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Biodiversity Theme (Mycology & Botany), Agriculture and Agri-Food Canada, 960 Carling Ave., Ottawa, Ontario, Canada, K1A 0C6
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ABSTRACT |
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Gliocephalis hyalina, a rarely seen micro-fungus with a morphology similar to the hyphomycete genus Aspergillus but with slimy conidia was found in a mixed microbial culture from soybean roots. This species has been reported sporadically since 1899, each time in association with other fungi or bacteria. Gliocephalis hyalina has not been maintained in monoxenic culture and requires other fungi to grow. Light and scanning electron microcope studies indicate that it is a biotrophic contact parasite of Fusarium species. The fungus may penetrate the cells but has no apparent deleterious effect on the growth or plant pathogenicity of its host. Phylogenetic analyses of partial nuclear small subunit rDNA sequences place G. hyalina near the Laboulbeniales, an order of obligate insect parasitic microfungi, and the related mycelial genus Pyxidiophora. Gliocephalis hyalina is mycoparasitic along with many Pyxidiophora species. These discoveries suggest that some "unculturable" microorganisms or "cryptic DNA" recovered from environmental DNA samples might represent obligate biotrophs that could be cultured and studied with simple techniques.
Key words: anamorphic ascomycete, evolution, Laboulbeniales
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONLITERATURE CITED |
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is a poorly understood hyphomycete first discovered on beet roots collected in France. After its initial description, the fungus was not mentioned again until Arnaud (1952) recorded G. hyalina on cones and branches of Pinus and on stems and roots of Cucumis melo. Barron (1968) made the most recent published collection of G. hyalina from a rotten potato tuber in soil from Ontario. A second species, Gliocephalis pulchella (Penz. & Sacc.) D. Hawksw., appears to be a saprobe on lichens (Hawksworth 1979).
Both species bear a remarkable morphological similarity to species of the much better known genus Aspergillus, but the conidia are produced in slime rather than in dry chains. In this respect, Gliocephalis has some similarity with species of Goidanichiella Barron ex Gams (Gams et al 1990), but in contrast to the latter genus both species of Gliocephalis lack septa in their conidiophore stipes and the dematiaceous pigments characteristic of Goidanichiella barronii. In fact, the fungus reported by Embree (1963) as G. hyalina in potting soil in San Francisco in all likelihood was G. barronii because the report notes the presence of pigmented, septate conidiophores.
In these reports attempts at in vitro culturing of G. hyalina were unsuccessful and it was assumed to be a parasite of soil bacteria or other fungi. Matruchot (1899) was unable to grow it in monoxenic culture. He eventually succeeded in growing it in co-culture with bacteria and hypothesized that it lived on bacterial waste metabolites. Barron (1968) was unable to establish pure cultures but maintained it for a limited period of time in association with a Fusarium species. Gams et al (1990) concluded that G. hyalina could not be grown without bacteria. When we isolated this fungus from soybean (Glycine max) roots collected in Ottawa, Canada, we also failed to maintain a living culture using standard monoxenic microbiological techniques. However, like previous investigators, we noticed that other fungi were present on the isolation plate, which in our case consisted of a species of Fusarium. The notion that G. hyalina might be a parasite of Fusarium was intriguing. The genus Fusarium (asexual stage of Gibberella, Hypocreales) includes some of the most economically important plant pathogens. Contamination of agricultural commodities with Fusarium toxins, such as zearalenone, deoxynivalenol (vomitoxin) and fumonisins, is monitored and regulated internationally (Summerell et al 2001).
We report here on the successful establishment of G. hyalina in dual culture with species of Fusarium and the successful preservation of the dual culture. The availability of living material let us study the interaction between G. hyalina and its host using light, scanning and transmission-electron microscopy. We also established the phylogenetic placement of this species using parsimony analysis of nuclear small subunit rDNA sequences and compared G. hyalina to Aspergillus terreus and other Aspergillus-like fungi such as Goidanichiella baronii, Custingophora olivacea, Escovopsis aspergillioides and Gondwannamyces proteae (anamorph: Knoxdaviesia proteae).
