Insects encounter variable temperature conditions in their natural habitats. Under non-optimal temperatures, they experience thermal stress and oxidative damage, which are mitigated by antioxidant enzymes like superoxide dismutase (SOD), catalase (CAT) and lipid peroxidation (LPO). While short-term effects of thermal stress on antioxidant enzyme activities in insects are well understood, the long-term effects are less explored. We investigated both short-term (3 and 6 h) and long-term (24 h) effects of thermal stress on SOD, CAT and LPO activities in the Parthenium beetle, Zygogramma bicolorata Pallister at cold (15°C), control/optimal (25°C) and hot (35°C) temperatures. Although Z. bicolorata is an effective biocontrol agent for noxious Parthenium weed, no prior study assessed the impact of thermal stress on antioxidant enzyme activities in this beetle. Our results revealed that antioxidant enzymes activities increased above control levels in both larvae and adults when exposed to thermal stress for short durations. Under long-term thermal stress, CAT and LPO activities decreased below control levels, while SOD activity increased. Regardless of temperature conditions, early larval instars exhibited higher enzyme activities compared to later instars. In adults, males showed higher SOD and CAT activities, whereas LPO activity did not differ significantly between sexes. Our findings suggest that short-term thermal stress can stimulate protective enzyme activity in these beetles and help them adapt to suboptimal temperatures. However, prolonged exposure may lead to excessive stimulation, potentially inhibiting protective enzyme activity and causing the beetles to activate alternative pathways to manage thermal stress. Moreover, fourth instars and adult females are the most thermal stress-tolerant stages for Parthenium biocontrol.
{"title":"Impact of short- and long-duration thermal stress on antioxidant enzyme activity in Parthenium beetles","authors":"Priyanka Yadav, Arvind Kumar Patel, Parinita Singh, Sourabh Verma, Ritabrata Chowdhury, Bhupendra Kumar","doi":"10.1111/phen.12475","DOIUrl":"10.1111/phen.12475","url":null,"abstract":"<p>Insects encounter variable temperature conditions in their natural habitats. Under non-optimal temperatures, they experience thermal stress and oxidative damage, which are mitigated by antioxidant enzymes like superoxide dismutase (SOD), catalase (CAT) and lipid peroxidation (LPO). While short-term effects of thermal stress on antioxidant enzyme activities in insects are well understood, the long-term effects are less explored. We investigated both short-term (3 and 6 h) and long-term (24 h) effects of thermal stress on SOD, CAT and LPO activities in the Parthenium beetle, <i>Zygogramma bicolorata</i> Pallister at cold (15°C), control/optimal (25°C) and hot (35°C) temperatures. Although <i>Z. bicolorata</i> is an effective biocontrol agent for noxious Parthenium weed, no prior study assessed the impact of thermal stress on antioxidant enzyme activities in this beetle. Our results revealed that antioxidant enzymes activities increased above control levels in both larvae and adults when exposed to thermal stress for short durations. Under long-term thermal stress, CAT and LPO activities decreased below control levels, while SOD activity increased. Regardless of temperature conditions, early larval instars exhibited higher enzyme activities compared to later instars. In adults, males showed higher SOD and CAT activities, whereas LPO activity did not differ significantly between sexes. Our findings suggest that short-term thermal stress can stimulate protective enzyme activity in these beetles and help them adapt to suboptimal temperatures. However, prolonged exposure may lead to excessive stimulation, potentially inhibiting protective enzyme activity and causing the beetles to activate alternative pathways to manage thermal stress. Moreover, fourth instars and adult females are the most thermal stress-tolerant stages for Parthenium biocontrol.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 2","pages":"139-151"},"PeriodicalIF":1.5,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143909463","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Olga V. Polenogova, Anastasia V. Simakova, Tatyana N. Klementeva, Anna A. Varenitsina, Yulia V. Andreeva, Irina B. Babkina, Yulia A. Frank
The presence of environmental microplastics (MPs) poses a significant threat to terrestrial and aquatic animals, including insects such as blood-sucking mosquitoes. The paper reports on the laboratory study of the effect of three different types of MPs, including fragmented high-density polyethylene (HDPE), polypropylene (PP) and polystyrene (PS), on the viability, innate immune responses, activity of detoxifying enzymes and malondialdehyde (MDA) concentration in Aedes aegypti (Linnaeus, 1762). The results showed that dietary administration of microfragments of PP, PS and HDPE at low concentrations (4 mg/L) had no effect on the survival rate of mosquito larvae, but was observed to suppress the larval immune response. The addition of MPs to the diet resulted in a significant suppression of phenoloxidase activity compared to the control. A decrease in the activity of the detoxifying enzymes glutathione-S-transferase and non-specific esterase was observed. Dietary administration of MPs did not cause any significant change in alkaline proteolytic enzyme activity in larvae compared to the control. However, we observed a twofold increase in the activity of acid proteolytic enzymes in all experiments compared to the control (p < 0.05). MDA levels in larval homogenates remained unchanged, while lysozyme-like activity showed a slight decrease compared to the control. The observed processes may be a consequence of intestinal obstruction by MPs, which may cause microtraumas to intestinal tissues and changes in the structure and composition of the microbiota. These changes may have a profound effect on the resistance of mosquito larvae to insecticides and pathogens.
