveys conducted in a nursery located in eastern Sicily, southern Italy, revealed the presence of plants of Vachellia nilotica (syn. Acacia arabica), V. farnesiana (syn. A. farnesiana) and Pithecellobium dulce showing symptoms of trunk and branch canker, shoot dieback and general decline. Laboratory fungal isolation from wood tissues showed high percentage of Diaporthe-like (60–62%) and Botryosphaeriaceae-like fungi (21–85%) constantly associated with the diseased samples. Subsequent molecular characterization of recovered isolates was based on sequencing of the complete internally transcribed spacer region (ITS), the translation elongation factor 1-alpha (tef1) and the beta-tubulin (tub2) regions, followed by multi-locus phylogenetic analyses. The isolates collected from symptomatic tissues were phylogenetically characterized as Diaporthe foeniculina and Neofusicoccum parvum. Pathogenicity tests were conducted on Acacia and P. dulce plants and results showed that both species were pathogenic, being able to induce necrotic lesions on the stem. To our knowledge this is the first report worldwide of D. foeniculina and N. parvum infecting A. arabica, A. farnesiana and P. dulce.
1. Introduction
Fabaceae (or Leguminosae) [1] is an economically and ecologically important plant family including close to 770 genera and over 19,500 species [2]. This family includes Acacia species, some of them re-ordered nowadays within the genus Vachellia—woody perennial trees native to Australia, with some of them naturalized and invasive [3]—and Pithecellobium dulce, an evergreen plant native to Mexico known for its nutritional and medicinal properties [4]. In Italy, Acacia and P. dulce are cultivated and widely distributed, especially in the southern regions, for ornamental purposes. No relevant diseases have been reported for P. dulce; in fact, only few fungal associations have been listed, most of which with no symptoms recorded [5]. Regarding Acacia species, many fungal diseases have been reported worldwide, especially in tropical regions [6]. Since nurseries represent a key location in the production of plants, particular attention needs to be given to all strategies for preventing diseases occurring during this phase. In fact, diseases occurring in the nursery, especially those caused by canker-causing pathogens, are not always immediately detectable. Symptomatology can remain hidden throughout the latency of canker pathogens, and diseases may only be fully expressed after transplanting in the field [7].
Major fungal diseases of Acacia spp. occurring in the nursery include foliar diseases such as Pestalotiopsis leaf spot, Phaeotrichoconis leaf spot, phyllode rust disease (Atelocauda digitata) and anthracnose (Colletotrichum sp.), as well as stem and root diseases including seedling dumping-off caused by species belonging to Pythium, Rhizoctonia and Fusarium and various agents of canker and dieback [8].
Moreover, extensive literature is focused on the canker and wilt pathogen Ceratocystis, considered an emerging and important threat for Acacia plantations around the world [9,10,11,12,13]. As previously mentioned, in Italy, Acacia species are cultivated for ornamental purposes, which is the reason why the ornamental nurseries represent a crucial point for the detection of diseases that could compromise the propagation processes as well as the longevity of the plants in urban landscapes. In Italy, phytopathological investigations have not been particularly extensive. In this regard, the first disease detected in Italy was in 2001 on A. retinoides, when symptomatic plants showed leaf spot and stem canker, caused by Calonectria pauciramosa (reported as Cylindrocladium pauciramosum) [14]. In 2022, new symptoms of necrotic sunken lesions and wood discoloration were observed at the stem level in both the rootstock and the scion, as well as at the graft union of young plants of A. dealbata grafted on A. retinodes in a nursery in eastern Sicily. Pathogenicity test revealed Lasiodiplodia citricola as the causal agent of the disease [15].
The Botryosphaeriaceae and Diaporthaceae families include important canker pathogens of numerous agricultural, forestry and ornamental crops [16,17]. Symptomatology includes twig and shoot dieback, stem and trunk cankers, bark cracking, gummosis, and tree decline. These pathogens are often defined as opportunistic, able to survive as endophytes within the host tissues until the onset of stress conditions [16,17].
Recently, new surveys conducted in a nursery of eastern Sicily revealed the presence of plants of Acacia arabica (nowadays as Vachellia nilotica), A. farnesiana (V. farnesiana) and P. dulce showing symptoms of twig and shoot canker and dieback. For this reason, the aim of our study was to investigate the etiology of the disease by (i) characterizing the fungal isolates recovered from diseased wood samples based on phylogenetic analyses and (ii) testing their pathogenicity.