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MATERIALS AND METHODS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONLITERATURE CITED |
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) and incubated in the dark or in incident light at 25 C. Fungal structures were mounted on slides in 85% lactic acid and photographed using phase or differential interference contrast microscopy. Gliocephalis hyalina (DAOM 229465, Canadian Collection of Fungal Cultures) was compared to several other Aspergillus-like fungi, including Goidanichiella baronii (DAOM 145402, DAOM 145918), Custingophora olivacea (CBS 335.68, Centraalbureau voor Schimmelcultures), Escovopsis aspergilioides (CBS 423.93) and the anamorph of Gondwan-namyces proteae (CMW 3757, Tree Pathology Cooperative Programme Culture Collection, MJ Wingfield). For scanning electron microscopy (SEM), blocks of agar about 5 mm across were cut from sporulating colonies and fixed in 4% glutaraldehyde and 0.5% osmium tetroxide in a 0.1 M phosphate buffer, dehydrated in a graded ethanol series, then critical-point dried (Tousimis SAMDRI PVT-3). Specimens were mounted and coated with gold palladium alloy (Technics Sputter Coater) and examined using a Phillips XL30 environmental scanning electron microscope. Preparations for transmission electron microscopy (TEM) were made by embedding the specimens in LR White and Spurr low viscosity embedding medium. Specimens were cut using a glass or diamond knife mounted in a microtome, and the thin sections were stained with uranyl acetate and lead citrate. These sections were examined using a Zeiss EM 902 analytical TEM microscope.
Infection studies were made on slide cultures (Cole et al 1969). Slides were sterilized by cleaning with 95% ethanol. Molten 10% water agar was dripped onto the slides and allowed to solidify. Conidia of Fusarium spp. were transferred to the slides and allowed to germinate. After ca. 12 h, Gliocephalis conidia were added to the slides and allowed to germinate. A cover slip was placed on the culture and the behavior of the germ tubes of G. hyalina was followed by light microscopy and pictures were taken at 1 h intervals.
Phylogenetic analysis.— –
The entire nuclear ribosomal small subunit (SSU) and internal transcribed spacer region (ITS) was amplified by the polymerase chain reaction using NS1 and ITS4 primers (White et al 1990) directly from spore suspensions of G. hyalina without DNA extraction. Amplicons were purified using Wizard fast-preps (BIO/CAN Scientific, Ontario, Canada). The NS1-NS4 sequence of the G. hyalina SSU rDNA was obtained using standard primers (White et al 1990) and direct sequencing of the PCR product on an ABI PRISM 310 automatic sequencer (Perkin Elmer Applied Biosystems, California). The alignment of the G. hyalina and SSU sequences of species representing different orders of the fungal kingdom was calculated using the Pileup algorithm of GCG 10.1 (Canadian Bioinformatics Resource http://www.cbr.nrc.ca/with a gap weight of 5 and a gap length penalty of 1) and adjusted by eye. The final alignment contained 1083 bases. For phylogenetic analysis, a region with only single-stranded sequence for G. hyalina data was excluded (85 bp). The aligned dataset consisted of 988 unweighted characters, with gaps treated as a fifth base resulting in 468 constant, 156 parsimony uninformative and 364 parsimony informative characters. Phylogenetic relationships were inferred using heuristic searches in PAUP* 4.0b8 (Swofford 2001), using tree-bisection-reconnection (TBR) branch swapping. Starting trees were obtained through simple stepwise addition. Confidence levels were estimated using a bootstrap analysis (1000 replicates). The confidence levels of the different nodes in the tree also were evaluated with Bayesian analysis of the dataset using the Markov Chain Monte Carlo algorithm (MrBayes 3, Huelsenbeck and Ronquist 2001). The analysis was run for 200 000 generations with every 10th tree sampled. The first 2000 trees were discarded because these were generated before convergence of the chains. Four cold chains were run simultaneously. The posterior probability of each node was calculated. The SSU sequence of G. hyalina was determined in duplicate and is deposited in GenBank under accession numbers (AF505620
[GenBank]
[5' end] and AF505621
[GenBank]
[3' end]).
