In invertebrates, the cuticle is the first and major protective barrier against predators and pathogen infections. While immune responses and behavioral defenses are also known to be important for insect protection, the potential of cuticle-associated microbial symbionts to aid in preventing pathogen entry during molting and throughout larval development remains unexplored. Here, we show that bacterial symbionts of the beetle Lagria villosa inhabit unusual dorsal invaginations of the insect cuticle, which remain open to the outer surface and persist throughout larval development. This specialized location enables the release of several symbiont cells and the associated protective compounds during molting. This facilitates ectosymbiont maintenance and extended defense during larval development against antagonistic fungi. One Burkholderia strain, which produces the antifungal compound lagriamide, dominates the community across all life stages, and removal of the community significantly impairs the survival probability of young larvae when exposed to different pathogenic fungi. We localize both the dominant bacterial strain and lagriamide on the surface of eggs, larvae, pupae, and on the inner surface of the molted cuticle (exuvia), supporting extended protection. These results highlight adaptations for effective defense of immature insects by cuticle-associated ectosymbionts, a potentially key advantage for a ground-dwelling insect when confronting pathogenic microbes.
Fungal pathogens are important natural enemies of insects and exert strong selective pressures on populations in both natural and agricultural settings [1, 2]. Adhesion and germination of entomopathogens on the insect surface is followed by direct penetration of the cuticle and secretion of toxins, attacking a major protective barrier of insects . In response, insects have evolved diverse defense mechanisms including elaborate immune responses, as well as behavioral, mechanical, and chemical defenses [4, 5]. While animals can often produce defensive compounds themselves, there is growing evidence that associated microorganisms can support protection against fungi and other enemies [6, 7]. Symbiotic microbes inhibit fungal infections in aphids [8, 9], eggs of Lagria beetles [10, 11], immature life stages of solitary wasps [12,13,14], fruit moths , and leaf-rolling weevils , as well as the nutritional resources of ants [17,18,19], termites  and ambrosia-beetles . Although numerous compounds produced by defensive symbionts have been identified [6, 22,23,24], there are only a few systems in which these have been spatially tracked [25,26,27,28], since their quantification and detection in situ remains challenging.
Symbiont-mediated defense might be especially important for animals with temporarily limited protection mechanisms, like insects with complete metamorphosis, in which the distinct life stages —adult, egg, larva, pupa— face different challenges and demand specific defense strategies. Eggs are particularly susceptible to predation, parasitism, and pathogen infection since behavioral defenses are limited by the lack of mobility . In Lagria villosa beetles, fungal infections are prevented by Burkholderia symbionts on the eggs, which produce different antimicrobial compounds [10, 11]. A similar strategy has been observed in squids , hoopoe birds , and lizards , indicating that egg protection through beneficial microorganisms has evolved in different environments for invertebrate and vertebrate hosts .
Insect larvae and pupae also face high infection risks, as they often inhabit pathogen-rich environments like soil or the phyllosphere. The leaf-rolling weevil Euops chinensis increases the survival of its larval offspring in leaf cradles by depositing the symbiotic fungus Penicillium herquei with the eggs . Also in solitary beewolf wasps, antibiotic-producing Streptomyces bacteria are incorporated into the cocoon silk protecting the pre-pupa from mold fungi [12, 13]. Therefore, symbiont-mediated defense might be a common defense strategy for immature stages. The localization of microbial symbionts on the host surface or in connection to the external environment could be especially convenient to prevent infections. Cuticle-associated host defenses, including melanization [34, 35] and immune factors in the molting fluid [36, 37] might be thus complemented by ectosymbionts. However, immature insects recurrently shed their cuticle during development, which has both advantages and potential risks. Molting can clear out detrimental but also beneficial microbes from the surface, and it might lead to temporal vulnerability to antagonists until a fully sclerotized and melanized cuticle is reestablished [38, 39]. While these tradeoffs are likely common across many invertebrates that shed their cuticle, research on defense strategies during molting phases is lacking.
In L. villosa beetles (Coleoptera: Tenebrionidae), ectosymbionts with high bioactive potential are associated with the insect throughout immature life stages [10, 11, 40] (Fig. 1a). This polyphagous beetle originates from sub-Saharan Africa and was introduced to South America, where it is found on several crop plants. Adults feed on leaves and flowers, while the larvae are mostly detritivorous . Hence, L. villosa beetles occur in soil and around decaying plant material, where they deposit eggs, and the larvae feed, molt (Fig. 1b, c), pupate (Fig. 1d), and emerge as adults, demanding effective defense mechanisms against a variety of potential pathogens throughout their lifetime. Concordantly, the beetles harbor a community of bacterial symbionts including several strains of Burkholderia gladioli (Gamma-Proteobacteria, previously Beta-Proteobacteria), which are vertically transmitted from female accessory glands onto the egg surface during oviposition [10, 40]. Multiple strains can infect the beetles, and at least two, B. gladioli Lv-StA and B. gladioli Lv-StB (henceforth “Lv-StA” and “Lv-StB”, respectively), are capable of producing antimicrobial compounds that inhibit fungal growth on the beetle eggs [10, 11]. Under field conditions, Lv-StB is consistently present in high abundance within female accessory glands and on the egg surface, where it is important for defense presumably by producing the antifungal polyketide lagriamide . The symbionts are absent in male adults but are present in both female and male larvae in the related species L. hirta , where they are housed as ectosymbionts in peculiar dorsal cuticular invaginations formed during embryonic development and so far described only in this insect genus .
Given the localization of the ectosymbionts in larvae in cuticle-lined organs of both sexes, we reasoned that, in addition to egg defense and transmission to the next generation, symbiont presence during larval development may be associated with the protection of molting stages. To test this, we investigated the functional role of antibiotic-producing B. gladioli symbionts in larvae and pupae of L. villosa beetles by (i) evaluating symbiont function in larval and pupal stages via bioassays against antagonistic fungi, (ii) characterizing and localizing the symbiont community in all life stages through 16 S rRNA gene amplicon sequencing, qPCR and FISH, and (iii) quantifying and localizing the bioactive secondary metabolite lagriamide in situ and monitoring its biosynthesis during development using high-performance liquid chromatography mass spectrometry (HPLC-MS) and mass-spectrometry imaging with a high-resolution atmospheric pressure scanning microprobe (AP-SMALDI-HR MSI). Thereby, we show prolonged antibiotic-mediated defense provided by a Burkholderia bacterial symbiont during the immature life stages of the beetles and highlight the symbiotic organs as unique host morphological adaptations that support the protective association.
Symbiont-mediated defense against entomopathogens in early larval and pupal stages
To assess the potential protective function of the symbionts after egg hatching, we carried out bioassays exposing larvae to different pathogenic fungi and monitored survival and fungal growth (Table S1). We evaluated the first days of larval development covering multiple molting events since freshly molted larvae are likely more susceptible to infections . First, we exposed young larvae to a fungal pathogen previously isolated from L. villosa beetles, Purpureocillium lilacinum . In these conditions, aposymbiotic larvae were less likely to survive compared to symbiotic individuals including those that were untreated, reinfected with the natural symbiont community recovered from eggs, or with the culturable symbiont strain Lv-StA (Fig. 2a, Table S2, Cox mixed effects model, p values: untreated: 0.0017, reinfected-egg wash: <0.001, reinfected-StA 0.023), while there was no significant difference between untreated and reinfected larvae (Table S2, p value: 0.2). In a second assay, we focused on the natural symbiont community dominated by Lv-StB and tested its protective effect against two generalist entomopathogens—Beauveria bassiana and Metarhizium anisopliae– applying fungal titers comparable to amounts of fungal conidia in other studies and agricultural applications of entomopathogens [45,46,47] or natural soil [48, 49]. Because there was no difference between untreated larvae and larvae reinfected with the natural community in the previous assay, we compared symbiont-free larvae to reinfected larvae in the following assays, controlling for the surface-sterilization procedure . To rule out the possibility that symbiotic larvae survived better because of a nutritional benefit by the symbionts, we added a control group that was not exposed to fungi. Again, when exposed to B. bassiana or M. anisopliae, symbiotic larvae were more likely to survive compared to aposymbiotic larvae (Fig. 2b, Table S3, Cox mixed effects model, p values: B. bassiana: 0.0028, M. anisopliae: 0.026). While the tested M. anisopliae strain was overall more virulent than that of B. bassiana and symbiont-conferred protection was weaker against M. anisopliae (Fig. 2b), the probability of fungal growth was significantly lower in symbiotic individuals for both fungi (Fig. 2c, Table S4, Cox mixed effects model, p values: B. bassiana: <0.001, M. anisopliae: <0.001), in line with a broad-spectrum defense. There were no differences in survival between symbiotic and aposymbiotic larvae in the absence of pathogenic fungi.
