Cargando…
Step-Specific Adaptation and Trade-Off over the Course of an Infection by GASP Mutation Small Colony Variants
During an infection, parasites face a succession of challenges, each decisive for disease outcome. The diversity of challenges requires a series of parasite adaptations to successfully multiply and transmit from host to host. Thus, the pathogen genotypes that succeed during one step might be counter...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7845629/ https://www.ncbi.nlm.nih.gov/pubmed/33436427 http://dx.doi.org/10.1128/mBio.01399-20 |
_version_ | 1783644592491462656 |
---|---|
author | Faucher, Christian Mazana, Vincent Kardacz, Marion Parthuisot, Nathalie Ferdy, Jean-Baptiste Duneau, David |
author_facet | Faucher, Christian Mazana, Vincent Kardacz, Marion Parthuisot, Nathalie Ferdy, Jean-Baptiste Duneau, David |
author_sort | Faucher, Christian |
collection | PubMed |
description | During an infection, parasites face a succession of challenges, each decisive for disease outcome. The diversity of challenges requires a series of parasite adaptations to successfully multiply and transmit from host to host. Thus, the pathogen genotypes that succeed during one step might be counterselected in later stages of the infection. Using the bacterium Xenorhabdus nematophila and adult Drosophila melanogaster flies as hosts, we showed that such step-specific adaptations, here linked to GASP (i.e., growth advantage in stationary phase) mutations in the X. nematophila master gene regulator lrp, exist and can trade off with each other. We found that nonsense lrp mutations had lowered the ability to resist the host immune response, while all classes of mutations in lrp were associated with a decrease in the ability to proliferate during early infection. We demonstrate that reduced proliferation of X. nematophila best explains diminished virulence in this infection model. Finally, decreased proliferation during the first step of infection is accompanied by improved proliferation during late infection, suggesting a trade-off between the adaptations to each step. Step-specific adaptations could play a crucial role in the chronic phase of infections in any disease organisms that show similar small colony variants (SCVs) to X. nematophila. |
format | Online Article Text |
id | pubmed-7845629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-78456292021-02-05 Step-Specific Adaptation and Trade-Off over the Course of an Infection by GASP Mutation Small Colony Variants Faucher, Christian Mazana, Vincent Kardacz, Marion Parthuisot, Nathalie Ferdy, Jean-Baptiste Duneau, David mBio Research Article During an infection, parasites face a succession of challenges, each decisive for disease outcome. The diversity of challenges requires a series of parasite adaptations to successfully multiply and transmit from host to host. Thus, the pathogen genotypes that succeed during one step might be counterselected in later stages of the infection. Using the bacterium Xenorhabdus nematophila and adult Drosophila melanogaster flies as hosts, we showed that such step-specific adaptations, here linked to GASP (i.e., growth advantage in stationary phase) mutations in the X. nematophila master gene regulator lrp, exist and can trade off with each other. We found that nonsense lrp mutations had lowered the ability to resist the host immune response, while all classes of mutations in lrp were associated with a decrease in the ability to proliferate during early infection. We demonstrate that reduced proliferation of X. nematophila best explains diminished virulence in this infection model. Finally, decreased proliferation during the first step of infection is accompanied by improved proliferation during late infection, suggesting a trade-off between the adaptations to each step. Step-specific adaptations could play a crucial role in the chronic phase of infections in any disease organisms that show similar small colony variants (SCVs) to X. nematophila. American Society for Microbiology 2021-01-12 /pmc/articles/PMC7845629/ /pubmed/33436427 http://dx.doi.org/10.1128/mBio.01399-20 Text en Copyright © 2021 Faucher et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Faucher, Christian Mazana, Vincent Kardacz, Marion Parthuisot, Nathalie Ferdy, Jean-Baptiste Duneau, David Step-Specific Adaptation and Trade-Off over the Course of an Infection by GASP Mutation Small Colony Variants |
title | Step-Specific Adaptation and Trade-Off over the Course of an Infection by GASP Mutation Small Colony Variants |
title_full | Step-Specific Adaptation and Trade-Off over the Course of an Infection by GASP Mutation Small Colony Variants |
title_fullStr | Step-Specific Adaptation and Trade-Off over the Course of an Infection by GASP Mutation Small Colony Variants |
title_full_unstemmed | Step-Specific Adaptation and Trade-Off over the Course of an Infection by GASP Mutation Small Colony Variants |
title_short | Step-Specific Adaptation and Trade-Off over the Course of an Infection by GASP Mutation Small Colony Variants |
title_sort | step-specific adaptation and trade-off over the course of an infection by gasp mutation small colony variants |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7845629/ https://www.ncbi.nlm.nih.gov/pubmed/33436427 http://dx.doi.org/10.1128/mBio.01399-20 |
work_keys_str_mv | AT faucherchristian stepspecificadaptationandtradeoffoverthecourseofaninfectionbygaspmutationsmallcolonyvariants AT mazanavincent stepspecificadaptationandtradeoffoverthecourseofaninfectionbygaspmutationsmallcolonyvariants AT kardaczmarion stepspecificadaptationandtradeoffoverthecourseofaninfectionbygaspmutationsmallcolonyvariants AT parthuisotnathalie stepspecificadaptationandtradeoffoverthecourseofaninfectionbygaspmutationsmallcolonyvariants AT ferdyjeanbaptiste stepspecificadaptationandtradeoffoverthecourseofaninfectionbygaspmutationsmallcolonyvariants AT duneaudavid stepspecificadaptationandtradeoffoverthecourseofaninfectionbygaspmutationsmallcolonyvariants |