Bacterial Pore-Forming Toxin

A special issue of Toxins (ISSN 2072-6651). This special issue belongs to the section "Bacterial Toxins".

Deadline for manuscript submissions: closed (30 November 2021) | Viewed by 3594

Special Issue Editor


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Guest Editor
Laboratory of molecular microbiology, G. K. Skryabin Institute of Biochemistry and physiology of microorganisms RAS, 5 Prospekt Nauki, Pushchino, Moscow Region 142290, Russia
Interests: bacterial pore-forming toxins; structure; function; evolution; regulation of toxin gene expression; monoclonal antibodies
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Special Issue Information

Dear Colleagues,

The presence of direct evidence of the distribution of pathogenic microorganisms resistant to a wide range of antibiotics and the effective horizontal transfer of resistance genes to them has led to a situation in which antibiotics do not always help to cope with the infection. This requires the development of new approaches in the fight against bacterial infections. The study of the regulation of the expression of bacterial toxins is a basis for the implementation of directed control of the pathogenesis process. Finding ways to disrupt the adaptation of bacteria to various conditions and/or to hinder the expression of toxins, their secretion from the bacterial cell, and the implementation of separate stages of pore formation is certainly urgent. Therefore, a detailed knowledge of the principles of pore formation from genes to obtaining a mature pore makes it possible to determine the places of possible restriction or complete blocking of both the expression of genes of such toxins and their functional activity. Hence, it makes it possible to create an alternative anti-virulent therapy for many diseases, the course of which is determined by bacterial pore-forming toxins. The development of anti-virulence approaches will make it possible to obtain an alternative treatment for bacterial infections by acting directly on pathogenic factors, and not on a pathogenic microorganisms, including the design of monoclonal antibodies, toxin-specific antibodies, and small-molecule inhibitors against pore-forming proteins.

This current Issue is specifically focused on publishing research activities towards developing novel strategies for the diagnosis and suppression of pore-forming toxins. The Issue is expected to publish original research articles, reviews, and short communications in the broad area of pore-forming toxins research.

Dr. Alexander Solonin
Guest Editor

Manuscript Submission Information

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Keywords

  • anti-virulence therapy
  • bacterial pore-forming toxins
  • monoclonal antibodies
  • toxin expression regulation

Published Papers (1 paper)

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Research

12 pages, 2113 KiB  
Article
A Novel and Efficient High-Yield Method for Preparing Bacterial Ghosts
by Yi Ma, Liu Cui, Meng Wang, Qiuli Sun, Kaisheng Liu and Jufang Wang
Toxins 2021, 13(6), 420; https://0-doi-org.brum.beds.ac.uk/10.3390/toxins13060420 - 13 Jun 2021
Cited by 8 | Viewed by 2842
Abstract
Bacterial ghosts (BGs) are empty cell envelopes possessing native extracellular structures without a cytoplasm and genetic materials. BGs are proposed to have significant prospects in biomedical research as vaccines or delivery carriers. The applications of BGs are often limited by inefficient bacterial lysis [...] Read more.
Bacterial ghosts (BGs) are empty cell envelopes possessing native extracellular structures without a cytoplasm and genetic materials. BGs are proposed to have significant prospects in biomedical research as vaccines or delivery carriers. The applications of BGs are often limited by inefficient bacterial lysis and a low yield. To solve these problems, we compared the lysis efficiency of the wild-type protein E (EW) from phage ΦX174 and the screened mutant protein E (EM) in the Escherichia coli BL21(DE3) strain. The results show that the lysis efficiency mediated by protein EM was improved. The implementation of the pLysS plasmid allowed nearly 100% lysis efficiency, with a high initial cell density as high as OD600 = 2.0, which was higher compared to the commonly used BG preparation method. The results of Western blot analysis and immunofluorescence indicate that the expression level of protein EM was significantly higher than that of the non-pLysS plasmid. High-quality BGs were observed by SEM and TEM. To verify the applicability of this method in other bacteria, the T7 RNA polymerase expression system was successfully constructed in Salmonella enterica (S. Enterica, SE). A pET vector containing EM and pLysS were introduced to obtain high-quality SE ghosts which could provide efficient protection for humans and animals. This paper describes a novel and commonly used method to produce high-quality BGs on a large scale for the first time. Full article
(This article belongs to the Special Issue Bacterial Pore-Forming Toxin)
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