2. Materials and Methods
2.1. Surveys and Fungal Isolation
Surveys were carried out in a nursery located in the eastern area of Sicily during 2022. Symptomatic woody samples were collected from ten Acacia plants (five A. arabica plants and five A. farnesiana plants) and five P. dulce plants consisting of necrotized shoot, branch and trunk tissues. After collecting, samples were brought to the laboratory of the Department of Agriculture, Food and Environment, University of Catania, for further analyses. Fungal isolation was conducted as follows: small sections (0.2 to 0.3 cm2) of symptomatic woody tissues were surface-sterilized for 1 min in 1.5% sodium hypochlorite, rinsed in sterile deionized water, dried on sterile absorbent paper under a laminar hood, placed on potato dextrose agar (PDA, Lickson, Vicari, Italy) amended with 100 mg L−1 of streptomycin sulfate (Sigma-Aldrich, St. Louis, MO, USA) (PDA-S) to prevent bacterial growth, and then incubated at 25 °C for 3–5 days until fungal colonies were large enough to be examined. The isolation frequency (IF) of the main fungal categories was calculated according to the formula IF = (Nfs/Nst) × 100, where Nfs is the number of samples from which the specific fungal category was isolated and Nst is the total number of samples on which fungal isolation was conducted. Subsequently, fungi were grouped according to the general genus-family morphology of the colony (shape, color, texture) and representative colonies of interest were transferred to PDA-S plates. Single-hyphal tip cultures were obtained from pure cultures and maintained on PDA-S at 25 °C. From this preliminary grouping, representative isolates were chosen for molecular characterization.
2.2. DNA Extraction, PCR Amplification and Sequencing
Fungal isolates were grown on PDA for seven days for the genomic DNA extraction. Mycelium was collected and processed using the Wizard Genomic DNA Purification Kit® (Promega Corporation, Madison, WI, USA) according to the manufacturer’s protocol. Extracted DNA was stored at 4 °C until use. The following gene regions were selected for amplification and sequencing: the complete internally transcribed spacer region (ITS1-5.8S-ITS2) rDNA gene region with primers ITS5 and ITS4 [18], the translation elongation factor 1-alpha (tef1) with primers EF1-728F and EF1-986R [19] and EF1-688F and EF1-1251R [20], and the beta-tubulin (tub2) region with primers Bt-2a and Bt-2b [21]. PCR conditions were set as follows: 30 s at 94 °C; 35 cycles each of 30 s at 94 °C; 1 min at 52 °C (ITS) or 55 °C (tef1 and tub2); 1 min at 68 °C; and a final cycle for 5 min at 68 °C. PCR products were visualized on 1% agarose gels (90 V for 40 min) stained with GelRed® Nucleic Acid GelStain (Biotium) to confirm the presence and size of PCR products. PCR amplicons were purified and sequenced in both direction by Macrogen Inc. (Seoul, Republic of Korea). The sequencing products were edited with Lasergene SeqMan Pro (DNASTAR, Madison, WI, USA) and deposited in GenBank (https://www.ncbi.nlm.nih.gov/). Isolates characterized in this study are listed in Table 1.
2.3. Phylogenetic Analysis
The sequences obtained in this study were compared with the NCBI GenBank nucleotide database using the standard nucleotide Basic Local Alignment Search Tool (BLAST) (https://blast.ncbi.nlm.nih.gov/Blast.cgi (accessed on 7 May 2024)). The newly generated sequences of each genomic region were aligned to reference sequences retrieved from recent and comprehensive phylogenetic studies for isolates in the genera Diaporthe [22] and Neofusicoccum [23] and downloaded from GenBank (Table 2). Sequence alignments for phylogenetic analyses were produced with the server version of MAFFT (https://mafft.cbrc.jp/alignment/server/ (accessed on 10 June 2025)) and checked and refined using BioEdit Sequence alignment Editor 7.7.1.0 [24]. Isolates in both genera were used for phylogenetic analyses within a combined matrix of ITS rDNA, tef1 and tub2 sequences. The loci were concatenated to a combined matrix using Phyutility v. 2.2 [25] (Smith and Dunn 2008). Sequences of Botryosphaeria dothidea and B. fabicerciana served as outgroup taxa in phylogenetic analyses of the family Botryosphaeriaceae, and Diaporthella corylina served as the outgroup taxon in phylogenetic analyses of the family Diaporthaceae. Maximum likelihood (ML) analyses were performed with RAxML [26], as implemented in raxmlGUI 2.0 [27], using the ML + rapid bootstrap setting and the GTRGAMMA+I substitution model which was selected as the most appropriate model by Modeltest. The matrix was partitioned for the different gene regions, and bootstrap analyses were performed with 1000 bootstrap replicates. For evaluation and interpretation of bootstrap support, values between 70% and 90% were considered moderate, above 90% as high, and 100% as the maximum. Maximum parsimony (MP) bootstrap analyses were performed with Phylogenetic Analyses Using Parsimony (PAUP) v. 4.0a169 [28]. A total of 1000 bootstrap replicates were implemented using five rounds of heuristic search with random sequence addition, followed by tree-bisection-reconnection (TBR) branch swapping. The MULTREES option was enabled, the steepest descent option was disabled, the COLLAPSE command was set to MINBRLEN, and each replicate was limited to 1 million rearrangements. All molecular characters were treated as unordered and assigned equal weight, with gaps considered as missing data. The COLLAPSE command was set to MINBRLEN.
