Metamorphic development of the olfactory system in the red flour beetle (Tribolium castaneum, HERBST)

Background: Insects depend on their olfactory sense as a vital system. Olfactory cues are processed by a rather complex system and translated into various types of behavior. In holometabolous insects like the red flour beetle Tribolium castaneum, the nervous system typically undergoes considerable remodeling during metamorphosis. This process includes the integration of new neurons, as well as remodeling and elimination of larval neurons. Results: We find that the sensory neurons of the larval antennae are reused in the adult antennae. Further, the larval antennal lobe gets transformed into its adult version. The beetle’s larval antennal lobe is already glomerularly structured, but its glomeruli dissolve in the last larval stage. However, the axons of the olfactory sensory neurons remain within the antennal lobe volume. The glomeruli of the adult antennal lobe then form from mid-metamorphosis independently of the presence of a functional OR/Orco complex but mature dependent on the latter during a postmetamorphic phase. Conclusions: We provide insights into the metamorphic development of the red flour beetle’s olfactory system and compared it to data on Drosophila melanogaster, Manduca sexta, and Apis mellifera. The comparison revealed that some aspects, such as the formation of the antennal lobe’s adult glomeruli at mid-metamorphosis, are common, while others like the development of sensory appendages or the role of Orco seemingly differ

Insecticidal genes of Yersinia spp.: taxonomical distribution, contribution to toxicity towards Manduca sexta and Galleria mellonella, and evolution

<p>Abstract</p> <p>Background</p> <p>Toxin complex (Tc) proteins termed TcaABC, TcdAB, and TccABC with insecticidal activity are present in a variety of bacteria including the yersiniae.</p> <p>Results</p> <p>The <it>tc </it>gene sequences of thirteen <it>Yersinia </it>strains were compared, revealing a high degree of gene order conservation, but also remarkable differences with respect to pseudogenes, sequence variability and gene duplications. Outside the <it>tc </it>pathogenicity island (<it>tc</it>-PAI^<it>Ye</it>) of <it>Y. enterocolitica </it>strain W22703, a pseudogene (<it>tccC2'</it>/<it>3'</it>) encoding proteins with homology to TccC and similarity to tyrosine phosphatases at its C-terminus was identified. PCR analysis revealed the presence of the <it>tc</it>-PAI^{<it>Ye </it>}and of <it>tccC2'</it>/<it>3'</it>-homologues in all biotype 2–5 strains tested, and their absence in most representatives of biotypes 1A and 1B. Phylogenetic analysis of 39 TccC sequences indicates the presence of the <it>tc</it>-PAI^{<it>Ye </it>}in an ancestor of <it>Yersinia</it>. Oral uptake experiments with <it>Manduca sexta </it>revealed a higher larvae lethality of <it>Yersinia </it>strains harbouring the <it>tc</it>-PAI^{<it>Ye </it>}in comparison to strains lacking this island. Following subcutaneous infection of <it>Galleria mellonella </it>larvae with five non-human pathogenic <it>Yersinia </it>spp. and four <it>Y. enterocolitica </it>strains, we observed a remarkable variability of their insecticidal activity ranging from 20% (<it>Y. kristensenii</it>) to 90% (<it>Y. enterocolitica </it>strain 2594) dead larvae after five days. Strain W22703 and its <it>tcaA </it>deletion mutant did not exhibit a significantly different toxicity towards <it>G. mellonella</it>. These data confirm a role of TcaA upon oral uptake only, and suggest the presence of further insecticidal determinants in <it>Yersinia </it>strains formerly unknown to kill insects.</p> <p>Conclusion</p> <p>This study investigated the <it>tc </it>gene distribution among yersiniae and the phylogenetic relationship between TccC proteins, thus contributing novel aspects to the current discussion about the evolution of insecticidal toxins in the genus <it>Yersinia</it>. The toxic potential of several <it>Yersinia </it>spp. towards <it>M. sexta </it>and <it>G. mellonella </it>demonstrated here for the first time points to insects as a natural reservoir for yersiniae.</p

HeFDI – Die landesweite Initiative zum Aufbau von Forschungsdateninfrastrukturen in Hessen

