Lichens are typically formed by the association of two partners. The fungus (mycobiont) usually comprises most of the lichen, while the photosynthetic algal or cyanobacterial partner is referred to as the photobiont. Many lichens contain more than one photobiont and other associates, the lichenicolous fungi, may also be involved. The spectrum of interactions is fascinating and ranges from mutualism, through commensalism, to situations where one, or sometimes more, of the associates is doomed by the antagonistic activities of an invading fungus. Furthermore, these interactions are dynamic over time. Many mycologists assume that once a lichen ascospore has contacted a suitable photobiont, or once a dual propagule such as a soredium, isidium or lichen fragment has landed on an appropriate surface, a lichen thallus will develop. Accepted dogma is that the thallus will grow to form a mature lichen surviving for tens, if not hundreds or even thousands of years. These are over-simplifications; in fact there is war in the world of lichens. Following a brief consideration of parasitism and other forms of symbiosis, this war will be illustrated under the headings of algal slaves, exploiters of two kingdoms, alien invaders, cosy niche seekers and take-over specialists. It is hoped that this review will encourage mycologists to study these interactions which, as yet, remain largely unexplored.

Catalase and ascorbate peroxidase enzymatic activities were examined during the interaction between Nicotiana tabacum and the arbuscular mycorrhizal Glomus mosseae. Transient enhancements of both enzymatic activities were detected in the inoculated plant roots coinciding in time with the stage of appressoria formation in the root surface. The analysis of free salicylic acid content in roots revealed that the increases in enzymatic activities were coincident in time with the accumulation of SA in inoculated roots. These data indicate that the first reaction of the root cells to the invasion of arbuscular mycorrhizal fungi is a defence response.

Accurate identification of small-spored Alternaria spp. is challenging because of morphological plasticity under non-standard conditions and the common misapplication of the name A. alternata to a variety of morphologically distinct taxa. A system used by some authors of naming phytotoxigenic alternarias as pathotypes of A. alternata has further clouded the meaning and usefulness of this specific epithet. Two hundred and sixty isolates of small-spored Alternaria, primarily from fruit substrates, were segregated into morphological groups and then subjected to RAPD-PCR analysis using total genomic DNA and three different primers. When cultured under defined conditions, the pattern of sporulation observed at 50 × magnification was predictive of genetic relatedness as determined by cluster analysis of RAPD fragment patterns. In RAPD analyses, morphological groups or species were resolved as distinct branches of the dendrogram: Alternaria gaisen (= A. kikuchiana, A. alternata Japanese pear pathotype, group 2), A. longipes (= A. alternata tobacco pathotype, group 5), the ‘tenuissima’ group (group 5), the arborescens group (group 3) and the ‘infectoria’ group (group 6). Isolates in groups for which there were only a few representatives clustered as a branch. Analysis of RAPD fragment patterns confirmed that when Alternaria isolates are cultured and observed under defined conditions, their phenotypic plasticity is minimized and valid taxonomic separations can be made upon morphological characteristics. We conclude that A. alternata, A. gaisen, A. longipes and other small-spored saprotrophic or perthotrophic taxa are recognizable as morphologically distinct taxa. We suggest that the ‘pathotype’ system of naming small-spored Alternaria taxa confers no predictive value relative to observable morphological and genetic characters, and should be abandoned.

Traditional taxonomy of aquatic hyphomycetes has been based on conidial morphology and development. Since the predominantly tetraradiate and sigmoid forms are due to convergent evolution, they are often phylogenetically non-informative. The comparison of nuclear small-subunit ribosomal DNA sequences of 30 species (22 new, eight previously published) assigned 22 to Leotiomycetes, four to Dothideomycetes, three to Sordariomycetes, and one to Orbiliomycetes. Eight species of Anguillospora were distributed among the Leotiomycetes, Dothideomycetes, and Orbiliomycetes. All three anamorphs connected with Massarina were assigned to the Pleosporales, however, Clavariopsis aquatica and Tumularia aquatica separated from Anguillospora longissima. The nSSU rDNA sequences of several species were identical (e.g. Anguillospora crassa and A. furtiva), suggesting the need to include less conservative genes for resolving such differences.

