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":"64 ","pages":"Article 101227"},"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":"64 ","pages":"Article 101225"},"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":"64 ","pages":"Article 101224"},"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}
Pub Date : 2024-06-20DOI: 10.1016/j.cois.2024.101222
Michelle Schinkel, Teun Bousema, Ronald P van Rij
Mosquito-borne diseases have a major impact on global human health. Biological agents that colonize the mosquito vector are increasingly explored as an intervention strategy to prevent vector-borne disease transmission. For instance, the release of mosquitoes carrying the endosymbiotic bacterium Wolbachia effectively reduced dengue virus incidence and disease. Insect-specific viruses are likewise considered as biocontrol agents against vector-borne diseases. While most studies focused on insect-specific viruses as an intervention against arthropod-borne viruses, we here consider whether mosquito-specific viruses may affect the transmission of the malaria-causing Plasmodium parasite by Anopheles mosquitoes. Although there is no direct experimental evidence addressing this question, we found that viral infections in dipteran insects activate some of the immune pathways that are antiparasitic in Anopheles. These findings suggest that indirect virus–parasite interactions could occur and that insect-specific viruses may modulate malaria transmission. Tripartite interactions between viruses, parasites, and Anopheles mosquitoes thus merit further investigation.
{"title":"Tripartite interactions between viruses, parasites, and mosquitoes","authors":"Michelle Schinkel, Teun Bousema, Ronald P van Rij","doi":"10.1016/j.cois.2024.101222","DOIUrl":"10.1016/j.cois.2024.101222","url":null,"abstract":"<div><p>Mosquito-borne diseases have a major impact on global human health. Biological agents that colonize the mosquito vector are increasingly explored as an intervention strategy to prevent vector-borne disease transmission. For instance, the release of mosquitoes carrying the endosymbiotic bacterium <em>Wolbachia</em> effectively reduced dengue virus incidence and disease. Insect-specific viruses are likewise considered as biocontrol agents against vector-borne diseases. While most studies focused on insect-specific viruses as an intervention against arthropod-borne viruses, we here consider whether mosquito-specific viruses may affect the transmission of the malaria-causing <em>Plasmodium</em> parasite by <em>Anopheles</em> mosquitoes. Although there is no direct experimental evidence addressing this question, we found that viral infections in dipteran insects activate some of the immune pathways that are antiparasitic in <em>Anopheles</em>. These findings suggest that indirect virus–parasite interactions could occur and that insect-specific viruses may modulate malaria transmission. Tripartite interactions between viruses, parasites, and <em>Anopheles</em> mosquitoes thus merit further investigation.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"64 ","pages":"Article 101222"},"PeriodicalIF":5.8,"publicationDate":"2024-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000646/pdfft?md5=ec9299ee6d90260ecb7ea5a3f7ca7f4b&pid=1-s2.0-S2214574524000646-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141440303","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 : 2024-06-20DOI: 10.1016/j.cois.2024.101223
Junwei J Zhu, Haichuan J Wang
Biting flies, including stable flies and horn flies, are considered important pests of livestock, companion animals, and humans by inflicting painful bites and interrupting normal animal behavior and human recreational/outdoor activities. It is estimated that they cause an annual loss of over 3 billion dollars in the US livestock industry. Both groups of pest flies further transmit various infectious diseases to animals and humans. The present review summarizes recent research advancements in stable and horn fly chemical and sensory ecology, especially in the discovery of novel attractants and repellents, as well as their controls for these blood-sucking flies and beyond.
