Hydrolysis of sex pheromone by antennal esterases of the cabbage looper, Trichoplusia ni

Esterases were isolated from chemosensory sensilla on the antennaeof Trichoplusia ni (Hübner). The disc gel electrophoreticpatterns of these esterases from males and females were similar;however, more bands were observed in the antennae than in 8other tissues examined. Most of the esterases detected in the100,000 g supernatant of the antennal preparation could be dissociatedfrom the 100,000 g membrane pellet. Esterases from both maleand female antennae hydrolyzed the sex attractant, (Z)-7-dodecen-l-olacetate, more rapidly than did the legs, fat body or Malpighiantubules. The enzymes primarily responsible for pheromone catabolismwere less sensitive to paraoxon, eserine and p-(hydroxymercuri)benzoatethan those hydrolyzing 1-napthyl acetate. This suggested thata major portion of the observed pheromone-hydrolytic activitywas due to acetylesterases. Measurement of pheromone hyrolysisin sections of disc gels that contained separated antennal orabdominal body wall esterases revealed 2 peaks of activity withboth tissues; however, the rate of pheromone hydrolysis by theabdominal esterases was slower than that of the antennae. Thesignificance of these findings is discussed in relation to thepossibility of antennal esterases having a functional role inthe olfactory process of males of T. ni.     

桃蚜对正[反]—β法尼烯的行为及电生理反应

[反]-β-法尼烯([E]-β-farnesene)是多种蚜虫的报警信息素成分。本文用触角分部切 断法,检测到桃蚜Myzus persicae触角对[反]-β-法尼烯的敏感部位在原生感觉圈。嗅觉反应表明[反]-北京吃网-β-法尼烯对桃蚜的驱拒效果极显著。触角电位检测结果表明成蚜对[反]-β-法尼烯的电生理反应比若蚜敏感。     

Orientation to sex pheromone in the American cockroach: Analysis of chemo-orientation mechanisms

Male Periplaneta americana were photographed in a 2.4 m diameter arena containing a female sex pheromone source in the centre. Orientation pathways were digitized and analysed with regard to chemo-orientation mechanisms employed. Indirect components of chemo-orientation include arrestment near the pheromone source owing to an increase in turning rate and decrease in rate of locomotion, and zig-zag motor patterns that facilitate localization of the source. Most males were successful in locating the source if they moved to within 30 cm. Direct components of chemo-orientation include looping and relatively sharp correcting turns.No significant differences in orientation were observed between intact and unilaterally-antennectomized males, except that correcting turns close to the pheromone source were significantly less precise in males with one antenna. These results indicate that males with two antennae have an advantage over males with one antenna in being able to employ simultaneous information processing close to the pheromone source. Males with crossed antennae were unable to locate the pheromone source, suggesting that the fixed position of their antennae interfered with sensory information input.     

Functional Specificity of Sex Pheromone Receptors in the Cotton Bollworm Helicoverpa armigera

Male moths can accurately perceive the sex pheromone emitted from conspecific females by their highly accurate and specific olfactory sensory system. Pheromone receptors are of special importance in moth pheromone reception because of their central role in chemosensory signal transduction processes that occur in olfactory receptor neurons in the male antennae. There are a number of pheromone receptor genes have been cloned, however, only a few have been functionally characterized. Here we cloned six full-length pheromone receptor genes from Helicoverpa armigera male antennae. Real-time PCR showing all genes exhibited male-biased expression in adult antennae. Functional analyses of the six pheromone receptor genes were then conducted in the heterologous expression system of Xenopus oocytes. HarmOR13 was found to be a specific receptor for the major sex pheromone component Z11-16:Ald. HarmOR6 was equally tuned to both of Z9-16: Ald and Z9-14: Ald. HarmOR16 was sensitively tuned to Z11-16: OH. HarmOR11, HarmOR14 and HarmOR15 failed to respond to the tested candidate pheromone compounds. Our experiments elucidated the functions of some pheromone receptor genes of H. armigera. These advances may provide remarkable evidence for intraspecific mating choice and speciation extension in moths at molecular level.     

