Cargando…
LytM Proteins Play a Crucial Role in Cell Separation, Outer Membrane Composition, and Pathogenesis in Nontypeable Haemophilus influenzae
LytM proteins belong to a family of bacterial metalloproteases. In Gram-negative bacteria, LytM factors are mainly reported to have a direct effect on cell division by influencing cleavage and remodeling of peptidoglycan. In this study, mining nontypeable Haemophilus influenzae (NTHI) genomes, three...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358004/ https://www.ncbi.nlm.nih.gov/pubmed/25714719 http://dx.doi.org/10.1128/mBio.02575-14 |
_version_ | 1782361227485249536 |
---|---|
author | Ercoli, Giuseppe Tani, Chiara Pezzicoli, Alfredo Vacca, Irene Martinelli, Manuele Pecetta, Simone Petracca, Roberto Rappuoli, Rino Pizza, Mariagrazia Norais, Nathalie Soriani, Marco Aricò, Beatrice |
author_facet | Ercoli, Giuseppe Tani, Chiara Pezzicoli, Alfredo Vacca, Irene Martinelli, Manuele Pecetta, Simone Petracca, Roberto Rappuoli, Rino Pizza, Mariagrazia Norais, Nathalie Soriani, Marco Aricò, Beatrice |
author_sort | Ercoli, Giuseppe |
collection | PubMed |
description | LytM proteins belong to a family of bacterial metalloproteases. In Gram-negative bacteria, LytM factors are mainly reported to have a direct effect on cell division by influencing cleavage and remodeling of peptidoglycan. In this study, mining nontypeable Haemophilus influenzae (NTHI) genomes, three highly conserved open reading frames (ORFs) containing a LytM domain were identified, and the proteins encoded by the ORFs were named YebA, EnvC, and NlpD on the basis of their homology with the Escherichia coli proteins. Immunoblotting and confocal analysis showed that while NTHI NlpD is exposed on the bacterial surface, YebA and EnvC reside in the periplasm. NTHI ΔyebA and ΔnlpD deletion mutants revealed an aberrant division phenotype characterized by an altered cell architecture and extensive membrane blebbing. The morphology of the ΔenvC deletion mutant was identical to that of the wild-type strain, but it showed a drastic reduction of periplasmic proteins, including the chaperones HtrA, SurA, and Skp, and an accumulation of β-barrel-containing outer membrane proteins comprising the autotransporters Hap, IgA serine protease, and HMW2A, as observed by proteomic analysis. These data suggest that EnvC may influence the bacterial surface protein repertoire by facilitating the passage of the periplasmic chaperones through the peptidoglycan layer to the close vicinity of the inner face of the outer membrane. This hypothesis was further corroborated by the fact that an NTHI envC defective strain had an impaired capacity to adhere to epithelial cells and to form biofilm. Notably, this strain also showed a reduced serum resistance. These results suggest that LytM factors are not only important components of cell division but they may also influence NTHI physiology and pathogenesis by affecting membrane composition. |
format | Online Article Text |
id | pubmed-4358004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-43580042015-03-17 LytM Proteins Play a Crucial Role in Cell Separation, Outer Membrane Composition, and Pathogenesis in Nontypeable Haemophilus influenzae Ercoli, Giuseppe Tani, Chiara Pezzicoli, Alfredo Vacca, Irene Martinelli, Manuele Pecetta, Simone Petracca, Roberto Rappuoli, Rino Pizza, Mariagrazia Norais, Nathalie Soriani, Marco Aricò, Beatrice mBio Research Article LytM proteins belong to a family of bacterial metalloproteases. In Gram-negative bacteria, LytM factors are mainly reported to have a direct effect on cell division by influencing cleavage and remodeling of peptidoglycan. In this study, mining nontypeable Haemophilus influenzae (NTHI) genomes, three highly conserved open reading frames (ORFs) containing a LytM domain were identified, and the proteins encoded by the ORFs were named YebA, EnvC, and NlpD on the basis of their homology with the Escherichia coli proteins. Immunoblotting and confocal analysis showed that while NTHI NlpD is exposed on the bacterial surface, YebA and EnvC reside in the periplasm. NTHI ΔyebA and ΔnlpD deletion mutants revealed an aberrant division phenotype characterized by an altered cell architecture and extensive membrane blebbing. The morphology of the ΔenvC deletion mutant was identical to that of the wild-type strain, but it showed a drastic reduction of periplasmic proteins, including the chaperones HtrA, SurA, and Skp, and an accumulation of β-barrel-containing outer membrane proteins comprising the autotransporters Hap, IgA serine protease, and HMW2A, as observed by proteomic analysis. These data suggest that EnvC may influence the bacterial surface protein repertoire by facilitating the passage of the periplasmic chaperones through the peptidoglycan layer to the close vicinity of the inner face of the outer membrane. This hypothesis was further corroborated by the fact that an NTHI envC defective strain had an impaired capacity to adhere to epithelial cells and to form biofilm. Notably, this strain also showed a reduced serum resistance. These results suggest that LytM factors are not only important components of cell division but they may also influence NTHI physiology and pathogenesis by affecting membrane composition. American Society of Microbiology 2015-02-24 /pmc/articles/PMC4358004/ /pubmed/25714719 http://dx.doi.org/10.1128/mBio.02575-14 Text en Copyright © 2015 Ercoli et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ercoli, Giuseppe Tani, Chiara Pezzicoli, Alfredo Vacca, Irene Martinelli, Manuele Pecetta, Simone Petracca, Roberto Rappuoli, Rino Pizza, Mariagrazia Norais, Nathalie Soriani, Marco Aricò, Beatrice LytM Proteins Play a Crucial Role in Cell Separation, Outer Membrane Composition, and Pathogenesis in Nontypeable Haemophilus influenzae |
title | LytM Proteins Play a Crucial Role in Cell Separation, Outer Membrane Composition, and Pathogenesis in Nontypeable Haemophilus influenzae |
title_full | LytM Proteins Play a Crucial Role in Cell Separation, Outer Membrane Composition, and Pathogenesis in Nontypeable Haemophilus influenzae |
title_fullStr | LytM Proteins Play a Crucial Role in Cell Separation, Outer Membrane Composition, and Pathogenesis in Nontypeable Haemophilus influenzae |
title_full_unstemmed | LytM Proteins Play a Crucial Role in Cell Separation, Outer Membrane Composition, and Pathogenesis in Nontypeable Haemophilus influenzae |
title_short | LytM Proteins Play a Crucial Role in Cell Separation, Outer Membrane Composition, and Pathogenesis in Nontypeable Haemophilus influenzae |
title_sort | lytm proteins play a crucial role in cell separation, outer membrane composition, and pathogenesis in nontypeable haemophilus influenzae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358004/ https://www.ncbi.nlm.nih.gov/pubmed/25714719 http://dx.doi.org/10.1128/mBio.02575-14 |
work_keys_str_mv | AT ercoligiuseppe lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT tanichiara lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT pezzicolialfredo lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT vaccairene lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT martinellimanuele lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT pecettasimone lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT petraccaroberto lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT rappuolirino lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT pizzamariagrazia lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT noraisnathalie lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT sorianimarco lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae AT aricobeatrice lytmproteinsplayacrucialroleincellseparationoutermembranecompositionandpathogenesisinnontypeablehaemophilusinfluenzae |