Common functional elements of Drosophila melanogaster seminal peptides involved in reproduction of Drosophila melanogaster and Helicoverpa armigera females

Sex peptide (SP) and Ductus ejaculatorius peptide (Dup) 99B are synthesized in the retrogonadal complex of adult male Drosophila melanogaster, and are transferred in the male seminal fluid to the female genital tract during mating. They have been sequenced and shown to exhibit a high degree of homology in the C-terminal region. Both affect subsequent mating and oviposition by female D. melanogaster. SP also increases in vitro juvenile hormone (JH) biosynthesis in excised corpora allata (CA) of D. melanogaster and Helicoverpa armigera. We herein report that the partial C-terminal peptides SP(8-36) and SP(21-36) of D. melanogaster, and the truncated N-terminal SP(6-20) do not stimulate JH biosynthesis in vitro in CA of both species. Both of these C-terminal peptides reduce JH-III biosynthesis significantly. Dup99B, with no appreciable homology to SP in the N-terminal region, similarly lacks an effect on JH production by H. armigera CA. In contrast, the N-terminal peptides - SP(1-11) and SP(1-22) - do significantly activate JH biosynthesis of both species in vitro. We conclude that the first five N-terminal amino acid residues at the least, are essential for allatal stimulation in these disparate insect species. We have previously shown that the full-length SP(1-36) depresses pheromone biosynthesis in H. armigera in vivo and in vitro. We now show that full-length Dup99B and the C-terminal partial sequence SP(8-36) at low concentrations strongly depress (in the range of 90% inhibition) PBAN-stimulated pheromone biosynthesis of H. armigera. In addition, the N-terminal peptide SP(1-22), the shorter N-terminal peptide SP(1-11) and the truncated N-terminal SP(6-20) strongly inhibit pheromone biosynthesis at higher concentrations.     

Female sex pheromone suppression and the fate of sex-peptide-like peptides in mated moths of Helicoverpa armigera

Insect males produce accessory gland (MAG) factors that are transferred in the seminal fluid to females during copulation, and elicit changes in the mated female's behavior and physiology. Our previous studies showed that the injection of synthetic Drosophila melanogaster sex-peptide (DrmSP) into virgin females of the moth Helicoverpa armigera causes a significant inhibition of pheromone production. In this and other moth species, pheromone production, correlated with female receptivity, is under neuroendocrine control due to the circadian release of the neuropeptide PBAN. In this study, we show that PBAN, present in the hemolymph during the scotophase in females, is drastically reduced after mating. We also identify 4 DrmSP-like HPLC peaks (Peaks A, S1, S2, and B) in MAGs, with increasing levels of DrmSP immunoreactivity during the scotophase, when compared to their levels observed during the photophase. In H. armigera MAGs, a significant reduction in the pheromonostatic peak (Peak B) was already evident after 15 min of copulation, and depletion of an additional peak (Peak S2) was evident after complete mating. Peak A is also detected in female brains, increasing significantly 1 h after mating, at which time inhibition of pheromone biosynthesis also occurs. However, changes corresponding to the other MAG peaks were not detected in mated female tissues.     

Control of pheromone biosynthesis in mated redbanded leafroller moths

Mating in the redbanded leafroller moth, Argyrotaenia velutinana, causes a permanent decline in pheromone titers. Three hours following the termination of mating, phermone titers were significantly decreased from premating levels, and titers remained low for at least four days after mating. Pheromone titers were similar in females that had been decapitated or mated for twenty-four hours. In the redbanded leafroller moth, two peptides control pheromone production. The pheromone biosynthesis activating neuropeptide is produced in the brain and the pheromonotropic bursa peptide is produced in the corpus bursae. Both peptides stimulated pheromone biosynthesis in mated females and extracts prepared from brains and bursae of mated females contained pheromonotropic activity. However, severing the ventral nerve cord before mating prevented the decline in pheromone titer that occurred in mated females. Hemolymph collected during scotophase from mated females did not have pheromonotropic activity, whereas hemolymph collected during scotophase from virgin females contained activity. These results indicate that mating produces a signal sent by the ventral nerve cord to the brain to stop the release of pheromone biosynthesis activating neuropeptide. © 1993 Wiley-Liss, Inc.     

