Pub Date : 2024-03-13DOI: 10.1016/j.cois.2024.101192
Brittany F Peterson
Insect gut bacteria have been implicated in a myriad of physiological processes from nutrient supplementation to pathogen protection. In fact, symbiont-mediated insecticide degradation has helped explain sudden control failure in the field to a range of active ingredients. The mechanisms behind the loss of susceptibility are varied based on host, symbiont, and insecticide identity. However, while some symbionts directly break down pesticides, others modulate endogenous host detoxification pathways or involve reciprocal degradation of insecticidal and bactericidal compounds both inspiring new questions and requiring the reexamination of past conclusions. Good steward of the chemical pesticide arsenal requires consideration of these ecological interactions from development to deployment.
{"title":"Microbiome toxicology — bacterial activation and detoxification of insecticidal compounds","authors":"Brittany F Peterson","doi":"10.1016/j.cois.2024.101192","DOIUrl":"10.1016/j.cois.2024.101192","url":null,"abstract":"<div><p>Insect gut bacteria have been implicated in a myriad of physiological processes from nutrient supplementation to pathogen protection. In fact, symbiont-mediated insecticide degradation has helped explain sudden control failure in the field to a range of active ingredients. The mechanisms behind the loss of susceptibility are varied based on host, symbiont, and insecticide identity. However, while some symbionts directly break down pesticides, others modulate endogenous host detoxification pathways or involve reciprocal degradation of insecticidal and bactericidal compounds both inspiring new questions and requiring the reexamination of past conclusions. Good steward of the chemical pesticide arsenal requires consideration of these ecological interactions from development to deployment.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000348/pdfft?md5=77047e6322e7f5dc9664f4b930b77938&pid=1-s2.0-S2214574524000348-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140136601","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-13DOI: 10.1016/j.cois.2024.101193
Leigh Boardman
Low temperatures are rarely experienced in isolation. The impacts of low temperatures on insects can be exacerbated or alleviated by the addition of other environmental factors, including, for example, desiccation, hypoxia, or infection. One way in which environmental factors can interact is through cross-talk where different factors enact common signaling pathways. In this review, I highlight the breadth of abiotic and biotic factors that can interact with low-temperature tolerance in both natural and artificial environments; and discuss some of the candidate pathways that are possibly responsible for cross-talk between several factors. Specifically, I discuss three interesting candidates: the neurohormone octopamine, circadian clock gene vrille, and microbes. Finally, I discuss applications of cross-talk studies, and provide recommendations for researchers.
{"title":"Cross-talk between low temperature and other environmental factors","authors":"Leigh Boardman","doi":"10.1016/j.cois.2024.101193","DOIUrl":"10.1016/j.cois.2024.101193","url":null,"abstract":"<div><p>Low temperatures are rarely experienced in isolation. The impacts of low temperatures on insects can be exacerbated or alleviated by the addition of other environmental factors, including, for example, desiccation, hypoxia, or infection. One way in which environmental factors can interact is through cross-talk where different factors enact common signaling pathways. In this review, I highlight the breadth of abiotic and biotic factors that can interact with low-temperature tolerance in both natural and artificial environments; and discuss some of the candidate pathways that are possibly responsible for cross-talk between several factors. Specifically, I discuss three interesting candidates: the neurohormone octopamine, circadian clock gene <em>vrille</em>, and microbes. Finally, I discuss applications of cross-talk studies, and provide recommendations for researchers.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140136600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-06DOI: 10.1016/j.cois.2024.101184
Jian Pu , Henry Chung
The continuous use of insecticides over the last eight decades has led to the development of resistance to these insecticides. Research in the last few decades showed that the mechanisms underlying resistance are diverse but can generally be classified under several modes of resistance such as target-site resistance, metabolic resistance, and penetration resistance. In this review, we highlight new discoveries in insecticide resistance research made over the past few years, including an emerging new mode of resistance, sequestration resistance, where the overexpression of olfactory proteins binds and sequesters insecticides in resistant strains, as well as recent research on how posttranscriptional regulation can impact resistance. Future research will determine the generality of these emerging mechanisms across insect species.
