Caroline Zanchi
Lai Ka Lo
Reshma R
Isabel Moritz2
Joachim Kurtz
Caroline Müller- 1Animal Evolutionary Ecology Group, Institute for Evolution and Biodiversity, University of Münster, Münster, Germany
- 2Department of Chemical Ecology, Faculty of Biology, Bielefeld University, Bielefeld, Germany
Larvae of the turnip sawfly Athalia rosae are a pest of Brassicacae plants, as their feeding can cause defoliation of various crops of economic importance. The larvae and the adults of this sawfly species are known to take up different classes of chemical compounds from their respective host plants, with potentially deterrent functions against predators. In addition, compounds taken up by the adults, the clerodanoids, are known for their antimicrobial activity. These features could be a challenge to biocontrol strategies. Several natural enemies of A. rosae have been identified, targeting larval and pupal stages of A. rosae, which could potentially be used as biocontrol agents. However, targeting the adult stage of a larval pest in addition to targeting the juvenile stages may improve population control. In this study, we ask whether a strain of the entomopathogenic fungus Beauveria bassiana shows biological activity against A. rosae adults. We also investigate whether the behavior of clerodanoid uptake by the adults, which is commonly found, affects their survival in response to a B. bassiana exposure. We found a clear dose-response relationship, i.e., with increasing fungal conidia concentrations survival of A. rosae decreased. However, there was only a low incidence of mycelial growth and sporulation from A. rosae cadavers, indicating that either the fungus is not successfully developing inside this host, or it is not able to re-emerge from it. Clerodanoid uptake decreased the survival of healthy adults; however, it did not increase their survival to B. bassiana. Our results revealed that this strain of B. bassiana if applied alone is probably not suitable for biocontrol of this sawfly species, because A. rosae showed a high baseline resistance against this fungus. The behavior of clerodanoid uptake is unlikely to have evolved as a defense against this entomopathogenic fungus.
Introduction
Insect herbivores can cause tremendous losses in agriculture, when feeding as larvae or adults on diverse plant parts of crops (Zalucki et al., 2012; Sharma et al., 2017). Natural enemies of insect pests are used as effective control agents against adult as well as juvenile stages of their herbivorous hosts (Kuhar et al., 2000; Laznik et al., 2010; Boivin et al., 2012). However, most examples of biological pest control involve targeting juvenile stages of insect pests. For example, the effectiveness of the most widely used biopesticide to date, Bacillus thuringiensis, decreases with increasing developmental stage of the insect host (Glare and O’Callaghan, 2000). Likewise, baculoviruses, applied mainly against lepidopteran pest species, target larval hosts (Inceoglu et al., 2001). In many cases, juvenile stages might be more accessible to a biocontrol agent, since they are the stages which aggregate in high densities in crop fields, and have a high feeding rate (Ohnesorge, 1979; Ferro et al., 1983). Manipulating the adult population has been shown to be an effective method of reducing the damage to crops (Hunt and Vernon, 2001; Cotes et al., 2018). However, adults are often the dispersing stage and might be harder to target (Vallat and Dorn, 2005; Lombaert et al., 2006). Another obstacle to the use of parasites and pathogens against adult insect pests is that several microbial control agents, such as B. thuringiensis and baculoviruses, need to be taken up orally by species which might not feed in the adult stage or feed on a food source which might not be a suitable vector for a biocontrol agent (Glare and O’Callaghan, 2000), preventing the uptake of oral pathogens.