{"title":"Effects of microplastics on the physiology of living organisms on the example of laboratory reared bloodsucking mosquitoes Aedes aegypti L.","authors":"Olga V. Polenogova, Anastasia V. Simakova, Tatyana N. Klementeva, Anna A. Varenitsina, Yulia V. Andreeva, Irina B. Babkina, Yulia A. Frank","doi":"10.1111/phen.12474","DOIUrl":"10.1111/phen.12474","url":null,"abstract":"<p>The presence of environmental microplastics (MPs) poses a significant threat to terrestrial and aquatic animals, including insects such as blood-sucking mosquitoes. The paper reports on the laboratory study of the effect of three different types of MPs, including fragmented high-density polyethylene (HDPE), polypropylene (PP) and polystyrene (PS), on the viability, innate immune responses, activity of detoxifying enzymes and malondialdehyde (MDA) concentration in <i>Aedes aegypti</i> (Linnaeus, 1762). The results showed that dietary administration of microfragments of PP, PS and HDPE at low concentrations (4 mg/L) had no effect on the survival rate of mosquito larvae, but was observed to suppress the larval immune response. The addition of MPs to the diet resulted in a significant suppression of phenoloxidase activity compared to the control. A decrease in the activity of the detoxifying enzymes glutathione-S-transferase and non-specific esterase was observed. Dietary administration of MPs did not cause any significant change in alkaline proteolytic enzyme activity in larvae compared to the control. However, we observed a twofold increase in the activity of acid proteolytic enzymes in all experiments compared to the control (<i>p</i> < 0.05). MDA levels in larval homogenates remained unchanged, while lysozyme-like activity showed a slight decrease compared to the control. The observed processes may be a consequence of intestinal obstruction by MPs, which may cause microtraumas to intestinal tissues and changes in the structure and composition of the microbiota. These changes may have a profound effect on the resistance of mosquito larvae to insecticides and pathogens.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 2","pages":"128-138"},"PeriodicalIF":1.5,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143909545","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Triacylglycerides (TAGs) are neutral lipids and are one of the major energy storage forms in an insect aiding in normal physiology including reproduction of the organism. Importance of TAG metabolism in gametogenesis has been investigated in insects like mosquitoes, silkworm and Drosophila. However, a direct association between TAG levels and egg-to-adult viability has not been explored. In this study, we have assessed both stored and circulating TAG levels and egg-to-adult viability in Drosophila melanogaster lines with varying genetic backgrounds established through inbreeding and recombinant inbreeding strategies. We found noticeable variation in egg-to-adult viability and in both stored and circulating TAG levels in D. melanogaster lines. Apparently the D. melanogaster lines with higher levels of circulating TAG also had a higher egg-to-adult viability. To validate this, analysis of these variations through supervised correlation and unsupervised K-means clustering showed that levels of circulating TAG are positively associated with egg-to-adult viability irrespective of gender. The findings suggest that levels of circulating TAG promotes successful transition of egg to an adult. Taken together, the findings not only have a potential application in husbandry of ecologically and economically important insects but also holds importance in translational research in fertility of vertebrates including humans.