{"title":"New and emerging mechanisms of insecticide resistance","authors":"Jian Pu , Henry Chung","doi":"10.1016/j.cois.2024.101184","DOIUrl":"10.1016/j.cois.2024.101184","url":null,"abstract":"<div><p>The continuous use of insecticides over the last eight decades has led to the development of resistance to these insecticides. Research in the last few decades showed that the mechanisms underlying resistance are diverse but can generally be classified under several modes of resistance such as target-site resistance, metabolic resistance, and penetration resistance. In this review, we highlight new discoveries in insecticide resistance research made over the past few years, including an emerging new mode of resistance, sequestration resistance, where the overexpression of olfactory proteins binds and sequesters insecticides in resistant strains, as well as recent research on how posttranscriptional regulation can impact resistance. Future research will determine the generality of these emerging mechanisms across insect species.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140065042","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-01DOI: 10.1016/j.cois.2024.101180
F Claire Rind
Detecting looming motion directly towards the insect is vital to its survival. Looming detection in two insects, flies and locusts, is described and contrasted. Pathways using looming detectors to trigger action and their topographical layout in the brain is explored in relation to facilitating behavioural selection. Similar visual stimuli, such as looming motion, are processed by nearby glomeruli in the brain. Insect-inspired looming motion detectors are combined to detect and avoid collision in different scenarios by robots, vehicles and unmanned aerial vehicle (UAV)s.
{"title":"Recent advances in insect vision in a 3D world: looming stimuli and escape behaviour","authors":"F Claire Rind","doi":"10.1016/j.cois.2024.101180","DOIUrl":"10.1016/j.cois.2024.101180","url":null,"abstract":"<div><p>Detecting looming motion directly towards the insect is vital to its survival. Looming detection in two insects, flies and locusts, is described and contrasted. Pathways using looming detectors to trigger action and their topographical layout in the brain is explored in relation to facilitating behavioural selection. Similar visual stimuli, such as looming motion, are processed by nearby glomeruli in the brain. Insect-inspired looming motion detectors are combined to detect and avoid collision in different scenarios by robots, vehicles and unmanned aerial vehicle (UAV)s.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000221/pdfft?md5=2e8861ff0ac60524835098292ac67567&pid=1-s2.0-S2214574524000221-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140016619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-29DOI: 10.1016/j.cois.2024.101183
Kohei Oguchi, Toru Miura
In social insects, interactions among colony members trigger caste differentiation with morphological modifications. During caste differentiation in termites, body parts and caste-specific morphologies are modified during postembryonic development under endocrine controls such as juvenile hormone (JH) and ecdysone. In addition to endocrine factors, developmental toolkit genes such as Hox- and appendage-patterning genes also contribute to the caste-specific body part modifications. These toolkits are thought to provide spatial information for specific morphogenesis. During social evolution, the complex crosstalks between physiological and developmental mechanisms should be established, leading to the sophisticated caste systems. This article reviews recent studies on these mechanisms underlying the termite caste differentiation and addresses implications for the evolution of caste systems in termites.
{"title":"Body part-specific development in termite caste differentiation: crosstalk between hormonal actions and developmental toolkit genes","authors":"Kohei Oguchi, Toru Miura","doi":"10.1016/j.cois.2024.101183","DOIUrl":"10.1016/j.cois.2024.101183","url":null,"abstract":"<div><p>In social insects, interactions among colony members trigger caste differentiation with morphological modifications. During caste differentiation in termites, body parts and caste-specific morphologies are modified during postembryonic development under endocrine controls such as juvenile hormone (JH) and ecdysone. In addition to endocrine factors, developmental toolkit genes such as Hox- and appendage-patterning genes also contribute to the caste-specific body part modifications. These toolkits are thought to provide spatial information for specific morphogenesis. During social evolution, the complex crosstalks between physiological and developmental mechanisms should be established, leading to the sophisticated caste systems. This article reviews recent studies on these mechanisms underlying the termite caste differentiation and addresses implications for the evolution of caste systems in termites.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-02-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140012364","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-23DOI: 10.1016/j.cois.2024.101181
Daniel G Lingeman, Kenneth L O’Dell Jr., Zainulabeuddin Syed
Historically, some of the most effective tools to counter vector-borne diseases have been those directed against the vectors. Ticks are undergoing a population explosion as evidenced by the recent expansion of their distribution range. Tick control has traditionally relied heavily on pesticides. However, sustained use of acaricides is resulting in resistant tick populations. Multipronged management strategies that build and expand upon innovative control methods are sorely needed. Behavior-modifying chemicals, referred to as semiochemicals, such as pheromones and repellents, offer a first line of personal protection against ticks. We review the current understanding of tick semiochemicals, and how such understanding is leading to the identification of novel chemistries that are effective and safe.