This setback is circumvented by entomopathogenic fungi, which infect their host by penetrating through its cuticle. In the case of Beauveria bassiana (Ascomycota: Hypocreales), the conidia attach, germinate and penetrate the cuticle of a broad range of insect hosts (Ortiz-Urquiza and Keyhani, 2013). When the hemolymph of the host is reached, the fungus differentiates into yeast-like cells called blastospores, which proliferate in the insect’s body cavity and use its nutrients. After host death, hyphae germinate, colonize host tissues, catabolize their remaining nutrients and breach the cuticle from the inside. After colonizing the insect surface and if the environmental conditions allow it, conidia will sporulate and complete the life-cycle of the fungus (Ortiz-Urquiza and Keyhani, 2013; Pedrini et al., 2013). The ease of production of B. bassiana on an industrial scale (Santa et al., 2005) as well as the fact that this is a necrotrophic parasite which needs to kill its host to complete its life-cycle made it a microorganism of interest in the context of biological control and integrated pest management (Lacey et al., 2015). However, its application in the field faces several challenges: Its speed of killing is sometimes considered as too slow to prevent significant damage to the crops by feeding insects (Inglis et al., 2001), and its lethality might also decrease as a result of environmental conditions (Rangel et al., 2008) and host defenses (Maistrou et al., 2018). Insect behavior can be an important line of defense against entomopathogenic fungi (Bonadies et al., 2019) including B. bassiana (Meyling and Pell, 2006), which might further jeopardize the success of biocontrol strategies.
The turnip sawfly, Athalia rosae (Hymenoptera: Tenthredinidae), is a feeding specialist on plants of Brassicaceae. The larvae feed on leaves and flowers (Bandeili and Müller, 2010) and can cause serious losses on crops of economic importance (Sawa et al., 1989), as they often occur in high densities, leading to complete defoliation (Riggert, 1939). The control of this pest includes the use of insecticides for coating seeds of Brassicacae, as well as for later pulverization in the field (Daniel and Ion, 2019). As an alternative or complement to chemical pesticides, several natural enemies of A. rosae have been described, including nematodes and insect parasitoids (ichneumonids, tachinids, and chalcidids), which exclusively infest the larval stages (Riggert, 1939). The adults of A. rosae feed on nectar of various plants, mostly belonging to the Apiaceae. In addition, adult males and females visit different plants of the Lamiales, on which they do not cause any visible damage but take up neo-cleradane diterpenoids (in the following called clerodanoids; Nishida et al., 2004). These compounds act as feeding stimulants (Opitz et al., 2012), but also affect the mating behavior, making particularly females more successful once they have had access to clerodanoids (Amano et al., 1999). Moreover, adults that have incorporated these compounds are better protected against diverse predators and seem to be bitter tasting (Nishida and Fukami, 1990). Thus, adults are pharmacophagous, as they take up these compounds for purposes other than nutrition, a behavior also called self-medication (Abbott, 2014). Clerodanoids isolated from different Lamiaceae are known to have antimicrobial activity in vitro (Bozov et al., 2015). However, it is to our knowledge unknown yet whether exposure to clerodanoids via uptake from leaves can also act antimicrobial in vivo.
Efforts to control the populations of A. rosae focus on egg and larval stages, probably because of their ease of collection in the field (Sáringer et al., 1996; Kamangar et al., 2010). However, controlling adults while they aggregate on plants for clerodanoid uptake and reproduction may reduce the number of ovipositing adult females on crop fields. Moreover, it is yet unknown whether entomopathogenic fungi could be an option for the control of A. rosae populations. In this study, we investigated whether B. bassiana could be a prospective biocontrol agent against adult A. rosae. Additionally, we investigated whether the lethality of the fungus is influenced by the behavior of clerodanoid uptake by the sawflies.
Materials and Methods
Insect Maintenance
Adults of the sawfly A. rosae were collected from Apiaceae in the surroundings of Bielefeld, Germany, and reared in the laboratory for several generations. Adults were provided with potted host plants of Sinapis alba for oviposition. Larvae were offered S. alba and Brassica rapa var. pekinensis for feeding. The host plants were grown in the greenhouse (about 20°C, 70% r.h., 16 h:8 h light:dark) and offered to the insects at a pre-flowering stage, when about 5–6 weeks old. The insects were kept on their host plants in large mesh cages (60 × 60 × 60 cm) at room temperature and 16 h:8 h light:dark until the last larval instar, the eonymphs, crawled into the soil. Pots with soil and eonymphs were removed to containers with a gauze-lid. Once adults emerged, they were collected and kept in groups of up to 10 adults in Petri dishes (9 cm diameter) lined with filter paper and a source of honey-water mixture (1:50) in a refrigerator until use.
