Fungal Reproduction Research Articles

E Pluribus Unum: The Fungal Kingdom as a Rosetta Stone for Biology and Medicine.

THE Genetics Society of America's (GSA's) Edward Novitski Prize recognizes a single experimental accomplishment or a body of work in which an exceptional level of creativity, and intellectual ingenuity, has been used to design and execute scientific experiments to solve a difficult problem in genetics. The 2019 recipient is Joseph Heitman, who is recognized for his work on fungal pathogens of humans and for ingenious experiments using yeast to identify the molecular targets of widely used immunosuppressive drugs. The latter work, part of Heitman's postdoctoral research, proved to be a seminal contribution to the discovery of the conserved Target of Rapamycin (TOR) pathway. In his own research group, a recurring theme has been the linking of fundamental insights in fungal biology to medically important problems. His studies have included defining fungal mating-type loci, including their evolution and links to virulence, and illustrating convergent transitions from outcrossing to inbreeding in fungal pathogens of plants and animals. He has led efforts to establish new genetic and genomic methods for studying pathogenesis in Cryptococcus species. Heitman's group also discovered unisexual reproduction, a novel mode of fungal reproduction with implications for pathogen evolution and the origins of sexual reproduction.

Inhibitory effect and mechanism of nitric oxide (NO) fumigation on fungal disease in Xinjiang Saimaiti dried apricots

Nitric oxide (NO) is a gaseous free radical molecule that is widely used for controlling postharvest diseases in fresh fruit. However, there have been few reports on its application in dried fruit. In this study, the inhibitory effect of NO on disease in dried apricots caused by Aspergillus flavus, Aspergillus niger and Penicillium italicum was investigated both in vivo and in vitro. Furthermore, the inhibitory effect of NO and sulfur dioxide (SO2) on the three fungi was compared in vitro. NO fumigation decreased the severity of disease in dried apricots in vivo and suppressed colony expansion and mycelial growth of the three fungi in vitro in a concentration-dependent manner. The antifungal activity of NO was similar or better than that of SO2in vitro. Further, Mechanistic studies showed that NO reduced mycelium biomass, increased cell membrane permeability, destroyed plasma membrane integrity, and changed the mycelium microscopic structure. The damage of the fungal cell membrane induced by NO fumigation inhibited fungal growth and reproduction. Our results demonstrate that NO plays a critical role in controlling fungal disease in Xinjiang Saimaiti dried apricots.

Intraspecific diversity affects stress response and the ecological performance of a cosmopolitan aquatic fungus

Abstract Fungi play an important role in organic matter turnover and ensure key ecosystem services in freshwaters. The relationships between intraspecific fungal diversity and key ecological processes remain largely unknown. We examined the effects of intraspecific diversity of Articulospora tetracladia, a cosmopolitan fungal decomposer thriving on plant detritus in streams. Alder leaves were inoculated with 1 or mixtures of 2–8 fungal strains for 35 d, and leaf litter decomposition and fungal reproduction were quantified in the presence and absence of 2 mg L−1 of cadmium (Cd), a common stressor in polluted streams. Intraspecific diversity and identity affected fungal reproduction, but not leaf decomposition. Under metal stress, leaf decomposition slightly increased with intraspecific diversity. Fungal reproduction increased with intraspecific diversity and was greater in mixed assemblages, either in the absence or presence of Cd. Effect size of intraspecific diversity was higher under Cd stress for fungal reproduction, but no differences were found for leaf mass loss, with or without metal. The impacts of intraspecific diversity loss may jeopardize fungal survival and fungal functions, namely microbial leaf decomposition and leaf litter condition for invertebrate shredders in streams, particularly under metal stress.

