scholarly journals Encystment Induces Down-Regulation of an Acetyltransferase-Like Gene in Acanthamoeba castellanii

Pathogens ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 321 ◽  
Author(s):  
Steven Rolland ◽  
Luce Mengue ◽  
Cyril Noël ◽  
Stéphanie Crapart ◽  
Anne Mercier ◽  
...  
Keyword(s):  
Bioinformatics Analysis ◽  
Acanthamoeba Castellanii ◽  
Acanthamoeba Keratitis ◽  
Free Living ◽  
Adverse Conditions ◽  
Genetic Modifications ◽  
Granulomatous Amoebic Encephalitis ◽  
Free Living Amoeba ◽  
Causative Agents

Acanthamoeba castellanii is a ubiquitous free-living amoeba. Pathogenic strains are causative agents of Acanthamoeba keratitis and granulomatous amoebic encephalitis. In response to adverse conditions, A. castellanii differentiate into cysts, which are metabolically inactive and resistant cells. This process, also named encystment, involves biochemical and genetic modifications that remain largely unknown. This study characterizes the role of the ACA1_384820 Acanthamoeba gene during encystment. This gene encodes a putative N-acetyltransferase, belonging to the Gcn5-related N-acetyltransferase (GNAT) family. We showed that expression of the ACA1_384820 gene was down-regulated as early as two hours after induction of encystment in A. castellanii. Interestingly, overexpression of the ACA1_384820 gene affects formation of cysts. Unexpectedly, the search of homologs of ACA1_384820 in the Eukaryota gene datasets failed, except for some species in the Acanthamoeba genus. Bioinformatics analysis suggested a possible lateral acquisition of this gene from prokaryotic cells. This study enabled us to describe a new Acanthamoeba gene that is down-regulated during encystment.

scholarly journals Isoniazid Conjugated Magnetic Nanoparticles Loaded with Amphotericin B as a Potent Antiamoebic Agent against Acanthamoeba castellanii

Antibiotics ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 276
Author(s):  
Kawish Iqbal ◽  
Sumayah Abdelnasir Osman Abdalla ◽  
Ayaz Anwar ◽  
Kanwal Muhammad Iqbal ◽  
Muhammad Raza Shah ◽  
...  
Keyword(s):  
Magnetic Nanoparticles ◽  
Amphotericin B ◽  
Central Nervous System Infection ◽  
Acanthamoeba Castellanii ◽  
Acanthamoeba Keratitis ◽  
Free Living ◽  
Granulomatous Amoebic Encephalitis ◽  
Nano Drug Delivery ◽  
Free Living Amoeba ◽  
Acanthamoeba Species

The pathogenic free-living amoeba, Acanthamoeba castellanii, is responsible for a rare but deadly central nervous system infection, granulomatous amoebic encephalitis and a blinding eye disease called Acanthamoeba keratitis. Currently, a combination of biguanides, amidine, azoles and antibiotics are used to manage these infections; however, the host cell cytotoxicity of these drugs remains a challenge. Furthermore, Acanthamoeba species are capable of transforming to the cyst form to resist chemotherapy. Herein, we have developed a nano drug delivery system based on iron oxide nanoparticles conjugated with isoniazid, which were further loaded with amphotericin B (ISO-NPs-AMP) to cause potent antiamoebic effects against Acanthamoeba castellanii. The IC50 of isoniazid conjugated with magnetic nanoparticles and loaded with amphotericin B was found to be 45 μg/mL against Acanthamoeba castellanii trophozoites and 50 μg/mL against cysts. The results obtained in this study have promising implications in drug discovery as these nanomaterials exhibited high trophicidal and cysticidal effects, as well as limited cytotoxicity against rat and human cells.

scholarly journals Vibrio cholerae O139 requires neither capsule nor LPS O side chain to grow inside Acanthamoeba castellanii

2009 ◽  
Vol 58 (1) ◽  
pp. 125-131 ◽  
Author(s):  
Hadi Abd ◽  
Amir Saeed ◽  
Andrej Weintraub ◽  
Gunnar Sandström
Keyword(s):  
Vibrio Cholerae ◽  
Acanthamoeba Castellanii ◽  
Side Chain ◽  
Wild Type ◽  
Intracellular Growth ◽  
Free Living ◽  
Growth And Survival ◽  
Free Living Amoeba ◽  
Vibrio Cholerae O139

Vibrio cholerae, the causative agent of cholera, has the ability to grow and survive in the aquatic free-living amoeba Acanthamoeba castellanii. The aim of the present study was to examine the ability of the clinical isolate V. cholerae O139 MO10 to grow in A. castellanii and to determine the effect of the bacterial capsule and LPS O side chain on intracellular growth. Results from co-cultivation, viable counts, a gentamicin assay, electron microscopy and statistical analysis showed that the association of V. cholerae O139 MO10 with A. castellanii did not inhibit growth of the amoeba, and enhanced growth and survival of V. cholerae O139 MO10 occurred. The wild-type V. cholerae O139 MO10 and a capsule mutant or capsule/LPS double mutant grew inside A. castellanii. Neither the capsule nor the LPS O side chain of V. cholerae O139 was found to play an important role in the interaction with A. castellanii, disclosing the ability of V. cholerae to multiply and survive inside A. castellanii, as well as the role of A. castellanii as an environmental host for V. cholerae.

