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Published on: March 4, 2020
Replication of Neisseria meningitidis within epithelial cells requires TonB-dependent acquisition of host cell iron
Jason A Larson1, Dustin L Higashi, Igor Stojiljkovic
1Department of Molecular Microbiology and Immunology, Oregon Health Sciences University, Portland, Oregon 97201, USA. larsonja@ohsu.edu
Abstract:
Neisseria meningitidis (meningococcus [MC]) is able to enter and replicate within epithelial cells. Iron, an essential nutrient for nearly all organisms, is an important determinant in the ability of MC to cause disease; however, its role in MC intracellular replication has not been investigated. We analyzed the growth of MC within the A431 human epithelial cell line and the dependence of this growth on iron uptake. We present evidence here that chelation of iron from infected tissue culture cells with Desferal strongly inhibited intracellular replication of wild-type (wt) MC. We also provide genetic evidence that iron must be acquired by MC from the host cell in order for it to replicate. An hmbR mutant that is unable to use hemoglobin iron and could not grow in tissue culture media without iron supplementation replicated more rapidly within epithelial cells than its wt parent strain. An fbpA mutant that is unable to utilize human transferrin iron or lactoferrin iron replicated normally within cells. In contrast, a tonB mutant could not replicate intracellularly unless infected cultures were supplemented with ferric nitrate. Taken together, these findings strongly suggest that MC intracellular replication requires TonB-dependent uptake of a novel host cell iron source.
Insights
Neisseria meningitidis (meningococcus) requires iron for intracellular replication within epithelial cells. Host cell iron uptake, particularly via the TonB system, is crucial for meningococcal growth inside host cells.
Area of Science:
- Microbiology
- Cell Biology
- Infectious Diseases
Background:
- Neisseria meningitidis (meningococcus) invades and replicates within epithelial cells.
- Iron is vital for bacterial growth, but its role in meningococcal intracellular replication is unknown.
Purpose of the Study:
- To investigate the role of iron uptake in the intracellular replication of Neisseria meningitidis within epithelial cells.
Main Methods:
- Analyzing meningococcal growth in A431 human epithelial cells.
- Using iron chelators (Desferal) and genetic mutants (hmbR, fbpA, tonB) to assess iron dependence.
Main Results:
- Iron chelation significantly inhibited wild-type meningococcal intracellular replication.
- Mutants lacking hemoglobin or transferrin iron uptake replicated differently, indicating specific iron source requirements.
- A tonB mutant's replication was restored by ferric nitrate supplementation, highlighting TonB-dependent iron acquisition.
Conclusions:
- Intracellular replication of Neisseria meningitidis is dependent on acquiring iron from the host epithelial cell.
- The TonB-dependent iron uptake system is essential for meningococcal intracellular growth.
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