To test if symbionts can also protect pupae, we exposed aposymbiotic and symbiotic individuals directly after pupation to fungi and used two set-ups (Table S1). One set-up used a combination of different fungi (fungus-mix: P. lilacinum, B. bassiana, M. anisopliae) which was applied to the environment and the other set-up used a topical application of M. anisopliae conidia onto the dorsal thorax of pupae. When we exposed pupae to the fungus-mix or only to M. anisopliae, there was no difference in emergence rate (Fig. S1a) or survival of adults after emergence between the treatments (Fig. S1b, c). However, we observed melanization spots on the pupal surface, likely as a reaction to fungi, which was significantly higher in aposymbiotic individuals infected with M. anisopliae (Fig. S1d, Cox proportional hazards regression model, p value = 0.037). Additionally, we observed a higher probability of visible fungal growth on pupae infected with M. anisopliae (Fig. S1e, Cox proportional hazards regression model, p value = 0.012). Although adult emergence rate and survival after emergence were not different between both groups infected with fungi (aposymbiotic and untreated), all emerged adults died within eight days (Fig. S1c) which is not expected given the usual longevity in absence of fungal infections (Fig. 1). This might be due to the high exposure to the pathogen, and/or the gradual decline in Lv-StB titers under laboratory conditions, which has been previously documented [40, 50]. Foreseeing this problem, we maintained the symbiotic individuals on soil and live plants, which decreases the risk of symbiont loss . However, only three out of five female pupae tested before the experiment still carried Burkholderia spp., and none of the adults that emerged (Fig. S1f). In summary, the natural symbiont community present in the dorsal organs and on the insect’s surface inhibited fungal infections in young larvae and pupae and increased the chances of larval survival in the presence of fungal pathogens.
Symbiont strain Lv-StB is maintained in special dorsal cuticle invaginations and becomes dominant during L. villosa development
To evaluate if protection in larval and pupal stages is mediated by the same symbionts as previously described in eggs, we investigated the bacteria associated to field-collected L. villosa individuals and tested whether Lv-StB dominates the community beyond the egg stage (Fig. 1a). As in female glands and on the egg surface , Burkholderiaceae were consistently present in larvae and pupae (Fig. S2a). While Enterobacteriaceae and Rhizobiaceae were also predominant in larvae, the profiles correspond to the full body, and these are therefore most likely associated with the gut. As observed directly by in situ localizations using microscopy, Burkholderia is present and becomes dominant in the dorsal structures of older larvae (Fig. S3). Lv-StB is particularly predominant in the community, being present in 95% of the samples and showing the highest relative abundance among Burkholderia ASVs (Amplicon Sequence Variants) in 82% of the 58 samples (Fig. 3a). The three individuals in which Lv-StB was not detected showed high relative titers of the ASV assigned to the culturable strain B. gladioli Lv-StA, or a closely related ASV (Fig. 3a, Fig. S2b). In early larvae, Lv-StB was present in very low abundance, judging from the absolute read counts in these samples (Fig. S2b) and FISH (Fig. S3a–c). While this might result from a bottleneck during vertical transmission or natural variation among individuals, we cannot rule out that the low titers are associated with laboratory conditions, since Burkholderia symbionts are often lost during controlled rearing [40, 50]. To identify potential differences in absolute symbiont abundance at a fine temporal scale during development, we quantified Lv-StB symbiont titer using qPCR across larval and pupal stages. Additionally, we considered both field-collected and laboratory-raised individuals for the life stages in which this was feasible (Fig. 3b). The mean abundances of Lv-StB copy numbers were the highest in females and tended to decrease in laboratory-raised individuals as host development advanced. As expected , Lv-StB titers of later timepoints were higher in field-collected individuals than in laboratory-raised individuals. Taken together, the results suggest that Lv-StB is the dominant Burkholderia strain across larval development and is consistently present throughout the life cycle (Fig. 3a). Additional involvement of other bacteria in protection is also possible, given the consistent presence of specific groups, albeit in lower relative abundance in symbiotic organs.
To localize Lv-StB in each life stage and further assess its dominance within the symbiotic organs, we carried out fluorescence in situ hybridization (FISH) with specific probes targeting this strain (Figs. S4, S5) on histological sections throughout host development (Fig. 4). After symbionts are transmitted from female accessory glands (Fig. 4a) to the egg surface (Fig. 4b), embryos develop three equally sized organs located dorsally, which likely originate as invaginations of the cuticle. From the first larval instar on (L1, Fig. 4c), the pouches are filled with symbionts. These peculiar organs remain open to the outside through a small cuticle-lined canal and are maintained throughout larval development, increasing in size as the insect grows  (Fig. 4d, e). In female pupae, symbionts can be found in the first dorsal pouch (Fig. 4f) and on the surface of the head region between bristles (Fig. 4g). To evaluate if ectosymbionts are released from the pouches, we carried out FISH on whole exuviae of the first (L1) and last larval instar (larva-to-pupa molt). We detected Burkholderia symbionts on the external surface of L1 exuviae (Fig. 4h), which might be explained by contact with the egg chorion during hatching. We also found high amounts of Burkholderia on the internal surface of larva-to-pupa exuviae (Fig. 4i) and the outside surface of pupae, as noted above (Fig. 4g). These findings indicate that the symbionts not only colonize the dorsal organs but are also present on the surface of early larvae and pupae. The probe used to target Lv-StB cells showed low-intensity unspecific labeling on a pure Lv-StA culture (Fig. S4 a, b), but a direct comparison on an egg wash (Fig. S4c, d) and tissue sections (Fig. S5) confirmed much more prominent labeling of Lv-StB cells, supporting the results observed by sequencing. In summary, Lv-StB is the most prevalent bacterial strain in symbiotic pouches during the life cycle of L. villosa, and symbionts are also released to the surface of larvae and pupae, as indicated by their presence on exuviae and pupal bristles.