Acanthamoeba spp. monoclonal antibody against a CPA2 transporter: a promising molecular tool for acanthamoebiasis diagnosis and encystment study

Parasitology ◽  
2020 ◽  
Vol 147 (14) ◽  
pp. 1678-1688
Author(s):  
Michele Martha Weber-Lima ◽  
Bianca Prado-Costa ◽  
Alessandra Becker-Finco ◽  
Adriana Oliveira Costa ◽  
Philippe Billilad ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Diagnostic Methods ◽  
Free Living ◽  
Immunoprecipitation Assay ◽  
Granulomatous Amoebic Encephalitis ◽  
Free Living Amoeba ◽  
Amoebic Keratitis ◽  
Low Sensitivity

AbstractFree-living amoeba of the genus Acanthamoeba are ubiquitous protozoa involved in opportunistic and non-opportunistic infection in humans, such as granulomatous amoebic encephalitis and amoebic keratitis. Both infections have challenging characteristics such as the formation of the resistant cysts in infected tissues, hampering the treatment and most usual diagnosis depending on time-consuming and/or low sensitivity techniques. The use of monoclonal antibodies presents itself as an opportunity for the development of more effective alternative diagnostic methods, as well as an important and useful tool in the search for new therapeutic targets. This study investigated the possibility of using a previously produced monoclonal antibody (mAb3), as a diagnostic tool for the detection of Acanthamoeba trophozoites by direct and indirect flow cytometry and immunofluorescence. Immunoprecipitation assay and mass spectrometry allowed the isolation of the antibody's target and suggested it is a transporter part of the CPA (cation: proton antiporter) superfamily. In vitro tests indicate an important role of this target in Acanthamoeba's encystment physiology. Our results support the importance of studying the role of CPA2 transporters in the context of acanthamoebiasis, as this may be a way to identify new therapeutic candidates.

scholarly journals Overexpression of a G-protein coupled receptor-like gene affects encystment of Acanthamoeba castellanii

2021 ◽  
Author(s):  
Steven Rolland ◽  
Anne Mercier ◽  
Luce Mengue ◽  
Yann Hechard ◽  
Ascel Samba-Louaka
Keyword(s):  
G Protein ◽  
Early Phase ◽  
Acanthamoeba Castellanii ◽  
Pathogenic Microorganisms ◽  
G Protein Coupled Receptor ◽  
Free Living ◽  
Vegetative Form ◽  
Free Living Amoeba ◽  
G Protein Coupled

Acanthamoeba castellanii is an amphizoic free-living amoeba as it can be found in humans and in the environment. This amoeba represents an important reservoir of pathogenic microorganisms. Persistence of A. castellanii in the environment or in humans is allowed by the ability of the vegetative form to differentiate under cysts when surrounding conditions are unfavorable. In this study, we investigate the role of the ACA1_383450 gene during encystment of A. castellanii. This gene encodes a putative G-protein coupled receptor, which shares homology with human GPR107 and murine GPR108. Expression of the ACA1_383450 gene is transiently repressed at the early phase of encystment and its overexpression affects encystment of A. castellanii. This study reveals a new Acanthamoeba gene which could affect the encystment process.

scholarly journals Molecular Identification of Pathogenic Free-Living Amoeba from Household Biofilm Samples in Iran: A Risk Factor for Acanthamoeba Keratitis

2021 ◽  
Vol 9 (10) ◽  
pp. 2098
Author(s):  
Maryam Norouzi ◽  
Reza Saberi ◽  
Maryam Niyyati ◽  
Jacob Lorenzo-Morales ◽  
Hamed Mirjalali ◽  
...  
Keyword(s):  
Contact Lenses ◽  
Opportunistic Infections ◽  
Acanthamoeba Keratitis ◽  
Free Living ◽  
Pathogenic Potential ◽  
Ability Test ◽  
Soft Contact Lenses ◽  
Increased Risk ◽  
Free Living Amoeba ◽  
Causative Agents