Antennal responses of Cydia pomonella (L.) exposed to surfaces treated with methoxyfenozide

Electroantennogram (EAG) measurements were recorded from the antennae of male and female codling moth, Cydia pomonella L., to determine whether adult moths exposed to surfaces treated with the ecdysteroid agonist methoxyfenozide experience a decline in their antennal reception and thus olfactory sensitivity. Such a phenomenon would offer a possible mechanism for the previously reported decreased responsiveness from moths treated with methoxyfenozide to pheromone‐ and plant volatile‐based monitoring lures. Mean EAG data revealed that the antennae from methoxyfenozide‐treated male moths appear to be just as sensitive to various doses of synthetic codlemone as the antennae from the control and surfactant‐treated moths, but they appeared to be less sensitive to the pheromone component 12OH (collected from female effluvia) than the control male antennae. Mean male EAG responses to the pheromone components E8,E10‐12Al and codlemone collected from methoxyfenozide‐treated females were significantly less than the responses towards those two pheromone components collected from the control and surfactant‐treated females. Female moth exposure to methoxyfenozide did not negatively impact the sensitivity of female antennae to the plant volatile pear ester, but it did towards the apple volatile butyl hexanoate. Data from this study show that adult C. pomonella exposure to methoxyfenozide‐treated surfaces does appear to negatively impact, in a minor way, the (i) olfactory sensitivity (or detection) of male antennae towards some components of the female sex pheromone, (ii) the female antennal sensitivity towards a key apple volatile and (iii) the attractiveness of female pheromone effluvia.     

Electroantennographic resolution of pulsed pheromone plumes in two species of moths with bipectinate antennae

Trains of 20-ms-duration pulses of pheromone were deliveredat rates of 1–33 Hz to antennal preparations of malesof Bombyx mori and Lymantria dispar, two moth species with bipectinateantennae. Resolution of rapidly pulsed plumes of pheromone wasnot compromised by a complex antennal morphology or by moderatechanges in wind speed (25–50 cm/s). Fourier analysis ofthe electroantennograms resolved the temporal structure of thesignal at frequencies up to 25 Hz for B. mori and up to 5 Hzfor L. dispar. The ability of these sensory structures to identifythe original (unchanged) frequency of the pulse train is particularlynoteworthy because air is slowed by about an order of magnitudeas it passes through bipectinate antennae. Although an unchangingfrequency in slowed airflow may be counterintuitive, this flowpattern, and its effects on odorant patch shape and spacing,is explained from fluid mechanical principles (i.e., the principleof continuity). An unchanging frequency suggests that as deceleratingair passes through a bipectinate antenna, the slowed patchesof odorant are stretched, thinned, and brought closer togetherby the same factor with which they are slowed.     

Sulfhydryl-reagent inhibition of olfaction in a moth and effects of exposure to pheromone compounds or a pheromone analogue

The effects on olfaction of N-ethylmaleimide (NEM), a specificreagent of free sulfhydryl groups, were studied in the mothMamestra brassicae. The antennae of male M.brassicae bear twotypes of specialist receptor neurons involved in pheromone communication.One type is tuned to (Z)-11-hexadecenyl acetate (Z11-16:Ac),the main pheromone component; the second type is tuned to (Z)-9-tetradecenylacetate (Z9-14:Ac), an interspecific inhibitor not producedby the females of this species. Vapours of NEM irreversiblyinhibited the electro-antennographic (EAG) responses to Z11-16:Acand Z9-14:Ac. When Zll-16:Ac was applied before and during NEMtreatment, the responses to Z9-14:Ac were preserved and someprotection was observed in the responses to Zll-16:Ac. In return,Z9-14:Ac partially prevented the disappearance of responsesto Zll-16:Ac but not to Z9-14:Ac. A third compound, hexadecylacetate (16:Ac), found in the pheromone gland, but not detectedby the antennal receptors, did not prevent the inhibition causedby NEM.     

Pheromone production, male abundance, body size, and the evolution of elaborate antennae in moths

The males of some species of moths possess elaborate feathery antennae. It is widely assumed that these striking morphological features have evolved through selection for males with greater sensitivity to the female sex pheromone, which is typically released in minute quantities. Accordingly, females of species in which males have elaborate (i.e., pectinate, bipectinate, or quadripectinate) antennae should produce the smallest quantities of pheromone. Alternatively, antennal morphology may be associated with the chemical properties of the pheromone components, with elaborate antennae being associated with pheromones that diffuse more quickly (i.e., have lower molecular weights). Finally, antennal morphology may reflect population structure, with low population abundance selecting for higher sensitivity and hence more elaborate antennae. We conducted a phylogenetic comparative analysis to test these explanations using pheromone chemical data and trapping data for 152 moth species. Elaborate antennae are associated with larger body size (longer forewing length), which suggests a biological cost that smaller moth species cannot bear. Body size is also positively correlated with pheromone titre and negatively correlated with population abundance (estimated by male abundance). Removing the effects of body size revealed no association between the shape of antennae and either pheromone titre, male abundance, or mean molecular weight of the pheromone components. However, among species with elaborate antennae, longer antennae were typically associated with lower male abundances and pheromone compounds with lower molecular weight, suggesting that male distribution and a more rapidly diffusing female sex pheromone may influence the size but not the general shape of male antennae.     

