Next Article in Journal
Food Security and Foodborne Mycotoxicoses—What Should Be the Adequate Risk Assessment and Regulation?
Previous Article in Journal
A Novel Regulator PepR Regulates the Expression of Dipeptidase Gene pepV in Bacillus thuringiensis
Previous Article in Special Issue
Successive Acanthamoeba Corneal Isolates Identified in Poland Monitored in Terms of In Vitro Dynamics
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Acanthamoeba spp. as Factors for Severe Infectious Diseases in Humans

1
Department of Medical Biology, Medical University of Warsaw, 00-575 Warsaw, Poland
2
Department of Ophthalmology, Independent Public Clinical Ophthalmology Hospital, Medical University of Warsaw, 00-576 Warsaw, Poland
3
Department of Public Health, Medical University of Warsaw, 02-097 Warsaw, Poland
*
Authors to whom correspondence should be addressed.
Microorganisms 2024, 12(3), 581; https://doi.org/10.3390/microorganisms12030581
Submission received: 1 March 2024 / Revised: 8 March 2024 / Accepted: 11 March 2024 / Published: 14 March 2024
(This article belongs to the Special Issue Acanthamoeba spp. as Factors for Severe Infectious Diseases in Humans)
Acanthamoeba spp., known as free-living organisms, occur in both natural and man-made habitats, including those in soil, air, water bodies of varying types, in health facilities, hospital environments, and on/in equipment. These heterotrophic organisms exist as trophozoites which feed on bacteria and as dormant cysts. Previously, Acanthamoeba spp. were considered to be harmless exozoic protists that develop without entering the human body; However, infections caused in humans by Acanthamoeba were reported in the 1960s and 1970s [1,2,3,4]. Frequent exposure to the amoebae result in the occurrence of IgG anti-Acanthamoeba antibodies in non-infected persons. Non-specific symptoms caused by Acanthamoeba spp., and endondosymbionts surviving in them, affect the diagnosis correctness of [4,5,6,7,8].
Acanthamoeba spp. present a serious risk for human health as causative factors of encephalitis and keratitis; the amoebae can also cause cutaneous and nasopharyngal infections.

1. Granulomatous Amoebic Encephalitis (GAE)

Granulomatous amoebic encephalitis (GAE), a rare but usually fatal disease exhibiting neurological symptoms resembling viral or bacterial meningitis, is the subject of epidemiology, physiology, diagnosis, and treatment studies [1,3,6,7,8]. A loss of consciousness and coma both result in a poor prognosis. GAE symptoms common to other of CNS diseases can cause misdiagnosis; magnetic resonance imaging and computed tomography are helpful for this reason. GAE develops in persons with HIV/AIDS and those who are immunocompromised or undergoing immunosuppressive therapy [8,9,10]. The amebae enter the human body through the nose and into to bloodstream, crossing blood–brain barrier and invade the CNS; infections via skin lesions or the respiratory tract are also likely. Complex therapy (ketoconazole, azithromycin, and pentamidine isethionate) is less effective due to the resistance of Acanthamoeba to chemicals and the inability of drugs to cross the blood–brain barrier [3,8,10]. Despite some success in treatment efforts, the prognosis for GAE is still poor.

2. Acanthamoeba Keratitis (AK)

Acanthamoeba keratitis (AK) initially shows non-specific and confusing clinical symptoms similar to viral, fungal, or bacterial keratitis: ring-shaped cornea infiltrations, characteristic of AK, occurs in ~50% of cases. It is considered a rare but devastating infection that occurs mainly in immunocompetent persons, and it is associated with a high risk of blindness. The main risk factor for this type of infection is poor hygiene when wearing contact lenses; micro-injuries to the cornea and foreign bodies in the eyes predispose people to AK [8,10,11]. The binding of amoebae to contact lenses and the cornea is the first step in the development of AK, which is usually unilateral. The use of a slit-lamp, in vivo confocal microscopy, direct microscopic examinations, in vitro cultures, and molecular techniques are common in related research and in medical practice to detect causative agents and assess pathological effects [11,12,13]. The recommended drugs for this infection belong to the diamides and biguanides groups. The presence of cysts in the eye despite treatment creates the risk of the emergence of trophozoites and AK recrudescence. Anti-adhesive agents are investigated with contact-lens solutions that are not effective enough against the amoebae [8,13,14,15]. Non-specific AK symptoms are common causes of misdiagnosis and ineffective therapy.

