Male Pheromone Production Research Articles

Individual Variation in Male Pheromone Production in Xylocopa sonorina Correlates with size and Gland Color.

Sex pheromones are species-specific chemical signals that facilitate the location, identification, and selection of mating partners. These pheromones can vary between individuals, and act as signals of mate quality. Here, we investigate the variation of male pheromones in the mesosomal glands of the large carpenter bee Xylocopa sonorina, within a Northern California population. We tested the hypothesis that morphological traits are correlated with the observed variation in chemical blend composition of these bees. We also conducted behavioral assays to test whether these male pheromones act as long-range attractants to conspecifics. We found that larger males with darker mesosomal glands have a higher pheromone amount in their glands. Our analysis also suggests that this pheromone blend functions as a long-range attractant to both males and females. We show that both male body size and sexual maturation are important factors influencing pheromone abundance, and that this pheromone blend acts as a long-range attractant. We hypothesize that this recorded variation in male pheromone could be important for female choice.

Interactions between oxidative stress and attractiveness to mates and individual mate choice in the beetle Tenebrio molitor

AbstractMale mating signals are sexual traits that may provide females with information about the physiological quality of the individual. Males of the yellow mealworm beetle, Tenebrio molitor, use pheromones to attract mating partners. The level of pheromone production in males has been identified as a signal of the male condition. We tested whether male sex pheromones also signal the oxidative stress status of their bearers. We used the herbicide paraquat to manipulate the oxidative stress status of individual beetles. We found that healthy males and females preferred healthy mates to those experiencing oxidative stress. If the individual choosing mates was experiencing oxidative stress, females but not males maintained their preference for healthy mating partners. Our study demonstrates a chemical signal indicating the oxidative stress status of a potential partner and reveals that the decisions based on this signal depend upon the condition and gender of the individual making a choice.

Male-specific features are reduced in Mecp2-null mice: analyses of vasopressinergic innervation, pheromone production and social behaviour.

Deficits in arginine vasopressin (AVP) and oxytocin (OT), two neuropeptides closely implicated in the modulation of social behaviours, have been reported in some early developmental disorders and autism spectrum disorders. Mutations in the X-linked methyl-CpG-binding protein 2 (MECP2) gene are associated to Rett syndrome and other neuropsychiatric conditions. Thus, we first analysed AVP and OT expression in the brain of Mecp2-mutant mice by immunohistochemistry. Our results revealed no significant differences in these systems in young adult Mecp2-heterozygous females, as compared to WT littermates. By contrast, we found a significant reduction in the sexually dimorphic, testosterone-dependent, vasopressinergic innervation in several nuclei of the social brain network and oxytocinergic innervation in the lateral habenula of Mecp2-null males, as compared to WT littermates. Analysis of urinary production of pheromones shows that Mecp2-null males lack the testosterone-dependent pheromone darcin, strongly suggesting low levels of androgens in these males. In addition, resident-intruder tests revealed lack of aggressive behaviour in Mecp2-null males and decreased chemoinvestigation of the intruder. By contrast, Mecp2-null males exhibited enhanced social approach, as compared to WT animals, in a 3-chamber social interaction test. In summary, Mecp2-null males, which display internal testicles, display a significant reduction of some male-specific features, such as vasopressinergic innervation within the social brain network, male pheromone production and aggressive behaviour. Thus, atypical social behaviours in Mecp2-null males may be caused, at least in part, by the effect of lack of MeCP2 over sexual differentiation.

Phenotypic plasticity in sex pheromone production in Bicyclus anynana butterflies.

