- 1Institut Pasteur de la Guadeloupe, Les Abymes, Guadeloupe, France
- 2Laboratoire Ecologie et Biologie des Interactions, Université de Poitiers, Unité Mixte de Recherche (UMR) Centre national de la recherche scientifique (CNRS) 7267, Poitiers, France
- 3Department of Comparative Pathobiology, College of Veterinary Medicine, Purdue University, West Lafayette, IN, United States
- 4Purdue Institute for Drug Discovery (PIDD), Purdue University, West Lafayette, IN, United States
- 5Purdue Institute of Inflammation, Immunology and Infectious Disease (PI4D), Purdue University, West Lafayette, IN, United States
Editorial on the Research Topic
New advances in the biology and pathogenesis of free-living amoebae
Introduction
Free-living amoebae (FLA) are fascinating unicellular eukaryotic microorganisms found worldwide in aquatic and soil habitats. They have an important role in the ecosystems, actively feeding mainly on bacteria and other microorganisms. FLA life cycle is mainly composed of two stages: the trophozoite (the metabolically and replicative form of the amoeba) and the persistent cyst (which is highly resistant to various adverse conditions such as water disinfection processes and therapeutic treatments). While being mainly non-pathogenic, some FLA (namely Acanthamoeba and Naegleria fowleri) are currently considered emerging opportunistic pathogens (Bartrand et al., 2014; Sente et al., 2016). FLA are also well-known reservoirs of amoeba-resistant bacteria (ARB), possibly contributing to the spread of pathogenic ARB (such as Legionella), which constitutes a potential threat to water quality and human health (Samba-Louaka et al., 2019; Chaúque et al., 2022). It is therefore crucial to increase awareness of these neglected waterborne pathogens and related diseases. This Research Topic presents recent research on several FLA topics and includes studies presented by participants who attended the 19th International Free-Living Amoebae Meeting (FLAM) held in Poitiers, France, in June 2023.
Summarizing the papers accepted
In this Research Topic, Naegleria fowleri extracellular vesicles (EVs) have garnered great interest in our community, with two papers by independent lab groups being published. Russell et al. and Retana Moreira et al. have both investigated EV characterization and their effect on various clinical isolates of Naegleria fowleri, as well as on host cells such as B103 neuroblastoma or primary cultures of mouse cell microglia, using SEM methods. Staying on the theme of N. fowleri, Nadeem et al. highlight the emerging threat and “outbreak” of N. fowleri in Pakistan. This review highlights the need for improved awareness, public health measures, and water surveillance. Dereeper et al. contributed six new high-quality Naegleria genomes to establish the Naegleria genus pangenome with a near-to-complete repertoire of core and accessory genes, highlighting new architecture and functional features in Naegleria.
Excitingly, there was a description of one new putative host species of mycobacteria, Rosculus vilicus, within the environment that was published by Jessu et al.. This may pose as a potential host and transmission route for Johne's disease and should be kept a close eye on in the future.
A review from Wang et al. describes the characteristics of Acanthamoeba infection, including biological characteristics, classification, disease, and pathogenic mechanism, in order to provide a scientific basis for the diagnosis, treatment, and prevention of Acanthamoeba infection.
Loufouma Mbouaka et al. used Realtime-Glo as a novel two-dimensional (2D) cytotoxicity viability assay, being able to monitor the cell health and the pathobiology of Acanthamoeba on feeder cells. This assay could be adapted for Balamuthia pathogenicity models as well, but because Naegleria can also metabolize the propriety reagent, it may be difficult to differentiate between the pathogen or host response in that model.
One study assessed the phylogenetic diversity of the mitochondrial genome ribosomal protein S3 (rps3) over 10 strains of B. mandrillaris. Law et al. proposed that due to the copy-number variations (CNVs) and highly variable sequences of the protein tandem repeats of rps3, this could be a perfect target for a clinical genotyping assay for B. mandrillaris.
Whangviboonkij et al. presented a three-dimensional (3D) human neurospheroid model to assess the cytotoxicity and pathobiology response of B. mandrillaris. Using 3D models that mimic the human central nervous system (CNS) can provide a more physiologically relevant environment than traditional 2D cell culture for studying the pathogenicity of amoeba. These models are particularly useful for reducing the need for experiments using animal models.
Sticking to the theme of 3D models, Campolo et al. describe the aggregation and encystment of Acanthamoeba's response on various contact lens materials under the same conditions. They found that some lenses will promote this aggregation phenotype, which will induce rapid encystment of some Acanthamoeba cells within a few hours to fully mature cysts, which they believe helps Acanthamoeba to withstand the disinfection process of contact lens care solutions.
Finally, to bring all the amoebae together, Ferrins et al. describe novel chemical pharmacophores that have various inhibitory activities against Acanthamoeba sp., Naegleria fowleri, or Balamuthia mandrillaris, which have been shown to cross the blood–brain barrier. This exciting physiological property is much needed for the development of any future anti-amoebic therapeutics for CNS disease. We cannot just stop at showing the amoeba inhibitory activity and stating that in vivo pharmacokinetic/pharmacodynamic or in vivo efficacy models are necessary to “validate the compounds future potential.”