2.4. Pathogenicity Test
Two species of Acacia, including A. arabica and A. farnesiana, and the species P. dulce were selected to conduct pathogenicity tests in order to fulfill Koch’s postulates. Regarding A. arabica and A. farnesiana, a total of six plants for each plant species were inoculated with the fungal isolates. Specifically, three plants were inoculated with D. foeniculina isolate ACA 91, and three plants with N. parvum isolate ACA 82. Likewise, three plants of P. dulce were inoculated with D. foeniculina isolate ACA 113 and three with N. parvum ACA 105. Three plants served as controls. Stem wounds were made with a sterilized 5 mm diameter cork borer to remove the bark, and a 5 mm diameter mycelium plug from a seven-day-old culture of the selected isolates was placed upside down into the wound. Wounds were then sealed with Parafilm® to prevent desiccation. Controls were inoculated with sterile PDA plugs. Plants were regularly watered. Total lesion lengths were measured 60 days after inoculation. Re-isolations were conducted as described above and identification was based on morphological characteristics (color, texture, growth rate and eventually spore features) of the colonies.
3. Results
3.1. Surveys and Fungal Isolation
Disease incidence observed in the nursery was about 9% based on a total of 2000 cultivated plants. Specifically, about 6% was observed for Acacia plants and 3% for P. dulce plants. The symptomatology on Acacia spp. and P. dulce consisted of typical apical shoot dieback and general decline of the plants (Figure 1A–D), as well as necrotic patches and external and internal necrotic lesions along the trunks and shoots and at the insertion of the main branches. The isolation frequency from Acacia plants consisted of 62% of Diaporthe-like colonies from dieback symptoms and 21% of Botryosphaeriaceae-like colonies from necrotic lesions on trunks and branches. For P. dulce plants, the isolation frequency showed 85% of Botryosphaeriaceae-like colonies from necrotic lesions on trunks and branches and 60% of Diaporthe-like from twig dieback. From fungal isolation, a total of 46 isolates (32 Diaporthe-like and 14 Neofusicoccum-like) were collected and stored in the fungal collection of the Department of Agriculture, Food and Environment, Laboratory of Plant Pathology. The isolates collected belonging to each genus (Diaporthe and Neofusicoccum) did not show any morphological differences. Thus, a total of 31 representative isolates (23 Diaporthe-like and 8 Neofusicoccum-like) were selected for further molecular analyses.
3.2. Phylogenetic Analysis
Since the Diaporthe isolates revealed identical sequences for the analyzed loci (ITS, tef1, tub2), except for some ITS polymorphisms, 14 representative isolates were selected for the phylogenetic analyses. The dataset used for the phylogenetic analyses of Diaporthe consisted of 48 taxa, including the isolates from Acacia spp. and P. dulce and the outgroup (D. corylina CBS 121124). The combined matrix of ITS-tef1-tub2 included 1610 characters (597 ITS, 428 tef1, 585 tub2), of which 871 were constant (399 ITS, 132 tef1, 340 tub2), 233 were variable but parsimony-uninformative (85 ITS, 62 tef1, 86 tub2) and 506 were parsimony informative (113 ITS, 134 tef1, 159 tub2). The ML tree (−lnL = 12,314.431617) obtained by RAxML is shown in Figure 2. The isolates ACA 91, ACA92, ACA 95, ACA97, ACA100-104, ACA 111-113, ACA 116 and ACA124 were collected from the symptomatic plants clustered with D. foeniculina with medium support (70% ML, 85% MP). However, two strongly supported lineages were distinguished within this clade, suggesting an intraspecific variability within D. foeniculina isolates.
The dataset of Neofusicoccum contained 40 taxa including the isolates from Acacia spp. and P. dulce and the outgroups (Botryosphaeria dothidea CBS 115476 and B. fabicerciana CBS 118831). The alignments included 1255 characters (534 ITS, 306 tef1, 415 tub2) of which 989 were constant (450 ITS, 196 tef1, 343 tub2), 84 were variable but parsimony-uninformative (29 ITS, 30 tef1, 25 tub2) and 182 parsimony informative (55 ITS, 80 tef1, 47 tub2). The ML tree (−lnL = 3893.049301) obtained by RAxML is shown in Figure 3. Maximum likelihood analyses resulted in a tree topology similar to that revealed by MP bootstrap analysis. Phylogenetic analyses did not show intraspecific variability among the ACA isolates, which were all resolved inside the N. parvum s. str. clade with moderate (73% ML, 71% MP) support. However, they were strongly supported (98% ML, 100% MP) within the N. parvum species complex, which includes N. hongkongense, N. occulatum, N. parvum, N. podocarpi, N. ribis and N. sinoeucalypti.
3.3. Pathogenicity Test
Results of pathogenicity test proved that both fungal species are pathogenic to Acacia plants as well as to P. dulce although with some slight differences (Figure 4). In particular, D. foeniculina isolate ACA 91 and N. parvum isolate ACA 82 induced lesions on A. arabica with an average length of 5.6 (standard deviation ± 2.4) cm and 5.1 (±2.2) cm, respectively. On A. farnesiana, D. foeniculina isolate ACA 91 induced lesions of an average of 7.5 (±4.7) cm, and N. parvum isolate ACA 82 of 5.7 (±4.1) cm. On P. dulce, D. foeniculina isolate ACA 113 and N. parvum isolate ACA 105 induced lesions of an average of 1.9 ± 1.0 cm and 1.9 ± 0.3 cm, respectively. Of note, gum production was observed from the inoculation point of A. farnesiana plants. Control plants did not produce any lesions, but a superficial discoloration that did not extend beyond the inoculation point was observed due to the oxidation of wounded tissue. Re-isolations from all inoculated plants confirmed the presence of the Diaporthe- and Neofusiccocum-like colonies, with cultural characteristics matching those of the inoculated isolates. No colonies resembling Diaporthe or Neofusicoccum were isolated from control plants.
