Judith K. Pell

Fungal Biocontrol of Acari

Mites and ticks are susceptible to pathogenic fungi, and there are opportunities to exploit these micro-organisms for biological control. We have collated records of 58 species of fungi infecting at least 73 species of Acari, either naturally or in experiments. Fungal pathogens have been reported to kill representatives of all three orders of the Actinotrichida (the Astigmata, Oribatida and Prostigmata) and the Ixodida and Mesostigmata in the Anactinotrichida. Most reports concern infections in the Prostigmata, particularly in the families Tetranychidae and Eriophyidae. Two species of Acari-specific pathogens - Hirsutella thompsonii and Neozygites floridana - are important natural regulators of pestiferous eriophyoid and tetranychid mites respectively. Research has been done to understand the factors leading to epizootics of these fungi and to conserve and enhance natural pest control. Hirsutella thompsonii was also developed as the commercial product Mycar for the control of eriophyoid mites on citrus, but was withdrawn from sale in the 1980s, despite some promising effects in the field. Beauveria bassiana , Metarhizium anisopliae, Paecilomyces farinosus, Paecilomyces fumosoroseus and Verticillium lecanii infect ixodid ticks in nature, and B. bassiana and M. anisopliae are being studied as biological control agents of cattle ticks in Africa and South America. Beauveria bassiana also has potential as a mycopesticide of the two-spotted spider mite, Tetranychus urticae . There is scope to develop fungal biocontrol agents against a range of acarine pests, both as stand-alone treatments and for use in integrated pest management. Further research is required to clarify the taxonomic status of fungal pathogens of Acari, to study their ecosystem function, and to develop efficient mass production systems for species of Hirsutella and Neozygites .

Interactions Between Entomopathogenic Fungi and Other Natural Enemies: Implications for Biological Control

Pathogens and arthropod natural enemies may contribute to the suppression of insect pest populations either as individual species or as species complexes. However, because natural enemies of insects have evolved and function in a multitrophic context it is important to assess interactions within complexes of natural enemies if they are to be exploited effectively in pest management. Natural enemies can interact either synergistically/additively (e.g. enhanced transmission and dispersal of insect pathogens) or antagonistically (e.g. parasitism/infection, predation and competition). In this paper, studies assessing the potential interactions between insect and fungal natural enemies are reviewed. In general, these studies indicate the positive nature of the interactions between arthropod natural enemies and fungal pathogens with respect to the control of insect populations. More work is required to investigate further the many ways in which the natural enemy community interacts in the agroecosystem

Detection and avoidance of an entomopathogenic fungus by a generalist insect predator

Abstract.  1. Increasing evidence suggests that insects can assess their environment based on cues related to mortality risks to themselves or their offspring. Limited knowledge is available on such abilities in relation to entomopathogenic fungi, which can cause significant mortality in insect populations. In laboratory bioassays, the ability of the generalist predator Anthocoris nemorum L. (Heteroptera: Anthocoridae) to detect the presence of its natural enemy, the fungal pathogen Beauveria bassiana (Balsamo) Vuillemin (Ascomycota: Hypocreales) was investigated.

Entomopathogenic fungi and insect behaviour: from unsuspecting hosts to targeted vectors

The behavioural response of an insect to a fungal pathogen will have a direct effect on the efficacy of the fungus as a biological control agent. In this paper we describe two processes that have a significant effect on the interactions between insects and entomopathogenic fungi: (a) the ability of target insects to detect and avoid fungal pathogens and (b) the transmission of fungal pathogens between host insects. The behavioural interactions between insects and entomopathogenic fungi are described for a variety of fungal pathogens ranging from commercially available bio-pesticides to non-formulated naturally occurring pathogens. The artificial manipulation of insect behaviour using dissemination devices to contaminate insects with entomopathogenic fungi is then described. The implications of insect behaviour on the use of fungal pathogens as biological control agents are discussed.

Conservation biological control using fungal entomopathogens

Conservation biological control relies on modification of the environment or management practices to protect and encourage natural enemies that are already present within the system, thereby enhancing and improving their ability to control pest populations in a reliable way. Such strategies are only possible when based on a strong understanding of the ecology of the species concerned at the individual, community and landscape scale. Conservation biological control with entomopathogenic fungi includes the manipulation of both the crop environment and also habitats outside the crop. Further investment in conservation biological control with entomopathogenic fungi could make a substantial contribution to sustainable crop production either as stand alone strategies or, more importantly, in support of other biological and integrated pest management strategies.

Influence of Pesticide Use on the Natural Occurrence of Entomopathogenic Fungi in Arable Soils in the UK: Field and Laboratory Comparisons

The spectrum and abundance of entomopathogenic fungi in agricultural soil receiving different pesticide applications were evaluated . Seven small field plots within a barley crop were selected . Each plot had received a different pesticide treatment at slightly higher than the field rate each year for the previous 12-19 years . The field plots received either benomyl (fungicide) , triadimefon (fungicide) , aldicarb (insecticide) , chlorfenvinphos (insecticide) , glyphosate (herbicide) , all five of these pesticides or no pesticides at all (control) . Soil sampled from each plot was baited with Galleria mellonella larvae at either 18 or 26 C . Five species of entomopathogenic fungi infected these larvae . Beauveria bassiana was the dominant species , and the only species for which infection levels were high enough to be analyzed statistically . Significantly fewer G. mellonella larvae became infected with B. bassiana in soil treated with benomyl than in other treatments . This deleterious effect was confir...