The impact of cover crop shoot decomposition on soil microorganisms in an apple orchard in northeast China

Mowing can facilitate the incorporation of cover crop shoots into soil and improve the properties of soils in apple orchards. This article evaluated how apple orchard soil responds to the decomposition of the shoot residues of three cover crops[native mixed herbs (NMS), red clover (RCS), and ryegrass (RES)] in terms of microbial metabolism and biomass, and discussed the relationships between microbial responses and shoot chemistry. The chemical composition of shoots was analysed and a buried bag experiment was carried out to simulate shoot decomposition in an apple orchard. The results revealed significant differences in the chemical compositions and shoot C:N ratios (NMS: 10.9, RCS: 19.1, and RES: 12.9) of the three cover crops. The decomposition of the cover crop shoots promoted microbial metabolism and boosted soil bacterial reproduction (increase in the biomass indicator muramic acid: 19.44, 124.15, and 14.83 mg kg−1, respectively. But there are different types of effects on soil fungal reproduction (change in the biomass indicator glucosamine: 712.51, 887.45, and 103.97 mg kg−1), and they are obviously negative, significantly positive, and non-significant respectively. Thus, the native mixed herbs and red clover are preferable swards for better shoot enhancement in apple orchard.

A new identified suppressor of Cdc7p/SepH kinase, PomA, regulates fungal asexual reproduction via affecting phosphorylation of MAPK-HogA

The septation initiation network (SIN), composed of a conserved SepH (Cdc7p) kinase cascade, plays an essential role in fungal cytokinesis/septation and conidiation for asexual reproduction, while the mitogen-activated protein kinase (MAPK) pathway depends on successive signaling cascade phosphorylation to sense and respond to stress and environmental factors. In this study, a SepH suppressor–PomA in the filamentous fungus A. nidulans is identified as a negative regulator of septation and conidiation such that the pomA mutant is able to cure defects of sepH1 in septation and conidiation and overexpression of pomA remarkably suppresses septation. Under the normal cultural condition, SepH positively regulates the phosphorylation of MAPK-HogA, while PomA reversely affects this process. In the absence of PbsB (MAPKK, a putative upstream member of HogA), PomA and SepH are unable to affect the phosphorylation level of HogA. Under the osmostress condition, the induced phosphorylated HogA is capable of bypassing the requirement of SepH, a key player for early events during cytokinesis but not for MobA/SidB, the last one in the core SIN protein kinase cascade, indicating the osmotic stimuli-induced septation is capable of bypassing requirement of SepH but unable to bypass the whole SIN requirement. Findings demonstrate that crosstalk exists between the SIN and MAPK pathways. PomA and SepH indirectly regulate HogA phosphorylation through affecting HogA-P upstream kinases.

Whole-Genome Sequence Data Uncover Widespread Heterothallism in the Largest Group of Lichen-Forming Fungi.

Fungal reproduction is regulated by the mating-type (MAT1) locus, which typically comprises two idiomorphic genes. The presence of one or both allelic variants at the locus determines the reproductive strategy in fungi—homothallism versus heterothallism. It has been hypothesized that self-fertility via homothallism is widespread in lichen-forming fungi. To test this hypothesis, we characterized the MAT1 locus of 41 genomes of lichen-forming fungi representing a wide range of growth forms and reproductive strategies in the class Lecanoromycetes, the largest group of lichen-forming fungi. Our results show the complete lack of genetic homothallism suggesting that lichens evolved from a heterothallic ancestor. We argue that this may be related to the symbiotic lifestyle of these fungi, and may be a key innovation that has contributed to the accelerated diversification rates in this fungal group.

The Cys2His2 zinc finger protein Zfp1 regulates sexual reproduction and virulence in Cryptococcus neoformans