Xylaria species are common endophytes in tropical plants. It is not known, however, whether transmission of Xylaria occurs horizontally or vertically, whether individual Xylaria strains have wide host ranges or are host-specific, or how they are dispersed. We compared frequency of Xylaria endophytes in leaves and seeds of two tree species in Puerto Rico, Casuarina equisetifolia (Australian pine) and Manilkara bidentata (ausubo). These trees were chosen because they differ markedly in morphology, habitat, distribution, and origin. In C. equisetifolia Xylaria was significantly more frequent in leaves than in seeds. Xylaria was isolated from seeds of trees in inland parks, but never from seeds of trees growing on beaches. This suggests that vertical transmission of Xylaria may be possible but is not necessary for infection. In M. bidentata, Xylaria was isolated from 97% of leaves but was never isolated from seeds, suggesting that transmission is entirely horizontal. Seedlings raised in a greenhouse far from other M. bidentata trees had a level of Xylaria infection as high as seedlings in the forest, suggesting that inocula can come from other sources and endophytic strains are not host-specific.

Culture media influenced the germination of conidia, appressorial development and mycelial growth of Metarhizium anisopliae. Although the addition of KCl to Sabouraud dextrose agar (SDAM) significantly reduced germination of the conidia of three isolates in vitro and lowered germination and appressorial development on the cuticles of Myzus persicae and Meligethes aeneus, conidia grown on SDAM and minimal medium (MM) were more aggressive than conidia derived from SDA or yeast extract agar. No relationship was found between either germination or appressorial development and LT50 values, suggesting that virulence depends on the speed of infection. Calcofluor staining and lectin binding showed that culture conditions also influenced the adhesion of Metarhizium anisopliae to insect cuticles through alteration of surface carbohydrates such as 1-4-β-glucans. Dark, pigmented conidia from MM bound less lectins and calcofluor whereas the paler conidia from the other media fluoresced more intensely. Conidia from SDAM fluoresced 20-fold brighter and adhered more readily to insect cuticle compared with conidia derived from MM. Although inocula from both media showed elevated pathogenic activity against aphid and pollen beetle, MM-grown conidia were more aggressive since high mortality was induced by comparatively fewer conidia. When fluorescent intensity of calcofluor-stained conidia was compared to the number of conidia adhering to the insect cuticles, the relationship was significant, indicating that this dye has practical implications for the assessment of fungal strains in screening programmes for commercial development.

The 18S rDNA data base for mainstream Peronosporomycetes has been substantially increased. The sub-class divide between the Peronosporomycetidae and the Saprolegniomycetidae is supported. The deep clade separation of the Leptomitales within the Peronosporomycetidae is reinforced and support is provided for divergences within the Phytophthora and Pythium lines. A new family for the Leptolegnia lineage is proposed from the Saprolegniaceae sensu lato.

A saprophytic, lignin-decomposing basidiomycete fungal isolate (BB1), identified as a member of the russuloid lineage closest to the genus Peniophora, plays a role in soil aggregation and stabilization. In liquid media this fungus secretes large amounts of extracellular materials or mucilage that act as soil binding agents. We investigated the nature of these materials using periodate treatment and lectin cytochemistry, and studied whether or not these materials are involved in soil aggregation. Water stability of artificial fungal amended soil aggregates was destroyed by periodate treatment suggesting that polysaccharides produced by the basidiomycete were involved in soil aggregation. Binding patterns of fluorescently labeled lectins were also investigated to determine specific carbohydrate moieties present in the fungal mucilage. Fluorescently conjugated lectins (Ulex europaeus Agglutinin I and Lotus tetragonolobus lectin) bound to extracellular mucilage indicating that this basidiomycete mucilage contains fucosyl sugar residues. We also demonstrated that water stability of artificial soil aggregates prepared with fungal mycelia pretreated with L(−)fucose lectins were significantly reduced. This study indicates that fungal-derived material containing fucosyl residues plays a role in soil adhesion.

The diversity and vertical transmission of double-stranded (ds) RNA in Helicobasidium mompa and Rosellinia necatrix was examined by electrophoresis and Northern hybridization. These two fungi share the similar niche as root rot pathogens of trees in forests and orchards, and had diverse dsRNAs. The detection frequency of dsRNA in both fungi was different; in H. mompa, 68.4% (132 out of 193 MCGs; mycelial compatibility groups) had dsRNA, whereas 20.9% (53 out of 254 MCGs) in R. necatrix. dsRNA banding patterns and Northern blot analyses revealed the presence of various dsRNA elements in both fungi. Hyphal tip isolation was mostly unsuccessful to remove dsRNA with some exceptions. Sexual reproduction functioned to remove dsRNA in both fungi since dsRNA was not detected from single sexual spore cultures. Possible explanations for the difference in the detection frequency of dsRNA are discussed in terms of the differences in their sexual reproduction and other factors.