Presence of lagriamide throughout the host life cycle and bioactive potential
As shown in Fig. 4, Lv-StB is highly abundant in larvae and pupae, the symbiotic pouches are connected to the outer surface and the symbionts are present on the outer and inner surface of exuviae. To gain further insight into the chemical basis and dynamics of defense observed in early larval and pupal stages, we investigated whether the Lv-StB bioactive secondary metabolite lagriamide (Fig. 5a) is also produced during these time points and where it is located in the host. We first analyzed crude extracts of field-collected individuals and offspring of field-collected females by HPLC-HRESI-MS and evaluated the presence of lagriamide by comparing retention time, UV absorbance, and high-resolution mass spectra to an authentic reference. We detected lagriamide in every life stage except in adult males (which lack symbionts), showing that lagriamide is consistently produced across symbiont-bearing life stages of L. villosa and is also present on shed exuviae (Fig. 5b). Using AP-SMALDI-HR MSI, we localized lagriamide on the egg surface, in larval and pupal symbiotic organs as well as distributed across the surface of exuviae from larval molts (Fig. 5c–h, Fig. S6), whereas we could not detect it on individuals without the natural symbiont community (Fig. S7). Thus, lagriamide co-localizes with Lv-StB throughout host development, i.e., in female accessory glands, on the egg surface, in symbiotic organs of larvae and pupae, and on exuviae. Although we did not detect lagriamide on the surface of larval sections via AP-SMALDI-profiling, possibly because the abundance resulting after histological sectioning is below the detection limit, HPLC-MS, and AP-SMALDI-profiling confirmed its presence on intact molted exuviae, and it spatially coincided with Lv-StB presence. Additionally, in vitro activity profiling of pure lagriamide revealed that it hinders the growth of B. bassiana and M. anisopliae on plate, showing partial inhibition (Fig. S8a, b). This observation is in line with the previously reported antifungal activity against P. lilacinum and Aspergillus niger , and the larval antifungal assays (Fig. 2). However, we did not observe antibacterial effects against the entomopathogen Bacillus thuringensis under these conditions (Fig. S8c). Taken together, these findings indicate that the dominant symbiont strain Lv-StB produces the antifungal polyketide lagriamide throughout the developmental stages of L. villosa from eggs to pupae.
L. villosa beetles are associated with a bacterial community dominated by Burkholderia  harbored in specialized symbiotic structures only absent in male adults. The symbionts are vertically transmitted, although sporadic acquisition from the environment likely occurs [9, 42]. Multiple Burkholderia strains can infect the beetles, occasionally simultaneously , and at least two —Lv-StB and Lv-StA— are known to produce antimicrobial compounds inhibiting fungal growth on the insect’s eggs and thereby enhance survival [10, 11]. Here, we show consistent presence of the antimicrobial lagriamide and its producer Lv-StB throughout the host life cycle. In situ localization of both Lv-StB and lagriamide confirms their presence within open symbiotic organs and their distribution across the surface of shed exuviae, demonstrating release of symbionts and the protective compound during larval molting. Reduced fungal growth and enhanced survival of young larvae in presence of Lv-StB, when confronted with different fungi and in vitro antifungal activity of pure lagriamide against fungi, demonstrate the protective role. These findings reveal a case of host adaptation to house ectosymbionts in specialized cuticular organs, which facilitate external release of bacteria and the associated compounds that aid in host protection. At the same time, these organs offer a suitable environment for growth and maintenance of antibiotic-producing ectosymbionts despite recurrent molting.
Like other arthropods living in the soil, L. villosa larvae and pupae face the challenge of fungal pathogens in the environment. This risk is particularly high in phases with reduced structural protection due to an incompletely sclerotized cuticle after molting [38, 39]. The cuticle is a key protective barrier against pathogenic fungi in almost all arthropods because of its rigidity , but also through the presence of antifungal proteins (e.g. glucanases, or proteinase- and chitinase-inhibitors), or small molecules with inhibitory activity, like cuticular fatty acids or benzoquinones [43, 51, 52]. For example, Galleria mellonella morphs with higher amounts of melanin, increased dihydroxyphenylalanine (DOPA) decarboxylase activity but lower amounts of hydrocarbons show reduced fungal attachment and germination, resulting in increased host survival in comparison to weakly melanized larvae . Yet, relying on the cuticle as a primary armor can involve important tradeoffs. While the phenomenon of molting practiced by ecdysozoans, including arthropods and nematodes, enables growth or reaching the next life stage, it also entails the cost of a temporarily softer and thinner integument. Right after molting, individuals might therefore be more susceptible to natural enemies, as described for some crustaceans [54, 55]. However, molting itself can shed off epibionts  or pathogens that were not able to penetrate the cuticle. In the crustacean Daphnia magna, for example, the bacterial pathogen Pasteuria ramosa has lower chances of a successful infection when the host molts soon after exposure to the pathogen . Also, in the diamondback moth Plutella xylostella, larvae inoculated with fungi early during an instar are more likely to die than if inoculated later during the same instar . It is also possible that fungi can breach the cuticle during vulnerable periods and proceed with infection within the insect host even after several molting events, as occurs in larvae of Colorado potato beetles . Taken together, such findings in different arthropods indicate that while the cuticle itself is the first major barrier against pathogens and molting can remove both beneficial and harmful microbes from the surface, the early period after ecdysis is particularly vulnerable due to a softer cuticle and/or the longer period available for pathogens to colonize and establish before the next molt.
Despite a long history of research on defense mechanisms of arthropods against fungal pathogens , the vulnerability of molting stages and adaptations for protection in these phases have rarely been studied, particularly in insects. However, studies in Bombyx mori and Tribolium castaneum show that the molting fluid that is secreted and accumulates during molting between the old and new cuticle  not only enables successful ecdysis but could also protect vulnerable postmolt insects against microbial pathogens . In L. villosa, critical phases where structural protection is limited are the first larval instar, which remains unmelanized for around 24 h, and the phases after each of the seven larval molts and during pupation, where individuals also lack mobility. By exposing symbiotic and aposymbiotic individuals to pathogens over the first 10 days after hatching and during pupation, respectively, we covered multiple molting events as well as metamorphosis and showed that cuticle-associated symbionts can persist despite recurrent molting and provide an effective means for protecting these life stages against fungal pathogens. Our setup does not directly demonstrate that fungal entry is occurring immediately after ecdysis in aposymbionts, yet the presence of both the symbionts and the antifungal lagriamide over extended areas of the inner surface of shed exuviae are in line with their role as a protective barrier to infections upon molting. In pupae, our results suggest a moderate inhibition of fungal growth by the symbionts, although we did not find a strong advantage in pupal emergence or survival shortly after emergence. This might be associated to the potential loss of symbionts after some time under laboratory conditions in untreated individuals, as previously reported for this insect , or an alternative line of defense in the pupal stage. As aposymbiotic beetles that are not challenged with fungal infections can fully develop and lay eggs in the laboratory , it is challenging to manipulate and individually track the symbiotic status of Lagria beetles up to the adult stage. However, the inhibition of fungal growth on pupae, the high abundance of Lv-StB symbionts on the pupal surface, and lagriamide detection inside the enlarged dorsal organ are in line with symbiont-mediated protection during pupation. Altogether, our results reveal symbiont-provided protection against fungal pathogens as an adaptive defense strategy of immature insect life stages, which likely supplements existing immune responses and structural defenses.
The evolution of the protective symbiosis in Lagria beetles likely relied on the dorsal cuticular invaginations as a morphological adaptation facilitating accommodation and release of ectosymbionts. The external location of symbionts makes defensive metabolites readily available for deterring antagonists that attack insects from the exterior , while the crypt-like structures grant shelter to symbionts and likely provide nourishment from surrounding glandular cells . Similarly, attine ants carry defensive Pseudonocardia bacteria in cuticular crypts on their surface, which protect both ants and their fungal gardens against pathogens [62,63,64]. Another structurally and functionally similar organ is found in solitary beewolf wasps, which harbor Streptomyces bacteria in cuticle-lined reservoirs of their antennae that protect the developing larva by producing an antibiotic cocktail [12, 13, 65, 66]. Also, ectosymbionts of marine ciliates defend their host against predators, and bacterial symbionts on developing embryos of certain shrimps and lobsters can inhibit infections by pathogenic fungi [67, 68]. Cuticular organs that foster symbiont colonization are also described in several other insects, and fungus-bearing mycangia of wood-boring and bark beetles, as well as leaf-rolling weevils, resemble pouches of L. villosa larvae . Interestingly, although the pouches of L. villosa larvae are invaginations of the cuticle and are connected to glandular cells, they are not shed off with the exuvia as usually seen in exocrine glands of insects . This prevents a complete loss of symbionts during molting, which is also reflected by similar symbiont titers from larvae after molting and intermolt stages (Fig. 3b, comparison between early L2 and mid L2). Similarly, other molting arthropods like nymphs of the phasmid Oreophoetes peruana do not discard the cuticular lining of their defensive glands during molting, conserving the costly secretion and keeping it available as a chemical defense directly after molting . The external location of the symbionts might be additionally favorable for the host to avoid contact with potentially harmful bioactive secondary metabolites produced by the bacteria .