Cryptococcus neoformans is a ubiquitous yeast pathogen that often infects the human central nervous system (CNS) to cause meningitis in immunocompromised individuals. Although numerous signaling pathways and factors important for fungal sexual reproduction and virulence have been investigated, their precise mechanism of action remains to be further elucidated. In this study, we identified and characterized a novel zinc finger protein Zfp1 that regulates fungal sexual reproduction and virulence in C. neoformans. qRT-PCR and ZFP1 promoter regulatory activity assays revealed a ubiquitous expression pattern of ZFP1 in all stages during mating. Subcellular localization analysis indicates that Zfp1 is targeted to the cytoplasm of C. neoformans. In vitro assays of stress responses showed that zfp1Δ mutants and the ZFP1 overexpressed strains ZFP1OE are hypersensitive to SDS, but not Congo red, indicating that Zfp1 may regulate cell membrane integrity. Zfp1 is also essential for fungal sexual reproduction because basidiospore production was blocked in bilateral mating between zfp1Δ mutants or ZFP1 overexpressed strains. Fungal nuclei development assay showed that nuclei in the bilateral mating of zfp1Δ mutants or ZFP1 overexpressed strains failed to undergo meiosis after fusion, indicating Zfp1 is important for regulating meiosis during mating. Although zfp1Δ mutants showed normal growth and produced normal major virulence factors, virulence was attenuated in a murine model. Interestingly, we found that the ZFP1 overexpressed strains were avirulent in a murine systemic-infection model. Overall, our study showed that the zinc finger protein Zfp1 is essential for fungal sporulation and virulence in C. neoformans.

N6-methyladenosine RNA methylation is involved in virulence of the rice blast fungus Pyricularia oryzae (syn. Magnaporthe oryzae).

N6-methyladenosine (m6A) RNA methylation is a conserved modification of RNA in eukaryotes. Pyricularia oryzae, a filamentous phytopathogenic fungus, is the cause of a destructive rice blast disease that can lead to significant declines in rice production. Here, we characterized the function of m6A RNA methylation in the development and virulence of P. oryzae by studying four genes with functional genomics. We found that PoIme4 is an N6-adenosine-methyltransferase, and deletion of PoIME4 led to decreased levels of m6A RNA methylation. PoYth1 and PoYth2 are two m6A-binding proteins, and deletion of PoYTH2 led to reduced conidiation. Co-localization experiments showed that PoAlkb1 (an mRNA:m6A demethylase) and PoYth1 were co-localized with PoDcp1 in the processing bodies involved in mRNA decay. Virulence tests showed that PoIME4, PoALKB1, PoYTH1 and PoYTH2 were involved in virulence on rice in P. oryzae. Therefore, these experimental evidences provide new and important information about the roles of m6A RNA methylation in fungal asexual reproduction and pathogenicity.

Periphytic algae decouple fungal activity from leaf litter decomposition via negative priming.

1. Well-documented in terrestrial settings, priming effects describe stimulated heterotrophic microbial activity and decomposition of recalcitrant carbon by additions of labile carbon. In aquatic settings, algae produce labile exudates which may elicit priming during organic matter decomposition, yet the directions and mechanisms of aquatic priming effects remain poorly tested. 2. We tested algal-induced priming during decomposition of two leaf species of contrasting recalcitrance, Liriodendron tulipifera and Quercus nigra, in experimental streams under light or dark conditions. We measured litter-associated algal, bacterial, and fungal biomass and activity, stoichiometry, and litter decomposition rates over 43 days. 3. Light increased algal biomass and production rates and increased bacterial abundance 141-733% and fungal production rates 20-157%. Incubations with a photosynthesis inhibitor established that algal activity directly stimulated fungal production rates in the short-term. 4. Algal-stimulated fungal production rates on both leaf species were not coupled to long-term increases in fungal biomass accrual or litter decomposition rates, which were 154-157% and 164-455% greater in the dark, respectively. The similar patterns on fast- vs. slow-decomposing L. tulipifera and Q. nigra, respectively, indicated that substrate recalcitrance may not mediate priming strength or direction. 5. In this example of negative priming, periphytic algae decoupled fungal activity from decomposition, likely by providing labile carbon invested toward greater fungal growth and reproduction instead of recalcitrant carbon degradation. If common, algal-induced negative priming could stimulate heterotrophy reliant on labile carbon yet suppress decomposition of recalcitrant carbon, modifying energy and nutrients available to upper trophic levels and enhancing organic carbon storage or export in well-lit aquatic habitats.