Electrophysiological basis for the behavioural response of male and female Trichoplusia ni to synthetic female pheromone

Electroantennogram (EAG) studies demonstrated that antennae of both male and female Trichoplusia ni have: (1) receptor-neurones sensitive to female pheromone, (2) a low response threshold, (3) an identical mean-percentage EAG curve over a broad concentration range of pheromone, and (4) a similar absolute recovery interval from adaptation to pheromonal stimulation. These factors suggest that antennae of male and female T. ni have homologous and homogeneous acceptor sites for the female pheromone. Pheromonal stimulation of female antennae elicited EAGs with only 25% of the amplitude of those elicited in males.     

Ethometric analysis of pheromone receptor function in cockroaches

Cockroach olfactory receptors were studied with respect to their rôle in mediating behavioural responses to aggregation pheromone and female sex pheromone by employing experimental cockroaches in bioassays for aggregation and courting activity.Using organ ablation and techniques combining ablation with colchicine treatment of antennae, the antennae were determined to be sensory organs for perception of both pheromones.Since proteins are thought to be implicated in the molecular mechanism of olfactory perception, chemicals known to affect proteins were applied to the antennae. Bathing antennae with saline, distilled water, vincristine, vinblastine, or colchicine resulted in no reduction in responses to aggregation pheromone, whereas responses to sex pheromone were reduced. Vinca alkaloids caused the greatest depression in responses, and of these, vincristine treatment required the longest time period for complete recovery. Full sexual display by vinca alkaloid-treated males was not apparent until 8 days after treatment.The effect of formaldehyde vapour treatment, habituation, or both produced differential results. Formaldehyde treatment reduced responses to aggregation pheromone, but did not affect responses to sex pheromone. Habituation alone had no effect on aggregation, but initially reduced responses to sex pheromone. Combined treatments did not affect responses to aggregation pheromone, but resulted in a complete loss of responses to sex pheromone requiring a recovery period of 8 days.The main conclusion drawn from this work is that although responses to sex and aggregation pheromone are mediated by antennal sensillae, their mechanisms must differ drastically.     

Investigation of a sex pheromone for the oriental cockroach,Blatta orientalis

A sex pheromone for adult male oriental cockroaches Blatta orientalis was isolated from the faeces of adult virgin female oriental cockroaches. It elicited a sexual response at 10 pg and 1 ng with B. orientalis and Periplaneta americana adult males, respectively. The site of production appers to be the crop, oesophagus, and proventriculus. Electroantennogram responses of male antennae toward the isolated pheromone were greater than those of the female antennae. The adult male oriental cockroach also responded to the American cockroach sex pheromone. The isolated pheromone with a mol. wt of 232 may be similar to one of the components of the American cockroach sex pheromone.     

Antennal-specific pheromone-degrading aldehyde oxidases from the moths Antheraea polyphemus and Bombyx mori

Female moths produce blends of odorant chemicals, called pheromones. These precise chemical mixtures both attract males and elicit appropriate mating behaviors. To locate females, male moths must rapidly detect changes in environmental pheromone concentration. Therefore, the regulation of pheromone concentration within antennae, their chief organ of smell, is important. We describe antennal-specific aldehyde oxidases from the moths Antheraea polyphemus and Bombyx mori that are capable of catabolizing long chain, unsaturated aldehydes such as their aldehyde pheromones. These soluble enzymes are associated uniquely with male and female antennae and have molecular masses of 175 and 130 kDa, respectively. The A. polyphemus aldehyde oxidase has been localized to the olfactory sensilla which contain the pheromone receptor cell dendrites. These same sensilla contain a previously described sensilla-specific esterase that degrades the acetate ester component of A. polyphemus pheromone. We propose that sensillar pheromone-degrading enzymes modulate pheromone concentration in the receptor space and hence play a dynamic role in the pheromone-mediated reproductive behaviors of these animals.     

Grasshopper sexual pheromone: a component of the defensive secretion in Taeniopoda eques

ABSTRACT. Both male and female Taeniopoda eques (Burmeister) emit a defensive secretion from their thoracic spiracles. The secretion from mature females was found to act as a sex pheromone, eliciting mating behaviour in males. Females became chemically attractive to males about 16–18 days after eclosion. The antennae are shown to be the site of pheromone reception in males. Feeding upon natural host plants was not a prerequisite for pheromone production.     

