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Published on: March 23, 2019
Effect of combined oxidative and nitrosative stress on Neisseria meningitidis
Abstract:
Reactive oxygen and nitrogen species are produced by the human immune system in response to infection. Methods to detoxify these reactive species are vital to the survival of human pathogens, such as Neisseria meningitidis, which is the major aetiological agent of bacterial meningitis. Following activation, macrophages produce superoxide (O(2)(-)), hydrogen peroxide (H(2)O(2)) and nitric oxide (NO). The toxicity of O(2)(-), generated using X/Xo (xanthine/xanthine oxidase), and H(2)O(2) was investigated in the presence and absence of the NO donor DEA-NONOate [2-(N,N-diethylamino)-diazenolate-2-oxide diethylammonium salt]. Most of the toxicity from X/Xo was due to H(2)O(2). In N. meningitidis, NO decreased the toxicity of the H(2)O(2). In contrast, in the enteric bacterium Escherichia coli, NO increased the toxicity of the H(2)O(2).
Insights
Pathogens like Neisseria meningitidis use detoxification methods against immune reactive species. Nitric oxide (NO) affects hydrogen peroxide (H2O2) toxicity differently in bacteria, decreasing it in N. meningitidis but increasing it in E. coli.
Area of Science:
- Microbiology
- Immunology
- Biochemistry
Background:
- The human immune system produces reactive oxygen and nitrogen species to combat infections.
- Pathogen survival often depends on their ability to detoxify these reactive species.
- Neisseria meningitidis, a key cause of bacterial meningitis, requires detoxification mechanisms.
Purpose of the Study:
- To investigate the toxicity of superoxide (O(2)(-)) and hydrogen peroxide (H(2)O(2)) generated by immune cells.
- To determine the role of nitric oxide (NO) in modulating the toxicity of reactive oxygen species in bacterial pathogens.
- To compare the effects of NO on reactive oxygen species toxicity in Neisseria meningitidis and Escherichia coli.
Main Methods:
- Generated superoxide (O(2)(-)) using xanthine/xanthine oxidase (X/Xo) system.
- Assessed hydrogen peroxide (H(2)O(2)) toxicity in the presence and absence of a nitric oxide (NO) donor (DEA-NONOate).
- Compared the impact of NO on reactive oxygen species toxicity in Neisseria meningitidis and Escherichia coli.
Main Results:
- Hydrogen peroxide (H(2)O(2)) was the primary toxic agent from the xanthine/xanthine oxidase (X/Xo) system.
- Nitric oxide (NO) reduced the toxicity of H(2)O(2) towards Neisseria meningitidis.
- Nitric oxide (NO) enhanced the toxicity of H(2)O(2) towards Escherichia coli.
Conclusions:
- Nitric oxide (NO) plays a differential role in modulating reactive oxygen species toxicity in bacterial pathogens.
- Understanding these interactions is crucial for developing strategies against bacterial meningitis and other infections.
- Bacterial species exhibit distinct responses to immune-derived reactive nitrogen species.
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