Fungi on submerged wood in streams are a diverse group, comprising taxa from various families. Fungal communities on submerged wood collected from Sungai Sitam in Brunei, Tai Po Kau Forest Stream in Hong Kong, and from a stream in Lipur Lentang Nature Reserve in Malaysia are reported. One hundred and forty-seven taxa were recorded. A higher species diversity including temperate and tropical species was recorded in Tai Po Kau Forest Stream in the subtropics. Ascomycetes and their asexual stages were dominant in tropical and subtropical freshwater habitats, while discomycetes were rare in these habitats. Distinct fungal communities are found on submerged wood in tropical, subtropical and temperate regions and these are discussed. Including the fungi identified in this study, over 1000 fungi has been recorded from freshwater habitats.

The colonisation intensity and composition of the mycorrhizal community in the aquatic plants Lobelia dortmanna and Littorella uniflora were studied. The mycorrhizal fungi were characterised by fungal specific nested PCR and sequencing using the 5′-end of the LSU rDNA as target. For this, primers for the clade of Acaulospora, the clade including Glomus mosseae and G. intraradices and the clade containing G. etunicatum and G. claroideum were used.

The nested PCR products were screened for different sequence types using single stranded conformation polymorphism (SSCP) and representatives for each type were sequenced. A phylogenetic analysis of the sequences showed two phylotypes of Acaulospora, one phylotype within the clade of G. etunicatum/G. claroideum and five within the G. mosseae/G. intraradices clade. The colonisation intensity was comparable to that seen in typical grassland vegetation. The neutral lipid fatty acid 16[ratio ]1ω5 was seen to be indicative of mycorrhizal colonisation with concentrations up to 35 nmol mg−1 root DW, which indicates that the fungi are active.

The widespread occurrence of vegetative incompatibility in fungi and the high level of incompatibility gene polymorphisms in fungal populations means that generally parents in a cross will be vegetatively incompatible. In Neurospora crassa the mating type locus even functions as a vegetative incompatibility locus assuring vegetative incompatibility in a cross. In this paper we have tested the effect of vegetative incompatibility on regulating transmission of mitochondrial plasmids and nuclear genes in sexual interactions of N. crassa. In the absence of mating type vegetative incompatibility between the parents, transmission of plasmids from the conidial paternal parent was found to be approximately ten times higher than in normal crosses. Control experiments in which conidia of a contaminating plasmid bearing strain of similar mating type as (and fully vegetatively compatible with) the established maternal culture were added together with the presumed paternal conidia (opposite mating type) showed plasmid transmission to ascospores. Since trichogynes do not fuse with conidia of the same mating type, it may be concluded that plasmids from the contaminating strain entered the maternal tissue by somatic fusion. The fate of conidial nuclei in such sexual interactions has been investigated as well, both under conditions of vegetative compatibility and incompatibility between the strains. These experiments demonstrated that conidia that are vegetatively compatible to the established protoperithecial strain manage to get access to the resources of the maternal culture and initiate new fruiting bodies. This type of nuclear parasitism was never observed when vegetatively incompatible conidia were used. We propose that vegetative incompatibility may function in sexual crosses to protect unfertilised cultures from looting of maternal resources.

Genetic variability within 69 biocontrol isolates of Trichoderma, obtained from different geographical locations and culture collections and selected as biocontrol agents, was studied. Sequence data, obtained from the ITS1 region of rDNA and a fragment of the translation elongation factor 1 (tef1) gene, were used in a phylogenetic analysis. Phylograms showing similar topologies were generated using alignments containing the ITS1 region or a portion of the tef1 gene. 21 distinct ITS1 sequence types and 17 distinct tef1 sequence types were identified among the 69 isolates. More than 50% of the potential biocontrol strains were grouped within Trichoderma sect. Pachybasium; of these, 81% were grouped within the cluster that included the ex-type strains of T. harzianum and T. inhamatum, and 16% were grouped with T. virens. Within T. sect. Trichoderma, which included 36% of the 69 strains, 56% were grouped with T. asperellum, and 24% with T. viride, T. atroviride or T. koningii. Only 10% of the strains studied were located in T. sect. Longibrachiatum.

