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Isolation and Chemical Characterization of Lipid A from Gram-negative Bacteria
Published on: September 16, 2013
Lipid a remodeling modulates outer membrane vesicle biogenesis by Porphyromonas gingivalis
Sarah R Alaei1, Alisa J King1, Karim Banani2
1Division of Science and Mathematics, School of Interdisciplinary Arts and Sciences, University of Washington, Tacoma, Washington, USA.
Abstract:
Outer membrane vesicles (OMVs) are small membrane enclosed sacs released from bacteria which serve as carriers of biomolecules that shape interactions with the surrounding environment. The periodontal pathogen, Porphyromonas gingivalis, is a prolific OMV producer. Here, we investigated how the structure of lipid A, a core outer membrane molecule, influences P. gingivalis OMV production, OMV-dependent TLR4 activation, and biofilm formation. We examined mutant strains of P. gingivalis 33277 deficient for enzymes that alter lipid A phosphorylation and acylation status. The lipid A C4'-phosphatase (lpxF)-deficient strain and strains bearing inactivating point mutations in the LpxF active site displayed markedly reduced OMV production relative to WT. In contrast, strains deficient for either the lipid A C1-phosphatase (lpxE) or the lipid A deacylase (PGN_1123; lpxZ) genes did not display alterations in OMV abundance compared to WT. These data indicate that lipid A C4'-phosphate removal is required for typical OMV formation. In addition, OMVs produced by ΔlpxF and ΔlpxZ strains, possessing only penta-acylated lipid A, stimulated robust TLR4 activation, whereas OMVs obtained from WT and ΔlpxE strains, containing predominantly tetra-acylated lipid A, did not. Hence, lipid A remodeling modulates the capacity of OMVs to engage host TLR4-dependent immunity. Finally, we demonstrate an inverse relationship between OMV abundance and biofilm density, with the ∆lpxF mutants forming denser biofilms than either WT, ΔlpxE, or ΔlpxZ strains. Therefore, OMVs may also contribute to pathogenesis by regulating biofilm formation and dispersal.IMPORTANCEPorphyromonas gingivalis is a bacterium strongly associated with periodontitis. P. gingivalis exports lipids, proteins, and other biomolecules that contribute to the bacterium's ability to persist in inflammatory conditions encountered during disease. These biomolecules are exported through several mechanisms, including via outer membrane vesicles (OMVs). Despite their ubiquity, the mechanisms that drive outer membrane vesicle production vary among bacteria and are not fully understood. In this study, we report that C4' dephosphorylation of lipid A, a major outer membrane molecule, is required for robust outer membrane vesicle production and biological function in P. gingivalis. This finding adds to the growing body of evidence that lipid A structure is an important factor in outer membrane vesicle biogenesis in diverse bacterial species.
Insights
Outer membrane vesicles (OMVs) production in Porphyromonas gingivalis is significantly reduced when the lipid A molecule lacks a C4 phosphate group. This lipid A modification also impacts OMV
Area of Science:
- Microbiology and Immunology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- Porphyromonas gingivalis is a key pathogen in periodontitis, utilizing outer membrane vesicles (OMVs) to export biomolecules.
- OMVs play crucial roles in bacterial interactions and pathogenesis, but OMV production mechanisms are not fully understood.
- Lipid A structure is a critical component of the outer membrane and can influence bacterial behavior and host interactions.
Purpose of the Study:
- To investigate how alterations in lipid A structure affect P. gingivalis OMV production.
- To determine the impact of lipid A modifications on OMV-mediated Toll-like receptor 4 (TLR4) activation.
- To assess the relationship between OMV production, lipid A structure, and biofilm formation in P. gingivalis.
Main Methods:
- Construction and analysis of P. gingivalis mutant strains deficient in enzymes modifying lipid A phosphorylation and acylation.
- Quantification of OMV production in wild-type and mutant strains.
- Assessment of TLR4 activation by OMVs from different strains and measurement of biofilm density.
Main Results:
- Deficiency in the lipid A C4'-phosphatase (lpxF) gene significantly reduced OMV production.
- OMVs from lpxF and lpxZ mutants (penta-acylated lipid A) induced robust TLR4 activation, unlike WT and lpxE mutants (tetra-acylated lipid A).
- Reduced OMV production correlated with increased biofilm density, suggesting OMVs regulate biofilm formation and dispersal.
Conclusions:
- C4' dephosphorylation of lipid A is essential for typical P. gingivalis OMV biogenesis.
- Lipid A structure remodeling by P. gingivalis modulates OMV immunogenicity and TLR4 engagement.
- OMVs produced by P. gingivalis contribute to pathogenesis by influencing biofilm dynamics and potentially host immune responses.
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