Acanthamoeba

''Acanthamoeba'' is a genus of amoebae that are commonly recovered from soil, fresh water, and other habitats.
The genus ''Acanthamoeba'' has two stages in its life cycle, the metabolically active trophozoite stage and a dormant, stress-resistant cyst stage. In nature, ''Acanthamoeba'' species are generally free-living bacterivores. However, they are also opportunistic pathogens able to cause serious and potentially fatal infections in humans and other animals.

Distribution

''Acanthamoeba'' spp. are among the most prevalent protozoa found in the environment. They are distributed worldwide, and have been isolated from soil, air, sewage, seawater, chlorinated swimming pools, domestic tap water, bottled water, dental treatment units, hospitals, air-conditioning units, and contact lens cases. Additionally, they have been isolated from human skin, nasal cavities, throats, and intestines, as well as plants and other mammals.

Role in disease

Diseases caused by ''Acanthamoeba'' include keratitis and granulomatous amoebic encephalitis
(GAE). The latter is often but not always seen in immunosuppressed patients. GAE is caused by the amoebae entering the body through an open wound and then spreading to the brain. The combination of host immune responses and secreted amoebal proteases causes massive brain swelling resulting in death in about 95% of those infected.

Granulomatous amoebic encephalitis (GAE)

Granulomatous amoebic encephalitis (GAE) is caused by amoebic infection of the central nervous system (CNS). It is characterized by neurological symptoms including headache, seizures, and mental-status abnormalities. These worsen progressively over weeks to months, leading to death in most patients. Infection is generally associated with underlying conditions such as immunodeficiency, diabetes, malignancies, malnutrition, systemic lupus erythematosus, and alcoholism. The parasite enters the body through cuts in the skin or by being inhaled into the upper respiratory tract. The parasite then spreads through the blood into the CNS. ''Acanthamoeba'' crosses the blood–brain barrier by means that are not yet understood. Subsequent invasion of the connective tissue and induction of pro-inflammatory responses leads to neuronal damage that can be fatal within days. Pure granulomatous lesions are rare in patients with AIDS and other related immunodeficiency states, as the patients do not have adequate numbers of CD+ve T-cells to mount a granulomatous response to ''Acanthamoeba'' infection in CNS and other organs and tissues. A perivascular cuffing with amoebae in necrotic tissue is usual finding in the AIDS and related T-cell immunodeficiency conditions.

Brain biopsy normally reveals severe oedema and hemorrhagic necrosis. A patient who has contracted this illness usually displays subacute symptoms, including altered mental status, headaches, fever, neck stiffness, seizures, and focal neurological signs (such as cranial nerve palsies and coma), all leading to death within one week to several months. Due to the rarity of this parasite and a lack of knowledge, no good diagnoses or treatments for ''Acanthamoeba'' infection are now known. ''Acanthamoeba'' keratitis cases in the past have resolved from a therapy consisting of atropine and some other drugs with no antimicrobial effects. Recent publications show atropine to interfere with the protist's CHRM1 receptor, causing cell death.

Infection usually mimics that of bacterial leptomeningitis, tuberculous meningitis, or viral encephalitis. The misdiagnosis often leads to erroneous, ineffective treatment. In the case that the ''Acanthamoeba'' is diagnosed correctly, the current treatments, such as amphotericin B, rifampicin, trimethoprim-sulfamethoxazole, ketoconazole, fluconazole, sulfadiazine, or albendazole, are only tentatively successful. Correct and timely diagnosis, as well as improved treatment methods and an understanding of the parasite, are important factors in improving the outcome of infection by ''Acanthamoeba''. A paper published in 2013 has shown substantial effects of some FDA-approved drugs with an ''in vitro'' kill rate above 90%. These results were ''in vitro'' effects, but as the drugs are already approved, human infections can be targeted after dose calculations in clinical trials done with these diverse groups of drugs.

Acanthamoebic keratitis

When present in the eye, ''Acanthamoeba'' strains can cause acanthamoebic keratitis, which may lead to corneal ulcers or even blindness. This condition occurs most often among contact lens wearers who do not properly disinfect their lenses, exacerbated by a failure to wash hands prior to handling the lenses. Multipurpose contact lens solutions are largely ineffective against ''Acanthamoeba'', whereas hydrogen peroxide-based solutions have good disinfection characteristics.