Digitale Forschungsdaten als Ressource sichern, aufbewahren und anderen zur Verfügung stellen: alle Phasen des Forschungsdatenzyklus adressiert das Projekt „Hessische Forschungsdateninfrastrukturen“ (HeFDI), in dem elf hessische Hochschulen und die HeBIS-Verbundzentrale unter Federführung der Philipps-Universität Marburg zusammenarbeiten. Das Hessische Ministerium für Wissenschaft und Kunst fördert dieses Vorhaben mit 3,4 Millionen Euro von 2016 bis 2020. Seit Oktober 2016 arbeitet ein Team von mehr als 20 Personen an den hessischen Hochschulen am Forschungsdatenmanagement, das heißt beispielsweise an Policies, Repositorien, Schulungen und unterstützenden Tools für das aktive Datenmanagement. Das Team berät zudem die Forschenden bedarfsorientiert zu ihren Datenmanagementstrategien entlang des gesamten Datenlebenszyklus und insbesondere bei der Einwerbung und Durchführung von Drittmittelprojekten. Ziel dieser Arbeit ist der Aufbau einer Forschungsdateninfrastruktur. Dazu werden die notwendigen organisatorischen Prozesse und technischen Entwicklungen zur Verankerung des Forschungsdatenmanagements – abhängig von den Anforderungen der beteiligten Hochschulen – angestoßen, koordiniert und etabliert. Das Projekt HeFDI nimmt dabei die strategisch bedeutsame Aufgabe der Sicherung und Bereitstellung von Forschungsdaten in einer koordinierten Gesamtstrategie an. Es vertritt einen Middle-out-Ansatz, bei dem Entscheidungs- und Arbeitsebenen systematisch miteinander verzahnt werden. Damit besitzt HeFDI Modellcharakter für institutionelle Kooperation und nachhaltige Governance-Strukturen im Bereich des Forschungsdatenmanagements; die in HeFDI erarbeiteten Lösungen stehen über Hessen hinaus exemplarisch für Synergie, Effizienz, Abstimmung und Arbeitsteilung. In a joint project called Hessian Research Data Infrastructures (HeFDI), eleven universities in the State of Hesse face the challenge to save digital research data as a resource, as well as to store and prepare digital research data for publication and re-use. HeFDI is funded by the Hessian Ministry for Science and the Arts with 3.4 million Euros, running from 2016 to 2020. Since October 2016, more than 20 experts are working together as a team to build up an infrastructure for research data management, e. g. by implementing policies, developing repositories, offering workshops and trainings and helping with tools for active data management. They also lend advice and support to researchers concerning data management strategies, especially with respect to third party funding at the early stage of project proposals. Thus, the HeFDI-project’s objective consists in establishing a research data infrastructure which encompasses necessary organizational processes as well as technical developments and implementations. While there is strong cooperation, those processes and implementations are always adapted to local and institutional needs and the requirements of each university. Overall, HeFDI aims at tackling the crucial task to save and publish digital data by developing a coordinated common strategy for all project partners. At the same time, HeFDI represents a middle out-strategy: decision making and action levels are closely intertwined, and cooperation is based on a reliable and functional governance system. Therefore, HeFDI serves as a role model for institutional cooperation and sustainable governance structures in research data management. Solutions developed within HeFDI reach out far beyond the federal state of Hesse as they can be taken as an example for possible synergies, efficiency, proper reconcilement and the distribution of tasks

3D-Reconstructions and Virtual 4D-Visualization to Study Metamorphic Brain Development in the Sphinx Moth Manduca Sexta

During metamorphosis, the transition from the larva to the adult, the insect brain undergoes considerable remodeling: new neurons are integrated while larval neurons are remodeled or eliminated. One well acknowledged model to study metamorphic brain development is the sphinx moth Manduca sexta. To further understand mechanisms involved in the metamorphic transition of the brain we generated a 3D standard brain based on selected brain areas of adult females and 3D reconstructed the same areas during defined stages of pupal development. Selected brain areas include for example mushroom bodies, central complex, antennal- and optic lobes. With this approach we eventually want to quantify developmental changes in neuropilar architecture, but also quantify changes in the neuronal complement and monitor the development of selected neuronal populations. Furthermore, we used a modeling software (Cinema 4D) to create a virtual 4D brain, morphing through its developmental stages. Thus the didactical advantages of 3D visualization are expanded to better comprehend complex processes of neuropil formation and remodeling during development. To obtain datasets of the M. sexta brain areas, we stained whole brains with an antiserum against the synaptic vesicle protein synapsin. Such labeled brains were then scanned with a confocal laser scanning microscope and selected neuropils were reconstructed with the 3D software AMIRA 4.1

Feeding-induced changes in allatostatin-A and short neuropeptide F in the antennal lobes affect odor-mediated host seeking in the yellow fever mosquito, <i>Aedes aegypti</i>