Juvenile hormone induction of pheromone gland PBAN-responsiveness in Helicoverpa armigera females

The maturation of corpora allata (CA) and the competence of pheromone glands in the adult moth Helicoverpa armigera, are both age-related and appear to be correlated. Sex pheromone glands of pharate adults do not produce sex pheromone independently, nor do they respond to exogenous PBAN. Newly emerged moths produce significantly less pheromone than day one moths. JH (juvenile hormone) II was found to be the main JH form produced by CA in vitro. JH II primed pheromone glands of pharate adults to respond to PBAN. In addition, injection or topical application of JH II to newly-emerged females induced pheromone production in the presence of PBAN. Our findings suggest that JH is involved in the initiation of pheromone production of Helicoverpa armigera.     

Biosynthetic maturation of the corpus allatum of the female adult medfly,Ceratitis capitata,and its putative control

The major juvenile hormone (JH) homolog synthesized in vitro by the adult female Medfly (Ceratitis capitata) corpus allatum (CA) is JHB(3), with JH-III the minor homolog. Methyl-incorporation in vitro in post-eclosion virgin females is age-dependent. Basal activity occurs during the first four days post-eclosion and increases significantly thereafter, peaking at five days. Biosynthetic maturation of the mated female CA is delayed by one day and reduced considerably. The delayed response may be due to direct cerebral or neural inhibition. Synthetic Drosophila melanogaster sex peptide depresses JH biosynthesis by the Medfly female CA in vitro. Male-derived accessory gland peptides of the Medfly are transferred to the female during mating and a Medfly SP-analog may be responsible for down-regulation of JH synthesis by the CA in mated Medfly females. Mevinolin, an inhibitor of the mevalonate pathway, significantly reduces the biosynthesis of JHB(3), while farnesoic acid, a proximate precursor of JHIII, significantly stimulates the biosynthesis of both JHB(3) and JHIII in vitro.     

Regulation of juvenile hormone biosynthesis in Heliothis virescens by Manduca sexta allatotropin

In Heliothis virescens, reproduction is strictly dependent on juvenile hormone (JH). In females, mating induces a sharp increase in JH titers, which stimulates increased vitellogenin biosynthesis and higher rates of egg production. JH biosynthesis is presumably stimulated by production and/or release of stimulatory neuropeptides such as allatotropins. There is evidence that allatotropin of H. virescens may be structurally related to Manduca sexta allatotropin (Manse-AT). In a radiochemical in vitro assay, synthetic Manse-AT stimulated JH biosynthesis by corpora allata (CA) of virgin H. virescens females in a dose-dependent manner, but had no effect on CA activity in H. virescens males. In females, the CA showed a transient increase in sensitivity to Manse-AT shortly after mating. Several structurally related peptides stimulated CA activity to a similar extent as Manse-AT. Corpora allata activity was stimulated by a Ca2+ ionophore, A23187. A membrane-permeable Ca2+ chelator, BAPTA/AM, antagonized the stimulatory effects of Manse-AT, suggesting that Manse-AT may enhance CA activity by increasing intracellular Ca2+ concentration.     

Mating in Heliothis virescens: Transfer of juvenile hormone during copulation by male to female and stimulation of biosynthesis of endogenous juvenile hormone

Studies were undertaken to determine whether adult males of Heliothis virescens transfer juvenile hormone (JH) to females during copulation, and an in vitro radiochemical assay was used to determine whether mating causes an allatotropic effect, i.e., stimulation of JH biosynthesis by corpora allata (CA). In vitro, CA from 3-day-old mated females synthesized and released approximately 2.5 times total JH as that of CA from comparably aged virgin females. Of the homologues, JH II exhibited significant increase in mated females; JH I also increased but not significantly. JH III remained similar to that of virgin females. This is the first demonstration of an allatotropic effect of mating in moths. In contrast to the female, CA of virgin males did not produce any JH, but accessory sex glands (ASG) in 3-day-old males synthesized small amounts of JH. Immediately after adult emergence, male ASG contained approximately 1.5 ng JH I and II, which increased by 12 h after emergence and remained at this high level up to 54 h after emergence. JH III was barely detected in ASG. JH in ASG of mated male immediately after uncoupling was depleted almost completely, and 24 h later recovered to levels comparable to that of 54-h-old virgin male. Virgin female bursa copulatrix did not contain any JH, but mated female bursa, immediately after uncoupling, had JH at levels comparable to that observed in virgin male ASG. By 6 h after uncoupling, JH levels decreased dramatically in mated female bursa. These data suggest the transfer of JH to females by the male. Arch. Insect Biochem. Physiol. 38:100–107, 1998. © 1998 Wiley-Liss, Inc.     