4. Discussion
The results of this study revealed the presence of D. foeniculina and N. parvum, causing cankers and dieback, on A. arabica, A. farnesiana and P. dulce in a nursery located in Sicily, southern Italy. These plant species are cultivated in Italy mainly for ornamental purposes, and some Acacia spp. are also recognized as alien and invasive species. For example, A. saligna was introduced for reforestation purposes and for dune stabilization, but it quickly became an invasive species across the entire national territory [29]. The attention to Acacia is testified in Italy by reforestation programs conducted during the 1950s–1960s in southern Italy with the species A. melanoxylon for its appreciable wood and botanical characteristic in preventing the spread of wildfire [30].
Wood diseases are increasingly becoming the subject of investigation of plant pathologists around the world due to the increasing complexity of their etiology and their wide host range and challenging management [31]. In our study, N. parvum (Botryosphaeriaceae) was consistently isolated from symptomatic tissues of A. arabica and A. farnesiana. This species is widely distributed around the world and well known to be a highly aggressive canker-causing pathogen on many different crops, including ornamental trees [32,33]. Its wide distribution, probably a result of the repeated introductions of agricultural and ornamental plant material [34], and its ability to attack many different hosts, characteristic of several Botryosphaeriaceae [17], make the report of this pathogen significant for the growers. In Sicily, N. parvum has been repeatedly reported in recent decades, demonstrating its highly polyphagous behavior for ornamental [35,36,37,38] and agricultural crops [39,40,41]. This species, with identification based only on the ITS gene region, was reported in Sicily on A. melanoxylon causing canker and dieback in 2016 [30]. However, for a proper identification of Neofusicoccum species, a multi-gene phylogenetic analysis is necessary, especially in the case of N. parvum, which is part of a cryptic species complex [23].
Similarly, the presence of D. foeniculina on both Acacia species is not unusual. Diaporthaceae are recognized as another important group of fungi causing wood diseases on several fruit and nut crops [31], and many associations of Diaporthe species with Acacia have been recorded [42]. Although D. foeniculina is reported worldwide as a primary canker-causing pathogen [43,44], some studies considered it as a weak pathogen, less aggressive compared to other fungal species [41,45,46,47]. On the contrary, in our study, lesions on A. arabica and A. farnesiana caused by D. foeniculina are similar, in terms of length, to those produced by N. parvum. Thus, results of our study do not suggest a clear demarcation between the two identified species in disease development. Discrepancies regarding the observed aggressiveness of the same fungal species around the world may be quite normal and can be attributed to different factors such as differences in isolate virulence and host response.
Concerning P. dulce, this study provides the first report of cankers and dieback caused by D. foeniculina and N. parvum. Until now, only a few diseases have been reported on this host, of which none seemed to be relevant in terms of limitation to its cultivation [5]. The results of our investigation highlight the need to not underestimate the risks derived by the development of wood diseases, especially in nurseries. Canker-causing pathogens, in fact, are characterized by phases of latency during the infection cycle [17] that make it almost impossible to ascertain their presence within the host, unless molecular techniques such as qPCR [48] are used. Latent infections of canker-causing pathogens establishing without notice in the nursery represent the initial inoculum from which further epidemics could develop in new fields [7], especially when plants are subjected to different types of stress like injuries, heat and drought [17]. This epidemiological statement was also evidenced, for example, in the cases of apple canker caused by Nectria galligena, Botryosphaeriaceae diseases on almond and prune, and grapevine infected by several wood pathogens [7,49,50]. In this regard, especially in nurseries and greenhouses, it is crucial to maintain high standards of hygiene during all delicate processes of propagation. Routine sanitation does not guarantee the complete absence of inoculum in plants but could be very helpful in keeping the potential inoculum under control. Monitoring of pathogen populations in diversified environments, like nurseries, where many plant species co-inhabit is crucial to avoid dangerous host jumps and intensification of disease levels.
To our knowledge, this is the first report of D. foeniculina and N. parvum causing canker and dieback on Acacia species and P. dulce worldwide, and these species also should be monitored in other areas where their hosts are planted to evaluate their spread and impact.
Author Contributions
Conceptualization, G.P. and D.A.; methodology, G.R.L., H.V. and L.V.; software, H.V. and G.R.L.; formal analysis, G.R.L. and G.G.; investigation, G.P. and D.A.; resources, G.P.; data curation, G.R.L., H.V. and G.G.; writing—original draft preparation, G.G. and G.R.L.; writing—review and editing, G.P., D.A., G.R.L., G.G., H.V. and L.V.; funding acquisition, G.P. All authors have read and agreed to the published version of the manuscript.
