Engineering a genome-reduced bacterium to eliminate Staphylococcus aureus biofilms in vivo
Author
Publication date
2021ISSN
1744-4292
Abstract
Bacteria present a promising delivery system for treating human diseases. Here, we engineered the genome-reduced human lung pathogen Mycoplasma pneumoniae as a live biotherapeutic to treat biofilm-associated bacterial infections. This strain has a unique genetic code, which hinders gene transfer to most other bacterial genera, and it lacks a cell wall, which allows it to express proteins that target peptidoglycans of pathogenic bacteria. We first determined that removal of the pathogenic factors fully attenuated the chassis strain in vivo. We then designed synthetic promoters and identified an endogenous peptide signal sequence that, when fused to heterologous proteins, promotes efficient secretion. Based on this, we equipped the chassis strain with a genetic platform designed to secrete antibiofilm and bactericidal enzymes, resulting in a strain capable of dissolving Staphylococcus aureus biofilms preformed on catheters in vitro, ex vivo, and in vivo. To our knowledge, this is the first engineered genome-reduced bacterium that can fight against clinically relevant biofilm-associated bacterial infections.
Document Type
Article
Document version
Published version
Language
English
Subject (CDU)
57 - Biological sciences in general
578 - Virology
616.9 - Communicable diseases. Infectious and contagious diseases, fevers
Keywords
Pages
20
Publisher
EMBO Press
Collection
17;
Is part of
Molecular Systems Biology
Citation
Garrido, Victoria; Piñero-Lambea, Carlos; Rodriguez-Arce, Irene [et al.]. Engineering a genome-reduced bacterium to eliminate Staphylococcus aureus biofilms in vivo. Molecular Systems Biology, 2021, 17, e10145. Disponible en: <https://www.embopress.org/doi/full/10.15252/msb.202010145>. Fecha de acceso: 16 dic. 2021. DOI: 10.15252/msb.202010145
Grant agreement number
info:eu-repo/grantAgreement/EU/H2020/670216
info:eu-repo/grantAgreement/EU/H2020/634942
Note
This work has been supported by the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program, under grant agreement 670216 (MYCOCHASSIS). We also acknowledge the support of the Spanish Ministry of Economy, Industry and Competitiveness (MEIC) to the EMBL partnership, the Centro de Excelencia Severo Ochoa, the CERCA Program from the Generalitat de Catalunya, the European Union’s Horizon 2020 research and innovation program under grant agreement 634942 (MycoSynVac), and the LaCaixa Fundation grant (Livetherapeutics HR18-00058). M.L.-S. acknowledges the support from FEDER project from Instituto Carlos III (ISCIII, Accion Estrat egica en Salud 2016) (reference CP16/00094). We also acknowledge the staff of CRG/UPF Proteomics Unit, which is part of the Spanish Infrastructure for Omics Technologies (ICTS OmicsTech) unit is a member of the ProteoRed PRB3 consortium, which is supported by grant PT17/0019 of the PE I + D+i 2013-2016 from the Instituto de Salud Carlos III (ISCIII) and ERDF. We also acknowledge Margarita Ecay for her assistance in the PET images analysis and Samuel Miravet-Verde for the bioinformatic support.
This item appears in the following Collection(s)
- Ciències Bàsiques [94]
Rights
2021 - The Authors. Published under the terms of the CC BY4.0 license.
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0/


