Interactions of Neisseria gonorrhoeae with adherent polymorphonuclear leukocytes
Mark P Simons1, William M Nauseef, Michael A Apicella
1Department of Microbiology, 3-403 Bowen Science Building, University of Iowa, 51 Newton Rd., Iowa City, IA 52242, USA.
Abstract:
Neisseria gonorrhoeae causes severe exudative urethritis. The exudates from infected individuals contain large numbers of polymorphonuclear leukocytes (PMN) with ingested gonococci. The fate of N. gonorrhoeae within PMN has been a topic of debate for years. In this study, we examined the interactions of N. gonorrhoeae with PMN adherent to surfaces as a system that better models events during clinical disease. Using chemiluminescence to measure reactive oxygen species (ROS), we found that N. gonorrhoeae stimulated PMN to produce a respiratory burst. Different kinetics were seen when PMN were stimulated with opsonized zymosan particles. In addition, ROS were produced predominantly inside the PMN in response to gonococci. Laser scanning confocal microscopy and transmission electron microscopy showed that N. gonorrhoeae rapidly associated with PMN under these experimental conditions and was internalized. Some gonococci were cleared in the first 30 to 60 min after phagocytosis, but a majority of the population persisted for 6 h after phagocytosis. Quantification of viable organisms showed that a significant portion of the population resisted killing. The viability of this subpopulation remained unchanged for 2 h after phagocytosis. A significant increase of viable gonococci from 1 to 6 h was also observed, suggesting intracellular replication. Four different N. gonorrhoeae strains demonstrated the same capacity to resist PMN-mediated killing, whereas Escherichia coli was rapidly killed by PMN under the same conditions. Taken together, these findings suggest that a subpopulation of N. gonorrhoeae resists killing and replicates within PMN phagosomes in spite of NADPH oxidase activation.
Insights
Neisseria gonorrhoeae evades killing by human immune cells called polymorphonuclear leukocytes (PMN). A subpopulation of gonococci survives and replicates inside PMN, despite the immune cells activating their respiratory burst to kill bacteria.
Area of Science:
- Microbiology
- Immunology
- Cell Biology
Background:
- Neisseria gonorrhoeae causes urethritis, with bacteria found within polymorphonuclear leukocytes (PMN) in patient exudates.
- The survival mechanisms of N. gonorrhoeae inside PMN are not fully understood and remain a subject of debate.
- Previous studies have not fully replicated the in vivo conditions of PMN-host interactions.
Purpose of the Study:
- To investigate the interaction between N. gonorrhoeae and surface-adherent PMN, modeling clinical scenarios.
- To determine the fate of N. gonorrhoeae following phagocytosis by PMN.
- To assess the role of reactive oxygen species (ROS) in PMN-mediated killing of N. gonorrhoeae.
Main Methods:
- Utilized chemiluminescence to measure ROS production in PMN stimulated with N. gonorrhoeae.
- Employed laser scanning confocal and transmission electron microscopy to visualize bacterial-PMN interactions and internalization.
- Quantified viable N. gonorrhoeae populations over time post-phagocytosis.
Main Results:
- N. gonorrhoeae stimulated PMN to produce ROS, with production occurring intracellularly.
- Gonococci were rapidly internalized by PMN, but a significant subpopulation resisted killing for up to 6 hours.
- Intracellular N. gonorrhoeae viability increased between 1 and 6 hours, suggesting replication.
- Unlike N. gonorrhoeae, Escherichia coli was rapidly killed by PMN under identical conditions.
Conclusions:
- A subpopulation of N. gonorrhoeae possesses mechanisms to resist killing by activated PMN.
- N. gonorrhoeae can survive and replicate within PMN phagosomes, contributing to persistent infection.
- These findings highlight bacterial resistance strategies against key innate immune responses.
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