Funding
This study was funded by Piano di incentivi per la ricerca di Ateneo DIME-SIECO 2024–2026 University of Catania (Italy) and by the University of Catania, a PhD grant to Giuseppa Rosaria Leonardi and mobility grants: Erasmus+ project “UNIVERSITIES FOR INNOVATION” (2022-1-IT02-KA131-HED-000055839) and “ERASMUS MOBILITY NETWORK” (2022-1-IT02-KA130-HED-000061416).
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
The original data presented in the study are openly available in GenBank (https://www.ncbi.nlm.nih.gov/genbank).
Conflicts of Interest
The authors declare no conflicts of interest.
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Figure 1.
Symptomatology of Acacia spp. and Pithecellobium dulce. (A), Acacia spp. plant decline. (B), apical shoot dieback on Acacia plant. (C), P. dulce dieback and canopy defoliation. (D), stem canker and necrosis on Acacia plant.
Figure 1.
Symptomatology of Acacia spp. and Pithecellobium dulce. (A), Acacia spp. plant decline. (B), apical shoot dieback on Acacia plant. (C), P. dulce dieback and canopy defoliation. (D), stem canker and necrosis on Acacia plant.
Figure 2.
Phylogram of the best ML tree (−lnL = 12,314.431617) revealed by RAxML from an analysis of the combined ITS-tef1-tub2 matrix of Diaporthe, showing the phylogenetic position of isolates from diseased Acacia arabica, A. farnesiana and Pithecellobium dulce plants (bold), with Diaporthella corylina (CBS 12114) selected as outgroup to root the tree. Maximum likelihood (ML) and maximum parsimony (MP) bootstrap support above 70% are given at first and second position, respectively, above or below the branches. T = ex-type.
Figure 2.
Phylogram of the best ML tree (−lnL = 12,314.431617) revealed by RAxML from an analysis of the combined ITS-tef1-tub2 matrix of Diaporthe, showing the phylogenetic position of isolates from diseased Acacia arabica, A. farnesiana and Pithecellobium dulce plants (bold), with Diaporthella corylina (CBS 12114) selected as outgroup to root the tree. Maximum likelihood (ML) and maximum parsimony (MP) bootstrap support above 70% are given at first and second position, respectively, above or below the branches. T = ex-type.
Figure 3.
Phylogram of the best ML tree (−lnL = 3893.049301) revealed by RAxML from an analysis of the combined ITS-tef1-tub2 matrix of Neofusicoccum, showing the phylogenetic position of isolates from diseased Acacia arabica, A. farnesiana and Pithecellobium dulce plants (bold), with Botryosphaeria dothidea (CBS 115476) and B. fabicerciana (CBS 118831) selected as outgroup to root the tree. Maximum likelihood (ML) and maximum parsimony (MP) bootstrap support above 70% are given at first and second position, respectively, above or below the branches. T = ex-type.
Figure 3.
Phylogram of the best ML tree (−lnL = 3893.049301) revealed by RAxML from an analysis of the combined ITS-tef1-tub2 matrix of Neofusicoccum, showing the phylogenetic position of isolates from diseased Acacia arabica, A. farnesiana and Pithecellobium dulce plants (bold), with Botryosphaeria dothidea (CBS 115476) and B. fabicerciana (CBS 118831) selected as outgroup to root the tree. Maximum likelihood (ML) and maximum parsimony (MP) bootstrap support above 70% are given at first and second position, respectively, above or below the branches. T = ex-type.
Figure 4.
Pathogenicity test. From left to right: non-inoculated control plant; external lesion caused by Diaporthe foeniculina isolate ACA 91 on Acacia arabica; gummosis starting from inoculation point of D. foeniculina isolate ACA 91 on Acacia farnesiana; internal lesion caused by D. foeniculina isolate ACA 91 on Acacia arabica; internal lesion on Acacia arabica inoculated with Neofusicoccum parvum isolate ACA 82.
Figure 4.
Pathogenicity test. From left to right: non-inoculated control plant; external lesion caused by Diaporthe foeniculina isolate ACA 91 on Acacia arabica; gummosis starting from inoculation point of D. foeniculina isolate ACA 91 on Acacia farnesiana; internal lesion caused by D. foeniculina isolate ACA 91 on Acacia arabica; internal lesion on Acacia arabica inoculated with Neofusicoccum parvum isolate ACA 82.
Table 1.
Isolates collected from symptomatic Acacia spp. and Pithecellobium dulce plants used in the molecular analyses.
Table 1.