Blue light exposure and nutrient conditions influence the expression of genes involved in simultaneous hyphal knot formation in Coprinopsis cinerea

Light and nutrients are crucial environmental factors influencing fungal sexual reproduction. Blue light induces simultaneous hyphal knot formation in Coprinopsis cinerea mycelia grown on low-glucose media but not in mycelia grown on high-glucose media. Many hyphal knots are visible in the arc near the edge of the colony one day after 15 min of blue light stimulation. These findings collectively suggest that blue light accelerates hyphal knot induction in nutrient-limited conditions. Transcriptome analysis revealed that gene expression after light exposure is divided into at least two major stages. In the first stage, genes coding for fasciclin (fas1), cyclopropane-fatty-acyl-phospholipid synthases (cfs1 and cfs2), and putative lipid exporter (nod1) are highly expressed after 1 h of light exposure in the mycelial region where the hyphal knot will be developed. These genes are upregulated by blue light and not influenced by glucose condition and mating. These results suggest that although some of the genes are critical for induction of the hyphal knots, they are not sufficient for hyphal knot development. In the second gene expression stage, genes encoding galectins (cgl1-3), farnesyl cysteine-carboxyl methyltransferases, mating pheromone-containing protein, nucleus protein (ich1), and laccase (lcc1) are specifically upregulated at 10–16 h after blue light exposure when the mycelia are cultivated on low-glucose media. These genes might be involved in the architecture of hyphal knots or signal transduction for further fruiting body development. These results contribute to the understanding of the effect of environmental factors on sexual reproduction in basidiomycetous fungi

Sleeping Beauties: Horizontal Transmission via Resting Spores of Species in the Entomophthoromycotina

Many of the almost 300 species of arthropod-pathogenic fungi in the Entomophthoromycotina (Zoopagomycota) are known for being quite host-specific and are able to cause epizootics. Most species produce two main types of spores, conidia and resting spores. Here, we present a review of the epizootiology of species of Entomophthoromycotina, focusing on their resting spores, and how this stage leads to horizontal transmission and persistence. Cadavers in which resting spores are produced can often be found in different locations than cadavers of the same host producing conidia. Resting spores generally are dormant directly after production and require specific conditions for germination. Fungal reproduction resulting from infections initiated by Entomophaga maimaiga resting spores can differ from reproduction resulting from conidial infections, although we do not know how commonly this occurs. Reservoirs of resting spores can germinate for variable lengths of time, including up to several months, providing primary infections to initiate secondary cycling based on conidial infections, and not all resting spores germinate every year. Molecular methods have been developed to improve environmental quantification of resting spores, which can exist at high titers after epizootics. Ecological studies of biological communities have demonstrated that this source of these spores providing primary inoculum in the environment can decrease not only because of germination, but also because of the activity of mycopathogens.

Interactive effects of dissolved nitrogen, phosphorus and litter chemistry on stream fungal decomposers.

The enrichment of ecosystems by nutrients such as nitrogen (N) and phosphorus (P) has important ecological consequences. These include effects on plant litter decomposition in forest soils and forested headwater streams, where fungi play a pivotal role. However, our understanding of nutrient relationships on fungal communities associated with decomposing litter remains surprisingly incomplete. We conducted a fully factorial microcosm experiment with known communities of fungal decomposers from streams to assess the importance of dissolved N and P supply, as well as the atomic nutrient ratio (N:P), on fungal community succession, diversity, biomass and reproduction on three leaf-litter species differing in nutrient and lignin concentrations. Fungal biomass accrual and spore production were strongly controlled by external N supply, whereas P supply was much less important. The magnitude of these effects was mediated by litter quality, with stronger effects of dissolved N and P on lignin-poor and high N:P litter. N supply also influenced fungal diversity and species composition, acting as a pacemaker of community succession. Collectively, our data indicate that N was in much greater demand than predicted by standard stoichiometric models. The most parsimonious explanation for this deviation relates to the need of litter fungi to invest large amounts of N into degradative exoenzymes.

