Abstract

BackgroundDuring infection, inflammation is partially driven by the release of mediators which facilitate intercellular communication. Amongst these mediators are small membrane vesicles (MVs) that can be released by both host cells and Gram-negative and -positive bacteria. Bacterial membrane vesicles are known to exert immuno-modulatory and -stimulatory actions. Moreover, it has been proposed that host cell-derived vesicles, released during infection, also have immunostimulatory properties. In this study, we assessed the release and activity of host cell-derived and bacterial MVs during the first hours following infection of THP-1 macrophages with the common respiratory pathogens non-typeable Haemophilus influenzae, Moraxella catarrhalis, Streptococcus pneumoniae, and Pseudomonas aeruginosa.ResultsUsing a combination of flow cytometry, tunable resistive pulse sensing (TRPS)-based analysis and electron microscopy, we demonstrated that the release of MVs occurs by both host cells and bacteria during infection. MVs released during infection and bacterial culture were found to induce a strong pro-inflammatory response by naive THP-1 macrophages. Yet, these MVs were also found to induce tolerance of host cells to secondary immunogenic stimuli and to enhance bacterial adherence and the number of intracellular bacteria.ConclusionsBacterial MVs may play a dual role during infection, as they can both trigger and dampen immune responses thereby contributing to immune defence and bacterial survival.

Highlights

  • During infection, inflammation is partially driven by the release of mediators which facilitate intercellular communication

  • To obtain clarity on the dynamics of membrane vesicles (MVs) shedding during infection, we studied the release kinetics and examined the functional activity of both host cell-derived and bacterial MVs released by THP-1 macrophages infected with non-typeable Haemophilus influenzae (NTHi), Moraxella catarrhalis (Mrc), Streptococcus pneumoniae (Spn), and Pseudomonas aeruginosa (Psa), which are well-known opportunistic pathogens most frequently involved in lower respiratory tract infections in humans [14,15,16]

  • To study vesicle release during short-term infection of THP-1 macrophages and during culture of NTHi, Mrc, Spn, and Psa, we first aimed to characterize MVs shed by unstimulated THP-1 macrophages and during culture

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Summary

Introduction

Inflammation is partially driven by the release of mediators which facilitate intercellular communication Amongst these mediators are small membrane vesicles (MVs) that can be released by both host cells and Gram-negative and -positive bacteria. Inflammation in response to bacterial infection results from contact of host cells with bacteria or bacterial products and this process is directed by an extensive communication between cells of the infected tissues, immune cells, and bacteria [1, 2] Involved in this communication are small soluble mediators as well as nanosized membrane vesicles (MVs) that are released by bacteria and by host cells [3,4,5,6]. Only a few studies assessed bacterial MV shedding during infection, and the kinetics for release as well as the Volgers et al BMC Microbiology (2017) 17:216 functionality of MVs shed during infection have remained poorly addressed [10,11,12]

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