{"title":"Semiochemicals and natural repellents in biting fly management","authors":"Junwei J Zhu, Haichuan J Wang","doi":"10.1016/j.cois.2024.101223","DOIUrl":"10.1016/j.cois.2024.101223","url":null,"abstract":"<div><p>Biting flies, including stable flies and horn flies, are considered important pests of livestock, companion animals, and humans by inflicting painful bites and interrupting normal animal behavior and human recreational/outdoor activities. It is estimated that they cause an annual loss of over 3 billion dollars in the US livestock industry. Both groups of pest flies further transmit various infectious diseases to animals and humans. The present review summarizes recent research advancements in stable and horn fly chemical and sensory ecology, especially in the discovery of novel attractants and repellents, as well as their controls for these blood-sucking flies and beyond.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"64 ","pages":"Article 101223"},"PeriodicalIF":5.8,"publicationDate":"2024-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141440302","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 : 2024-06-05DOI: 10.1016/j.cois.2024.101219
Ratna Chaturvedi, Patrick Emery
Sleep is conserved across the animal kingdom, and Drosophila melanogaster is a prime model to understand its intricate circadian and homeostatic control. GABA (gamma-aminobutyric acid), the brain’s main inhibitory neurotransmitter, plays a central role in sleep. This review delves into GABA’s complex mechanisms of actions within Drosophila’s sleep-regulating neural networks. We discuss how GABA promotes sleep, both by inhibiting circadian arousal neurons and by being a key neurotransmitter in sleep homeostatic circuits. GABA’s impact on sleep is modulated by glia through astrocytic GABA recapture and metabolism. Interestingly, GABA can be coexpressed with other neurotransmitters in sleep-regulating neurons, which likely contributes to context-based sleep plasticity.
{"title":"Fly into tranquility: GABA’s role in Drosophila sleep","authors":"Ratna Chaturvedi, Patrick Emery","doi":"10.1016/j.cois.2024.101219","DOIUrl":"10.1016/j.cois.2024.101219","url":null,"abstract":"<div><p>Sleep is conserved across the animal kingdom, and <em>Drosophila melanogaster</em> is a prime model to understand its intricate circadian and homeostatic control. GABA (gamma-aminobutyric acid), the brain’s main inhibitory neurotransmitter, plays a central role in sleep. This review delves into GABA’s complex mechanisms of actions within <em>Drosophila’s</em> sleep-regulating neural networks. We discuss how GABA promotes sleep, both by inhibiting circadian arousal neurons and by being a key neurotransmitter in sleep homeostatic circuits. GABA’s impact on sleep is modulated by glia through astrocytic GABA recapture and metabolism. Interestingly, GABA can be coexpressed with other neurotransmitters in sleep-regulating neurons, which likely contributes to context-based sleep plasticity.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"64 ","pages":"Article 101219"},"PeriodicalIF":5.3,"publicationDate":"2024-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141287866","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 : 2024-06-05DOI: 10.1016/j.cois.2024.101220
Harshad Vijay Mayekar, Subhash Rajpurohit
Declines in insect populations have gained formidable attention. Given their crucial role in the ecosystem, the causes of declining insect populations must be investigated. However, the insect clade has been associated with low extinction and high diversification rates. It is unlikely that insects underwent mass extinctions in the past. However, the pace of current climate change could make insect populations vulnerable to extinction. We propose genome size (GS) and transposable elements (TEs) to be rough estimates to assess extinction risk. Larger GS and/or proliferating TEs have been associated with adaptation in rapid climate change scenarios. We speculate that unstable, stressful environmental conditions are strongly associated with GS and TE expansion, which could be further correlated with adaptations. Alternately, stressful conditions trigger TE bursts that are not purged in smaller populations. GS and TE loads could be indicators of small effective populations in the wild, likely experiencing bottlenecks or drastic climatic perturbations, which calls for an urgent assessment of extinction risk.
昆虫数量的减少已经引起了极大的关注。鉴于昆虫在生态系统中的关键作用,必须对昆虫数量下降的原因进行调查。然而,昆虫类群的灭绝率很低,而多样化率却很高。昆虫在过去不太可能发生大规模灭绝。然而,当前的气候变化可能使昆虫种群容易灭绝。我们建议将基因组大小(GS)和可转座元素(TE)作为评估灭绝风险的粗略估计值。具体来说,较大的基因组大小和/或增殖的转座元素数量与快速气候变化情景下的适应有关。我们推测,不稳定、压力大的环境条件与GS和TE的扩张密切相关,而GS和TE的扩张又与适应进一步相关。另一种情况是,压力条件会引发 TE 爆发,而这些 TE 在较小的种群中不会被清除。GE和TE可能是野外小规模有效种群可能遭遇瓶颈的指标,因此需要进行灭绝风险评估。
{"title":"No single rescue recipe: genome complexities modulate insect response to climate change","authors":"Harshad Vijay Mayekar, Subhash Rajpurohit","doi":"10.1016/j.cois.2024.101220","DOIUrl":"10.1016/j.cois.2024.101220","url":null,"abstract":"<div><p>Declines in insect populations have gained formidable attention. Given their crucial role in the ecosystem, the causes of declining insect populations must be investigated. However, the insect clade has been associated with low extinction and high <em>diversification</em> rates. It is unlikely that insects underwent mass extinctions in the past. However, the pace of current climate change could make insect populations vulnerable to extinction. We propose genome size (GS) and transposable elements (TEs) to be rough estimates to assess extinction risk. Larger GS and/or proliferating TEs have been associated with adaptation in rapid climate change scenarios. We speculate that unstable, stressful environmental conditions are strongly associated with GS and TE expansion, which could be further correlated with adaptations. Alternately, stressful conditions trigger TE bursts that are not purged in smaller populations. GS and TE loads could be indicators of small effective populations in the wild, likely experiencing bottlenecks or drastic climatic perturbations, which calls for an urgent assessment of extinction risk.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"64 ","pages":"Article 101220"},"PeriodicalIF":5.3,"publicationDate":"2024-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141287867","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 : 2024-06-03DOI: 10.1016/j.cois.2024.101218
Islam S Sobhy , Geoff M Gurr , T Hefin Jones
In response to herbivory, plants employ several inducible defenses to mitigate herbivore damage. These plant-induced responses can trigger subtle changes in plant metabolite composition, altering the profiles of plant-produced exudates such as (extra-) floral nectar and plant guttation. Natural enemies consume these plant-produced exudates, which serve as consistent and nutrient-dense food sources. There is mounting evidence that natural enemies’ access to plant-produced exudates impacts their fitness, performance, and life history traits. Nonetheless, the role of induced plant defense on plant-produced exudates and the subsequent effect on natural enemies remains under-researched. This review, thus, highlights the potential role of induced plant defense on the profiles of plant-produced exudates, with a particular emphasis on altered metabolic changes affecting resource nutritional value and consequently the fitness and performance of natural enemies. Future directions and potential implications in biological control practices are also highlighted.
{"title":"Induced plant resistance and its influence on natural enemy use of plant-derived foods","authors":"Islam S Sobhy , Geoff M Gurr , T Hefin Jones","doi":"10.1016/j.cois.2024.101218","DOIUrl":"10.1016/j.cois.2024.101218","url":null,"abstract":"<div><p>In response to herbivory, plants employ several inducible defenses to mitigate herbivore damage. These plant-induced responses can trigger subtle changes in plant metabolite composition, altering the profiles of plant-produced exudates such as (extra-) floral nectar and plant guttation. Natural enemies consume these plant-produced exudates, which serve as consistent and nutrient-dense food sources. There is mounting evidence that natural enemies’ access to plant-produced exudates impacts their fitness, performance, and life history traits. Nonetheless, the role of induced plant defense on plant-produced exudates and the subsequent effect on natural enemies remains under-researched. This review, thus, highlights the potential role of induced plant defense on the profiles of plant-produced exudates, with a particular emphasis on altered metabolic changes affecting resource nutritional value and consequently the fitness and performance of natural enemies. Future directions and potential implications in biological control practices are also highlighted.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"64 ","pages":"Article 101218"},"PeriodicalIF":5.3,"publicationDate":"2024-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000609/pdfft?md5=99d80498325c35f552efaa35f0534eae&pid=1-s2.0-S2214574524000609-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141260978","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 : 2024-05-29DOI: 10.1016/j.cois.2024.101207
Jette T Knudsen , Rickard Ignell
The common bed bug, Cimex lectularius (Cimicidae, Hemiptera), is obligate haematophagous and can carry pathogens but is not known to transmit diseases to humans in natural settings. Bed bugs are activated and guided by semiochemicals and heat by potential hosts, as well as by an aggregation pheromone when searching for food and home. No sexual pheromone has been detected in bed bugs, which mate through traumatic insemination. First, after mounting, males are able to distinguish between large nymphs, other males, and females. To avoid unwanted traumatic inseminations, nymphs and adults emit an alarm pheromone. The olfactory system of bed bugs has relatively few odorant and ionotropic receptors, which likely reflects the simple environment that bed bugs live in, and use to search for hosts and conspecifics.
