Open Access
| Issue |
Med Sci (Paris)
Volume 41, Number 10, Octobre 2025
|
|
|---|---|---|
| Page(s) | 743 - 752 | |
| Section | M/S Revues | |
| DOI | https://doi.org/10.1051/medsci/2025140 | |
| Published online | 19 November 2025 | |
- Salazar-Ardiles C, Asserella-Rebollo L, Andrade DC. Free-living amoebas in extreme environments: the true survival in our planet. BioMed Res Int 2022 ; 2022 : 2359883. [Google Scholar]
- Samba-Louaka A, Delafont V, Rodier M-H, et al. Free-living amoebae and squatters in the wild: ecological and molecular features. FEMS Microbiol Rev 2019 ; 43 : 415–34. [Google Scholar]
- Visvesvara GS, Moura H, Schuster FL. Pathogenic and opportunistic free-living amoebae: Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri, and Sappinia diploidea. FEMS Immunol. Med Microbio. 2007 ; 50 : 1–26. [Google Scholar]
- Anderson OR. A Half-century of research on free-living Amoebae (1965-2017): review of biogeographic, ecological and physiological studies. Acta Protozool 2018 ; 2018 : 1–28. [Google Scholar]
- Walochnik J. Amoebae. In : Florin-Christensen M, Schnittger L, editors. Parasitic Protozoa of Farm Animals and Pets. Cham : Springer International Publishing, 2018 : 389–412. [Google Scholar]
- Vingataramin Y, Delumeau A, Quétel I, et al. Characterization of the natural bacterial microbiota of pathogenic free-living amoebae (Acanthamoeba spp. and Naegleria fowleri) isolated from rivers and tap water in Guadeloupe. Sci Total Environ 2025 ; 975 : 179204. [Google Scholar]
- Sykora JL, Keleti G, Martinez AJ. Occurrence and pathogenicity of Naegleria fowleri in artificially heated waters. Appl. Environ. Microbiol. 1983 ; 45 : 974–9. [Google Scholar]
- Delumeau A, Quétel I, Harnais F, et al. Bacterial microbiota management in free-living amoebae (Heterolobosea lineage) isolated from water: the impact of amoebae identity, grazing conditions, and passage number. Sci Total Environ 2023 ; 900 : 165816. [Google Scholar]
- Biglarnia F, Solhjoo K, Rezanezhad H, et al. Isolation and identification of potentially pathogenic free-living amoeba in dialysis fluid samples of hydraulic systems in hemodialysis units. Trans R Soc Trop Med Hyg 2022 ; 116 : 454–61. [Google Scholar]
- Jalilehvand M, Hajialilo E, Ghiasi Y, et al. Isolation and identification of free living Amoeba from patients and contact lens users in Iran. Iran J Parasitol 2022 ; 17 : 167–73. [Google Scholar]
- Khatoonaki H, Solhjoo K, Rezanezhad H, et al. Isolation and identification of potentially pathogenic free-living amoeba in dental-unit water samples. J Water Health 2022 ; 20 : 1126–36. [Google Scholar]
- Reynaud Y, Gelasse A, Multigner L, et al. Looking for pathogens in Dust from North Africa arriving in the french West Indies using metabarcoding and cultivable analysis. Microorganisms 2024 ; 12 : 2111. [Google Scholar]
- Thomas V, McDonnell G, Denyer SP, et al. Free-living amoebae and their intracellular pathogenic microorganisms: risks for water quality. FEMS Microbiol Rev 2010 ; 34 : 231–59. [Google Scholar]
- Pánek T, Simpson AGB, Brown MW, et al. Heterolobosea. In : Archibald JM, Simpson AGB, Slamovits CH, et al., editors. Handbook of the Protists Cham : Springer International Publishing, 2017 : 1–42. [Google Scholar]
- Mathavarajah S, Flores A, Huber RJ. Dictyostelium discoideum: a model system for cell and developmental biology. Curr Protoc Essent Lab Tech 2017 ; 15 : 14.1.1–19. [Google Scholar]
- Shmakova L, Bondarenko N, Smirnov A. viable species of Flamella (Amoebozoa: Variosea) isolated from ancient Arctic permafrost sediments. Protist 2016 ; 167 : 13–30. [Google Scholar]
- Adl SM, Simpson Alastair G, Lane CE, et al. The revised classification of eukaryotes. J Eukaryot Microbiol 2012 ; 59 : 429–93. [Google Scholar]