{"title":"Circulating triacylglycerides influence egg-to-adult viability in Drosophila melanogaster","authors":"Ayesha Aslam, Urooj Javed, Mushtaq Hussain","doi":"10.1111/phen.12473","DOIUrl":"10.1111/phen.12473","url":null,"abstract":"<p>Triacylglycerides (TAGs) are neutral lipids and are one of the major energy storage forms in an insect aiding in normal physiology including reproduction of the organism. Importance of TAG metabolism in gametogenesis has been investigated in insects like mosquitoes, silkworm and <i>Drosophila</i>. However, a direct association between TAG levels and egg-to-adult viability has not been explored. In this study, we have assessed both stored and circulating TAG levels and egg-to-adult viability in <i>Drosophila melanogaster</i> lines with varying genetic backgrounds established through inbreeding and recombinant inbreeding strategies. We found noticeable variation in egg-to-adult viability and in both stored and circulating TAG levels in <i>D. melanogaster</i> lines. Apparently the <i>D. melanogaster</i> lines with higher levels of circulating TAG also had a higher egg-to-adult viability. To validate this, analysis of these variations through supervised correlation and unsupervised K-means clustering showed that levels of circulating TAG are positively associated with egg-to-adult viability irrespective of gender. The findings suggest that levels of circulating TAG promotes successful transition of egg to an adult. Taken together, the findings not only have a potential application in husbandry of ecologically and economically important insects but also holds importance in translational research in fertility of vertebrates including humans.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 2","pages":"119-127"},"PeriodicalIF":1.5,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143909570","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kimberly Przybyla, Baptiste Martinet, Denis Michez, Michel Bocquet, Dalel Askri, Philippe Bulet
Wildlife faces an increasing threat from extreme climatic events, such as heatwaves, which can have a severe impact on various species, including crucial pollinators like bumblebees. Bumblebees are cold-adapted and heterothermic, possessing the ability to regulate their internal temperature. The impact of heat stress seems species specific in bumblebees. While most species are impacted, some bumblebee species manage to survive, potentially by employing physiological mechanisms, including the modulation of their protein profile (e.g. Heat Shock Proteins). However, there is limited understanding of how their protein profiles are associated with heat exposure. In this study, we examined the global variation in the protein profile of males from two bumblebee species sampled in the wild: the heat-tolerant Bombus terrestris and the heat-sensitive Bombus magnus. After subjecting them to heat stupor at 40°C in controlled condition, it was observed that nearly all B. terrestris survived the stress, while over 50% of B. magnus individuals succumbed to the heat exposure. Through off-gel bottom-up proteomics and LC–MS/MS analysis of the hemolymph proteome, we identified 164 proteins in both species with a large part of differentially expressed proteins after heat exposure. Additionally, quantitative analysis of fat bodies revealed that the relative mass was stable in B. terrestris, while it was significantly lower in B. magnus exposed to heat stress. Our data suggest that compared with B. magnus, B. terrestris displays a higher adaptability of its hemolymph proteome in response to heat stress. This adaptability could be a key factor contributing to the high physiological resistance of B. terrestris and its ability to adapt to new, stressful environments expected due to climate change. Understanding these mechanisms of protein regulation in bumblebees could provide valuable insights into their resilience and vulnerability facing environmental stresses.
