Salma Younes1,2
Nouran Zein2
Shaden Abunasser2
Layla Kamareddine1,2
Natalia V. Kirienko3
Gheyath K. Nasrallah1,2*- 1Biomedical Research Center, Qatar University, Doha, Qatar
- 2Biomedical Sciences Department, College of Health Sciences, Qatar University, Doha, Qatar
- 3Department of BioSciences, Rice University, Houston, TX, United States
Editorial on the Research Topic
Unconventional animal models in infectious disease research, volume II
Infectious diseases remain a serious health threat globally, an actuality that necessitates ongoing research in this field. Among different research modalities, the use of animal models to unravel host-pathogen interactions that contribute to infectious diseases pathogenesis is on the rise. By means of simple manipulation, these model organisms could be used to study host and microbial factors contributing to disease progression, host defensive strategies, and mechanisms of pathogenic dissemination. Recent advancements in the genetics discipline has further enhanced the utilization of both conventional and unconventional animal models in research. In this launched Research Topic, we provide valuable insight on the particular use of several less-common model organisms in infectious disease research.
Among several studies published in this Research Topic, Longhuan et al. explored how different Bordetella species interact with the phagocytic predatory amoeba Dictyostelium discoideum and revealed that the human pathogen Bordetella bronchiseptica has evolved to exploit this amoeba’s life cycle to propagate and spread. Interestingly, this trait was shared by a handful of other Bordetella species as well but not by all members of this genus, as the bird pathogen B. avium and the human-restricted species B. pertussis and B. parapertussis lack this ability and do not seem able to thrive in D. discoideum. Moreover, the genome-wide association study (GWAS) conducted for this paper identified 83 genes associated with the ability of Bordetella species to evade amoebic predation. Based on these findings, the authors speculate that the Bordetella species followed different evolutionary trajectories, with some increasingly adapting to single hosts while others remained more cosmopolitan in their spread. A better understanding of how Bordetella species resist amoeba predation may reveal promising targets for interventions to treat and prevent the diseases they cause.
Another area that has benefitted from the use of unconventional animal models is studying host-pathogen interactions, particularly to investigate diseases originating from pathogens that utilize insect vectors (such as mosquitoes) to spread and infect humans. Wide-spread adoption of intense insecticidal treatment in an apparently vain attempt to eradicate this vector has driven mosquitoes to develop resistance to this treatment approach. This has encouraged scientists to score for other vector control alternatives, one of which is targeting the immune system of insect vectors to minimize the ability of a pathogen to reside inside the insect host (Habtewold et al., 2008; Edgerton et al., 2020). Around the fundamentals of this notion, the study submitted by Morejon and Michel to our Research Topic aimed to investigate the role of antimicrobial peptides (AMPs) and Toll pathway components in the antimicrobial activity of Anopheles gambiae hemolymph by developing a novel assay for measuring AMP production via growth inhibition of bacteria on agar plates. AMPs are produced by innate immune genes, and their upregulation depends on signaling pathways like Toll and Imd. The authors of the paper leverage this useful, ex vivo, medium-throughput assay to show that bacterial challenge with Micrococcus luteus in A. gambiae drives defensin 1-mediated AMP expression. Interestingly, they determined that a sterile challenge (i.e., sterile water) primed the innate immune system for a stronger reaction, suggesting that the host is engaging in some sort of immune surveillance for breaches of its body cavity. A more detailed understanding of the regulation of the mosquito immune system’s antimicrobial activity could lead to the development of innovative strategies for minimizing host infection and disease transfer.
Another insect gaining popularity for infectious disease research is the lepidopteran Galleria mellonella also known as the greater wax or the honeycomb moth. This organism has several advantages, including its moderate conservation of innate immune pathways, comparative experimental simplicity, and low cost (Bismuth et al., 2019). In one of the studies submitted to our Research Topic, Felix et al. investigated the potentiality of α-mangostin, a natural xanthone molecule, to kill methicillin-resistant Staphylococcus aureus (MRSA) persisters and to disrupt established biofilm and prevent its future formation. The authors found that the minimum inhibitory concentration for α-mangostin in persister cells was 2 µg/ml and that it quickly permeabilized the cell membrane. Although α-mangostin was found to be non-toxic to liver-derived HepG2 and lung-derived A549 cells at 8 times this concentration, it also lysed 50% of human erythrocytes. In vivo, α-mangostin increased the survival rate of Galleria mellonella larvae infected with MRSA persisters by up to 75% after 120 hours. This study presented Galleria mellonella as a potential model organism for studying infectious diseases. However, it is also a cautionary tale, reminding us that studies in closer organisms are often needed to more thoroughly assess compound toxicity before considering systemic administration. Despite this, the authors foresee some aptitude for α-mangostin as a treatment option for MRSA-related topical infections.
