As ectotherms, many insects spend the winter months in a state of suspended animation (i.e., diapause), lowering their metabolic rates to subsist on a limited store of energy reserves. The ability to lower metabolic rate during diapause relies, in part, on cold winter temperatures to intrinsically lower metabolic rate. Winter warming associated with global climate change may pose a challenge to diapausing insects by intrinsically increasing metabolic rate, potentially leading to the exhaustion of energetic reserves. We used stop-flow respirometry to measure oxygen consumption in response to temperatures representative of both acute and chronic winter warming scenarios in diapausing Pieris rapae pupae. Metabolic rate increased with increasing temperature in diapausing pupae, but metabolic rate depended on both pupal age and warming severity, with older pupae having lower metabolic rates overall. Despite the increases in metabolic rate, pupae recovered metabolic rate within 24-hours after short-term acute-warming exposure. In contrast, chronic exposure to warming over weeks and months led to significant decreases in metabolic rate later in diapause, as well as reductions in pupal mass. These results demonstrate that while respiration was thermally responsive, warming did not lead to sustained increases in metabolic rate. Instead, diapausing P. rapae appear to acclimate to higher temperature by lowering their metabolic rates in response to months of chronic warming. Overall, these patterns suggest that this species could be resilient to winter warming, at least in the context of energetics. However, the precise mechanisms underlying these responses remain to be characterized. Thus, future research-e.g., on the genetic underpinnings of energetics in the context of warming-could further elucidate the relative vulnerability of diapausing insects to future winter warming.
In response to high temperatures, insect metabolic rates increase, favoring the release of higher amounts of reactive oxygen species (ROS). These ROS need to be counteracted by antioxidants to avoid oxidative stress, which can lead to cell damage and death. In this manuscript, we review evidence in insects showing the effects of high temperatures on ROS production, the antioxidant defenses reported in insects in response to high and extremely high temperatures and the extent to which they contribute to preventing oxidative damage. Endogenously produced antioxidants can be enzymatic or non-enzymatic and are involved in heat responses in at least seven insect orders. Our review indicates that evidence is very limited for the effect of high temperature on ROS production, but it clearly shows that at least one antioxidant is upregulated during short-term heat exposure. However, the effects of antioxidants in effectively reducing oxidative damage in biomolecules are still poorly supported by evidence. Dietary-dependent antioxidants show strong potential for coping with heat stress, but evidence is limited, although numerous plants produce antioxidant compounds and a great number of insect species feed on plants. The role of antioxidants in heat acclimation and adaptation is promising but evidence is still very limited in insects. Antioxidants also protect from other prooxidant conditions such as pesticide exposure, nutrient stress, or new biotic interactions, which often act in combination. Potential trade-offs between antioxidant use to different functions could define insect survival and pace of life in response to multiple stressors, including high temperatures. Our literature review indicates that there is only limited evidence of the role of antioxidants in preventing oxidative damage caused by heat, opening the possibility that ROS production might be mitigated by the action of uncoupling proteins or degradation of mitochondria. Finally, we conclude by proposing promising research avenues to gain a deeper understanding of the role of ROS and antioxidants in the oxidative balance of insects exposed to mild and extreme heat.