Inhibition of pheromone biosynthesis in Helicoverpa armigera by pheromonostatic peptides

Male insect accessory glands contain factors that are transferred during mating to the female, some inducing post-mating behavior, including the cessation of pheromone production, non-receptivity and the initiation of oviposition. One such factor is the Drosophila melanogaster sex-peptide (DrmSP). A pheromone suppression peptide, termed HezPSP, was identified in the moth Helicoverpa zea, isolated by HPLC and the active peak sequenced, but the activity of the synthesized peptide has not been reported to date. HezPSP bears no sequence homology to DrmSP. However, both peptides contain a disulfide bridge separated by an equal number, but dissimilar, amino acids. We herein report on the pheromonostatic activity of HezPSP partial peptides in the moth Helicoverpa armigera.     

Termination of sex pheromone production in mated females of the silkworm moth

A mating duration of more than 6 h was necessary to permanently terminate the production of the sex pheromone (bombykol) in the silkworm moth, Bombyx mori L. (Lepidoptera: Bombycidae), although the female formed a bursa copulatrix including a spermatophore and laid fertilized eggs even after mating for only 0.5 h. The 6-h mated female again produced bombykol if given an injection of synthetic pheromonotropic neuropeptide (PBAN), which is known to activate pheromone biosynthesis in a virgin female. Extracts of brain-suboesophageal ganglion (SG) complexes, which were removed from 6- and 24-h mated females, showed strong pheromonotropic activities. These results indicated that the pheromone gland of the mated female maintained its ability to biosynthesize bombykol; however, it could not produce pheromone due to a suppression of PBAN secretion from the SG. Furthermore, bombykol titers did not decrease after mating in females with a transected ventral nerve cord, even after the injection of a spermatophore extract, suggesting that the suppression of PBAN secretion was mediated by a neural signal and not by a substance in the spermatophore. The mated females accumulated (10E, 12Z)-10,12-hexadecadienoic acid, a precursor of bombykol biosynthesis, in their pheromone glands as did decapitated females. © 1996 Wiley-Liss, Inc.     

豆野螟成虫行为学特征及性信息素产生与释放节律

豆野螟Maruca vitrata (Fabricius)是一种严重的泛热带豆类蔬菜害虫。本文在（29±1）℃、相对湿度75%～80%、光周期14L∶10D条件下研究了豆野螟成虫的羽化、交尾行为以及雌蛾性信息素的释放节律。结果表明：其羽化行为全天可见,在雌蛾中,86%于暗期羽化; 在雄蛾中,73%于暗期羽化。雌雄蛾羽化行为在暗期第4、5和8 h差异达到显著 (t>4; P<0.05)。交尾活动发生在暗期19：00到5：00之间,交尾持续时间最短约为20 min,最长约为90 min,3日龄进入暗期第5 h具有最高的交尾率。1、6和7日龄成虫具有单个交尾高峰,2到5日龄成虫具有两个交尾高峰。同一日龄成虫交尾在暗期前半段平均花费的时间要明显高于在后半段花费的时间。低龄和高龄的成虫用于交尾的时间明显高于中龄的性成熟成虫。成虫的开始交尾时间随着日龄的增加逐渐前移。雄蛾对进入暗期后第5 h和第9 h处女雌蛾的性腺提取物和空气收集性信息素的触角电位反应最强,对 3日龄处女雌蛾的性腺提取物和空气收集性信息素的触角电位反应最强。处女雌蛾田间诱蛾试验表明：23：00-01：00为诱蛾高峰期,3日龄处女雌蛾的诱蛾效果最好。该蛾的羽化、交尾及性信息素产生与释放均存在节律上的一致性。雌蛾的性信息素释放的时间较长,见于整个暗期,然而交尾行为发生时间较短,主要发生于两个交尾高峰之间。     