Targeted Dispersal of the Aphid Pathogenic Fungus Erynia neoaphidis by the Aphid Predator Coccinella septempunctata

The potential of adult and larval C. septempunctata to vector the aphid-specific entomopathogenic fungus E. neoaphidis was assessed through a series of laboratory and field experiments. The ability of coccinellids to vector conidia from a colony of E. neoaphidis -infected pea aphids, Acyrthosiphon pisum, to a colony of uninfected A. pisum was demonstrated in a laboratory study. Adult coccinellids which had previously foraged on plants infested with different densities of sporulating cadavers (1, 5, 15, 30 cadavers per plant) initiated infection in a proportion of uninfected pea aphids (4, 0, 2 and 8%, respectively) when subsequently allowed to forage on A. pisum infested bean plants. Further laboratory studies demonstrated that fourth instar larvae and adult coccinellids artificially inoculated with conidia initiated infection in 11 and 13% of an A. pisum population in which they foraged, respectively. Furthermore, a proportion of A. pisum placed on bean plants which had previously been foraged on by inoculated larval and adult coccinellids also died from infection (3 and 10% of A. pisum, respectively). However, although coccinellid adults inoculated with conidia initiated infection in 19% of A. pisum, cereal aphids, S. avenae , exposed to the inoculated coccinellids did not become infected. A further laboratory study demonstrated that infection of A. pisum only occurred if inoculated coccinellids were transferred to A. pisum populations immediately post inoculation. However, a proportion of A. pisum placed on bean plants which had been foraged on by inoculated coccinellids transferred 0, 4 and 24 h post inoculation died from infection (9, 3 and 7%, respectively). A field study further demonstrated the potential of coccinellids to vector E. neoaphidis. Single spring sown field bean plants (Long Hoos Experimental Plots, IACRRothamsted Farm) were enclosed within nylon mesh bags and 25 adult A. pisum were added to each bag with one of the following treatments: no further addition (control), coccinellid adult (control), inoculated coccinellid adult, inoculated A. pisum or sporulating A. pisum cadavers. No aphids died of E. neoaphidis in the control treatments; 5, 16 and 33% of aphids were infected with E. neoaphidis on the other treatments, respectively.

Field and laboratory evaluation of a sex pheromone trap for the autodissemination of the fungal entomopathogen Zoophthora radicans (Entomophthorales) by the diamondback moth, Plutella xylostella (Lepidoptera: Yponomeutidae)

The effectiveness of a sex pheromone trap designed specifically to deliver conidia (infective fungal propagules) of the entomopathogenic fungus Zoophthora radicans Brefeld (Zygomycetes: Entomophthorales) to male Plutella xylostella (Linnaeus) was investigated. In field experiments in the Cameron Highlands of Malaysia, synthetic pheromone lures attracted adult males P. xylostella at all times of the day whereas lures of virgin female moths attracted males only between the hours of dusk and dawn, when females are known to produce their pheromone. Adult male moths attracted to traps baited with synthetic pheromone spent a geometric mean time of 88 seconds within the inoculation chamber, a time compatible with the period adults must spend within a shower of Z. radicans conidia produced by uniform mycelial mats in order to become infected. The field longevity of male and female P. xylostella adults was found to be similar, with individuals living for a mean time of 4.9 days. This was sufficient time for male moths to respond to the pheromone, enter the trap, become infected with Z. radicans and succumb to that infection in the field (3-3.5 days) thereby releasing infective conidia into the cabbage crop.

Dissemination of beneficial microbial agents by insects

Recent trends in pest management show an increased shift from insecticidal sprays towards the use of transgenic crops with insecticidal properties. This shift is partly due to the development of insect resistance to conventional insecticides and the large and increasing costs of developing and registering new chemicals. However, the long-term effectiveness of transgenic crops remains a hotly-debated issue. This scenario confronts and challenges entomologists to develop and evaluate other methods of pest management.

Challenges in modelling complexity of fungal entomopathogens in semi-natural populations of insects

The use of fungal entomopathogens as microbial control agents has driven studies into their ecology in crop ecosystems. Yet, there is still a lack of understanding of the ecology of these insect pathogens in semi-natural habitats and communities. We review the literature on prevalence of fungal entomopathogens in insect populations and highlight the difficulties in making such measurements. We then describe the theoretical host-pathogen models available to examine the role that fungal entomopathogens could play in regulating insect populations in semi-natural habitats, much of the inspiration for which has been drawn from managed systems, particularly forests. We further emphasise the need to consider the complexity, and particularly the heterogeneity, of semi-natural habitats within the context of theoretical models and as a framework for empirical studies. We acknowledge that fundamental gaps in understanding fungal entomopathogens from an ecological perspective coupled with a lack of empirical data to test theoretical predictions is impeding progress. There is an increasing need, especially under current rapid environmental change, to improve our understanding of the role of fungi in insect population dynamics beyond the context of forestry and agriculture.