- Dinda SK, Hazra S, De A, et al. Amoebae: beyond pathogens-exploring their benefits and future potential. Front Cell Infect Microbiol 2024 ; 14 : 1518925. [Google Scholar]
- Rossine FW, Vercelli GT, Tarnita CE, et al. Structured foraging of soil predators unveils functional responses to bacterial defenses. Proc Natl Acad Sci USA. 2022 ; 119 : e2210995119. [Google Scholar]
- Choi A, Seong JW, Kim JH, et al. Presence and diversity of free-living amoebae and their potential application as water quality indicators. Parasites Hosts Dis 2024 ; 62 : 180–92. [Google Scholar]
- Steinert M. Pathogen-host interactions in Dictyostelium, Legionella, Mycobacterium and other pathogens. Semin Cell Dev Biol 2011 ; 22 : 70–6. [Google Scholar]
- Thewes S, Soldati T, Eichinger L. Editorial: Amoebae as host models to study the interaction with pathogens. Front Cell Infect Microbiol 2019 ; 9 : 47. [Google Scholar]
- Price CTD, Hanford HE, Al-Quadan T, et al. Amoebae as training grounds for microbial pathogens. mBio 2024 ; 15 : e00827–24. [Google Scholar]
- Rojo JU, Rajendran R, Nyangau EM, et al. Seroprevalence of Naegleria fowleri in the Houston-Galveston Texas population. Parasitol Res 2024 ; 123 : 421. [Google Scholar]
- Sarink MJ, Meijs NL van der, Denzer K, et al. Three encephalitis-causing amoebae and their distinct interactions with the host. Trends Parasitol 2022 ; 38 : 230–45. [Google Scholar]
- Bhosale NK, Parija SC. Balamuthia mandrillaris: An opportunistic, free-living ameba – An updated review. Trop Parasitol 2021 ; 11 : 78–88. [Google Scholar]
- Abdouni B, Lehoux M, Wolf L, et al. Encéphalite granulomateuse amibienne : à propos d’un cas. Prat Neuro. - FMC 2022 ; 13 : 124–9. [Google Scholar]
- Salazar-Ardiles C, Paredes Valencia K, Andrade DC. Amoebas: the omnipotent organism and silent assassin. Mol Biol Rep 2025 ; 52 : 160. [Google Scholar]
- Greub G, Raoult D. Microorganisms resistant to free-living amoebae. Clin Microbiol Rev 2004 ; 17 : 413–33. [Google Scholar]
- Steenbergen JN, Nosanchuk JD, Malliaris SD, et al. Cryptococcus neoformans virulence is enhanced after growth in the genetically malleable host Dictyostelium discoideum. Infect Immun 2003 ; 71 : 4862–72. [Google Scholar]
- Aoki K, Hagiwara R, Akashi M, et al. Fifteen Marseilleviruses newly isolated from three water samples in Japan reveal local diversity of Marseilleviridae. Front Microbiol 2019 ; 10. [Google Scholar]
- Winiecka-Krusnell J, Dellacasa-Lindberg I, Dubey JP, et al. Toxoplasma gondii: uptake and survival of oocysts in free-living amoebae. Exp Parasitol 2009 ; 121 : 124–31. [Google Scholar]
- Rowbotham TJ. Preliminary report on the pathogenicity of Legionella pneumophila for freshwater and soil amoebae. J Clin Pathol 1980 ; 33 : 1179–83. [Google Scholar]
- Shi Y, Queller DC, Tian Y, et al. The ecology and evolution of Amoeba-Bacterium interactions. Appl Environ Microbiol 2021 ; 87 : e01866–20. [Google Scholar]
- Van der Henst C, Scrignari T, Maclachlan C, et al. An intracellular replication niche for Vibrio cholerae in the amoeba Acanthamoeba castellanii. ISME J. 2016 ; 10 : 897–910. [Google Scholar]
- Girard-Misguich F, Laencina L, Dubois V, et al. ESX-4, un système de sécrétion mycobactérien ancestral, essentiel pour la croissance de Mycobacterium abscessus dans les phagocytes environnementaux et humains. Med Sci 2018 ; 34 : 795–7. [Google Scholar]
- Colson P, Scola BL, Raoult D. Giant viruses of Amoebae: a journey through innovative research and paradigm changes. Annu Rev Virol 2017 ; 4 : 61–85. [Google Scholar]
- Claverie J-M, Abergel C. Les virus géants - État des connaissances, énigmes, controverses et perspectives. Med Sci (Paris) 2016 ; 32 : 1087–96. [Google Scholar]
