Christopher M. Wallis
Mark S. Sisterson- Crop Diseases, Pest and Genetics Research Unit, San Joaquin Valley Agricultural Sciences Center, U.S. Department of Agriculture – Agricultural Research Service, Parlier, CA, United States
Novel tactics for controlling insect pests in perennial fruit and nut crops are needed because target pests often display decreased susceptibility to chemical controls due to overreliance on a handful of active ingredients and regulatory issues. As an alternative to chemical controls, entomopathogenic fungi could be utilized as biological control agents to manage insect pest populations. However, development of field ready products is hampered by a lack of basic knowledge. Development of field ready products requires collecting, screening, and characterizing a greater variety of potential entomopathogenic fungal species and strains. Creation of a standardized research framework to study entomopathogenic fungi will aid in identifying the potential mechanisms of biological control activity that fungi could possess, including antibiotic metabolite production; strains and species best suited to survive in different climates and agroecosystems; and optimized combinations of entomopathogenic fungi and novel formulations. This mini review therefore discusses strategies to collect and characterize new entomopathogenic strains, test different potential mechanisms of biocontrol activity, examine ability of different species and strains to tolerate different climates, and lastly how to utilize this information to develop strains into products for growers.
1 Introduction
Acreage of perennial crops, including grapevines, fruit trees, and nut crops is increasing because perennial fruit and nut crops provide greater returns than field and forage crops. However, preventing pests and diseases from reducing yields in monocultures held for a decade or longer is challenging. Abundance of insect pests, and the pathogens they may transmit, may increase each season leading to a gradual decline in yields, eventually resulting in complete vineyard or orchard removal (Mustu et al., 2015). Most pest management programs rely on synthetic chemical controls. However, overreliance on a handful of active ingredients has resulted in decreased susceptibility in target pests, particularly when active ingredients are utilized repeatedly (Mustu et al., 2015; Sharma et al., 2018). In addition, regulatory agencies have called for the reduction or limitation of synthetic chemical-based pesticides due to environmental and human health concerns, and, coupled with the increased cost of developing new, safer synthetic pesticides (up to $250 million), there is an increasingly smaller variety of such products on the market (Glare et al., 2012). As a result, an increasing number of growers are turning to non-synthetic pesticides and other organic practices to serve a burgeoning market (Glare et al., 2012; Lacey et al., 2015). Therefore, there is a need to develop alternative methods to decrease pest insect populations that reduce fruit and nut crop yields.
One tactic to manage insect pests that has demonstrated some success is the use of biopesticides developed from entomopathogenic fungi (Lacey et al., 2001; Da Silva Santos et al., 2022; Irsad et al., 2023). Several entomopathogenic products are available on the market targeting a range of pests in perennial fruit and nut crops (Faria and Wraight, 2007; Da Silva Santos et al., 2022). Most currently available products involve one of four fungal genera: Beauveria (e.g. De La Rosa et al., 2000; Wraight et al., 2007a, 2007b; Keller et al., 2003; Brownbridge et al., 2006; Townsend et al., 2010), Isaria (e.g. Wraight et al., 2007b; Zimmermann, 2008; Lacey et al., 2011), Akanthomyces (formerly Lecanicillium) (e.g. Goettel et al., 2008; Kim et al., 2009), or Metarhizium (e.g. De La Rosa et al., 2000; Lomer et al., 2001; Chandler et al., 2005; Lacey et al., 2011; Jaronski and Jackson, 2012). However, formulations involving other species also have been developed such as Aschersonia aleyrodis, Conidiobolus thromboides, Hirsutella thompsonii and Nomuraea rileyi (Faria and Wraight, 2007; Lacey et al., 2015).
While commercial formulations for entomopathogenic fungi are available, including those using species in the genera Beauveria sp., Isaria sp., and Metarhizium sp., additional screening and testing is needed to identify novel virulent isolates and expand the overall diversity of described strains. Further research is warranted to clarify entomopathogenic fungi-host-microbiota interactions using modern molecular biology techniques such next-generation sequencing. Recent progress on understanding the role of environment on the effectiveness of entomopathogenic fungi, as review by Lacey et al. (2015), should continue as it will be needed to ensure overall effectiveness of products. Similarly, testing of mixtures of isolates is needed to identify synergistic effects as only a handful of studies have reported on research utilizing this approach (e.g. Spescha et al., 2023a, 2023b). Furthermore, once virulent isolates are identified, considerable testing is required to optimize formulations, application rates and methods using up-to-date research approaches. Here in this mini-review, the current state of entomopathogenic fungi research is examined, with the ultimate focus on improvement of the use of fungal biological control agents to limit abundance of insect pests in perennial crops.
