Insect Sensory Organs Research Articles

Drosophila HCN mediates gustatory homeostasis by preserving sensillar transepithelial potential in sweet environments.

Establishing transepithelial ion disparities is crucial for sensory functions in animals. In insect sensory organs called sensilla, a transepithelial potential, known as the sensillum potential (SP), arises through active ion transport across accessory cells, sensitizing receptor neurons such as mechanoreceptors and chemoreceptors. Because multiple receptor neurons are often co-housed in a sensillum and share SP, niche-prevalent overstimulation of single sensory neurons can compromise neighboring receptors by depleting SP. However, how such potential depletion is prevented to maintain sensory homeostasis remains unknown. Here, we find that the Ih-encoded hyperpolarization-activated cyclic nucleotide-gated (HCN) channel bolsters the activity of bitter-sensing gustatory receptor neurons (bGRNs), albeit acting in sweet-sensing GRNs (sGRNs). For this task, HCN maintains SP despite prolonged sGRN stimulation induced by the diet mimicking their sweet feeding niche, such as overripe fruit. We present evidence that Ih-dependent demarcation of sGRN excitability is implemented to throttle SP consumption, which may have facilitated adaptation to a sweetness-dominated environment. Thus, HCN expressed in sGRNs serves as a key component of a simple yet versatile peripheral coding that regulates bitterness for optimal food intake in two contrasting ways: sweet-resilient preservation of bitter aversion and the previously reported sweet-dependent suppression of bitter taste.

Involvement of Chemosensory Protein CrufCSP3 in Perception of the Host Location in a Parasitic Wasp Cotesia ruficrus.

Chemosensory proteins (CSPs) constitute a class of olfactory proteins localized in insect sensory organs that serve a crucial function in decoding external chemical stimuli. This study aims to elucidate the involvement of CrufCSP3 in olfactory perception within the context of Cotesia ruficrus, an indigenous endoparasitoid targeting the invasive pest Spodoptera frugiperda. Through fluorescence-competitive binding assays and site-directed mutagenesis, we pinpointed four amino acids as pivotal residues involved in the interaction between CrufCSP3 and five host-related compounds. Subsequent RNA interference experiments targeting CrufCSP3 unveiled a reduced sensitivity to specific host-related compounds and a decline in the parasitism rate of the FAW larvae. These findings unequivocally indicate the essential role of CrufCSP3 in the chemoreception process of C. ruficrus. Consequently, our study not only sheds light on the functional importance of CSPs in parasitic wasp behavior but also contributes to the development of eco-friendly and efficacious wasp behavior modifiers for effectively mitigating pest population surges.

Reconstructing the ecology of a Cretaceous cockroach: destructive and high-resolution imaging of its micro sensory organs.

Animals highly depend on their sensory organs to detect information about their surrounding environment. Among animal sensory organs, those of insects have a notable ability to detect information despite their small size, which might be, therefore, one of the reasons for the evolutionary success of insects. However, insect sensory organs are seldom fossilized in sediments due to their small size and fragility. A potential solution for this problem is the study of exceptionally well-preserved fossil material from amber. Unfortunately, the resolution of existing non-destructive analysis is insufficient to observe details of these micro sensory organs even with amber preservation. Here, we focus on the analysis of the micro sensory organs of an extinct male cockroach (Huablattula hui Qiu et al., 2019) in Cretaceous amber by combining destructive and non-destructive methods. Compared to extant species inhabiting dark environments, H. hui has relatively large compound eyes, and all the antennal sensilla for detecting multimodal information observed here are fewer or smaller. The characteristics of these sensory organs support the diurnality of the bright habitats of H. hui in contrast to many extant cockroaches. Like extant male mantises, grooved basiconic type sensilla exist abundantly on the antenna of the fossilized specimen. The abundance of grooved basiconic sensilla in mantid males results from using sex pheromones, and therefore, H. hui may have likewise used mantis-like intersexual communication. These lines of evidence suggest that the ecology and behavior of Cretaceous cockroaches were more diverse than those of related extant species.