{"title":"Differential expression of hemolymph proteins in wild bumblebees provides insights into species-specific impacts of heat stress","authors":"Kimberly Przybyla, Baptiste Martinet, Denis Michez, Michel Bocquet, Dalel Askri, Philippe Bulet","doi":"10.1111/phen.12470","DOIUrl":"10.1111/phen.12470","url":null,"abstract":"<p>Wildlife faces an increasing threat from extreme climatic events, such as heatwaves, which can have a severe impact on various species, including crucial pollinators like bumblebees. Bumblebees are cold-adapted and heterothermic, possessing the ability to regulate their internal temperature. The impact of heat stress seems species specific in bumblebees. While most species are impacted, some bumblebee species manage to survive, potentially by employing physiological mechanisms, including the modulation of their protein profile (e.g. Heat Shock Proteins). However, there is limited understanding of how their protein profiles are associated with heat exposure. In this study, we examined the global variation in the protein profile of males from two bumblebee species sampled in the wild: the heat-tolerant <i>Bombus terrestris</i> and the heat-sensitive <i>Bombus magnus</i>. After subjecting them to heat stupor at 40°C in controlled condition, it was observed that nearly all <i>B. terrestris</i> survived the stress, while over 50% of <i>B. magnus</i> individuals succumbed to the heat exposure. Through off-gel bottom-up proteomics and LC–MS/MS analysis of the hemolymph proteome, we identified 164 proteins in both species with a large part of differentially expressed proteins after heat exposure. Additionally, quantitative analysis of fat bodies revealed that the relative mass was stable in <i>B. terrestris</i>, while it was significantly lower in <i>B. magnus</i> exposed to heat stress. Our data suggest that compared with <i>B. magnus</i>, <i>B. terrestris</i> displays a higher adaptability of its hemolymph proteome in response to heat stress. This adaptability could be a key factor contributing to the high physiological resistance of <i>B. terrestris</i> and its ability to adapt to new, stressful environments expected due to climate change. Understanding these mechanisms of protein regulation in bumblebees could provide valuable insights into their resilience and vulnerability facing environmental stresses.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 1","pages":"105-117"},"PeriodicalIF":1.5,"publicationDate":"2024-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143120178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Toby Bruce, Thies H. Büscher, Fiona Clissold, Nicholas Teets, Nicky Wybouw
<p><i>Physiological Entomology</i> considers how insects function and cope with their environment. We address these proximate questions in insect physiology across all biological levels and disciplines, including molecular genetics, morphology and ecology. The mission of <i>Physiological Entomology</i> is broad and not restricted to one particular field within insect physiology. <i>Physiological Entomology</i> further welcomes research that focuses on non-insect arthropods, such as crustaceans and arachnids.</p><p>For the past century, <i>Physiological Entomology</i> has published original high-quality research that carries broad implications for the field of entomology. Although our emphasis is centred on research manuscripts, we also welcome reviews. Review manuscripts are expected to provide a comprehensive and timely review of the study area. We are also encouraging the community to submit proposals for Special Issues. Together with Wiley, we will support Guest Editors of these Special Issues throughout the entire process. Finally, we now also provide researchers with a <i>Methods</i> platform to promote the development and dissemination of novel methods in insect physiology.</p><p><i>Physiological Entomology</i> is a Royal Entomological Society journal and contributes to the society's goal to support the broad research community and the study and practice of insect science. To support this mission, we have a prize for the best research by an Early Career researcher award, which will be awarded soon on a biannual basis. To be eligible, authors must be the lead author and an early career researcher, which the RES defines as any researcher who is within 10 years of completing their undergraduate degree or with less than 10 years working in entomology in any capacity, with or without a degree. Time for career breaks is not counted in the 10-year time period. We will also shortly be introducing a competition for timely review articles written by early career researchers.</p><p>In February 2024, Thies Büscher (Kiel University), Nick Teets (University of Kentucky) and Nick Wybouw (Ghent University) joined our editorial board as new Editors-in-Chief. Thies Büscher is a functional morphologist who researches the evolution and biomechanics of insect attachment systems to elucidate how they interact with and are adapted to surfaces in their environment. Nick Teets focuses on adaptations to variable and extreme environmental conditions, including mechanisms underlying thermal tolerance and overwintering, and the implications of environmental variation for pest control. Nick Wybouw is an evolutionary geneticist who studies the molecular-genetic basis of complex traits within the broader fields of endosymbiosis, herbivory and speciation. This new set of complementary expertise in our editorial board will enable us to continue publishing impactful and high-quality studies. To further ensure the publication of high-quality studies across the broad scope of