Parnassius smintheus is an alpine butterfly that overwinters as a first-instar caterpillar within its egg and often beneath the snow. While extreme temperatures in early winter appear pivotal to year-to-year population change of P. smintheus in the Rocky Mountains of Canada, the sources of mortality for these eggs are unclear. Here we tested three hypotheses about the vulnerability of eggs to warming and extreme weather in early winter (i.e. upper quartile of daily maximum and minimum microclimate temperatures in November): (1) warming disrupts the acquisition of cold tolerance, making eggs susceptible to subsequent cold snaps; (2) warming drives premature development and hatch, such that precocious hatchlings either starve or freeze; and (3) warming depletes the energy stores of dormant eggs. We then used these hypotheses to guide a simulation of the risk of winter mortality for eggs over the last half-century (1971 - 2020) in the Rocky Mountains of Canada. Early winter warming did not interrupt the acquisition of cold tolerance by freeze-avoidant eggs. Eggs did risk lethal freezing in simulated winters when extreme low temperatures coincided with an absence of snow cover. Early winter warming increased the risk of subsequent hatching, and precocious larvae were less cold-tolerant than eggs. Our simulation found that precocious larvae risked freezing during snow-free cold snaps in spring. Early winter warming did not appreciably drawdown energy stores, and we found that P. smintheus could not only fuel overwintering but tolerate several days of starvation after hatch. We conclude that eggs risk precocious development after early winter warming and are likely vulnerable in winters that lack persistent snow cover. Together, these sources of winter mortality may explain year-to-year change in P. smintheus populations. Identifying unidirectional thresholds, such as hatching and freezing, may be important for predicting the susceptibility of some alpine insects to future winter warming.
Globally, the area of protected cropping has grown exponentially in the past 25 years. Concomitantly, the number of greenhouse crop species has increased, and a substantial proportion of these rely on, or benefit from, bee pollination. Both in crops grown outside and under cover, diversity in pollinating species could create resilience in this important service. Here we review, for the first time, the utility and use of solitary bee species for crop pollination in protected cropping environments. An increasing number of bee species, including solitary bees, are managed for pollination of crops grown outside, and our review shows that there is no shortage of solitary species able to pollinate crops grown under protective covers. Despite this, only four solitary species are used on a small commercial scale, and only in orchard crops, while pollination in greenhouses worldwide is delivered by a few, often introduced, bumble bee species. We argue that there are two impediments to the use of solitary bees for pollination in protective cropping environments: (a) Bumble bees satisfy most current greenhouse requirements, and (b) There are intrinsic difficulties in relation to husbandry and reliable large-scale supply of solitary bees, in particular when they are required year-round. We explore the possibility to overcome the second impediment by selecting species with suitable life-history traits or by deploying multiple species. Structured Abstract Purpose To review the utility and use of solitary bee species for pollination of crops grown under covers, and to investigate what could be done to enhance the use of solitary bees in such environments. Basic Procedures Using a systematic literature search, we review the solitary bee species that have been experimentally tested for their efficacy as pollinators of greenhouse and protected orchard crops. Studies included measured efficacy as increased seed/fruit set, fruit quality, pollen deposition or, where appropriate, buzz pollination activity, relative to controls. We also searched the literature for evidence of use of solitary bees in the pollination of crops under cover. Main findings The pollination efficacy of 45 solitary bee species had been tested in 98 bee-crop species combinations, with 87% of tests yielding positive outcomes. Representatives of different bee families differed in their efficacy for the pollination of different crop species. Despite their utility, only four species are used commercially in orchards, and none in greenhouses, because (a) bumble bees satisfy most current requirements; (b) there are intrinsic difficulties in relation to husbandry and reliable year-round supplies of solitary bees in sufficient numbers. New and important aspects We provide a global review and juxtapose utility and use of solitary bees. We also explore, for the first time, the difficulties posed by life-history traits on the deployment of solitary bees for the pollination of greenhouse crops and discuss whether and how these could be overcome.
