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Open AccessJournal ArticleDOI

Antibiotics Stimulate Formation of Vesicles in Staphylococcus aureus in both Phage-Dependent and -Independent Fashions and via Different Routes

TLDR
It is shown that antibiotics can induce MVs through different routes in the important human pathogen Staphylococcus aureus, and evidence that the amount of DNA associated with MVs formed by phage lysis is greater than that for MV formed by β-lactam antibiotic-induced blebbing is presented.
Abstract
Bacterial membrane vesicle research has so far focused mainly on Gram-negative bacteria. Only recently have Gram-positive bacteria been demonstrated to produce and release extracellular membrane vesicles (MVs) that contribute to bacterial virulence. Although treatment of bacteria with antibiotics is a well-established trigger of bacterial MV formation, the underlying mechanisms are poorly understood. In this study, we show that antibiotics can induce MVs through different routes in the important human pathogen Staphylococcus aureus DNA-damaging agents and antibiotics inducing the SOS response triggered vesicle formation in lysogenic strains of S. aureus but not in their phage-devoid counterparts. The β-lactam antibiotics flucloxacillin and ceftaroline increased vesicle formation in a prophage-independent manner by weakening the peptidoglycan layer. We present evidence that the amount of DNA associated with MVs formed by phage lysis is greater than that for MVs formed by β-lactam antibiotic-induced blebbing. The purified MVs derived from S. aureus protected the bacteria from challenge with daptomycin, a membrane-targeting antibiotic, both in vitro and ex vivo in whole blood. In addition, the MVs protected S. aureus from killing in whole blood, indicating that antibiotic-induced MVs function as a decoy and thereby contribute to the survival of the bacterium.

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Cracking Open Bacterial Membrane Vesicles.

TL;DR: This review will discuss recent progress in understanding the biochemical composition and properties of MVs, and show the potential for applications in various fields.
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Extracellular Vesicle Biogenesis and Functions in Gram-Positive Bacteria.

TL;DR: The latest findings on the biogenesis and functions of EVs from Gram-positive bacteria are reviewed and key areas for future research are identified.
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Microbiota-derived extracellular vesicles in interkingdom communication in the gut.

TL;DR: In this article, the authors review current knowledge on microbiota EVs and specifically highlight their role in controlling host metabolism, intestinal barrier integrity and immune training, and highlight their importance in the development of the human intestine.
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Staphylococcus aureus membrane vesicles contain immunostimulatory DNA, RNA and peptidoglycan that activate innate immune receptors and induce autophagy.

TL;DR: In this article, the authors examined the morphology, contents and immunostimulatory functions of MVs produced by three Staphylococcus aureus strains; a methicillin resistant clinical isolate, a methicity sensitive clinical isolate and a laboratory-adapted strain.
Journal ArticleDOI

Answers to naysayers regarding microbial extracellular vesicles.

TL;DR: In this review, doubts that have been verbalized to us and answers to counter them are provided to highlight the most pressing topics in the authors' understanding of the biological processes underlying these structures.
References
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Journal ArticleDOI

Staphylococcus aureus infections.

TL;DR: In an elegant series of clinical observations and laboratory studies published in 1880 and 1882, Ogston described staphylococcal disease and its role in sepsis and abscess formation.
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Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances

TL;DR: The aim of broth and agar dilution methods is to determine the lowest concentration of the assayed antimicrobial agent (minimal inhibitory concentration, MIC) that, under defined test conditions, inhibits the visible growth of the bacterium being investigated.
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The toxic shock syndrome exotoxin structural gene is not detectably transmitted by a prophage

TL;DR: It is shown here that TSSE is not demonstrably transferred by lysogeny; moreover, the gene is cloned and the cloned product is serologically and biologically indistinguishable from the native protein, and that the TSSE determinant is associated with a larger DNA segment that is absent or rearranged in TSSE− strains.
Journal ArticleDOI

Outer-membrane vesicles from Gram-negative bacteria: biogenesis and functions

TL;DR: This Review discusses recent advances in the study of OMVs, focusing on new insights into the mechanisms of biogenesis and the functions of these vesicles.
Journal ArticleDOI

Through the wall: extracellular vesicles in Gram-positive bacteria, mycobacteria and fungi

TL;DR: The current status of vesiculogenesis research in thick-walled microorganisms is described and the cargo and functions associated with EVs in these species are discussed.
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