Immunological and inflammatory responses in the kidneys in experimental acanthamoebiasis

ABSTRACT The pathomechanisms of Acanthamoeba spp. infection are still poorly understood. The aim of the study was to determine the expression of the NLR family pyrin domain-containing protein 3 (NLRP3), prostaglandin-endoperoxide synthase 2 (PTGS2, commonly known as cyclooxygenase-2, COX-2), and var...

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Main Authors: Karolina Kot, Patrycja Tomasiak, Maciej Tarnowski, Danuta Kosik-Bogacka, Natalia Łanocha-Arendarczyk
Format: Article
Language:English
Published: American Society for Microbiology 2025-08-01
Series:Microbiology Spectrum
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Online Access:https://journals.asm.org/doi/10.1128/spectrum.00243-25
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author Karolina Kot
Patrycja Tomasiak
Maciej Tarnowski
Danuta Kosik-Bogacka
Natalia Łanocha-Arendarczyk
author_facet Karolina Kot
Patrycja Tomasiak
Maciej Tarnowski
Danuta Kosik-Bogacka
Natalia Łanocha-Arendarczyk
author_sort Karolina Kot
collection DOAJ
description ABSTRACT The pathomechanisms of Acanthamoeba spp. infection are still poorly understood. The aim of the study was to determine the expression of the NLR family pyrin domain-containing protein 3 (NLRP3), prostaglandin-endoperoxide synthase 2 (PTGS2, commonly known as cyclooxygenase-2, COX-2), and various cytokines in the kidneys of immunocompetent and immunosuppressed mice infected with Acanthamoeba sp. (T16 genotype). The proteins were analyzed by quantitative reverse transcription PCR. In immunocompetent mice, we observed increased mRNA levels of interferon gamma (IFNγ), tumor necrosis factor alpha (TNFα), PTGS2/COX-2, and interleukin (IL)-17A at the beginning of infection. While in the late stages, we found decreased levels of NLRP3, IL-1β, IL-10, IL-17A, IL-21, IL-23, IFNγ, TNFα, and macrophage inflammatory protein-2 (MIP-2) in the kidneys of infected hosts compared to uninfected ones. In immunosuppressed mice, we noted higher expressions of NLRP3, PTGS2/COX-2, IL-1β, IL-10, IL-17A, IL-21, IFNγ, TNFα, and MIP-2, and lower expression of IL-18 in the infected mice compared to the control group. The basic understanding of the immune response during Acanthamoeba sp. infection is critical to improving clinical outcomes and also has significant implications for developing therapeutic interventions. Here, we have reported the inflammatory responses in the kidneys infected with Acanthamoeba sp. However, additional studies are needed to understand the specific beneficial and detrimental roles of the cytokine response.IMPORTANCEAcanthamoeba spp. are significant biological factors and can cause rare infections characterized by high mortality and difficulty with treatment. One of the reasons Acanthamoeba spp. persist so effectively in the body is a lack of knowledge about the pathomechanisms and pathophysiology of infections. Recent studies showed that Acanthamoeba spp. can also infect the kidneys in the hosts, being an important cause of medical complications. A better understanding of the mechanisms by which Acanthamoeba spp. cause kidney injury could lead to more effective treatments for systemic acanthamoebiasis.
