Skip to main navigation Skip to search Skip to main content

Comparative neuropathology of granulomatous amoebic encephalitis caused by Acanthamoeba spp. across species

  • Ruqaiyyah Siddiqui*
  • , Sutherland K Maciver
  • , David Lloyd
  • , Naveed Ahmed Khan*
  • *Corresponding author for this work

    Research output: Contribution to journal › Review article › peer-review

    Abstract

    Acanthamoeba species are free-living amoebae that cause granulomatous amoebic
    encephalitis, a rare but frequently fatal infection of the central nervous system that
    predominantly affects immunocompromised individuals. The disease is characterised by a
    subacute to chronic course, diagnostic difficulty, and marked heterogeneity in clinical
    presentation. Here, we describe a comparative analysis of the neuropathology of
    Acanthamoeba encephalitis across humans and animals, highlighting conserved features of
    haematogenous dissemination, perivascular tropism, granulomatous inflammation, and chronic
    tissue destruction. Across species, both trophozoites and cysts persist within neural tissue,
    reflecting prolonged host–pathogen interaction rather than acute cytolysis. Despite variability
    in lesion distribution and disease kinetics, the fundamental pathological signature of
    Acanthamoeba encephalitis is remarkably conserved. These observations validate the use of
    animal models for mechanistic investigation and therapeutic development and clarify key
    processes underlying this devastating opportunistic infection.
    Original languageEnglish
    JournalParasitology
    DOIs
    Publication statusAccepted/In press - 12 Aug 2026

    Keywords

    • Granulomatous amoebic encephalitis
    • Acanthamoeba
    • Comparative pathology
    • Neuroinflammation
    • Opportunistic infection

    Fingerprint

    Dive into the research topics of 'Comparative neuropathology of granulomatous amoebic encephalitis caused by Acanthamoeba spp. across species'. Together they form a unique fingerprint.

    Cite this