Molecular elements of pheromone detection in the female moth,Heliothis virescens

Pheromones play pivotal roles in the reproductive behavior of moths, most prominently for the mate finding of male moths. Accordingly, the molecular basis for the detection of female‐released pheromones by male moths has been studied in great detail. In contrast, little is known about how females can detect pheromone components released by themselves or by conspecifics. In this study, we assessed the antenna of female Heliothis virescens for elements of pheromone detection. In accordance with previous findings that female antennae respond to the sex pheromone component (Z)‐9‐tetradecenal, we identified olfactory sensory neurons that express its cognate receptor, the receptor type HR6. All HR6 cells coexpressed the “sensory neuron membrane protein 1” (SNMP1) and were associated with supporting cells expressing the pheromone‐binding proteins PBP1 and PBP2. These features are reminiscent to male antennae and point to congruent mechanisms for pheromone detection in the two sexes. Further analysis of the SNMP1‐expressing cells revealed a higher number in females compared to males. Moreover, in females, the SNMP1 neurons were arranged in clusters, which project their dendrites into a common sensillum, whereas in males there were only solitary SNMP1‐neurons and only 1 per sensillum. Not all SNMP1 positive cells in female antennae expressed HR6 but instead the putative pheromone receptors HR11 and HR18, respectively. Neurons expressing 1 of the 3 receptor types were assigned to different sensilla. Together the data indicate that on the antenna of females, sensory neurons in a subset of sensilla trichodea are equipped with molecular elements, which render them responsive to pheromones.     

A receptor and binding protein interplay in the detection of a distinct pheromone component in the silkmoth Antheraea polyphemus

Male moths respond to conspecific female-released pheromones with remarkable sensitivity and specificity, due to highly specialized chemosensory neurons in their antennae. In Antheraea silkmoths, three types of sensory neurons have been described, each responsive to one of three pheromone components. Since also three different pheromone binding proteins (PBPs) have been identified, the antenna of Antheraea seems to provide a unique model system for detailed analyzes of the interplay between the various elements underlying pheromone reception. Efforts to identify pheromone receptors of Antheraea polyphemus have led to the identification of a candidate pheromone receptor (ApolOR1). This receptor was found predominantly expressed in male antennae, specifically in neurons located beneath pheromone-sensitive sensilla trichodea. The ApolOR1-expressing cells were found to be surrounded by supporting cells co-expressing all three ApolPBPs. The response spectrum of ApolOR1 was assessed by means of calcium imaging using HEK293-cells stably expressing the receptor. It was found that at nanomolar concentrations ApolOR1-cells responded to all three pheromones when the compounds were solubilized by DMSO and also when DMSO was substituted by one of the three PBPs. However, at picomolar concentrations, cells responded only in the presence of the subtype ApolPBP2 and the pheromone (E,Z)-6,11-hexadecadienal. These results are indicative of a specific interplay of a distinct pheromone component with an appropriate binding protein and its related receptor subtype, which may be considered as basis for the remarkable sensitivity and specificity of the pheromone detection system.     

赤松毛虫性信息素次要组分的鉴定——组分、电生理和田间效果

用带有极性和非极性毛细柱的气相色谱(GC)分析赤松毛虫Dendrolimus spectabilis性信息素腺体提取物,发现腺体中除含有已鉴定的性信息素(顺,反)-5,7-十二碳二烯醇(Z5,E7-12∶OH)外,还有微量的(顺,反)-5,7-十二碳二烯醛(Z5,E7-12∶Ald)和(顺,反)-5,7-十二碳二烯乙酸酯(Z5,E7-12∶Oac),三种成分以100∶5-6±5-4∶3-2±1-8的比例存在。使用气相色谱-质谱选择性离子检测法（GC-MS-SIM）分析赤松毛虫腺体提取物,发现腺体中确实含有微量的Z5,E7-12∶Oac和痕量的Z5,E7-12∶Opr。赤松毛虫腺体提取物的气相色谱和触角电位检测联用（GC-EAD）分析发现只有Z5,E7-12∶OH能激起EAD反应,然而使用较高剂量的标准化合物进行GC-EAD分析发现Z5,E7-12∶OH、Z5,E7 12∶Oac和(顺,反)-5,7-十二碳二烯丙酸酯(Z5,E7-12∶Opr)均能刺激起EAD反应,而Z5,E7-12∶Ald则不能。触角电位（EAG）剂量-反应关系研究表明,当剂量变化范围在0.01～1 μg时,雄虫触角对Z5,E7-12∶OH最敏感,对Z5,E7-12∶Oac和Z5,E7-12∶Opr次之。田间试验表明,由Z5,E7-12∶OH, Z5,E7-12∶Oac和Z5,E7-12∶Opr配制的三组分诱芯,其诱蛾量显著高于由Z5,E7-12∶OH组成的单组分或是它与其乙酸酯或丙酸酯组成的两组分诱芯,当Z5,E7-12∶OH,Z5,E7-12∶Oac和Z5,E7-12∶Opr的比例为100∶3∶25时,诱蛾效果最佳。在上述三组分混合物中加入一定量的Z5,E7-12∶Ald,则对诱蛾有明显的抑制作用。上述事实表明,Z5,E7-12∶Oac和Z5,E7-12∶Opr是赤松毛虫性信息素的两种次要组分,而Z5,E7-12∶Ald则是信息素的抑制剂。     

