» Articles » PMID: 33456336

Acanthamoeba - Pathogen and Vector of Highly Pathogenic Bacteria Strains to Healthy and Immunocompromised Individuals

Overview
Publisher Termedia
Date 2021 Jan 18
PMID 33456336
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Acanthamoeba is a free-living protist pathogen, which is present in every place on Earth. 50 to 100 percent of the adult population has serum antibodies, specific for Acanthamoeba antigens. Acanthamoeba is an etiological agent of keratitis and encephalitis diagnosed in human. Acanthamoeba keratitis occurs in healthy persons and may lead to visual impairment and blindness, because corneal infection with this parasite fails to induce cell-mediated immune response due to the absence of resident antigen-presenting cells in the cornea. Systemic immunization with Acanthamoeba antigens induces Th1 cell-mediated immunity and serum IgG antibody, but do not prevent the development of keratitis. Immunization via mucosal surfaces stimulates IgA antibodies in tears and protects against the development of keratitis. Amoebae feed mainly on bacteria, fungi, and algae. By transferring intracellular bacteria, amoeba contributes to the spread of diseases dangerous to humans. Some microorganisms have evolved to become resistant to protist, since they are not internalized or able to survive, grow, and exit free-living protists after internalization. In many cases, the bacteria inside living amoebae survive longer, and multiply better, showing higher virulence. There is a hypothesis, which assumes that Acanthamoeba and symbiontic bacteria survive and multiply better in moist soil, rich in nitrogen compounds, particularly in the vicinity of the root systems of Alnus glutinosa, infected with nitrogen-fixing bacteria Frankia alni. Impact of soil environment created by nitrogen-fixing bacterium Frankia alni on specific relations between protists Acanthamoeba and highly pathogenic bacteria strains in Alnus glutinosa habitats in Poland continue to be established.

Citing Articles

The role of PPAR in fungal keratitis.

Zhou H, Zhang H, Bi M, Zhang W Front Immunol. 2025; 15:1454463.

PMID: 39763659 PMC: 11700800. DOI: 10.3389/fimmu.2024.1454463.


Metagenomic next-generation sequencing-assisted diagnosis of a rare case of primary cutaneous acanthamoebiasis in an HIV patient: a case report.

Fan W, Li P, Wei Q, Liu X, Cai Y, Li B Front Cell Infect Microbiol. 2024; 14:1356095.

PMID: 38863830 PMC: 11165212. DOI: 10.3389/fcimb.2024.1356095.


Monitoring potentially pathogenic protists in sewage sludge using Metataxonomics.

Rozo-Montoya N, Bedoya-Urrego K, Alzate J Food Waterborne Parasitol. 2023; 33:e00210.

PMID: 37808003 PMC: 10558727. DOI: 10.1016/j.fawpar.2023.e00210.


Sublethal Exposure to Plasma-Activated Water Influences the Morphological Characteristics, Phagocytic Ability, and Virulence of Acanthamoeba castellanii.

Bahrami S, Darvishi M, Zarei M, Sabaeian M, Henriquez F Acta Parasitol. 2023; 68(3):582-592.

PMID: 37338633 DOI: 10.1007/s11686-023-00691-0.


Both the microbiome and the macrobiome can influence immune responsiveness in psoriasis.

Kierasinska M, Donskow-Lysoniewska K Cent Eur J Immunol. 2022; 46(4):502-508.

PMID: 35125950 PMC: 8808298. DOI: 10.5114/ceji.2021.110314.


References
1.
Kot K, Lanocha-Arendarczyk N, Kosik-Bogacka D . Amoebas from the genus Acanthamoeba and their pathogenic properties. Ann Parasitol. 2019; 64(4):299-308. View

2.
Lass A, Szostakowska B, Idzinska A, Chomicz L . The first genotype determination of Acanthamoeba potential threat to human health, isolated from natural water reservoirs in Poland. Parasitol Res. 2014; 113(7):2693-9. PMC: 4058056. DOI: 10.1007/s00436-014-3925-6. View

3.
Greub G, Raoult D . Microorganisms resistant to free-living amoebae. Clin Microbiol Rev. 2004; 17(2):413-33. PMC: 387402. DOI: 10.1128/CMR.17.2.413-433.2004. View

4.
Abd H, Johansson T, Golovliov I, Sandstrom G, Forsman M . Survival and growth of Francisella tularensis in Acanthamoeba castellanii. Appl Environ Microbiol. 2003; 69(1):600-6. PMC: 152416. DOI: 10.1128/AEM.69.1.600-606.2003. View

5.
Bielawska-Drozd A, Niemcewicz M, Gawel J, Bartoszcze M, Graniak G, Joniec J . [Real time PCR hybridization for the rapid and specific identification of Francisella tularensis]. Med Dosw Mikrobiol. 2011; 62(4):351-60. View