Phenotypic plasticity refers to the environmental control of phenotypes. Cues experienced during development (developmental plasticity) or during adulthood (acclimatization) can both affect adult phenotypes. Phenotypic plasticity has been described in many traits but examples of developmental plasticity in physiological traits, in particular, remain scarce. We examined developmental plasticity and acclimatization in pheromone production in the butterfly Bicyclus anynana in response to rearing temperature. B. anynana lives in the African tropics where warm rearing temperatures of the wet season produce active males that court and females that choose, whereas cooler temperatures of the dry season lead to choosy less active males and courting females. We hypothesized that if male pheromone production is costly, it should be reduced in the dry season form. After describing the ultrastructure of pheromone producing cells, we showed that dry season males produced significantly less sex pheromones than wet season males, partly due to acclimatization and partly due to developmental plasticity. Variation in levels of one of the compounds is associated with differential regulation of a pheromone biosynthetic enzyme gene. This plasticity might be an adaptation to minimize pheromone production costs during the stressful dry season.

The fatty acid elongase Bond is essential for Drosophila sex pheromone synthesis and male fertility.

Insects use a spectacular variety of chemical signals to guide their social behaviours. How such chemical diversity arises is a long-standing problem in evolutionary biology. Here we describe the contribution of the fatty acid elongase Bond to both pheromone diversity and male fertility in Drosophila. Genetic manipulation and mass spectrometry analysis reveal that the loss of bond eliminates the male sex pheromone (3R,11Z,19Z)-3-acetoxy-11,19-octacosadien-1-ol (CH503). Unexpectedly, silencing bond expression severely suppresses male fertility and the fertility of conspecific rivals. These deficits are rescued on ectopic expression of bond in the male reproductive system. A comparative analysis across six Drosophila species shows that the gain of a novel transcription initiation site is correlated with bond expression in the ejaculatory bulb, a primary site of male pheromone production. Taken together, these results indicate that modification of cis-regulatory elements and subsequent changes in gene expression pattern is one mechanism by which pheromone diversity arises.

A Wolbachia-Sensitive Communication between Male and Female Pupae Controls Gamete Compatibility in Drosophila

Gamete compatibility is fundamental to sexual reproduction. Wolbachia are maternally inherited endosymbiotic bacteria that manipulate gamete compatibility in many arthropod species. In Drosophila, the fertilization of uninfected eggs by sperm from Wolbachia-infected males often results in early developmental arrest. This gamete incompatibility is called cytoplasmic incompatibility (CI). CI is highest in young males, suggesting that Wolbachia affect sperm properties during male development. Here, we show that Wolbachia modulate testis development. Unexpectedly, this effect was associated with Wolbachia infection in females, not males. This raised the possibility that females influenced testis development by communicating with males prior to adulthood. Using a combinatorial rearing protocol, we provide evidence for such a female-to-male communication during metamorphosis. This communication involves the perception of female pheromones by male olfactory receptors. We found that this communication determines the compatibility range of sperm. Wolbachia interfere with this female-to-male communication through changes in female pheromone production. Strikingly, restoring this communication partially suppressed CI in Wolbachia-infected males. We further identified a reciprocal male-to-female communication at metamorphosis that restricts the compatibility range of female gametes. Wolbachia also perturb this communication by feminizing male pheromone production. Thus, Wolbachia broaden the compatibility range of eggs, promoting thereby the reproductive success of Wolbachia-infected females. We conclude that pheromone communication between pupae regulates gamete compatibility and is sensitive to Wolbachia in Drosophila.

A novel mechanism regulating a sexual signal: The testosterone-based inhibition of female sex pheromone expression in garter snakes

Vertebrates communicate their sex to conspecifics through the use of sexually dimorphic signals, such as ornaments, behaviors and scents. Furthermore, the physiological connection between hormones and secondary sexual signal expression is key to understanding their dimorphism, seasonality and evolution. The red-sided garter snake (Thamnophis sirtalis parietalis) is the only reptile for which a described pheromone currently exists, and because garter snakes rely completely on the sexual attractiveness pheromone for species identification and mate choice, they constitute a unique model species for exploring the relationship between pheromones and the endocrine system. We recently demonstrated that estrogen can activate female pheromone production in male garter snakes. The purpose of this study was to determine the mechanism(s) acting to prevent female pheromone production in males. We found that castrated males (GX) are courted by wild males in the field and produce appreciable amounts of female sex pheromone. Furthermore, pheromone production is inhibited in castrates given testosterone implants (GX+T), suggesting that pheromone production is actively inhibited by the presence of testosterone. Lastly, testosterone supplementation alone (T) increased the production of several saturated methyl ketones in the pheromone but not the unsaturated ketones; this may indicate that saturated ketones are testosterone-activated components of the garter snake's skin lipid milieu. Collectively, our research has shown that pheromone expression in snakes results from two processes: activation by the feminizing steroid estradiol and inhibition by testosterone. We suggest that basal birds and garter snakes share common pathways of activation that modulate crucial intraspecific signals that originate from skin.