Dung fungi as a proxy for megaherbivores: opportunities and limitations for archaeological applications

The use of spores of coprophilous fungi from sedimentary sequences as proxy evidence for large herbivore abundance has garnered pronounced attention and scrutiny over the past three decades. In response to the rapid rate at which new information is being discovered on this topic, this paper presents a brief review of the archaeological applications so far, and outlines opportunities and limitations of using Sporormiella as a proxy for herbivore abundance. Specific archaeological uses of this proxy include understanding megaherbivore extinctions and human land use patterns such as pastoralism and agriculture. We analyse how dung fungal records are formed and review the mycological literature to outline factors affecting spore reproduction and preservation. These include how strongly each commonly used dung fungal taxon relies on dung as a substrate and environmental factors affecting dung fungal reproduction and coprophilous fungi deposition. Certain laboratory preparation techniques adversely affect spore representation on pollen slides. The methods of analysis and quantification of spore records also impact our understanding. We describe good practice to increase precision of analytical methods. Due to limitations imposed by some of these factors, it is possible that an absence of dung fungi from a palaeoecological record does not imply an absence of herbivores. However, consideration of these factors and inclusion of as wide a range of coprophilous spore records as possible increases the reliability of such inferences.

Understanding photoreception in fungi and its role in fungal development with focus on phytopathogenic fungi

Like other environmental factors, light can influence various developmental processes in fungal species. Most of the fungi can respond to different wavelengths of light such as blue (475 nm), near UV (300–380 nm) and red light (650 nm). Blue light has been found to be the most associated light quality with fungal development. The most commonly investigated photoregulatory receptors in fungi are the white collar complex proteins (WC-1, WC-2) in the light oxygen voltage domain which sense and regulate the effects of blue light on fungal development and reproduction. The sequencing of several fungal genomes has led to the identification of other photoreceptor genes and their products, such as phytochromes (for red light), cryptochromes (for blue light) and blue and green light absorbing rhodopsins in some ascomycetes and basidiomycetes. Although similar types of regulatory mechanisms appear to be involved in signalling light responses in fungal species, nevertheless, there may be other hitherto undiscovered mechanisms responsible for regulating light perception. It warrants further investigations on photoreception in more fungal species including plant pathogenic fungi to better understand the underlying mechanisms controlling light perception at the metabolic level. Certain circadian rhythms have been found to play crucial role in fungal perception and adaptation to light. The information has led to the use of certain photoselective materials for control of some plant diseases.

Comparative transcriptomics of Pleurotus eryngii reveals blue-light regulation of carbohydrate-active enzymes (CAZymes) expression at primordium differentiated into fruiting body stage

Blue light is an important environmental factor which could induce mushroom primordium differentiation and fruiting body development. However, the mechanisms of Pleurotus eryngii primordium differentiation and development induced by blue light are still unclear. The CAZymes (carbohydrate-active enzymes) play important roles in degradation of renewable lignocelluloses to provide carbohydrates for fungal growth, development and reproduction. In the present research, the expression profiles of genes were measured by comparison between the Pleurotus eryngii at primordium differentiated into fruiting body stage after blue light stimulation and dark using high-throughput sequencing approach. After assembly and compared to the Pleurotus eryngii reference genome, 11,343 unigenes were identified. 539 differentially expressed genes including white collar 2 type of transcription factor gene, A mating type protein gene, MAP kinase gene, oxidative phosphorylation associated genes, CAZymes genes and other metabolism related genes were identified during primordium differentiated into fruiting body stage after blue light stimulation. KEGG results showed that carbon metabolism, glycolysis/gluconeogenesis and biosynthesis of amino acids pathways were affected during blue light inducing primordia formation. Most importantly, 319 differentially expressed CAZymes participated in carbon metabolism were identified. The expression patterns of six representative CAZymes and laccase genes were further confirmed by qRT-PCR. Enzyme activity results indicated that the activities of CAZymes and laccase were affected in primordium differentiated into fruiting body under blue light stimulation. In conclusion, the comprehensive transcriptome and CAZymes of Pleurotus eryngii at primordium differentiated into fruiting body stage after blue light stimulation were obtained. The biological insights gained from this integrative system represent a valuable resource for future genomic studies on this commercially important mushroom.

