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H2S, a Bacterial Defense Mechanism against the Host Immune Response.


ABSTRACT: The biological mediator hydrogen sulfide (H2S) is produced by bacteria and has been shown to be cytoprotective against oxidative stress and to increase the sensitivity of various bacteria to a range of antibiotic drugs. Here we evaluated whether bacterial H2S provides resistance against the immune response, using two bacterial species that are common sources of nosocomial infections, Escherichia coli and Staphylococcus aureus Elevations in H2S levels increased the resistance of both species to immune-mediated killing. Clearances of infections with wild-type and genetically H2S-deficient E. coli and S. aureus were compared in vitro and in mouse models of abdominal sepsis and burn wound infection. Also, inhibitors of H2S-producing enzymes were used to assess bacterial killing by leukocytes. We found that inhibition of bacterial H2S production can increase the susceptibility of both bacterial species to rapid killing by immune cells and can improve bacterial clearance after severe burn, an injury that increases susceptibility to opportunistic infections. These findings support the role of H2S as a bacterial defense mechanism against the host response and implicate bacterial H2S inhibition as a potential therapeutic intervention in the prevention or treatment of infections.

SUBMITTER: Toliver-Kinsky T 

PROVIDER: S-EPMC6300618 | biostudies-literature | 2019 Jan

REPOSITORIES: biostudies-literature

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H<sub>2</sub>S, a Bacterial Defense Mechanism against the Host Immune Response.

Toliver-Kinsky Tracy T   Cui Weihua W   Törö Gabor G   Lee Seung-Jin SJ   Shatalin Konstantin K   Nudler Evgeny E   Szabo Csaba C  

Infection and immunity 20181219 1


The biological mediator hydrogen sulfide (H<sub>2</sub>S) is produced by bacteria and has been shown to be cytoprotective against oxidative stress and to increase the sensitivity of various bacteria to a range of antibiotic drugs. Here we evaluated whether bacterial H<sub>2</sub>S provides resistance against the immune response, using two bacterial species that are common sources of nosocomial infections, <i>Escherichia coli</i> and <i>Staphylococcus aureus</i> Elevations in H<sub>2</sub>S level  ...[more]

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