Conclusion
In conclusion, this Research Topic brings together diverse examples of the ongoing research on FLA regarding (i) FLA biology and pathogenesis (such as Naegleria pangenome or Balamuthia mandrillaris' mitochondrial heterogeneity), the role of extracellular vesicles in N. fowleri–host interaction, (ii) FLA as hosts of zoonotic bacteria, (iii) drug development against FLA (namely brain permeable therapeutics against Acanthamoeba, Naegleria, or Balamuthia), various newly described 2D and 3D pathobiological models for brain organoid, cytotoxicity, or Acanthamoeba aggregation models, and (iv) FLA epidemiology. While this surely represents a glimpse of the ongoing research worldwide, we believe that increased research in disease, epidemiology, diagnostics, and treatment of pathogenic FLA species and the characterization of other emerging FLA should be encouraged, namely within the One Health concept.
Furthermore, we expect the emergence of the use of artificial intelligence (AI) in amoebae research. Indeed, the development and application of machine learning (ML) in the field of infectious diseases have gained massive attention in recent years, including other protozoans such as Plasmodium and Trypanosoma (Hu et al., 2022). We caught a glimpse of machine learning with Dr. Rice's (unpublished data) and Dr. Debnath's (Shing et al., 2022) novel Acanthamoeba cysticidal methodologies at the recent FLAM 2023 conference. Although the European Parliament and the US administration are trying to impose obligations for general-purpose AI to mitigate possible risks to health, fundamental rights, and democracy, we are assisting in the boost of AI in research and innovation. How AI will impact research in free-living amoebae is worth investigating. Beyond the identification of trophozoites or cysts, will AI be able to predict genera of amoebae present within the water or soil during sampling campaigns? Regarding the virulence factors identified in some pathogenic amoebae, will AI suggest human outcomes or some area to investigate, interrogate, and suggest optimal patient-specific treatment options? How deep will this rapidly advancing generative AI turn our field upside down? The next FLAM to be held in Mexico City, Mexico, in 2025, could be a place for an exchange around the impact of AI on the study of amoebae.
Author contributions
IM: Writing—original draft, Writing—review & editing. AS-L: Writing—original draft, Writing—review & editing. CR: Writing—original draft, Writing—review & editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was partially funded by the EU project FEDER-Une Santé (IM).
Acknowledgments
We thank the authors of this Research Topic for their valuable contributions. We also thank all the reviewers who have given up their precious time to diligently peer-review and make impactful suggestions to the contributing authors.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's note
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References
Bartrand, T. A., Causey, J. J., and Clancy, J. L. (2014). Naegleria fowleri: An emerging drinking water pathogen. J. Am. Water Works Assoc. 106, E418–E432. doi: 10.5942/jawwa.20l4.106.0140
Chaúque, B. J. M., dos Santos, D. L., Anvari, D., and Rott, M. B. (2022). Prevalence of free-living amoebae in swimming pools and recreational waters, a systematic review and meta-analysis. Parasitol. Res. 121, 3033–3050. doi: 10.1007/s00436-022-07631-3
Hu, R. S., Hesham, A. E. L., and Zou, Q. (2022). Machine learning and its applications for protozoal pathogens and protozoal infectious diseases. Front. Cell. Infect. Microbiol. 12:882995. doi: 10.3389/fcimb.2022.882995
Samba-Louaka, A., Delafont, V., Rodier, M. H., Cateau, E., and Héchard, Y. (2019). Free-living amoebae and squatters in the wild: ecological and molecular features. FEMS Microbiol. Rev. 43, 415–434. doi: 10.1093/femsre/fuz011
Sente, C., Erume, J., Naigaga, I., Magambo, P. K., Ochwo, S., Mulindwa, J., et al. (2016). Occurrence and genetic characterisation of Acanthamoeba spp. from environmental and domestic water sources in Queen Elizabeth Protected Area, Uganda. Parasit. Vectors 9:127. doi: 10.1186/s13071-016-1411-y
Keywords: free-living amoebae, pathogenesis, FLAM 2023, Naegleria, Acanthamoeba, Balamuthia, reviews, novel methods
Citation: Marcelino I, Samba-Louaka A and Rice CA (2024) Editorial: New advances in the biology and pathogenesis of free-living amoebae. Front. Microbiol. 15:1401217. doi: 10.3389/fmicb.2024.1401217
Received: 14 March 2024; Accepted: 09 April 2024;
Published: 29 April 2024.
Edited and reviewed by: Axel Cloeckaert, Institut National de recherche pour l'agriculture, l'alimentation et l'environnement (INRAE), France
Copyright © 2024 Marcelino, Samba-Louaka and Rice. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Isabel Marcelino, IMarcelino@pasteur-guadeloupe.fr; Ascel Samba-Louaka, ascel.samba@univ-poitiers.fr; Christopher A. Rice, carice@purdue.edu