Pub Date : 2024-07-15DOI: 10.1016/j.cois.2024.101235
Pest arthropods cause significant crop damage or are vectors of pathogens for both plants and animals. The current standard of pest management prevents against crop losses and protects human and animal health, but shortcomings exist, such as insecticide resistance and environmental damage to nontarget organisms. New management methods are therefore needed. The development of new tools, such as site-specific gene editing, has accelerated the study of gene function and phenotype in nonmodel arthropod species and may enable the development of new strategies for pathogen and arthropod control. Here, the most recent developments in gene editing in arthropod pests are briefly reviewed. Additionally, technological advances that could be applicable to new species or enhance the success rates of gene editing in species with already established protocols are highlighted.
{"title":"Gene editing in agricultural, health, and veterinary pest arthropods: recent advances","authors":"","doi":"10.1016/j.cois.2024.101235","DOIUrl":"10.1016/j.cois.2024.101235","url":null,"abstract":"<div><p>Pest arthropods cause significant crop damage or are vectors of pathogens for both plants and animals. The current standard of pest management prevents against crop losses and protects human and animal health, but shortcomings exist, such as insecticide resistance and environmental damage to nontarget organisms. New management methods are therefore needed. The development of new tools, such as site-specific gene editing, has accelerated the study of gene function and phenotype in nonmodel arthropod species and may enable the development of new strategies for pathogen and arthropod control. Here, the most recent developments in gene editing in arthropod pests are briefly reviewed. Additionally, technological advances that could be applicable to new species or enhance the success rates of gene editing in species with already established protocols are highlighted.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141632951","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 : 2024-07-06DOI: 10.1016/j.cois.2024.101231
While genomic resources for social insects have vastly increased over the past two decades, we are still far from understanding the genetic and molecular basis of eusociality. Here, we briefly review three scientific advancements that, when integrated, can be highly synergistic for advancing our knowledge of the genetics and evolution of eusocial traits. Population genomics provides a natural way to quantify the strength of natural selection on coding and regulatory sequences, highlighting genes that have undergone adaptive evolution during the evolution or maintenance of eusociality. Genome-wide association studies (GWAS) can be used to characterize the complex genetic architecture underlying eusocial traits and identify candidate causal variants. Concurrently, CRISPR/Cas9 enables the precise manipulation of gene function to both validate genotype–phenotype associations and study the molecular biology underlying interesting traits. While each approach has its own advantages and disadvantages, which we discuss herein, we argue that their combination will ultimately help us better understand the genetics and evolution of eusocial behavior. Specifically, by triangulating across these three different approaches, researchers can directly identify and study loci that have a causal association with key phenotypes and have evidence of positive selection over the relevant timescales associated with the evolution and maintenance of eusociality in insects.
{"title":"An integrative genomic toolkit for studying the genetic, evolutionary, and molecular underpinnings of eusociality in insects","authors":"","doi":"10.1016/j.cois.2024.101231","DOIUrl":"10.1016/j.cois.2024.101231","url":null,"abstract":"<div><p>While genomic resources for social insects have vastly increased over the past two decades, we are still far from understanding the genetic and molecular basis of eusociality. Here, we briefly review three scientific advancements that, when integrated, can be highly synergistic for advancing our knowledge of the genetics and evolution of eusocial traits. Population genomics provides a natural way to quantify the strength of natural selection on coding and regulatory sequences, highlighting genes that have undergone adaptive evolution during the evolution or maintenance of eusociality. Genome-wide association studies (GWAS) can be used to characterize the complex genetic architecture underlying eusocial traits and identify candidate causal variants. Concurrently, CRISPR/Cas9 enables the precise manipulation of gene function to both validate genotype–phenotype associations and study the molecular biology underlying interesting traits. While each approach has its own advantages and disadvantages, which we discuss herein, we argue that their combination will ultimately help us better understand the genetics and evolution of eusocial behavior. Specifically, by triangulating across these three different approaches, researchers can directly identify and study loci that have a causal association with key phenotypes and have evidence of positive selection over the relevant timescales associated with the evolution and maintenance of eusociality in insects.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000737/pdfft?md5=def5feae1854413d419a230e3ae428cb&pid=1-s2.0-S2214574524000737-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141558338","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 : 2024-07-04DOI: 10.1016/j.cois.2024.101230
We often consider mosquitoes through an ‘anthropocentric lens’ that disregards their interactions with nonhuman and nonpathogenic organisms, even though these interactions can be harnessed for mosquito control. Mosquitoes have been recognized as floral visitors, and pollinators, for more than a century. However, we know relatively little about mosquito–plant interactions, excepting some nutrition and chemical ecology-related topics, compared with mosquito–host interactions, and frequently use flawed methodology when investigating them. Recent work demonstrates mosquitoes use multimodal sensory cues to locate flowers, including ultraviolet visual cues, and we may underestimate mosquito pollination. This review focuses on current knowledge of how mosquitoes locate flowers, floral visitation assay methodology, mosquito pollination, and implications for technologies such as sterile male mosquito release through genetic control programs or Wolbachia infection.
