Evolutionary unique N-glycan-dependent protein quality control system plays pivotal roles in cellular fitness and extracellular vesicle transport in Cryptococcus neoformans

  1. Department of Life Science, Chung-Ang University, Seoul, Republic of Korea
  2. Department of Systems Biotechnology, Chung-Ang University, Anseong-Si, Republic of Korea
  3. Department of Biomedical-Chemical Engineering, The Catholic University of Korea, Bucheon-Si, Republic of Korea
  4. Department of Biotechnology, The Catholic University of Korea, Bucheon-Si, Republic of Korea
  5. Digital OMICs Research Center, Korea Basic Science Institute, Cheongju-si, Republic of Korea
  6. Department of Biotechnology, Yonsei University, Seoul, Republic of Korea
  7. Department of Medicine, Duke University, Durham, USA

Peer review process

Not revised: This Reviewed Preprint includes the authors’ original preprint (without revision), an eLife assessment, public reviews, and a provisional response from the authors.

Read more about eLife’s peer review process.

Editors

  • Reviewing Editor
    Lysangela Alves
    Instituto Carlos Chagas, Curitiba, Brazil
  • Senior Editor
    Silke Hauf
    Virginia Tech, Blacksburg, United States of America

Reviewer #1 (Public review):

Summary:

Using gene deletion analysis, the authors confirm the molecular function of putative components of an N-glycan-dependent endoplasmic reticulum protein quality control (ERQC) system (UGG1, MNS1, MNS101, MNL1, and MNL2), in the basidiomycetous fungal pathogen Cryptococcus neoformans. Specifically, they confirm the essential role of these components in the ERQC system and their role in ER stress which contributes to cellular fitness and pathogenicity.

The second part of the study links the components to secretion, mainly EV biogenesis and composition. However, this part of the study is less convincing.

Strengths:

Although it is unclear why ER stress in the mutants would not manifest into a classical secretion defect, this is a rigorous, well-controlled study, with the use of complemented strains that demonstrate phenotypic restoration. The diagram in Figure 1 is very useful in orientating the reader to a complex subject matter, although the legend could be more descriptive.

Weaknesses:

A major weakness is the sheer volume of data presented (in the main text and supplement), which makes the results difficult to follow and retain: the work could essentially be two separate studies.
Another major weakness is the lack of mechanistic insight into the role of the ERQC system in EV secretion and its disconnection to "classical" secretion, which is difficult to reconcile. Some insight into why EV secretion is decreased, and classical secretion is unaffected, would strengthen the significance of the findings. No mechanism is provided to explain why the ERQC mutants (Ugg1 mutant in particular) would have reduced and heterogeneously sized EVs. Furthermore, it is not convincing that the EV content changes would greatly impact fitness and virulence. The proteomics data showing reduced cargo in the Ugg1 mutant is not convincing and difficult to follow.

Reviewer #2 (Public review):

Summary:

This study investigates the molecular function of the N-glycan-dependent endoplasmic reticulum protein quality control system (ERQC) in Cryptococcus neoformans and correlates this pathway with key features of C. neoformans virulence, especially those mediated by extracellular vesicle transport. The findings provide valuable insights into the connection between this pathway and the biogenesis of C. neoformans extracellular vesicles.

Strengths:

The strength of this study lies primarily in the careful selection of appropriate and current methodologies, which provide a solid foundation for the authors' results and conclusions across all presented data. All experiments are supported by well-designed and established controls in the study of C. neoformans, further strengthening the validity of the results and conclusions drawn from them. The study presents novel data on this important pathway in C. neoformans, establishing its connection with C. neoformans virulence. Interestingly, the findings led the authors to understand the relationship between this pathway and the transport of key fungal virulence factors via extracellular vesicles. This was demonstrated in the study, paving the way for a deeper understanding of extracellular vesicle biogenesis-a field still filled with gaps but one to which this study contributes solid data, helping to clarify aspects of this process.

Weaknesses:

I do not see significant weaknesses in this study. The experiments are well-grounded, and the results are clearly presented. I believe the only weakness is that the paper could be condensed. Sections like the discussion, for instance, are extremely lengthy, which may make reading and, consequently, understanding more challenging for many readers. Regarding the presentation of the results, while clear, the figures contain a lot of information, and I believe that some of this content could be moved to supplementary figures.

Reviewer #3 (Public review):

Summary:

Cryptococcus neoformans is a global critical threat pathogen and the manuscript by Mota et al demonstrates that the pathogen's N-glycan-dependent protein quality control system regulates the capacity of the fungus to cause disease. The system makes sure that glycoproteins are folded correctly. The system is involved in the fitness and virulence of the fungus by regulating aspects of cellular robustness and the trafficking of virulence-associated compounds outside of the cell via transport in extracellular vesicles.

Strengths:

The investigators use multiple modalities to demonstrate that the system is involved in cryptococcal pathogenesis. The investigators generated mutant C. neoformans to explore the role of genes involved in the protein folding system. Basic microbiology, genetic analyses, proteomics, fluorescence and transmission microscopy, nanotracking analyses, and murine studies were performed. The validity of the findings are thus very high. Hypotheses are robustly demonstrated.

Weaknesses:

Aspects of the results should be better explained. Some results are extrapolated in their meaning beyond the extent of the data.

Author response:

Reviewer #1:

We thank the reviewer for recognizing the impact of our work on the pivotal roles of N-glycan-dependent ERQC in cellular fitness and pathogenicity and providing valuable comments to be considered to improve the manuscript. As suggested, we will rearrange data, reduce text volume, and discuss the possibility of how ERQC mutation decreases EV secretion without significant defect in conventional secretion. Regarding the proteomics data, we have already initiated a comparative analysis of total intracellular and EV-associated proteins to determine whether the reduced cargo loading in the Ugg1 mutant is specific to EV-associated proteins. Additionally, we may extend the analysis to include total secretion, enabling a clearer comparison between classical secretion and EV-mediated secretion to better evaluate the extent of classical secretion defects in the Ugg1 mutant.

Reviewer #2:

We sincerely thank the reviewer for the positive evaluation of our work. As recommended, we will reduce the text and reorganize the data to enhance the manuscript's readability.

Reviewer #3:

We sincerely thank the reviewer for the high appreciation of our work. As recommended, we will provide a more detailed explanation of the results with improved interpretation, strongly grounded on the obtained data.

  1. Howard Hughes Medical Institute
  2. Wellcome Trust
  3. Max-Planck-Gesellschaft
  4. Knut and Alice Wallenberg Foundation