Clerodanoid Exposure
Within 2 days after adult hatching, adult males and females were individually placed in small Petri dishes (5 cm diameter) lined with slightly moistened filter paper and placed at room temperature. Throughout the experiment, we did not further consider the sex of the animals but randomly distributed males and females into all treatments. They were provided with the honey-water mixture and half of the individuals were offered a small piece (1 × 1 cm) of a leaf of Ajuga reptans (Lamiaceae). Plants used for this experiment were kept outside in pots and were flowering. Adults usually start within less than 20 min to voraciously “nibble” on the leaves (Müller, personal observation) and take up clerodanoid compounds in that way (Nishida et al., 2004; Paul et al., 2021). We refer to this experimental manipulation as “exposure treatment.” After 48 h, the leaf was removed from the Petri dish and the bioassay was initiated (see below). Even though we do not have a direct quantification of the amount of compounds taken up after nibbling on the leaves, we know that nibbling on A. reptans leaves for a short time leads to qualitative changes in the chemical profiles of adults. After such exposure, adults become attractive to their conspecifics, which exhibit a nibbling behavior only on exposed but not on non-exposed conspecifics (Paul et al., 2021). We observed this behavior toward insects exposed to clerodanoids in our experiment, but not toward insects of the non-exposed treatment.
Culture of Beauveria bassiana and Condidia Suspension
A Beauveria bassiana strain (KVL 03-122) was collected from an agroecosystem in Denmark (Meyling et al., 2009) isolated from Leptoterna dolobrata (Homoptera: Miridae). It was kept at −80°C in a culture collection at University of Copenhagen before cultivation. Isolates were cultivated on quarter-strength Sabouraud Dextrose Agar + Yeast 10% (SDAY) and incubated for 10 days at 23°C to allow for sporulation. Conidia were collected by scraping the surface of the culture with a sterile loop and transferred in sterile 1 ml phosphate buffered saline (PBS) with 0.05% of Triton-X. The resulting solution was centrifuged twice at 23°C, 4000 rpm for 3.5 min and the supernatant discarded in order to remove agar and hyphae. The pellet was resuspended in 1 ml PBS/Triton-X 0.05%, and the conidia concentration assessed with a hemocytometer (Neubauer Improved). The concentration of the inoculum was adjusted through serial dilutions before exposing the adults of A. rosae.
We chose to expose the sawflies to 2.107, 2.108, and 2.109 conidia/ml. In a preliminary assay, 2.106 conidia/ml did not cause any mortality significantly different from control insects (Supplementary Figure S1). We, therefore, chose to focus our sampling efforts on the three aforementioned inoculum concentrations.
After each infection bout (replicate), the germination rate of the inoculum was assessed by plating 100 μl of a 105 conidia/ml solution on quarter strength SDAY 10% plates. After incubation for 24 h at 23°C, the germination of 3 × 100 conidia was counted to ensure that the germination rate or the inoculum was higher than 90%.
We chose the strain KVL 03-122 based on previous bioassays performed on Tenebrio molitor (Coleoptera: Tenebrionidae), which showed that KVL 03-122 was one of the most virulent strains we had access to, maybe because of its fast germination on the insect cuticle (unpublished data). Its host range is unknown but is likely to be broad, since it infects species of different orders, including beetles and mirids. Whether it has been in contact with populations of A. rosae in the field is unknown, but the ecology of B. bassiana makes the existence of an adaptation to the latter unlikely (Ortiz-Urquiza and Keyhani, 2013). Another strain, KVL 03-144, showing an intermediate virulence to T. molitor, did not cause a mortality significantly different from control animals in a preliminary experiment on A. rosae despite the relatively high concentration of the inoculum (2.108 conidia/ml, Supplementary Figure S2).
