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Updated: Jul 11, 2026

Visualisation and Quantification of Intracellular Interactions of Neisseria meningitidis and Human α-actinin by Confocal Imaging
Published on: October 24, 2010
A functional two-partner secretion system contributes to adhesion of Neisseria meningitidis to epithelial cells
Corinna Schmitt1, David Turner, Maria Boesl
1University of Wuerzburg, Institute of Hygiene and Microbiology, Josef-Schneider-Str. 2, E1, 97080 Wuerzburg, Germany.
Abstract:
Neisseria meningitidis is a frequent commensal of the human nasopharynx causing severe invasive infections in rare cases. A functional two-partner secretion (TPS) system in N. meningitidis, composed of the secreted effector protein HrpA and its cognate transporter HrpB, is identified and characterized in this study. Although all meningococcal strains harbor at least one TPS system, the hrpA genes display significant C-terminal sequence variation. Meningococcal genes encoding the TPS effector proteins and their transporters are closely associated and transcribed into a single mRNA. HrpA proteins are translocated across the meningococcal outer membrane by their cognate transporters HrpB and mainly released into the environment. During this process, HrpA is proteolytically processed to a mature 180-kDa form. In contrast to other known TPS systems, immature HrpA proteins are stable in the absence of HrpB and accumulate within the bacterial cell. A small percentage of mature HrpA remains associated with the bacteria and contributes to the interaction of meningococci with epithelial cells.
Insights
Neisseria meningitidis utilizes a two-partner secretion (TPS) system, involving HrpA and HrpB proteins, for outer membrane translocation. This system influences bacterial interaction with epithelial cells, with variations in HrpA affecting function.
Area of Science:
- Microbiology
- Molecular Biology
- Bacterial Pathogenesis
Background:
- Neisseria meningitidis is a common nasopharyngeal bacterium that can cause invasive diseases.
- Two-partner secretion (TPS) systems are crucial for protein transport in various bacteria.
Purpose of the Study:
- To identify and characterize the functional two-partner secretion (TPS) system in Neisseria meningitidis.
- To investigate the role of the HrpA effector protein and HrpB transporter in N. meningitidis.
Main Methods:
- Genetic analysis of TPS system components (hrpA and hrpB genes).
- Protein translocation and processing assays.
- Bacterial interaction assays with epithelial cells.
Main Results:
- A functional TPS system, comprising HrpA and HrpB, was identified in N. meningitidis.
- HrpA undergoes proteolytic processing to a mature 180-kDa form during translocation.
- Immature HrpA accumulates intracellularly in the absence of HrpB.
- Mature HrpA associated with bacteria contributes to epithelial cell interaction.
Conclusions:
- The study elucidates the mechanism and function of the TPS system in N. meningitidis.
- Variations in HrpA C-terminal sequences were observed.
- The TPS system plays a role in the interaction of N. meningitidis with host epithelial cells.
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