- Colson P, La Scola B, Levasseur A, et al. Mimivirus: leading the way in the discovery of giant viruses of amoebae. Nat Rev Microbiol 2017 ; 15 : 243–54. [Google Scholar]
- Mattana A, Serra C, Mariotti E, et al. Acanthamoeba castellanii promotion of in vitro survival and transmission of coxsackie b3 viruses. Eukaryot Cell 2006 ; 5 : 665–71. [Google Scholar]
- Steenbergen JN, Nosanchuk JD, Malliaris SD, et al. Interaction of Blastomyces dermatitidis, Sporothrix schenckii, and Histoplasma capsulatum with Acanthamoeba castellanii. Infect Immun 2004 ; 72 : 3478–88. [Google Scholar]
- Heilmann A, Rueda Z, Alexander D, et al. Impact of climate change on amoeba and the bacteria they host. J Assoc Med Microbiol Infect Dis Can 2024 ; 9 : 1–5. [Google Scholar]
- Wannasan A, Uparanukraw P, Songsangchun A, et al. Potentially pathogenic free-living amoebae in some flood-affected areas during 2011 chiang mai flood. Rev Inst Med Trop São Paulo 2013 ; 55 : 411–6. [Google Scholar]
- Moussa M, Tissot O, Guerlotté J, et al. Soil is the origin for the presence of Naegleria fowleri in the thermal recreational waters. Parasitol Res 2015 ; 114 : 311–5. [Google Scholar]
- Silva TCB da, Chaúque BJM, Benitez GB, et al. Global prevalence of potentially pathogenic free-living amoebae in sewage and sewage-related environments-systematic review with meta-analysis. Parasitol Res 2024 ; 123 : 48. [Google Scholar]
- Muchesa P, Mwamba O, Barnard TG, et al. Detection of free-living Amoebae using Amoebal enrichment in a wastewater treatment plant of Gauteng province, South Africa. BioMed Res Int 2014 ; 2014 : 575297. [Google Scholar]
- Meisler DM, Rutherford I, Bican FE, et al. Susceptibility of Acanthamoeba to surgical instrument sterilization techniques. Am J Ophthalmol 1985 ; 99 : 724–5. [Google Scholar]
- Moreno-Mesonero L, Soler P, Alonso JL, et al. Assessment of pathogenic protozoa in a drinking water treatment plant with UV treatment. J Environ Manage 2024 ; 366 : 121897. [Google Scholar]
- Sundermann CA, Estridge BH. Inactivation of Giardia lamblia cysts by cobalt-60 irradiation. J Parasitol 2010 ; 96 : 425–8. [Google Scholar]
- Zahid MT, Mustafa G, Sajid R, et al. Surviving chlorinated waters: bleaching sensitivity and persistence of free-living amoebae. Environ Sci Pollut Res Int 2024 ; 31 : 48073–84. [Google Scholar]
- Bornier F, Zas E, Potheret D, et al. Environmental free-living Amoebae can predate on diverse antibiotic-resistant human pathogens. Appl Environ Microbiol 2021 ; 87 : e00747–21. [Google Scholar]
- Samba-Louaka A. Amoebae as targets for toxins or effectors secreted by mammalian pathogens. Toxins 2021 ; 13 : 526. [Google Scholar]
- Charrat B, Durrmeyer M, Jaouad W, et al. Dictyostelium discoideum - Un modèle novateur pour l’étude de la phagocytose. Med Sci (Paris) 2024 ; 40 : 688–91. [Google Scholar]
- Long JJ, Luna EK, Jackson M, et al. Interactions of free-living amoebae with the rice fungal pathogen, Rhizoctonia solani. BMC Res Notes 2019 ; 12 : 746. [Google Scholar]
- Zhang Y, Xu X, Wei Z, et al. The global epidemiology and clinical diagnosis of Acanthamoeba keratitis. J Infect Public Health 2023 ; 16 : 841–52. [Google Scholar]
- Kalra SK, Sharma P, Shyam K, et al. Acanthamoeba and its pathogenic role in granulomatous amebic encephalitis. Exp Parasitol 2020 ; 208 : 107788. [Google Scholar]
- Lorenzo-Morales J, Cabello-Vílchez AM, Martín-Navarro CM, et al. Is Balamuthia mandrillaris a public health concern worldwide? Trends Parasitol 2013 ; 29 : 483–8. [Google Scholar]
- Gharpure R, Bliton J, Goodman A, et al. Epidemiology and clinical characteristics of primary Amebic Meningoencephalitis caused by Naegleria fowleri: a global review. Clin Infect Dis Off Publ Infect Dis Soc Am 2021 ; 73 : e19–e27. [Google Scholar]
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