2 Improving collection strategies to obtain a greater diversity of entomopathogenic fungi
Entomopathogenic fungi are typically collected from a single location at a single point in time. The procedure involves collecting the target pest, surface sterilizing bodies, and holding surface sterilized bodies on isolation medium (Da Silva Santos et al., 2022). This approach has been used to identify numerous entomopathogenic fungi that have been tested as pure strains, with studies targeting piercing-sucking insects (Brownbridge et al., 2001; Meekers et al., 2002; Cuthbertson and Walters, 2005; Nielsen and Hajek, 2005; Labbe et al., 2009; Lacey et al., 2011), chewing insects (Zimmermann, 1992; Lomer et al., 1999, 2001; De La Rosa et al., 2000; Thomas, 2000; Wraight and Ramos, 2002; Chandler and Davidson, 2005; Brownbridge et al., 2006; Dolci et al., 2006; Hajek, 2007; Moscardi and Sosa-Gomez, 2007; Townsend et al., 2010; Thakre et al., 2011), and other arthropods such as mites (Chandler et al., 2000, 2005; Wekesa et al., 2005; Abolins et al., 2007). Despite these efforts, most strains have been isolated from insect pests of non-woody host plants. However, there are a limited number of studies conducted on pests of woody plants such as those conducted by Hajek (2007) that targeted the spongy moth, Lymantria dispar. Further, many studies focus on optimizing use of entomopathogenic fungi to control pests in a contained environment such as a greenhouse, with research often on whiteflies (Aleyrodidae) and mites (Chandler et al., 2005; Labbe et al., 2009).
Recently, some entomopathogenic fungal strains have been isolated from insect pests of woody crops and tested for virulence. For instance, Beauveria bassiana, Isaria fumosorosea, Metarhizium anisopliae and/or Metarhizium robertsii strains have been identified that kill pests of grapevine including the European grapevine moth (Lobesia botrana) (Aguilera Sammaritano et al., 2018; Aguilera Sammaritano et al., 2021; Lopez Plantey et al., 2019; Beris et al., 2024), planthoppers (Moussa et al., 2021), vine mealybug (Rondot and Reineke, 2018), and grapevine aphid (Sayed et al., 2020). For orchard pests, Beauveria bassiana, Isaria fumosorosea, Metarhizium anisopliae and/or Podonectria sp. strains have been isolated from fruit flies (Goble et al., 2011), moths (Coombes et al., 2016), psyllids (Gandarilla-Pacheco et al., 2013), scale insects (Dao et al., 2016), and others (Shapiro-Ilan et al., 2003; Pereault et al., 2009).
Despite recent progress, considerable advancement is needed to realize the full potential of using entomopathogenic fungi to control pests in perennial fruit and nut crops. A concerted effort to obtain and evaluate a greater number of entomopathogenic fungi from woody perennial plants would aid in developing a more diverse collection and associated data that could be used to improve understanding about entomopathogenic fungi in many ways (Figure 1A). While studies should continue to isolate fungi directly from target pests, additional sampling to isolate fungi directly from plant tissue or the environment should also be conducted. Indeed, recent attempts to discover strains that may manage vineyard and orchard pest populations have used isolates collected from plants or the environment (often soil) (Goble et al., 2011; Lopez Plantey et al., 2019). For the former, plant tissues could be pulverized after surface sterilization, and then mixed into sterile media (Ownley et al., 2008; Da Silva Santos et al., 2022). For the latter, soil could serially diluted and plated on selective media (containing specific compounds or antibiotics) (Luz et al., 2007; Rocha and Luz, 2009). Insect baits could also be used to acquire entomopathogenic fungi from soil (Goble et al., 2010; Vega et al., 2012; Lopez Plantey et al., 2019).
Figure 1 Research needed to robustly develop entomopathogenic fungi as biopesticides: (A) collection of new strains, (B) characterizing how certain fungal strains limit insect populations, (C) examining fungal-environmental interactions, and (D) screening of strains. Colors indicate areas that are well-researched, involve emerging interest, or where research is still lacking. Note that other research efforts beyond these are needed, and overlap exists between these types of research.
Isolates are typically collected from a single growing region and climate. However, strains that can be marketed to a wider consumer base, for instance in multiple regions and climates, are more likely to be viewed as economically viable because mass production of entomopathogenic fungi can be expensive (de Faria and Wraight, 2007; Jaronski and Mascarin, 2017; Marrone, 2019). Thus, it would be useful to identify strains that could be applied across wide geographic areas, and this requires collaboration across countries and continents (Kabaluk et al., 2010).