The first cure of a corneal infection was achieved in 1985 at Moorfields Eye Hospital.

In May 2007, Advanced Medical Optics, manufacturer of Complete Moisture Plus Contact Lens Solution products, issued a voluntary recall of their Complete Moisture Plus solutions. The fear was that contact lens wearers who used their solution were at higher risk of acanthamoebic keratitis than contact lens wearers who used other solutions. The manufacturer recalled the product after the Centers for Disease Control in the United States found that 21 people had possibly received an ''Acanthamoeba'' infection after using Complete Moisture Plus in the month prior to diagnosis.

As a bacterial reservoir

Several species of bacteria that can cause human disease are also able to infect and replicate within ''Acanthamoeba'' species. These include ''Legionella pneumophila'', ''Pseudomonas aeruginosa'', and some strains of ''Escherichia coli'' and ''Staphylococcus aureus''. For some of these bacteria, replication inside ''Acanthamoeba'' has been associated with enhanced growth in macrophages, and increased resistance to some antibiotics. Furthermore, due to the high prevalence of ''Acanthamoeba'' in the environment, these amoebae have been proposed to serve as an environmental reservoir for some human pathogens.

Ecology

''A. castellanii'' can be found at high densities in various soil ecosystems. It preys on bacteria, but also fungi and other protozoa.

This species is able to lyse bacteria and produce a wide range of enzymes, such as cellulases or chitinases, and probably contributes to the breakdown of organic matter in soil, contributing to the microbial loop.

Physiology

Role as a model organism

Because ''Acanthamoeba'' does not differ greatly at the ultrastructural level from a mammalian cell, it is an attractive model for cell-biology studies; it is important in cellular microbiology, environmental biology, physiology, cellular interactions, molecular biology, biochemistry, and evolutionary studies, due to the organisms' versatile roles in the ecosystem and ability to capture prey by phagocytosis, act as vectors and reservoirs for microbial pathogens, and to produce serious human infections. In addition, ''Acanthamoeba'' has been used extensively to understand the molecular biology of cell motility and cancer cell dormancy by in-depth exploration of the process of encystation.

The recently available ''Acanthamoeba'' genome sequence revealed several orthologs of genes employed in meiosis of sexual eukaryotes. These genes included ''Spo11, Mre11, Rad50, Rad51, Rad52, Mnd1, Dmc1, Msh'', and '' Mlh''. This finding suggests that ''Acanthamoeba'' is capable of some form of meiosis and may be able to undergo sexual reproduction.

Owing to its ease and economy of cultivation, the Neff strain of ''A. castellanii'', discovered in a pond in Golden Gate Park in the 1960s, has been effectively used as a classic model organism in the field of cell biology. From just 30 L of simple medium inoculated with ''A. castellanii'', about 1 kg of cells can be obtained after several days of aerated culture at room temperature. Pioneered in the laboratory of Edward D. Korn at the National Institutes of Health (NIH), many important biological molecules have been discovered and their pathways elucidated using the ''Acanthamoeba'' model. Thomas Dean Pollard applied this model at the NIH, Harvard Medical School, Johns Hopkins University School of Medicine, and the Salk Institute for Biological Studies to discover and characterize many proteins that are essential for cell motility, not only in amoebae, but also in many other eukaryotic cells, especially those of the human nervous and immune systems, the developing embryo, and cancer cells. ''Acanthamoeba'' also has served as a model to study the evolution of certain G-proteins. This unicellular eukaryote expresses few GPCRs over its cell membrane that serve vital role for the microorganism, structural homology bioinformatics tools have been used to show the presence of a homolog of human M1-muscarinic receptor in ''A. castellanii''. Blocking these muscarinic receptors in past studies has proven to be amoebicidal in Acanthamoeba spp. More recently, voltage-gated calcium channels in ''Acanthamoeba'' spp. (CavAc) have been reported to have similarities with human voltage-gated calcium channels such as TPC-1 and L-type calcium channels and respond to Ca-channel blockers such as loperamide. This model microbe has been studied to understand complex neurodegenerative states including Alzheimer's disease. Scientists have isolated a neurotransmitter acetylcholine in ''Acanthamoeba'' and the enzymatic machinery needed for its synthesis.