Isolates collected from symptomatic Acacia spp. and Pithecellobium dulce plants used in the molecular analyses.
| Species | Strain a | Host | Country | GenBank Accession Number b | ||
|---|---|---|---|---|---|---|
| ITS | tef1 | tub2 | ||||
| Diaporthe foeniculina | ACA 91 | Acacia arabica | Italy, Giarre | PX649194 | PX662033 | PX662010 |
| Diaporthe foeniculina | ACA 92 | Acacia arabica | Italy, Giarre | PX644738 | PX662034 | PX662011 |
| Diaporthe foeniculina | ACA 95 | Acacia arabica | Italy, Giarre | PX649195 | PX662035 | PX662012 |
| Diaporthe foeniculina | ACA 96 | Acacia arabica | Italy, Giarre | PX644739 | PX662036 | PX662013 |
| Diaporthe foeniculina | ACA 97 | Acacia arabica | Italy, Giarre | PX644740 | PX662037 | PX662014 |
| Diaporthe foeniculina | ACA 98 | Acacia arabica | Italy, Giarre | PX644741 | PX662038 | PX662015 |
| Diaporthe foeniculina | ACA 99 | Acacia farnesiana | Italy, Giarre | PX644742 | PX662039 | PX662016 |
| Diaporthe foeniculina | ACA 100 | Acacia farnesiana | Italy, Giarre | PX644743 | PX662040 | PX662017 |
| Diaporthe foeniculina | ACA 101 | Acacia farnesiana | Italy, Giarre | PX649196 | PX662041 | PX662018 |
| Diaporthe foeniculina | ACA 102 | Acacia farnesiana | Italy, Giarre | PX649197 | PX662042 | PX662019 |
| Diaporthe foeniculina | ACA 103 | Acacia farnesiana | Italy, Giarre | PX649198 | PX662043 | PX662020 |
| Diaporthe foeniculina | ACA 104 | Acacia farnesiana | Italy, Giarre | PX644744 | PX662044 | PX662021 |
| Diaporthe foeniculina | ACA 111 | Pithecellobium dulce | Italy, Giarre | PX644745 | PX662045 | PX662022 |
| Diaporthe foeniculina | ACA 112 | Pithecellobium dulce | Italy, Giarre | PX644746 | PX662046 | PX662023 |
| Diaporthe foeniculina | ACA 113 | Pithecellobium dulce | Italy, Giarre | PX644747 | PX662047 | PX662024 |
| Diaporthe foeniculina | ACA 116 | Pithecellobium dulce | Italy, Giarre | PX644748 | PX662048 | PX662025 |
| Diaporthe foeniculina | ACA 117 | Pithecellobium dulce | Italy, Giarre | PX649199 | PX662049 | PX662026 |
| Diaporthe foeniculina | ACA 118 | Pithecellobium dulce | Italy, Giarre | PX649200 | PX662050 | PX662027 |
| Diaporthe foeniculina | ACA 119 | Pithecellobium dulce | Italy, Giarre | PX644749 | PX662051 | PX662028 |
| Diaporthe foeniculina | ACA 122 | Pithecellobium dulce | Italy, Giarre | PX644750 | PX662052 | PX662029 |
| Diaporthe foeniculina | ACA 123 | Pithecellobium dulce | Italy, Giarre | PX649201 | PX662053 | PX662030 |
| Diaporthe foeniculina | ACA 124 | Pithecellobium dulce | Italy, Giarre | PX644751 | PX662054 | PX662031 |
| Diaporthe foeniculina | ACA 126 | Pithecellobium dulce | Italy, Giarre | PX644752 | PX662055 | PX662032 |
| Neofusicoccum parvum | ACA 80 | Acacia arabica | Italy, Giarre | PX651383 | PX662056 | PX662064 |
| Neofusicoccum parvum | ACA 82 | Acacia arabica | Italy, Giarre | PX651384 | PX662057 | PX662065 |
| Neofusicoccum parvum | ACA 83 | Acacia arabica | Italy, Giarre | PX651385 | PX662058 | PX662066 |
| Neofusicoccum parvum | ACA 85 | Acacia farnesiana | Italy, Giarre | PX651386 | PX662059 | PX662067 |
| Neofusicoccum parvum | ACA 105 | Pithecellobium dulce | Italy, Giarre | PX651387 | PX662060 | PX662068 |
| Neofusicoccum parvum | ACA 106 | Pithecellobium dulce | Italy, Giarre | PX651388 | PX662061 | PX662069 |
| Neofusicoccum parvum | ACA 108 | Pithecellobium dulce | Italy, Giarre | PX651389 | PX662062 | PX662070 |
| Neofusicoccum parvum | ACA 110 | Pithecellobium dulce | Italy, Giarre | PX651390 | PX662063 | PX662071 |
a Isolates and sequences used in the phylogenetic analyses are shown in bold font; b ITS, internal transcribed spacer; tef1, translation elongation factor 1-α; tub2, beta-tubulin.
Table 2.
