Journal of insect physiology最新文献

{"title":"Gene regulation by mating depends on time, diet, and body region in female Aedes aegypti","authors":"Ferdinand Nanfack-Minkeu ,&nbsp;Jelmer W. Poelstra ,&nbsp;Laura K. Sirot","doi":"10.1016/j.jinsphys.2024.104715","DOIUrl":"10.1016/j.jinsphys.2024.104715","url":null,"abstract":"<div><div><em>Aedes aegypti</em> is a major vector of several arboviruses that cause human mortality and morbidity. One method for controlling the spread of these viruses is to control mosquito reproduction. During mating, seminal fluid molecules and sperm are transferred and these stimuli influence female post-mating physiology and behavior. Yet, little is known about the mechanisms underlying these post-mating responses. To fill this gap, short-read RNA sequencing was used to identify differentially expressed genes between unmated (control) and mated females in the head/thorax (HT), abdomen (Ab) and the lower reproductive tract (LRT), of mosquitoes reared with 3% and 12% sucrose. The results revealed that at 3% sucrose, four, 408 and 415 significantly differential expressed genes (DEGs) were identified in the HT, Ab and LRT, respectively, at six hours post mating (hpm). The number of DEGs dropped dramatically at 24 hpm with no DEGs in the HT, three in the Ab, and 112 in the LRT. In contrast, the number of DEGs was lower at 6 hpm than 24 hpm in the LRT at 12% sucrose. Comparing our results to a similar study which used 10% sucrose revealed evidence in support of condition-dependent regulation of gene expression by mating in this species. This study shows that mating-induced transcriptional changes depend on time point after mating, body region, and diet. Our results provide foundational knowledge for future functional analyses to identify genes and pathways involved in the post-mating behavioral and physiological changes of female mosquitoes.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"159 ","pages":"Article 104715"},"PeriodicalIF":2.3,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142467626","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Phenotypical aspects of Culex pipiens biotype pipiens during diapause: Lipid utilization, body size, insemination, and parity","authors":"Rody Blom ,&nbsp;Jeroen Spitzen ,&nbsp;Tessa de Haan ,&nbsp;Constantianus J.M. Koenraadt","doi":"10.1016/j.jinsphys.2024.104714","DOIUrl":"10.1016/j.jinsphys.2024.104714","url":null,"abstract":"<div><div>In temperate regions, female <em>Culex pipiens</em> biotype <em>pipiens</em> mosquitoes undergo diapause in winter. Diapausing biotype <em>pipiens</em> mosquitoes are potentially important winter reservoirs for mosquito-borne viruses, such as West Nile virus (WNV), Usutu virus (USUV), and Sindbis virus (SINV). Mosquitoes in diapause have not taken a bloodmeal prior to winter. Therefore, they do not become infected by taking an infectious bloodmeal and as a consequence, vertical transmission is considered the primary mechanism of mosquito-borne virus overwintering. Prior to winter, biotype <em>pipiens</em> mosquitoes build up fat reserves, which they utilize throughout winter. Furthermore, earlier studies have indicated that larger body size is correlated with increased survival during winter. However, not much is known about lipid utilization and body size of wild biotype <em>pipiens</em> mosquitoes in diapause. Therefore, we performed monthly collections of diapausing biotype <em>pipiens</em> mosquitoes in two consecutive winters (2020/2021 and 2021/2022) in bunkers of the New Hollandic Waterline in the Netherlands. Every month, we checked the proportion of inseminated and parous females via microscopy. In addition, we measured wing length as proxy for body size, and assessed total lipid content. Furthermore, we monitored indoor temperature in the overwintering locations. We show that the overwintering sites in our study provide relatively stable environments, in which temperatures rarely drop below 0 °C. The vast majority of biotype <em>pipiens</em> females were inseminated (84.1 %) and nulliparous (97.5 %). We detected differences in body size between but not within the two years of sampling. Additionally, we detected a difference in lipid content between the sampling years. We confirm that the vast majority of diapausing biotype <em>pipiens</em> females are inseminated and