Inhibition and evasion of neutrophil microbicidal responses by Legionella longbeachae

ABSTRACT Legionella species evade degradation and proliferate within alveolar macrophages as an essential step for the manifestation of disease. However, most intracellular bacterial pathogens are restricted in neutrophils, which are the first line of innate immune defense against invading pathogens...

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Main Authors: Hannah E. Hanford, Christopher T. D. Price, Silvia Uriarte, Yousef Abu Kwaik
Format: Article
Language:English
Published: American Society for Microbiology 2025-02-01
Series:mBio
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Online Access:https://journals.asm.org/doi/10.1128/mbio.03274-24
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author Hannah E. Hanford
Christopher T. D. Price
Silvia Uriarte
Yousef Abu Kwaik
author_facet Hannah E. Hanford
Christopher T. D. Price
Silvia Uriarte
Yousef Abu Kwaik
author_sort Hannah E. Hanford
collection DOAJ
description ABSTRACT Legionella species evade degradation and proliferate within alveolar macrophages as an essential step for the manifestation of disease. However, most intracellular bacterial pathogens are restricted in neutrophils, which are the first line of innate immune defense against invading pathogens. Bacterial degradation within neutrophils is mediated by the fusion of microbicidal granules to pathogen-containing phagosomes and the generation of reactive oxygen species (ROS) by the phagocyte NADPH oxidase complex. Here, we show that human neutrophils fail to trigger microbicidal processes and, consequently, fail to restrict L. longbeachae. In addition, neutrophils infected with L. longbeachae fail to undergo a robust pro-inflammatory response, such as degranulation and IL-8 production. Here, we identify three strategies employed by L. longbeachae for evading restriction by neutrophils and inhibiting the neutrophil microbicidal response to other bacteria co-inhabiting in the same cell. First, L. longbeachae excludes the cytosolic and membrane-bound subunits of the phagocyte NADPH oxidase complex from its phagosomal membrane independent of the type 4 secretion system (T4SS). Consequently, infected neutrophils fail to generate robust ROS in response to L. longbeachae. Second, L. longbeachae impedes the fusion of azurophilic granules to its phagosome and the phagosomes of bacteria co-inhabiting the same cell through T4SS-independent mechanisms. Third, L. longbeachae protects phagosomes of co-inhabiting bacteria from degradation by ROS through a trans-acting T4SS-dependent mechanism. Collectively, we conclude that L. longbeachae evades restriction by human neutrophils via T4SS-independent mechanisms and utilizes trans-acting T4SS-dependent mechanisms for inhibition of neutrophil ROS generation throughout the cell cytosol.IMPORTANCELegionella longbeachae is commonly found in soil environments where it interacts with a wide variety of protist hosts and microbial competitors. Upon transmission to humans, L. longbeachae invades and replicates within alveolar macrophages, leading to the manifestation of pneumonia. In addition to alveolar macrophages, neutrophils are abundant immune cells acting as the first line of defense against invading pathogens. While most intracellular bacterial species are killed and degraded by neutrophils, we show that L. longbeachae evades degradation. The pathogen impairs the major neutrophils’ microbicidal processes, including the fusion of microbicidal granules to the pathogen-containing vacuole. By inhibiting of assembly of the phagocyte NADPH oxidase complex, the pathogen blocks neutrophils from generating microbicide reactive oxygen species. Overall, L. longbeachae employs unique virulence strategies to evade the major microbicidal processes of neutrophils.
