2016-11-03T14:11:40

Entomopathogenic fungi routinely kill their hosts before releasing infectious spores, but a few species keep insects alive while sporulating, which enhances dispersal. Transcriptomics- and metabolomics-based studies of entomopathogens with post-mortem dissemination from their parasitized hosts have unraveled infection processes and host responses. However, the mechanisms underlying active spore transmission by Entomophthoralean fungi in living insects remain elusive. Here we report the discovery, through metabolomics, of the plant-associated amphetamine, cathinone, in four Massospora cicadina -infected periodical cicada populations, and the mushroom-associated tryptamine, psilocybin, in annual cicadas infected with Massospora platypediae or Massospora levispora , which likely represent a single fungal species. The absence of some fungal enzymes necessary for cathinone and psilocybin biosynthesis along with the inability to detect intermediate metabolites or gene orthologs are consistent with possibly novel biosynthesis pathways in Massospora . The neurogenic activities of these compounds suggest the extended phenotype of Massospora that modifies cicada behavior to maximize dissemination is chemically-induced.

Brachycybe (Wood) is a genus of fungivorous millipedes. To date, the fungal associates of these millipedes have never been characterized. In an attempt to resolve these relationships, culture-based approaches combined with DNA barcode sequencing were used. Sampling of 313 individuals collected from three of four B. lecontii clades and 20 sites across seven states uncovered at least 183 genera in 40 orders from four fungal phyla. At least seven putative new species were recovered in this study, despite the use of more classical culture-based approaches. Three of these fungi were phylogenetically resolved using ITS + LSU and include two new species, aff. Fonsecaea sp., Mortierella aff. ambigua, and a new genus related to Apophysomyces. Overall, the results of this study highlight the vast amount of undescribed fungal biodiversity associated with millipedes. Twelve fungal genera from nine orders showed high connectivity across the entire B. lecontii-associated fungal network, indicating a central role for these fungi in their association with these millipedes. These twelve include the two putative new species described above. The ecology of these and other fungal associates were also explored, using fungal cohort pairings and entomopathogenicity trials. Over 40% of all fungal pairings resulted in competitive interactions, a majority of which involved inhibition or overgrowth by fungi in the Hypocreales and Polyporales, respectively. The abundance of these competitive interactions in these two orders indicate differing ecological strategies. Hypocreales used chemical warfare to competitively exclude other fungi, while Polyporales physically overgrew their competitors. Mucoromycotan fungi used a similar strategy to the Polyporales. Results of a series of entomopathogenicity trials indicated that B. lecontii was less susceptible to entomopathogenic Hypocreales than an insect model (Galleria mellonella), even though these fungi are known to attack several classes of arthropods. Furthermore, the absence of a negative interaction between B. lecontii and entomopathogenic Hypocreales may indicate a beneficial relationship. When challenged with Polyporales, B. lecontii exhibited high mortality, while G. mellonella was unaffected. This stands in sharp contrast to previous casual observations of the feeding behavior of B. lecontii. Recent discoveries of previously overlooked fungal diversity have been groundbreaking and hint at substantial cryptic fungal biodiversity across the globe. The 200-300 million-year-old association between fungi and the Colobognatha, which includes Brachycybe lecontii, provides an ideal system to uncover biodiversity and examine function of these fungi in a highly understudied and ancient association.

ABSTRACT Genomic sequence data indicate that certain fungi in the genus Metarhizium have the capacity to produce lysergic acid-derived ergot alkaloids, but accumulation of ergot alkaloids in these fungi has not been demonstrated previously. We assayed several Metarhizium species grown under different conditions for accumulation of ergot alkaloids. Isolates of M. brunneum and M. anisopliae accumulated the lysergic acid amides lysergic acid α-hydroxyethyl amide, ergine, and ergonovine on sucrose-yeast extract agar but not on two other tested media. Isolates of six other Metarhizium species did not accumulate ergot alkaloids on sucrose-yeast extract agar. Conidia of M. brunneum lacked detectable ergot alkaloids, and mycelia of this fungus secreted over 80% of their ergot alkaloid yield into the culture medium. Isolates of M. brunneum, M. flavoviride, M. robertsii, M. acridum, and M. anisopliae produced high concentrations of ergot alkaloids in infected larvae of the model insect Galleria mellonella, but larvae infected with M. pingshaense, M. album, M. majus, and M. guizhouense lacked detectable ergot alkaloids. Alkaloid concentrations were significantly higher when insects were alive (as opposed to killed by freezing or gas) at the time of inoculation with M. brunneum. Roots of corn and beans were inoculated with M. brunneum or M. flavoviride and global metabolomic analyses indicated that the inoculated roots were colonized, though no ergot alkaloids were detected. The data demonstrate that several Metarhizium species produce ergot alkaloids of the lysergic acid amide class and that production of ergot alkaloids is tightly regulated and associated with insect colonization. IMPORTANCE Our discovery of ergot alkaloids in fungi of the genus Metarhizium has agricultural and pharmaceutical implications. Ergot alkaloids produced by other fungi in the family Clavicipitaceae accumulate in forage grasses or grain crops; in this context they are considered toxins, though their presence also may deter or kill insect pests. Our data report ergot alkaloids in Metarhizium species and indicate a close association of ergot alkaloid accumulation with insect colonization. The lack of accumulation of alkaloids in spores of the fungi and in plants colonized by the fungi affirms the safety of using Metarhizium species as biocontrol agents. Ergot alkaloids produced by other fungi have been exploited to produce powerful pharmaceuticals. The class of ergot alkaloids discovered in Metarhizium species (lysergic acid amides) and their secretion into the growth medium make Metarhizium species a potential platform for future studies on ergot alkaloid synthesis and modification.

The millipede Brachycybe lecontii Wood, 1864 is a fungivorous social millipede known for paternal care of eggs and forming multi-generational aggregations. We investigated the life history, paternal care, chemical defence, feeding and social behaviour of B. lecontii and provided morphological and anatomical descriptions, using light and scanning electron microscopy. Based on observations of B. lecontii from 13 locations throughout its distribution, we report the following natural history aspects. The oviposition period of B. lecontii lasted from mid-April to late June and the incubation period lasted 3–4 weeks. Only males cared for the eggs and subsequent care of juveniles was not observed. In one case, the clutches of two males became combined and they were later cared for by only one of the males. The defensive compound of B. lecontii is stored in large glands occupying a third of the paranotal volume and were observed only in stadia II millipedes and older. We observed B. lecontii feeding on fungi of the order Polyporales and describe a cuticular structure on the tip of the labrum that may relate to fungivory. We found that their stellate-shaped aggregations (pinwheels) do not form in the absence of fungus and suggest the aggregation is associated with feeding. We describe and illustrate a previously undescribed comb-like structure on the tibia and tarsi of the six anterior-most leg-pairs and measure the colour and spectral reflectance of the B. lecontii exoskeleton.