{"title":"Mosquito floral visitation and pollination","authors":"","doi":"10.1016/j.cois.2024.101230","DOIUrl":"10.1016/j.cois.2024.101230","url":null,"abstract":"<div><p>We often consider mosquitoes through an ‘anthropocentric lens’ that disregards their interactions with nonhuman and nonpathogenic organisms, even though these interactions can be harnessed for mosquito control. Mosquitoes have been recognized as floral visitors, and pollinators, for more than a century. However, we know relatively little about mosquito–plant interactions, excepting some nutrition and chemical ecology-related topics, compared with mosquito–host interactions, and frequently use flawed methodology when investigating them. Recent work demonstrates mosquitoes use multimodal sensory cues to locate flowers, including ultraviolet visual cues, and we may underestimate mosquito pollination. This review focuses on current knowledge of how mosquitoes locate flowers, floral visitation assay methodology, mosquito pollination, and implications for technologies such as sterile male mosquito release through genetic control programs or <em>Wolbachia</em> infection.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141544689","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 : 2024-06-27DOI: 10.1016/j.cois.2024.101226
Norah Saabna , Tamar Keasar
This review focuses on biological control interactions in arid areas and is motivated by the need to devise sustainable agricultural practices for a warming and drying world. Parasitoids, important natural enemies of crop pests, are diverse and abundant in natural arid habitats. Dryland croplands, which are usually irrigated, are also rich in local parasitoids. Nevertheless, biological control projects in arid croplands mostly involve imported parasitoids (classical biological control) rather than the conservation of native species. Dryland parasitoids experience heat, drought, low relative humidity, sparse vegetation, and low host densities. Heat resistance combines local genetic adaptations, behavioral and physiological flexibility, and microbial symbioses, but how parasitoids cope with other aridity-related challenges is insufficiently understood. How dryland conditions impact host–parasitoid population dynamics also requires further study.
{"title":"Parasitoids for biological control in dryland agroecosystems","authors":"Norah Saabna , Tamar Keasar","doi":"10.1016/j.cois.2024.101226","DOIUrl":"10.1016/j.cois.2024.101226","url":null,"abstract":"<div><p>This review focuses on biological control interactions in arid areas and is motivated by the need to devise sustainable agricultural practices for a warming and drying world. Parasitoids, important natural enemies of crop pests, are diverse and abundant in natural arid habitats. Dryland croplands, which are usually irrigated, are also rich in local parasitoids. Nevertheless, biological control projects in arid croplands mostly involve imported parasitoids (classical biological control) rather than the conservation of native species. Dryland parasitoids experience heat, drought, low relative humidity, sparse vegetation, and low host densities. Heat resistance combines local genetic adaptations, behavioral and physiological flexibility, and microbial symbioses, but how parasitoids cope with other aridity-related challenges is insufficiently understood. How dryland conditions impact host–parasitoid population dynamics also requires further study.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141466822","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 : 2024-06-27DOI: 10.1016/j.cois.2024.101228
Luis Abdala-Roberts , Xoaquín Moreira
The ecological effects of plant diversity have been well studied, but the extent to which they are driven by variation in specialized metabolites is not well understood. Here, we provide theoretical background on phytochemical diversity effects on herbivory and its expanded consequences for higher trophic levels. We then review empirical evidence for effects on predation and parasitism by focusing on a handful of studies that have undertaken manipulative approaches and link back their results to theory on mechanisms. We close by summarizing key aspects for future research, building on knowledge gained thus far.