{"title":"How insects work—Linking genotype to phenotype","authors":"Toby Bruce, Thies H. Büscher, Fiona Clissold, Nicholas Teets, Nicky Wybouw","doi":"10.1111/phen.12472","DOIUrl":"10.1111/phen.12472","url":null,"abstract":"<p><i>Physiological Entomology</i> considers how insects function and cope with their environment. We address these proximate questions in insect physiology across all biological levels and disciplines, including molecular genetics, morphology and ecology. The mission of <i>Physiological Entomology</i> is broad and not restricted to one particular field within insect physiology. <i>Physiological Entomology</i> further welcomes research that focuses on non-insect arthropods, such as crustaceans and arachnids.</p><p>For the past century, <i>Physiological Entomology</i> has published original high-quality research that carries broad implications for the field of entomology. Although our emphasis is centred on research manuscripts, we also welcome reviews. Review manuscripts are expected to provide a comprehensive and timely review of the study area. We are also encouraging the community to submit proposals for Special Issues. Together with Wiley, we will support Guest Editors of these Special Issues throughout the entire process. Finally, we now also provide researchers with a <i>Methods</i> platform to promote the development and dissemination of novel methods in insect physiology.</p><p><i>Physiological Entomology</i> is a Royal Entomological Society journal and contributes to the society's goal to support the broad research community and the study and practice of insect science. To support this mission, we have a prize for the best research by an Early Career researcher award, which will be awarded soon on a biannual basis. To be eligible, authors must be the lead author and an early career researcher, which the RES defines as any researcher who is within 10 years of completing their undergraduate degree or with less than 10 years working in entomology in any capacity, with or without a degree. Time for career breaks is not counted in the 10-year time period. We will also shortly be introducing a competition for timely review articles written by early career researchers.</p><p>In February 2024, Thies Büscher (Kiel University), Nick Teets (University of Kentucky) and Nick Wybouw (Ghent University) joined our editorial board as new Editors-in-Chief. Thies Büscher is a functional morphologist who researches the evolution and biomechanics of insect attachment systems to elucidate how they interact with and are adapted to surfaces in their environment. Nick Teets focuses on adaptations to variable and extreme environmental conditions, including mechanisms underlying thermal tolerance and overwintering, and the implications of environmental variation for pest control. Nick Wybouw is an evolutionary geneticist who studies the molecular-genetic basis of complex traits within the broader fields of endosymbiosis, herbivory and speciation. This new set of complementary expertise in our editorial board will enable us to continue publishing impactful and high-quality studies. To further ensure the publication of high-quality studies across the broad scope of ","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"49 4","pages":"279-280"},"PeriodicalIF":1.5,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/phen.12472","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142596399","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Insects attach to various surfaces that differ, among others, in roughness and wettability. Identifying surface characteristics that allow or prevent insects from attaching are an important research avenue of pest control. Here we take an experimental approach to analyse the attachment of common bed bugs, Cimex lectularius Linnaeus (1758), to Perspex (PMMA) substrates. We construct a reliable centrifuge device that allows the measurement of attachment forces at substrate roughnesses, Ra, between 0.02 and 1.3 μm and at two wettabilities. Our results suggest that bed bug attachment to surfaces is minimal at a substrate roughness of 0.2 and 0.4 μm on normal PMMA, where the lowest attachment force was 0.8 mN and the safety factor 15. At lower and higher roughness, attachment forces were higher and the safety factor increased to a maximum of 133. On PMMA that was made superhydrophobic by spray-coating, attachment was lowest (0.2 mN) at the lowest roughness and continuously increased with increasing roughness, reaching 2.5 mN and a safety factor of 46. For every roughness, attachment forces were lower on superhydrophobic than on normal PMMA. This knowledge may inspire the development of repelling substrates for bed bug control.
{"title":"Surface wettability affects attachment of male bed bugs Cimex lectularius to rough Perspex substrates","authors":"Rob Dwyer-Joyce, Dagmar Voigt, Klaus Reinhardt","doi":"10.1111/phen.12471","DOIUrl":"10.1111/phen.12471","url":null,"abstract":"<p>Insects attach to various surfaces that differ, among others, in roughness and wettability. Identifying surface characteristics that allow or prevent insects from attaching are an important research avenue of pest control. Here we take an experimental approach to analyse the attachment of common bed bugs, <i>Cimex lectularius</i> Linnaeus (1758), to Perspex (PMMA) substrates. We construct a reliable centrifuge device that allows the measurement of attachment forces at substrate roughnesses, Ra, between 0.02 and 1.3 μm and at two wettabilities. Our results suggest that bed bug attachment to surfaces is minimal at a substrate roughness of 0.2 and 0.4 μm on normal PMMA, where the lowest attachment force was 0.8 mN and the safety factor 15. At lower and higher roughness, attachment forces were higher and the safety factor increased to a maximum of 133. On PMMA that was made superhydrophobic by spray-coating, attachment was lowest (0.2 mN) at the lowest roughness and continuously increased with increasing roughness, reaching 2.5 mN and a safety factor of 46. For every roughness, attachment forces were lower on superhydrophobic than on normal PMMA. This knowledge may inspire the development of repelling substrates for bed bug control.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 1","pages":"96-104"},"PeriodicalIF":1.5,"publicationDate":"2024-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/phen.12471","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143117185","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Gerben Debruyn, Thies H. Büscher, Michaël P. J. Nicolaï, Jessica L. Dobson, Wanjie Xie, Karen De Clerck, Liliana D'Alba, Matthew D. Shawkey
Colours in nature can be pigmentary, structural or a combination of both. The prevalence, function and nanostructural origin of structural coloration in eggs is largely unknown. Stick and leaf insect eggs display a wide variety of colours, most of which are produced by pigments. The eggs of Myronides glaucus (Phasmida: Lonchodidae; Hennemann, 2021), however, show a clear purple to green iridescence. Here, we use micro-spectrophotometry, Fourier-transform infrared reflectance, transmission- and scanning electron microscopy, atomic force microscopy, finite-difference time-domain optical simulations and experimental approaches to elucidate the mechanism for iridescence in M. glaucus eggshells, which together reveal that iridescence is caused by thin-film interference by a 200- to 450-nm-thick outermost layer. These results highlight the diversity of phasmid eggs and the need to study the different mechanisms and functions of structural coloration.