While identifying strains that can be applied across a large geographic scale is important, optimizing control requires understanding effects of microclimate on performance of entomopathogens (Marrone, 2014; Maina et al., 2018). Because sampling at the microenvironmental scale is key to understanding interactions between strains of entomopathogenic fungi and the environment, this topic will be discussed in more detail later in this review.
3 Entomopathogenic fungi-host-microbiota interactions
Often, entomopathogenic fungi that show promise in controlled laboratory settings fail to be successful in the field or nature settings (Vega et al., 2012). Poor performance of entomopathogenic fungi could be due to environmental effects (discussed later) or due to intricate insect-fungal interactions. To better understand fungal-insect interactions, studies have been conducted to identify how fungi colonize the host insect and mechanisms of insect resistance (Da Silva Santos et al., 2022). The mechanisms that entomopathogenic fungi utilized have been well reviewed (e.g. Inglis et al., 2001; Charnley, 2003; Charnley and Collins, 2007; Ortiz-Urquiza and Keyhani, 2013; Singh et al., 2017; Ma et al., 2024). Likewise, research on insect immune response to infection has been conducted (Qu and Wang, 2018; Da Silva Sanots et al., 2022). Mechanisms that entomopathogenic fungi use to overcome insect immune response include masking colonization (Wang and Leger, 2006), possessing resistance to antifungal compounds (Lu et al., 2015), production of enzymes that better penetrate insect cuticles and tissues (Ali et al., 2010), and production of secondary metabolites that weaken host immune responses (Pal et al., 2007; Xu et al., 2017). Additional screening of metabolites for inclusion in novel formulations of biopesticides is needed as such compounds could affect insect behavior, development, or survival.
In addition to studies on how entomopathogenic fungi may act as direct predators or produce toxic metabolites that kill insects, research on the interaction of entomopathogenic fungi with the microbial community in and around the insect is needed (Figure 1B). Wei et al. (2017) observed how Beauveria bassiana interacted with insect gut microbiota in mosquito hosts to ultimately result in death. Accordingly, research to identify and describe interactions among fungal community members found in vineyard and orchard settings is warranted. Studies should focus on determining whether microbial endophytes or epiphytes of insects interact with entomopathogenic fungi to have synergistic effects. Utilizing next-generation sequencing technologies to examine insect microbiomes could greatly increase understanding of accessory microbes that work with entomopathogenic fungi to infect hosts (Gurung et al., 2019; Gupta and Nair, 2020).
4 Research to clarify environmental adaptations of fungi
Key to commercially producing and deploying entomopathogenic fungi as biopesticides is understanding how entomopathogenic fungi survive and thrive in different environments. Several studies have examined effects of environmental conditions on entomopathogenic fungi such as effects of soil composition (Milner et al., 2003; Bruck, 2005; Quesada-Moraga et al., 2007; Roy et al., 2010a, 2010b), agricultural practices (Hummel et al., 2002; Townsend et al., 2003), and the capacity of entomopathogenic fungi to grow on or in the plants that the targeted pests feed upon (Inyang et al., 1998; Ownley et al., 2004, 2010; Ugine et al., 2007a, 2007b; Olleka et al., 2009; Cory and Ericsson, 2010). The ability of entomopathogenic fungi to colonize plants is of particular interest because it may provide the opportunity to kill target pests and prevent colonization of the plant by bacterial, fungal, nematode, or viral pathogens (Cherry et al., 2005; Ownley et al., 2004; Ownley et al., 2010; Brownbridge, 2006; Quesada-Moraga et al., 2009; Kim et al., 2009; Koike et al., 2011).
Despite a collection of research focused on understanding microclimatic effects on entomopathogenic fungi and the capacity of some fungal strains to adopt different lifestyles (i.e. as an endophyte in crop plants or ability to dwell in the soil as a saprophyte), little is known about the temporal dynamics on entomopathogenic fungal populations, especially whether they peak with targeted pest populations, what the fate of the entomopathogenic fungi is during the dormant season, and how populations may flux over multiple years (Figure 1C). Most applications of entomopathogenic fungi are made in response to observations of high pest abundance (Lacey et al., 2015). Yet, with perennial crops it would be advantageous to develop entomopathogenic fungi that could colonize the vineyard or orchard for multiple years, avoiding the need for re-applications and providing a baseline level of control (Meyling and Eilenberg, 2007; Pell, 2007). Some research has been conducted on approaches to conserve entomopathogenic fungi in the environment, thereby facilitating natural epizootics (Steinkraus, 2007a, 2007b; Pell et al., 2010). Sampling throughout the year for entomopathogenic fungi in different areas of the orchard could reveal where entomopathogenic fungi dwell when their insect hosts are not present (Lacey et al., 2015). Likewise, monitoring the dynamics of applied or natural entomopathogenic fungi over years in a vineyard or orchard environment may reveal which fungi are best suited for long-term, baseline control for insect pests (Lacey et al., 2015).