Host range experiments.— – Host specificity was tested by inoculating growing cultures of host fungi with 1 spore drop of G. hyalina in the center of the colony. Cultures were checked by light microscopy after 5 d for sporulation and formation of contact cells. The experiment was run in duplicate. Several species of Fusarium and some common soil fungi were tested as potential hosts for G. hyalina, namely Fusarium sporotrichioides DAOM 213383, F. oxysporum DAOM 197539, F. poae DAOM 13714, F. verticillioides KAS 99M-6, F. merismoides DAOM 167040, F. culmorum DAOM 211723, F. tumidum BBA 63572, F. sambucinum DAOM 214958, F. venenatum DAOM 64537, F. solani DAOM 193421, F. torulosum BBA 64988, Epicoccum purpurascens DAOM 185649, Cladosporium cladosporioides DAOM 196948, Botrytis cinerea DAOM 189076, Trichoderma viride JBT1003 and Alternaria alternata DAOM 216376. To ensure that pure spore drops of G. hyalina were used for host-range experiments, each aquaeous spore suspension was plated on CMA without any host to check that no mycelial growth occurred.
Pot culture experiments.— –
A bioassay originally designed to study the interaction of Fusarium graminearum and roots of wheat seedlings (Chongo et al 2001) was adapted to determine whether G. hyalina would reduce the pathogenic effects of Fusarium on wheat seedlings grown in a sterile, environment without soil. Wheat seeds with a low incidence of natural Fusarium infection (variety AC Brio, collected at New Liskeard, Ontario) were surface sterilized using 10% chlorine bleach (5 min), 100% ethanol (5 min) and water (10 min). Thirty seeds per treatment were soaked in concentrated spore suspensions of (i) F. graminearum (DAOM 180378), (ii) F. graminearum and Gliocephalis hyalina and (iii) water. Seeds were planted in approximately 30 mL of a presterilized, soilless mix in potting trays, and plants were grown in a growth chamber with 12 h of light/dark cycles at 22 C and were watered as required. Seed germination and growth were assessed 16 d after planting, and stem and root lengths as well as stem dry weights were measured. The experiment was done in duplicate. The data were analysed using ANOVA as implemented in SAS 6.0.
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RESULTS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONLITERATURE CITED |
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). Best results were obtained with G. hyalina in a mixed culture with an unidentified Fusarium sp. (DAOM 229465) on CMA (FIG. 2). Fusarium spp. sporulated sparsely on this medium and the conidiophores of the parasite were easily observed and studied. Colonies of G. hyalina were colorless and conidiophores were produced randomly over the host colony (FIGS. 1–2).
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), having an unbranched, aseptate, hyaline conidiophore terminating in a swollen vesicle, (8–)9–14(–17) µm, giving rise to 1–2 series of metulae, bearing conidiogenous cells (FIGS. 4–5). Conidiophores are (154–)226– 408(– 476) µm long. Each metula terminates in 2–3 cylindrical conidiogenous cells, (10–)12–16(–20) µm long, 2–3 µm wide, that produce conidia in basipetal chains (Cole and Samson 1979) (FIGS. 5–6). The conidia are hyaline, cylindrical with rounded apices and have slightly truncate bases, 6–9 µm x 2–3 µm (FIG. 7). They accumulate in clear, watery masses at the apices of the conidiophores; they become white as the culture ages. The bases of the conidiophores are slightly swollen (FIG. 8). In older colonies lateral, aseptate cells are produced directly on the hyphae. These cells resemble chlamydospores, and we speculate that they are survival structures (FIGS. 9–10).
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Parasitic interaction.— –
Time-lapse photography of slide cultures using light microscopy (LM) showed that spores of G. hyalina would germinate only when mycelium of Fusarium was present. Then the spores swelled and sent out single germ tubes, which grew directly toward the Fusarium hyphae. At contact the Gliocephalis hyphae seemed to attach to the Fusarium cells (FIG. 13). Multiple lateral contact points developed between the narrow growing hyphae of Gliocephalis and the broader Fusarium hyphae. No evidence of specialized attachment or penetration structures using LM was found (FIG. 11
). With SEM, we found clear evidence of specialized structures growing from Gliocephalis and "grabbing" the hyphae of Fusarium (FIG. 12). These attachment structures (haustoria), consisted of slightly swollen ends of otherwise normal-looking hyphae or hyphal branches. No evidence of hyphal collapse or erosion of the host cell wall was seen with SEM. Erosion of the host cell wall was seen in some ultrathin serial sections of the haustorium/host interface using trasmission electron microscopy (FIGS. 14–15), but no penetration structures or plasmodesmata were observed.