GenBank accession numbers of isolates used in the phylogenetic analyses.
| Species | Strain a | Host | Country | GenBank Accession Number b | ||
|---|---|---|---|---|---|---|
| ITS | tef1 | tub2 | ||||
| Botryosphaeria dothidea | CBS 115476 T | Prunus sp. | Switzerland | AY236949 | AY236898 | AY236927 |
| Botryosphaeria fabicerciana | CBS 118831 | Syzygium cordatum | South Africa | DQ316084 | MT592032 | MT592468 |
| Diaporthe acericola | MFLUCC 17-0956 | Acer negundo | Italy | KY964224 | KY964180 | KY964074 |
| Diaporthe ampelina | CBS 114016 | Vitis vinifera | France | AF230751 | GQ250351 | JX275452 |
| Diaporthe amygdali | CBS 126679 | Prunus dulcis | Portugal | KC343022 | KC343748 | KC343990 |
| Diaporthe australafricana | CBS 111886 | Vitis vinifera | Australia | KC343038 | KC343764 | KC344006 |
| Diaporthe brasiliensis | CBS 133183 T | Aspidosperma tomentosus | Brazil | KC343042 | KC343768 | KC344010 |
| Diaporthe caatingaensis | CBS 141542 T | Tacinga inamoena | Brazil | KY085926 | KY115603 | KY115600 |
| Diaporthe chamaeropis | CBS 454.81 | Chamaerops humilis | Greece | KC343048 | KC343774 | KC344016 |
| Diaporthe canthii | CBS 132533 | Canthium inerme | South Africa | JX069864 | KC843120 | KC843230 |
| Diaporthe citri | CBS 135422 | Citrus sp. | USA | KC843311 | KC843071 | KC843187 |
| Diaporthe cytosporella | CBS 137020 | Citrus limon | Spain | KC843307 | KC843116 | KC843221 |
| Diaporthe eres | CBS 116953 | Pyrus pyrifolia | New Zealand | KC343147 | KC343873 | KC344115 |
| Diaporthe foeniculina | CBS 111553 T | Foeniculum vulgare | Portugal | KC343101 | KC343827 | KC344069 |
| Diaporthe foeniculina | CBS 129528 | Rhus pendulina | South Africa | JF951146 | KC843100 | KC843205 |
| Diaporthe foeniculina | CBS 123208 | Foeniculum vulgare | Portugal | EU814480 | GQ250315 | JX275464 |
| Diaporthe foeniculina | CBS 136972 | Vaccinium corymbosum | Italy | KJ160565 | KJ160597 | MF418509 |
| Diaporthe foeniculina | AR5151 | Citrus latifolia | USA | KC843303 | KC843112 | KC843217 |
| Diaporthe forlicesenica | MFLUCC 17-1015 | Dorycnium hirsutum | Italy | KY964215 | KY964171 | KY964099 |
| Diaporthe hongkongensis | CBS 115448 T | Dichroa febrifuga | China | KC343119 | KC343845 | KC344087 |
| Diaporthe heterophyllae | CBS 143769 T | Acacia heterophylla | France | MG600222 | MG600224 | MG600226 |
| Diaporthe inconspicua | CBS 133813 T | Maytenus ilicifolia | Brazil | KC343123 | KC343849 | KC344091 |
| Diaporthe limonicola | CBS 142549 T | Citrus limon | Malta | MF418422 | MF418501 | MF418582 |
| Diaporthe longicolla | ATCC 60325 | Glycine max | USA | KJ590728 | KJ590767 | KJ610883 |
| Diaporthe melitensis | CBS 142551 T | Citrus limon | Malta | MF418424 | MF418503 | MF418584 |
| Diaporthe notophagi | BRIP54801 T | Notophagus cunninghamii | Australia | JX862530 | JX862536 | KF170922 |
| Diaporthe novem | CBS 127271 T | Glycine max | Croatia | KC343156 | KC343882 | KC344124 |
| Diaporthe parvae | PSCG034 | Pyrus bretschneideri | China | MK626919 | MK654858 | MK691248 |
| Diaporthe phoenicicola | CBS 161.64 T | Areca catechu | India | KC343032 | KC343758 | KC344000 |
| Diaporthe pterocarpi | CBS 137021 | Pterocarpus indicus | Thailand | JQ619901 | JX275418 | JX275462 |
| Diaporthe pterocarpicola | CBS 135432 T | Pterocarpus indicus | Thailand | JQ619887 | JX275403 | JX275441 |
| Diaporthe rudis | CBS 113201 | Vits vinifera | Portugal | KC343234 | KC343960 | KC344202 |
| Diaporthe sojae | FAU 635 | Glycine max | USA | KJ590719 | KJ590762 | KJ610875 |
| Diaporthe saccarata | CBS 116311 | Protea repens | South Africa | KC343190 | KC343916 | KC344158 |
| Diaporthe thunbergiae | CBS 135769 T | Thunbergia laurifolia | Thailand | JQ619893 | JX275409 | JX275449 |
| Diaporthella corylina | CBS 12114 T | Corylus sp. | China | KC343004 | KC343730 | KC343972 |
| Neofusicoccum buxi | CBS 113714 | Buxus sempervirens | Sweden | KX464164 | KX464677 | KX464954 |
| Neofusicoccum australe | CMW 6837 | Acacia sp. | Australia | AY339262 | AY339270 | AY339254 |
| Neofusicoccum eucalypticola | CBS 115679 T | Eucalyptus grandis | Australia | AY615141 | AY615133 | AY615125 |