About 35 Trichoderma species are currently recognised on the basis of morphological and molecular characters. Besides the role of a few of these species in biotechnology, several seem to play prominent roles in soil ecosystems. With a goal of investigating global biodiversity in Trichoderma, we report on the occurrence of Trichoderma spp. in Russia (Moscow and Ural areas), Siberia (Krasnoyarsk area) and the Himalayan mountains – areas from which no Trichoderma isolates are so far available. The ITS 1 and 2 sequence of the rDNA cluster of the 75 isolates obtained was compared with that of ex-type strains and taxonomically established isolates of Trichoderma. Thirty-nine isolates were positively identified as T. atroviride, T. virens, T. hamatum, T. asperellum, T. koningii and T. oblongisporum. A further 26 isolates yielded six closely related ITS1/2 sequence types, which are highly similar yet different from the ex-(neo)type strains of T. harzianum and T. inhamatum. Some of these genotypes (i.e. 1 and 2a) occurred only in Russia/Siberia, whereas others (2b, 3, 4 and 5) were found only in the Himalayas. RAPD analysis was consistent with these genotypes, and revealed genetic homogeneity even between strains from widely separated areas. Parsimony analysis placed these five genotypes, together with T. harzianum, T. inhamatum and the mushroom-aggressive T. harzianum ‘biotype 2’ in a large, unresolved ‘harzianum’ clade. Ten isolates were not safely alignable within known species, and five of them may be undescribed taxa: one isolate from 2700 m elevation in the Himalayas, which clustered in parsimony analysis at a basal position in section Longibrachiatum; and four isolates, displaying two closely related sequence types, forming a separate clade with T. stromaticum. The five remaining isolates also exhibited three unique ITS1 and 2 sequence patterns, but parsimony analysis placed them into the unresolved ‘harzianum’ clade, and their relationship to T. harzianum is thus unclear. The study shows that molecular screening of uninvestigated geographic areas can lead to the identification of isolates with new ITS1 and ITS2 sequence patterns, some of which may be new taxa. It also reveals that T. harzianum is at present the genetically most diverse member of the genus.

The hydrophobin SC4 was isolated from the medium of a dikaryon from Schizophyllum commune with disrupted SC3 genes. Although not glycosylated, its biophysical properties were similar to those of SC3. As the hydrophobins SC3 from S. commune and ABH1 and ABH3 from Agaricus bisporus, SC4 self-assembled at hydrophilic-hydrophobic interfaces into an SDS insoluble amphipathic film with a typical rodlet structure at its hydrophobic face, and also proved to be a powerful surfactant. Similar rodlet structures were observed in the fruiting body plectenchyma. By immunodetection SC4 could be localized lining air channels within this tissue. A similar localization was found for the ABH1 hydrophobin in fruiting bodies of A. bisporus. Probably, these hydrophobin coatings prevent collapse of air channels allowing efficient gas exchange even under wet conditions.

Phialocephala fortinii is a common root endophytic fungus with a wide geographic distribution and little, if any, host specificity. Little is known about its habitat specificity, although there is evidence to suggest that high water tables may restrict the occurrence of P. fortinii in wetlands. We tested this hypothesis by determining the distribution of P. fortinii along a sand dune – wetland complex. Isolates of P. fortinii, identified on the basis of cultural and morphological characteristics, were obtained from the roots of vascular plants across the moisture gradient. Three ‘cultural groups’ were recognized among these isolates. Thirty-three of these isolates were compared among themselves and to strains of known identity using PCR/RFLP analysis of the ITS region and a portion of the 28S subunit of rDNA. The restriction digest profiles of all isolates were identical to those of P. fortinii for 4 restriction enzymes. DNA sequences, from a subset of these strains, showed a low percent sequence divergence confirming the reliability of the RFLP data. The same analyses were done with two strains of Leptodontidium orchidicola, a culturally similar root endophyte, to ensure that this taxon was not among the transect isolates. DNA data showed a clear difference between P. fortinii and L. orchidicola but did not discriminate among cultural groups. Thus, P. fortinii showed no habitat specificity and occurred in both xeric and hydric sites. RFLP profiles and ITS sequences showed little variation among isolates of P. fortinii and among the isolates of L. orchidicola.

Strains of Colletotrichum species derived from diseased strawberry plants from a wide geographical range were studied using mitochondrial and ribosomal DNA RFLPs, and acetyl and propionyl esterase isoenzymes. Two major species aggregates were detected, centred on C. acutatum and C. gloeosporioides respectively, with significant further subdivision. There were apparent discrepancies in the hierarchical nesting of some taxon groups based on the different molecular techniques. Strains assigned to C. acutatum fell into several rDNA RFLP groups, but there was less variation in mtDNA RFLP band patterns. There appears to be at least one probably clonal population in the U.S.A. which is also present in Europe, and a less well-defined series of groups which are at least sometimes sexually reproducing. Strains assigned to C. fragariae were found not to have distinct rDNA band patterns from the teleomorph linked strains studied, which had been referred to as C. gloeosporioides. They did vary in this respect from C. gloeosporioides associated with Citrus, its type host. It was, therefore, concluded that all the strains studied with cylindrical conidia should be placed within C. fragariae, which is confirmed as separate from C. gloeosporioides and recognized as a holomorphic taxon. Nevertheless, a separate asexually reproducing infraspecific group was distinguishable using mtDNA information. An epitype is designated for C. fragariae.