The main insect chemoreceptors are olfactory receptors (ORs), gustatory receptors (GRs) and ionotropic receptors (IRs). The odorant binding sites of many insect ORs appear to be occluded and inaccessible from the surface of the receptor protein, based on the three-dimensional structure of OR5 from the jumping bristletail Machilis hrabei (MhraOR5) and a survey of a sample of vinegar fly (Drosophila melanogaster) OR structures obtained from artificial intellegence (A.I.) modeling. Molecular dynamics simulations revealed that the occluded site can become accessible through tunnels that transiently open and close. The present study extends this analysis to examine seventeen ORs and one GR docking with ligands that have known valence: nine that signal attraction and nine that signal aversion. All but one of the receptors displayed occluded ligand binding sites analogous to MhraOR5, and docking software predicted the known attractant and repellent ligands will bind to the occluded sites. Docking of the repellent DEET was examined, and more than half of the OR ligand sites were predicted to bind DEET, including receptors that signal aversion as well as those that signal attraction. However, DEET may not actually have access to all the attractant binding sites. The larger size and lower flexibility of repellent molecules may restrict their passage through the tunnel bottlenecks, which could act as filters to select access to the ligand binding sites. In contrast to ORs and GRs, the IR ligand binding site is in an extracellular domain known to undergo a large conformational change from an open to a closed state. A.I. models of two D. melanogaster IRs of known valence and two blacklegged tick (Ixodes scapularis) IRs having unknown ligands were computationally tested for attractant and repellent binding. The ligand-binding sites in the closed state appear inaccessible to the protein surface, so attractants and repellents must bind initially at an accessible site in the open state before triggering the conformational change. In some IRs, repellent binding sites were identified at exterior sites adjacent to the ligand-binding site. These may be allosteric sites that, when occupied by repellents, can stabilize the open state of an attractant IR, or stabilize the closed state of an IR in the absence of its activating ligand. The model of D. melanogaster IR64a suggests a possible molecular mechanism for the activation of this IR by H+. The amino acids involved in this proposed mechanism are conserved in IR64a from several Dipteran pest species and disease vectors, potentially offering a route to discovery of new repellents that act via the allosteric site.
The calcium dependent Calpain proteases are modulatory enzymes with important roles in cell cycle control, development and immunity. In the fly model Drosophila melanogaster Calpain A cleaves Cactus/IkappaB and consequently modifies Toll signals during embryonic dorsal-ventral (DV) patterning. Here we explore the role of Calpains in the hemiptera Rhodnius prolixus, an intermediate germband insect where the Bone Morphogenetic Protein (BMP) instead of the Toll pathway plays a major role in DV patterning. Phylogenetic analysis of Calpains in species ranging from Isoptera to Diptera indicates an increase of Calpain sequences in the R. prolixus genome and other hemimetabolous species. One locus encoding each of the CalpC, CalpD and Calp7 families, and seven Calpain A/B loci are present in the R. prolixus genome. Several predicted R. prolixus Calpains display a unique architecture, such as loss of Calcium-binding EF-hand domains and loss of catalytic residues in the active site CysPc domain, yielding catalytically dead Calpains A/B. Knockdown for one of these inactive Calpains results in embryonic DV patterning defects, with expansion of ventral and lateral gene expression domains and consequent failure of germ band elongation. In conclusion, our results reveal that Calpains may exert a conserved function in insect DV patterning, despite the changing role of the Toll and BMP pathways in defining gene expression territories along the insect DV axis.
Foraging behavior of pollinators is shaped by, among other factors, the conflict between maximizing resource intake and minimizing predation risk; yet, empirical studies quantifying variation in both forces are rare, compared to those investigating each separately. Here, we discuss the importance of simultaneously assessing bottom-up and top-down forces in the study of plant-pollinator interactions, and propose a conceptual and testable graphical hypothesis for pollinator foraging behavior and plant fitness outcomes as a function of varying floral rewards and predation risk. In low predation risk scenarios, no noticeable changes in pollinator foraging behavior are expected, with reward levels affecting only the activity threshold. However, as predation risk increases we propose that there is a decrease in foraging behavior, with a steeper decline as plants are more rewarding and profitable. Lastly, in high predation risk scenarios, we expect foraging to approach zero, regardless of floral rewards. Thus, we propose that pollinator foraging behavior follows an inverse S-shape curve, with more pronounced changes in foraging activity at intermediate levels of predation risk, especially in high reward systems. We present empirical evidence that is consistent with this hypothesis. In terms of the consequences for plant fitness, we propose that specialized plant-pollinator systems should be more vulnerable to increased predation risk, with a steeper and faster decline in plant fitness, compared with generalist systems, in which pollinator redundancy can delay or buffer the effect of predators. Moreover, whereas we expect that specialist systems follows a similar inverse S-shape curve, in generalist systems we propose three different scenarios as a function not only of reward level but also compatibility, mating-system, and the interplay between growth form and floral display. The incorporation of trade-offs in pollinator behavior balancing the conflicting demands between feeding and predation risk has a promising future as a key feature enabling the development of more complex foraging models.