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Given the apparent specificity of G. hyalina for a Fusarium host, we studied the interaction in a more natural system. Fusarium graminearum adversely affects germination of wheat seeds (Chongo et al 2001), so we inoculated a spore suspension of G. hyalina into sterile soil in small pots containing wheat grains, either alone or in mixture with a virulent strain of F. graminearum to determine the effectiveness of G. hyalina as a biocontrol agent. After 16 d we observed no statistically significant difference in seed survival and germination, seedling root length or leaf length between experimental treatments and the control (FIG. 17). Gliocephalis hyalina was seemingly unable to protect wheat from the germination-inhibiting effects of F. graminearum, although a small but significant increase (P = 0.0073) in dry weight for plants treated with the mycoparasite was noted.
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONLITERATURE CITED |
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). The Laboulbeniales were considered phylogenetic orphans until their relationship with Pyxidiophora was discovered (Blackwell 1994, Weir and Blackwell 2001). The discovery of the relationship of G. hyalina to Pyxidiophora provides another link between the mycelial ascomycetes and the Laboulbeniales. Gliocephalis hyalina is a sister taxon of Pyxidiophora in this dataset. The placement of these taxa suggests that, although they are closely related to the Laboulbeniales, there is evidence for the separation of the Laboulbeniales, which lack hyphae, and the mycelial Pyxidiophorales. This relationship has an ecological consistency because many species of Pyxidiophora are considered mycoparasites (Lundqvist 1980, Blackwell and Malloch 1989). One species, P. lundqvistii, was discovered in cultures of Fusarium poae (Corlett 1986).
The conidiogenous cells of G. hyalina are phialides, and they are somewhat similar to those of the anamorphs of some species of Pyxidiophora (Lundqvist 1980) that have been ascribed to Thielaviopsis or Chalara. The phialides are hyaline and cylindrical and do not have the apical constriction that characterizes the phialides of some other Aspergillus-like genera. The phialides lack a well-developed collarette and conspicuous periclinal thickening. Despite the similarity in the conidiogenous cells and conidia between G. hyalina and the anamorphs of Pyxidiophora, none of the anamorphs of Pyxidiophora described by Lundqvist (1980) and Blackwell and Malloch (1989) have vesiculate conidiophores like those of G. hyalina.
The conidiophores of Gliocephalis spp. are similar to those of species of the genus Aspergillus (Matruchot 1899, Barron 1968). Species of both genera produce unbranched, aseptate conidiophores with swollen apical vesicles from which metulae and phialides develop. The genera are distinguished easily because conidia of Aspergillus species are produced in dry, basipetal chains and those of Gliocephalis spp. occur in slimy masses. The monotypic genus Goidanichiella also is similar to Gliocephalis, and the two have been confused sometimes. However, the conidiophores of Gliocephalis spp. are aseptate and hyaline, while those of Goidanichiella barronii are septate and darkly pigmented. Phylogenetic analysis confirms the significance of these characters. Aspergillus-like conidiophores have arisen several times in fungal evolution and occur in the Eurotiales (Aspergillus), Hypocreales (Escovopsis), Pyxidiophorales (Gliocephalis) and Microascales (Custingophora, Knoxdaviesia and Goidanichiella). A few remaining fungi with similar conidiophores, such as Heterocephalum aurantiacum, have uncertain phylogenetic affinities.