{"title":"Thin-film iridescence in the eggshell of a stick insect (Myronides glaucus)","authors":"Gerben Debruyn, Thies H. Büscher, Michaël P. J. Nicolaï, Jessica L. Dobson, Wanjie Xie, Karen De Clerck, Liliana D'Alba, Matthew D. Shawkey","doi":"10.1111/phen.12469","DOIUrl":"10.1111/phen.12469","url":null,"abstract":"<p>Colours in nature can be pigmentary, structural or a combination of both. The prevalence, function and nanostructural origin of structural coloration in eggs is largely unknown. Stick and leaf insect eggs display a wide variety of colours, most of which are produced by pigments. The eggs of <i>Myronides glaucus</i> (Phasmida: Lonchodidae; Hennemann, 2021), however, show a clear purple to green iridescence. Here, we use micro-spectrophotometry, Fourier-transform infrared reflectance, transmission- and scanning electron microscopy, atomic force microscopy, finite-difference time-domain optical simulations and experimental approaches to elucidate the mechanism for iridescence in <i>M. glaucus</i> eggshells, which together reveal that iridescence is caused by thin-film interference by a 200- to 450-nm-thick outermost layer. These results highlight the diversity of phasmid eggs and the need to study the different mechanisms and functions of structural coloration.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 1","pages":"88-95"},"PeriodicalIF":1.5,"publicationDate":"2024-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143117184","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Charles J. Mason, April Grummer, Michael Bosch, Ikkei Shikano
Ingested toxins formulated as baits can be effective in the management of insect pests, but their efficacy may be influenced by insect foraging alongside active ingredients. There are several components that might influence insect consumption of toxic baits, one of which being prior nutritional exposure. In our study, we investigated how protein deprivation following adult emergence influences lethal and sublethal effects of boric acid on the pest tephritid melon fly, Zeugodacus cucurbitae. We performed a series of experiments to address the impact of prior diet on mortality, diet consumption, enzymes involved in detoxification and antioxidation and fly activity. Newly emerged melon fly adults were provided either diet containing 3:1 sucrose/yeast hyrdrolysate or just sucrose for three days prior to bioassays. Overall, protein deprivation had a strong effect on fly interactions with boric acid. In two separate experiments (continuous exposure and short duration feeding), insects only pre-fed sucrose had significantly higher mortality compared with those pre-fed protein. Insects that were pre-fed only sucrose removed more liquid diet over the same duration of the experiments, suggesting compensatory foraging behaviours. Adults pre-fed sucrose had higher catalase (1.5×) and superoxide dismutase (1.7×) activities compared with adults pre-fed sucrose-yeast, but we found no effect of boric acid on their activity or that of glutathione-S-transferase or acetylcholinesterase activity. Boric acid consumption also significantly reduced the activity of melon flies. Overall, our results demonstrate that prior diet in fly adulthood can impact subsequent exposure to and efficacy of ingested toxicants.
