Endocrine scaffolds and peptide networks: How is the molt cycle and ecdysis programme controlled in crustaceans?

Lead Research Organisation: Aberystwyth University
Department Name: IBERS

Abstract

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Technical Summary

In contrast to insects, our understanding of the neuropeptide networks involved in crustacean ecdysis is rudimentary. However, our recent research has identified novel potential control mechanisms that promise to revolutionise our understanding of crustacean molt control. The overarching objective of this work is to develop a much more detailed model of the neuroendocrine control of crustacean molting, by functional analysis of neuroendocrine scaffolds and networks, comparing with insects. Three interrelated themes will be investigated: 1) The control of ecdysteroid synthesis, and entry into premolt, 2) The initiation of the "ecdysis cassette" via a proposed ecdysis-triggering hormone/eclosion hormone (ETH/EH) signalling network. 3) The interaction of these peptides in regulating sequential release of the hormones critical in integrating successful ecdysis in or crab model, Carcinus maenas.
PacBio Iso-Seq transcriptomes will be produced (specific-YO and epidermis and whole crab), and analysed to identify full-length transcripts for receptors (MIH, CHH, ETH and EH) and peptides (ETH, EH). The receptors will be functionally deorphaned by transient expression in cell-based assays (GPCRs- aequorin Ca2+ reporting, mGCs, cGMP measurement). The cells (neurones and peripheral non-neuronal ETH producing cells) expressing the receptor and peptide transcripts will be identified using RNAScope, quantitative PCR (dd-PCR) and IHC by developing antisera for ETH and EH. Functional analysis of neuropeptide networks with be done by using RNAi, peptide injections and measurement of perturbations of neuropeptide cascades in the ecdysis cassette and ultrasensitive TR-FIA for ETH, EH and CRZ. CRZ abrogation of MIH and CHH signalling in the YO will be investigated using ecdysteroid and cGMP RIA. By using these multifaceted approaches, we aim to answer a big question in arthropod endocrinology-How does neuropeptide signalling integrate molting processes in crustaceans?

Planned Impact

The research questions posed in this proposal are firstly of interest to academic groupings, in Biological Sciences and particularly to invertebrate endocrinologists and neuroscientists. We are attempting to answer outstanding, fundamental questions in arthropod neuroendocrinology and physiology, by taking a comparative approach; the work is unifying, in that we are using the considerable body of knowledge that is available for insect model systems, to investigate these in a well-established crustacean non-model. It is now becoming clear that arthropods possess a common "toolbox" of neuropeptides and receptors, as befits their shared ancestry. Intuitively, for the most pervading phenomena in the life history of arthropods- growth and ecdysis, we should expect that common neuroendocrine control mechanisms are ubiquitous. Counterintuitively, some are very different (for example in the control of molting hormone synthesis in the two subphyla), yet others are instantly recognisable (the hormonal control of exuviation- the "ecdysis cassette"). By identifying core neuropeptide signalling pathways involved in crustacean ecdysis, we are trying to answer a big question that impacts upon every aspect of arthropod physiology and development. Thus, we have every confidence that the results from our studies will, in the near future, appear in biology textbooks. Publishing primary papers and reviews in high impact journals, presenting our work at national and international meetings, will disseminate our findings. We anticipate that the proposed work will lead to up to eight high quality, primary research papers. Crustaceans and insects are immensely charismatic animals. Crustacean ecdysis and insect metamorphosis and eclosion are fascinating behaviours that capture interest, as evidenced by our BBC coverage of crab ecdysis, (The One Show). Thus, we plan to maximise public exposure to our research (see Pathways to Impact statement). Both DCW and SGW are passionate about public engagement and have had extensive media coverage. To summarise; we will engage public interest by taking advantage of, and creating available opportunities. Relevance and impact to industry. The proposed work has a direct impact on crustacean aquaculture. Firstly, the current shrimp (penaeid) industry, presently worth 39 billion USD pa, is being transformed by development of environmentally sustainable indoor recirculating aquaculture systems (RAS) as opposed to extensive culture, which has many negative environmental and disease issues. Furthermore, the by-product of molting- the old exuviae are used to extract chitosan for pharmaceutical processes- a market worth 1.5 billion USD, which is set to grow to over 17 billion USD in the next 5 years. At the moment, we know very little regarding the hormonal control of molting in penaeid shrimp, yet we have a huge body of research in crabs, which is translational and can be directly applied to shrimp aquaculture, and quite fundamental issues which dramatically decrease productivity, such as molt-related mortality. Further potential impacts relate firstly to animal welfare issues, particularly during transportation of live crustaceans, the responses due to stress, indicated by our research implicates a common set of neuropeptides that are involved in the control of molting, and the stress response, and are probably involved in the considerable mortality of crustaceans during transport to market. Finally, a future, but possibly critical impact relates to issues involving the use of stable pseudopeptide mimetics in insect pest control. There is a renewed interest in developing these to target groups or single species of insects, and those associated with disruption of growth and ecdysis are ones that are currently demanding attention. Thus, knowledge of possible off target effects on crustaceans, with regard to disruption of molting will be vital in assessing the potential impact of these on non-target organisms.