Endosymbionts

''Acanthamoeba'' spp. contain diverse bacterial endosymbionts that are similar to human pathogens, so they are considered to be potential emerging human pathogens. The exact nature of these symbionts and the benefit they represent for the amoebic host still have to be clarified. These include ''Legionella'' and ''Legionella''-like pathogens.

Giant viruses

The giant viruses ''Mimivirus, Megavirus'', and ''Pandoravirus'' infect ''Acanthamoeba''.

Members of the genus ''Acanthamoeba'' are unusual in serving as hosts for a variety of giant viruses (that have more than 1000 protein-coding genes; for instance, ''Pandoravirus'', which has about 2500 protein-coding genes in its genome).

Diversity

''Acanthamoeba'' can be distinguished from other genera of amoebae based on morphological characteristics. However, differentiating one species of ''Acanthamoeba'' from another by morphology has proven difficult. Based on 18S rDNA sequencing, known ''Acanthamoeba'' strains can be organized into 12 groups, denoted T1-T12. Most disease-causing isolates belong to type T4.

Below is a list of described species of ''Acanthamoeba'', with sequence types noted where known. Species that have been identified in diseased patients are marked with *.
*''A. astronyxis'' (Ray & Hayes 1954) Page 1967 * (T7)
*''A. byersi'' Qvarnstrom, Nerad & Visvesvara 2013 *
*''A. castellanii'' Volkonski 1931 * (T4) 'A. terricola'' Pussard 1964*''A. comandoni'' Pussard 1964 (T9)
*''A. culbertsoni'' (Singh & Das 1970) Griffin 1972 * (T10)
*''A. divionensis'' Pussard & Pons 1977 (T4)
*''A. echinulata'' Pussard & Pons 1977
*''A. gigantea'' Schmöller 1964
*''A. glebae'' (Dobell 1914)
*''A. gleichenii'' Volkonsky 1931
*''A. griffini'' Sawyer 1971 (T3)
*''A. hatchetti'' Sawyer, Visvesvara & Harke 1977 * (T11)
*''A. healyi'' Moura, Wallace & Visvesvara 1992 (T12)
*''A. hyalina'' Dobel & O'connor 1921
*''A. jacobsi'' Sawyer, Nerad & Visvesvara 1992
*''A. keratitis'' *
*''A. lenticulata'' Molet & Ermolieff-braun 1976 (T3)
*''A. lugdunensis'' Pussard & Pons 1977 * (T4)
*''A. mauritaniensis'' Pussard & Pons 1977 (T4)
*''A. micheli'' Corsaro et al. 2015
*''A. palestinensis'' (Reich 1933) Page 1977 * (T1)
*''A. paradivionensis'' Pussard & Pons 1977 (T4)
*''A. pearcei'' Nerad et al. 1995
*'' A. polyphaga'' (Puschkarew 1913) Volkonsky 1931 * (T4)
*''A. pustulosa'' Pussard & Pons 1977 (T2)
*'' A. pyriformis'' (Olive & Stoianovitch 1969) Spiegel & Shadwick 2016
*''A. quina'' Pussard & Pons 1977 *
*''A. rhysodes'' (Singh 1952) Griffin 1972 * (T4)
*''A. royreba'' Willaert, Stevens & Tyndall 1978
*''A. sohi'' Kyung-il & Shin 2003
*''A. stevensoni'' Sawyer et al. 1993 (T11)
*''A. triangularis'' Pussard & Pons 1977 (T4)
*''A. tubiashi'' Lewis & Sawyer 1979 (T8)

Etymology

From the Greek ''akantha'' (spike/thorn), which was added before "amoeba" (change) to describe this organism as having a spine-like structure (acanthopodia). This organism is now well known as Acanthamoeba, an amphizoic, opportunistic, and nonopportunistic protozoan protist widely distributed in the environment.

See also

* ''Acanthamoeba'' infection
* '' Balamuthia mandrillaris''

References

External links

''Acanthamoeba''
– Centers for Disease Control and Prevention
Video of Acanthamoeba from contact lens keratitis
*

on Amoeba
Eye health and AcanthamoebaAcanthamoeba pictures and illustrations

{{Authority control

Amoebozoa genera
Discosea
Parasitic amoebozoa
Taxa described in 1931