New pest management solutions are needed to control soil invertebrates (insects, nematodes, mollusks) in order to implement the goals of the European Green Deal. Natural volatile organic compounds (VOCs) such as 1-octen-3-ol and 3-octanone, emitted by the entomopathogenic fungus Metarhizium brunneum could be part of the solution. Three major crop pests, Agriotes lineatus (wireworm), Diabrotica virgifera virgifera (corn rootworm) and Phyllopertha horticola (garden chafer), were susceptible to fumigation with 1-octen-3-ol and 3-octanone. The toxicity of the VOCs was tested in soil-free arenas and in soils which differed in moisture content and porosity. The mortality rates were dependent on the interaction between the VOC treatment, dose and pest species. The insects differed in their sensitivity to these VOCs. A dose of 1.25 µl of 1-octen-3-ol applied in a closed glass tube was sufficient to kill D. v. virgifera and P. horticola in soil trials whereas 5 µl was needed to kill A. lineatus. The highest dose (20 µl) was highly toxic to all insects. Soil moisture content slightly influenced mortality rates whereas porosity had no obvious impact. The mode of action of the VOCs is unknown but the compounds are likely to cause tissue damage and loss of body fluids. This may explain the shrivelled appearance of corn rootworm and garden chafer and melanisation in wireworm. Both 1-octen-3-ol and 3-octanone show promise as biofumigants.

Inundative mass application of Metarhizium brunneum BIPESCO 5 (Hypocreales, Clavicipitaceae) is used for the biological control of Diabrotica v. virgifera (Coleoptera, Chrysomelidae). Long-term field trials were performed in three Austrian maize fields—with different cultivation techniques and infestation rates—in order to evaluate the efficacy of the treatment to control the pest larvae. In addition, the indigenous Metarhizium spp. population structure was assessed to compare the different field sites with BIPESCO 5 mass application. Annual application of the product Granmet-P^TM (Metarhizium colonized barley kernels) significantly increased the density of Metarhizium spp. in the treated soil above the upper natural background level of 1000 colony forming units per gram dry weight soil. Although a decrease in the pest population over time was not achieved in heavily infested areas, less damage occurred in treated field sites in comparison to control sites. The Metarhizium population structure was significantly different between the treated field sites. Results showed that inundative mass application should be repeated regularly to achieve good persistence of the biological control agent, and indicated that despite intensive applications, indigenous populations of Metarhizium spp. can coexist in these habitats. To date, crop rotation remains the method of choice for pest reduction in Europe, however continuous and preventive application of M. brunneum may also present an alternative for the successful biological control of Diabrotica.

The volatile organic compounds (VOCs) 1-octen-3-ol and 3-octanone produced by the entomopathogenic fungus Metarhizium brunneum are known to have pesticidal properties at high doses against a range of invertebrate pests. Very little is known about their behavior-modifying (semiochemical) properties. This study focused on investigating the behavioral responses of three subterranean crop pests, wireworm (Agriotes lineatus), western corn rootworm (Diabrotica virgifera virgifera), and garden chafer (Phyllopertha horticola), to relatively low doses of 1-octen-3-ol and 3-octanone. The behavior of wireworms and corn rootworms were slightly influenced by the VOCs, yet not significantly. Western corn rootworms appeared to be slightly attracted by 100 µl and 200 µl 1-octen-3-ol and 100 µl dose of 3-octanone, respectively but slightly repelled by the higher dose of 3-octanone. Wireworms appeared to be slightly repelled by 1-octen-3-ol and high dose 3-octanone, but slightly attracted by the 100 µl dose of 3-octanone. The VOCs had no significant impact on garden chafer. In silico studies showed that corn rootworm odorant binding proteins (OBPs) had a strong binding affinity of 1-octen-3-ol and high dose 3-octanone, indicating that these VOCs can be detected and recognized by corn rootworm. OBPs are well conserved between species; thus, wireworm and garden chafer OBPs should also be able to bind with the VOCs. Further trials will be done to confirm that VOCs could be used as semiochemicals. Appropriate formulation of the VOCs should increase their efficacy and prevent rapid dissipation of the VOCs.

The mass occurrence of the sugar beet weevil (Asproparthenis punctiventris, previously Bothynoderes punctiventris) has been endangering sugar beet cultivation in Austria for centuries. Exacerbated by climatic and political changes (warmer, drier spring and limited access to chemical pesticides), new approaches are needed to counter the problem. The aim of our work was to test whether the bioinsecticide Metarhizium brunneum Ma 43 (formerly M. anisopliae var. anisopliae BIPESCO 5/F52) can be used as a sustainable plant protection product against the sugar beet weevil. Our goal was to control the pest in all its development stages through multiple applications. Therefore, GranMet^TM-P, a granular formulation of M. brunneum Ma 43, was applied in spring to establish the fungus in the soil, whereas GranMet^TM-WP, a liquid formulation of the production strain, was used in early summer on trap ditches and leaves to target the adult weevils. Soil and plant samples as well as weevils were collected during the planting season from the trial sites to evaluate the development of the fungus and the mycosis of the treated weevils. In addition, data on hibernating weevils and their emigration from untreated field sites was collected. In all field sites, the Metarhizium spp. abundance increased above the background level (<1000 CFU g⁻¹ soil dry weight) after application of the product. With an increasing number of treatments per plot, and thus an increased contact possibility between pest and the fungus, a rise in the mycosis rate was observed. In conclusion, the various Metarhizium application strategies, which are already available or in testing, must be implemented to ensure control in both old and new sugar beet fields. Metarhizium is a further asset in the successful control of this sugar beet pest.

Due to their versatile lifestyle as saprophytes, endophytes and entomopathogens, fungi of the genera Metarhizium and Beauveria are exposed to varying illumination conditions in their natural habitats, which makes a thorough adaptation to light very likely. While the few available studies for these genera support this assumption, research in this field is still in its infancy and the data material restricted to only a few fungal species. Thus, the aim of this work was to explore how light influences growth, conidial production and secondary metabolite formation of two industrial relevant strains of M. brunneum (MA 43, formerly M. anisopliae var. anisopliae BIPESCO 5/F52) and B. brogniartii (BIPESCO 2). To achieve this, we constructed an easily adjustable illumination device for highly standardized photophysiological studies of fungi on Petri dishes, the so-called LIGHT BOX. With the aid of this device, M. brunneum and B. brongniartii were grown on S4G or S2G agar at 25°C for 14 days either in complete darkness or under constant illumination with red light (λ_peak = 635 nm), green light (λ_peak = 519 nm) or blue light (λ_peak = 452 nm). In addition, for each wavelength the effect of different illumination intensities was tested, i.e., intensities of red light ranging from 22.1 ± 0.1 to 136.5 ± 0.3 µW cm^-², green light from 16.5 ± 0.1 to 96.2 ± 0.1 µW cm^-², and blue light from 56.1 ± 0.2 to 188.9 ± 0.6 µW cm^-². Both fungi strongly responded in terms of growth, conidial production, pigmentation and morphology to changes in the wavelength and irradiation intensity. The wavelength-dependent production of the well-known secondary metabolite oosporein which is secreted by the genus Beauveria in particular, was also increased under green and blue light exposure. The established LIGHT BOX system allows not only to optimize spore production yields with these biotechnologically relevant fungi, but also allows the photobiological exploration of other fungi.