| Neofusicoccum eucalyptorum | CBS 115791 | Eucalyptus grandis | South Africa | AF283686 | AY236891 | AY236920 |
| Neofusicoccum hellenicum | CERC 1947 T | Pistacia vera | Greece | KP217053 | KP217061 | KP217069 |
| Neofusicoccum hongkongense | CERC 2973 T | Araucaria cunninghamii | China | KX278052 | KX278157 | KX278261 |
| Neofusicoccum hongkongense | CERC 2967 | Araucaria cunninghamii | China | KX278050 | KX278155 | KX278259 |
| Neofusicoccum hongkongense | CERC 2968 | Araucaria cunninghamii | China | KX278051 | KX278156 | KX278260 |
| Neofusicoccum mangiferae | CBS 118531 T | Mangifera indica | Australia | AY615185 | DQ093221 | AY615172 |
| Neofusicoccum mediterraneum | CBS 113083 T | Pistacia vera | U.S.A. | KX464186 | KX464712 | KX464998 |
| Neofusicoccum microconidium | CGMCC 3.18750 T | Eucalyptus urophylla × E. grandis | China | KX278053 | KX278158 | KX278262 |
| Neofusicoccum occulatum | CBS 128008 T | Eucalyptus grandis | Australia | EU301030 | EU339509 | EU339472 |
| Neofusicoccum parvum | CBS 138823 T | Populus nigra | New Zealand | AY236943 | AY236888 | AY236917 |
| Neofusicoccum parvum | CBS 137504 | Vitis vinifera | Algeria | KJ657702 | KJ657715 | KX505915 |
| Neofusicoccum parvum | CBS 140887 | Vitis vinifera cv. Alfrocheiro | Portugal | MT587448 | MT592158 | MT592648 |
| Neofusicoccum parvum | CBS 139672 | Bruguiera gymnorhiza | South Africa | MT587446 | MT592156 | MT592646 |
| Neofusicoccum parvum | BOT 1A | Citrus limon | Italy | MW727244 | MW789904 | MW789889 |
| Neofusicoccum parvum | CAA 322 | Malus domestica | Portugal | KX505906 | KX505894 | KX505916 |
| Neofusicoccum parvum | CPC 32275 | Pomaderris aspera | Australia | MT587451 | MT592160 | MT592651 |
| Neofusicoccum parvum | CPC 35861 | Aloe sp. | South Africa | MT587449 | MT592159 | MT592649 |
| Neofusicoccum parvum | CBS 139671 | Bruguiera gymnorhiza | South Africa | MT587445 | MT592155 | MT592645 |
| Neofusicoccum podocarpi | CBS 131677 | Podocarpus henkelii | South Africa | MT587508 | MT592223 | MT592715 |
| Neofusicoccum podocarpi | CBS 115065 | Wollemia nobilis | Australia | MT587507 | MT592222 | MT592714 |
| Neofusicoccum podocarpi | CBS 131678 | Podocarpus henkelii | South Africa | MT587509 | MT592224 | MT592716 |
| Neofusicoccum protearum | CBS 114176 T | Leucadendron salignum | South Africa | AF452539 | KX464720 | KX465006 |
| Neofusicoccum ribis | CBS 115475 T | Ribes sp. | USA | AY236935 | AY236877 | AY236906 |
| Neofusicoccum ribis | CBS 124924 | Terminalia catappa | Cameroon | FJ900607 | FJ900653 | FJ900634 |
| Neofusicoccum sinense | CGMCC 3.18315 T | Unknown woody plant | China | KY350148 | KY817755 | KY350154 |
| Neofusicoccum sinoeucalypti | CERC2005 T | Eucalyptus urophylla × E. grandis | China | KX278061 | KX278166 | KX278270 |
| Neofusicoccum variabile | CBS 143481 T | Mimusops caffra | South Africa | MH558610 | MH576586 | MH569155 |
a T = ex-type isolates. b ITS, internal transcribed spacer; tef1, translation elongation factor 1-α; tub2, beta-tubulin.
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Leonardi, G.R.; Vecchio, L.; Gusella, G.; Aiello, D.; Voglmayr, H.; Polizzi, G. New Records of Canker-Causing Pathogens of Acacia spp. and Pithecellobium dulce in Southern Italy. J. Fungi 2025, 11, 874. https://doi.org/10.3390/jof11120874
AMA Style
Leonardi GR, Vecchio L, Gusella G, Aiello D, Voglmayr H, Polizzi G. New Records of Canker-Causing Pathogens of Acacia spp. and Pithecellobium dulce in Southern Italy. Journal of Fungi. 2025; 11(12):874. https://doi.org/10.3390/jof11120874
Chicago/Turabian StyleLeonardi, Giuseppa Rosaria, Laura Vecchio, Giorgio Gusella, Dalia Aiello, Hermann Voglmayr, and Giancarlo Polizzi. 2025. "New Records of Canker-Causing Pathogens of Acacia spp. and Pithecellobium dulce in Southern Italy" Journal of Fungi 11, no. 12: 874. https://doi.org/10.3390/jof11120874
APA StyleLeonardi, G. R., Vecchio, L., Gusella, G., Aiello, D., Voglmayr, H., & Polizzi, G. (2025). New Records of Canker-Causing Pathogens of Acacia spp. and Pithecellobium dulce in Southern Italy. Journal of Fungi, 11(12), 874. https://doi.org/10.3390/jof11120874
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