The pine needle blight pathogen Dothistroma septosporum produces a polyketide toxin, dothistromin. This paper reports that loss of the ability to produce dothistromin did not affect the pathogenicity of D. septosporum to Pinus radiata in a laboratory-based pathogenicity test. However, dothistromin synthesis provided an advantage to the D. septosporum wild-type, compared to dothistromin-deficient mutants, in growth competition with other fungi in vitro . Other pine-needle inhabitants, such as the latent pathogen Cyclaneusma minus and the endophyte Lophodermium conigenum , were inhibited by dothistromin-producing D. septosporum . Therefore, it was concluded that dothistromin is not a pathogenicity factor, but that it may play a role in competition of D. septosporum with other fungi in its ecological niche.

The most abundant metabolite of the eucalyptus leaf spot pathogen Mycosphaerella cryptica was extracted from agar cultures. The structure of the compound was elucidated by detailed studies of NMR and MS data and by comparison with derivatives. The compound is a previously undescribed diphenylether structurally related to pannaric acid found in lichens. Culture extracts from another species of Mycosphaerella isolated from the same environment yielded 5-hydroxymethylfuran-3-carboxylic acid, a furan acidic compound previously isolated from a basidiomycete fungus. Assays for bioactivity of these metabolites revealed no evidence for antimicrobial activity. Some phytotoxicity was seen on newly emerged leaves of Eucalyptus globulus, but not on juvenile or adult leaves, when treated with either metabolite.