Another published article in our launched Research Topic by Ménard et al., reviewed the broader use of Galleria mellonella as a model for bacterial infection, focusing on immunological and microbiological aspects. The authors emphasized virulence and new therapies for many important pathogenic bacteria and discussed directions for further improvement of this model. This paper, along with other recent reviews (Junqueira, 2012; Asai et al., 2023) illustrate Galleria mellonella’s significant potential in host-pathogen interaction studies.
Honeybees are also emerging as a potential model organism in infectious disease research. In one of the articles submitted to our Research Topic, Chang et al. investigated the effect of Escherichia coli LF82, an inflammatory bowel disease-associated bacterium, on the cognitive abilities of honeybees. Exposure to LF82 increased gut permeability, impaired learning and memory, and reduced tryptophan metabolism in the gut. The study also examined transcriptome changes in the honeybee brain and found that LF82 colonization altered the expression of 255 host genes. The study suggested that LF82 can induce enteritis-like manifestations and cognitive impairment through escape of gut metabolites, causing transcriptional changes in the brain. This study expands our understanding of the link between gut microbiota and neurological disorders, a field of increasing interest (Cryan et al., 2019; Zou et al., 2023).
In conclusion, the articles highlight significant progress in infectious disease research using unconventional animal models, leading to exciting discoveries and therapies. We anticipate increased utilization of these models, driving faster progress and deeper insights into infectious diseases. Exploring unconventional animal models will advance our knowledge and interventions.
Acknowledgments
We acknowledge everyone that has contributed to the success of this volume of our Research Topic.
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
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
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Bismuth, H., Aussel, L., Ezraty, B. (2019). [The greater wax moth, galleria mellonella to study host-pathogen interactions]. Med. Sci. (Paris). 35 (4), 346–351. doi: 10.1051/medsci/2019071
Cryan, J. F., O’Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., et al. (2019). The microbiota-Gut-Brain axis. Physiol. Rev. 99 (4), 1877–2013. doi: 10.1152/physrev.00018.2018
Edgerton, E. B., McCrea, A. R., Berry, C. T., Kwok, J. Y., Thompson, L. K., Watson, B., et al. (2020). Activation of mosquito immunity blocks the development of transmission-stage filarial nematodes. Proc. Natl. Acad. Sci. 117 (7), 3711–3717. doi: 10.1073/pnas.1909369117
Habtewold, T., Povelones, M., Blagborough, A. M., Christophides, G. K. (2008). Transmission blocking immunity in the malaria non-vector mosquito anopheles quadriannulatus species a. PloS Pathogens. 4 (5), e1000070. doi: 10.1371/journal.ppat.1000070
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Keywords: animal models, infectious diseases, antimicrobial peptides, Galleria mellollella, host-pathogen interactions, Bordetella species, phagocytic predatory amoeba, Dictyostelium discoideum
Citation: Younes S, Zein N, Abunasser S, Kamareddine L, Kirienko NV and Nasrallah GK (2023) Editorial: Unconventional animal models in infectious disease research, volume II. Front. Cell. Infect. Microbiol. 13:1225129. doi: 10.3389/fcimb.2023.1225129
Received: 18 May 2023; Accepted: 01 June 2023;
Published: 14 June 2023.
Edited and Reviewed by:
Thomas Rudel, Julius Maximilian University of Würzburg, GermanyCopyright © 2023 Younes, Zein, Abunasser, Kamareddine, Kirienko and Nasrallah. 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: Gheyath K. Nasrallah, Z2hleWF0aC5uYXNyYWxsYWhAcXUuZWR1LnFh