Acanthamoeba
contributed by R. Neal Band and Frededrick L. Schuster
Acanthamoeba spp. are found in a variety of soil, freshwater and brackish
water environments, and some members of the genus are opportunistic pathogens
of humans. In soil, they are part of a collection of organisms referred to as
small amebae (compared to Amoeba proteus and other "large"
amebae) which constitute a significant component of the soil habitat, reaching
up to a million amebae per gram of soil. The Acanthamoeba life-cycle
is comprised of a trophic (actively feeding) stage, and a thick-walled cystic
(dormant) stage which forms under conditions of adversity, such as desiccation
and lack of food. The trophic ameba has distinctive fine-pointed pseudopods
(acanthopodia) that project from the surface. Cysts have been reported to remain
viable under laboratory conditions for twenty-four years. With return of conditions
optimal for growth, cysts germinate to give rise to trophic amebae. Differences
in cyst morphology have been used to distinguish species of Acanthamoeba.
Ecology: Acanthamoeba spp. are found in virtually every type of soil
and water habitat, and have even been isolated from Antarctic soil samples.
The organism can also be isolated from home aquaria, humidifiers, flower pots,
domestic water supplies and water taps, and other locations, which puts them
in close contact with humans. Amebae isolated from nature are often found to
harbor bacteria, implicating them as vectors of potentially pathogenic bacteria.
They may, for example, play a role in the survival of bacteria such as Legionella,
the causal agent of legionellosis, and may explain the ability of these bacteria
to survive in air conditioning cooling towers and hospital water supplies.
In the soil habitat, acanthamebae feed on bacteria and other microorganisms.
But soil amebae are also subject to the degradative activities of other soil
microbes, such as yeasts and fungi. Cysts of soil amebae, such as Acanthamoeba,
are destroyed in the presence of other soil microbes.
Nutrition and cultivation: Acanthamoeba spp can be grown in the laboratory
under a variety of conditions. Amebae proliferate when grown with bacteria,
but will also grow in bacteria-free (axenic) conditions in an enriched culture
medium (peptone, yeast extract, and glucose), reaching numbers of more than
a million amebae per milliliter. Under optimal laboratory growth conditions,
amebae have a doubling time of several hours. Defined media, in which all components
of the growth medium are known, are also available for more exacting studies
on nutritional requirements. Their ease of cultivation and the ability of their
cysts to be freeze-dried for long-term storage, make Acanthamoeba an
organism of choice for cellular and molecular studies, as well as more conventional
studies on ecology, pathogenesis, and nutrition.
Evolutionary relationships: In the 1930s, Andre Lwoff and his collaborators
identified thiamine as a vitamin requirement. Subsequent work by others identified
vitamin B12 and biotin as additional vitamin requirements, which could be consistent
with an algal origin of acanthamebae. This was called into question, however,
when the herbicide Trifluralin was found to inhibit the growth of Naegleria
but not Acanthamoeba, indicating that microtubules of the former
were plant-like while those of Acanthamoeba were animal-like. But the Acanthamoeba
cyst wall contains cellulose, a carbohydrate usually associated with plants.
Recent studies have made use of the 18S ribosomal RNA gene to determine evolutionary
relationships among Acanthamoeba species and strains, as well as relationships
to other eukaryotic organisms.
Cytology: Acanthamoeba has a nucleus with a large, central nucleolus.
Mitosis, termed mesomitosis, differs from the typical eukaryotic pattern in
that centrioles are not present although spindle fibers do terminate in centrosomes.
Acanthamoebae have a high degree of resistance to radiation and mutagenic agents,
suggesting that they may have a polyploid chromosomal complement or, alternatively,
they possess a very efficient DNA repair mechanism.
Pathogenesis: Acanthamoeba spp., although free-living organisms, are
also opportunistic pathogens of humans, causing systemic acanthamebiasis (encephalitis,
cutaneous, disseminated and nasopharyngeal infections), as well as amebic keratitis.
Groups at high risk for systemic infections include immunocompromised and immunosuppressed
individuals, while keratitis occurs in otherwise healthy individuals. Several
different strains and species of Acanthamoeba have been implicated in
these infections, unlike Naegleria where pathogenicity is associated
with a single species, N. fowleri.
In Acanthamoeba encephalitis and other systemic infections, the portals
of entry are through the respiratory tract and wounds, with passage to the brain
and other sites via the circulatory system. Cysts of Acanthamoeba in
the soil can be carried by the wind to the nasal passages, and amebae have been
isolated from the nasal mucosa of healthy humans. They can also enter the body
through breaks in the skin (cutaneous acanthamebiasis) that become contaminated
with soil containing cysts. Many of the victims of systemic Acanthamoeba
infections have been AIDS patients, whose immune system has been weakened
by the human immunodeficiency virus. Immunocompetent individuals have been shown
to have antibodies against Acanthamoeba, indicating that many persons
may be exposed to these amebae but do not develop disease.
In Acanthamoeba keratitis, in which the amebae attack the corneal surface
and stroma of the eye, infection occurs as the result of corneal trauma or,
more commonly, because of poor hygiene in care of contact lenses, particularly
the extended wear variety. A major source of infection for contact lens users
is home-made saline solutions, prepared from non-sterile tap or distilled water
containing bacteria and encysted Acanthamoeba. The cysts germinate, giving
rise to trophic amebae, which feed on bacteria and proliferate on the contact
lens surface or in the lens case. When the lens is placed in the eye, the amebae
are then transferred to the corneal surface. Once established in the cornea,
they are difficult to eliminate due to the cyst, which is not permeable to many
antimicrobial agents.
Antimicrobial therapy for Acanthamoeba infections: Systemic Acanthamoeba
infections are often fatal, in part because of difficulty in diagnosing the
disease, and in part due to delayed use of antimicrobial therapy. Among the
drugs that have been used successfully to treat systemic Acanthamoeba
infections are 5-fluorocytosine, fluconazole, and pentamidine isethionate. Optimal
drug therapy, however, has not yet been determined.
Acanthamoeba keratitis has been successfully treated with topical applications
of chlorhexidine or polyhexamethylene biguanide, with and without propamidine
isethionate.
CODENET - website from recent EU project on coccolithophores, includes listing
of largest available culture collection.
Pathogenic potential: Pathogenicity and virulence are often associated with
production of destructive enzymes or toxins. In N. fowleri, prolonged
cultivation in axenic medium causes a significant loss of virulence which can
be traced to several differentially expressed genes, one of which codes for
a serine protease. Similar studies are lacking for genetic localization of virulence
in Acanthamoeba, although secretion of ribonuclease, proteolytic enzymes,
and lipases may play a role in determining destructive potential of the amebae.
Most clinical isolates of Acanthamoeba are able to tolerate and grow
at 37oC, suggesting that temperature tolerance is an important factor in determining
pathogenic potential. There are, however, strains that grow at 37oC and are
not pathogenic, and some of the keratitis isolates grow better at 30oC than
at 37oC.