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  Phages as the ultimate puppeteers of bacterial metabolism


   Department of Genetics and Genome Biology

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  Prof M Clokie, Dr H Yesilkaya  No more applications being accepted  Competition Funded PhD Project (Students Worldwide)

About the Project

Bacteriophages, or phages are bacterial viruses, and are the most abundant and diverse biological entities on Earth. Throughout the biosphere they outnumber their bacterial hosts by at least 10 to 1 and strikingly, the majority of the functions of most genes encoded by phages remains unknown. What is known is that their impact on life ranges from the maintenance of healthy microbiota to the promotion of biodiversity in soil and oceans. Phages also have a plethora of potential practical uses, from the treatment of infections caused by antibiotic resistant bacteria to preventing antibiotic resistance build up within food animals and increasing the shelf life of food products to reduce global food waste.

To optimise and extend the applications of phages within food security and disease settings, it is important to understand how different phages impact their host bacteria, particularly how they manipulate their metabolism. Our lab and work of others have shown using metabolomic profiling experiments that phages can profoundly alter the metabolites that bacteria express [1-2] and reviewed and contextualised in our review [3]. However, our understanding of the underlying molecular and genetic mechanisms by which this happens is really limited. To unravel this during this exciting PhD project, the student will work in an interdisciplinary way both in a phage-focused laboratory, in an analytical chemistry lab, and within a group focused on determining how metabolism impacts bacterial phenotype.

Aims and Objectives

In this project, we aim to test the hypothesis that particular phage types target specific bacterial pathways and determine the mechanistic basis for such targeting, which will help us better develop phages for therapy.

Specific Objectives are:

  1. Determine how phages impact bacterial metabolism by using RNASeq and qPCR and analytical chemistry in order to probe infected transcriptomes
  2. By comparative analysis of transcriptomic data, identify phage specific infection strategies for the phages tested, for example establish if phages that are equally aggressive impact the same metabolic pathways
  3. Make bacterial knockout mutants of whole or partial metabolic pathways targeted by phages and determine how phages interact with these bacterial mutants
  4. Establish the impact of a) infected cells and b) phage resistant mutants on bacterial virulence and eukaryotic host response in a range of models including biofilm generation, capsule synthesis, and virulence.

In order to answer these objectives, in this project we will use Klebsiella and it’s phages as a model system. We will study the impact of our diverse, well characterised Klebsiella phage collection on its bacterial host metabolism. Klebsiella are Gram-negative bacteria, some of which cause diseases and others are found in the environment as free-living microbes. They have diverse metabolic adaptive capabilities including the ability to fix nitrogen. K. pneumoniae can also cause many diseases including pneumonia, urinary tract infection, bacteremia, and septicaemia in humans and animals, showing that the microbe is environmentally adept very likely due to its inherent metabolic flexibility. Worryingly, many strains are antibiotic resistant thus pose a serious health threat, hence it is one of the few pathogens for which there is an urgent need for effective antibiotics as declared by the WHO.

Importance

This project aims to provide a fundamental understanding of the relationship of specific phages to their bacterial hosts and in doing so to compare how the host takeover strategies differ between phages, and how the subsequent behaviour of the infected bacteria is affected when challenged with different phages. This dataset and outputs from the thesis would provide the proof of a novel method by which to assess phages for therapeutic and industrial applications.

Entry requirements:

  • Those who have a 1st or a 2.1 undergraduate degree in a relevant field are eligible.
  • Evidence of quantitative training is required. For example, AS or A level Maths, IB Standard or Higher Maths, or university level maths/statistics course.
  • Those who have a 2.2 and an additional Masters degree in a relevant field may be eligible.
  • Those who have a 2.2 and at least three years post-graduate experience in a relevant field may be eligible.
  • Those with degrees abroad (perhaps as well as postgraduate experience) may be eligible if their qualifications are deemed equivalent to any of the above.

For further information please contact [Email Address Removed]

Application advice:

To apply please refer the application instructions at

https://le.ac.uk/study/research-degrees/funded-opportunities/bbsrc-mibtp

You will need to apply for the PhD place at University of Leicester and also submit your online application notification to MIBTP.  Links for both are on the above web page.

Project / Funding Enquiries: For further information please contact [Email Address Removed]

Application enquiries to [Email Address Removed] 

Biological Sciences (4)

Funding Notes

All MIBTP students will be provided with a 4 years studentship.
Studentships include:
Tuition fees at UK rate*
• a tax free stipend of at least £15,609* p.a (to rise in line with UKRI recommendation)
• a travel allowance in year 1
• a travel / conference budget
• a generous consumables budget
• use of a laptop for the duration of the programme.
* International students are welcome to apply but must be able to fund the difference between UK
and International fees for the duration of their studies.

References

1. Howard-Varona, C., Lindback, M.M., Bastien, G.E. et al. Phage-specific metabolic reprogramming of virocells. ISME J 14, 881–895 (2020). https://doi.org/10.1038/s41396-019-0580-z
2. De Smet, J., Zimmermann, M., Kogadeeva, M. et al. High coverage metabolomics analysis reveals phage-specific alterations to Pseudomonas aeruginosa physiology during infection. ISME J 10, 1823–1835 (2016).https://doi.org/10.1038/ismej.2016.3
3. Francesca E. Hodges, Thomas Sicheritz-Pontén, and Martha R.J. Clokie. PHAGE.Mar 2021.16-25.http://doi.org/10.1089/phage.2020.0041
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