Bioassay
Adults with or without clerodanoid exposure were transferred individually from their Petri dishes to medicine cups (Carl Roth, Karlsruhe, Germany) containing 2 × 2 cm filter paper dipped in a filter-sterilized solution of honey in distilled water (1:50 v:v).
One microliter of conidia suspension of a given concentration was applied with a micropipette laterally where the legs are connected to the thorax, in order to facilitate the adsorption of the droplet during the movement of the adults. As a control, individuals received an application of PBS/Triton-X 0.05% only (referred to as “Triton” treatment). Care was taken that the whole droplet was adsorbed on the cuticle before including each individual in the experiment and closing the lid of the medicine cup. The medicine cups of a whole replicate were then kept in an incubator at 20°C and with a natural photoperiod. Every 2nd day, we transferred the individuals into a clean medicine cup with a fresh filter paper soaked in honey water. The experiments were carried out between April and May 2020. The day of inoculation was counted as day 0, and we refer to this experimental manipulation as “inoculation treatment.” Per treatment combination, between 17 and 34 individuals were set up (Table 1).
Table 1. Number of adult sawflies, which where either exposed or not to the plant Ajuga reptans, for uptake of clerodanoids, and then inoculated with different concentrations of B. bassiana conidia.
Individual sawflies were checked daily for movement, in which case, they were scored as alive. On the contrary, individuals lying at the bottom of the cup and showing no leg movement, or individuals showing a paralyzed and dehydrated look (characteristic of the death by B. bassiana) were scored as dead. Dead individuals were transferred into a new sterile medicine up and kept with a 3 × 3 cm piece of filter paper dipped in filter-sterilized distilled water, and kept in similar conditions. We checked daily for the re-emergence of the mycelium from the cadavers for 20 days.
Each fungal inoculation treatment concentration was performed twice in two separate inoculation sessions (replicates). Due to the number of insects we could obtain for each inoculation session, we could test only two concentrations simultaneously, alongside the corresponding Triton control. Therefore, the number of insects is higher in the Triton inoculation treatment.
Statistics
All statistical analyses and graphical representations were performed with the R software (R Core Team, 2013).
The survival of A. rosae when inoculated with different concentrations of conidia showed non-proportional hazards. We analyzed the survival data with an accelerated failure time model fitted for a Weibull distribution with the “survreg” function of the “survival” package (Therneau and Grambsch, 2000; Therneau, 2015). Between-group comparisons were performed using the method of contrasts (Crawley, 2007).
Regarding the proportion of sawfly individuals from which we could see mycelium germinating on the external surface of the cadaver, we analyzed presence or absence of mycelium on the cadaver with a generalized linear model (GLM) fitted for a binomial distribution, with presence or absence of mycelium being the response variable, and the clerodanoid exposure (or no exposure) and concentration of the inoculum of conidia as explanatory variables. Since the adults inoculated with Triton never showed any mycelial growth on their surface after death, we excluded them from the analysis.
For both analyses, we started with the most complex models including two-way interactions between the inoculation and the exposure treatments as well as the inoculation session as a frailty term in the survival analysis, and as a random factor. We performed model selection by comparing Akaike’s information criterion (AIC) of the full models and all possible nested models, including the null one. We kept as optimal models the ones with the lowest AICs (Akaike, 1976). The figures were made with the “ggplot2” and “survminer” packages (Wickham, 2016; Kassambara and Kosinski, 2018).
Results
Survival of Athalia rosae Adults to Beauveria bassiana KVL 03-122 and in Depedence of Clerodanoid Exposure
The mortality of the experimental sawflies population showed a clear dose response to the concentration of conidia present in the inoculum, with the longevity of the sawflies decreasing with increasing concentrations of the inoculum between the treatment groups (Figure 1; Supplementary Table S3 for post hoc comparisons).
