The pneumococcal two-component system SirRH is linked to enhanced intracellular survival of Streptococcus pneumoniae in influenza-infected pulmonary cells.

The virus-bacterial synergism implicated in secondary bacterial infections caused by Streptococcus pneumoniae following infection with epidemic or pandemic influenza A virus (IAV) is well documented. However, the molecular mechanisms behind such synergism remain largely ill-defined. In pneumocytes i...

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Main Authors: Nicolás M Reinoso-Vizcaíno, Melina B Cian, Paulo R Cortes, Nadia B Olivero, Mirelys Hernandez-Morfa, Germán E Piñas, Chandan Badapanda, Ankita Rathore, Daniel R Perez, José Echenique
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-08-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1008761
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author Nicolás M Reinoso-Vizcaíno
Melina B Cian
Paulo R Cortes
Nadia B Olivero
Mirelys Hernandez-Morfa
Germán E Piñas
Chandan Badapanda
Ankita Rathore
Daniel R Perez
José Echenique
author_facet Nicolás M Reinoso-Vizcaíno
Melina B Cian
Paulo R Cortes
Nadia B Olivero
Mirelys Hernandez-Morfa
Germán E Piñas
Chandan Badapanda
Ankita Rathore
Daniel R Perez
José Echenique
author_sort Nicolás M Reinoso-Vizcaíno
collection DOAJ
description The virus-bacterial synergism implicated in secondary bacterial infections caused by Streptococcus pneumoniae following infection with epidemic or pandemic influenza A virus (IAV) is well documented. However, the molecular mechanisms behind such synergism remain largely ill-defined. In pneumocytes infected with influenza A virus, subsequent infection with S. pneumoniae leads to enhanced pneumococcal intracellular survival. The pneumococcal two-component system SirRH appears essential for such enhanced survival. Through comparative transcriptomic analysis between the ΔsirR and wt strains, a list of 179 differentially expressed genes was defined. Among those, the clpL protein chaperone gene and the psaB Mn+2 transporter gene, which are involved in the stress response, are important in enhancing S. pneumoniae survival in influenza-infected cells. The ΔsirR, ΔclpL and ΔpsaB deletion mutants display increased susceptibility to acidic and oxidative stress and no enhancement of intracellular survival in IAV-infected pneumocyte cells. These results suggest that the SirRH two-component system senses IAV-induced stress conditions and controls adaptive responses that allow survival of S. pneumoniae in IAV-infected pneumocytes.
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spelling doaj.art-ab734bcf423d4b4196a38de2df195b732022-12-21T21:35:20ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742020-08-01168e100876110.1371/journal.ppat.1008761The pneumococcal two-component system SirRH is linked to enhanced intracellular survival of Streptococcus pneumoniae in influenza-infected pulmonary cells.Nicolás M Reinoso-VizcaínoMelina B CianPaulo R CortesNadia B OliveroMirelys Hernandez-MorfaGermán E PiñasChandan BadapandaAnkita RathoreDaniel R PerezJosé EcheniqueThe virus-bacterial synergism implicated in secondary bacterial infections caused by Streptococcus pneumoniae following infection with epidemic or pandemic influenza A virus (IAV) is well documented. However, the molecular mechanisms behind such synergism remain largely ill-defined. In pneumocytes infected with influenza A virus, subsequent infection with S. pneumoniae leads to enhanced pneumococcal intracellular survival. The pneumococcal two-component system SirRH appears essential for such enhanced survival. Through comparative transcriptomic analysis between the ΔsirR and wt strains, a list of 179 differentially expressed genes was defined. Among those, the clpL protein chaperone gene and the psaB Mn+2 transporter gene, which are involved in the stress response, are important in enhancing S. pneumoniae survival in influenza-infected cells. The ΔsirR, ΔclpL and ΔpsaB deletion mutants display increased susceptibility to acidic and oxidative stress and no enhancement of intracellular survival in IAV-infected pneumocyte cells. These results suggest that the SirRH two-component system senses IAV-induced stress conditions and controls adaptive responses that allow survival of S. pneumoniae in IAV-infected pneumocytes.https://doi.org/10.1371/journal.ppat.1008761
spellingShingle Nicolás M Reinoso-Vizcaíno
Melina B Cian
Paulo R Cortes
Nadia B Olivero
Mirelys Hernandez-Morfa
Germán E Piñas
Chandan Badapanda
Ankita Rathore
Daniel R Perez
José Echenique
The pneumococcal two-component system SirRH is linked to enhanced intracellular survival of Streptococcus pneumoniae in influenza-infected pulmonary cells.
PLoS Pathogens
title The pneumococcal two-component system SirRH is linked to enhanced intracellular survival of Streptococcus pneumoniae in influenza-infected pulmonary cells.
title_full The pneumococcal two-component system SirRH is linked to enhanced intracellular survival of Streptococcus pneumoniae in influenza-infected pulmonary cells.
title_fullStr The pneumococcal two-component system SirRH is linked to enhanced intracellular survival of Streptococcus pneumoniae in influenza-infected pulmonary cells.
title_full_unstemmed The pneumococcal two-component system SirRH is linked to enhanced intracellular survival of Streptococcus pneumoniae in influenza-infected pulmonary cells.
title_short The pneumococcal two-component system SirRH is linked to enhanced intracellular survival of Streptococcus pneumoniae in influenza-infected pulmonary cells.
title_sort pneumococcal two component system sirrh is linked to enhanced intracellular survival of streptococcus pneumoniae in influenza infected pulmonary cells
url https://doi.org/10.1371/journal.ppat.1008761
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