Realistic heat pulses protect frogs from disease under simulated rainforest frog thermal regimes

Abstract Recent emergences of fungal diseases have caused catastrophic global losses of biodiversity. Temperature is one of the most important factors influencing host–fungus associations but the effects of temperature variability on disease development are rarely examined. The chytrid pathogen Batrachochytrium dendrobatidis (Bd) has had severe effects on populations of hundreds of rainforest‐endemic amphibian species but we know little about the effects of rainforest‐specific host body temperature cycles on infection patterns. To address this challenge, we used body temperature regimes experienced in nature by frogs in the Australian Wet Tropics to guide a controlled experiment investigating the effects of body temperature fluctuations on infection patterns in a model host (Litoria spenceri), with emphasis on exposing frogs to realistic “heat pulses” that only marginally exceed the thermal optimum of the fungus. We then exposed cultured Bd to an expanded array of heat pulse treatments and measured parameters of population growth to help resolve the role of host immunity in our in vivo results. Infections developed more slowly in frogs exposed to daily 4‐hr heat pulses of 26°C or 29°C than in frogs in constant temperature treatments without heat pulses (control). Frogs that experienced heat pulses were also less likely to exceed infection intensities at which morbidity and mortality become likely. Ten of 11 (91%) frogs from the daily 29°C heat pulse treatment even cleared their infections after approximately 9 weeks. Cultured Bd also grew more slowly when exposed to heat pulses than in constant‐temperature control treatments, suggesting that mild heat pulses have direct negative effects on Bd growth in nature, but precluding us from determining whether there was a concurrent benefit of heat pulses to host immunity. Our results suggest that even in habitats where average temperatures may be suitable for fungal growth and reproduction, infection risk or the outcome of existing infections may be heavily influenced by short but frequent exposures to temperatures that only slightly exceed the optimum for the fungus. Our findings provide support for management interventions that promote warm microenvironments for hosts, such as small‐scale removal of branches overhanging critical habitat or provision of artificial heat sources. A plain language summary is available for this article.

Temperature modulates AgNP impacts on microbial decomposer activity

Silver nanoparticles (AgNP)s can have toxic effects on aquatic species and compromise important ecosystem processes. AgNP impacts have been the focus of much research, but their effects under different environmental contexts, such as the increase in global temperature are difficult to predict. The aim of this study was to evaluate the interactive effects of AgNPs and temperature on the activity and diversity of microbial decomposers of plant litter in streams. Litter-associated microbial communities were exposed in microcosms to increased concentrations of AgNPs (50 to 75000μgL−1) and AgNO3 (5 to 7500μgL−1) and kept for 21days at 10°C, 16°C and 23°C. Effects of AgNPs and AgNO3 were assessed based on leaf mass loss and litter-associated microbial communities by measuring microbial diversity, the activity of fungal extracellular enzymes, and fungal biomass and reproduction. Increase in temperature stimulated leaf mass loss, but not fungal biomass and reproduction. Increased AgNP and AgNO3 concentrations inhibited fungal reproduction and diversity, particularly at 23°C. Activities of the extracellular enzymes phenol oxidase and β-glucosidase were generally higher at 23°C. Microbial communities were mainly structured by AgNP and AgNO3 concentrations more than by temperature. The negative effects of nano and ionic Ag on microbial activity were more pronounced at 10 and 23°C. The behavior of AgNPs was more related to water physical and chemical characteristics (pH) than to temperature. Results highlight the importance of considering different environmental scenarios when examining NP toxicity to freshwater biota and ecosystem processes.