Current and potential biotechnological applications of odorant-binding proteins

Odorant-binding proteins (OBPs) are small soluble proteins whose biological function is believed to be facilitating olfaction by assisting the transport of volatile chemicals in both vertebrate and insect sensory organs, where they are secreted. Their capability to interact with a broad range of hydrophobic compounds combined with interesting features such as being small, stable, and easy to produce and modify, makes them suitable targets for applied research in various industrial segments, including textile, cosmetic, pesticide, and pharmaceutical, as well as for military, environmental, health, and security field applications. In addition to reviewing already established biotechnological applications of OBPs, this paper also discusses their potential use in prospecting of new technologies. The development of new products for insect population management is currently the most prevailing use for OBPs, followed by biosensor technology, an area that has recently seen a significant increase in studies evaluating their incorporation into sensing devices. Finally, less typical approaches include applications in anchorage systems and analytical tools. KEY POINTS: • Odorant-binding proteins (OBPs) present desired characteristics for applied research. • OBPs are mainly used for developing new products for insect population control. • Incorporation of OBPs into chemosensory devices is a growing area of study. • Less conventional uses for OBPs include anchorage systems and analytical purposes. Graphical Abstract.

Convergent evolution of ramified antennae in insect lineages from the Early Cretaceous of Northeastern China.

Antennae are important, insect sensory organs that are used principally for communication with other insects and the detection of environmental cues. Some insects independently evolved ramified (branched) antennae, which house several types of sensilla for motion detection, sensing olfactory and chemical cues, and determining humidity and temperature levels. Though ramified antennae are common in living insects, occasionally they are present in the Mesozoic fossil record. Here, we present the first caddisflies with ramified antennae, the earliest known fossil sawfly, and a scorpionfly also with ramified antennae from the mid-Lower Cretaceous Yixian Formation of Northeastern China, dated at 125 million years ago (Ma). These three insect taxa with ramified antennae consist of three unrelated lineages and provide evidence for broad structural convergence that historically has been best demonstrated by features such as convergent mouthparts. In addition, ramified antennae in these Mid-Mesozoic lineages likely do not constitute a key innovation, as they are not associated with significantly increased diversification compared with closely related lineages lacking this trait, and nor are they ecologically isolated from numerous, co-occurring insect species with unmodified antennae.

Developmental expression patterns of four chemosensory protein genes from the Eastern spruce budworm, Chroistoneura fumiferana

Chemosensory proteins (CSPs) are associated with insect sensory organs, including the sensillum lymph in some cases. However, they are also commonly expressed in nonsensory tissues that lack gustatory and olfactory neurones. We characterized the sex and development specific expression patterns of four CSP genes from the Eastern spruce budworm (ESB) using Northern blots. CfumAY426540.2 was detected at high levels in adult moths. Conversely, CfumAY426538 was expressed in all stages except adult moths, and was most abundant during late stages of the 6th instar. CfumAY701858 was expressed in all stages, while CfumAY426539 was detected less frequently, at specific developmental stages such as the 5th to 6th instar moult. During a natural moult, and a premature moult induced by the ecdysteroid agonist tebufenozide, CfumAY701858 and CfumAY426539 were up-regulated, while CfumAY426538 appeared to be down-regulated. Our results suggest that some members of the CSP gene family from the ESB may be involved in development, including moulting.

Developmental evolutionary biology of the vertebrate ear

This brief overview shows that a start has been made to molecularly dissect vertebrate ear development and its evolutionary conservation to the development of the insect hearing organ. However, neither the patterning process of the ear nor the patterning process of insect sensory organs is sufficiently known at the moment to provide more than a first glimpse. Moreover, hardly anything is known about otocyst development of the cephalopod molluscs, another triploblast lineage that evolved complex 'ears'. We hope that the apparent conserved functional and cellular components present in the ciliated sensory neurons/hair cells will also be found in the genes required for vertebrate ear and insect sensory organ morphogenesis (Fig. 3). Likewise, we expect that homologous pre-patterning genes will soon be identified for the non-sensory cell development, which is more than a blocking of neuronal development through the Delta/Notch signaling system. Generation of the apparently unique ear could thus represent a multiplication of non-sensory cells by asymmetric and symmetric divisions as well as modification of existing patterning process by implementing novel developmental modules. In the final analysis, the vertebrate ear may come about by increasing the level of gene interactions in an already existing and highly conserved interactive cascade of bHLH genes. Since this was apparently achieved in all three lineages of triploblasts independently (Fig. 3), we now need to understand how much of the morphogenetic cascades are equally conserved across phyla to generate complex ears. The existing mutations in humans and mice may be able to point the direction of future research to understand the development of specific cell types and morphologies in the formation of complex arthropod, cephalopod, and vertebrate 'ears'.