Animals, including insects, need oxygen for aerobic respiration and eventually asphyxiate without it. Aerobic respiration, however, produces reactive oxygen species (ROS), which contribute to dysfunction and aging. Animals appear to balance risks of asphyxiation and ROS by regulating internal oxygen relatively low and stable, but sufficient levels. How much do levels vary among species, and how does variation depend on environment and life history? We predicted that lower internal oxygen levels occur in insects with either limited access to environmental oxygen (i.e., insects dependent on aquatic respiration, where low internal levels facilitate diffusive oxygen uptake, and reduce asphyxiation risks) or consistently low metabolic rates (i.e., inactive insects, requiring limited internal oxygen stores). Alternatively, we predicted insects with long life-stage durations would have internal oxygen levels > 1 kPa (preventing high ROS levels that are believed to occur under tissue hypoxia). We tested these predictions by measuring partial pressures of oxygen (PO2) in tissues from juvenile and adult stages across 15 species comprising nine insect orders. Tissue PO2 varied greatly (from 0 to 18.8 kPa) and variation across species and life stages was significantly related to differences in habitat, activity level, and life stage duration. Individuals with aquatic respiration sustained remarkably low PO2 (mean = 0.88 kPa) across all species from Ephemeroptera (mayflies), Plecoptera (stoneflies), Trichoptera (caddisflies), and Diptera (true flies), possibly reflecting a widespread, but hitherto unknown, adaptation for extracting sufficient oxygen from water. For Odonata (dragonflies), aquatic juveniles had higher PO2 levels (mean = 6.12 kPa), but these were still lower compared to terrestrial adults (mean = 13.3 kPa). Follow-up tests in juvenile stoneflies showed that tissue PO2 remained low even when exposed to hyperoxia, suggesting that levels were down-regulated. This was further corroborated since levels could be modulated by ambient oxygen levels in dead individuals. In addition, tissue PO2 was positively related to activity levels of insect life stages across all species and was highest in stages with short durations. Combined, our results support the idea that internal PO2 is an evolutionarily labile trait that reflects the balance between oxygen supply and demand within the context of the environment and life-history of an insect.
Pyrethroids are the most widely used insecticides for controlling insect vectors carrying medically and economically significant pathogens. In Colombia, studies on triatomine insecticide resistance are limited. Due to the increasing challenge of insecticide resistance, this work focuses on determining resistance to different pyrethroid insecticides in populations of Triatoma dimidiata from Colombia. To define the possible causes of resistance, three potential molecular mechanisms were explored: 1) mutations in the coding region of the voltage-gated sodium channel gene (vgsc), the insecticide target site; 2) modulation of enzymatic activity associated with metabolic resistance; and 3) changes in the mRNA profiles using RNA-seq. The results showed that the field population of T. dimidiata was resistant to lambda-cyhalothrin and deltamethrin insecticides. Insects surviving sublethal doses of insecticides did not exhibit the classical mutations in the vgsc gene. Transcriptomic profile analyses of T. dimidiata revealed differentially regulated genes in field and laboratory populations under selective pressure with lambda-cyhalothrin. Gene enrichment analysis showed the positive regulation of transcripts related to detoxifying enzymes and mitochondrial proteins, which could play a significant role in insecticide resistance. This comprehensive investigation is crucial for providing insights into resistance mechanisms and generating strategies to manage these critical vector species.