Establishing abiotic and biotic factors necessary for reliable male pheromone production and attraction to pheromones by female plum curculiosConotrachelus nenuphar(Coleoptera: Curculionidae)

AbstractThe plum curculio (PC),Conotrachelus nenupharHerbst (Coleoptera: Curculionidae), is a key pest of stone and pome fruit in North America. Though grandisoic acid (GA) was identified as a male-produced aggregation pheromone for this species, other components likely exist, as have been identified for various curculionids. To better determine these components, an understanding of the conditions necessary for optimum pheromone production and attraction is needed, this is essential for the improvement of monitoring techniques and to achieve better biological control. The goal of this study was to determine the biotic and abiotic factors influencing both the response to pheromones and pheromone production. Tests were conducted in a dual-choice still-air vertical olfactometer using live male PCs as odour sources and live females as responders, to determine which physiological factors (age, number of males, mating status) influenced female response to males. Head-space collections of GA production under various conditions (airflow rate and frequency, collection zone strata, variation of humidity, temperature, and presence of a harbourage) were also done, as were electroantennograms (EAG) using synthetic pheromone mixtures. Results revealed that for both strains, the odour of two virgin mature males elicited significantly greater and more consistent attraction from mature virgin females than other ages and numbers of males when compared with the control. Head-space collections indicate that male PC have increased production of GA under high humidity in the presence of fruit, indicating that these conditions are necessary for optimal pheromone production and collection. EAG studies revealed significant responses to GrandLures I, II, III/IV and to the positive enantiomer of GA, and the amplitude of the signal varied with concentration. Our data identify the optimal physiological state and conditions at which pheromone collections should be performed, and what physiological life stages respond to these stimuli. These results have implications for optimising monitoring tools for this serious crop pest. This species has a northern univoltine strain and a southern multivoltine strain, both of which were examined in this study.

MiR-124 controls male reproductive success in Drosophila

Many aspects of social behavior are controlled by sex-specific pheromones. Gender-appropriate production of the sexually dimorphic transcription factors doublesex and fruitless controls sexual differentiation and sexual behavior. miR-124 mutant males exhibited increased male-male courtship and reduced reproductive success with females. Females showed a strong preference for wild-type males over miR-124 mutant males when given a choice of mates. These effects were traced to aberrant pheromone production. We identified the sex-specific splicing factor transformer as a functionally significant target of miR-124 in this context, suggesting a role for miR-124 in the control of male sexual differentiation and behavior, by limiting inappropriate expression of the female form of transformer. miR-124 is required to ensure fidelity of gender-appropriate pheromone production in males. Use of a microRNA provides a secondary means of controlling the cascade of sex-specific splicing events that controls sexual differentiation in Drosophila. DOI:http://dx.doi.org/10.7554/eLife.00640.001.

Molecular Mechanisms Underlying Insect Behaviors: Receptors, Peptides, and Biosynthetic Pathways

Molecular Mechanisms Underlying Insect Behaviors: Receptors, Peptides, and Biosynthetic Pathways

Pheromone Gland Development and Pheromone Production in Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae)

