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The enigma of Calonectria species occurring on leaves of Ilex aquifolium in Europe
IMA Fungus volume 1, pages101–108(2010)
Species of Calonectria are common saprobes and plant pathogens on a wide range of hosts occurring in subtropical to tropical regions of the world. The aim of the present study was to resolve the status of new Calonectria collections obtained on Ilex leaves from France. Based on DNA sequence data of their (3-tubulin and histone gene regions, as well as morphology, the new collections matched the ex-type strain of Cylindrocladium ilicicola. On the host and in culture, yellow to brownish-yellow perithecia were observed that did not strain red in 3 % KOH. Based on these results, C. ilicicola and its purported teleomorph, Ca. pyrochroa, were shown to represent two distinct species, as the latter has bright red perithecia that strain purple in KOH. A new combination, Ca. lauri, based on Tetracytum lauri, is subsequently proposed for C. ilicicola. Calonectria lauri is distinct from Ca. ilicicola, a pathogen commonly associated with Cylindrocladium black rot of peanut. Finally, Ca. canadiana is proposed as new name for Cy. canadiense, which is a nursery pathogen involved with root rot of several tree genera in Quebec, Canada.
Species of Calonectria are members of Nectriaceae (Hypocreales, Ascomycetes) (Lombard 2010a–c). Nectriaceae are characterised by having uniloculate, orange to purple, superficial ascomata (Rossman et al. 1999). Calonectria is easily distinguished from other members of the family based on its Cylindrocladium anamorphs. Formerly Cylindrocladium also included members of Cylindrocladiella, a genus that accommodates Cylindrocladium-like species with small conidia (Boesewinkel 1982, Victor et al. 1998) and Nectricladiella teleomorphs (Schoch et al. 2000). Other morphologically similar genera that have also since been separated from this complex include Xenocylindrocladium (Decock et al. 1997), Curvicladiella (Crous et al. 2006a) and Dematiocladium (Crous et al. 2005). Following the approach of Crous et al. (2006b, 2008, 2009a, b) with other fungal groups, Lombard et al. (2009, 2010a–d) chose to use the older Calonectria name for the genus, irrespective whether the teleomorph or Cylindrocladium anamorph, unnamed microconidial, megaconidial, or chlamydospore-like synanamorph was observed. All taxa are since accommodated in Calonectria, which is a monophyletic genus (Lombard et al. 2010a–c).
Most species of Calonectria occur commonly in soil, especially in subtropical to tropical regions of the world. Although the genus was originally regarded as saprobic (Graves 1915), taxa have since been proven to be important plant pathogens, associated with a wide host range of plants, causing disease symptoms ranging from leaf spots to stem cankers, damping off, cutting rot, root and fruit rot (Crous et al. 2004b, 2006a, Lombard et al. 2009, 2010a, d). Major diseases attributed to Calonectria infections include Cylindrocladium black rot of Arachis hypogea (peanut), and red crown rot of Glycine max (soybean) (Crous et al. 1993, Wright et al. 2010), as well as root rot and leaf diseases of numerous diverse hosts (Crous et al. 2004b, 2006a).
Over the past few years, a species of Calonectria was collected from leaves of Ilex aquifolium in France. Presently four species of Calonectria have been described from Ilex (Aquifoliaceae), namely Calonectria morganii on Ilex paraguayensis in Argentina, and Ilex vomitoria in Florida (USA); Calonectria avesiculata on Ilex spp. in Georgia and Florida (USA), Cylindrocladium ilicicola (as Calonectria pyrochroa) on Ilex aquifolium on Clare Island (Ireland), and Calonectria spathulata on Ilex paraguariensis in Brazil (Crous 2002). Hawksworth & Sivanesan (1976) also reported a Calonectria species on Ilex aquifolium from Slapton, South Devon, England, which appears to be undescribed, with ascospores 3-septate, 14–22 ×3–4 µm. The collection obtained from France and treated in this study, is morphologically distinct from taxa presently reported from Ilex.
In recent years there have been several revisions focused on either Calonectria or its anamorph genus, Cylindrocladium (Rossman 1979, Peerally 1991, Crous & Wingfield 1994, Crous 2002). The first attempt to provide a molecular phylogeny of the genus was that of Schoch et al. (2001) based on β-tubulin DNA sequences. This gene region, however, proved insufficiently variable to reliably distinguish all species complexes in the genus (Kang et al. 2001a, b, Henricot & Culham 2002, Crous et al. 2004b, 2006a). Since then, a concerted effort has been made to generate a multi-gene phylogeny for taxa in the genus, and identify the best suited gene for species delimitation (Lombard et al. 2009, 2010a–d). Based on these findings, a combination of β-tubulin DNA sequence data, supplemented with either calmodulin or elongation factor 1-α, proved the most effective in distinguishing all known taxa.
