Cargando…

Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation

Anti-virulence strategy has been considered as one of the most promising approaches to combat drug-resistant bacterial infections. Pore-forming toxins (PFTs) are the largest class of bacterial toxins, inflicting their virulence effect through creating pores on the cell membrane. However, current sol...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Chunying, Ruan, Shuangrong, He, Ying, Li, Xuejing, Zhu, Yuefei, Wang, Honglan, Huang, Hanwei, Pang, Zhiqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643297/
https://www.ncbi.nlm.nih.gov/pubmed/36386467
http://dx.doi.org/10.1016/j.apsb.2022.03.015
_version_ 1784826491745337344
author Liu, Chunying
Ruan, Shuangrong
He, Ying
Li, Xuejing
Zhu, Yuefei
Wang, Honglan
Huang, Hanwei
Pang, Zhiqing
author_facet Liu, Chunying
Ruan, Shuangrong
He, Ying
Li, Xuejing
Zhu, Yuefei
Wang, Honglan
Huang, Hanwei
Pang, Zhiqing
author_sort Liu, Chunying
collection PubMed
description Anti-virulence strategy has been considered as one of the most promising approaches to combat drug-resistant bacterial infections. Pore-forming toxins (PFTs) are the largest class of bacterial toxins, inflicting their virulence effect through creating pores on the cell membrane. However, current solutions for eliminating PFTs are mostly designed based on their molecular structure, requiring customized design for different interactions. In the present study, we employed erythroliposome (denoted as RM-PL), a biomimetic platform constructed by artificial lipid membranes and natural erythrocyte membranes, to neutralize different hemolytic PFTs regardless of their molecular structure. When tested with model PFTs, including α-hemolysin, listeriolysin O, and streptolysin O, RM-PL could completely inhibit toxin-induced hemolysis in a concentration-dependent manner. In vivo studies further confirmed that RM-PL could efficiently neutralize various toxins and save animals’ lives without causing damage to organs or tissues. In addition, we explored the underlying mechanisms of this efficient detoxification ability and found that it was mainly macrophages in the spleen and the liver that took up RM-PL-absorbed toxins through a variety of endocytosis pathways and digested them in lysosomes. In summary, the biomimetic RM-PL presented a promising system for broad-spectrum and powerful toxin neutralization with a mechanism of lysosome-mediated toxin degradation.
format Online
Article
Text
id pubmed-9643297
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-96432972022-11-15 Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation Liu, Chunying Ruan, Shuangrong He, Ying Li, Xuejing Zhu, Yuefei Wang, Honglan Huang, Hanwei Pang, Zhiqing Acta Pharm Sin B Original Article Anti-virulence strategy has been considered as one of the most promising approaches to combat drug-resistant bacterial infections. Pore-forming toxins (PFTs) are the largest class of bacterial toxins, inflicting their virulence effect through creating pores on the cell membrane. However, current solutions for eliminating PFTs are mostly designed based on their molecular structure, requiring customized design for different interactions. In the present study, we employed erythroliposome (denoted as RM-PL), a biomimetic platform constructed by artificial lipid membranes and natural erythrocyte membranes, to neutralize different hemolytic PFTs regardless of their molecular structure. When tested with model PFTs, including α-hemolysin, listeriolysin O, and streptolysin O, RM-PL could completely inhibit toxin-induced hemolysis in a concentration-dependent manner. In vivo studies further confirmed that RM-PL could efficiently neutralize various toxins and save animals’ lives without causing damage to organs or tissues. In addition, we explored the underlying mechanisms of this efficient detoxification ability and found that it was mainly macrophages in the spleen and the liver that took up RM-PL-absorbed toxins through a variety of endocytosis pathways and digested them in lysosomes. In summary, the biomimetic RM-PL presented a promising system for broad-spectrum and powerful toxin neutralization with a mechanism of lysosome-mediated toxin degradation. Elsevier 2022-11 2022-03-29 /pmc/articles/PMC9643297/ /pubmed/36386467 http://dx.doi.org/10.1016/j.apsb.2022.03.015 Text en © 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Liu, Chunying
Ruan, Shuangrong
He, Ying
Li, Xuejing
Zhu, Yuefei
Wang, Honglan
Huang, Hanwei
Pang, Zhiqing
Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation
title Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation
title_full Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation
title_fullStr Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation
title_full_unstemmed Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation
title_short Broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation
title_sort broad-spectrum and powerful neutralization of bacterial toxins by erythroliposomes with the help of macrophage uptake and degradation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643297/
https://www.ncbi.nlm.nih.gov/pubmed/36386467
http://dx.doi.org/10.1016/j.apsb.2022.03.015
work_keys_str_mv AT liuchunying broadspectrumandpowerfulneutralizationofbacterialtoxinsbyerythroliposomeswiththehelpofmacrophageuptakeanddegradation
AT ruanshuangrong broadspectrumandpowerfulneutralizationofbacterialtoxinsbyerythroliposomeswiththehelpofmacrophageuptakeanddegradation
AT heying broadspectrumandpowerfulneutralizationofbacterialtoxinsbyerythroliposomeswiththehelpofmacrophageuptakeanddegradation
AT lixuejing broadspectrumandpowerfulneutralizationofbacterialtoxinsbyerythroliposomeswiththehelpofmacrophageuptakeanddegradation
AT zhuyuefei broadspectrumandpowerfulneutralizationofbacterialtoxinsbyerythroliposomeswiththehelpofmacrophageuptakeanddegradation
AT wanghonglan broadspectrumandpowerfulneutralizationofbacterialtoxinsbyerythroliposomeswiththehelpofmacrophageuptakeanddegradation
AT huanghanwei broadspectrumandpowerfulneutralizationofbacterialtoxinsbyerythroliposomeswiththehelpofmacrophageuptakeanddegradation
AT pangzhiqing broadspectrumandpowerfulneutralizationofbacterialtoxinsbyerythroliposomeswiththehelpofmacrophageuptakeanddegradation