The sand fly Lutzomyia longipalpis (Lutz & Neiva) (Diptera: Psychodidae: Phlebotominae) is the main vector of American visceral leishmaniasis. Adult males produce a terpenoid sex pheromone that in some cases also acts as male aggregation pheromone. We have analyzed the correlation between male pheromone production levels and pheromone gland cell morphogenesis after adult emergence from pupae. The abdominal tergites of L. longipalpis males were dissected and fixed in glutaraldehyde for transmission electron microscopy, or the pheromone was extracted in analytical grade hexane. Pheromone chemical analysis was carried out at 3- to 6-h intervals during the first 24 h after emergence and continued daily until the seventh day. All extracts were analyzed by gas chromatography. For the morphological analysis, we used insects collected at 0-6, 9-12, 12-14, and 96 h after emergence. Ultrastructural data from 0- to 6-h-old adult males revealed smaller pheromone gland cells with small microvilli at the end apparatus. Lipid droplets and peroxisomes were absent or very rare, but a large number of mitochondria could be seen. Lipid droplets started to appear in the gland cells cytoplasm approximately 9 h after adult emergence, and their number and size increased with age, together with the presence of several peroxisomes, suggesting a role for these organelles in pheromone biosynthesis. At 12-15 h after emergence, the lipid droplets were mainly distributed near the microvilli but were smaller than those in mature older males (4 d old). Pheromone biosynthesis started around 12 h after emergence and increased continuously during the first 3 d, stabilizing thereafter, coinciding with the period when males are more able to attract females.

Two Regulatory Mechanisms of Monoterpenoid Pheromone Production in Ips spp. Of Bark Beetles

Bark beetles use aggregation pheromones to coordinate host colonization and mating. These monoterpenoid chemical signals are produced de novo in midgut cells via the mevalonate pathway, and pheromone production is induced when an adult beetle feeds on phloem of a host tree. In Ips pini, juvenile hormone (JH) III influences key regulatory enzymes along the mevalonate pathway that leads to pheromone production. In fact, topically applied JH III is sufficient to stimulate pheromone production in unfed males. In this study, we explore the influence of feeding and JH III treatment on pheromone production in male Ips confusus, the pinyon Ips. We also characterize the influence of feeding and JH III treatment on transcript levels and activity of three key enzymes involved in pheromone biosynthesis: 3-hydroxy-3-methylglutaryl-CoA (HMG) synthase (HMGS), HMG-CoA reductase (HMGR) and geranyl diphosphate synthase (GPPS). We also extend the current understanding of the regulation of pheromone biosynthesis in I. pini, by measuring the influence of feeding and JHIII treatment on enzymatic activity of HMGS and GPPS. Feeding on host phloem alone strongly induces pheromone production in male I. confusus, while JH III treatment has no effect. However, feeding and JH III both significantly up-regulate mRNA levels of key mevalonate pathway genes. Feeding up-regulates these genes to a maximum at 32 h, whereas with JH III-treatment, they are up-regulated at 4, 8, and 16 h, but return near to non-treatment levels at 32 h. Feeding, but not JH III treatment, also increases the activity of all three enzymes in I. confusus, while both feeding or treatment with JH III increase HMGS and GPPS activity in I. pini. Our data suggest that pheromone production in Ips is not uniformly controlled by JH III and feeding may stimulate the release of some other regulatory factor, perhaps a brain hormone, required for pheromone production.

Structure and juvenile hormone-mediated regulation of the HMG-CoA reductase gene from the Jeffrey pine beetle, Dendroctonus jeffreyi

In several pine bark beetle species, juvenile hormone (JH) III regulated 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-R) gene expression has an important role in monoterpenoid pheromone production in males. We investigated the structure and regulated expression of the HMG-R gene ( HMG-R) in the Jeffrey pine beetle, Dendroctonus jeffreyi. cDNA and genomic sequences were recovered using a combination of library screening and PCR. The transcribed portion of the gene spans 9.8 kb and is interrupted by 13 introns. When compared to vertebrate HMG-Rs, the distribution of intron sites suggests a functional role for those in the 5′ untranslated region and membrane anchor domains. Northern blots show that topically applied JH III stimulates HMG-R expression up to 30-fold in male D. jeffreyi, compared to untreated insects, in both a dose- and time-dependent manner. There was no increase in expression levels in similarly treated female insects. The expression pattern is consistent with the production of monoterpenoid pheromone components in male D. jeffreyi, and suggests the utility of the system as a new tool for studying the mechanism of JH action.