Publications

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Description Although the project has been active since 2020, it is still in its relatively early stages at Aberystwyth and significantly impacted by the covid crisis due to restricted laboratory access and field work in that time. However, I have managed to get into the labs begun to investigate the role of the hormone corazonin in regulating moulting in the crab Carcinus maenas. Our (Aberystwyth) work to date has been given over mostly to developing reagents and strategies to disrupt the corazonin signalling to the so-called Y-organs (YOs) of the crab which produce moulting hormone, or ecdysone. The consensus view on moult control in crabs is that YOs are negatively regulated by a neuropeptide hormone called moult-inhibiting hormone (MIH) which is synthesised and released from the optic ganglia of the crab nervous system. We have recently challenged this view by proposing that corazonin may play a stimulatory function. Our working hypothesis is that corazonin may abrogate the effects of MIH on ecdysone production at the YOs because we discovered that the receptor for corazonin is dramatically upregulated in the YOs just before moulting occurs. We have developed highly selective and sensitive assays to measure the absolute levels of corazonin receptor mRNA in the YOs using digital droplet PCR (ddPCR) and we are in the process for generating gene suppression reagents (dsRNA and siRNA) to explore the effects of corazonin signal perturbation on moult regulation. Whilst we develop these, we have shown that removing MIH signalling by eyestalk ablation in the crab Carcinus results in elevated corazonin receptor at the YOs, hinting at the interplay between the MIH and corazonin signalling pathways. This work is still very new and continually developing as we regain full access to the laboratories. Work in our partnering group at Bangor University is monitoring the effects of corazonin application to in vitro YO preparations on ecdysone synthesis. In due course we will combine our data to elucidate the mechanisms of corazonin and MIH control of moulting.
In recent months we have been applying the highly sensitive and specific 'digital PCR' assay for measuring 'carcikinin' gene expression analysis across the crab moulting cycle. Our collaborators in Bangor (Webster) have mapped the nerve cells that synthesise the carcikinin peptide (small protein). Therefore, we now have stronger evidence that carcikinin likely plays a key role in the moulting process because levels of gene activity increase at critical times in the moult process. We also know from this meticulous genetic and cellular work that carcikinin is found primarily in the central nervous system (ventral nerve ganglia) and also in the eyes and brain (to a lesser extent). These pieces of evidence are now enabling us to define the function of this molecule that could have important implications for understanding the moult process. In coming months over summer 2022 I will be developing also highly sensitive an specific methods (in situ hybridization- 'RNAScope') to localise where key hormone receptor genes are being expressed throughout the crab. This will be another indicator for the function for some of the hormone-receptor pathways that control moulting in this model species.

March 2023- We have now developed the hybridization chain reaction in situ hybridization probes and reagents to localise crustacean cardioactive peptide (CCAP) and CCAP receptor, Ecdysis triggering hormone (ETHR) and its receptor, Allatostatins and their receptors and two circadian clock gene targets (period and timeless) that will help us search for interaction of the circadian clock and moult control. These reagents are working very nicely and we are preparing images for publication at the time of writing.
Exploitation Route It is still too early on in our endeavours to unlock the full regulatory programme of moulting but we anticipate that our work will, in the medium to longer-term inform strategies for managing moulting control in crustaceans.
Sectors Agriculture, Food and Drink,Other

 
Title Digital droplet PCR assays 
Description I have developed digital droplet PCR assays on the BioRad QX200 platform for the measurement of gene expression of corazonin receptor, carcikinin and refrence genes ELF1a and uniquitin E3 ligase. More recently (2021/22) I have added a suite a circadian clock genes to this assay inventory inclusing Period, timeless, clock, bmal and cryptochrome2. More gene targets are in progress. These will facilitate high senstivity and high resolution gene absolute gene expression quantification and link rhythmic biology to the ecdysis programme- there is evidence that corazonin, which we believe plays a pivotal role in ecdysis, colocalises with clock transcripts indicating a link between the chronobiology and moult regulation (these animals molt periodixally and in phase with tides, daily and lunar events). 
Type Of Material Technology assay or reagent 
Year Produced 2021 
Provided To Others? No  
Impact None yet, the research questions for which these assays have been developed are ongoing but, slowed by restricted access to the laboratory (covid) 
 
Title Hybridization chain reaction reagents 
Description We have developed a suite of hybridization chain reaction (HCR) in situ hybridization probes and reagents for localising neurohormone and receptor mRNA expression in tissues of the target species, Carcinus maenas. These reagents allow multi-channel fluorescent localization for simultaneous labelling of multiple target transcripts in wholemount crab samples. 
Type Of Material Technology assay or reagent 
Year Produced 2022 
Provided To Others? No  
Impact As detailed in the original proposal, we will utilise these reagents to obtain high resolution spatial expression patterns on neuropeptide hormones and their cognate receptors in our model species. This will contribute significantly to our understanding of the inter-endocrine pathways in crustacean moulting. The sensitivity and specificity of the probes enable us to visualise mRNAs expressed at low levels. 
 
Description Exeter University 
Organisation University of Exeter
Country United Kingdom 
Sector Academic/University 
PI Contribution We are providing the resources and materials to conduct PacBio sequencing of the mRNA transcripit from a variety of tissues that will be aligned to the draft Carcinus maenas genome to identify GPCR splice variants. The PacBio reads will also be used to confirm and gap-fill genomic sequences in the draft genome.
Collaborator Contribution Eduarda M Santos is collaborating with us on the crab Carcinus maenas PacBio sequencing to elucidate GPCR splice variants. The Exeter group, together with CEFAS (Dr Van Aerle) have sequenced the genome (unpublished) of this species that they will provide access to and support in assembling our PacBio reads to the genome.
Impact None as yet- due to the covid pandemic we are still waiting to begin the PacBio sequencing on this project.
Start Year 2020