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spelling doaj-art-d92598a72e1f487896b98e0b9efd837f2025-02-05T14:00:48ZengAmerican Society for MicrobiologymBio2150-75112025-02-0116210.1128/mbio.03274-24Inhibition and evasion of neutrophil microbicidal responses by Legionella longbeachaeHannah E. Hanford0Christopher T. D. Price1Silvia Uriarte2Yousef Abu Kwaik3Department of Microbiology and Immunology, College of Medicine, University of Louisville, Louisville, Kentucky, USADepartment of Microbiology and Immunology, College of Medicine, University of Louisville, Louisville, Kentucky, USADepartment of Microbiology and Immunology, College of Medicine, University of Louisville, Louisville, Kentucky, USADepartment of Microbiology and Immunology, College of Medicine, University of Louisville, Louisville, Kentucky, USAABSTRACT Legionella species evade degradation and proliferate within alveolar macrophages as an essential step for the manifestation of disease. However, most intracellular bacterial pathogens are restricted in neutrophils, which are the first line of innate immune defense against invading pathogens. Bacterial degradation within neutrophils is mediated by the fusion of microbicidal granules to pathogen-containing phagosomes and the generation of reactive oxygen species (ROS) by the phagocyte NADPH oxidase complex. Here, we show that human neutrophils fail to trigger microbicidal processes and, consequently, fail to restrict L. longbeachae. In addition, neutrophils infected with L. longbeachae fail to undergo a robust pro-inflammatory response, such as degranulation and IL-8 production. Here, we identify three strategies employed by L. longbeachae for evading restriction by neutrophils and inhibiting the neutrophil microbicidal response to other bacteria co-inhabiting in the same cell. First, L. longbeachae excludes the cytosolic and membrane-bound subunits of the phagocyte NADPH oxidase complex from its phagosomal membrane independent of the type 4 secretion system (T4SS). Consequently, infected neutrophils fail to generate robust ROS in response to L. longbeachae. Second, L. longbeachae impedes the fusion of azurophilic granules to its phagosome and the phagosomes of bacteria co-inhabiting the same cell through T4SS-independent mechanisms. Third, L. longbeachae protects phagosomes of co-inhabiting bacteria from degradation by ROS through a trans-acting T4SS-dependent mechanism. Collectively, we conclude that L. longbeachae evades restriction by human neutrophils via T4SS-independent mechanisms and utilizes trans-acting T4SS-dependent mechanisms for inhibition of neutrophil ROS generation throughout the cell cytosol.IMPORTANCELegionella longbeachae is commonly found in soil environments where it interacts with a wide variety of protist hosts and microbial competitors. Upon transmission to humans, L. longbeachae invades and replicates within alveolar macrophages, leading to the manifestation of pneumonia. In addition to alveolar macrophages, neutrophils are abundant immune cells acting as the first line of defense against invading pathogens. While most intracellular bacterial species are killed and degraded by neutrophils, we show that L. longbeachae evades degradation. The pathogen impairs the major neutrophils’ microbicidal processes, including the fusion of microbicidal granules to the pathogen-containing vacuole. By inhibiting of assembly of the phagocyte NADPH oxidase complex, the pathogen blocks neutrophils from generating microbicide reactive oxygen species. Overall, L. longbeachae employs unique virulence strategies to evade the major microbicidal processes of neutrophils.https://journals.asm.org/doi/10.1128/mbio.03274-24granuleslysosomesROSNADPH oxidaseazurphilic granules
spellingShingle Hannah E. Hanford
Christopher T. D. Price
Silvia Uriarte
Yousef Abu Kwaik
Inhibition and evasion of neutrophil microbicidal responses by Legionella longbeachae
mBio
granules
lysosomes
ROS
NADPH oxidase
azurphilic granules
title Inhibition and evasion of neutrophil microbicidal responses by Legionella longbeachae
title_full Inhibition and evasion of neutrophil microbicidal responses by Legionella longbeachae
title_fullStr Inhibition and evasion of neutrophil microbicidal responses by Legionella longbeachae
title_full_unstemmed Inhibition and evasion of neutrophil microbicidal responses by Legionella longbeachae
title_short Inhibition and evasion of neutrophil microbicidal responses by Legionella longbeachae
title_sort inhibition and evasion of neutrophil microbicidal responses by legionella longbeachae
topic granules
lysosomes
ROS
NADPH oxidase
azurphilic granules
url https://journals.asm.org/doi/10.1128/mbio.03274-24
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