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Nigel Groome Studentship: The Impact of Neonicotinoid Pesticide Resistance on The Role of Nicotinic Acetylcholine Receptors in Food-related Reward Signalling

Oxford Brookes University - Faculty of Health and Life Sciences - School of Biological and Medical Sciences

Qualification Type: PhD
Location: Oxford
Funding for: UK Students, EU Students, International Students
Funding amount: £19,237
Hours: Full Time
Placed On: 3rd December 2024
Closes: 17th January 2025

3 Year, full-time funded PhD Studentship

Eligibility: Home UK/EU and International applicants

Bursary p.a.: Bursary equivalent to UKRI national minimum stipend plus fees (current 2024/25 bursary rate is £19,237)

Fees and Bench fees: will be met by the University for the 3 years of the funded Studentship. Visa and associated costs are not funded. International applicants can visit https://www.brookes.ac.uk/students/isat/ for further information

Closing date: Friday 17th January 2025 – Midday

Start Date: September / October 2025

Project Title: Nigel Groome Studentship: The impact of neonicotinoid pesticide resistance on the role of nicotinic acetylcholine receptors in food-related reward signalling                       

Requirements:

Applicants should have a first or upper second-class honours degree from a Higher Education Institution in the UK or acceptable equivalent qualification. EU Applicants must have a valid IELTS Academic test certificate (or equivalent) with an overall minimum score of 6.5 to 7.0 and no score below 6.0 issued in the last 2 years by an approved test centre.

The studentship requires you to undertake the equivalent of up to 6 hrs teaching per week on average, during semester time, and to include preparation and marking (but no more than 20 hrs per week), and to participate in a teaching skills course without further remuneration.    

Project Description:

On average, smokers weigh 4 to 5 kg less than non-smokers while gaining 4.5 kg within a year after quitting. Bees show addiction to sub-lethal doses of neonicotinoids (insecticides that mimic nicotine), resulting in difficulties with feeding and foraging and overall lower food intake. The molecular mechanisms underlying the effect of nicotine on body weight are complex and poorly understood. Nicotine acts on nicotinic receptors, which are expressed in parts of the brain that mediate food intake. Furthermore, nicotinic receptor expression increases in the reward circuitry of the brain upon sugar intake. Conversely, we have shown that nicotinic receptor expression decreases in the brain of the fruit fly upon starvation.

This study aims to elucidate the role of nicotinic receptors in food-related reward signalling and to evaluate the effects of insecticide resistance-causing mutations in these receptors on food intake to understand potential fitness costs arising from these mutations.

This is a collaborative project between the labs of Dr Andrew Jones, a leading expert in Cys-loop ligand-gated ion channels (CysLGICs) in insects and Dr Korneel Hens, an expert on fly genetics, CRISPR modification and feeding behaviour.

It is an exciting opportunity to use state-of-the-art molecular techniques to answer a very timely research question. You will use CRISPR to tag nicotinic receptors that change expression upon starvation in the fly brain and fly genetics to study the role of these receptors in reward signalling. You will also evaluate the effect of mutations in these receptors causing neonicotinoid resistance on food choice and food intake.

Application process: Please contact hls-applications@brookes.ac.uk for details of how to apply via the above ‘Apply’ button.

Director of Studies: Dr Andrew Jones

Supervisors: Dr Korneel Hens, Dr Andrew Jones

Project Contact: Dr Korneel Hens: khens@brookes.ac.uk

Contact hls-applications@brookes.ac.uk with any queries.

This project is advertised on a competitive basis alongside other current Nigel Groome PhD studentship advertisements for School of Biological and Medical Sciences projects. Part time MPhil/PhD study will be exceptionally considered.

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