Introduction to microscopy in Mexico

Microscopy Research and TechniqueVolume 40, Issue 1 p. 1-1 Topical Paper Introduction to microscopy in Mexico William Krakow, William KrakowSearch for more papers by this authorMiguel José Yacamán, Miguel José YacamánSearch for more papers by this author William Krakow, William KrakowSearch for more papers by this authorMiguel José Yacamán, Miguel José YacamánSearch for more papers by this author First published: 07 December 1998 https://doi.org/10.1002/(SICI)1097-0029(19980101)40:1<1::AID-JEMT1>3.0.CO;2-0AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume40, Issue1Special Issue: Insect Sensory Organs as a Model System in Sensory Physiology and Developmental Biology1 January 1998Pages 1-1 RelatedInformation

Introduction to microscopy in Mexico

Microscopy Research and TechniqueVolume 40, Issue 1 p. 1-1 Topical Paper Introduction to microscopy in Mexico William Krakow, William KrakowSearch for more papers by this authorMiguel José Yacamán, Miguel José YacamánSearch for more papers by this author William Krakow, William KrakowSearch for more papers by this authorMiguel José Yacamán, Miguel José YacamánSearch for more papers by this author First published: 07 December 1998 https://doi.org/10.1002/(SICI)1097-0029(19980101)40:1<1::AID-JEMT1>3.0.CO;2-0AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume40, Issue1Special Issue: Insect Sensory Organs as a Model System in Sensory Physiology and Developmental Biology1 January 1998Pages 1-1 RelatedInformation

Ontogentetic changes in the cuticular scales of a jumping spider

Microscopy Research and TechniqueVolume 40, Issue 1 p. 79-80 Short Communication Ontogentetic changes in the cuticular scales of a jumping spider V. R. Townsend Jr., Corresponding Author V. R. Townsend Jr. Department of Biology, University of Southwestern Louisiana, Lafayette, Louisiana 70504-2451Department of Biology, University of Southwestern Louisiana, Lafayette, Louisiana 70504-2451Search for more papers by this authorB. E. Felgenhauer, B. E. Felgenhauer Department of Biology, University of Southwestern Louisiana, Lafayette, Louisiana 70504-2451Search for more papers by this author V. R. Townsend Jr., Corresponding Author V. R. Townsend Jr. Department of Biology, University of Southwestern Louisiana, Lafayette, Louisiana 70504-2451Department of Biology, University of Southwestern Louisiana, Lafayette, Louisiana 70504-2451Search for more papers by this authorB. E. Felgenhauer, B. E. Felgenhauer Department of Biology, University of Southwestern Louisiana, Lafayette, Louisiana 70504-2451Search for more papers by this author First published: 07 December 1998 https://doi.org/10.1002/(SICI)1097-0029(19980101)40:1<79::AID-JEMT11>3.0.CO;2-QCitations: 4AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume40, Issue1Special Issue: Insect Sensory Organs as a Model System in Sensory Physiology and Developmental Biology1 January 1998Pages 79-80 RelatedInformation

Introduction to insect sensory organs as a model system in sensory physiology and developmental biology.

Introduction to insect sensory organs as a model system in sensory physiology and developmental biology.

The tympanal hearing organ of the parasitoid fly Ormia ochracea (Diptera, Tachinidae, Ormiini)

Tympanate hearing has evolved in at least 6 different orders of insects, but had not been reported until recently in the Diptera. This study presents a newly discovered tympanal hearing organ, in the parasitoid tachinid fly, Ormia ochracea. The hearing organ is described in terms of external and internal morphology, cellular organization of the sensory organ and preliminary neuroanatomy of the primary auditory afferents. The ear is located on the frontal face of the prothorax, directly behind the head capsule. Conspicuously visible are a pair of thin cuticular membranes specialized for audition, the prosternal tympanal membranes. Directly attached to these membranes, within the enlarged prosternal chamber, are a pair of auditory sensory organs, the bulbae acusticae. These sensory organs are unique among all auditory organs known so far because both are contained within an unpartitioned acoustic chamber. The prosternal chamber is connected to the outside by a pair of tracheae. The cellular anatomy of the fly's scolopophorous organ was investigated by light and electron microscopy. The bulba acustica is a typical chordotonal organ and it contains approximately 70 receptor cells. It is similar to other insect sensory organs associated with tympanal ears. The similarity of the cellular organization and tympanal morphology of the ormiine ear to the ears of other tympanate insects suggests that there are potent constraints in the design features of tympanal hearing organs, which must function to detect high frequency auditory signals over long distances. Each sensory organ is innervated by a branch of the frontal nerve of the fused thoracic ganglia. The primary auditory afferents project to each of the pro-, meso-, and metathoracic neuropils. The fly's hearing organ is sexually dimorphic, whereby the tympanal membranes are larger in females and the spiracles larger in males. The dimorphism presumably reflects differences in the acoustic behavior in the two sexes.

