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Mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung

The genetic disease cystic fibrosis (CF) frequently leads to chronic lung infections by bacteria and fungi. We identified three individuals with CF with persistent lung infections dominated by Clavispora (Candida) lusitaniae. Whole genome sequencing analysis of multiple isolates from each infection...

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Autores principales: Murante, Daniel, Demers, Elora G., Kurbessoian, Tania, Ruzic, Marina, Ashare, Alix, Stajich, Jason E., Hogan, Deborah A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104081/
https://www.ncbi.nlm.nih.gov/pubmed/37066389
http://dx.doi.org/10.1101/2023.04.05.535776
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author Murante, Daniel
Demers, Elora G.
Kurbessoian, Tania
Ruzic, Marina
Ashare, Alix
Stajich, Jason E.
Hogan, Deborah A.
author_facet Murante, Daniel
Demers, Elora G.
Kurbessoian, Tania
Ruzic, Marina
Ashare, Alix
Stajich, Jason E.
Hogan, Deborah A.
author_sort Murante, Daniel
collection PubMed
description The genetic disease cystic fibrosis (CF) frequently leads to chronic lung infections by bacteria and fungi. We identified three individuals with CF with persistent lung infections dominated by Clavispora (Candida) lusitaniae. Whole genome sequencing analysis of multiple isolates from each infection found evidence for selection for mutants in the gene MRS4 in all three distinct lung-associated populations. In each population, we found one or two unfixed, non-synonymous mutations in MRS4 relative to the reference allele found in multiple environmental and clinical isolates including the type strain. Genetic and phenotypic analyses found that all evolved alleles led to loss of function of Mrs4, a mitochondrial iron transporter. RNA Seq analyses found that Mrs4 variants with decreased activity led to increased expression of genes involved in iron acquisition mechanisms in both low iron and replete iron conditions. Furthermore, surface iron reductase activity and intracellular iron was much higher in strains with Mrs4 loss of function variants. Parallel studies found that a subpopulation of a CF-associated Exophiala dermatiditis infection also had a non-synonymous loss of function mutation in MRS4. Together, these data suggest that MRS4 mutations may be beneficial during chronic CF lung infections in diverse fungi perhaps for the purposes of adaptation to an iron restricted environment with chronic infections.
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spelling pubmed-101040812023-04-15 Mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung Murante, Daniel Demers, Elora G. Kurbessoian, Tania Ruzic, Marina Ashare, Alix Stajich, Jason E. Hogan, Deborah A. bioRxiv Article The genetic disease cystic fibrosis (CF) frequently leads to chronic lung infections by bacteria and fungi. We identified three individuals with CF with persistent lung infections dominated by Clavispora (Candida) lusitaniae. Whole genome sequencing analysis of multiple isolates from each infection found evidence for selection for mutants in the gene MRS4 in all three distinct lung-associated populations. In each population, we found one or two unfixed, non-synonymous mutations in MRS4 relative to the reference allele found in multiple environmental and clinical isolates including the type strain. Genetic and phenotypic analyses found that all evolved alleles led to loss of function of Mrs4, a mitochondrial iron transporter. RNA Seq analyses found that Mrs4 variants with decreased activity led to increased expression of genes involved in iron acquisition mechanisms in both low iron and replete iron conditions. Furthermore, surface iron reductase activity and intracellular iron was much higher in strains with Mrs4 loss of function variants. Parallel studies found that a subpopulation of a CF-associated Exophiala dermatiditis infection also had a non-synonymous loss of function mutation in MRS4. Together, these data suggest that MRS4 mutations may be beneficial during chronic CF lung infections in diverse fungi perhaps for the purposes of adaptation to an iron restricted environment with chronic infections. Cold Spring Harbor Laboratory 2023-04-06 /pmc/articles/PMC10104081/ /pubmed/37066389 http://dx.doi.org/10.1101/2023.04.05.535776 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Murante, Daniel
Demers, Elora G.
Kurbessoian, Tania
Ruzic, Marina
Ashare, Alix
Stajich, Jason E.
Hogan, Deborah A.
Mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung
title Mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung
title_full Mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung
title_fullStr Mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung
title_full_unstemmed Mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung
title_short Mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung
title_sort mrs4 loss of function in fungi during adaptation to the cystic fibrosis lung
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104081/
https://www.ncbi.nlm.nih.gov/pubmed/37066389
http://dx.doi.org/10.1101/2023.04.05.535776
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