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Protein domain-dependent vesiculation of Lipoprotein A, a protein that is important in cell wall synthesis and fitness of the human respiratory pathogen Haemophilus influenzae

Jalalvand, Farshid LU ; Su, Yu Ching LU ; Manat, Guillaume LU ; Chernobrovkin, Alexey ; Kadari, Mahendar LU ; Jonsson, Sandra LU orcid ; Janousková, Martina LU ; Rutishauser, Dorothea ; Semsey, Szabolcs and Løbner-Olesen, Anders , et al. (2022) In Frontiers in cellular and infection microbiology 12.
Abstract

The human pathogen Haemophilus influenzae causes respiratory tract infections and is commonly associated with prolonged carriage in patients with chronic obstructive pulmonary disease. Production of outer membrane vesicles (OMVs) is a ubiquitous phenomenon observed in Gram-negative bacteria including H. influenzae. OMVs play an important role in various interactions with the human host; from neutralization of antibodies and complement activation to spread of antimicrobial resistance. Upon vesiculation certain proteins are found in OMVs and some proteins are retained at the cell membrane. The mechanism for this phenomenon is not fully elucidated. We employed mass spectrometry to study vesiculation and the fate of proteins in the outer... (More)

The human pathogen Haemophilus influenzae causes respiratory tract infections and is commonly associated with prolonged carriage in patients with chronic obstructive pulmonary disease. Production of outer membrane vesicles (OMVs) is a ubiquitous phenomenon observed in Gram-negative bacteria including H. influenzae. OMVs play an important role in various interactions with the human host; from neutralization of antibodies and complement activation to spread of antimicrobial resistance. Upon vesiculation certain proteins are found in OMVs and some proteins are retained at the cell membrane. The mechanism for this phenomenon is not fully elucidated. We employed mass spectrometry to study vesiculation and the fate of proteins in the outer membrane. Functional groups of proteins were differentially distributed on the cell surface and in OMVs. Despite its supposedly periplasmic and outer membrane location, we found that the peptidoglycan synthase-activator Lipoprotein A (LpoA) was accumulated in OMVs relative to membrane fractions. A mutant devoid of LpoA lost its fitness as revealed by growth and electron microscopy. Furthermore, high-pressure liquid chromatography disclosed a lower concentration (55%) of peptidoglycan in the LpoA-deficient H. influenzae compared to the parent wild type bacterium. Using an LpoA-mNeonGreen fusion protein and fluorescence microscopy, we observed that LpoA was enriched in “foci” in the cell envelope, and further located in the septum during cell division. To define the fate of LpoA, C-terminally truncated LpoA-variants were constructed, and we found that the LpoA C-terminal domain promoted optimal transportation to the OMVs as revealed by flow cytometry. Taken together, our study highlights the importance of LpoA for H. influenzae peptidoglycan biogenesis and provides novel insights into cell wall integrity and OMV production.

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publishing date
type
Contribution to journal
publication status
published
subject
keywords
Haemophilus influenzae, lipoprotein A, LpoA, outer membrane vesicles (OMV), respiratory pathogen
in
Frontiers in cellular and infection microbiology
volume
12
article number
984955
publisher
Frontiers Media S. A.
external identifiers
  • scopus:85140348268
  • pmid:36275016
ISSN
2235-2988
DOI
10.3389/fcimb.2022.984955
language
English
LU publication?
yes
id
3c7a3722-62c5-4b72-b384-4c23811974da
date added to LUP
2022-12-13 15:08:42
date last changed
2024-06-13 21:37:06
@article{3c7a3722-62c5-4b72-b384-4c23811974da,
  abstract     = {{<p>The human pathogen Haemophilus influenzae causes respiratory tract infections and is commonly associated with prolonged carriage in patients with chronic obstructive pulmonary disease. Production of outer membrane vesicles (OMVs) is a ubiquitous phenomenon observed in Gram-negative bacteria including H. influenzae. OMVs play an important role in various interactions with the human host; from neutralization of antibodies and complement activation to spread of antimicrobial resistance. Upon vesiculation certain proteins are found in OMVs and some proteins are retained at the cell membrane. The mechanism for this phenomenon is not fully elucidated. We employed mass spectrometry to study vesiculation and the fate of proteins in the outer membrane. Functional groups of proteins were differentially distributed on the cell surface and in OMVs. Despite its supposedly periplasmic and outer membrane location, we found that the peptidoglycan synthase-activator Lipoprotein A (LpoA) was accumulated in OMVs relative to membrane fractions. A mutant devoid of LpoA lost its fitness as revealed by growth and electron microscopy. Furthermore, high-pressure liquid chromatography disclosed a lower concentration (55%) of peptidoglycan in the LpoA-deficient H. influenzae compared to the parent wild type bacterium. Using an LpoA-mNeonGreen fusion protein and fluorescence microscopy, we observed that LpoA was enriched in “foci” in the cell envelope, and further located in the septum during cell division. To define the fate of LpoA, C-terminally truncated LpoA-variants were constructed, and we found that the LpoA C-terminal domain promoted optimal transportation to the OMVs as revealed by flow cytometry. Taken together, our study highlights the importance of LpoA for H. influenzae peptidoglycan biogenesis and provides novel insights into cell wall integrity and OMV production.</p>}},
  author       = {{Jalalvand, Farshid and Su, Yu Ching and Manat, Guillaume and Chernobrovkin, Alexey and Kadari, Mahendar and Jonsson, Sandra and Janousková, Martina and Rutishauser, Dorothea and Semsey, Szabolcs and Løbner-Olesen, Anders and Sandblad, Linda and Flärdh, Klas and Mengin-Lecreulx, Dominique and Zubarev, Roman A. and Riesbeck, Kristian}},
  issn         = {{2235-2988}},
  keywords     = {{Haemophilus influenzae; lipoprotein A; LpoA; outer membrane vesicles (OMV); respiratory pathogen}},
  language     = {{eng}},
  publisher    = {{Frontiers Media S. A.}},
  series       = {{Frontiers in cellular and infection microbiology}},
  title        = {{Protein domain-dependent vesiculation of Lipoprotein A, a protein that is important in cell wall synthesis and fitness of the human respiratory pathogen Haemophilus influenzae}},
  url          = {{http://dx.doi.org/10.3389/fcimb.2022.984955}},
  doi          = {{10.3389/fcimb.2022.984955}},
  volume       = {{12}},
  year         = {{2022}},
}