Effects of Sunflower Phenolamides on Infected Bumblebees: History
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Contributor:
Antoine Gekière
,
Irène Semay
,
,
Denis Michez
,
Pascal Gerbaux
,
Maryse Vanderplanck

Bees may forage on specific floral resources to face parasite infection. Such natural resources are comparable to ‘natural pharmacies’ and may be favoured in bee conservation strategies. Consumption of sunflower pollen, despite being detrimental for larval development, has been recently shown to reduce the load of a widespread bumble bee gut parasite in the common eastern bumble bee. Although the underlying mechanisms remain unknown, it has been suggested that sunflower phenolamides—a family of molecules found in most flowering plants—may be responsible for such a reduction in parasite load. 

  • Crithidia bombi
  • Bombus terrestris
  • Helianthus annuus
  • Specialised metabolites
  • Microcolony performance
  • Phenotypic variation
  • Immunocompetence

1. Introduction

Bees rely on floral resources, mainly pollen, to meet the nutritional requirements for their development, reproduction and survival [1]. Pollen consists of both central (i.e., phytochemicals involved in plant growth and development such as proteins, amino acids, lipids and carbohydrates) [2] and specialised metabolites (i.e., phytochemicals involved in plant abiotic and biotic interactions such as alkaloids, phenolics and terpenoids) [3]. Whereas bee–plant interactions are often regarded as a ‘perfect mutualism’, they actually hide a silent conflict in which bees act concurrently as pollinators, essential to plant reproduction, and palynivores, compromising the plant reproductive success (i.e., pollen dilemma [4]). This conflict of interest has been proposed as an explanation for the occurrence of specialised metabolites in pollen that may be toxic or deterrent to some bee species, which limits excessive pollen harvesting (e.g., [5][6]). Indeed, some specialised metabolites are detrimental to unspecialised bees by impeding larval development [7], leading to gut damage in adults [5], inducing malaise behaviours [8], weakening the immune system [9] and, in some instance, killing larvae and adults [8]. Moreover, other hypotheses have been put forward to explain the presence of specialised metabolites in pollen, such as pleiotropy (i.e., non-adaptative genetic or physiological leakage from other tissues) and protection against biotic (e.g., pathogens) or abiotic (e.g., UV radiation) stressors [10][11]. Along with pollen nutrients, it is likely that pollen-specialised metabolites shape bee–plant interactions.
Bees, even generalist species, do not forage randomly on all available plant species but rather display a selective foraging behaviour, favouring floral resources that meet their nutritional and physiological requirements [12]. Actually, feeding on suitable resource may help bees face environmental stressors such as heat stress [13], pesticide exposure [14] but also parasite infection [15][16]. Indeed, wild bees are challenged with a vast range of parasites, parasitoids and pathogens including metazoans, protozoans, bacteria and viruses [17][18]. Infection outcomes greatly differ regarding enemy species: while some bees’ enemies were found to only have sublethal effects (e.g., impaired flower handling and foraging behaviour [19]), some significantly reduced their host survival (e.g., [20]). Further, outcomes vary depending on the host species and its physiology, including its nutritional state [21][22].
How specific pollen help bees to deal with an infection remains mostly unknown, but studies have suggested that the consumption of particular resources can either impede parasite development (e.g., flagellum removal [23]) or boost bee immunity (e.g., greater fat body content and pro-phenoloxidase production [24]). Notably, the consumption of specific pollen-specialised metabolites has been shown to reduce parasite load in bumble bees [25] and help honeybees to face infection [26]. For instance, sunflower pollen (Helianthus annuus; Asterids: Asteraceae) has been shown to reduce Crithidia bombi (Euglenozoa: Trypanosomatidae) infection in the common eastern bumble bee Bombus impatiens (Hymenoptera: Apidae) [27]. This observation was consistent among several sunflower cultivars and populations [28] but differed according to the timing and duration of exposure to sunflower pollen [29] as well as to the caste of the infected bumble bees [30]. Sunflower pollen has, therefore, been suggested as a suitable resource for infected bumble bees despite its low nutritional quality [31]. Yet, the mechanism underlying such a parasite load reduction remains unknown [32], although it has been recently suggested that it could be due to a more rapid excretion induced by sunflower pollen consumption, and more especially by its phenolamides [33], a major class of phenylpropanoid metabolites evolutionarily conserved across angiosperms [34][35].

2. Phenolamide Allocation in Sunflower

While no detectable phenolamide occurred in sunflower leaves and corolla, significant differences in phenolamide profiles were found between sunflower pollen and nectar. Although the roles of phenolamides in plant development and resistance against abiotic (e.g., UV radiation) and biotic (e.g., pathogens and herbivores) stressors are well-documented [34], no function has been clearly attributed for their large amount in pollen (coat) and nectar [36]. However, the evidence is that phenolamides in sunflower floral resources do not ‘simply’ result from a pleiotropic effect as none of them were detected in vegetative parts. Moreover, since sunflower nectar is a phloem derivative [37], it suggests that pre-nectar from the vascular system is free of phenolamides, which are then probably synthesised in the nectariferous tissues. The origin of phenolamides in sunflower pollen is not clear as they can arise from both leakage from anthers [38] and biosynthesis in pollen cytoplasm [39]. Regardless, such an occurrence of phenolamides in floral resources obviously exposes bees to their effects, especially since these specialised metabolites are widespread among flowering plants [34].