Trypanosomatids, obligate parasites capable of impacting insects' hindgut, have recently obtained considerable attention, especially about their effects on bees. While Crithidia mellificae and C. bombi were initially discovered and studied in honey bees and bumblebees, respectively, molecular techniques revealed Lotmaria passim as the predominant trypanosomatid in honey bees globally. New species like C. expoeki and C. acanthocephali have also been identified. These parasites have complex life cycles involving various host developmental stages and are transmitted horizontally within and outside colonies through direct contact, oral interactions, and contaminating flowers with infected faeces. The impact of trypanosomatids on honey bee colony health remains uncertain. In bumblebees, studies highlighted the widespread presence of C. bombi, affecting colony and individual fitness, development, and foraging behaviour. Bee trypanosomatids have been detected in various species, including other insects, and mammals, suggesting diverse epidemiological pathways and potential effects that warrant further investigation. Biotic factors, including co-infections, gut microbiota, food contamination, and abiotic factors like environmental conditions, pesticides, and urbanization, play crucial roles in infection dynamics. This review aimed to summarise key research on trypanosomatid transmission and infection in both managed and wild bees, focusing on the influence of biotic and abiotic factors. The work highlights significant gaps in current knowledge and provides a valuable foundation for future studies. Understanding the pathogenicity and infection dynamics of trypanosomatids, along with the impact of environmental factors, is essential for developing effective conservation strategies that support pollinator health and overall ecosystem resilience.
Cold temperatures can play a significant role in the range and impact of pest insects. Severe cold events can reduce the size of insect outbreaks and perhaps even cause outbreaks to end. Measuring the precise impact of cold events, however, can be difficult because estimates of insect mortality are often made at the end of the winter season. In late January 2023 long-term climate models predicted a significant cold event to occur over eastern North America. We used this event to evaluate the immediate impact on hemlock woolly adelgid (Adelges tsugae Annand) overwintering mortality at four sites on the northern edge of the insects invaded range in eastern North America. We observed complete mortality, partial mortality and no effects on hemlock woolly adelgid mortality that correlated with the location of populations and strength of the cold event. Our data showed support for preconditioning of overwintering adelgids having an impact on their overwintering survival following this severe cold event. Finally, we compared the climatic conditions at our sites to historical weather data and previous observations of mortality in Nova Scotia. The cold event observed in February 2023 resulted in the coldest temperatures observed at these sites, including the period within which hemlock woolly adelgid invaded, suggesting cold conditions, especially under anthropogenic climate forcing, may not be a limiting factor in determining the ultimate northern range of hemlock woolly adelgid in eastern North America.
The triatomine bug Rhodnius prolixus is a hematophagous hemipteran and a primary vector of Trypanosoma cruzi, the causative agent of Chagas' disease (CD), in Central America and Northern South America. Blood-feeding poses significant challenges for hematophagous organisms, particularly due to the release of high doses of pro-oxidant free heme during hemoglobin digestion. In this arthropod, most of the free heme in the gut is aggregated into hemozoin (Hz), an inert and non-oxidative biocrystal. Two major components present in the perimicrovillar membranes (PMM) of triatomine insects have been previously implicated in heme crystallization: lipids and the biochemical marker of the PMM, the enzyme α-glucosidase. In this study, we investigated the role of R. prolixus α-glucosidase isoform G (Rp-αGluG) in heme detoxification and the effects of its knockdown on the insect physiology. The effect of α-glucosidase isoform G (αGluG) knockdown on T. cruzi proliferation and metacyclogenesis was also investigated. Initially, a 3D structure of Rp-αGluG was predicted by comparative modeling and then subjected to molecular docking with the heme molecule, providing in silico support for understanding the process of Hz biocrystallization. Next, adult females of R. prolixus were challenged with RNAi against Rp-αGluG (dsαGluG) to assess physiological and phenotypic changes caused by its knockdown. Our data show that the group challenged with dsαGluG produced less Hz, resulting in more intact hemoglobin available in the digestive tract. These animals also laid fewer eggs, which had a lower hatching rate. In addition, T. cruzi metacyclogenesis was significantly lower in the dsαGluG group. The present work demonstrates the importance of Rp-αGluG in heme detoxification, the digestive and reproductive physiology of R. prolixus, as well as its influence on the life cycle of T. cruzi. Since heme neutralization is a vital process for hematophagous bugs, our study provides useful information for the development of new strategies targeting the Hz formation and potentially affecting the vectorial transmission of Chagas disease.