Mycoparasites are classified either as necrotrophic parasites or biotrophic parasites (Barnett and Binder 1973). Necrotrophic parasites destroy their hosts (Barnett and Binder 1973) but biotrophic parasites are not destructive, instead interacting with their hosts in three different ways (Barnett and Binder 1973; Hoch 1977a, b). The parasites can live inside the host cell, as in the case of some chytrids. On the other hand they can produce haustoria on the host cell or parasitism can occur through contact points on the host cell without the production of haustoria or internal hyphae (Barnett and Binder 1973; Hoch 1977a, b). We conclude from our observations that Gliocephalis hyalina is a biotrophic contact parasite of Fusarium species because it does not destroy its host. In our experiments it grew with all the Fusarium species tested but did not grow with other soil fungi. According to Gams (personal communication), a culture of G. hyalina was preserved in 1993 as CBS 642.93 in co-culture with Cylindrocarpon destructans, an anamorphic species also classified in the Nectriaceae. Therefore it is possible that the host range of G. hyalina is slightly broader than we determined, including a broader range of species in the Nectriaceae. It also might be that different strains of the species have different host preferences.
Only 10 fungal species are reported as biotrophic contact parasites, namely Melanospora zamiae Zimm., Harzia acremonioides (Harz.) Cost., Woronina pythii Goldie-Smith, Nematogonum ferrugineum (Pers.) Hughes, Calcarisporium parasiticum Barnett, Gonatobotrys simplex Corda, Gonatobotryum fuscum Sacc., Gonatorhodiella higheili Smith, Olpitrichum tenellum (Berk. & M.A. Curtis) Hol.-Jech. and Stephanoma phaeospora Butler & McCain, (Hoch 1977a, b; Hoch 1978; Walker et al 1982; Dylewski and Miller 1983; Urbasch 1986; Jordan and Barnett 1978; Li and Shen 1996). As is the case with the other contact mycoparasites, G. hyalina has no visible effect on the growth and sporulation of the host fungi. Using TEM no infection structures or penetration of the host hyphae were found, although a slight invasion of the host cytoplasm was observed in some cases (FIGS. 14–15). This is similar to the parasitic behavior of Stephanoma phaeospora, also a biotrophic contact parasite on Fusarium (Hoch 1978). Biotrophic parasites of plant pathogenic fungi might seem like promising candidates for biological control agents because of their relative specificity, but it would be difficult to produce inoculum and separate it from the host mycelium on a commercial scale. In our pot experiments G. hyalina had little detectable effect on the pathogenicity of Fusarium graminearum to wheat seedlings (FIG. 17), so its possible benefits as a bio-control agent are not obvious, at least in the assay that we used.
In this study we have shown that G. hyalina can be maintained in dual culture only by using Fusarium species as hosts among those tested. Some "unculturable’ micro-organisms detected by extracting environmental DNA (Hugenholtz et al 1998, Vandenkoornhuyse et al 2002) might be obligate biotrophs that could be isolated and propagated by growing in association with a compatible host. Gliocephalis hyalina is an example of an organism whose DNA would be considered novel if recovered from a soil sample. As mycologists continue the search for "missing fungi’ (Hyde 2001) and as ecologists explore environmental DNA, it is important to remember that sequence data are available currently for only about 10% of the fungal species now known to science and that many microfungi are known only from dried herbarium specimens for which no living cultures or DNA samples exist.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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1 Corresponding author. Current address: Department of Microbiology, University of Stellenbosch, Private Bag X1, Matieland, 7602, South Africa. E-mail: kj{at}sun.ac.za
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LITERATURE CITED |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONLITERATURE CITED |
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Barron GL. 1968. The genera of hyphomycetes from soil. Baltimore: William and Wilkins.
Barnett HL, Binder FL. 1973. The fungal host-parasite relationship. Annual Review of Phytopathology 11:273–292.[CrossRef]
Blackwell M. 1994. Minute mycological mysteries: the influence of arthropods on the lives of fungi. Mycologia 86: 1–17.[CrossRef]
———, Malloch D. 1989. Pyxidiophora (Pyxidiophoraceae): a link between the Laboulbeniales and the hyphal ascomycetes. Mem NY Bot Gard 49:23–32.
Chongo G, Gossen BD, Kutcher HR, Gilbert J, Turkington TK, Fernandez MR, McLaren D. 2001. Reaction of seedling roots of 14 crop species of Fusarium graminearum from wheat heads. Can J Plant Pathol 23:132–137.
Cole GT, Nag Raj TR, Kendrick WB. 1969. A simple technique for time-lapse photomicrography of microfungi in plate culture. Mycologia 61:726–730.[CrossRef][Medline]
———, Samson RA. 1979. Patterns of development and conidial fungi. London: Pitman Publishing.