3. Effects of Sunflower Pollen and Phenolamides on Bumble Bees

Sunflower pollen is not suitable for bumble bee development mainly due to nutritional deficiencies [40] but also to the occurrence of potentially toxic specialised metabolites (e.g., alkaloids [3]) and to the peculiar morphology of exine, which is typical of Asteraceae [41][42]. As no compensatory feeding behaviour (i.e., increased pollen collection) has been highlighted, it suggests that unsuitability may be due to pollen toxicity or low digestibility rather than to nutritional deficiencies (e.g., [5]). Actually, microcolonies fed a supplemented diet also produced a reduced number of males and a restricted offspring mass, suggesting that phenolamides may partly explain sunflower unsuitability (Figure 1). They also displayed a higher pollen dilution, which is known as a behaviour allowing for mitigation of unfavourable pollen properties (e.g., [43]). However, neither natural nor supplemented diets induced mortality among the B. terrestris workers. Such unsuitable but sublethal effects of sunflower phenolamides might arise from their antifungal and antibacterial properties [44][45] that may disrupt the bumble bee microbiota (e.g., by boosting/depleting some phylotypes [46]). Moreover, phenolamides are known to upregulate some genes in bees that are homologous to those that stimulate rapid excretion in other insects [47], suggesting that phenolamides might negatively alter bumble bee physiology.

Microcolony development across treatments.

Figure 1. Microcolony development across treatments.

Alongside these effects reported in the literature, the bioassays highlighted that phenolamides also induced a reduction in fat body content, which is a major component of the immune system [48]. Indeed, individuals fed a supplemented or natural diet displayed lower fat body content compared to those fed a control diet (Figure 2). As natural and supplemented diets have different nutritive composition (i.e., one based on sunflower pollen, the other based on willow pollen as for the control diet), this effect cannot arise from differences in pollen nutrients or digestibility. The only valid explanation would be the contribution of the fat body in the detoxification of allelochemical compounds [49]. Actually, the occurrence of phenolamides in both natural and supplemented diets could have activated detoxification pathways, leading to metabolic costs associated with a reduction in lipid reserves (i.e., fat body).

Regarding phenotypic variation, the occurrence of phenolamides in the pollen diet also impacted the shape of the forewing and increased shape fluctuating asymmetry (FA) in newly emerged males (i.e., significant differences among males reared on different diets). Such effects of specialised metabolites on male wing shape have already been highlighted in similar bioassays using sinigrin and amygdalin-supplemented diets [50] and can be indicative of changes in environmental conditions or presence of stressors [51]. By contrast, levels of FA are often lower under controlled conditions [50], and the increase in FA in stressful conditions is indicative of a lesser developmental stability, meaning that males are challenged during their development, which leads to deviations from perfect symmetry between each side [52]. The mechanism explaining such modifications under various stressors remains unclear, but it has been proposed that a shift in energy allocation (e.g., activation of detoxification pathways) can occur and then weaken the homeostasis, ultimately impacting the phenotype [53].

4. Infection Costs of a Gut Parasite on Bumble Bees

While diet effects on microcolonies were strongly pronounced, only mild effects of the gut parasite Crithidia bombi were observed since infected microcolonies did not display neither higher mortality nor higher stress responses than uninfected ones. Actually, C. bombi is known to be a highly prevalent but not too virulent gut parasite [54]. While a compensatory feeding behaviour (i.e., increased pollen collection) and reduced survival have been highlighted in infected Bombus impatiens workers [55], these effects were not observed herein for B. terrestris, suggesting that differences in susceptibility occur among bumble bee species.

As expected, due to the immune challenge, parasite infection resulted in a significant decrease in fat body content (Fig 2). However, such an effect has never been highlighted in previous laboratory studies investigating the impact of the parasite on bumble bees’ fat bodies, probably because of the experimental design that implied isolating each individual for a short period [21][56]. Individuals were maintained within microcolonies and likely constantly reinfected themselves via nestmate faeces and brood with a continuous exposure for 35 days [57], which could have resulted in a greater immune challenge than in previous studies.

Fat body content in Bombus terrestris individuals

Figure 2. Fat body content in bumble bee individuals.

Regarding the phenotypic variation, the parasite did not impact any of the measured parameters (i.e., centroid size, wing shape, size FA, and shape FA). This result contrasts with a previous study showing that Apicystis bombi (Apicomplexa: Neogregarinorida) impacted wing size and shape as well as size FA [50]. This discrepancy could be explained by the difference in parasites’ host life stages. Indeed, A. bombi infects all brood stages as well as adults, challenging the bumble bees during their development, whereas C. bombi only infects adults without any developmental challenge [57]. 