Although it was previously demonstrated that multiple Burkholderia strains (including Lv-StA) can coinfect single L. villosa beetles  and FISH revealed occasional presence of other bacteria and strains in the organs of younger larvae (Fig. S3a–c), Lv-StB is generally predominant and shows signs of a tight association with its host. Possibly, host provisions support its proliferation and enable it to remain in the organs despite its reduced genome . The dominance of this strain also underlines the putative importance of the bioactive polyketide lagriamide for host protection or competitive exclusion of coinfecting microorganisms. However, other Burkholderia strains and community members might also contribute to host protection, as they were either shown to be capable of producing bioactive metabolites [10, 72, 73] or to carry gene clusters for putative defensive molecules . Such coinfections by closely related symbiont strains in a single individual as observed in L. villosa are rare in insects, or so far understudied. However, defensive symbioses are often described as dynamic and can be shaped by multiple coinfections throughout a population or by symbiont replacements , offering an opportunity to acquire multiple defensive partners. Like other insects harboring defensive symbionts with a broad bioactive potential [12, 13], Lagria beetles are not challenged by a single antagonist, but rather by a variety of pathogens in the soil. Having the possibility for symbiont uptake via a mixed-mode symbiont transmission and simultaneously a tight association to one specific defensive symbiont strain, the beetle might have evolved a flexible strategy to adapt to various antagonists. Thus, the protective effect of the dominant symbiont Lv-StB through the production of lagriamide may be complemented by other compounds of associated microorganisms.
In conclusion, we show that in L. villosa, the adaptations to house antifungal-producing Burkholderia bacteria in cuticular invaginations in larvae and pupae enable defense against entomopathogens throughout development including multiple molting phases. These structures foster a specialized association with a specific defensive symbiont strain while maintaining flexibility to acquire additional protective strains from the environment. In contrast to highly intimate nutritional symbioses in which morphological adaptations such as bacteriomes have evolved, defensive symbioses usually have intrinsically different constraints regarding where and how microorganisms are maintained for effective protection, especially if deploying bioactive compounds. Cuticle-associated ectosymbionts can therefore be an effective and dynamic defense strategy influencing antagonistic interactions between arthropods and pathogenic microbes.
Materials and methods
Insect collecting and rearing
L. villosa individuals were collected in plantations of various crops in the states of São Paulo and Paraná, Brazil, from 2017 to 2020 (Table S7). Individuals were reared in plastic containers in a climate chamber (16:8 L:D light regime with 0.5 h dusk, 26 °C, and 60% humidity). Adult beetles were fed with iceberg lettuce, soybean, and kidney bean leaves, and larvae were fed with dry soybean and kidney bean leaves. Centrifuge tubes with autoclaved tap water and cotton on top and centrifuge tube lids with moist cotton were provided for humidity control and as egg-laying substrate.
Bacterial community profiling via 16 S rRNA gene amplicon sequencing
L. villosa specimens were collected directly from the field or recovered in the lab as offspring of field-collected females in case of eggs and small larvae and preserved in ethanol or methanol. Accessory glands of female specimens were dissected before DNA extraction. Eggs were extracted as full clutches or a fraction of a single clutch (min. 18 eggs per clutch), while small larvae were extracted individually and later pooled by clutch combining DNA from either three (10 days old) or two (15 days old) individuals. All other samples were extracted individually. The Epicenter MasterPure Complete DNA and RNA Purification Kit was used for DNA extraction of a total of 58 samples following the manufacturer’s instructions and including lysozyme treatment before protein digestion. The V4 region of the 16 S rRNA gene was sequenced by a commercial provider (StarSeq, Mainz, Germany) on a MiSeq platform (Illumina), using primers 515 F  and 806bR [75, 76], double indexing, and a paired end approach with a read length of 300 nt. Amplicon sequence variants (ASVs) were inferred using the R package DADA2  with default parameters including dereplication, chimera removal, and trimming lengths of 250 and 140 nt for forward and reverse reads, respectively. This corresponded to a 253 bp fragment of the V4 region. Taxonomy was assigned using the pre-trained classifier SILVA 132 [78, 79] with subsequent removal of reads classified as chloroplast or mitochondria. For graphical representation, only ASVs were shown that reached 1% or more of the reads per sample, in at least one sample. ASVs within Burkholderiaceae classified as “Burkholderia-Caballeronia-Paraburkholderia” or not assigned at the genus level were evaluated manually to detect previously described Burkholderia symbiont strains [11, 71], for which whole-genome or Metagenome-assembled Genome (MAG) references are available. In the evaluated region, Lv-StB shows a pairwise dissimilarity of at least 9 nucleotides with respect to the other reference sequences in the database. Four of the obtained ASV sequences had a pairwise identity of 100% to a sequence in the local database and another four ASVs were between 98 and 99.6% in similarity. These ASVs were assigned accordingly. All others were below 93% in similarity to the reference sequences in the database.
Quantification of Lv-StB throughout beetle life stages
Different developmental stages (Table S5) of L. villosa individuals from the field and the 1st lab generation were collected in replicates and frozen at –80 °C before nucleic acid extraction. Females were dissected beforehand to obtain only the symbiont-bearing structures. Samples were homogenized with liquid nitrogen and nucleic acids were extracted using the innuPREP DNA/RNA Mini Kit (Analytik Jena) following the manufacturer’s guidelines. qPCRs were carried out with the DNA targeting the trans-AT PKS/NRPS lgaG region of the lagriamide gene cluster with the specific primers LgaG_3_fwd (CGCCGTATCGAGCAGTTTC) and LgaG_3_rev (CAACTGGTCGAGCGTATCAA) under the following conditions: Initial activation at 95 °C for 15 min, denaturation at 95 °C for 15 s, annealing at 65 °C for 15 s and elongation at 72 °C for 15 s. qPCRs were carried out using the 5x HOT FIREPol EvaGreen HRM Mix EvaGreen (Solis BioDyne) on a RotorGene-Q cycler (Qiagen) in 10 µL reactions including 0.5 µL of each primer and 1 µL template DNA. Standard curves were generated by amplifying the fragment, followed by purification and determination of the DNA concentration using a Qubit fluorometer (Thermo Fisher). Afterwards, a standard containing 1 ng/µL was generated and 1:10 serial dilutions to 10−8 ng/µL were prepared. All standards were included in the qPCR run for absolute quantification. qPCR copy numbers were corrected for the number of individuals extracted in each sample (Table S5). Influence of the different life stages on the symbiont titer was analyzed by a Kruskal-Wallis and a posthoc Dunn’s test using the PMCMRplus package (Version 1.9.0) in RStudio (Version 1.2.5042). Plots were created using the ggplot2 package (Version 3.3.0) and Adobe Illustrator (Adobe, Version 14.1, CC 2020).
Symbiont localization by fluorescence in situ hybridization (FISH)
FISH was either performed on entire tissue (whole-mount), on semithin sections of L. villosa individuals, on an egg wash, or pure symbiont culture (Lv-StA). Either field-collected individuals (female, bigger larvae, pupae, larva-pupa-exuvia) or offspring of field-collected females (egg, L1 larva, L1 exuvia) were used. Before FISH, L. villosa individuals and exuviae were fixed in 4% formaldehyde for at least 3 days, while the egg wash and symbiont culture were fixed on glass slides with ethanol. Embedding, semithin sectioning, and FISH were performed as described previously  using a hybridization temperature of 50 °C. The Cy3- or Cy5-labeled Burk16S probe (5ʹTGCGGTTAGACTAGCCACTʹ3) was used to mark all Burkholderia strains, and the Cy5-labeled Burk16S_StB_2 probe (5ʹGGCAACCCTTTGTTTTGACCʹ3) was used for the symbiont strain Lv-StB, Cy5-labeled Burk16S_StA probe (5ʹGCACCCTCAGATCTCTCCAAGG3) was used for symbiont strain Lv-StA and Cy3-labeled EUB338 probe  (5ʹGCTGCCTCCCGTAGGAGTʹ3) was used for general eubacteria. DAPI (40,6-diamidino-2-phenylindole) was used to label the host cell nuclei and as counterstaining. Images were taken on an AxioImager.Z2 fluorescence microscope (Zeiss, Jena, Germany).
