Ulrich Kück
Richard J. Bennett
Linqi Wang
Paul S. Dyer- 1Allgemeine & Molekulare Botanik, Ruhr-University, Bochum, Germany
- 2Department of Molecular Microbiology and Immunology, Brown University, Providence, RI, United States
- 3State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China
- 4School of Life Sciences, University of Nottingham, Nottingham, United Kingdom
Editorial on the Research Topic
Sexual and Parasexual Reproduction of Human Fungal Pathogens
In recent years, human fungal pathogens have received increasing attention, with several of these species responsible for prevalent diseases that are associated with high mortality rates. The major human pathogens belong to the genera Candida, Aspergillus, and Cryptococcus, although a wide variety of highly diverse fungal species are clinically relevant. This increased interest has arisen due to a number of factors such as the presence of ever higher numbers of clinically vulnerable patients who are susceptible to fungal infections, better identification and diagnosis of fungal diseases, and the emergence and spread of isolates showing resistance to commonly used antifungal drugs. It is therefore of both fundamental interest and medical importance to understand how human fungal pathogens can generate variation and evolve over time.
Historically, most human fungal pathogens were thought to propagate primarily through clonal asexual reproduction. During this process, cells can still accumulate mutations and can undergo a variety of genomic rearrangements and ploidy alterations. Such changes can contribute to adaptive changes associated with enhanced pathogenicity, resistance to antifungal drugs, and persistence in chronic infections. Two reviews summarize our current view on parasexual propagation in various Candida species.
Mishra et al., (2021) provide a comprehensive review of current understanding of parasexual reproduction, the underlying molecular mechanisms governing its regulation, and its relevance to Candida biology. The article reminds us that the discovery of parasexuality in Candida albicans roughly two decades ago has served as a model for other Candida species for which sexual cycles have not been described. In particular, parallels between parasexual cycles in C. albicans and meiotic divisions in other fungi are emphasized, and their relevance to natural populations are illustrated.
Xu (2021) addresses the question of how genetic diversity is generated in natural populations of Candida tropicalis. The article reviews current understanding of the potential modes of reproduction in this species and describes the expectations of modes of sexual, parasexual, and asexual reproduction, comparing them with the patterns of genetic variation observed in natural populations.
Full sexual cycles can also impact the evolution of important fungal attributes such as pathogenicity and antifungal drug resistance, as well as provide a valuable tool for genetic analysis. Although long overlooked, discoveries of complete sexual cycles in species such as Aspergillus fumigatus have widened our understanding of how sex occurs and how it may contribute to pathogenesis. Such discoveries are greatly assisted by insights from pioneering genome sequencing projects in the early 2000s and followed previous studies that provided indirect evidence for sexual reproduction in natural populations.
The sexual cycle of A. fumigatus had previously only been demonstrated under laboratory conditions and there has been much speculation as to if and where mating might occur in nature. Zhang et al., (2021) demonstrate that flower bulb waste material from stockpiles undergoing composting can provide the environmental conditions necessary for sexual reproduction in A. fumigatus. Specialist membranes and fluorescent stains were used to demonstrate the presence of sexual ascospores within the waste material and it was further shown that ascospores can germinate after exposure to 70°C for periods of up to several days in contrast to asexual conidiospores, which lost viability. Finally, it was confirmed that flower bulb waste material could serve as a natural substrate for sex by the demonstration that such material could be utilized successfully to perform sexual crosses in the laboratory.
Ashton et al., (2022) also demonstrate that the sexual cycle can be used for genetic analysis. They used the ‘bulk segregant analysis (BSA)’ technique together with next-generation sequencing and a newly developed bioinformatic pipeline to investigate the underlying basis of monogenic traits in A. fumigatus. Using a clinical isolate exhibiting monogenic resistance to the azole antifungal itraconazole in a cross with a sensitive partner strain, they identified 123 genes in F1 progeny that are potentially responsible for resistance to itraconazole. They then used a combination of backcrossing and an increased number of progeny in the BSA pools to narrow this down to just 20 candidate genes and were then able to that show a change of methionine to lysine codon in the cyp51A gene was responsible for antifungal resistance. This study shows great promise for future applications of BSA in A. fumigatus and beyond.
Sexual reproduction is also evident in the opportunistic yeast-like pathogen Cryptococcus neoformans, where it can promote the generation of hyper-virulent and drug-resistant strains and produces infectious meiospores. The article by Wu et al., (2022) addresses the question of how the ubiquitin-proteasome system regulates sexual reproduction in C. neoformans. The article revealed that the F-box protein Cdc4 is critical for fungal virulence and sexual reproduction in C. neoformans. In particular, Cdc4 regulates cell membrane integrity and repair of DNA damage in this pathogen. Moreover, when used in bilateral mating experiments, cdc4 deletion mutants showed a block in their ability to undergo meiosis after nuclear fusion within the basidia, ultimately failing to form meiospores.
In conclusion, the articles and reviews in this Research Topic expand our understanding of how sexual and parasexual reproduction of human fungal pathogens can drive the adaptive genetic changes that contribute to key traits, including those impacting antifungal drug resistance and pathogenesis in the mammalian host. They also highlight how sexual reproduction provides powerful tools with which to genetically dissect key aspects of fungal biology.
Author Contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
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
Ashton, GD, Blythe, M, Sang, F, Zadik, D, Holmes, N, Malla, S, et al. Use of Bulk Segregant Analysis for Determining the Genetic Basis of Azole Resistance in the Opportunistic Pathogen Aspergillus fumigatus. Front. Cell Infect. Microbiol. (2022). doi: 10.3389/fcimb.2022.841138
Mishra, A, Forche, A, Anderson, MZ. Parasexuality of Candida Species. Front. Cell Infect. Microbiol. (2021) 11:796929. doi: 10.3389/fcimb.2021.796929
Xu, J. Is Natural Population of Candida tropicalis Sexual, Parasexual, and/or Asexual? Front. Cell Infect. Microbiol. (2021) 11:751676. doi: 10.3389/fcimb.2021.751676
Zhang, J, Verweij, PE, Rijs, AJMM, Debets, AJM, Snelders, E. Flower Bulb Waste Material Is a Natural Niche for the Sexual Cycle in Aspergillus fumigatus. Front. Cell Infect. Microbiol. (2022) 11:785157. doi: 10.3389/fcimb.2021.785157
Keywords: human fungal pathogens, propagation, sexual cycles, genetics, fungal reproduction
Citation: Kück U, Bennett RJ, Wang L and Dyer PS (2022) Editorial: Sexual and Parasexual Reproduction of Human Fungal Pathogens. Front. Cell. Infect. Microbiol. 12:934267. doi: 10.3389/fcimb.2022.934267
Received: 02 May 2022; Accepted: 10 May 2022;
Published: 28 June 2022.
Edited and reviewed by:
Joseph Heitman, Duke University, United StatesCopyright © 2022 Kück, Bennett, Wang and Dyer. 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: Ulrich Kück, dWxyaWNoLmt1ZWNrQHJ1Yi5kZQ==