5. Effects of Sunflower Pollen and Phenolamides on a Gut Parasite

It was shown that sunflower pollen did not reduce C. bombi load in the bumble bee B. terrestris (Figure 3). This observation is quite surprising and unexpected given the plethora of previous studies that systematically found a medicinal effect of sunflower pollen in infected bumble bees in different experimental designs (i.e., different sunflower cultivars, different parasite strains, workers housed individually or in microcolonies) [27][28][29][30][31][32]. One explanation would be the difference in the host bumble bee species as this entry used B. (Bombus) terrestris whereas previous studies used B. (Pyrobombus) impatiens, which modifies the host genotype x parasite genotype x environment interacting factor in the Bombus–Crithidia system [22]. Such a discrepancy has recently been demonstrated by Fowler et al. [58] who showed that sunflower pollen reduced Crithidia load in B. impatiens, B. bimaculatus and B. vagans (subgenus Pyrobombus) but not in B. griseocollis (subgenus Cullumanobombus). Another difference in the experimental design is the delay between parasite inoculation and consumption of sunflower pollen, which seems to be a crucial parameter when assessing the medicinal effect of pollen diet. Indeed, previous studies indicated that infected bumble bees fed sunflower pollen 3.5 days after inoculation did not display any reduced parasite load compared to control, whereas infected bumble bees fed sunflower pollen right after inoculation displayed a reduced parasite load after seven days [29]. Discrepancies may also arise from difference in pollen used as the control diet, namely willow and buckwheat or wildflower mix in previous ones [27][28][29][30][31][32].

While no effect of sunflower pollen has been highlighted for parasite infection, phenolamides benefited the parasite as infected workers fed a supplemented diet displayed an increased parasite load (Figure 3). Such a parasite-facilitating effect of phenolamides has been already observed in a previous study, though it was less pronounced than herein, probably because of some differences between the experimental designs [32]. This effect could arise from different biological activities of phenolamides: (i) their antifungal and antibacterial properties [44][45] that may disrupt the gut microbiota and then weaken a crucial non-immunological defence [59]; (ii) their antioxidant and radical scavenging activities that may lead to a decrease in reactive oxygen species and an immunosuppressed state [60]; and (iii) their potential toxic activities that could result in activation of defence pathways (i.e., detoxification system), altering bee physiology, consuming their energy reserves and then weakening the whole organism that would not be disposed to face an immune challenge (e.g., [61]). While these results cannot unravel the mechanisms favouring parasite development in microcolonies fed a supplemented diet, it can however be proposed that phenolamides are not responsible for medicinal effects of sunflower as recently suggested by [33], that put forward a reduction in parasite load through more rapid excretion after sunflower pollen consumption.

Figure 3. Parasite load among diet treatments for 31 days (mean ± SE).

6. Focus for Future Research

Since all pollen diets display specialised metabolites with differing biological activities and potential physical properties, no one can clearly rule out potential effects of their control pollen diet on parasite load (i.e., favouring or impeding effects). One solution would be to use an artificial diet free of specialised metabolites and physical barriers, and suitable for microcolony development, or to clearly establish the absence of medicinal effects of the natural control pollen diet prior to bioassays (e.g., examining parasite growth through in vitro assays), which has never been thoroughly done. Besides this issue, the definition of ‘medicinal effects’ itself may be confusing. Importantly, a medicinal effect may occur either by benefiting the host or by hampering parasite growth. While some have claimed that a diet must compulsorily be detrimental to the parasite to be considered as medicinal [62], others have argued that it is not mandatory and proposed that medicinal diets could either increase host resistance or tolerance to infection [63]. Furthermore, detrimental effects on unicellular parasites cannot be only assessed based on cells count but should also be considered through molecular impacts on parasite cells such as impairment of protein synthesis, intercalation in DNA, disruption of cell wall, induction of apoptosis, or any other mechanism impeding parasite fitness such as flagellum loss (e.g., [23]). Experiments seeking the most suitable control diet when addressing medicinal effects of pollen on infected bees as well as experiments testing the molecular effects of pollen-specialised metabolites on parasite cells promise to bring new insights into the mechanisms underlying medicinal effects of pollen. Untangling such mechanisms would shed light on the way bees could use floral resources to overcome parasite challenge.

7. Conclusions

It was showed that some phenolamides are found in sunflower floral resources (i.e., nectar and pollen) while they are absent from sunflower leaves and corolla and are therefore collected by bumble bees when foraging. Both sunflower pollen and its phenolamides had detrimental effects on Bombus terrestris, but phenolamides had milder effects. Conversely, sunflower pollen and its phenolamides had surprising diverging effects on Crithidia bombi load (Figure 4). On the one hand, sunflower pollen did not alter parasite load, which contrasts with previous studies conducted on B. impatiens. On the other hand, sunflower phenolamides increased parasite load, which discredits hypotheses made in previous studies. Because in plant–bee–parasite studies control diets and biological models differ greatly, this entry cautions against comparisons that could be drawn and encourages future research to develop a proper standardised framework.
Graphical abstract
Figure 4. Graphical abstract.
 

This entry is adapted from the peer-reviewed paper 10.3390/biology11040545

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