Figure 1. Survival of Athalia rosae adults inoculated with Beauveria bassiana and depending on clerodanoid exposure. Kaplan-Meier curve showing the proportion of live individuals over 14 days of A. rosae adults inoculated with several concentrations of conidia of B. bassiana strain KVL 03-122. Orange lines: 0.05% Triton X-PBS (triton); pink lines: 2.107; blue lines: 2.108; green lines: 2.199 conidial/ml. Dashed lines represent adults allowed to take up clerodanoids (Cl) from a leaf of Ajuga reptans prior to inoculation (NonCl); survival of adults treated with Cl-triton was significantly different from those of the NonCl-triton treatment. There was no difference between survival of Cl and NonCl individuals in the other inoculation treatments with different concentrations of B. bassiana. Survival decreased with increasing concentrations of the inoculation treatment. See Supplementary Table S3 for post hoc comparisons.
The effect of clerodanoid exposure on the survival of A. rosae adults over 14 days differed depending on the inoculation with B. bassiana conidia (inoculation treatment*exposure treatment: deviance = 10.13; p = 0.018; df = 9,182). Individuals that were exposed to clerodanoids prior to inoculation with the non-infectious control (0.05% Triton X-PBS) died after a shorter time compared to those not exposed to clerodanoids. In contrast, when the individuals were inoculated with conidia of B. bassiana, there was no difference between individuals exposed to clerodanoids or not (Figure 1; Supplementary Table S3 for post hoc comparisons).
Sporulation of Beauveria bassiana From Adult Sawfly Cadavers
We found a very low incidence of mycelial growth and sporulation from cadavers of A. rosae that had been inoculated with different concentrations of conidia. The proportion of cadavers from which fungal sporulation occurred was between 10 and 26% in the different experimental groups (Figure 2). Among the adult sawflies inoculated with conidia, neither the clerodanoid exposure nor the concentration of conidia of the inoculum explained the incidence of mycelial growth on the cadavers (inoculation treatment∗exposure treatment: deviance = 2.51; p = 0.28; df = 5,119; inoculation treatment: deviance = 0.4; p = 0.82; df = 2,122; exposure treatment: deviance = 0.43; p = 0.51; df = 1,123). As expected, no mycelium germinated on the external surface of adults not exposed to conidia.
Figure 2. Mycelial colonization of the cadavers of A. rosae. Stacked bar graph representing the proportion of A. rosae cadavers showing mycelial colonization, i.e., mycosis (yes) or not (none) by B. bassiana KVL 03-122 depending on the inoculation and exposure treatments: Non-Cl, no clerodanoids exposure, Cl, clerodanoids exposure; triton, 2.107, 2.108, and 2.109 represent the inoculation control and the inoculum concentration in conidial/ml. Neither the inoculation nor the clerodanoids exposure treatments significantly affected the proportion of cadavers showing mycelial colonization.
Discussion
This study aimed at assessing the virulence of a B. bassiana strain against adult sawflies of A. rosae, which are known to expose themselves to clerodanoids in their natural environment. Manipulating both the amount of conidia the sawfly individuals received and whether or not they were allowed to take up clerodanoids enabled us to gather data on both the sawfly-fungus interaction and the potential benefit of clerodanoid uptake.
The inoculum concentrations of B. bassiana we had to use to induce mortality significantly higher than in control individuals of A. rosae were relatively high compared to lethal concentrations used in other insect-B. bassiana interactions (Maistrou et al., 2018, 2020). This indicates that adults of A. rosae have a rather high baseline resistance against this fungus. This species is indeed often confronted with entomopathogenic fungi, as the larvae bury themselves in the soil, where they pupate. Thus, also the emergence of the young adults happens in the soil, where entomopathogenic fungi are omnipresent (Clifton et al., 2015). This constant pressure could explain the evolution of a high level of constitutive resistance against such pathogens in A. rosae.
