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Recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation
Bacterial secretion systems mediate the selective exchange of macromolecules between bacteria and their environment, playing a pivotal role in processes such as horizontal gene transfer or virulence. Among the different families of secretion systems, Type III, IV and VI (T3SS, T4SS and T6SS) share t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025392/ https://www.ncbi.nlm.nih.gov/pubmed/36949816 http://dx.doi.org/10.3389/fcimb.2023.1146000 |
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author | Guzmán-Herrador, Dolores L. Fernández-Gómez, Andrea Llosa, Matxalen |
author_facet | Guzmán-Herrador, Dolores L. Fernández-Gómez, Andrea Llosa, Matxalen |
author_sort | Guzmán-Herrador, Dolores L. |
collection | PubMed |
description | Bacterial secretion systems mediate the selective exchange of macromolecules between bacteria and their environment, playing a pivotal role in processes such as horizontal gene transfer or virulence. Among the different families of secretion systems, Type III, IV and VI (T3SS, T4SS and T6SS) share the ability to inject their substrates into human cells, opening up the possibility of using them as customized injectors. For this to happen, it is necessary to understand how substrates are recruited and to be able to engineer secretion signals, so that the transmembrane machineries can recognize and translocate the desired substrates in place of their own. Other factors, such as recruiting proteins, chaperones, and the degree of unfolding required to cross through the secretion channel, may also affect transport. Advances in the knowledge of the secretion mechanism have allowed heterologous substrate engineering to accomplish translocation by T3SS, and to a lesser extent, T4SS and T6SS into human cells. In the case of T4SS, transport of nucleoprotein complexes adds a bonus to its biotechnological potential. Here, we review the current knowledge on substrate recognition by these secretion systems, the many examples of heterologous substrate translocation by engineering of secretion signals, and the current and future biotechnological and biomedical applications derived from this approach. |
format | Online Article Text |
id | pubmed-10025392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100253922023-03-21 Recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation Guzmán-Herrador, Dolores L. Fernández-Gómez, Andrea Llosa, Matxalen Front Cell Infect Microbiol Cellular and Infection Microbiology Bacterial secretion systems mediate the selective exchange of macromolecules between bacteria and their environment, playing a pivotal role in processes such as horizontal gene transfer or virulence. Among the different families of secretion systems, Type III, IV and VI (T3SS, T4SS and T6SS) share the ability to inject their substrates into human cells, opening up the possibility of using them as customized injectors. For this to happen, it is necessary to understand how substrates are recruited and to be able to engineer secretion signals, so that the transmembrane machineries can recognize and translocate the desired substrates in place of their own. Other factors, such as recruiting proteins, chaperones, and the degree of unfolding required to cross through the secretion channel, may also affect transport. Advances in the knowledge of the secretion mechanism have allowed heterologous substrate engineering to accomplish translocation by T3SS, and to a lesser extent, T4SS and T6SS into human cells. In the case of T4SS, transport of nucleoprotein complexes adds a bonus to its biotechnological potential. Here, we review the current knowledge on substrate recognition by these secretion systems, the many examples of heterologous substrate translocation by engineering of secretion signals, and the current and future biotechnological and biomedical applications derived from this approach. Frontiers Media S.A. 2023-03-06 /pmc/articles/PMC10025392/ /pubmed/36949816 http://dx.doi.org/10.3389/fcimb.2023.1146000 Text en Copyright © 2023 Guzmán-Herrador, Fernández-Gómez and Llosa https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Guzmán-Herrador, Dolores L. Fernández-Gómez, Andrea Llosa, Matxalen Recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation |
title | Recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation |
title_full | Recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation |
title_fullStr | Recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation |
title_full_unstemmed | Recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation |
title_short | Recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation |
title_sort | recruitment of heterologous substrates by bacterial secretion systems for transkingdom translocation |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025392/ https://www.ncbi.nlm.nih.gov/pubmed/36949816 http://dx.doi.org/10.3389/fcimb.2023.1146000 |
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