3. Conclusions

Infections caused by Acanthamoeba strains posing a public-health threat worldwide are detected and reported with constantly increasing frequency.
Microorganisms is one of the leading journals in this area of research, in which the Special Issue
Acanthamoeba spp. as Factors for Severe Infectious Diseases in Humans” includes papers on the serious infections caused in people by amphizoic amoebae. The publications in this Special Issue cover an important spectrum of current research subjects: mainly, the problems relating to the fatal granulomatous encephalitis and Acanthamoeba keratitis, connected by their associated high risk of visual deterioration. There are many challenges associated with the extreme resistance of Acanthamoeba cysts to chemicals. Preventive actions are major factors inhibiting the risk of GAE and AK; however, the ability to inhibit the spread of Acanthamoeba infections is limited, due to the common occurrence of the amoebae in various environments.
There is an urgent need for further research work to develop effective and reliable Acanthamoeba diagnostic tests.
Future studies will make significant impacts by identifying novel agents/drugs that are able to cross the blood–brain barrier and will be extremely important for progression in terms of treatment efficacy.
Innovative concepts in the search for anti-adhesive agents are needed to improve the prevention of amoebic infection in humans.
Taking proper care in the handling of contact lenses is extremely important for the reasons we have described.
Moreover, advanced research is needed in order to enhance the anti-adhesive activity of contact-lens solutions.
Further studies are also needed to examine the ability of amphizoic amoebae in dispersing endosymbionts that are pathogenic to humans.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Červa, L.; Novak, K. Amoebic meningoencephalitis: Sixteen fatalities. Science 1968, 160, 92. [Google Scholar] [CrossRef] [PubMed]
  2. Naginton, J.; Watson, P.G.; Playfair, T.J.; McGill, J.; Jones, B.R.; Steele, A.D. Amoebic infection of the eye. Lancet 1974, 2, 1537–1540. [Google Scholar] [CrossRef] [PubMed]
  3. Martinez, A.J.; Visvesvara, G.S. Free-living, amphizoic and opportunistic amoebas. Brain Pathol. 1997, 7, 583–598. [Google Scholar] [CrossRef] [PubMed]
  4. Walochnik, J.; Obwaller, A.; Aspöck, H. Correlations between morphological, molecular biological, and physiological characteristics in clinical and nonclinical isolates of Acanthamoeba spp. Appl. Environ. Microbiol. 2000, 66, 4408–4413. [Google Scholar] [CrossRef] [PubMed]
  5. Brindley, N.; Matin, A.; Khan, N.A. Acanthamoeba castellanii: High antibody prevalence in racially and ethnically diverse populations. Exp. Parasitol. 2009, 121, 254–256. [Google Scholar] [CrossRef] [PubMed]
  6. Marciano-Cabral, F.; Cabral, G. Acanthamoeba spp. as agents of disease in humans. Clin. Microbiol. Rev. 2003, 16, 273–307. [Google Scholar] [CrossRef] [PubMed]
  7. Schuster, F.L.; Visvesvara, G.S. Free-living amoebae as opportunistic and non-opportunistic pathogens of humans and animals. Int. J. Parasitol. 2004, 34, 1001–1027. [Google Scholar] [CrossRef] [PubMed]
  8. Khan, N.A. Acanthamoeba: Biology and Pathogenesis, 2nd ed.; Caister Academic Press: Wymondham, UK, 2015. [Google Scholar]
  9. Damhorst, G.L.; Watts, A.; Hernandez-Romieu, A.; Mel, N.; Palmore, M.; Ali, I.K.M.; Neil, S.G.; Kalapila, A.; Cope, J.R. Acanthamoeba castellanii encephalitis in a patient with AIDS: A case report and literature review. Lancet Infect. Dis. 2022, 22, e59–e65. [Google Scholar] [CrossRef] [PubMed]
  10. Mazur, T.; Jóźwiak, M. Extracerebral infections Acanthamoeba spp. in mice. Wiad. Parazytol. 1993, 39, 357–360. [Google Scholar] [PubMed]
  11. Lorenzo-Morales, J.; Khan, N.A.; Walochnik, J. An update on Acanthamoeba keratitis: Diagnosis, pathogenesis and treatment. Parasite 2015, 22, 10–15. [Google Scholar] [CrossRef] [PubMed]
  12. Iovieno, A.; Ledee, D.R.; Miller, D.; Alfonso, E.C. Detection of bacterial endosymbionts in clinical Acanthamoeba isolates. Ophthalmology 2010, 117, 445–452. [Google Scholar] [CrossRef] [PubMed]
  13. Muthukumar, V.; Shi, L.; Chai, N.; Langenbucher, A.; Becker, S.L.; Seitz, B.; Orosz, E.; Stachon, T.; Kiderlen, A.F.; Bischoff, M.; et al. Efficacy of Off-Label Anti-Amoebic Agents to Suppress Trophozoite Formation of Acanthamoeba spp. on Non-Nutrient Agar Escherichia Coli Plates. Microorganisms 2022, 10, 1642. [Google Scholar] [CrossRef] [PubMed]
  14. Niederkorn, J.Y. The Biology of Acanthamoeba Keratitis. Exp. Eye Res. 2021, 202, 108365. [Google Scholar] [CrossRef] [PubMed]
  15. Padzik, M.; Chomicz, L.; Bluszcz, J.; Maleszewska, K.; Grobelny, J.; Conn, D.B.; Hendiger, E.B. Tannic Acid-Modified Silver Nanoparticles in Conjunction with Contact Lens Solutions Are Useful for Progress against the Adhesion of Acanthamoeba spp. to Contact Lenses. Microorganisms 2022, 10, 1076. [Google Scholar] [CrossRef] [PubMed]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Chomicz, L.; Szaflik, J.P.; Baltaza, W. Acanthamoeba spp. as Factors for Severe Infectious Diseases in Humans. Microorganisms 2024, 12, 581. https://doi.org/10.3390/microorganisms12030581

AMA Style

Chomicz L, Szaflik JP, Baltaza W. Acanthamoeba spp. as Factors for Severe Infectious Diseases in Humans. Microorganisms. 2024; 12(3):581. https://doi.org/10.3390/microorganisms12030581

Chicago/Turabian Style

Chomicz, Lidia, Jacek P. Szaflik, and Wanda Baltaza. 2024. "Acanthamoeba spp. as Factors for Severe Infectious Diseases in Humans" Microorganisms 12, no. 3: 581. https://doi.org/10.3390/microorganisms12030581

APA Style

Chomicz, L., Szaflik, J. P., & Baltaza, W. (2024). Acanthamoeba spp. as Factors for Severe Infectious Diseases in Humans. Microorganisms, 12(3), 581. https://doi.org/10.3390/microorganisms12030581

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop