RESUMEN
Pea aphids, Acyrthosiphon pisum, reproduce parthenogenetically and are wing-dimorphic such that offspring can develop into winged (alate) or unwinged (apterous) adults. Alate induction is maternal and offspring phenotype is entirely determined by changes in the physiology and environment of the mother. Juvenile hormones (JHs) have been implicated in playing a role in wing differentiation in aphids, however until recently, methods were not available to accurately quantify these insect hormones in small insects such as aphids. Using a novel LC-MS approach we were able to quantify JH III in pea aphids that were either producing a high proportion of winged morphs among their offspring or mainly unwinged offspring. We measured JH III titres by pooling the hemolymph of 12 or fewer individuals (1 microL hemolymph) treated identically. Levels of JH ranged from 30 to 163 pg/microL. While aphids in the two treatments strongly differed in the proportion of winged morphs among their offspring, their JH III titres did not differ significantly. There was also no correlation between JH III titre and the proportion of winged offspring in induced aphids. This supports earlier findings that wing dimorphism in aphids may be regulated by other physiological mechanisms.
Asunto(s)
Áfidos/fisiología , Inducción Embrionaria , Sesquiterpenos/metabolismo , Alas de Animales/crecimiento & desarrollo , AnimalesRESUMEN
The juvenile hormone (JH) titer was measured by liquid chromatography-mass spectrometry (LC-MS) with electrospray ionization (ESI). Three JH homologs, the JH I-III were detected in various amounts in larvae, prepupae and virgin adult females of Spodoptera frugiperda. In penultimate larvae, the JH II and III titers were relatively high, but decreased continuously during the 3 days of that stage, whereas JH I was detectable at low amounts only on the first 2 days. At the beginning of the last larval stage almost no JH could be detected but thereafter, a consistent low amount of JH III was present until the prepupal stage. In adult virgins, the JH titer peaked on the 2nd and 6th day after the imaginal molt. The measured hormone titers well agree with general lepidopteran physiology, because in larvae the JH titer should be high to prevent premature metamorphosis, but decrease in last instar larvae before pupation, whereas in adults JH returns to control various aspects of reproduction. JH biosynthesis is thought to be the main factor influencing the JH titer in the hemolymph and there is evidence that neuropeptides either act stimulatory (allatotropins) or inhibitory (allatostatins) on this process. After silencing of either the allatostatin AS-C-type (Spofr/Manse-AS) or the allatotropin AT 2 (Spofr-AT 2) gene the transcript level was reduced in brain and gut of last instar larvae as well as of adult S. frugiperda. This suppression led to an increased JH titer in larvae, suggesting an allatostatic activity of both the peptides in this stage. As a result of the elevated hormone titer, the last larval stage was prolonged. In prepupae, the JH titer was decreased, but the animals pupated and molted normally. In adult female virgin moths the effect on the JH titer was inversely dependent on the age of the moths and varied among the JH homologs, indicating that the peptides act either allatostatic or allatotropic. For both peptides, gene silencing clearly reduced the oviposition rates of adult females.
Asunto(s)
Hemolinfa/metabolismo , Hormonas de Insectos/metabolismo , Hormonas Juveniles/análisis , Neuropéptidos/metabolismo , Spodoptera/genética , Spodoptera/metabolismo , Animales , Cromatografía Liquida , Femenino , Inyecciones , Hormonas de Insectos/genética , Soluciones Isotónicas , Larva/crecimiento & desarrollo , Larva/metabolismo , Larva/fisiología , Espectrometría de Masas , Muda , Neuropéptidos/genética , Oviposición , Interferencia de ARN , ARN Bicatenario/farmacología , Solución de Ringer , Transcripción Genética/efectos de los fármacos , Aumento de PesoRESUMEN
Despite their abundance and their enormous significance for various ecological processes, endocrine systems of microcrustaceans have been poorly investigated. Here, we used a highly sensitive radioimmunoassay (RIA) to determine free and conjugated ecdysteroid levels in whole-body extracts of adult Daphnia magna during a complete molt cycle. Ecdysteroid levels were predominated by free ecdysteroids. Starting from basal levels in the postmolt stage the concentration of free ecdysteroids increased sharply in the early premolt stage, followed by a sharp decline back to basal levels just prior to ecdysis. Polar and apolar ecdysteroid conjugates were found in rather low amounts with little variation during the molt cycle. Only small amounts of ecdysteroids were found in newly deposited eggs of D. magna, which suggest a sparing investment of maternal ecdysteroids into the eggs for early embryogenesis. As in whole-body extracts, free ecdysteroids were the predominant ecdysteroids found in eggs of D. magna, together with small amounts of polar and intermediary amounts of apolar conjugates. Hence, the pathways leading to polar and apolar ecdysteroid conjugates appear to be of minor importance in D. magna. Analyses of the immunodetectable peak in free ecdysteroids by liquid chromatography-mass spectrometry (LC-MS) revealed that molting is induced most probably by an increased level of 20-hydroxyecdysone. Microcrustaceans of the genus Daphnia are key components in freshwater food webs. Examination of the functional role of ecdysteroids in controlling developmental processes might help to understand the performance of the herbivorous grazer in its environment, in particular with regard to the adverse effects of environmental xenobiotics acting as endocrine disrupters.
Asunto(s)
Daphnia/metabolismo , Ecdisteroides/metabolismo , Muda , Animales , Cromatografía Liquida/métodos , Daphnia/crecimiento & desarrollo , Espectrometría de Masas/métodos , Radioinmunoensayo/métodos , Reproducibilidad de los ResultadosRESUMEN
A simple, fast and sensitive method was developed for routine determination of juvenile hormone (JH), JH diols and JH acids in insect haemolymph, by liquid chromatography-mass spectrometry (LC-MS). Sample clean-up involves the precipitation of proteins by methanol/isooctane (1:1, v/v), centrifugation and partial evaporation of the organic solvents. Since JH is bound to a carrier protein in the haemolymph, a binding protein (BP) assay was performed to ensure JH is removed during precipitation. The JH compounds were separated on a C(18) column (ReproSil-Pur ODS-3) by gradient elution with water and methanol in less than 22 min and analysed by electrospray mass spectrometry. Due to the high abundance of Na(+) in insect haemolymph, [M+Na](+) is primarily formed. The limit of detection and quantification was 6 and 20 pg for JHs, and 8 and 25 pg for JH diols, respectively. To demonstrate the applicability of the method to different insect orders, haemolymph samples from the Mediterranean field cricket ( Gryllus bimaculatus), the fall armyworm ( Spodoptera frugiperda), the pea aphid ( Acyrthosiphon pisum) and an ant species ( Myrmicaria eumenoides) were analysed.