Outer membrane protein A, peptidoglycan-associated lipoprotein, and murein lipoprotein are released by Escherichia coli bacteria into serum
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Updated: Aug 11, 2026

Monitoring the Assembly of a Secreted Bacterial Virulence Factor Using Site-specific Crosslinking
Published on: December 17, 2013
J Hellman1, P M Loiselle, M M Tehan
1Department of Infectious Diseases, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA. hellman@etherdome.mgh.harvard.edu
Abstract:
Complexes containing lipopolysaccharide (LPS) and three outer membrane proteins (OMPs) are released by gram-negative bacteria incubated in human serum and into the circulation in an experimental model of sepsis. The same OMPs are bound by immunoglobulin G (IgG) in the cross-protective antiserum raised to Escherichia coli J5 (anti-J5 IgG). This study was performed to identify the three OMPs. The 35-kDa OMP was identified as outer membrane protein A (OmpA) by immunoblotting studies using OmpA-deficient bacteria and recombinant OmpA protein. The 18-kDa OMP was identified as peptidoglycan-associated lipoprotein (PAL) based on peptide sequences from the purified protein and immunoblotting studies using PAL-deficient bacteria. The 5- to 9-kDa OMP was identified as murein lipoprotein (MLP) based on immunoblotting studies using MLP-deficient bacteria. The studies identify the OMPs released into human serum and into the circulation in an experimental model of sepsis as OmpA, PAL, and MLP.
Insights
Gram-negative bacteria release outer membrane proteins (OMPs) during sepsis. This study identifies these OMPs as outer membrane protein A (OmpA), peptidoglycan-associated lipoprotein (PAL), and murein lipoprotein (MLP).
Area of Science:
- Microbiology and Immunology
- Bacterial Outer Membrane Proteins
- Sepsis Pathogenesis
Background:
- Gram-negative bacteria release outer membrane protein (OMP) and lipopolysaccharide (LPS) complexes during sepsis.
- These OMPs are targeted by immunoglobulin G (IgG) in protective antisera, suggesting a role in immune response.
- Identifying these specific OMPs is crucial for understanding sepsis mechanisms and developing therapeutic strategies.
Purpose of the Study:
- To identify the three specific outer membrane proteins (OMPs) released by gram-negative bacteria in the presence of human serum and during experimental sepsis.
- To characterize the molecular identity of OMPs recognized by cross-protective antibodies.
Main Methods:
- Immunoblotting techniques were employed to identify the OMPs.
- Studies utilized OmpA-deficient and PAL-deficient bacteria, alongside purified recombinant OmpA and peptide sequencing of purified proteins.
- Murein lipoprotein (MLP)-deficient bacteria were also used for identification.
Main Results:
- The 35-kDa OMP was identified as outer membrane protein A (OmpA).
- The 18-kDa OMP was identified as peptidoglycan-associated lipoprotein (PAL).
- The 5- to 9-kDa OMP was identified as murein lipoprotein (MLP).
Conclusions:
- The study successfully identified the three major OMPs released by gram-negative bacteria in human serum and circulation during experimental sepsis.
- These identified OMPs are OmpA, PAL, and MLP, providing critical targets for further immunological investigation and potential therapeutic development in sepsis.
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