In vivo bioassays with L. villosa larvae
Larval bioassays (Table S1) were carried out at 26 °C in small Petri dishes prepared as follows: Sterile vermiculite (1–2 mm) was distributed over the bottom of the dish and humidified with sterile water. Sterile filter paper inoculated either with 100 µL sterile water (no-fungus-treatment) or 100 µL of a fungal conidial suspension in sterile water (75 conidia/µL of P. lilacinum (LV1, Accession number: KY630747, KY630748, KY630749), or 104 conidia/µL of B. bassiana (LESF477, Database Identifier: CRM 1216, CRM - UNESP) or M. anisopliae (LESF 206, Database Identifier: CRM 530, CRM - UNESP), respectively) was added. In each dish, maximum five 1st instar larvae were placed according to their treatment and single-blind monitored for 10 days. UV-sterilized dried soybean and kidney bean leaves were provided as food sources every other day. To obtain aposymbiotic and differently reinfected 1st instar L. villosa larvae, 1–2 day(s) old egg clutches of field-collected females were divided into different groups. One part of the clutch was used as a control with the natural microbial community (untreated). Remaining eggs were first washed with sterile PBS, slightly shaken for 5 min in 70% ethanol, washed 2 times with sterile water, immersed for 30 s in 12% NaClO, and washed three times with sterile water. Eggs were then inoculated with PBS to obtain symbiont-free individuals (aposymbiotic), with the previously obtained egg-wash that contains the natural microbial community (reinfected-egg wash, previously named “reinfected-natural” ), or with a PBS suspension of a cultured symbiotic strain of L. villosa beetles (106 cells/µL) — B. gladioli Lv-StA (reinfected-LvStA). While this strain is only occasionally found in the beetles in natural conditions, we included it in this first assay to evaluate its protective potential, since it has been previously shown to chemically inhibit fungal growth on L. villosa eggs . The P. lilacinum assay was carried out with larvae from eight clutches laid by different L. villosa field-collected females in two consecutive years. Survival of hatching larvae was observed for 10 days in a single-blind assay. B. gladioli and Lv-StB presence on the egg clutches was verified via qPCR using B. gladioli specific primers Burk16S_1_F (GTTGGCCGATGGCTGATT) and Burk16S_1_R (AAGTGCTTTACAACCCGAAGG) and Lv-StB specific primers LgaG_3_fwd and LgaG_3_rev on the five clutches from the 2020 population. The corresponding qPCR reactions were carried out under the following conditions: Initial activation at 95 °C for 15 min, denaturation at 95 °C for 15 s, annealing at 65 °C for 15 s and elongation at 72 °C for 15 s.
The assay including B. bassiana, M. anisopliae, and the no-fungus-control was carried out with four clutches laid by different L. villosa field-collected females comparing aposymbiotic and reinfected-egg wash individuals. Given the inconsistent occurrence of Lv-StA in natural conditions and giving priority to the naturally dominant strain Lv-StB, a Lv-StA reinfection treatment was not included in this assay to guarantee a robust sample size per group. After hatching, larvae were observed for 10 days monitoring survival, developmental time, and fungal infection in a single-blind assay. To assess fungal growth, larvae were monitored under a stereoscope for visible fungal hyphae and sporulating fungus on the larval surface. Fungal and bacterial strains were grown on King B Agar plates or King B liquid medium. Symbiont presence of Lv-StB on the original eggs and larvae was verified via qPCRs of DNA extracts from a subset of untreated eggs and surviving larvae from each treatment using Lv-StB specific primers LgaG_3_fwd and LgaG_3_rev.
To determine the effect of different treatments on survival and fungal growth probability on L. villosa larvae, a Cox mixed effects model with treatment and fungus as fixed effect and a random intercept per clutch and per year was fitted using the coxme package (Version 2.2-16) in RStudio (Version 1.2.5042) (Table S2-S4). Plots were obtained with the rms package (Version 5.1-4), making use of the Kaplan–Meier-estimator, and Adobe Illustrator (Adobe, Version 14.1, CC 2020).
In vivo bioassays with L. villosa pupae
The pupal bioassays (Table S1) were carried out at 26 °C with no light in 24 well-plates. Each well was prepared with soil that was inoculated with 100 µL of fungus suspension 2–4 days before the experiment. The fungus mix for the first assay contained 106 conidia of each of the three fungi B. bassiana, M. anisopliae, and P. lilacinum. For the second assay, 106 conidia of M. anisopliae were inoculated into the soil and additional 106 conidia were inoculated onto the dorsal thorax of the pupae directly after pupation. Aposymbiotic and untreated pupae from the first lab generation were randomly placed in each well as soon as they emerged. Melanization and fungal growth were observed single-blind until emergence. Aposymbiotic individuals were obtained through the egg sterilization procedure described above and kept in a semi-sterile box until pupal emergence (around seven weeks). Symbiotic individuals were reared in a small terrarium on natural soil with growing soybean plants until the last larval stage. To determine the effect of the different treatments on survival, visible fungal infection, and melanization of L. villosa pupae, a Cox model was fitted to the data using the survival package (Version 2.2-16) in RStudio (Version 1.2.5042). Plots were obtained with the rms package (Version 5.1-4), making use of the Kaplan–Meier-estimator, and Adobe Illustrator (Adobe, Version 14.1, CC 2020).
Chemical extraction and quantification of lagriamide
L. villosa specimens (Table S6) were collected in the field or recovered in the lab as offspring of field-collected females in the case of eggs and larvae of the two first instars. Eggs were extracted as a fraction of the clutch including up to 60 eggs. First and second instar larvae were combined in multiple pools of up to 22 individuals for extraction. Field-collected larvae, pupae, and exuviae were extracted individually. For female adult specimens, the ovipositor and both accessory glands were dissected. For adult males, the full reproductive system was dissected. Replicate numbers for each sample type are indicated in Table S6. Each sample was extracted in a known amount of methanol (200–600 μL) for at least 24 h. Extracts were kept at 10 °C until further processing. Crude extracts were analyzed by LC-MS on an Exactive Orbitrap High Performance Benchtop LC-MS (Thermo Fisher Scientific) with an electron spray ion source and an Accela HPLC System, C18 column (Betasil C18 5 µm, 150 × 2.1 mm, Thermo Fisher Scientific), solvents: acetonitrile and water (both supplemented with 0.1% formic acid), flow rate: 0.2 mL min−1; program: hold 1 min at 5 % acetonitrile, 1–16 min 5–98% acetonitrile, hold 3 min 98% acetonitrile. Lagriamide amounts were measured by integration of the peak areas of the extracted mass traces (m/z = 747.4769 – 747.4843 [M-H]−) (ICIS integration algorithm in XCalibur, Thermo Fisher Scientific).
Lagriamide localization by AP-SMALDI-HR MSI experiments
L. villosa specimens were collected in the field or recovered in the lab as offspring of field-collected females in the case of eggs and exuviae. Aposymbiotic individuals were collected from a culture of the 6th lab generation. All samples were analyzed using an atmospheric pressure—scanning microprobe matrix-assisted laser desorption ionization (AP-SMALDI10, TransMIT, Gießen, Germany) ion source equipped with a UV (337 nm) nitrogen laser (LTB MNL-106, LTB, Germany). AP-SMALDI10 was coupled to a mass spectrometer Q‐Exactive Plus (Thermo Fisher Scientific, Bremen, Germany) providing high‐resolution mass spectra. Raw MS data were collected via Xcalibur software v.2.8 Build 2806 (Thermo Fisher Scientific), while the acquisition of spatial scans, predefined by the user in x‐ and y‐directions as a rectangular sample region, was controlled by the Master Control Program (TransMIT ).