{"title":"Adult dietary experience influences mortality of the pest melon fly, Zeugodacus cucurbitae (Diptera: Tephritidae), to an ingested toxin","authors":"Charles J. Mason, April Grummer, Michael Bosch, Ikkei Shikano","doi":"10.1111/phen.12468","DOIUrl":"10.1111/phen.12468","url":null,"abstract":"<p>Ingested toxins formulated as baits can be effective in the management of insect pests, but their efficacy may be influenced by insect foraging alongside active ingredients. There are several components that might influence insect consumption of toxic baits, one of which being prior nutritional exposure. In our study, we investigated how protein deprivation following adult emergence influences lethal and sublethal effects of boric acid on the pest tephritid melon fly, <i>Zeugodacus cucurbitae</i>. We performed a series of experiments to address the impact of prior diet on mortality, diet consumption, enzymes involved in detoxification and antioxidation and fly activity. Newly emerged melon fly adults were provided either diet containing 3:1 sucrose/yeast hyrdrolysate or just sucrose for three days prior to bioassays. Overall, protein deprivation had a strong effect on fly interactions with boric acid. In two separate experiments (continuous exposure and short duration feeding), insects only pre-fed sucrose had significantly higher mortality compared with those pre-fed protein. Insects that were pre-fed only sucrose removed more liquid diet over the same duration of the experiments, suggesting compensatory foraging behaviours. Adults pre-fed sucrose had higher catalase (1.5×) and superoxide dismutase (1.7×) activities compared with adults pre-fed sucrose-yeast, but we found no effect of boric acid on their activity or that of glutathione-S-transferase or acetylcholinesterase activity. Boric acid consumption also significantly reduced the activity of melon flies. Overall, our results demonstrate that prior diet in fly adulthood can impact subsequent exposure to and efficacy of ingested toxicants.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 1","pages":"77-87"},"PeriodicalIF":1.5,"publicationDate":"2024-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143113542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Vitellogenin (Vg) has been recognized as a co-opted gene involved in social colonies where it is associated with reproduction in the queen and task transitions in workers. The Solenopsis invicta genome harbours four Vg genes, Vg1, Vg2, Vg3 and Vg4, and this study explored the regional expression of these genes in the brain and head of the worker caste in different subcaste and social contexts. Transcriptomic analyses of the worker brain while in the presence or absence of brood revealed differential expression of genes involved with social behaviours. Among these, we found higher expression of Vg2 and Vg3 in the brains of workers in the absence of brood. The influence of brood on expression of Vg between worker castes was also investigated. RT-qPCR revealed higher expression of Vg in the head of workers in the absence of brood. Further studies demonstrated that Vg was also differentially expressed in the heads of workers conducting specific tasks and differing between subcastes. Nurses maintained higher Vg expression than foragers. We conclude worker Vg expression may be linked to the brood and/or nutritional state. Vg expression changes when workers are deprived of protein suggesting it is regulated by nutritional signalling and the presence of brood.
{"title":"Differential expression of vitellogenin in the brain of Solenopsis invicta workers based on social and nutritional context","authors":"Chloe Hawkings, Cecilia Tamborindeguy","doi":"10.1111/phen.12467","DOIUrl":"10.1111/phen.12467","url":null,"abstract":"<p>Vitellogenin (Vg) has been recognized as a co-opted gene involved in social colonies where it is associated with reproduction in the queen and task transitions in workers. The <i>Solenopsis invicta</i> genome harbours four Vg genes, Vg1, Vg2, Vg3 and Vg4, and this study explored the regional expression of these genes in the brain and head of the worker caste in different subcaste and social contexts. Transcriptomic analyses of the worker brain while in the presence or absence of brood revealed differential expression of genes involved with social behaviours. Among these, we found higher expression of Vg2 and Vg3 in the brains of workers in the absence of brood. The influence of brood on expression of Vg between worker castes was also investigated. RT-qPCR revealed higher expression of Vg in the head of workers in the absence of brood. Further studies demonstrated that Vg was also differentially expressed in the heads of workers conducting specific tasks and differing between subcastes. Nurses maintained higher Vg expression than foragers. We conclude worker Vg expression may be linked to the brood and/or nutritional state. Vg expression changes when workers are deprived of protein suggesting it is regulated by nutritional signalling and the presence of brood.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 1","pages":"64-76"},"PeriodicalIF":1.5,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/phen.12467","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143116482","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Xiaoming Qiu, Yongwen Lin, Jing Huang, Komivi S. Akutse
Opisthoplatia orientalis Burmeister is a traditional medicinal insect in China that is mass-produced by entrepreneur farmers. However, low temperatures pose a serious threat to the survival and quality of this insect, causing economic losses to the farmers. This study aimed to test the hypothesis that low temperatures induce a trade-off between immunity and physical condition of O. orientalis. The phenoloxidase activity and hemocyte concentration of O. orientalis under 25°C and 5°C were measured by micro-determination and haemocytometre, respectively. The immunocompetence of the insect was also evaluated by inoculating it with Metarhizium anisopliae M11, an entomopathogenic fungus. The physical factors (protein content, fatty acid content and body weight) of O. orientalis were determined accordingly. The results showed that phenoloxidase activity and hemocyte concentration increased from 9.21 mOD/min and 122.30 hemocyte/ml to 3.64 mOD/min and 55.70 hemocyte/ml when temperature down-regulated from 25 to 5°C. However, the insects at 5°C had higher protein and fatty acid content, but lower body weight, than those at 25°C. Moreover, there was a significant negative correlation between immunity and protein or fatty acid content, indicating a trade-off between immunity and physical condition in O. orientalis under low temperatures. This study provides useful insights for improving the efficiency of insect breeding and enhancing the quality of this medicinal insect.