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spelling doaj-art-d2eae38691bf413986503f62eb77e1df2025-08-20T04:00:44ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972025-08-0113810.1128/spectrum.00243-25Immunological and inflammatory responses in the kidneys in experimental acanthamoebiasisKarolina Kot0Patrycja Tomasiak1Maciej Tarnowski2Danuta Kosik-Bogacka3Natalia Łanocha-Arendarczyk4Department of Biology, Parasitology, and Pharmaceutical Botany, Pomeranian Medical University in Szczecin, Szczecin, PolandInstitute of Physical Culture Sciences, University of Szczecin, Szczecin, PolandDepartment of Physiology in Health Sciences, Pomeranian Medical University in Szczecin, Szczecin, PolandDepartment of Biology, Parasitology, and Pharmaceutical Botany, Pomeranian Medical University in Szczecin, Szczecin, PolandDepartment of Biology, Parasitology, and Pharmaceutical Botany, Pomeranian Medical University in Szczecin, Szczecin, PolandABSTRACT The pathomechanisms of Acanthamoeba spp. infection are still poorly understood. The aim of the study was to determine the expression of the NLR family pyrin domain-containing protein 3 (NLRP3), prostaglandin-endoperoxide synthase 2 (PTGS2, commonly known as cyclooxygenase-2, COX-2), and various cytokines in the kidneys of immunocompetent and immunosuppressed mice infected with Acanthamoeba sp. (T16 genotype). The proteins were analyzed by quantitative reverse transcription PCR. In immunocompetent mice, we observed increased mRNA levels of interferon gamma (IFNγ), tumor necrosis factor alpha (TNFα), PTGS2/COX-2, and interleukin (IL)-17A at the beginning of infection. While in the late stages, we found decreased levels of NLRP3, IL-1β, IL-10, IL-17A, IL-21, IL-23, IFNγ, TNFα, and macrophage inflammatory protein-2 (MIP-2) in the kidneys of infected hosts compared to uninfected ones. In immunosuppressed mice, we noted higher expressions of NLRP3, PTGS2/COX-2, IL-1β, IL-10, IL-17A, IL-21, IFNγ, TNFα, and MIP-2, and lower expression of IL-18 in the infected mice compared to the control group. The basic understanding of the immune response during Acanthamoeba sp. infection is critical to improving clinical outcomes and also has significant implications for developing therapeutic interventions. Here, we have reported the inflammatory responses in the kidneys infected with Acanthamoeba sp. However, additional studies are needed to understand the specific beneficial and detrimental roles of the cytokine response.IMPORTANCEAcanthamoeba spp. are significant biological factors and can cause rare infections characterized by high mortality and difficulty with treatment. One of the reasons Acanthamoeba spp. persist so effectively in the body is a lack of knowledge about the pathomechanisms and pathophysiology of infections. Recent studies showed that Acanthamoeba spp. can also infect the kidneys in the hosts, being an important cause of medical complications. A better understanding of the mechanisms by which Acanthamoeba spp. cause kidney injury could lead to more effective treatments for systemic acanthamoebiasis.https://journals.asm.org/doi/10.1128/spectrum.00243-25Acanthamoeba sp.COX-2cytokinesimmunological statuskidneysNLRP3
spellingShingle Karolina Kot
Patrycja Tomasiak
Maciej Tarnowski
Danuta Kosik-Bogacka
Natalia Łanocha-Arendarczyk
Immunological and inflammatory responses in the kidneys in experimental acanthamoebiasis
Microbiology Spectrum
Acanthamoeba sp.
COX-2
cytokines
immunological status
kidneys
NLRP3
title Immunological and inflammatory responses in the kidneys in experimental acanthamoebiasis
title_full Immunological and inflammatory responses in the kidneys in experimental acanthamoebiasis
title_fullStr Immunological and inflammatory responses in the kidneys in experimental acanthamoebiasis
title_full_unstemmed Immunological and inflammatory responses in the kidneys in experimental acanthamoebiasis
title_short Immunological and inflammatory responses in the kidneys in experimental acanthamoebiasis
title_sort immunological and inflammatory responses in the kidneys in experimental acanthamoebiasis
topic Acanthamoeba sp.
COX-2
cytokines
immunological status
kidneys
NLRP3
url https://journals.asm.org/doi/10.1128/spectrum.00243-25
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AT patrycjatomasiak immunologicalandinflammatoryresponsesinthekidneysinexperimentalacanthamoebiasis
AT maciejtarnowski immunologicalandinflammatoryresponsesinthekidneysinexperimentalacanthamoebiasis
AT danutakosikbogacka immunologicalandinflammatoryresponsesinthekidneysinexperimentalacanthamoebiasis
AT nataliałanochaarendarczyk immunologicalandinflammatoryresponsesinthekidneysinexperimentalacanthamoebiasis