The aim of the present study was to compare the new collections on Ilex from France to all species known in the genus, using morphology and DNA sequence analysis of their β-tubulin and histone gene regions in order to determine if it represented a novel taxon.
Materials and Methods
Single ascospore isolates were obtained from leaves of Ilex aquifolium as explained in Crous & Wingfield (1994). Isolates were incubated on plates of 2% malt extract agar (MEA), 2% potato-dextrose agar (PDA) and oatmeal agar (OA) (Crous et al. 2009c) for 7 d at 25 °C under continuous near-UV light, to promote sporulation. Reference strains are maintained in the CBS-KNAW Fungal Biodiversity Centre (CBS) Utrecht, The Netherlands.
DNA isolation, amplification and analyses
Genomic DNA was isolated from fungal mycelium grown on MEA, using the UltraCleanTM Microbial DNA Isolation Kit (MoBio Laboratories, Inc., Solana Beach, CA, USA) according to the manufacturer’s protocol. Two loci were amplified and sequenced as explained in Crous et al. (2004b) and Lombard et al. (2010c), namely, part of the β-tubulin gene (TUB), amplified with primers T1 (O’Donnell & Cigelnik 1997) and CYLTUBIR (Crous et al. 2004b); and part of the histone H3 gene (HIS) using primers CYLH3F and CYLH3R (Crous et al. 2004b). Part of the nuclear rDNA operon spanning the ′ end of the 18S nrRNA gene (SSU), the first internal transcribed spacer (ITS1), the 5.8S nrRNA gene, the second ITS region (ITS2) and the 5′ end of the 28S nrRNA gene (LSU) was amplified for some isolates as explained in Lombard et al. (2010c). The generated sequences were compared with other fungal DNA sequences from NCBI’s GenBank sequence database using a blastn search; TUB sequences with high similarity were added to the alignment and the result of sequences of the other loci were used as confirmation (not shown). The additional GenBank sequences were manually aligned using Sequence Alignment Editor v. 2.0a11 (Rambaut 2002). Phylogenetic analyses of the aligned sequence data were performed using PAUP (Phylogenetic Analysis Using Parsimony) v. 4.0b10 (Swofford 2003) and consisted of neighbour-joining analyses with the uncorrected (“p”), the Kimura 2-parameter and the HKY85 substitution models. Alignment gaps were treated as missing data and all characters were unordered and of equal weight. Any ties were broken randomly when encountered. For parsimony analyses, alignment gaps were treated as a fifth character state and all characters were unordered and of equal weight. Maximum parsimony analysis was performed using the heuristic search option with 100 random (ITS) or simple (LSU) taxa additions and tree bisection and reconstruction (TBR) as the branch-swapping algorithm. Branches of zero length were collapsed and all multiple, equally parsimonious trees were saved. The robustness of the trees obtained was evaluated by 1 000 bootstrap replications (Hillis 6 Bull 1993). Tree length (TL), consistency index (CI), retention index (RI) and rescaled consistency index (RC) were calculated. Sequences derived in this study were lodged at GenBank (<https://doi.org/ncbi.nlm.nih.gov>), the alignment in TreeBASE (<https://doi.org/treebase.org/treebase/index.html>), and taxonomic novelties in MycoBank (<https://doi.org/MycoBank.org>; Crous et al. 2004a).
Characteristics in culture were determined after 7 d on MEA, PDA and OA (Crous et al. 2009c). Morphological descriptions were based on sporulating cultures on synthetic nutrient-poor agar (SNA) (Nirenburg 1981, Lombard et al. 2009) and carnation leaf agar (CLA) (Crous et al. 2009c). Slide preparations were made from sporulating cultures (SNA for anamorph, CLA for teleomorph) in clear lactic acid, with 30 measurements determined per structure, and observations made with a Nikon SMZ1500 dissecting microscope, and with a Zeiss Axioscope 2 microscope using differential interference contrast (DIC) illumination. Colony characters and pigment production were noted after 7 d of growth on MEA, PDA and OA (Crous et al. 2009c) incubated at 25 °C. Colony colours (surface and reverse) were rated according to the colour charts of Rayner (1970).
Approximately 600,480and680 bases were determined for the isolates indicated in Table 1 for TUB, HIS and ITS, respectively. Of the β-tubulin gene, 522 bases were used for phylogenetic analyses in the manually adjusted alignment containing 32 isolates (including the outgroup sequence). Of these 522 characters (including alignment gaps), 180 were parsimony-informative, 47 were variable and parsimony-uninformative, and 295 were constant. Neighbour-joining analysis using the three substitution models, as well as the parsimony analysis, yielded trees with exactly the same topologies. Parsimony analysis of the alignment yielded a single most parsimonious tree (TL = 381 steps; CI = 0.816; RI = 0.953; RC = 0.778), which is shown in Fig. 1.
Calonectria lauri (Vanderw.) Lechat & Crous, comb. nov.
Basionym: Tetracytum lauri Vanderw., Parasitica 1: 145. 1945. (as “laurii”).
= Candelospora ilicicola Hawley, Proc. Roy. Irish Acad. 31: 11. 1912. [non Calonectria ilicicola Boedijn & Reitsma, 1950]
= Cylindrocladium ilicicola (Hawley) Boedijn & Reitsma, Reinwardtia 1: 57. 1950.
Typus: Ireland, Clare Island, Ilex aquifolium, Hawley, K (M) 61269!, holotype of Cy. ilicicola, IMI 76542 isotype. Netherlands, South-East Limburg, Vijlenerbos, Vijlen, Ilex aquifolium, Aug. 1970, H.A van der Aa, epitype CBS H-15110, ex-epitype culture CBS 749.70.
Ascomata perithecial, solitary, scattered, subglobose to ovoid, 450–550 Lim high × 380–420 µm diam, superficial, not obviously stromatic but difficult to remove from the subtratum because basal cells of ascomata remain immersed in the substratum, yellow to brownish-yellow, dark-red at base, not changing colour in 3% KOH or lactic acid, warted except at ostiolar region, ostiole papillate, composed of palisade-like, cylindrical to narrowly ellipsoidal cells. Ascomatal wall 50–65 µm thick of two regions; outer region comprising warts 50–55 µm thick, composed of globose to nearly angular, thick-walled cells, 10–30 × 5–16 µm, yellow, wall 1.5–2 µm thick; inner region 5–10 µm thick, composed of flattened, ellipsoidal cells, 12–18 × 3–5 µm, hyaline; warts globose to subglobose 25–40 × 15–30 µm, yellow. Asci clavate, long stipitate, 110–130 × 17–22 µm, 8-spored, multiseriate. Ascospores narrowly fusiform with rounded ends, lightly curved, guttulate, hyaline, smooth, (53–)60–86(–89) × 6.5–8(–9) µm, 3-septate, not conctricted at the septa or constricted when overmature. Conidiophores consisting of a stipe bearing a penicillate arrangement of fertile branches, a stipe extension, and a terminal vesicle; stipe septate, hyaline, smooth, 40–150 × 3–5 µm; stipe extensions septate, straight to flexuous, 120–200 µm long, 2.5–3 µm wide at the apical septum, terminating in an obpyriform to ellipsoid vesicle, (5–) 7–8(–10) µm diam. Conidiogenous apparatus with primary branches aseptate or 1-septate, 15–20 × 4–5 µm; secondary branches aseptate, 8–15 × 4–5 µm; tertiary branches aseptate, 10–15 × 4–5 µm, each terminal branch producing 2–4 phialides; phialides doliiform to reniform, hyaline, aseptate, 6–12 × 2.5–4 µm; apex with minute periclinal thickening and inconspicuous collarette. Conidia cylindrical, rounded at both ends, straight, (45–) 55–68(–73) × (4–)5–6(–7) µm (av. = 60 × 5.5 µm), (1–)3-septate, lacking a visible abscission scar, held in parallel cylindrical clusters by colourless slime. Megaconidia and microconidia unknown.
Culture characteristics: Colonies on MEA sienna to brick on the surface, and sienna in reverse; sienna on OA (surface); sienna to umber on PDA (surface), and umber in reverse; chlamydospores on MEA moderate, occurring throughout the medium, with sparse to moderate sporulation on aerial mycelium.
Additional specimens examined: Netherlands, Hilversum, on leaves of Ilex aquifolium, 11 Nov. 2008, W. Gams, CPC 15683 = CBS 128031, CPC 15684, CPC 15685. France, Pressigny (52), on leaves of Ilex aquifolium, 05 Dec. 2009, A. Gardiennet, AG09308, CBS H-20476, culture CPC 17978 = CBS 126269; Forêt de Chizé, Villiers en Bois (79) on leaves of Ilex aquifolium, 19 Sept. 2006, C. Lechat, CLL696. Belgium, Gent, on roots of Buxus sempervirens, July 1969, A. Roos, IMI 299390 = CBS 553.69.
Notes: The name Calonectria ilicicola is already occupied, and thus the next available epithet for this species in Calonectria is that of Tetracytum lauri. Calonectria lauri is phylogenetically closely related to Ca. citri (known on Citrus from Florida). Morphologically the two species can be separated in that Ca. citri has ellipsoid to pyriform or obovoid vesicles, and 3-septate conidia that are slightly shorter and narrower, (25–)53–60(–65) × 3–4(–5) µm (Crous 2002).
The genus Calonectria is based upon Calonectria pyrochroa (on Platanus leaf litter, France, lectotype BPI), which Rossman (1979) found to be indistinguishable from Ca. daldiniana (on Magnolia grandiflora leaf litter, Italy, holotype RO). A separate collection from decaying leaves of Pittosporum undulatum collected in Madeira (CUP-MM 2407) produced a Cylindrocladium anamorph with clavate vesicles, which later led Rossman (1983) to conclude that the oldest anamorph epithet that could be linked to Ca. pyrochroa was C. ilicicola.
Brayford & Chapman (1987) reported a wilting disease of Laurus nobilis in nurseries on the Isles of Scilly, and later on Arbutus andrachnoides and Gaultheria shallon in West Devon, UK. The causal organism was identified as C. ilicicola, but incorrectly linked to the teleomorph name, Ca. ilicicola. Based on a molecular comparison of ex-type strains, Crous et al. (1993) showed Ca. ilicicola was the teleomorph of C. parasiticum, a major pathogen associated with Cylindrocladium black rot of peanut. In a later study, Crous & Wingfield (1994) accepted the relationship between Ca. pyrochroa and C. ilicicola, as there were no cultures available at the time to refute this proposed link (Crous 2002). Following a revision of Cylindrocladium strains in the CBS culture collection, Crous et al. (2006a) discovered a strain linked to a specimen that closely matched the type of C. ilicicola, and subsequently designated CBS 749.70 (on Ilex aquifolium, the Netherlands) as ex-epitype strain for C. ilicicola. Sequence data derived from the ex-epitype strain, and morphology, proved to be identical to that of the new collection obtained from France (Figs 1–2), confirming it to be C. ilicicola.
However, isolate CBS 126269 produced a Calonectria teleomorph in culture, which is clearly distinct from Ca. pyrochroa. The latter species (and its synonyms) have scarlet-red perithecia, which turn purple in 2% KOH (Rossman 1979). The present collection (on the host and on CLA in culture), forms yellow to brownish yellow perithecia that do not discolour in KOH (except at the perithecial base). The teleomorph of C. ilicicola could therefore not be Ca. pyrochroa as currently accepted (Lombard et al. 2010c). Because the name Ca. ilicicola is already occupied by the pathogen causing Cylindrocladium black rot of peanut (Crous et al. 1993), a new name, Ca. lauri, is proposed for this species, which appears to occur commonly on Laurus, Ilex, as well as several other hosts in Europe (Brayford & Chapman 1987). Presently no cultures are available of Ca. pyrochroa, and further collections will have to be made from Platanus leaf litter in France to help clarify the morphology of its Cylindrocladium anamorph.
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The authors thank the technical staff, Arien van Iperen (cultures), Marjan Vermaas (photo plates), and Mieke Starink-Willemse (DNA isolation, amplification and sequencing) for their invaluable assistance. Drew Minnis (USDA, Beltsville, USA) is also thanked for bringing the homonym associated with epithet “canadensis” to our attention. Finally, we thank Alain Gardiennet for the supply of specimens.
In the recent treatment of the genus Calonectria, Lombard et al. (2010c) allocated the name Cylindrocladium canadense to Calonectria as Ca. canadensis (J.C. Kang, Crous & C.L. Schoch) L. Lombard, M.J. Wingf. & Crous, but overlooked the older existing name, Ca. canadensis (Ellis & Everh.) Berl. & Voglino. A new combination is required to resolve this homonym as follows:
Calonectria canadiana L. Lombard, M.J. Wingf. & Crous, nom. nov.
Basionym: Cylindrocladium canadense J.C. Kang, Crous & C.L. Schoch, Syst. Appl. Microbiol. 24: 210. 2001.
= Calonectria canadensis (J.C. Kang, Crous & C.L. Schoch) L. Lombard, M.J. Wingf. & Crous, Stud. Mycol. 66: 56. 2010, non Calonectria canadensis (Ellis & Everh.) Berl. & Voglino, Addendum to Syll. Fung. 4: 212. 1886.
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Lechat, C., Crous, P.W. & Groenewald, J.Z. The enigma of Calonectria species occurring on leaves of Ilex aquifolium in Europe. IMA Fungus 1, 101–108 (2010). https://doi.org/10.5598/imafungus.2010.01.02.01
- Ilex aquifolium