GAP-AK

  • Research type

    Research Study

  • Full title

    Investigation of the genetic diversity, pathogenicity, and therapeutic targets in Acanthamoeba species isolated from patients with Acanthamoeba Keratitis

  • IRAS ID

    353842

  • Contact name

    Michael Leroy Kwame Ansah

  • Contact email

    ma29@sanger.ac.uk

  • Sponsor organisation

    Wellcome Sanger Institute

  • Duration of Study in the UK

    2 years, 8 months, 31 days

  • Research summary

    The aim of this investigation is to develop a better understanding of the genome of Acanthamoeba, a genus of microscopic single-celled organisms that are commonly found in water, soil and household dust. Acanthamoeba cause the eye infection Acanthamoeba keratitis (AK) in immunocompetent individuals. AK is characterised by inflammation and destruction of corneal tissue, resulting in damage to the cornea and in severe cases, irreversible sight loss. This study will look at the genome and the genetic factors that may contribute to pathogenicity, disease progression and poor treatment outcome in the disease Acanthamoeba keratitis. This will include investigating species/strains commonly found in clinical isolates and cultured strains, investigating any amoeba resistant organisms found with isolates, comparing the genomes of clinical isolates to similar species found in the environment or non-pathogenic Acanthamoeba species to identify genes associated with pathogenicity. Through whole-genome sequencing of both free-living and pathogenic Acanthamoeba strains, this research seeks to identify genes and proteins essential for the organism’s survival and pathogenicity, and their influence on keratitis severity, potentially highlighting new avenues for therapeutic targets. Additionally, we aim to explore Acanthamoeba’s interactions with other organisms within the corneal environment, investigating how these interactions might influence infection dynamics and outcomes.

  • REC name

    London - Hampstead Research Ethics Committee

  • REC reference

    25/PR/0460

  • Date of REC Opinion

    29 Apr 2025

  • REC opinion

    Further Information Favourable Opinion