Sample heterogeneity required minor changes in specific parameters of the AP-SMALDI-HR MSI method. Therefore, egg samples (cryosections and intact eggs) were imaged with a step size of 10 - 15 μm. Exuviae samples were analyzed based on their size using 25 μm - 45 μm. Sagittal cryosections of pupae and larvae sections were analyzed with a step size of 30 μm. The lagriamide standard (30% DMSO at a concentration of 168 ng/µL) was pipetted on hexane extracted fine paper tissue in a volume of 1 μL/mm2. All samples were imaged with the number of laser shots per spot set to 30 (approximately 1.1 μJ × shot−1 to analyze the egg samples; 1.0 μJ × shot−1 for exuviae samples and 1.2 μJ × shot−1 for the pupae and larvae sections) within a laser frequency of 60 Hz. A mass range was set from m/z 100 to m/z 1000 with a resolving power of 140,000. AP-SMALDI-HR MS profiling of lagriamide standard was performed in positive ion mode with several laser shots per spot set to 30 (approximately 13 μJ × shot−1) within a laser frequency of 60 Hz, a mass range was set from m/z 700 to m/z 850 with a resolving power of 280,000. Ion intensity maps of selected m/z values were generated using a Mirion 3D V188.8.131.52 software package  with an m/z width of 0.01 u. Ion maps were normalized separately to the highest intensity for each ion species. All acquisitions were performed in positive polarity and in laser desorption ionization mode (LDI) without applying the MALDI matrix to the sample.
Samples were prepared as follows: exuviae samples were cut open along the dorsal posterior region to flatten them on a double-sided adhesive tape (3 M, Maplewood, MN, USA) using a fine tweezer (Fig. S9a, b). This was attached to a microscope glass slide (25 mm × 15 mm, Thermo Scientific, Menzel‐Gläser, VWR, Darmstadt, Germany) and finally fixed on the AP-SMALDI metal target. Intact eggs were carefully picked up from a clutch using a clean tweezer and fixed on a double-sided tape attached to a microscope glass slide (25 mm × 15 mm). Glass slides with egg samples were mounted on an AP-SMALDI metal target and promptly placed into the AP-SMALDI ion chamber to be analyzed. Because of the conditions in the ion chamber and the nature of the egg samples, a negative effect of drying and shape distortion was observed (Fig. S9c, d). For sectioning, samples were embedded in O.C.T. medium (Tissue‐Tek O.C.T. Compound; Sakura Finetek, Torrance, CA, USA), frozen in liquid nitrogen, and cut into 30 µm sections using a Leica cryomicrotome (Leica CM1850, Leica Mikrosysteme Vertrieb GmbH, Germany). Fresh sections were transferred from a cryomicrotome chamber (–20 °C) into a desiccator (filled with potassium hydroxide as a drying agent) to dry without a vacuum for 20 min.
The identity of acquired lagriamide-related ions from L. villosa samples, which was based on exact mass, was supported by best matching chemical formulas and isotope patterns generated via Qual Browser/Xcalibur software 3.0.63. This enabled to putatively assign the peaks to lagriamide (C41H68N2O10) adducts (∆ error <1 ppm), which was confirmed with AP-SMALDI-HR MS profiling of a lagriamide standard (Fig. S9e). In total, 3 µL of the lagriamide standard (30% DMSO at concentration 168 ng/µL) was pipetted in three parts onto small pieces of tissue paper glued to a clean microscope glass slide. Except for the potassium adduct, which was predominantly found in MS/MSI datasets, ions representing the [M + H]+ or [M + Na]+ adducts were detected. Presence of all three lagriamide adducts was demonstrated on an extract obtained from an L. villosa larval exuvia (Fig. S9f).
In vitro assays for lagriamide antimicrobial activity
Antimicrobial activity of lagriamide was studied by agar diffusion assays against Bacillus thuringiensis DSM2048, Beauveria bassiana ST000047, and Metarhizium anisopliae STH00420 (ATCC 24942). For the fungal assays, fifty microliters of a solution of lagriamide (168 ng/µL in 30% DMSO in methanol) were filled in agar holes of 9 mm diameter (malt extract agar, Merck, seeded with a spore suspension). After incubation at 23 °C for 4 d, the inhibition zone was evaluated. For the antibacterial assay, nutrient agar plates (Standard I nutrient agar, Merck) seeded with the bacterial culture were used and incubation took place at 30 °C. The inhibition zones were determined after 24 h.
Raw sequence data generated in this study and used for 16 S rRNA gene bacterial community profiling of L. villosa life stages is available in the GenBank SRA database under the BioProject accession number PRJNA790999.
Wang C, Wang S. Insect pathogenic fungi: genomics, molecular interactions, and genetic improvements. Annu Rev Entomol. 2017;62:73–90.
Lacey LA, Grzywacz D, Shapiro-Ilan DI, Frutos R, Brownbridge M, Goettel MS. Insect pathogens as biological control agents: Back to the future. J Invertebr Pathol. 2015;132:1–41.
Butt TM, Coates CJ, Dubovskiy IM, Ratcliffe NA Entomopathogenic fungi: new insights into host-pathogen interactions. Advances in Genetics. 2016. Elsevier Ltd.
Lu HL, St. Leger RJ. Insect immunity to entomopathogenic fungi. Adv Genet. 2016;94:251–85.
Yuan S, Tao X, Huang S, Chen S, Xu A. Comparative immune systems in animals. Annu Rev Anim Biosci. 2014;2:235–58.
Flórez LV, Biedermann PHW, Engl T, Kaltenpoth M. Defensive symbioses of animals with prokaryotic and eukaryotic microorganisms. Nat Prod Rep. 2015;32:904–36.
Oliver KM, Smith AH, Russell JA. Defensive symbiosis in the real world - advancing ecological studies of heritable, protective bacteria in aphids and beyond. Funct Ecol. 2014;28:341–55.
Scarborough CL, Ferrari J, Godfray HC. Aphid protected from pathogen. Science 2005;310:1781.
Łukasik P, van Asch M, Guo H, Ferrari J, Charles H. Unrelated facultative endosymbionts protect aphids against a fungal pathogen. Ecol Lett. 2013;16:214–8.
Flórez LV, Scherlach K, Gaube P, Ross C, Sitte E, Hermes C, et al. Antibiotic-producing symbionts dynamically transition between plant pathogenicity and insect-defensive mutualism. Nat Commun. 2017;8:15172.
Flórez LV, Scherlach K, Miller IJ, Rodrigues A, Kwan JC, Hertweck C, et al. An antifungal polyketide associated with horizontally acquired genes supports symbiont-mediated defense in Lagria villosa beetles. Nat Commun. 2018;9:2478.
Kaltenpoth M, Göttler W, Herzner G, Strohm E. Symbiotic bacteria protect wasp larvae from fungal infestation. Curr Biol. 2005;15:475–9.
Kroiss J, Kaltenpoth M, Schneider B, Schwinger MG, Hertweck C, Maddula RK, et al. Symbiotic streptomycetes provide antibiotic combination prophylaxis for wasp offspring. Nat Chem Biol. 2010;6:261–3.
Kaltenpoth M, Goettler W, Koehler S, Strohm E. Life cycle and population dynamics of a protective insect symbiont reveal severe bottlenecks during vertical transmission. Evol Ecol. 2010;24:463–77.
Wang X, Yang X, Zhou F, Tian ZQ, Cheng J, Michaud JP, et al. Symbiotic bacteria on the cuticle protect the oriental fruit moth Grapholita molesta from fungal infection. Biol Control. 2022;169:104895.