5 Improving entomopathogenic fungi-based product formulations
Selecting the best entomopathogenic fungi and determining the optimal formulation to make and disperse inoculum is key for their use as biopesticides (Santoro et al., 2005; Da Silva Santos et al., 2022). Selection generally involves the following: observing fungal virulence, quantifying reproductive capacity, assessing ability to mass produce, evaluating viability during storage and application, and rating effectiveness and survival after application (Ambethgar, 2009; Lopes et al., 2011).
Methods to perform the screening described above are well established (Da Silva Santos et al., 2022). However, the advent of modern genomic approaches and next-generation sequencing presents new opportunities to not only improve selections via traditional screenings but also by providing new tools to conduct novel experiments to advance our understanding of fungal genetic diversity and assessing entire microbial communities (Figure 1D). For instance, examination of effective and less-effective strains of the same or different entomopathogenic fungi species could identify genes and quantitative trait loci that are linked to improved virulence, reproduction, and survival in vineyards or orchards. Once these genes are discovered, newly collected strains could be quickly screened to observe if desired traits are present.
A combination of entomopathogenic fungi, or other non-fungal insect pathogens may be incorporated into products, providing synergistic effects (Malusa et al., 2021; Spescha et al., 2023a, 2023b). Knowledge about which microorganisms naturally co-occur in the environment is key to determining which microorganisms may need to be included together in a final product designed to have persistent, long-term control. Indeed, this has been attempted on several occasions with studies targeting soil pests (Bueno-Pallero et al., 2018; Spescha et al., 2023a), greenhouse pests (Shapiro-Ilan et al., 2004), and moths (Wang et al., 2021). Using next-generation sequencing of genomic DNA extracted from insect pests, crop plants, and the environment may reveal species that naturally co-occur, suggesting consideration for inclusion in a multiple-microorganism biopesticide formulation (Spescha et al., 2023b).
In addition to combinations of microorganisms, formulations of biopesticides could also contain biorational or other compounds, produced naturally by fungal isolates, to improve pest control. Such compounds could be identified via metabolomics studies of the different entomopathogenic fungi or associated fungi/microorganisms, and then added to the formulations for improved control (Berestetskiy and Hu, 2021). Accordingly, research should aim to isolate and identify metabolites from entomopathogenic fungi that possess insecticidal activity, via chromatography-based techniques such as those described by Elbanhawy et al. (2019) that analyzed methanolic extracts and quantified specific fatty acids. Follow-up research to then mass-produce and incorporate metabolites into biopesticide formulations would then need to occur.
6 Conclusions
Decreased effectiveness of overused insecticides and regulatory issues make controlling many insect pests in perennial crops challenging. Entomopathogenic fungal products provide an alternative strategy that could be integrated into management programs. Recent advances in genomics, proteomics, and metabolomics provide important tools that can be leveraged to identify useful strains and synergistic interactions.
Author contributions
CW: Writing – original draft, Writing – review & editing. MS: Writing – review & editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The work was supported in part via funds allocated to the U.S. Department of Agriculture – Agricultural Research Service projects #2034–22000-014–00D and #2034–22000-015–00D.
Acknowledgments
Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture. USDA is an equal opportunity provider and employer.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
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Keywords: biological control, entomopathogenic fungi, Beauveria spp., Metarhizium spp., grapevine, citrus, Prunus spp.
Citation: Wallis CM and Sisterson MS (2024) Opportunities for optimizing fungal biological control agents for long-term and effective management of insect pests of orchards and vineyards: a review. Front. Fungal Biol. 5:1443343. doi: 10.3389/ffunb.2024.1443343
Received: 03 June 2024; Accepted: 18 July 2024;
Published: 01 August 2024.
Edited by:
Jose Luis Ramirez, United States Department of Agriculture (USDA), United StatesReviewed by:
Seema Ramniwas, Chandigarh University, IndiaCopyright © 2024 Wallis and Sisterson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Christopher M. Wallis, Y2hyaXN0b3BoZXIud2FsbGlzQHVzZGEuZ292