光强度对棉铃虫交配行为的影响

【目的】为阐明光强度对棉铃虫Helicoverpa armigera (Hübner)交配行为的影响。【方法】本实验设置4个光照强度(0,0.5,5.0和50.0 lx),观察记录不同光照强度下棉铃虫雌蛾的求偶行为;分别通过单个腺体性信息素提取法和解剖雌虫受精囊的方式,检测不同光照强度下棉铃虫的雌蛾性信息素滴度和交配率。【结果】在强光(50.0 lx)下,棉铃虫雌蛾求偶起始时间最长,求偶持续时间最短,求偶次数最少,雌蛾性信息素滴度始终处于较低水平,交配率也属于最低。在微光(0.5 lx)下,雌蛾求偶起始时间最短,求偶持续时间最长,求偶次数最多;雌蛾性信息素始终处于较低水平,但暗期后段求偶率高达40%。【结论】强光(50.0 lx)可以抑制棉铃虫雌蛾的求偶行为、性信息素的合成及交配;微光(0.5 lx)可以促进棉铃虫雌蛾的求偶行为;相对黑暗环境(0 lx),微光(0.5 lx)还可以促进棉铃虫快速(1 h)完成交配,微光(0.5 lx)对棉铃虫的交配行为具有重要意义;求偶和性信息素的合成没有必然联系。本研究可为探讨光对夜蛾交配行为的影响提供一定的理论基础,也可为利用物理、化学通讯信息调控夜蛾行为提供一定的参考。     

Identification of Differentially Expressed Genes in the Pheromone Glands of Mated and Virgin Bombyx mori by Digital Gene Expression Profiling

Background

Mating decreases female receptivity and terminates sex pheromone production in moths. Although significant progress has been made in elucidating the mating-regulated inactivation of pheromone biosynthesis-activating neuropeptide (PBAN) secretion, little is known about the mating induced gene expression profiles in pheromone glands (PGs). In this study, the associated genes involved in Bombyx mori mating were identified through digital gene expression (DGE) profiling and subsequent RNA interference (RNAi) to elucidate the molecular mechanisms underlying the mating-regulated gene expression in PGs.

Results

Eight DGE libraries were constructed from the PGs of mated and virgin females: 1 h mating (M1)/virgin (V1) PGs, 3 h mating (M3)/virgin (V3) PGs, 24 h mating (M24)/virgin (V24) PGs and 48 h mating (M48)/virgin (V48) PGs (M48 and V48). These libraries were used to investigate the gene expression profiles affected by mating. DGE profiling revealed a series of genes showing differential expression in each set of mated and virgin female samples, including immune-associated genes, sex pheromone synthesis-associated genes, juvenile hormone (JH) signal-associated genes, etc. Most interestingly, JH signal was found to be activated by mating. Application of the JH mimics, methoprene to the newly-emerged virgin females leaded to the significant reduction of sex pheromone production. RNAi-mediated knockdown of putative JH receptor gene, Methoprene tolerant 1 (Met1), in female pupa resulted in a significant decrease in sex pheromone production in mature females, suggesting the importance of JH in sex pheromone synthesis.

Conclusion

A series of differentially expressed genes in PGs in response to mating was identified. This study improves our understanding of the role of JH signaling on the mating-elicited termination of sex pheromone production.     