Wang L, Feng Y, Tian J, Xiang M, Sun J, Ding J, et al. Farming of a defensive fungal mutualist by an attelabid weevil. ISME J. 2015;9:1793–801.
Currie CR, Stuart AE. Weeding and grooming of pathogens in agriculture by ants. Proc R Soc B Biol Sci. 2001;268:1033–9.
Currie CR, Scottt JA, Summerbell RC, Malloch D. Fungus-growing ants use antibiotic-producing bacteria to control garden parasites. Nature 1999;398:701–4.
Currie CR, Bot ANM, Boomsma JJ. Experimental evidence of a tripartite mutualism: Bacteria protect ant fungus gardens from specialized parasites. Oikos 2003;101:91–102.
Um S, Fraimout A, Sapountzis P, Oh D-CC, Poulsen M. The fungus-growing termite Macrotermes natalensis harbors bacillaene-producing Bacillus sp. that inhibit potentially antagonistic fungi. Sci Rep. 2013;3:3250.
Grubbs KJ, Surup F, Biedermann PHW, McDonald BR, Klassen JL, Carlson CM, et al. Cycloheximide-producing streptomyces associated with xyleborinus saxesenii and xyleborus affinis fungus-farming ambrosia beetles. Front Microbiol. 2020;11:1–12.
Piel J. Metabolites from symbiotic bacteria. Nat Prod Rep. 2009;26:338–62.
Van Arnam EB, Currie CR, Clardy J. Defense contracts: Molecular protection in insect-microbe symbioses. Chem Soc Rev. 2018;47:1638–51.
Beemelmanns C, Guo H, Rischer M, Poulsen M. Natural products from microbes associated with insects. Beilstein J Org Chem. 2016;12:314–27.
Lackner G, Peters EE, Helfrich EJN, Piel J. Insights into the lifestyle of uncultured bacterial natural product factories associated with marine sponges. Proc Natl Acad Sci USA. 2017;114:E347–E356.
Schoenian I, Spiteller M, Ghaste M, Wirth R, Herz H, Spiteller D. Chemical basis of the synergism and antagonism in microbial communities in the nests of leaf-cutting ants. Proc Natl Acad Sci USA. 2011;108:1955–60.
Kaltenpoth M, Strupat K, Svatoš A. Linking metabolite production to taxonomic identity in environmental samples by (MA)LDI-FISH. ISME J. 2016;10:527–31.
Geier B, Sogin EM, Michellod D, Janda M, Kompauer M, Spengler B, et al. Spatial metabolomics of in situ host–microbe interactions at the micrometre scale. Nat Microbiol. 2020;5:498–510.
De Roode JC, Lefèvre T. Behavioral immunity in insects. Insects 2012;3:789–820.
Kerwin AH, Gromek SM, Suria AM, Samples RM, Deoss DJ, O’Donnell K, et al. Shielding the next generation: Symbiotic bacteria from a reproductive organ protect bobtail squid eggs from fungal fouling. mBio. 2019;10:e02376-19.
Soler JJ, Martín-Vivaldi M, Ruiz-Rodríguez M, Valdivia E, Martín-Platero AM, Martínez-Bueno M, et al. Symbiotic association between hoopoes and antibiotic-producing bacteria that live in their uropygial gland. Funct Ecol. 2008;22:864–71.
Bunker ME, Elliott G, Martin MO, Arnold AE, Weiss SL. Vertically transmitted microbiome protects eggs from fungal infection and egg failure. Anim Microbiome. 2021;3:43.
Nyholm SV. In the beginning: Egg-microbe interactions and consequences for animal hosts: Egg microbiomes in animals. Philos Trans R Soc B Biol Sci. 2020;375:20190593.
Smith DFQ, Dragotakes Q, Kulkarni M, Hardwick M, Casadevall A, Microbiology M, et al. Melanization is an important antifungal defense mechanism in Galleria mellonella hosts. bioRxiv 2022.04.02.486843.
Yokoi K, Hayakawa Y, Kato D, Minakuchi C, Tanaka T, Ochiai M, et al. Prophenoloxidase genes and antimicrobial host defense of the model beetle, Tribolium castaneum. J Invertebr Pathol. 2015;132:190–200.
Zhang J, Huang W, Yuan C, Lu Y, Yang B, Wang CY, et al. Prophenoloxidase-mediated ex vivo immunity to delay fungal infection after insect ecdysis. Front Immunol. 2017;8:1–14.
Zhang J, Lu A, Kong L, Zhang Q, Ling E. Functional analysis of insect molting fluid proteins on the protection and regulation of ecdysis. J Biol Chem. 2014;289:35891–906.
Soluk DA. Postmolt susceptibility of ephemerella larvae to predatory stoneflies: constraints on defensive armour. Oikos 1990;58:336.
Kanyile SN, Engl T, Kaltenpoth M. Nutritional symbionts enhance structural defence against predation and fungal infection in a grain pest beetle. J Exp Biol. 2022;225:1–9.
Flórez LV, Kaltenpoth M. Symbiont dynamics and strain diversity in the defensive mutualism between Lagria beetles and Burkholderia. Environ Microbiol. 2017;19:3674–88.
Uberti A, Smaniotto MA, Giacobbo CL, Lovatto M, Lugaresi A, Girardi GC. Novo inseto praga na cultura do pessegueiro: biologia de Lagria villosa Fabricius, 1783 (Coleoptera: Tenebrionidae) alimentados com pêssego. Sci Electron Arch. 2017;10:72–76.
Stammer HJ. Die Symbiose der Lagriiden (Coleoptera). Z für Morphol und Ökologie der Tiere. 1929;15:1–34.
Boucias DG, Pendland JC Principles of Insect Pathology. 1998. Springer Science + Business Media, LLC, New York.
Garcia MA, Pierozzi IJ. Aspectos da biologia e ecologia de Lagria villosa Fabricius, 1781 (Coleoptera, Lagriidae). Rev Bras Biol. 1982;42:415–20.
Vega FE, Posada F, Catherine Aime M, Pava-Ripoll M, Infante F, Rehner SA. Entomopathogenic fungal endophytes. Biol Control. 2008;46:72–82.
Kabaluk JT, Ericsson JD. Metarhizium anisopliae seed treatment increases yield of field corn when applied for wireworm control. Agron J. 2007;99:1377–81.
Hallouti A, Ait Hamza M, Zahidi A, Ait Hammou R, Bouharroud R, Ait Ben Aoumar A, et al. Diversity of entomopathogenic fungi associated with Mediterranean fruit fly (Ceratitis capitata (Diptera: Tephritidae)) in Moroccan Argan forests and nearby area: impact of soil factors on their distribution. BMC Ecol. 2020;20:1–13.
Iwanicki NS, Pereira AA, Botelho ABRZ, Rezende JM, Moral RDA, Zucchi MI, et al. Monitoring of the field application of Metarhizium anisopliae in Brazil revealed high molecular diversity of Metarhizium spp in insects, soil and sugarcane roots. Sci Rep. 2019;9:1–12.
Roberts DW, St. Leger RJ. Metarhizium spp., cosmopolitan insect-pathogenic fungi: Mycological aspects. Adv Appl Microbiol. 2004;54:1–70.
Wierz JC, Gaube P, Klebsch D, Kaltenpoth M, Flórez LV. Transmission of bacterial symbionts with and without genome erosion between a beetle host and the plant environment. Front Microbiol. 2021;12:715601.
Gillespie JP, Bailey AM, Cobb B, Vilcinskas A. Fungi as elicitors of insect immune responses. Arch Insect Biochem Physiol. 2000;44:49–68.
Ortiz-Urquiza A, Keyhani NO. Action on the surface: Entomopathogenic fungi versus the insect cuticle. Insects 2013;4:357–74.