Free-living amoeba (FLA) are ubiquitously distributed in the environment. However, they are also the causative agents of opportunistic infections in humans and other animals. A biofilm comprises any syntrophic consortium of microorganisms in which cells stick to each other and often also to a surface. Moreover, FLA have been detected in various biofilms around the world. Therefore, the present study aimed to check for presence of FLA in samples from household biofilms in Iran and to characterize them at the molecular level. A total of 69 biofilm samples collected from showerheads, kitchen areas, and bathroom sinks were analyzed. Positive samples for FLA were characterized at the morphological and molecular levels. Furthermore, the results of morphology analysis indicated that 26.08% (18/69) of biofilm samples were positive for Acanthamoeba spp., Vermamoeba genus, and Vahlkampfiids. According to sequence analysis, five strains of Acanthamoeba isolates related to the T4 genotype and two strains belonged to the T2 genotype. In addition, the pathogenic potential of Acanthamoeba-positive isolates was conducted using the tolerance ability test. The results of BLASTn of Vermamoeba sequences were similar to what was expected for Vermamoeba vermiformis. The above-mentioned reasons revealed that the relative high contamination of household biofilm samples with FLA may pose a risk for people using soft contact lenses and for patients with traumatic cataract. Our finding proposes that filtration should be performed in shower heads and indicates the need to monitor people at increased risk of Acanthamoeba keratitis.

Comparative analyses of different genetic markers for the detection of Acanthamoeba spp. isolates

2014 ◽  
Vol 59 (3) ◽  
Author(s):  
Monika Derda ◽  
Agnieszka Wojtkowiak-Giera ◽  
Edward Hadaś
Keyword(s):  
Genetic Markers ◽  
Tap Water ◽  
Correct Diagnosis ◽  
Specific Marker ◽  
Pcr Assay ◽  
Free Living ◽  
Detection And Identification ◽  
Granulomatous Amoebic Encephalitis ◽  
Free Living Amoeba ◽  
Treatment Of Infection

AbstractAcanthamoeba are widespread free-living amoebae which may cause granulomatous amoebic encephalitis (GAE), keratitis, skin ulcerations and disseminated tissue infection. An important diagnostic and prognostic factor for the treatment of infection is a quick and correct diagnosis of amoebae strains. The aim of our study was to develop a rapid method for detection and identification of pathogenic Acanthamoeba spp. strains from diagnostic material collected from water. In this study we analysed five amplification-based genetic markers (Aca 16S, Ac6/210, GP, JDP, Nelson) used for identification of pathogenic Acanthamoeba spp. strains isolated in water sources in Poland, Iceland and Sweden. Our results demonstrated the presence of pathogenic Acanthamoeba strains in tap water. PCR assay appeared to be a more rapid and sensitive method to detect the presence of amoebae than the limited conventional techniques. Based on our observations, we can confirm that the use of four out of five genetic markers (Aca 16S, Ac 6/210, JDP, GP, Nelson) may be helpful in identification of Acanthamoeba spp. strains, but only one Aca 16S primer pair is a highly specific marker that distinguishes between pathogenic strains of Acanthamoeba and other free-living amoeba families.

scholarly journals Mitigation of Expression of Virulence Genes in Legionella pneumophila Internalized in the Free-Living Amoeba Willaertia magna C2c Maky

Pathogens ◽  
2020 ◽  
Vol 9 (6) ◽  
pp. 447 ◽  
Author(s):  
Rayane Mouh Mameri ◽  
Jacques Bodennec ◽  
Laurent Bezin ◽  
Sandrine Demanèche
Keyword(s):  
Gene Expression ◽  
Legionella Pneumophila ◽  
Virulence Genes ◽  
Natural Habitat ◽  
Acanthamoeba Castellanii ◽  
Severe Form ◽  
Aquatic Environments ◽  
Free Living ◽  
Intracellular Parasites ◽  
Free Living Amoeba

Legionella pneumophila is a human pathogen responsible for a severe form of pneumonia named Legionnaire disease. Its natural habitat is aquatic environments, being in a free state or intracellular parasites of free-living amoebae, such as Acanthamoeba castellanii. This pathogen is able to replicate within some amoebae. Willaertia magna C2c Maky, a non-pathogenic amoeba, was previously demonstrated to resist to L. pneumophila and even to be able to eliminate the L. pneumophila strains Philadelphia, Lens, and Paris. Here, we studied the induction of seven virulence genes of three L. pneumophila strains (Paris, Philadelphia, and Lens) within W. magna C2c Maky in comparison within A. castellanii and with the gene expression level of L. pneumophila strains alone used as controls. We defined a gene expression-based virulence index to compare easily and without bias the transcript levels in different conditions and demonstrated that W. magna C2c Maky did not increase the virulence of L. pneumophila strains in contrast to A. castellanii. These results confirmed the non-permissiveness of W. magna C2c Maky toward L. pneumophila strains.