Phytochemical Screening and Antifungal Efficacy of Closely Related Senna obtusifolia and Senna tora on Some Phytopathogenic Fungi

The antifungal activity of crude methanolic leaf extract of closely related Senna obtusifolia and Senna tora of family Caesalpiniaceae was evaluated by growth inhibition analysis on four phytopathogenic fungi viz. Alternaria helianthii, Pythium aphanidermatum, Fusarium oxysporum and Aspergillus niger. In spite of morphological similarities, the methanolic leaf extracts of these species show qualitative and quantitative differences in their chemical profiles establishing them as two distinct chemo-types. The methanolic extract of both the species contain two or more antifungal compounds that act synergistically, inhibiting fungal growth and reproduction. Senna obtusifolia have shown better antifungal efficacy as compared to its close relative S. tora on all the fungal phytopathogens investigated. Scanning electron microscopy observations reveal that the crude methanolic extract induced shrinkage and distortion of fungal mycelium adversely affecting the development of reproductive structures. These results can be correlated with synergistic or additive effect imposed by two or more antifungal compounds present in the crude extract. Statistical analysis support the characteristic difference in antifungal efficacy of methanolic extract of these species. This difference may be due to different permutations and combinations of antifungal compounds present in the extract of these closely related species.

Fungal Volatiles Can Act as Carbon Sources and Semiochemicals to Mediate Interspecific Interactions Among Bark Beetle-Associated Fungal Symbionts.

Mountain pine beetle (Dendroctonus ponderosae) has killed millions of hectares of pine forests in western North America. Beetle success is dependent upon a community of symbiotic fungi comprised of Grosmannia clavigera, Ophiostoma montium, and Leptographium longiclavatum. Factors regulating the dynamics of this community during pine infection are largely unknown. However, fungal volatile organic compounds (FVOCs) help shape fungal interactions in model and agricultural systems and thus may be important drivers of interactions among bark beetle-associated fungi. We investigated whether FVOCs can mediate interspecific interactions among mountain pine beetle’s fungal symbionts by affecting fungal growth and reproduction. Headspace volatiles were collected and identified to determine species-specific volatile profiles. Interspecific effects of volatiles on fungal growth and conidia production were assessed by pairing physically-separated fungal cultures grown either on a carbon-poor or -rich substrate, inside a shared-headspace environment. Fungal VOC profiles differed by species and influenced the growth and/or conidia production of the other species. Further, our results showed that FVOCs can be used as carbon sources for fungi developing on carbon-poor substrates. This is the first report demonstrating that FVOCs can drive interactions among bark beetle fungal symbionts, and thus are important factors in beetle attack success.

Ethanol and phenanthrene increase the biomass of fungal assemblages and decrease plant litter decomposition in streams

Fungi, particularly aquatic hyphomycetes, have been recognized as playing a dominant role in microbial decomposition of plant litter in streams. In this study, we used a microcosm experiment with different levels of fungal diversity (species number and identity) using monocultures and combinations with up to five aquatic hyphomycete species (Articulospora tetracladia, Tricladium splendens, Heliscus submersus, Tetrachaetum elegans and Flagellospora curta) to assess the effects of ethanol and phenanthrene on three functional measures: plant litter decomposition, fungal biomass accrual and reproduction. Alder leaves were conditioned by fungi for 7days and then were exposed to phenanthrene (1mgL−1) dissolved in ethanol (0.1% final concentration) or ethanol (at the concentration used to solubilise phenanthrene) for further 24days. Exposure to ethanol alone or in combination with phenanthrene decreased leaf decomposition and fungal reproduction, but increased fungal biomass produced. All aspects of fungal activity varied with species number. Fungal activity in polycultures was generally higher than that expected from the sum of the weighted performances of participating species in monoculture, suggesting complementarity between species. However, the activity of fungi in polycultures did not exceed the activity of the most productive species either in the absence or presence of ethanol alone or with phenanthrene.