Grizanova EV, Coates CJ, Dubovskiy IM, Butt TM. Metarhizium brunneum infection dynamics differ at the cuticle interface of susceptible and tolerant morphs of Galleria mellonella. Virulence 2019;10:999–1012.
Eaton WD, Love DC, Botelho C, Meyers TR, Imamura K, Koeneman T. Preliminary results on the seasonality and life cycle of the parasitic dinoflagellate causing bitter crab disease in Alaskan Tanner crabs (Chionoecetes bairdi). J Invertebr Pathol. 1991;57:426–34.
Field RH, Chapman CJ, Taylor AC, Neil DM, Vickerman K. Infection of the Norway lobster Nephrops norvegicus by a Hematodinium-like species of dinoflagellate on the west coast of Scotland. Dis Aquat Organ. 1992;13:1–15.
Threlkeld ST, Chiavelli DA, Willey RL. The organization of zooplankton epibiont communities. Trends Ecol Evol. 1993;8:317–21.
Duneau D, Ebert D. The role of moulting in parasite defence. Proc R Soc B Biol Sci. 2012;279:3049–54.
Vandenberg JD, Ramos M, Altre JA. Dose-Response and Age- and Temperature-Related Susceptibility of the Diamondback Moth (Lepidoptera: Plutellidae) to Two Isolates of Beauveria bassiana (Hyphomycetes: Moniliaceae). Environ Entomol. 1998;27:1017–21.
Vey A, Fargues J. Histological and ultrastructural studies of Beauveria bassiana infection in Leptinotarsa decemlineta larvae during ecdysis. J Invertebr Pathol. 1977;30:207–15.
Reynolds SE, Samuels RI. Physiology and biochemistry of insect moulting fluid. Adv Insect Phys. 1996;26:157–232.
Lopanik NB. Chemical defensive symbioses in the marine environment. Funct Ecol. 2014;28:328–40.
Sen R, Ishak HD, Estrada D, Dowd SE, Hong E, Mueller UG. Generalized antifungal activity and 454-screening of Pseudonocardia and Amycolatopsis bacteria in nests of fungus-growing ants. Proc Natl Acad Sci USA. 2009;106:17805–10.
Currie CR, Poulsen M, Mendenhall J, Boomsma JJ, Billen J. Coevolved crypts and exocrine glands support mutualistic bacteria in fungus-growing ants. Science 2006;311:81–3.
Li H, Sosa-Calvo J, Horn HA, Pupo MT, Clardy J, Rabeling C, et al. Convergent evolution of complex structures for ant-bacterial defensive symbiosis in fungus-farming ants. Proc Natl Acad Sci USA. 2018;115:10720–5.
Kaltenpoth M, Roeser-Mueller K, Koehler S, Peterson A, Nechitaylo TY, Stubblefield JW, et al. Partner choice and fidelity stabilize coevolution in a Cretaceous-age defensive symbiosis. Proc Natl Acad Sci. 2014;111:6359–64.
Engl T, Kroiss J, Kai M, Nechitaylo TY, Svatoš A, Kaltenpoth M. Evolutionary stability of antibiotic protection in a defensive symbiosis. Proc Natl Acad Sci USA. 2018;115:E2020–E2029.
Gil-Turnes MS, Hay ME, Fenical W. Symbiotic marine bacteria chemically defend crustacean embryos from a pathogenic fungus. Science 1989;246:116–8.
Gil-Turnes MS, Fenical W. Embryos of Homarus americanus are protected by epibiotic bacteria. Biol Bull. 1992;182:105–8.
Hoffmann KH Insect Molecular Biology and Ecology. 2015. CRC Press.
Eisner T, Morgan RC, Attygalle AB, Smedley SR, Herath KB, Meinwald J. Defensive production of quinoline by a phasmid insect (Oreophoetes peruana). J Exp Biol. 1997;200:2493–2500.
Waterworth SC, Flórez LV, Rees ER, Hertweck C, Kaltenpoth M, Kwan JC. Horizontal gene transfer to a defensive symbiont with a reduced genome in a multipartite beetle microbiome. mBio. 2020;11:e02430-19.
Niehs SP, Kumpfmüller J, Dose B, Little RF, Ishida K, Flórez LV, et al. Insect‐associated bacteria assemble the antifungal butenolide gladiofungin by non‐canonical polyketide chain termination. Angew Chem. 2020;132:23322–6.
Dose B, Niehs SP, Scherlach K, Flórez LV, Kaltenpoth M, Hertweck C. Unexpected bacterial origin of the antibiotic icosalide: two-tailed depsipeptide assembly in multifarious Burkholderia symbionts. ACS Chem Biol. 2018;13:2414–20.
Parada AE, Needham DM, Fuhrman JA. Every base matters: Assessing small subunit rRNA primers for marine microbiomes with mock communities, time series and global field samples. Environ Microbiol. 2016;18:1403–14.
Caporaso JG, Lauber CL, Walters WA, Berg-Lyons D, Huntley J, Fierer N, et al. Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms. ISME J. 2012;6:1621–4.
Caporaso JG, Lauber CL, Walters WA, Berg-Lyons D, Lozupone CA, Turnbaugh PJ, et al. Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample. Proc Natl Acad Sci USA. 2011;108:4516–22.
Callahan BJ, McMurdie PJ, Rosen MJ, Han AW, Johnson AJA, Holmes SP. DADA2: High-resolution sample inference from Illumina amplicon data. Nat Methods. 2016;13:581–3.
Quast C, Pruesse E, Yilmaz P, Gerken J, Schweer T, Yarza P, et al. The SILVA ribosomal RNA gene database project: Improved data processing and web-based tools. Nucleic Acids Res. 2013;41:590–6.
Yilmaz P, Parfrey LW, Yarza P, Gerken J, Pruesse E, Quast C, et al. The SILVA and ‘all-species Living Tree Project (LTP)’ taxonomic frameworks. Nucleic Acids Res. 2014;42:643–8.
Weiss B, Kaltenpoth M. Bacteriome-localized intracellular symbionts in pollen-feeding beetles of the genus Dasytes (Coleoptera, Dasytidae). Front Microbiol. 2016;7:1–10.
Amann RI, Binder BJ, Olson RJ, Chisholm SW, Devereux R, Stahl DA. Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations. Appl Environ Microbiol. 1990;56:1919–25.
Paschke C, Leisner A, Hester A, Maass K, Guenther S, Bouschen W, et al. Mirion - A software package for automatic processing of mass spectrometric images. J Am Soc Mass Spectrom. 2013;24:1296–306.
We thank Ramya Ganesan for carrying out DNA extractions and supporting insect collection, Benjamin Weiss for assistance and advice during the preparation of histological sections, Dagmar Klebsch and Christiane Gross for support in insect rearing, and Andrea Perner for MS measurements. We are thankful to the responsible Brazilian institutions for granting the following permits for access, collection, and export of insect specimens: ICMBio (SISBio) authorization 45742-5 and 45742-7—45742-10, CNPq process 01300.0013848/2017-33, and IBAMA exportation permits # 20BR034265/DF and 20BR035212/DF. This study also complies with Brazilian-Nagoya Protocol regulations: SISGen genetic patrimony access permit A412E4B and shipping permits R665BAC, RB1A835, RD32745, R8A3857, RD947ED, and R0A30D2. This research was supported by funding from the German Science Foundation (DFG) Research Grants FL1051/1-1, KA2846/6-1, and Project-ID 239748522—SFB 1127 (ChemBioSys), as well as a Consolidator Grant of the European Research Council (ERC CoG 819585 ‘SYMBeetle’) and the Novo Nordisk Foundation (NNF20OC0064385).
The authors declare no competing interests.
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Janke, R.S., Kaftan, F., Niehs, S.P. et al. Bacterial ectosymbionts in cuticular organs chemically protect a beetle during molting stages. ISME J 16, 2691–2701 (2022). https://doi.org/10.1038/s41396-022-01311-x