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Review
. 2020 Oct 5;7(12):312-322.
doi: 10.15698/mic2020.12.737.

Extracellular vesicles: An emerging platform in gram-positive bacteria

Affiliations
Review

Extracellular vesicles: An emerging platform in gram-positive bacteria

Swagata Bose et al. Microb Cell. .

Abstract

Extracellular vesicles (EV), also known as membrane vesicles, are produced as an end product of secretion by both pathogenic and non-pathogenic bacteria. Several reports suggest that archaea, gram-negative bacteria, and eukaryotic cells secrete membrane vesicles as a means for cell-free intercellular communication. EVs influence intercellular communication by transferring a myriad of biomolecules including genetic information. Also, EVs have been implicated in many phenomena such as stress response, intercellular competition, lateral gene transfer, and pathogenicity. However, the cellular process of secreting EVs in gram-positive bacteria is less studied. A notion with the thick cell-walled microbes such as gram-positive bacteria is that the EV release is impossible among them. The role of gram-positive EVs in health and diseases is being studied gradually. Being nano-sized, the EVs from gram-positive bacteria carry a diversity of cargo compounds that have a role in bacterial competition, survival, invasion, host immune evasion, and infection. In this review, we summarise the current understanding of the EVs produced by gram-positive bacteria. Also, we discuss the functional aspects of these components while comparing them with gram-negative bacteria.

Keywords: HGT; antibiotic resistance; biofilm; extracellular DNA; immune response; pathogenesis; peptidoglycan; quorum sensing; vaccine; virulence.

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Conflict of interest statement

Conflict of interest: Authors declare that they have read the contents of the paper and do not have any competing interests.

Figures

Figure 1
Figure 1. FIGURE 1: Origin and composition of gram-positive EVs.
(A) The release of EVs involves diversified events depending on the cell lytic enzyme viz. PGN degradation followed by cytoplasmic membrane bleb protrusion via endolysins and PGN remodelling via hydrolyzing enzyme autolysins. (B) The internal structure of EVs comprising of nucleic acids, virulence factors, and intracellular proteins.

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