Corlett M. 1986. Pyxidiophora lundqvistii n. sp. (Hypomycetales, Ascomycetes). Can J Bot 64:805–807.[CrossRef]
Dylewski DP, Miller CE. 1983. Systematic and host range studies of Woronina pythii (Plamodiophoromycetes) and host, Pythium species from axenic culture. Mycologia 73:412–422.
Embree RW. 1963. The status of Gliocephalis. Mycologia 55: 127, 28.[CrossRef]
Gams W, Hoekstra ES, Aproot A. 1998 CBS Course of Mycology. 4th ed. Centraalbureau voor Schimmelcultures, Baarn, Delft, Netherlands.
———, Steiman R, Seigle-Murandi F. 1990. The hyphomycete genus Goidanichiella. Mycotaxon 38:149–159.
Hawksworth DL. 1979. The lichenicolous hyphomycetes. Bull Br Mus (Nat His), Bot Ser 6:183–300.
Hoch HC. 1977a. Mycoparasitic relationships: Gonatobotrys simplex parasitic on Alternaria tenuis. Phytopathology 67:309–314.
———. 1977b. Mycoparasitic relationships. III. Parasitism of Physalospora obtusa by Calcarisporium parasiticum. Can J Bot 55:198–207.
———. 1978. Mycoparasitic relationships. IV. Stephanoma phaeospora parasitic on a species of Fusarium. Mycologia 70:370–379.[CrossRef]
Huelsenbeck JP, Ronquist F. 2001. MrBayes: Baysian inference of phylogenetic trees. Bioinformatics applications note 17:754–755.
Hugenholtz P, Goebel BM, Pace NR. 1998. Impact of culture-independent studies on the emerging phylogenetic view of bacterial diversity. J Bacteriol 180:4765–4774.
Hyde KD (ed.). 2001. Where are the missing fungi? Mycol Res 105:1422–1518.[CrossRef]
Jordan EG, Barnett HL. 1978. Nutrition and parasitism of Melanospora zamiae. Mycologia 70:301–312.
Li DC, Shen CY. 1996. Olpitrichum tenellum as a biotrophic contact mycoparasite. Can J Bot 74:2014–2016.[CrossRef]
Lundqvist N. 1980. On the genus Pyxidiophora sensu lato (Pyrenomycetes). Bot Not 133:121–144.
Matruchot ML. 1899. Notes mycologiques. I. Gliocephalis hyalina. Bull Soc Mycol France 15:254–262.
Minter DW, Kirk PM, Sutton BC. 1983. Thallic phialides. Trans Br Mycol Soc 80:39–66.
Summerell BA, Leslie JG, Backhouse D, Bryden WL, Burgess LW. 2001. Fusarium, Paul E. Nelson Symposium. American Phytopathological Society, Minneapolis.
Swofford DL. 2001. PAUP* (4.0) Phylogenetic Analysis Using Parsimony (*and other methods). Sunderland, Massachusetts: Sinauer Associates.
Tavares II. 1985. Laboulbeniales. Mycologia Mem 9:1–627.
Urbasch I. 1986. Harzia acremonioides als biotropher Kontakt-Mykoparasit an Stemphylium botryosum. [Harzia acremonioides as biotropic contact mycoparasite on Stemphylium botryosum]. J Pl Dis Prot 93:392–396.
Vandenkoornhuyse P, Baldauf SL, Leyval C, Straczek J, Young JPW. 2002. Extensive fungal diversity in plant roots. Science 295:2051.
Walker JC, Jones TG, Hedger JN. 1982. Preliminary studies on the contact mycoparasite Nematogonum ferrugineum. Trans Br Mycol Soc 78:374–378.
Weir A, Blackwell M. 2001. Molecular data support the Laboulbeniales as a separate class of Ascomycota, Laboulbeniomycetes. Mycol Res 105:1182–1190.[CrossRef]
White TJ, Bruns T, Lee S, Taylor J. 1990. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis AM, Gelfand DH, Sninsky JJ, White TJ, eds. PCR Protocols: a guide to methods and applications. San Diego, USA: Academic Press. p 315–322.
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