Aedes aegypti is a model species in which the endogenous regulation of odor-mediated host seeking behavior has received some attention. Sugar feeding and host seeking in female A. aegypti are transiently inhibited following a blood meal. This inhibition is partially mediated by short neuropeptide F (sNPF). The paired antennal lobes (ALs), as the first processing centers for olfactory information, has been shown to play a significant role in the neuropeptidergic regulation of odor-mediated behaviors in insects. The expression of sNPF, along with other peptides in the ALs of A. aegypti, indicate parallel neuromodulatory systems that may affect olfactory processing. To identify neuropeptides involved in regulating the odor-mediated host seeking behavior in A. aegypti, we use a semi-quantitative neuropeptidomic analysis of single ALs to analyze changes in the levels of five individual neuropeptides in response to different feeding regimes. Our results show that the level of sNPF-2, allatostatin-A-5 (AstA-5) and neuropeptide-like precursor-1-5 (NPLP-1-5), but not of tachykinin-related-peptides and SIFamide (SIFa), in the AL of female mosquitoes, changes 24 h and 48 h post-blood meal, and are dependent on prior access to sugar. To assess the role of these neuropeptides in modulating host seeking behavior, when systemically injected individually, sNPF-2 and AstA-5 significantly reduced host seeking behavior. However, only the injection of the binary mixture of the two neuropeptides lead to a host seeking inhibition similar to that observed in blood fed females. We conclude that modulation of the odor mediated host seeking behavior of A. aegypti is likely regulated by a dual neuropeptidergic pathway acting in concert in the ALs

Neuropeptides in the Antennal Lobe of the Yellow Fever Mosquito, Aedes aegypti.

For many insects, including mosquitoes, olfaction is the dominant modality regulating their behavioral repertoire. Many neurochemicals modulate olfactory information in the central nervous system, including the primary olfactory center of insects, the antennal lobe. The most diverse and versatile neurochemicals in the insect nervous system are found in the neuropeptides. In the present study, we analyzed neuropeptides in the antennal lobe of the yellow fever mosquito, Aedes aegypti, a major vector of arboviral diseases. Direct tissue profiling of the antennal lobe by matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry indicated the presence of 28 mature products from 10 different neuropeptide genes. In addition, immunocytochemical techniques were used to describe the cellular location of the products of up to seven of these genes within the antennal lobe. Allatostatin A, allatotropin, SIFamide, FMRFamide-related peptides, short neuropeptide F, myoinhibitory peptide, and tachykinin-related peptides were found to be expressed in local interneurons and extrinsic neurons of the antennal lobe. Building on these results, we discuss the possible role of neuropeptide signaling in the antennal lobe of Ae. aegypti. J. Comp. Neurol. 522:592-608, 2014. (c) 2013 Wiley Periodicals, Inc

3D Standard Brain of the Red Flour Beetle Tribolium Castaneum: A Tool to Study Metamorphic Development and Adult Plasticity

The red flour beetle Tribolium castaneum is emerging as a further standard insect model beside Drosophila. Its genome is fully sequenced and it is susceptible for genetic manipulations including RNA-interference. We use this beetle to study adult brain development and plasticity primarily with respect to the olfactory system. In the current study, we provide 3D standard brain atlases of freshly eclosed adult female and male beetles (A0). The atlases include eight paired and three unpaired neuropils including antennal lobes (ALs), optic lobe neuropils, mushroom body calyces and pedunculi, and central complex. For each of the two standard brains, we averaged brain areas of 20 individual brains. Additionally, we characterized eight selected olfactory glomeruli from 10 A0 female and male beetles respectively, which we could unequivocally recognize from individual to individual owing to their size and typical position in the ALs. In summary, comparison of the averaged neuropil volumes revealed no sexual dimorphism in any of the reconstructed neuropils in A0 Tribolium brains. Both, the female and male 3D standard brain are also used for interspecies comparisons, and, importantly, will serve as future volumetric references after genetical manipulation especially regarding metamorphic development and adult plasticity

Morphological and Transcriptomic Analysis of a Beetle Chemosensory System Reveals a Gnathal Olfactory Center

OR gene tissue expression and their chromosomal localization. a Venn diagram showing the number of ORs expressed (RPKM ≥ 0.5) in the different body parts: antennae, legs, mouthparts (as piece of the head capsule anterior of the antennae), heads (the whole head capsule including mouthparts but excluding the antennae), and bodies (excluding head and legs). b Venn diagram comparing our results (yellow, green) with data from Engsontia et al. [115] (blue, red). Number of expressed ORs, defined by RPKM ≥ 0.5 (yellow), by RT-PCR (blue), not expressed RPKM < 0.5 (green), or with no RT-PCR amplicon (red). ORs of the brown group were not previously tested by Engsontia et al. c Chromosomal localization of T. castaneum ORs. Based on the Georgia GA-2 strain genome assembly 3.0 [81], only chromosomal linkage groups containing an IR or SNMP are depicted. Gene clusters are indicated by a number referring to the chromosome and a letter conveys the relative position on the chromosome. The number of genes within this cluster is indicated in the square brackets. (PDF 277 kb