Hannah Agnew

Miss Hannah Agnew

Higher Degree by Research Candidate

PhD Candidate

School of Biological Sciences

Faculty of Sciences, Engineering and Technology


My research investigates the differences between closely related clinical isolates of Streptococcus pneumoniae, which have been taken from different anatomical niches, in hopes of identifying mechanisms that influence the disease tropism.  

Streptococcus pneumoniae is a commensal Gram-positive bacterium that is commonly found in the normal human microflora. However, the pneumococci can switch to cause both local (otitis media) and invasive diseases (meningitis) leading to high rates of morbidity and mortality. One important factor in pneumococcal pathogenesis is the capacity to metabolise different carbohydrates. Different niches of the body vary in their nutrient composition, which requires adaptation by pneumococci to survive, such as the switching between different metabolic pathways. My research aims to examine metabolic differences between closely related paediatric clinical isolates from different anatomical niches. This project will elucidate the molecular mechanisms that contribute to tissue tropism, which may lead to improved vaccines and therapeutic strategies.

Streptococcus pneumoniae is a commensal Gram-positive bacterium that is commonly found in the normal human microflora. However, the pneumococci can switch to cause both local (otitis media) and invasive diseases (meningitis) leading to high rates of morbidity and mortality. 

In the last 2 years, our lab has received clinical isolates of Streptococcus pneumoniae from the German National Reference Center for Streptococci (Aachen) collected in Germany over 17 years, from 2002 to 2019. These isolates were acquired from children, aged 4 months to over 6 years old, admitted to hospital with otitis media, pneumonia, sepsis and meningitis. Specifically, children with otitis media had both ear and nasopharynx isolates collected, whilst children with sepsis or meningitis had both blood and cerebral spinal fluid (CSF) isolates collected. 

These new isolates are being grouped based on clonal lineage and phenotypically characterised to determine any differences. In particular, the metabolic capabilities of the isolates are being closely examined due to research undertaken previously in the Paton lab that identified genetic differences in metabolic genes within closely related isolates from different niches, which influenced disease tropism. 

My research aims to identify metabolic differences, in vitro and in vivo, between clinical isolates of the same clonal lineage collected from different anatomical niches. Identification of these differences will elucidate the molecular mechanisms that contribute to tissue tropism, which may lead to improved vaccines and therapeutic strategies.

  • Appointments

    Date Position Institution name
    2022 - ongoing Doctor of Philosophy Candidate University of Adelaide
    2022 - 2022 Practical Demonstrator University of Adelaide
    2021 - 2022 Master of Philosophy Candidate University of Adelaide
    2019 - ongoing Private tutor Self-employed
  • Awards and Achievements

    Date Type Title Institution Name Country Amount
    2020 Scholarship Adelaide Summer Research Scholarship The University of Adelaide Australia -
    2020 Award Outstanding Academic Achievement Award The University of Adelaide Australia -
    2019 Award Outstanding Academic Achievement Award The University of Adelaide Australia -
    2018 Award Outstanding Academic Achievement Award The University of Adeliade Australia -
  • Language Competencies

    Language Competency
    English Can read, write, speak, understand spoken and peer review
  • Education

    Date Institution name Country Title
    2018 - 2020 The University of Adelaide Australia Bachelor of Science (Advanced)
  • Research Interests

  • Position: PhD Candidate
  • Email: hannah.agnew@adelaide.edu.au
  • Campus: North Terrace
  • Building: Molecular Life Sciences, floor 4
  • Org Unit: Molecular and Biomedical Science

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