低剂量60Co-γ辐射对棉铃虫蛾羽化、寿命、趋光行为和性信息素滴度的影响

为阐明低剂量辐射对棉铃虫Helicoverpa armigera (Hübner)生长发育、 成虫趋光行为和性信息素滴度的影响, 本试验设置5个辐照剂量, 记录棉铃虫蛾羽化率、 畸形率及寿命; 通过趋光行为学试验和单个腺体性信息素提取法, 检测了辐照(50 Gy)前后棉铃虫蛾趋光率和性信息素滴度的变化。结果表明： (1)在20 Gy剂量辐照下, 雌雄棉铃虫羽化率与对照相比分别降低了16.67%和20.00%, 畸形率均升高了10.00%,10,30,40和50 Gy辐照对棉铃虫蛾羽化率、 畸形率、 寿命均没有显著影响。(2)无论是光期还是暗期, 辐照后的棉铃虫蛾趋光率和性信息素滴度均有所上升, 其中趋光率提升幅度最大的是光期3日龄雌虫(28.33%±3.33%至91.67%±4.41%); 性信息素滴度提升量最大的是暗期5日龄雌蛾(36.27±4.26 ng至59.13±4.63 ng)。50 Gy辐照剂量会促进棉铃虫蛾的趋光行为和信息素的合成, 且棉铃虫蛾趋光率在设置的5个辐照剂量下无显著性差异。(3)棉铃虫蛾趋光率和性信息素滴度随着羽化日龄的增加有一个先上升后下降的变化趋势, 其中趋光率变化最大的是辐照组光期雌虫和辐照组暗期雄虫(二者均为91.67%±4.41%至3.33%±1.67%); 性信息素滴度变化最大的是辐照组暗期雌虫(71.00±5.22 ng至3.63±1.47 ng)。(4)在大多数处理中, 羽化率、 畸形率、 寿命及趋光率不存在雌雄差异。本研究为探讨辐照后棉铃虫趋光行为和体内生理生化的变化提供一定的理论基础依据, 同时也为利用物理、 化学通讯信息调控棉铃虫行为提供了新思路, 对害虫综合防治具有一定的参考价值。     

Sex pheromone titre in the glands of Spodoptera litura females: circadian rhythm and the effects of age and mating

The present study investigates the effects of age and mating status on the circadian variations of gland sex pheromone titre in female Spodoptera litura Fabricius. Similar to other nocturnal moths, S. litura females exhibit circadian variations of gland sex pheromone contents, with higher levels during scotophase and lower levels during photophase. The sex pheromone titre in the glands peaks during the first scotophase after eclosion and sharply declines afterwards. Higher pheromone contents during scotophase may facilitate female reproductive activities, and the negative relationship between pheromone titre and female calling is likely the result of pheromone release during female calling. Interestingly, the present study demonstrates that mated S. litura females have significantly higher sex pheromone titre in their pheromone glands (PGs) than virgin females. This finding contrasts with all previous studies of other insect species, in which mating generally reduces the sex pheromone titre in female PGs. In S. litura, mating and male accessory gland fluids can suppress female calling behaviours and re‐matings. These results suggest that the suppression of female calling behaviours by mating and male accessory gland fluids may significantly reduce the release of sex pheromones and thus result in higher sex pheromone titre in the PGs of mated females.     

Diel periodicity and influence of age and mating on female sex pheromone titre in Estigmene acrea (Lep., Arctiidae)

Abstract:  Calling behaviour, diel periodicity, and effect of age and mating on female sex pheromone titre in Estigmene acrea (Drury) were studied under laboratory conditions. Forty-five per cent of females started calling during the first scotophase, but the highest number of calling females was observed during the second, third and fourth scotophases. Calling behaviour occurred from the third hour after dark until just before the end of the scotophase. However, females exhibited a bimodal pattern of calling with the first peak occurring between 4 and 6 h and a second peak at 10 h after the onset of scotophase. The mean onset of calling time differed significantly with age. Older females showed a tendency to call longer, but there was no significant difference. The amount of (Z,Z)-3,6-cis-9, 10-epoxyheneicosadiene in females was quantified from the first scotophase following emergence, until the fifth scotophase. Glands of 0-day-old females presented a higher content of pheromone compared with that found in glands of 1-, 2-, 3- and 4-day-old females. Pheromone titre was determined at 2-h intervals throughout the third scotophase and photophase. (Z,Z)-3,6-cis-9,10-epoxyheneicosadiene was found in the gland during the scotophase as well as the photophase. However, there was no consistent pattern of pheromone production throughout the scotophase or photophase. Mated females of E. acrea produced significantly less pheromone than virgin females.     

Effect of temperature and photoperiod on juvenile hormone biosynthesis and sexual maturation in the cotton bollworm, Helicoverpa armigera: implications for life history traits

The Israeli population of the cotton bollworm, Helicoverpa armigera (Hübner), undergoes a short-day, low-temperature pupal diapause and is also suspected of being a seasonal migrant in the eastern Mediterranean region. H. armigera were reared in the laboratory under several constant temperature and photoperiodic combinations which simulate average conditions encountered in the spring, summer, early-autumn and late-autumn in Israel. Juvenile hormone (JH) biosynthesis, the onset of calling behavior, sex pheromone production and ovarian development were examined in virgin female moths subsequent to eclosion. Allatal maturation, defined as acquisition of competence to synthesize JH, was significantly delayed in moths reared under simulated spring conditions. This was probably the cause for the observed delay in ovarian development and the onset of calling behavior, and to the reduction in sex pheromone biosynthesis. The delay in female sexual maturation, commonly associated with migratory flight, is consistent with presumptive pre-reproductive migration in H. armigera.     