{"title":"Semiochemicals modulating bed bug behaviour","authors":"Jette T Knudsen , Rickard Ignell","doi":"10.1016/j.cois.2024.101207","DOIUrl":"10.1016/j.cois.2024.101207","url":null,"abstract":"<div><p>The common bed bug, <em>Cimex lectularius</em> (Cimicidae, Hemiptera), is obligate haematophagous and can carry pathogens but is not known to transmit diseases to humans in natural settings. Bed bugs are activated and guided by semiochemicals and heat by potential hosts, as well as by an aggregation pheromone when searching for food and home. No sexual pheromone has been detected in bed bugs, which mate through traumatic insemination. First, after mounting, males are able to distinguish between large nymphs, other males, and females. To avoid unwanted traumatic inseminations, nymphs and adults emit an alarm pheromone. The olfactory system of bed bugs has relatively few odorant and ionotropic receptors, which likely reflects the simple environment that bed bugs live in, and use to search for hosts and conspecifics.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"64 ","pages":"Article 101207"},"PeriodicalIF":5.3,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141184161","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 : 2024-05-29DOI: 10.1016/j.cois.2024.101208
Cameron M Hudson , Dominic Stalder , Christoph Vorburger
Insects are frequently infected with heritable bacterial endosymbionts. Some of them confer resistance to parasitoids. Such defensive symbionts are sensitive to variation in temperature. Drawing predominantly from the literature on aphids and flies, we show that temperature can affect the reliability of maternal transmission and the strength of protection provided by defensive symbionts. Costs of infection with defensive symbionts can also be temperature-dependent and may even turn into benefits under extreme temperatures, for example, when defensive symbionts increase heat tolerance. Alone or in combination, these mechanisms can drive temperature-associated (latitudinal) clines of infection prevalence with defensive symbionts. This has important consequences for host–parasitoid coevolution, as the relative importance of host-encoded vs. symbiont-provided defenses will shift along such clines.
{"title":"Clines of resistance to parasitoids: the multifarious effects of temperature on defensive symbioses in insects","authors":"Cameron M Hudson , Dominic Stalder , Christoph Vorburger","doi":"10.1016/j.cois.2024.101208","DOIUrl":"10.1016/j.cois.2024.101208","url":null,"abstract":"<div><p>Insects are frequently infected with heritable bacterial endosymbionts. Some of them confer resistance to parasitoids. Such defensive symbionts are sensitive to variation in temperature. Drawing predominantly from the literature on aphids and flies, we show that temperature can affect the reliability of maternal transmission and the strength of protection provided by defensive symbionts. Costs of infection with defensive symbionts can also be temperature-dependent and may even turn into benefits under extreme temperatures, for example, when defensive symbionts increase heat tolerance. Alone or in combination, these mechanisms can drive temperature-associated (latitudinal) clines of infection prevalence with defensive symbionts. This has important consequences for host–parasitoid coevolution, as the relative importance of host-encoded vs. symbiont-provided defenses will shift along such clines.</p></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"64 ","pages":"Article 101208"},"PeriodicalIF":5.3,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214574524000506/pdfft?md5=9cb4d689eefb47f6123d8742fadf7d25&pid=1-s2.0-S2214574524000506-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141184114","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}