{"title":"Effects of phytochemical diversity on multitrophic interactions","authors":"Luis Abdala-Roberts , Xoaquín Moreira","doi":"10.1016/j.cois.2024.101228","DOIUrl":"10.1016/j.cois.2024.101228","url":null,"abstract":"<div><p>The ecological effects of plant diversity have been well studied, but the extent to which they are driven by variation in specialized metabolites is not well understood. Here, we provide theoretical background on phytochemical diversity effects on herbivory and its expanded consequences for higher trophic levels. We then review empirical evidence for effects on predation and parasitism by focusing on a handful of studies that have undertaken manipulative approaches and link back their results to theory on mechanisms. We close by summarizing key aspects for future research, building on knowledge gained thus far.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141466819","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 : 2024-06-27DOI: 10.1016/j.cois.2024.101229
Michal Segoli , Miriam Kishinevsky , Jeffrey A Harvey
Anthropogenic climate change, including temperature extremes, is having a major impact on insect physiology, phenology, behavior, populations, and communities. Hyperparasitoids (insects whose offspring develop in, or on, the body of a primary parasitoid host) are expected to be especially impacted by such effects due to their typical life history traits (e.g. low fecundity and slow development), small populations (being high on the food chain), and cascading effects mediated via lower trophic levels. We review evidence for direct and indirect temperature and climate-related effects mediated via plants, herbivores, and the primary parasitoid host species on hyperparasitoid populations, focusing on higher temperatures. We discuss how hyperparasitoid responses may feed back to the community and affect biological control programs. We conclude that despite their great importance, very little is known about the potential effects of climate change on hyperparasitoids and make a plea for additional studies exploring such responses.
{"title":"Climate change, temperature extremes, and impacts on hyperparasitoids","authors":"Michal Segoli , Miriam Kishinevsky , Jeffrey A Harvey","doi":"10.1016/j.cois.2024.101229","DOIUrl":"10.1016/j.cois.2024.101229","url":null,"abstract":"<div><p>Anthropogenic climate change, including temperature extremes, is having a major impact on insect physiology, phenology, behavior, populations, and communities. Hyperparasitoids (insects whose offspring develop in, or on, the body of a primary parasitoid host) are expected to be especially impacted by such effects due to their typical life history traits (e.g. low fecundity and slow development), small populations (being high on the food chain), and cascading effects mediated via lower trophic levels. We review evidence for direct and indirect temperature and climate-related effects mediated via plants, herbivores, and the primary parasitoid host species on hyperparasitoid populations, focusing on higher temperatures. We discuss how hyperparasitoid responses may feed back to the community and affect biological control programs. We conclude that despite their great importance, very little is known about the potential effects of climate change on hyperparasitoids and make a plea for additional studies exploring such responses.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141466818","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 : 2024-06-25DOI: 10.1016/j.cois.2024.101227
Kelsey Adams , Olivier Roux
Swarming behavior is the cornerstone of the anopheline mating system. At dusk, males congregate in monospecific swarms in which females come to find a mate once in their lives. Although many Anopheles species coexist in sympatry, hybrids are infrequent, suggesting the existence of strong premating reproductive barriers. Chemical cues, particularly pheromones, often play a crucial role in bringing sexes together in a species-specific manner among insects. While the existence of sexual pheromones in Anopheles species has been postulated, only a few studies developed experimental designs to investigate their presence. Here, we discuss the contrasting and debatable findings regarding both long-range and contact sex pheromones in the context of swarm ecology in Anopheles species.