{"title":"Developing attractants and repellents for ticks: promises and challenges","authors":"Daniel G Lingeman, Kenneth L O’Dell Jr., Zainulabeuddin Syed","doi":"10.1016/j.cois.2024.101181","DOIUrl":"10.1016/j.cois.2024.101181","url":null,"abstract":"<div><p>Historically, some of the most effective tools to counter vector-borne diseases have been those directed against the vectors. Ticks are undergoing a population explosion as evidenced by the recent expansion of their distribution range. Tick control has traditionally relied heavily on pesticides. However, sustained use of acaricides is resulting in resistant tick populations. Multipronged management strategies that build and expand upon innovative control methods are sorely needed. Behavior-modifying chemicals, referred to as semiochemicals, such as pheromones and repellents, offer a first line of personal protection against ticks. We review the current understanding of tick semiochemicals, and how such understanding is leading to the identification of novel chemistries that are effective and safe.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-02-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139944020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-23DOI: 10.1016/j.cois.2024.101182
Ayako Wada-Katsumata , Coby Schal
The German cockroach is a valuable model for research on indoor pest management strategies and for understanding mechanisms of adaptive evolution under intense anthropogenic selection. Under the selection pressure of toxic baits, populations of the German cockroach have evolved a variety of physiological and behavioral resistance mechanisms. In this review, we focus on glucose aversion, an adaptive trait that underlies a behavioral resistance to baits. Taste polymorphism, a change in taste quality of glucose from sweet to bitter, causes cockroaches to avoid glucose-containing baits. We summarize recent findings, including the contribution of glucose aversion to olfactory learning-based avoidance of baits, aversion to other sugars, and assortative mating under sexual selection, which underscores the behavioral phenotype to all oligosaccharides that contain glucose. It is a remarkable example of how anthropogenic selection drove the evolution of an altered gustatory trait that reshapes the foraging ecology and sexual communication.
{"title":"Glucose aversion: a behavioral resistance mechanism in the German cockroach","authors":"Ayako Wada-Katsumata , Coby Schal","doi":"10.1016/j.cois.2024.101182","DOIUrl":"10.1016/j.cois.2024.101182","url":null,"abstract":"<div><p>The German cockroach is a valuable model for research on indoor pest management strategies and for understanding mechanisms of adaptive evolution under intense anthropogenic selection. Under the selection pressure of toxic baits, populations of the German cockroach have evolved a variety of physiological and behavioral resistance mechanisms. In this review, we focus on glucose aversion, an adaptive trait that underlies a behavioral resistance to baits. Taste polymorphism, a change in taste quality of glucose from sweet to bitter, causes cockroaches to avoid glucose-containing baits. We summarize recent findings, including the contribution of glucose aversion to olfactory learning-based avoidance of baits, aversion to other sugars, and assortative mating under sexual selection, which underscores the behavioral phenotype to all oligosaccharides that contain glucose. It is a remarkable example of how anthropogenic selection drove the evolution of an altered gustatory trait that reshapes the foraging ecology and sexual communication.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-02-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139954025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-21DOI: 10.1016/j.cois.2024.101179
Giles E Duffield
Mosquitoes express a rich repertoire of daily 24-hour rhythms in biochemistry, physiology, and behavior. The nocturnal Anopheles and Culex and diurnal Aedes mosquitoes are major vectors of human disease, transmitting parasites and arboviruses, such as malaria and dengue. In this review, we explore the role that 24-hour diel and circadian rhythms play in shaping the temporal life of the mosquito. We focus on recent advances in our understanding of behavioral rhythms, focusing on locomotor/flight activity, host-seeking, biting/blood feeding, and mating. We examine the molecular circadian clock, photocycle, and light signals, which in combination shape the mosquito 24-hour temporal program. We address species- and sex-specific differences and highlight important selective pressures from dynamically changing environments. This work also provides new insights into disease transmission, insect control, and future experimental design.