Another surprising result is that very few cadavers supported the re-emergence of our strain of B. bassiana. The mycosis developing at the surface of the insect cadaver is often used by invertebrate pathologists as a means of confirming that the insect died of the inoculated fungus instead of dying of a co-occuring opportunistic infection (Goettel and Inglis, 1997). In this context, it may seem that very few sawflies directly died of our strain of B. bassiana. However, this is unlikely, because their survival showed a clear dose-response to the concentration of conidia in the inoculum. Combined with the fact that we needed to inoculate the sawflies with a high dose of conidia, this confirms, as proposed by Maistrou et al. (2020), that the ability of one strain of B. bassiana to develop mycosis on the cadaver of the host is a fitness trait, which is correlated with other virulence traits, such as its ability to kill the host. It has been proposed that the ability to cause mycosis on the insect cadaver relies strongly on the ability to outcompete bacterial growth after host death (Fan et al., 2017). More experiments are required to explore this hypothesis in A. rosae adults in order to know whether this can explain a significant reduction in lifespan of the individuals compared to control with a low occurrence of mycosis on cadavers.
Interestingly, we observed no protective effect of the prior exposure of individual sawflies to clerodanoids, neither in the presence, nor absence of the fungus. This is an unexpected result considering that some clerodanoids show antifungal activity (reviewed by Li et al., 2016; Qing et al., 2017). The lack of a protective effect in this interaction suggests that the in vitro antimicrobial activity reported for some clerodanoids does not necessarily translate into a better protection against a potential pathogen in vivo. The activity may thus depend on the specific structure of the clerodanoids or other factors that modulate the insect’s physiology when incorporating compounds from A. reptans. There was moreover a slightly negative effect of clerodanoid uptake on survival of sawflies in the absence of fungal inoculation, as these insects showed a lower survival than the control. This corroborates results found by Kubo et al. (1982) who found insecticidal activities of two ajugarins, which are clerodanoids from Ajuga plants. Clerodanoids have been shown to affect insect physiology both by cuticular contact and feeding (Abbaszadeh et al., 2012). Thus, clerodanoid uptake may also come with some costs.
In contrast to the slightly negative effect of clerodanoids on adult survival, clerodanoid uptake has been shown to increase the mating success of female A. rosae (Amano et al., 1999), indicating a fitness benefit. A trade-off between reproduction and longevity has been observed in several insect species (Ellers, 1995; Hunt et al., 2006), and pharmacophagous uptake of plant compounds may have both costs and benefits (Erb and Robert, 2016). Moreover, in our study, the sawflies were not allowed to mate and had no opportunity to lay any eggs, as no host plant was provided. This may have affected their longevity as well. The longevity of the control animals treated with 0.05% Triton-X only was highly similar to the life-span observed for A. rosae in other studies, in which adult longevity had been investigated in dependence of the larval host plant quality (Müller and Sieling, 2006: on average 14 days; Bandeili and Müller, 2010: ranging from 9 to 17 days). Considering this relatively short adult lifespan of this species, the ability to reproduce during this time window is crucial for the individuals. Further studies should assess the effects of clerodanoid uptake on other life history traits such as fecundity and its relationship to longevity.
A negative effect of clerodanoids on the survival was not visible when the insects were inoculated with conidia, indicating that the deleterious effect of B. bassiana overwrites a potential negative effect of clerodanoids on A. rosae. In our system, we could not control for the amount of clerodanoids taken up by the adult sawflies during exposure. However, as A. rosae start within a very short time to nibble on leaves and as they had access to a leaf for 48 h, we can ensure that all insects had sufficient chance to take up clerodanoids. This was confirmed by the characteristic nibbling behavior conspecifics exhibited toward insects of the clerodanoids-exposed treatment. Adult sawflies could have either incorporated plant compounds and/or spread some over the surface of their cuticle when contacting the leaves or while cleaning themselves (Paul et al., 2021). Further experiments are needed to determine the exact location of clerodanoids in and/or on the individual sawflies.