scholarly journals Enhanced Killing of Acanthamoeba Cysts with a Plant Peroxidase-Hydrogen Peroxide-Halide Antimicrobial System

2003 ◽  
Vol 69 (5) ◽  
pp. 2563-2567 ◽  
Author(s):  
Reanne Hughes ◽  
Peter W. Andrew ◽  
Simon Kilvington
Keyword(s):  
Hydrogen Peroxide ◽  
Horseradish Peroxidase ◽  
Contact Lens ◽  
Acanthamoeba Keratitis ◽  
Free Living ◽  
Soybean Peroxidase ◽  
Plant Peroxidase ◽  
Time Points ◽  
Free Living Amoeba ◽  
Care Systems

ABSTRACT The activity of H2O2 against the resistant cyst stage of the pathogenic free-living amoeba Acanthamoeba was enhanced by the addition of KI and either horseradish peroxidase or soybean peroxidase or, to a lesser degree, lactoperoxidase. This resulted in an increase in the cysticidal activity of 3% (wt/vol) H2O2, and there was >3-log killing in 2 h, compared with the 6 h required for comparable results with the peroxide solution alone (P < 0.05). With 2% H2O2, enhancement was observed at all time points (P < 0.05), and total killing of the cyst inoculum occurred at 4 h, compared with 6 h for the peroxide alone. The activity of sublethal 1% H2O2 was enhanced to give 3-log killing after 8 h of exposure (P < 0.05). No enhancement was obtained when KCl or catalase was used as a substitute in the reaction mixtures. The H2O2 was not neutralized in the enhanced system during the experiments. However, in the presence of a platinum disk used to neutralize H2O2 in contact lens care systems, the enhanced 2% H2O2 system gave 2.8-log killing after 6 h or total cyst killing by 8 h, and total neutralization of the H2O2 occurred by 4 h. In contrast, 2% H2O2 alone resulted in <0.8-log killing of cysts in the presence of the platinum disk due to rapid (<1 h) neutralization of the peroxide. Our observations could result in significant improvement in the efficacy of H2O2 contact lens disinfection systems against Acanthamoeba cysts and prevention of acanthamoeba keratitis.

scholarly journals Legionella pneumophila Contains a Type II General Secretion Pathway Required for Growth in Amoebae as Well as for Secretion of the Msp Protease

1999 ◽  
Vol 67 (7) ◽  
pp. 3662-3666 ◽  
Author(s):  
Laura M. Hales ◽  
Howard A. Shuman
Keyword(s):  
Legionella Pneumophila ◽  
Acanthamoeba Castellanii ◽  
Gram Negative Bacteria ◽  
Type Ii ◽  
Free Living ◽  
Gram Negative ◽  
Secretion Pathway ◽  
Free Living Amoeba ◽  
Substitution Mutation

ABSTRACT We report the identification of a set of Legionella pneumophila genes that encode products with homology to proteins of the type II general secretion pathway of gram-negative bacteria. A strain containing a deletion-substitution mutation of two of these genes was unable to secrete the Msp protease. This strain was unable to multiply within the free-living amoeba Acanthamoeba castellanii yet was able to kill HL-60-derived macrophages. Because Msp is not required for growth in amoebae, other proteins which are important for growth in amoebae are likely secreted by this pathway.

Synthesis of diphosphoinositide by a supernatant fraction from Acanthamoeba castellanii

1976 ◽  
Vol 54 (9) ◽  
pp. 772-777 ◽  
Author(s):  
J. Thomas Buckley
Keyword(s):  
Acanthamoeba Castellanii ◽  
Supernatant Fraction ◽  
Two Dimensional ◽  
Free Living ◽  
Low Concentrations ◽  
Free Living Amoeba

Homogenates of the free-living amoeba Acanthamoeba castellanii incorporate phosphate from [γ-32P]ATP into a lipid which co-chromatographs with diphosphoinositide on one- and two-dimensional chromatography. Incorporation into lipids similar in mobility to triphosphoinositide is not detected. The product co-chromatographs with diphosphoinositide whether exogenous phosphatidylinositol or total amoeba lipid is the substrate. The inositide kinase is almost entirely located in the supernatant fraction after centrifugation at 100 000 g. Incorporation of phosphate from [γ-32P]ATP is linear for at least 15 min in the presence of 0.5 mM phosphatidylinositol. The enzyme requires Mg2+ or Mn2+ as well as ATP and it is not affected by low concentrations of Ca2+. The apparent Km for phosphatidylinositol is 2 mM. Both ADP and cAMP inhibit the reaction.

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