nulliparous. This indicates that they did not blood feed prior to winter, which underscores the likeliness of vertical transmission being the primary mechanism behind virus overwintering. The detected difference in body size between years can most likely be attributed to differences in summer conditions the mosquitoes were exposed to as larvae, although this needs confirmation. The difference in lipid depletion could not be explained by differences in climatic conditions. To shed more light on the links between climatic conditions, body size, lipid depletion and the consequences for mosquito population dynamics and arbovirus transmission, future experimental work, for example by arbovirus exposure followed by artificially induced diapause, is desired.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"159 ","pages":"Article 104714"},"PeriodicalIF":2.3,"publicationDate":"2024-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142437866","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Nutritional quality regulates postnatal wing morph in pea aphids","authors":"Xi Wang ,&nbsp;Zhi-Fu Liu ,&nbsp;Ming-Zhen Pan ,&nbsp;Zhaozhi Lu ,&nbsp;Tong-Xian Liu ,&nbsp;He-He Cao","doi":"10.1016/j.jinsphys.2024.104713","DOIUrl":"10.1016/j.jinsphys.2024.104713","url":null,"abstract":"<div><div>Aphids can produce winged or wingless offspring in response to environmental changes. Host nutrition is one of the extensively studied environmental factors influencing the plasticity of wing morphs of aphids. In this study, we found that the pea aphid, <em>Acyrthosiphon pisum</em>, produced a low proportion of winged offspring when fed on plants, but a significantly higher proportion on the artificial diet. Interestingly, when newly born nymphs were transferred back to the artificial diet after feeding on plants for six hours or longer, most nymphs became wingless. These results suggest that the wing morph state of pea aphids can change postnatally, potentially determined by the nutritional quality of their food. Furthermore, aphids feeding on the artificial diet exhibited higher levels of glucose and stronger insulin signaling activity compared with aphids on plants. Conversely, the amino acid levels were lower, and TOR signaling was weaker in aphids fed on the artificial diet. Insulin and the target of rapamycin (TOR) are the primary nutrient-sensing signaling pathways involved in controlling organism growth and have been implicated in regulating aphid wing morph plasticity. We tested whether these nutrient responsive pathways were involved in postanal wing determination of aphids. However, reducing amino acid content in the diet or inhibiting TOR with rapamycin resulted in a decrease of the winged morph, suggesting that the lower amino acid levels or TOR activity was not responsible for the higher proportion of winged morph on the artificial diet. These results suggest that nutritional quality, particularly sugars like sucrose and glucose, may regulate the postnatal wing morph of the pea aphid, likely via the insulin signaling pathway.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"159 ","pages":"Article 104713"},"PeriodicalIF":2.3,"publicationDate":"2024-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142391102","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Corrigendum to \"Cellular dynamics of host - parasitoid interactions: Insights from the encapsulation process in a partially resistant host\" [J. Insect Physiol. 155 (2024) 104646].","authors":"Samuel Gornard, Florence Mougel, Isabelle Germon, Véronique Borday-Birraux, Pascaline Venon, Salimata Drabo, Laure Kaiser","doi":"10.1016/j.jinsphys.2024.104711","DOIUrl":"10.1016/j.jinsphys.2024.104711","url":null,"abstract":"","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":" ","pages":"104711"},"PeriodicalIF":2.3,"publicationDate":"2024-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142307935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Multigenerational expression of antimicrobial peptides in Aedes aegypti exposed to Metarhizium anisopliae: Is trans-generational immune priming involved?","authors":"Ricardo de Oliveira Barbosa Bitencourt ,&nbsp;Huarrisson Azevedo Santos ,&nbsp;Nicolas Salcedo-Porras ,&nbsp;Carl Lowenberger ,&nbsp;Nathália Alves de Senne ,&nbsp;Patrícia Silva Gôlo ,&nbsp;Vânia Rita Elias Pinheiro Bittencourt ,&nbsp;Isabele da Costa Angelo","doi":"10.1016/j.jinsphys.2024.104712","DOIUrl":"10.1016/j.jinsphys.2024.104712","url":null,"abstract":"<div><div>We assessed, for the first time, a multigenerational expression of antimicrobial peptides (AMPs) in <em>Aedes aegypti</em> larvae exposed to the entomopathogenic fungus, <em>Metarhizium anisopliae,</em> and correlated it with a possible involvement in <em>trans</em>-generational immune priming (TGIP). <em>Aedes aegypti</em> larvae were first exposed to blastospores or conidia of <em>M. anisopliae</em> CG 489 for 24 and 48 h, and the relative expression of AMPs were measured using quantitative Real-Time PCR. A suspension of conidia was prepared, and two different survival tests were conducted with different larval generations (F0, F1, and F2). In the first bioassay, the survival curves of the three generations were conducted separately and compared with their respective control groups. In the other bioassay, the survival curves of the F0, F1, and F2 generations were compared simultaneously against a naïve group exposed to Tween 80. In both survival tests, the F0 generation was more susceptible to <em>M. anisopliae</em> than subsequent generations. For molecular analyses related to TGIP, F0, F1, and F2 larvae were exposed to conidia, and their expression of AMPs was compared with their control groups and a naïve group. There was no differential expression of <em>cecropin</em>, <em>defensin A</em> or <em>cathepsin B</em> between generations. <em>Lysozyme C</em>, however, showed an increase in expression across generations, suggesting a role in TGIP. These discoveries may help us develop biological insecticides against mosquito larvae based on entomopathogenic fungi.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"159 ","pages":"Article 104712"},"PeriodicalIF":2.3,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142289258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Larval stress affects adult Drosophila behavior and metabolism","authors":"Evgenia K. Karpova,&nbsp;Margarita A. Bobrovskikh,&nbsp;Elena V. Burdina,&nbsp;Natalya V. Adonyeva,&nbsp;Maksim A. Deryuzhenko,&nbsp;Lyudmila P. Zakharenko,&nbsp;Dmitriy V. Petrovskii,&nbsp;Nataly E. Gruntenko","doi":"10.1016/j.jinsphys.2024.104709","DOIUrl":"10.1016/j.jinsphys.2024.104709","url":null,"abstract":"<div><div>In this study, we raised the following question: “Does metamorphosis, being a “reboot” of all systems of the organism, erase the changes that occurred at earlier stages of insect development?” To answer this question, we investigated several behavioral, metabolic and neuroendocrine parameters in <em>Drosophila melanogaster</em> imago that had undergone heat stress at the 3rd larval instar (32 °C, 48 h). We discovered that larval stress negatively affected feeding and locomotor behavior, as well as total lipid content in adult flies. At the same time, these flies demonstrated a considerable increase in carbohydrate content and expression level of insulin/insulin-like growth factor signaling (IIS) pathway genes, <em>dfoxo</em>, <em>dilp6</em> and <em>dInR</em>. The data obtained allow us to conclude that metamorphosis does not erase the effect of stress exposure at early developmental stages and causes dramatic changes in carbohydrate and lipid metabolism as well as locomotor activity of adult insects, which is at least in part due to changes in IIS activity.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"159 ","pages":"Article 104709"},"PeriodicalIF":2.3,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142289257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Ecdysone promotes gene- and pathogen-specific immune responses to Micrococcus luteus and Bacillus subtilis in Drosophila S2 cells","authors":"Mona Ghassah ,&nbsp;Yulia A. Polunina ,&nbsp;Victor K. Chmykhalo ,&nbsp;Lyubov A. Lebedeva ,&nbsp;Yulii V. Shidlovskii ,&nbsp;Zaur M. Kachaev","doi":"10.1016/j.jinsphys.2024.104710","DOIUrl":"10.1016/j.jinsphys.2024.104710","url":null,"abstract":"<div><p>In <em>Drosophila</em>, the 20-hydroxyecdysone (20E) hormone regulates numerous essential biological processes. Here, we studied the contribution of 20E to the activity of immune signaling pathways and antimicrobial activity using the model <em>Drosophila</em> S2 cells. We found that while 20E alone has no essential effect on this system, pretreating S2 cells with 20E followed by incubation with <em>Escherichia coli</em> or <em>Micrococcus luteus</em> stimulates the induction of a limited number of antimicrobial peptide (AMP) genes, such as <em>Diptericin (Dpt)</em> and <em>Drosomycin (Drs).