To attract insects for sexual reproduction, some fungi can induce the formation of pseudoflowers on their hosts. Pseudoflowers are rosettes of yellow host leaves upon which the fungus presents gametes in sweet nectar. Eleven species of the fungus complex Uromyces pisi can induce pseudoflowers on the host Euphorbia cyparissias. The taxonomy of these species is based on the choice of the alternate host, a species of Fabaceae, as well as on teliospore morphology on the Fabaceae hosts. Morphological identification of the fungi on E. cyparissias is impossible. To identify the fungal species on infected E. cyparissias, we compared sequences from the ITS region of the rDNA to the DNA from five identified fungal species on Fabaceae. From 43 specimens on E. cyparissias, collected in 1997–99 in Switzerland, 24 specimens could be identified as U. pisi s. str. and 16 specimens as U. striatus. Two specimens were identified as U. laburni and U. loti, respectively, and one specimen could not be identified. We therefore conclude that fungal pseudoflowers are typically induced by U. pisi s. str. on U. striatus in Switzerland, although other species do sometimes occur. The ITS sequences were then used to reconstruct the phylogenetic relationship among species in the U. pisi complex and two closely related microcyclic rust species of the complex Uromyces scutellatus. Phylogenetic analyses indicated that the microcyclic species may be descendants from macrocyclic U. pisi s.l. ancestors. The ITS region sequenced in this study was found to be appropriate for answering phylogenetic, as well as ecological questions, and provided valuable markers for future studies.

To investigate the spatial and temporal diversity in the fungal community of the Dead Sea, we collected Dead Sea water samples at eight near-shore localities and at different stations offshore over a 1-year period (1999–2000). In addition, depth profiles were sampled at a deep station (304 m) in the centre of the sea. In the course of the study we obtained 476 isolates, comprising 38 species from 19 genera of Oomycota (1), Zygomycota (2), Ascomycota (13), and mitosporic fungi (3). This brings the total number of species recovered from the Dead Sea to 55. Approximately 43% of the isolates belonged to the genera Aspergillus and Eurotium. Most of the species found appeared only in winter. Fungal diversity increased near the outlets of less saline springs near the shore. The species Aspergillus terreus, A. sydowii, A. versicolor, Eurotium herbariorum, Penicillium westlingii, Cladosporium cladosporoides and C. sphaerospermum were isolated consistently and probably form a stable core of the community. The results suggest that a remarkably diverse fungal diversity may be found in the hypersaline Dead Sea waters. To what extent the fungal diversity recovered was present as dormant spores or as vegetative mycelia remains to be determined.

Phylogeny inferred from ITS DNA sequence resolved isolates of Australian Ganoderma into five terminal clades. The phylogenetic analysis was considered superior to sequence variation statistics for delineating species as intra and inter-specific variation were dissimilar across the taxa studied. The analysis also revealed that a number of isolates had been misnamed. Phylogeny inferred from the sequence data supported the retention of Elfvingia and Ganoderma as subgenera of Ganoderma, and the placement of the G. chalceum complex within subgenus Ganoderma. These findings were, however, poorly supported by decay analysis. G. adspersum, a European species considered to be a synonym of G. australe (a species which is in need of neotypification) by some authors, was not synonymous with G. australe from Australia. G. incrassatum from Northern Australia formed a clade with isolates named G. gibbosum from China and an isolate named G. australe from Taiwan. G. weberianum from Australia, originally identified by R. L. Steyaert, formed a terminal clade that was closely related to a second terminal clade comprised of two G. weberianum isolates and an isolate of G. microsporum from Asia. It was concluded that the clades represented two allopatric populations of G. weberianum and that G. microsporum was a synonym of G. weberianum. Isolates determined as G. chalceum by R. L. Steyaert and referred to here as G. cupreum formed a distinct terminal clade most closely related to material identified as G. sinense. A species mistaken for G. lucidum from Australia and Indonesia, a species from temperate and South East Asia containing commercially cultivated strains, and an Argentinean species showed evidence of allopatric speciation. Nomenclatural problems and the implications of our study on the pharmaceutical and commercial exploitation of Ganoderma in Australia are discussed.