Rhythmicity of sex pheromone content in female Heliothis virescens: impact of mating

Abstract Pheromone production in virgin females of Heliothis virescens (F.) (Lepidoptera: Noctuidae) peaked between the fourth and seventh hours of scotophase on the second, third, fourth and fifth days following eclosion. The highest peak (186 ng) occurred on day 3 after eclosion. Z-11-Hexadecenal comprised the highest proportion of seven components in the pheromone glands. Disproportionately higher amounts of hexadecanal and Z-11-hexadecenol occurred during photo-phase and other periods when low quantities of total pheromone were recorded.
Mating suppressed pheromone production which remained low until 48 h after mating. Coupling females with males mated three times previously or with 6-day-old males was less effective in causing a drop in pheromone content which peaked again 24 h after mating. This suggests the transfer of a male factor, a pheromonostatic factor, that suppresses pheromone production in mated females and that the factor from older and previously mated males is less effective.     

Regulation of sex pheromone biosynthesis in the oriental tobacco budworm,Helicoverpa assulta (Lepidoptera: Noctuidae)

The five components, Z9-16:Ald, 16:Ald, Z11-16:Ald, Z9-16:Ac and Z11-16:Ac, of the sex pheromone in Helicoverpa assulta were mostly detected during the scotophase, with their titer peaking at the 4th hour during the scotophase under a 15L/9D regime. They were not detected during the photophase, but were produced during the photophase when decapitated females were injected with extracts of virgin female (FHE), male heads (MHE), homogenates of the brain-suboesophageal ganglion complex (Br-SOG), or synthetic Hez-PBAN. Production of Z9-16:Ald increased during the first 45min after FHE injection and then declined to a very low level after 2h during the photophase. Synthetic Hez-PBAN stimulated the sex pheromone glands for at least 2h and the effect was more or less proportional to the concentration of the peptide. From the present results, we suggest the following: PBAN is released continuously into the haemolymph to stimulate pheromone biosynthesis at least during the first half of the scotophase, PBAN is synthesized and accumulated independent of photoperiod or sex, and the release starts just prior (about 1h) to the beginning of the scotophase.     

竹织叶野螟成虫求偶行为及其雌蛾性信息素分泌腺超微结构

【目的】蛾类昆虫性信息素的合成和释放与求偶行为的发生是一致的,其合成和释放的器官是性信息素腺体。为深入了解竹织叶野螟性信息素的分泌生理,开展了竹织叶野螟求偶行为及其性信息素腺体超微结构的研究。【方法】在光周期14L:10D、温度26±2℃、相对湿度80%±10％的室内条件下,观察研究了竹织叶野螟的求偶行为;依据求偶规律研究结果,选取最活跃日龄雌蛾,在暗期求偶高峰时间段,充分挤压其腹部末端,然后于第8节处横向切下,将切下的腹末标本处理后,借助显微镜和扫描电镜观察性信息素腺体的表面特征及超微结构。【结果】竹织叶野螟雌雄蛾求偶均具一定的程序性,且求偶行为只发生在暗期,暗期前5 h内雌蛾求偶率较低,6 h后求偶率明显升高,并在暗期7-8 h达到求偶高峰;求偶率与雌蛾日龄有密切关系,3日龄雌蛾求偶率最高,持续时间也最长。竹织叶野螟性信息素分泌腺位于腹部第8-9节节间膜上,是一完整的环状结构,显微镜下观察其分泌腺为一乳白色囊状体,扫描电镜下其腹面囊状体迂回褶皱多,大体分为3个褶皱区,除第1褶皱区外,其余褶皱区表面密布乳突、凹陷沟和刺状物,且刺状物顶端有孔;背面囊状体皱褶少,其表面形态与第2和第3褶皱区相似。【结论】研究结果有助于了解竹织叶野螟性信息素合成和释放的时辰节律,也为该虫性信息素的准确提取和鉴定、性信息素的生物合成及利用提供了科学依据。