Time-course haemolymph juvenile hormone titres in solitarious and gregarious adults of Schistocerca gregaria, and their relation to pheromone emission, CA volumetric changes and oocyte growth

The haemolymph JH III titres in solitarious and gregarious adult desert locusts, Schistocerca gregaria, were examined in relation to corpus allatum (CA) volumes, aggregation–maturation pheromone production in males and oocyte growth in females. The JH titres of gregarious females were generally higher than those of solitarious females at all ages studied. The titre patterns, however, were similar: relatively high on day 10, dropping to low levels between days 20 and 25, before rising again by day 25. In the solitarious males, the JH titre was very low on day 10 after fledging, but increased gradually and reached a maximal amount on day 30. The JH titre in gregarious males was low on day 10, elevated on day 15 coinciding with the start of the production of the pheromone, and dropped to a relatively low level on day 20 around the time of maximal pheromone production, then rising again by day 25. These results suggest that biosynthesis of the pheromone is associated with a high JH titre peak in the haemolymph. Although a clear relationship was found during the first gonadotropic cycle between JH titres, on one hand, and CA volume and oocyte growth, on the other, in both phases, no such correlation could be discerned in the second cycle.

Differential application of lambda-cyhalothrin to control the sandfly Lutzomyia longipalpis.

To study the impact of residual pyrethroid insecticide on the abundance and distribution of peridomestic Lutzomyia longipalpis, the sandfly vector of visceral leishmaniasis in Brazil, lambda-cyhalothrin was applied at 20 mg a.i.m-2 in the following interventions: (i) spraying of all animal pens in a village (blanket coverage); (ii) treatment of a subset of animal pens, either by spraying, or by installation of insecticide-impregnated 1 m2 cotton sheets as 'targets' (focal coverage). By sampling with CDC light traps, and using a novel analytical approach, we detected a 90% reduction in Lu.longipalpis abundance in sprayed sheds of the focal intervention. However, there was no discernible effect on the abundance of other phlebotomines trapped in sheds, or on the abundance of Lu.longipalpis in untreated dining-huts and houses. This differential impact on Lu.longipalpis abundance is explained in terms of the disruption of male pheromone production. Treated targets were approximately half as effective as residual spraying in reducing the abundance of Lu.longipalpis in sheds. Following blanket intervention, the abundance of Lu.longipalpis in traps fell by only 45% (not significant): catches at untreated dining-huts actually increased, possibly because the blanket coverage diverted Lu.longipalpis away from major aggregation sites at animal pens. It is recommended that care be taken during vector control programmes to ensure that all potential aggregation sites are treated. The possible consequences of leaving some sites untreated include poor control of peridomestic sandfly abundance and an increase in the biting rate on dogs and humans.

Starvation of Cabbage Looper Moths (Lepidoptera: Noctuidae) Increases Attraction to Male Pheromone

We compared the attraction of fed versus unfed cabbage looper moths, Trichoplusia ni (Hübner), to male pheromone. Significantly more starved females and starved males were attracted to male pheromone than were females or males that were provided a sugar-honey mixture. Food availability did not affect male attractiveness or male pheromone production, only female responsiveness. Female T. ni that were fed either honey, fructose, glucose, maltose, or sucrose were less likely to respond to male pheromone, compared to females that were not fed. Cabbage looper moth attraction to male pheromone may be related to foodfinding behavior.