{"title":"No sexual pheromones in Anopheles mosquitoes?","authors":"Kelsey Adams , Olivier Roux","doi":"10.1016/j.cois.2024.101227","DOIUrl":"10.1016/j.cois.2024.101227","url":null,"abstract":"<div><p>Swarming behavior is the cornerstone of the anopheline mating system. At dusk, males congregate in monospecific swarms in which females come to find a mate once in their lives. Although many <em>Anopheles</em> species coexist in sympatry, hybrids are infrequent, suggesting the existence of strong premating reproductive barriers. Chemical cues, particularly pheromones, often play a crucial role in bringing sexes together in a species-specific manner among insects. While the existence of sexual pheromones in <em>Anopheles</em> species has been postulated, only a few studies developed experimental designs to investigate their presence. Here, we discuss the contrasting and debatable findings regarding both long-range and contact sex pheromones in the context of swarm ecology in <em>Anopheles</em> species.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000695/pdfft?md5=1a328e5a463b1ca4b34dbd68c5071e24&pid=1-s2.0-S2214574524000695-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141466821","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 : 2024-06-25DOI: 10.1016/j.cois.2024.101225
Katherine H Malinski , Megan Elizabeth Moore , Joel G Kingsolver
Ongoing climate change is increasing the frequency and magnitude of high-temperature events (HTEs), causing heat stress in parasitoids and their hosts. We argue that HTEs and heat stress should be viewed in terms of the intersecting life cycles of host and parasitoid. Recent studies illustrate how the biological consequences of a given HTE may vary dramatically depending on its timing within these lifecycles. The temperature sensitivity of host manipulation by parasitoids, and by viral endosymbionts of many parasitoids, can contribute to differing responses of hosts and parasitoids to HTEs. In some cases, these effects can result in reduced parasitoid success and increased host herbivory and may disrupt the ecological interactions between hosts and parasitoids. Because most studies to date involve endoparasitoids of aphid or lepidopteran hosts in agricultural systems, our understanding of heat responses of host–parasitoid interactions in natural systems is quite limited.
{"title":"Heat stress and host–parasitoid interactions: lessons and opportunities in a changing climate","authors":"Katherine H Malinski , Megan Elizabeth Moore , Joel G Kingsolver","doi":"10.1016/j.cois.2024.101225","DOIUrl":"10.1016/j.cois.2024.101225","url":null,"abstract":"<div><p>Ongoing climate change is increasing the frequency and magnitude of high-temperature events (HTEs), causing heat stress in parasitoids and their hosts. We argue that HTEs and heat stress should be viewed in terms of the intersecting life cycles of host and parasitoid. Recent studies illustrate how the biological consequences of a given HTE may vary dramatically depending on its timing within these lifecycles. The temperature sensitivity of host manipulation by parasitoids, and by viral endosymbionts of many parasitoids, can contribute to differing responses of hosts and parasitoids to HTEs. In some cases, these effects can result in reduced parasitoid success and increased host herbivory and may disrupt the ecological interactions between hosts and parasitoids. Because most studies to date involve endoparasitoids of aphid or lepidopteran hosts in agricultural systems, our understanding of heat responses of host–parasitoid interactions in natural systems is quite limited.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141466820","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 : 2024-06-24DOI: 10.1016/j.cois.2024.101224
Hema Somanathan
Two bee species, the European honeybee and the buff-tailed bumblebee, are well-developed models of visual behaviour and ecology. How representative of bees across phylogeny and geography are these two species? Bee sensory systems likely differ between temperate and tropical species due to differences in the intensity or the types of selection pressures. Differences in temperate and tropical floral diversity, abundance and seasonality can influence sensory adaptations and behaviours. Niche partitioning in the speciose tropics along the microhabitat and temporal axes is increasingly reported to involve special visual adaptations in bees. Inclusive approaches encompassing other bee species and building on lessons from the ‘model’ bees will inform how ecology shapes bee senses, and, in turn, the structure of plant–bee mutualisms.
{"title":"Why diversity matters for understanding the visual ecology and behaviour of bees","authors":"Hema Somanathan","doi":"10.1016/j.cois.2024.101224","DOIUrl":"10.1016/j.cois.2024.101224","url":null,"abstract":"<div><p>Two bee species, the European honeybee and the buff-tailed bumblebee, are well-developed models of visual behaviour and ecology. How representative of bees across phylogeny and geography are these two species? Bee sensory systems likely differ between temperate and tropical species due to differences in the intensity or the types of selection pressures. Differences in temperate and tropical floral diversity, abundance and seasonality can influence sensory adaptations and behaviours. Niche partitioning in the speciose tropics along the microhabitat and temporal axes is increasingly reported to involve special visual adaptations in bees. Inclusive approaches encompassing other bee species and building on lessons from the ‘model’ bees will inform how ecology shapes bee senses, and, in turn, the structure of plant–bee mutualisms.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":null,"pages":null},"PeriodicalIF":5.8,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141455784","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}