In nature, plants and insects engage in intricate interactions. Despite the increasing knowledge of the microbiomes of plants and insects, the extent to which they exchange and alter each other's microbiomes remains unclear. In this work, the bacterial community associated with nymphs of Philaenus spumarius (Hemiptera: Aphrophoridae), the stems of Coleostephus myconis where the nymphs were feeding, and the foam produced by the nymphs, were studied by culture-dependent and -independent approaches, with an attempt to elucidate the exchange of bacteria between plants and insects. The results suggest that both approaches complement each other, as many bacterial genera identified by metabarcoding were not detected by culturing, and vice versa. Overall, stems and foam exhibited higher bacterial diversity than nymphs, with all the samples showing enrichment in bacteria known to provide diverse benefits to their host. Stems and foam were the most similar in bacterial composition, but Burkholderiaceae and Moraxellaceae dominated the stems, whereas Rhizobiaceae and Sphingobacteriaceae dominated the foam. Nymphs exhibit the most distinct bacterial composition, yet more similar to that found in the stem compared to the foam. Indeed, nymphs were enriched on endosymbiotic bacteria, mostly Candidatus Sulcia and Sodalis, not found in the stem and foam. Nevertheless, during feeding, nymphs appeared to exchange several bacteria genera with C. myconis, with a significant number being incorporated into the bacteriome of the nymph. The genera Curvibacter, Cutibacterium, Methylobacterium, Pseudomonas and Rhizobium are likely the most exchanged. Nymphs also appear to exchange bacteria to the foam, notably species from the Enhydrobacter, Pseudomonas, Rhizobium and Roseomonas genera. More studies to infer the functions of the shared bacteria between P. spumarius-C. myconis are needed.
Aphids are valuable models for studying the functional diversity of bacterial symbiosis in insects. In addition to their ancestral obligate nutritional symbiont Buchnera aphidicola, these insects can host a myriad of so-called facultative symbionts. The diversity of these heritable bacterial associates is now well known, and some of the ecologically important traits associated with them have been well documented. Some twenty years ago, it was suggested that facultative symbionts could play an important role in aphid nutrition, notably by improving feeding performance on specific host plants, thus influencing the adaptation of these insects to host plants. However, the underlying mechanisms have never been elucidated, and the nutritional role that facultative symbionts might perform in aphids remains enigmatic. In this opinion piece, I put forward a series of arguments in support of the hypothesis that facultative symbionts play a central role in aphid nutrition and emphasize methodological considerations for testing this hypothesis in future work. In particular, I hypothesize that the metabolic capacities of B. aphidicola alone may not always be able to counterbalance the nutritional deficiencies of phloem sap. The association with one or several facultative symbionts with extensive metabolic capabilities would then be necessary to buffer the insect from host plant-derived nutrient deficiencies, thus enabling it to gain access to certain host plants.