Overall, our data suggest that the behavior of clerodanoid uptake did not evolve as a means to increase survival to an exposure to entomopathogenic fungi, at least not toward this B. bassiana strain. Since its deleterious effect on control individuals represents a cost which might be non-negligible in natural populations, we can assume that other benefits selected for the evolution and persistence of this trait in A. rosae. The above-mentioned benefit in mating and a reduction in the predation by birds and reptiles in insects which had taken up clerodanoids are some of these benefits (Nishida and Fukami, 1990).
To conclude, our study did not reveal our strain of B. bassiana to be a good candidate as a biocontrol agent of A. rosae, since it was only able to cause significant mortality at high doses. More importantly, our strain was not able to cause mycosis on the cadavers. This means that in the eventuality of a massive release of conidia of this strain on A. rosae populations, the fitness of the fungus would be almost zero, since the persistence of B. bassiana in the environment has been shown to rely mainly on conidia production (Vänninen, 1995). In case of a massive release of conidia for biocontrol, the lack of their persistence in the environment would prevent the infection of non-target species, as well as prevent the disruption of the microbial community of the soil, or select for resistance in pest populations. A suitable strategy may be to test other strains of B. bassiana in order to identify more virulent ones or some in which virulence may be decoupled from the ability to cause mycosis. Another lead would be to combine B. bassiana with cuticle-disrupting agents, like entomopathogenic nematodes or diatomaceous earth, which are known to have a synergistic effect with B. bassiana on host mortality (Barberchek and Kaya, 1990; Riasat and Wakil, 2011). These agents might increase host death without enabling the fungus to compete against bacteria after host death. Finally, the pharmacophagous uptake of clerodanoids did not reveal to improve resistance of A. rosae individuals against this fungus but may be an effective self-medication against other microorganisms and pathogens.
Data Availability Statement
The raw data supporting the conclusions of this article is provided in the Supplementary Table S4.
Author Contributions
CZ, JK, and CM conceived the experiments. CZ, LL, RR, and IM performed the experiments. CZ analyzed the data. CZ and CM wrote the manuscript, with inputs from LL, RR, and JK. CM and JK acquired funding. All authors contributed to the article and approved the submitted version.
Funding
This project was funded by the German Research Foundation (DFG) as part of the SFB TRR 212 (NC3) – project number 396777467 (granted to CM) and 396780003 (granted to JK).
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.
Acknowledgments
We thank Savina Maistrou and Nicolai Vitt Meyling for providing us with the strains and their feedback on fungal biology, and Sarah Catherine Paul for technical and conceptual help. We also thank two referees for improving this manuscript during the revision process.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphys.2021.637617/full#supplementary-material
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Keywords: Athalia rosae, Beauveria bassiana, Ajuga reptans, clerodanoids, pharmacophagy, phytochemicals, chemical ecology
Citation: Zanchi C, Lo LK, R R, Moritz I, Kurtz J and Müller C (2021) Survival of the Sawfly Athalia rosae Upon Infection by an Entomopathogenic Fungus and in Relation to Clerodanoid Uptake. Front. Physiol. 12:637617. doi: 10.3389/fphys.2021.637617
Edited by:
Everton Kort Kamp Fernandes, Universidade Federal de Goiás, BrazilReviewed by:
Letian Xu, Hubei University, ChinaSergio Angeli, Free University of Bozen-Bolzano, Italy
Copyright © 2021 Zanchi, Lo, R, Moritz, Kurtz and Müller. 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: Caroline Zanchi, caroline.zanchi@uni-muenster.de; caroline.zanchi@fu-berlin.de; Caroline Müller, caroline.müller@uni-bielefeld.de