Interspecific activity of semiochemicals among sibling species ofPissodes (Coleoptera: Curculionidae)

Pissodes strobi, P. approximatus, andP. nemorensis are sibling species of pine weevils that can hybridize in the laboratory but are presumed to be reproductively isolated in nature. Males of all three species produce the terpenoids grandisol and grandisal; these compounds serve as an aggregation pheromone forP. approximatus andP. nemorensis when deployed with odors from pine bolts. A series of field experiments examined the possibility of cross-attraction among the three species. Tests in New York and Florida found that parapatrically distributedP. approximatus andP. nemorensis were cross-attractive, but different photoperiodic conditioning was required for pheromone production in males of the two species. Long-day pheromone production (P. approximatus-type.) was inherited in interspecific hybrids. Other tests showed thatP. strobi males, or hybrid males from crosses ofP. strobi withP. approximatus, were not attractive to sympatricP. approximatus. When the response ofP. strobi was assessed to males of eitherP. strobi orP. approximatus confined on white pine leaders (the breeding site ofP. strobi), no evidence of cross-attraction or pheromone activity was found;P. strobi were caught in equal numbers onP. strobi-baited leaders,P. approximatus-baited leaders, and unbaited leaders. Tests of interspecific interactions found that maleP. strobi produce an allelochemical signal that interrupts the response ofP. approximatus to its natural or synthetic aggregation pheromone. This interspecific response is apparently adaptive for members of both species (classified as an allomone-kairomone or synomone) because it may ultimately serve to prevent interspecific matings that would lower the fitness of the parents.

The effect of staphylococcal enterotoxin B on pheromone production in fat bodies isolated from male boll weevils

In this study we treated fat bodies excised from 1- to 10-day-old male boll weevils with staphylococcal enterotoxin B. After the compound was incubated with fat bodies for 2 hr, the incubating medium was extracted and analyzed for boll weevil sex pheromone production by gas chromatographic analysis. Of the four compounds that make up the boll weevil male sex pheromone, differences were found between the control (no enterotoxin) and test groups in production of the two aldehydes. We concluded from this that the staphylococcal enterotoxin does affect male pheromone production in boll weevils.

Induction of female sex pheromone production in male houseflies by ovary implants or 20-hydroxyecdysone

Implanting ovaries or injecting 20-hydroxyecdysone into male houseflies induced sex pheromone production, including (Z)-9-tricosene (muscalure), 9,10-epoxytricosane and (Z)-14-tricosen-10-one, which normally occurs only in vitellogenic females. Control males did not produce detectable amounts of these compounds. Injection of 20-hydroxyecdysone (5 μg/insect per day) for 3 days resulted in the accumulation of 1.81 μg/insect of ( Z)-9-tricosene, 0.97 μg/insect of 9,10-epoxytricosane and 0.12 μg/insect ( Z)-14-tricosen-10-one. Multiple injections of 20-hydroxyecdysone at doses as low as 50 ng resulted in the accumulation of 23:1, C 23 epoxide and C 23 ketone; shifted the distribution of label within the alkenes from 27:1 to 23:1 and decreased the amount of label in the hydrocarbon fractions as alkenes. Structures of the C 23 alkene and epoxide produced by the males were verified by gas chromatography-mass spectrometry. Radioactivity from [1- 14C] acetate was incorporated into the C 23 alkene, epoxide and ketone in male insects after ovaries were implanted or they were injected with 20-hydroxyecdysone. Synthesis of the C 23 pheromone components decreased rapidly within several days after the administration of 20-hydroxyecdysone ceased, indicating that the enzymes involved in sex pheromone production were not permanently induced by hormone treatment. Ecdysone was also effective in initianing pheromone production in males, whereas inokosterone and cholesterol were not effective. Data presented demonstrate that male houseflies possess the metabolic capability to produce the sex pheromone components, and this suggests that 20-hydroxyecdysone alters the production of cuticular hydrocarbons such that the C 23 sex pheromone components become major products.

Laboratory and Insectary Studies on the Use of Antibiotics and Antimicrobial Agents in Mass-Rearing of Boll Weevils12

Antibiotics were used to shield the growth medium of larvae of Anthonomus grandis grandis Boheman from microbial contamination without detectable adverse effects on boll weevil development, egg production, hatch, and male pheromone production. The standard diet overlain with medicated sand yielded 86–97% newly-emerged weevils with less than 500 bacteria/weevil as compared with 18% from diet with unmedicated sterile sand.