Existing theories make different predictions regarding the effect of a pathogenic infection on the host capacity to reproduce. Terminal investment theory suggests that due to the increased risk of mortality, and the associated risk of losing future opportunity to reproduce, infected individuals would increase their investment towards reproduction. Life-history theory posits that due to energetic and resource costs associated with mounting an immune defense, hosts would decrease their investment towards reproduction, and reallocate resources towards defense and survival. Additionally, Somatic damage incurred by the host due to the infection is also expected to compromise the host capacity to reproduce. We explored these possibilities in Drosophila melanogaster females experimentally infected with pathogenic bacteria. We tested if the effect of infection on female fecundity is pathogen specific, determined by infection outcome, and variable between individual infected females. We observed that the mean, population level change in post-infection female fecundity was pathogen specific, but not correlated with mortality risk. Furthermore, infection outcome, i.e., if the infected female died or survived the infection, had no effect on fecundity at this level. At individual resolution, females that died after infection exhibited greater variation in fecundity compared to ones that survived the infection. This increased variation was bidirectional, with some females reproducing in excess while others reproducing less compared to the controls. Altogether, our results suggest that post-infection female fecundity is unlikely to be driven by risk of mortality and is probably determined by the precise physiological changes that an infected female undergoes when infected by a specific pathogen.
Herbivory is a major fitness pressure for plants and a key driver of crop losses in agroecosystems. Dense monocultures are expected to favor specialist herbivorous insects, particularly those who primarily consume crop species; yet, levels and types of herbivory are not uniform within regional cropping systems. It is essential to determine which local and regional ecological factors drive variation in herbivory in order to support functional agroecosystems that rely less on chemical inputs. Crops in the genus Cucurbita host a suite of both generalist and specialist herbivores that inflict significant damage, yet little is known about the relative contribution of these herbivores to variation in herbivory and how local- and landscape-scale Cucurbita resource concentrations, management practices, and natural enemies mediate this relationship. In this study, we tested whether three foundational ecological hypotheses influenced Cucurbita herbivory across 20 pumpkin fields in the semi-arid Southern High Plains Region of Texas. We used generalized linear mixed models and confirmatory path analysis to assess whether the Density-dependent Herbivory Hypothesis, Resource Concentration Hypothesis, or the Natural Enemies Hypothesis, could explain variation in Cucurbita herbivory and insect dynamics in the context of conventional agronomic practices. We found that herbivory increased over time, indicating that herbivores were causing sustained damage throughout the growing season. We also found that fields with higher local Cucurbita resources had lower herbivory, suggesting a resource dilution effect. Natural enemy communities were more abundant and taxonomically rich in sites with greater generalist herbivore abundance, though predator abundance declined over time, indicating that late-season crop fields are most at risk given high herbivory and low natural enemy-based control. Our findings also suggest that while local resource availability may drive the abundance and richness of arthropod communities, additional agronomic and phenological information is needed to anticipate herbivory risk in an agriculturally dominated landscape.
Insects are valuable models for studying innate immunity and its role in combating infections. The silkworm Bombyx mori L., a well-studied insect model, is susceptible to a range of pathogens, including bacteria, fungi, viruses, and microsporidia. Their susceptibility makes it a suitable model for investigating host-pathogen interactions and immune responses against infections and diseases. This review focuses on the humoral immune response and the production of antimicrobial peptides (AMPs), the phenoloxidase (PO) system, and other soluble factors that constitute the primary defense of silkworms against microbial pathogens. The innate immune system of silkworms relies on pattern recognition receptors (PRRs) to recognize pathogen-associated molecular patterns (PAMPs), which then activate various immune pathways including Imd, Toll, JAK/STAT, and RNA interference (RNAi). Their activation triggers the secretion of AMPs, enzymatic defenses (lysozyme and PO), and the generation of reactive oxygen species (ROS). Collectively, these pathways work together to neutralize and eliminate pathogens, thereby contributing to the defense mechanism of silkworms. Understanding the innate immunity of silkworms can uncover conserved molecular pathways and key immune components shared between insects and vertebrates. Additionally, it can provide valuable insights for improving sericulture practices, developing strategies to control diseases affecting silk production, and providing a theoretical foundation for developing pest control measures.