Opisthoplatia orientalis Burmeister是中国传统的药用昆虫,由企业家农民大量生产。然而,低温对这种昆虫的生存和品质造成了严重威胁,给农民造成了经济损失。本研究旨在验证低温诱导东方花免疫和生理状态之间的权衡的假设。采用微量测定法和血细胞计法分别测定了25℃和5℃条件下东方红酚氧化酶活性和血细胞浓度。用金龟子绿僵菌(Metarhizium anisopliae M11)对其免疫能力进行了评价。据此测定了东方葵的蛋白质含量、脂肪酸含量和体质量等物理因子。结果表明,当温度从25℃降至5℃时,酚氧化酶活性和血细胞浓度从9.21 mOD/min和122.30血细胞/ml增加到3.64 mOD/min和55.70血细胞/ml。与25℃处理相比,5℃处理的昆虫蛋白质和脂肪酸含量较高,但体重较低。此外,蛋白质和脂肪酸含量与免疫力呈显著负相关,表明低温条件下东方花的免疫力与身体状况存在权衡关系。本研究为提高药用昆虫的育种效率和提高药用昆虫的品质提供了有益的见解。
{"title":"The trade-off between immunity and product quality of Opisthoplatia orientalis (Blattodea: Blaberidae) under low temperatures","authors":"Xiaoming Qiu, Yongwen Lin, Jing Huang, Komivi S. Akutse","doi":"10.1111/phen.12466","DOIUrl":"10.1111/phen.12466","url":null,"abstract":"<p><i>Opisthoplatia orientalis</i> Burmeister is a traditional medicinal insect in China that is mass-produced by entrepreneur farmers. However, low temperatures pose a serious threat to the survival and quality of this insect, causing economic losses to the farmers. This study aimed to test the hypothesis that low temperatures induce a trade-off between immunity and physical condition of <i>O. orientalis</i>. The phenoloxidase activity and hemocyte concentration of <i>O. orientalis</i> under 25°C and 5°C were measured by micro-determination and haemocytometre, respectively. The immunocompetence of the insect was also evaluated by inoculating it with <i>Metarhizium anisopliae</i> M11, an entomopathogenic fungus. The physical factors (protein content, fatty acid content and body weight) of <i>O. orientalis</i> were determined accordingly. The results showed that phenoloxidase activity and hemocyte concentration increased from 9.21 mOD/min and 122.30 hemocyte/ml to 3.64 mOD/min and 55.70 hemocyte/ml when temperature down-regulated from 25 to 5°C. However, the insects at 5°C had higher protein and fatty acid content, but lower body weight, than those at 25°C. Moreover, there was a significant negative correlation between immunity and protein or fatty acid content, indicating a trade-off between immunity and physical condition in <i>O. orientalis</i> under low temperatures. This study provides useful insights for improving the efficiency of insect breeding and enhancing the quality of this medicinal insect.</p>","PeriodicalId":20081,"journal":{"name":"Physiological Entomology","volume":"50 1","pages":"57-63"},"PeriodicalIF":1.5,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143112427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}