{"title":"Circadian and daily rhythms of disease vector mosquitoes","authors":"Giles E Duffield","doi":"10.1016/j.cois.2024.101179","DOIUrl":"10.1016/j.cois.2024.101179","url":null,"abstract":"<div><p>Mosquitoes express a rich repertoire of daily 24-hour rhythms in biochemistry, physiology, and behavior. The nocturnal <em>Anopheles</em> and <em>Culex</em> and diurnal <em>Aedes</em> mosquitoes are major vectors of human disease, transmitting parasites and arboviruses, such as malaria and dengue. In this review, we explore the role that 24-hour diel and circadian rhythms play in shaping the temporal life of the mosquito. We focus on recent advances in our understanding of behavioral rhythms, focusing on locomotor/flight activity, host-seeking, biting/blood feeding, and mating<em>.</em> We examine the molecular circadian clock, photocycle, and light signals, which in combination shape the mosquito 24-hour temporal program. We address species- and sex-specific differences and highlight important selective pressures from dynamically changing environments. This work also provides new insights into disease transmission, insect control, and future experimental design.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139939816","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-13DOI: 10.1016/j.cois.2024.101177
Caleb B Hubbard, Amy C Murillo
Identifying and understanding behavioral resistance to insecticides is vital for maintaining global food security, public health, and ecological balance. Behavioral resistance has been documented to occur in a multitude of insect taxa dating back to the 1940s, but has not received significant research attention due primarily to the complexities of studying insect behavior and a lack of any clear definition of behavioral resistance. In recent years, a systematic effort to investigate the mechanism(s) of behavioral resistance in pest taxa (e.g. the German cockroach and the house fly) has been undertaken. Here, we practically define behavioral resistance, describe the efforts taken by research groups to elucidate resistance mechanisms, and provide insight on designing appropriate bioassays for investigating behavioral resistance mechanisms in the future.
{"title":"Behavioral resistance to insecticides: current understanding, challenges, and future directions","authors":"Caleb B Hubbard, Amy C Murillo","doi":"10.1016/j.cois.2024.101177","DOIUrl":"10.1016/j.cois.2024.101177","url":null,"abstract":"<div><p>Identifying and understanding behavioral resistance to insecticides is vital for maintaining global food security, public health, and ecological balance. Behavioral resistance has been documented to occur in a multitude of insect taxa dating back to the 1940s, but has not received significant research attention due primarily to the complexities of studying insect behavior and a lack of any clear definition of behavioral resistance. In recent years, a systematic effort to investigate the mechanism(s) of behavioral resistance in pest taxa (e.g. the German cockroach and the house fly) has been undertaken. Here, we practically define behavioral resistance, describe the efforts taken by research groups to elucidate resistance mechanisms, and provide insight on designing appropriate bioassays for investigating behavioral resistance mechanisms in the future.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000191/pdfft?md5=8fe2e9c06894a765a449b52cc804cad4&pid=1-s2.0-S2214574524000191-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139734702","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The Aedes mosquito, which transmits the dengue fever virus and other viruses, has acquired resistance to pyrethroid insecticides in a naturally selective manner. Massive use of insecticides has led to the worldwide expansion of resistant populations. The major factor in pyrethroid resistance is knockdown resistance (kdr) caused by amino acid mutation(s) in the voltage-gated sodium channel, which is the target site of this insecticide group. Some kdr mutations can lead to a dramatic increase in resistance, and multiple mutations can increase the level of pyrethroid resistance by 10 to several-hundred. In this review, we summarize the kdr identified in Aedes mosquitoes with a focus on the recent advances in the study of kdr.
{"title":"Recent advances in the study of knockdown resistance mutations in Aedes mosquitoes with a focus on several remarkable mutations","authors":"Nozomi Uemura, Kentaro Itokawa, Osamu Komagata, Shinji Kasai","doi":"10.1016/j.cois.2024.101178","DOIUrl":"10.1016/j.cois.2024.101178","url":null,"abstract":"<div><p>The <em>Aedes</em> mosquito, which transmits the dengue fever virus and other viruses, has acquired resistance to pyrethroid insecticides in a naturally selective manner. Massive use of insecticides has led to the worldwide expansion of resistant populations. The major factor in pyrethroid resistance is knockdown resistance (kdr) caused by amino acid mutation(s) in the voltage-gated sodium channel, which is the target site of this insecticide group. Some <em>kdr</em> mutations can lead to a dramatic increase in resistance, and multiple mutations can increase the level of pyrethroid resistance by 10 to several-hundred. In this review, we summarize the <em>kdr</em> identified in <em>Aedes</em> mosquitoes with a focus on the recent advances in the study of kdr.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.3,"publicationDate":"2024-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000208/pdfft?md5=eb6711e849535c35c116f2b90d675463&pid=1-s2.0-S2214574524000208-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139721991","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}