</em> Contrary to this, cells pretreatment with 20E simulates the activity of numerous <em>Bacillus subtilis</em>-induced AMP genes. Interestingly, it also significantly promotes the expression of components of both the Toll (<em>Dif, Dorsal</em>, etc.) and the IMD pathways (<em>Relish, IMD</em>, etc.) in the presence of <em>Bacillus subtilis</em>. Unexpectedly, simultaneous treatment of S2 cells by 20E and all three bacteria shows another pattern of activity and leads to a suppression of <em>Drosocin (Dro)</em> induction, in particular. Our study reveals that the contribution of 20E to immune genes activity varies for different genes and depends on the mode of 20E interplay with the pathogen and the nature of the pathogen itself.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"159 ","pages":"Article 104710"},"PeriodicalIF":2.3,"publicationDate":"2024-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142239114","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Dying of thirst: Osmoregulation by a hawkmoth pollinator in response to variability in ambient humidity and nectar availability","authors":"Ajinkya Dahake ,&nbsp;Steven G. Persaud ,&nbsp;Marnesha N. Jones ,&nbsp;Joaquín Goyret ,&nbsp;Goggy Davidowitz ,&nbsp;Robert A. Raguso","doi":"10.1016/j.jinsphys.2024.104700","DOIUrl":"10.1016/j.jinsphys.2024.104700","url":null,"abstract":"<div><p>Climate-induced shifts in flowering phenology can disrupt pollinator-floral resource synchrony, especially in desert ecosystems where rainfall dictates both. However, baseline metrics to gauge pollinator health in the wild amidst rapid climate change are lacking. Our laboratory-based study establishes a baseline for pollinator physiological state by exploring how osmotic conditions influence survivorship in a desert hawkmoth pollinator, <em>Manduca sexta</em>. We sampled hemolymph osmolality from over 1000 lab-grown moths at 20 %, 50 %, and 80 % ambient humidity levels. Starved moths maintained healthy osmolality of 350–400 mmol/kg for 1–3 days after eclosion regardless of ambient humidity, but it sharply rose to 550 mmol/kg after 4–5 days in low and moderate humidity, and after 5 days in high humidity. Starved moths in low humidity conditions perished within 5 days, while those in high humidity survived twice as long. Moths fed synthetic <em>Datura wrightii</em> nectar, synthetic <em>Agave palmeri</em> nectar, or water, maintained osmolality within a healthy range of 350–400mmol/kg. The same was true for moths fed authentic floral nectars from <em>Datura</em> and <em>Agave</em> plants, although moths consumed more synthetic than authentic nectars, possibly due to non-sugar constituents. Simulating a 4-day mismatch between pollinator emergence and nectar availability, a single nectar meal osmotically rescued moths under dry ambient conditions. Our findings highlight hemolymph osmolality as a rapid and accurate biomarker distinguishing dehydrated from hydrated states in insect pollinators.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"159 ","pages":"Article 104700"},"PeriodicalIF":2.3,"publicationDate":"2024-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S002219102400088X/pdfft?md5=09eca8269cc5e561136d652a517b30ab&pid=1-s2.0-S002219102400088X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142162523","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Dietary potassium and cold acclimation additively increase cold tolerance in Drosophila melanogaster","authors":"Bassam Helou ,&nbsp;Marshall W. Ritchie ,&nbsp;Heath A. MacMillan ,&nbsp;Mads Kuhlmann Andersen","doi":"10.1016/j.jinsphys.2024.104701","DOIUrl":"10.1016/j.jinsphys.2024.104701","url":null,"abstract":"<div><p>In the cold, chill susceptible insects lose the ability to regulate ionic and osmotic gradients. This leads to hemolymph hyperkalemia that drives a debilitating loss of cell membrane polarization, triggering cell death pathways and causing organismal injury. Biotic and abiotic factors can modulate insect cold tolerance by impacting the ability to mitigate or prevent this cascade of events. In the present study, we test the combined and isolated effects of dietary manipulations and thermal acclimation on cold tolerance in fruit flies. Specifically, we acclimated adult <em>Drosophila melanogaster</em> to 15 or 25 °C and fed them either a K⁺-loaded diet or a control diet. We then tested the ability of these flies to recover from and survive a cold exposure, as well as their capacity to protect transmembrane K⁺ gradients, and intracellular Na⁺ concentration. As predicted, cold-exposed flies experienced hemolymph hyperkalemia and cold-acclimated flies had improved cold tolerance due to an improved maintenance of the hemolymph K⁺ concentration at low temperature. Feeding on a high-K⁺ diet improved cold tolerance additively, but paradoxically reduced the ability to maintain extracellular K⁺ concentrations. Cold-acclimation and K⁺-feeding additively increased the intracellular K⁺ concentration, aiding in maintenance of the transmembrane K⁺ gradient during cold exposure despite cold-induced hemolymph hyperkalemia. There was no effect of acclimation or diet on intracellular Na⁺ concentration. These findings suggest intracellular K⁺ loading and reduced muscle membrane K⁺ sensitivity as mechanisms through which cold-acclimated and K⁺-fed flies are able to tolerate hemolymph hyperkalemia.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"159 ","pages":"Article 104701"},"PeriodicalIF":2.3,"publicationDate":"2024-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0022191024000891/pdfft?md5=7374511cd6a1aa6a5bada385330ef47c&pid=1-s2.0-S0022191024000891-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142169176","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Male condition and seminal fluid affect female host-marking behavior in the Mexican fruit fly","authors":"Guadalupe Córdova-García ,&nbsp;Ana Salazar-Suárez,&nbsp;Perla Paloma Cabrera-Ferral,&nbsp;Francisco Díaz-Fleischer ,&nbsp;Maurilio López-Ortega ,&nbsp;Diana Pérez-Staples","doi":"10.1016/j.jinsphys.2024.104699","DOIUrl":"10.1016/j.jinsphys.2024.104699","url":null,"abstract":"<div><p>Mating and the transfer of seminal fluid components including male accessory glands (MAGs) proteins can affect oviposition behavior in insects. After oviposition, some species of fruit flies deposit a host-marking pheromone (HMP) on the fruit that discourages oviposition by other females of the same or different species or genus and reduces competition between larvae. However, we know very little about how mating, receiving seminal fluid, or male condition can affect female host marking behavior. Here, we tested how the physiological state of females (mated or unmated), the receipt of seminal fluid, and the condition of the male (wild or sterile) affect oviposition and host-marking behavior (HMB) in <em>Anastrepha ludens</em> (Diptera: Tephritidae). We also determined the efficiency of the host-marking pheromone from mated or unmated females in deterring oviposition. In a further examination of how seminal fluid may be affecting HMB we assessed if there were differences in the size of wild or sterile MAGs and the protein quantity transferred during mating. Our results indicate that receiving seminal fluid increased egg laying and increased time invested in host-marking (HM). Unmated females laid fewer eggs than mated females but invested the same amount of time in depositing host-marking pheromone, which had similar effectiveness in deterring oviposition as that of mated females. Females that mated with sterile males laid the same number of eggs as females that mated with wild males but spent less time depositing host-marking pheromone, which suggests that females detect the condition of the male and invest less in marking hosts. Finally, sterile males had larger accessory glands and transferred more MAGs proteins during mating compared to wild males. Seminal proteins could be manipulating HM behavior and female investment into their current reproductive effort. We are only beginning to understand how male condition and seminal fluid can affect female physiology and maternal investment in HMP.</p></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"158 ","pages":"Article 104699"},"PeriodicalIF":2.3,"publicationDate":"2024-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142093520","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}