Electroantennogram responses to the sex pheromone and other odours in the American cockroach

Electroantennogram responses of adult American cockroaches were recorded for the sex pheromone and 30 kinds of monoterpenoids. Strong responses to the sex pheromone were obtained from the antennae of male adults, but not from females. The compounds possessing a hydroxyl or carbonyl group produced significant EAG responses in the antennae. Bornyl acetate, however, was an exception and gave strong responses in both male and female antennae. There was basically no difference between the antennal responsiveness to monoterpenoids tested in both sexes.     

旋花蛾性信息素成分的鉴定

提取和鉴定了杂草田旋花Convolvulus arvensis的天敌旋花蛾Tyta luctuosa的性信息素主要成分,并应用风洞实验对雄蛾进行了测试。结果表明,腺体提取物和雌蛾求偶时所释放的主要性信息素成分均为2种化合物：顺-9-十四碳烯醛（Z9-14∶Ald）和顺-11-十六碳烯醛（Z11-16∶Ald）。腺体提取物中2种化合物的总量在个体间差异很大（22～167 ng）,但二者的比率相对稳定（Z9-14∶Ald/Z11-16∶Ald=0.3±0.15）。雌蛾所释放的性信息素量及比率在个体间也存在差异。每只雌蛾求偶时平均每小时释放94 ng Z9-14∶Ald和45 ng Z11-16∶Ald,平均比率为2.2。风洞实验结果显示,48%的雄蛾可被合成的性信息素混合物（0.4 μg Z9-14∶Ald, 2 μg Z11-16∶Ald）引诱完成逆风飞行并最终触及刺激源,而2种对照组（以求偶期雌蛾或性信息素腺体提取物为刺激源）的引诱率则分别为62%和44%。     

Electrophysiological investigations of sex pheromone reception and release in Bruchidius atrolineatus

ABSTRACT. Male antennal sensitivity to female sex pheromone in Bruchidius atrolineatus was investigated electrophysiologically (EAG). The existence of receptors for this pheromone was shown in the antennae of males. (No such receptors exist in the antennae of females.) Young (age < 24h) males gave an EAG of amplitude 25–30% of the response of older males. Diapausing males several days old gave a much smaller response than active males of the same age.
EAGs were used to test the production/release of pheromone by groups of twenty females. Before they are 24 h old, active females do not produce/release the pheromone; older females release it at an almost constant rate. Sexually diapausing females do not produce and/or release the sex pheromone.
In sexually active females, mating inhibits pheromone release almost immediately. There is a correlation between reproductive status of the females (development of ovaries, oogenesis) and the production or release of the pheromone. A corresponding correlation also exists in the males whose antennae show a very low sensitivity when they are young or when they are in reproductive diapause.     

Olfactory attraction to aggregation pheromone is mediated by disti-flagellum of antennal segments in Riptortus pedestris

Riptortus pedestris (Hemiptera: Alydidae) is a serious pest of soybean and sweet persimmon and uses male produced aggregation pheromone, (E)-2-hexenyl (Z)-3-hexenoate, (E)-2-hexenyl (E)-2-hexenoate, and tetradecyl isobutyrate to facilitate food location and recognition by conspecifics. Using electroantennogram (EAG) and greenhouse bioassay, we determined which antennal segment is involved in the detection of their aggregation pheromone. In the first EAG test using individual antennal segments, significant EAG responses to 1:1:1 mixture of the aggregation pheromone were observed only from the disti-flagellum segments of both male and female antennae at both pheromone doses tested (1 µg and 100 µg). In the following EAG tests using gradually removed antennal segment(s), EAG response was still maintained when the distal half of a disti-flagellum was surgically removed, while EAG response was lost when whole segment of disti-flagellum or other whole segments were gradually removed from intact antenna of both sexes. In greenhouse experiment, removing one or both segment(s) of disti-flagellum from male or female antennae resulted in significant reduction in their attraction to the aggregation pheromone. Together, these findings support that the disti-flagellum of R. pedestris houses olfactory neurons associated with attraction to their aggregation pheromone.