Fine structure of the tibiotarsal and pretarsal sensory organs in Monobella grassei banyulensis Deharveng (Collembola : Neanuridae)

The fine structure of the tibiotarsal and pretarsal sensory organs of Monobella grassei banyulensis Deharveng (Collembola : Neanuridae) has been examined by electron microscopy. Three types of sensory organs have been observed. (1) the most numerous setae of the tibiotarsus are classic mechanosensitive setae with one bipolar sensory cell, whose distal outer segment ends in a tubular body. (2) Two small setae are arranged on each side of the basal part of the claw; they show 3 sensory cells, 2 of which are mechanosensitive cells of the scolopidial type; the outer segments of the 2 mechanosensitive cells end at the base of the sensory hair. The dendrite of the 3rd sensory cell extends into the hair shaft. (3) Two similar chordotonal sensilla link the tibiotarsus and the pretarsus; each sensillum is composed of 2 bipolar sensory cells enveloped in sheath cells. The first type of sensory organ shows the characteristics of insect exteroceptive mechanosensitive hairs. The mechanosensitive cells of the 2nd and 3rd tibiotarsus sensory organs are probably proprioceptive and control the movements of the pretarsus in relation to the tibiotarsus. Two features are noteworthy: (1) the association of the scolopidial cells with a chemosensitive one has never been observed in other insect sensory organs, except in the Collembola; and (2) there is an important morphological diversity in the ciliary roots of the various scolopidial cells, which are in other respects very similar.

Ultrastructure of sensilla on the distal antennal segment of adult Oncopeltus fasciatus (Dallas) (Hemiftera : Lygaeidae)

The sensilla on the distal antennal segment of adult Oncopeltus fasciatus were studied with the scanning and transmission electron microscopes. The result has been an elucidation of the ultrastructure of 7 morphologically distinct sensory organs. These include smooth, grooved, and two-chambered pegs, symmetrical and asymmetrical hairs, a pit-peg, and a tactile bristle. Pore tubules are described in the tactile bristle and the uninnervated channel of the two-chambered peg. Dendritic protrusions which extend into the fluid channels of the symmetrical hair have also been identified. A more complete knowledge of insect sensory organs has resulted from the morphological considerations presented in this paper. Heretofore pore tubules have only been described in olfactory sensilla, and few olfactory organs have been shown to possess pores containing dendrites.

A light and electron microscopic study of sensory organs and associated structures in the foreleg tibia of the cricket, Gryllus assimilis.

AbstractEarly descriptions of insect sensory organs included three presumed mechanotransducers in the tibia of Orthoptera, namely the subgenual organ, the intermediate organ, and the tympanal organ. This investigation re‐evaluates the light microscopic appearances of these organs in the foreleg tibia of the cricket, Gryllus assimilis, initially described by Herbig in 1902.The study also examines the fine structure of the subgenual and intermediate organs and provides the first fine structure analysis of these structures.The subgenual and intermediate organs are typical scolopophorus organs suspended perpendicular to each other within the dorsal hemolymph canal. Each is innervated by dendrites from the anterior ganglion. Neither the subgenual, intermediate, nor tympanal organ is structurally related to the larger posterior tympanic membrane.The study shows that the tibial tympanal organ in the cricket is not a scolopophorus organ, but consists of highly modified epithelium, associated with the anterior tympanic membrane, and receiving innervation from the anterior ganglion.

An electron microscopic study of the tympanal organ and associated structures in the foreleg tibia of the cricket, Gryllus assimilis.

AbstractEarly descriptions of insect sensory organs included three presumed mechanotransducers in the tibia of Orthoptera, namely the subgenual organ, the intermediate organ, and the tympanal organ. The following study examines the fine structure of the tympanal organ in the foreleg tibia of the cricket, Gryllus assimilis. This investigation provides the first fine structure analysis of this structure and shows that the tibial tympanal organ is not a scolopophorus organ. It consists of highly modified epithelium, associated with the anterior tympanic membrane, and receives innervation from the anterior ganglion.