Aditya S. Paul
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- Department of Immunology and Infectious Diseases, School of Public Health, Harvard University, Boston, MA, United States
Editorial on the Research Topic
Chemical-genetics to study microbial pathogen basis of infection and drug targets
Infection microbiology is challenging because pathogens develop adaptations that elude straightforward analogy with non-pathogens. Experimental methods for pathogens typically lag behind model systems, with few “off-the-shelf” approaches for direct study. Nonetheless, dedicated activity by smaller communities of researchers has over time yielded tools for study that are proving powerful for detailed understanding of infection processes. Reverse genetic approaches and chemical probe inhibitors are providing insights into pathogenic mechanisms. Identification of chemical susceptibilities of microbial pathogens has clear relevance for therapeutic interventions and drug development.
We have gathered 5 articles that utilize chemical biology and reverse genetic approaches to study infectious fungi, parasitic protists, and parasitic worms. The through line across the studies is the use of inhibitors in assays of infection, allowing researchers to study the basis of chemical susceptibility in poorly understood pathogenic organisms. Readers will appreciate the specialized approaches required to sustain these systems in the lab and make them amenable to measurements of growth and infection in controlled environments.
The phylum Apicomplexa comprise a diverse group of parasites of widespread medical and veterinary importance. Despite the longstanding need for interventions, drugs and treatments are few. Cryptosporidiosis is a diarrheal disease, for which there exists one FDA-approved chemotherapy (Sparks et al., 2015). Over the past decade, methods for continuous propagation of Cryptosporidium parasites in a lab setting have come online (Vinayak et al., 2015), enabling experimental approaches to study biology and chemical susceptibility. Here, Hanna et al. carry out an elegant set of chemical-genetic studies to prove a target of a potent antiparasitic inhibitor in Cryptosporidium parvum, one of the species that cause human disease. Following chemoproteomics, the researchers use knockdown, overexpression, and site-directed mutagenesis, to demonstrate specific targeting of a tRNA-synthetase in C. parvum. This study, with an earlier report from another group (Vinayak et al., 2020), expanded the set of selectable markers in C. parvum to include resistant alleles of parasite tRNA-synthetases. Also within Apicomplexa, the sister genera Plasmodium and Babesia are home to parasite species with specific tropism for red blood cells; in humans these parasites cause malaria and babesiosis, respectively. While treatments have tended to focus on molecular targets within the parasites, Groomes et al. undertook a screen of Plasmodium and Babesia parasites with drugs and advanced clinical-stage inhibitors annotated for targets in the host red blood cell. The researchers identified micromolar-IC50 potency inhibitors amongst these compounds, with higher potency generally displayed toward the Plasmodium parasites. In addition to the potential for repurposing, the study utilized assays that provide direct experimental for host cell targeting required for antiproliferative action.
Candida auris is a recently emerged fungal pathogen present in healthcare settings (Lockhart et al., 2017), with drug-resistance being a major issue (Du et al., 2020). Following a chemical screen in C. auris that identified an aryl-carbohydrazide inhibitor of proliferation, Tebbji et al. carry out a chemical-genetic haploinsufficiency profiling screen in the better established laboratory model Candida albicans. The researchers show that C. albicans cells with reduced expression of the fatty acid desaturase Ole1 gene exhibit increased susceptibility to the inhibitor. Subsequent fatty acid metabolism studies as well as supplementation experiments supported the Ole1-pathway as a target of the inhibitor in C. albicans and C. auris. In a moth larva model (Galleria mellonella) of systemic candidiasis caused by infection with C. auris or C. albicans, administration of the original hit compound or an analog improved survival.
We included in this Research Topic a study on parasitic Fasciola flukes, the causative agent of the zoonotic disease fascioliasis. Though not a microorganism (the worms can grow up to several centimeters in length), the use of chemical inhibitors to study trematode parasite development throughout the course of host infection aligns well with the research theme. Juvenile worms mature into adults in their journey from the stomach towards the liver, as the surroundings become increasingly anaerobic. Based on analogy to nematodes (Iwata et al., 2008), Tashibu et al. use a combination of biochemistry and chemical biology to find that juvenile and adult worms differ in their modes of mitochondrial respiration. The researchers found that juveniles carry out conventional ubiquinone-dependent respiration in the presence of oxygen, but can also perform a non-canonical, rhodoquinone-dependent mode of fumarate respiration to produce ATP. Adults, by contrast, predominantly utilize the fumarate mode of respiration. The chemical biology approach in this study was critical in demonstrating changes in mitochondrial metabolism during worm maturation, tracking with changes in oxygen within developmental niches in the host organism.
A translational framework also touches on improved pipelines for screening antimicrobial therapies. Guarnieri et al., in their studies of lactic acid bacteria (LAB) as a topical anti-infective, introduce the use of G. mellonella as an alternative to vertebrate animals for facile screening of LAB for burn wounds.
Chemical biology is a growing area for study of pathogens and infection biology. In some systems, the availability and implementation of genetics has allowed researchers to study the modes of action of compounds in live microbes, a powerful adjunct to traditional biochemical approaches. The implications are significant, especially given that frequently the related diseases have few treatments. Identification of a target can shed light on infection mechanisms and may inform new drug development efforts.
Author contributions
AP: Writing – original draft, Writing – review & editing.
Conflict of interest
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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The author(s) declare that no Generative AI was used in the creation of this manuscript.
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References
Du, H., Bing, J., Hu, T., Ennis, C. L., Nobile, C. J., Huang, G. (2020). Candida auris: Epidemiology, biology, antifungal resistance, and virulence. PLoS Pathog. 16, e1008921. doi: 10.1371/journal.ppat.1008921
Iwata, F., Shinjyo, N., Amino, H., Sakamoto, K., Islam, M. K., Tsuji, N., et al. (2008). Change of subunit composition of mitochondrial complex II (succinate–ubiquinone reductase/quinol–fumarate reductase) in Ascaris suum during the migration in the experimental host. Parasitol. Int. 57, 54–61. doi: 10.1016/j.parint.2007.08.002
Lockhart, S. R., Etienne, K. A., Vallabhaneni, S., Farooqi, J., Chowdhary, A., Govender, N. P., et al. (2017). Simultaneous emergence of multidrug-resistant candida auris on 3 continents confirmed by whole-genome sequencing and epidemiological analyses. Clin. Infect. Dis. 64, 134–140. doi: 10.1093/cid/ciw691
Sparks, H., Nair, G., Castellanos-Gonzalez, A., White, A. C. (2015). Treatment of cryptosporidium: what we know, gaps, and the way forward. Curr. Trop. Med. Rep. 2, 181–187. doi: 10.1007/s40475-015-0056-9
Vinayak, S., Pawlowic, M. C., Sateriale, A., Brooks, C. F., Studstill, C. J., Bar-Peled, Y., et al. (2015). Genetic modification of the diarrheal pathogen Cryptosporidium parvum. Nature 523, 477–480. doi: 10.1038/nature14651
Keywords: pathogen, Plasmodium, Babesia, Cryptosporidium, Candida, Fasciola, Galleria mellonella
Citation: Paul AS (2025) Editorial: Chemical-genetics to study microbial pathogen basis of infection and drug targets. Front. Cell. Infect. Microbiol. 15:1582879. doi: 10.3389/fcimb.2025.1582879
Received: 25 February 2025; Accepted: 10 March 2025;
Published: 19 March 2025.
Edited and Reviewed by:
Yong-Sun Bahn, Yonsei University, Republic of KoreaCopyright © 2025 Paul. 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: Aditya S. Paul, YXBhdWxAaHNwaC5oYXJ2YXJkLmVkdQ==