Why are some species sexually dimorphic while other closely related species are not? While all females in genus Strauzia share a multiply-banded wing pattern typical of many other true fruit flies, males of four species have noticeably elongated wings with banding patterns "coalesced" into a continuous dark streak across much of the wing. We take an integrative phylogenetic approach to explore the evolution of this dimorphism and develop general hypotheses underlying the evolution of wing dimorphism in flies. We find that the origin of coalesced and other darkened male wing patterns correlate with the inferred origin of host plant sharing in Strauzia. While wing shape among non-host-sharing species tended to be conserved across the phylogeny, shapes of male wings for Strauzia species sharing the same host plant were more different from one another than expected under Brownian models of evolution and overall rates of wing shape change differed between non-host-sharing species and host-sharing species. A survey of North American Tephritidae finds just three other genera with specialist species that share host plants. Host-sharing species in these genera also have wing patterns unusual for each genus. Only genus Eutreta is like Strauzia in having the unusual wing patterns only in males, and of genera that have multiple species sharing hosts, only in Eutreta and Strauzia do males hold territories while females search for mates. We hypothesize that in species that share host plants, those where females actively search for males in the presence of congeners may be more likely to evolve sexually dimorphic wing patterns.
Chironomus riparius midge larvae are ubiquitous in freshwater ecosystems throughout the Northern Hemisphere. Recently, freshwater in temperate regions has experienced a threat from salinization due to the use of road de-icers. As ambient temperatures fluctuate, snow and ice melt carry the de-icers into nearby freshwater and significantly raise salt levels. Recently, organic de-icers including brine beet juice de-icer (BBJD) have been implemented as an "ecofriendly" alternative to traditional road salt. Not much is known about the effects of BBJD on freshwater invertebrates. Aquatic insects respond to salinity by adjusting the ion transport functions of osmoregulatory organs. A key component in insect osmoregulation is the presence of water channel proteins known as aquaporins (AQPs) that allow movement of water along an osmotic gradient. To date, there is limited knowledge on the effects of salinity on AQP function in aquatic insects. In this study, we characterized a water-specific AQP known as CrAQP2 (a PRIP homolog) in the osmoregulatory organs of C. riparius larvae. CrAQP2 was immunolocalized in osmoregulatory organs with greatest transcript abundance in the Malpighian tubules. NaCl caused differential Craqp2 transcript expression in some of the organs, whereas BBJD had little effect on Craqp2 transcript levels. Craqp2 knockdown decreased total body water regardless of treatment and reduced survival of larvae in BBJD and NaCl. Therefore, CrAQP2 appears to be important in maintaining total body water levels stable and likely plays a role in the ability of midge larvae to respond to salinity.
There is a growing body of evidence that invertebrates can generate improved secondary responses after a primary challenge. This immunological memory can be primed by a range of pathogens, including bacteria. The generation of immunological memory has been demonstrated in mosquitoes, with the memory primed by a range of initial stimuli. This study aimed to examine whether insecticide resistance affects the capacity to generate immunological memory. The primary hypothesis was tested by examining the capacity of genetically related laboratory-reared Anopheles arabiensis strains that differ by insecticide resistant phenotype to generate immunological memory. The competing hypothesis tested was that the bacterial virulence was the key determinant in generating immunological memory. Immune memory was generated in F1 females but not males. Immunological memory was demonstrated in both laboratory strains, but the efficacy differed by the insecticide resistant phenotype of the strain. An initial oral challenge provided by a blood meal resulted generated better memory than an oral challenge by sugar. The efficacy of memory generation between the two bacterial strains differed between the two mosquito strains. Regardless of the challenge, the two strains differed in their capacity to generate memory. This study therefore demonstrated that insecticide resistant phenotype affected the capacity of the two strains to generate immunological memory. Although this study needs to be replicated with wild mosquitoes, it does suggest that a potential role for insecticide resistance in the functioning of the immune system and memory generation of An. arabiensis.