Acanthamoeba: Difference between revisions
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Acanthamoeba
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==Background== |
==Background== |
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===Microbiology=== |
===Microbiology=== |
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*Seventeen genotypes (T1-T17), of which 10 have caused disease in humans |
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*Most common is ''[[Acanthamoeba castellanii]]'' complex (T4) |
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*Species traditionally organized morphologically into 3 groups |
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{| class="wikitable" |
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!Group |
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!Species |
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!Trophozoite Size |
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!Cyst Size |
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|I |
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|''A. astronyxis'', ''A. comandoni'', ''A. tubiashi'', ''A. byersi'' |
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|30-125 μm |
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|16-35 μm |
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|II |
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|''A. castellanii'', ''A. polyphaga'', ''A. rhysodes'', ''A. hatchetti'' |
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|15-45 μm |
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|≤18 μm |
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|III |
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|''A. culbertsoni'', ''A. royreba'', ''A. lenticulata'' |
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|15-45 μm |
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|<18 μm with different morphologies |
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|} |
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===Life Cycle=== |
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*Cysts and trophozoites can cause disease |
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===Epidemiology=== |
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*More common in immunocompromised patients, with risk factors including [[AIDS]], liver disease, diabetes, organ transplantation, corticosteroid use, chemotherapy, and rituximab |
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===Granulomatous amebic encephalitis=== |
===Granulomatous amebic encephalitis=== |
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*Subacute presentation of encephalitis (fever, headache, nuchal rigidity, behaviour changes, altered level of conciousness, focal neurological deficiets) |
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*Often preceded by cutaneous lesions by months |
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**May include ulcers, nodules, and subcutaneous abscesses |
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**Amoebic granulomas on biopsy |
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===Non-neurological disseminated acanthamoebiasis=== |
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*Rarely, patients may have disseminated disease without evidence of CNS involvement |
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*Mostly seen in patients with AIDS, transplant, or prolonged corticosteroid use |
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*Most commonly involves skin, but can involve liver, lungs, and bones |
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===Amoebic keratitis=== |
===Amoebic keratitis=== |
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*Sight- and eye-threatening infection |
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*Often secondary to corneal trauma or improper contact lens hygiene |
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*Present with severe pain, photophobia, tearing |
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*May see dendiform epitheliopathy or stromal ring |
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== Diagnosis == |
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* Ameba culture on nutrient agar with layer of gram-negative bacteria at 30ºC (cornea/skin) or 37–C (brain/lung) |
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* Species identification done with 18S rDNA sequencing |
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==Management== |
==Management== |
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===Granulomatous amebic encephalitis=== |
===Granulomatous amebic encephalitis=== |
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===Amoebic keratitis=== |
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*Can be treated with any of: |
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**[[Is treated by::PHMB]] |
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**[[Is treated by::Chlorhexadine]] |
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**Topical and oral [[Is treated by::voriconazole]] |
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**[[Is treated by::Propamidine]] |
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**[[Is treated by::Hexamidine]] |
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[[Category:Protozoa]] |
[[Category:Protozoa]] |
Latest revision as of 16:47, 25 January 2022
Background
Microbiology
- One of the free-living amoebae
- Seventeen genotypes (T1-T17), of which 10 have caused disease in humans
- Most common is Acanthamoeba castellanii complex (T4)
- Species traditionally organized morphologically into 3 groups
Group | Species | Trophozoite Size | Cyst Size |
---|---|---|---|
I | A. astronyxis, A. comandoni, A. tubiashi, A. byersi | 30-125 μm | 16-35 μm |
II | A. castellanii, A. polyphaga, A. rhysodes, A. hatchetti | 15-45 μm | ≤18 μm |
III | A. culbertsoni, A. royreba, A. lenticulata | 15-45 μm | <18 μm with different morphologies |
Life Cycle
- Cysts and trophozoites can cause disease
Epidemiology
- More common in immunocompromised patients, with risk factors including AIDS, liver disease, diabetes, organ transplantation, corticosteroid use, chemotherapy, and rituximab
Clinical Manifestations
Granulomatous amebic encephalitis
- Subacute presentation of encephalitis (fever, headache, nuchal rigidity, behaviour changes, altered level of conciousness, focal neurological deficiets)
- Often preceded by cutaneous lesions by months
- May include ulcers, nodules, and subcutaneous abscesses
- Amoebic granulomas on biopsy
Non-neurological disseminated acanthamoebiasis
- Rarely, patients may have disseminated disease without evidence of CNS involvement
- Mostly seen in patients with AIDS, transplant, or prolonged corticosteroid use
- Most commonly involves skin, but can involve liver, lungs, and bones
Amoebic keratitis
- Sight- and eye-threatening infection
- Often secondary to corneal trauma or improper contact lens hygiene
- Present with severe pain, photophobia, tearing
- May see dendiform epitheliopathy or stromal ring
Diagnosis
- Ameba culture on nutrient agar with layer of gram-negative bacteria at 30ºC (cornea/skin) or 37–C (brain/lung)
- Species identification done with 18S rDNA sequencing
Management
Granulomatous amebic encephalitis
- Can consider a combinaction of pentamidine, azoles, flucytosine, sulfadiazine, miltefosine, amikacin, and voriconazole
Amoebic keratitis
- Can be treated with any of:
- PHMB
- Chlorhexadine
- Topical and oral voriconazole
- Propamidine
- Hexamidine