Interaction with the host: the role of fibronectin and extracellular matrix proteins in the adhesion of Gram-negative bacteria.
Adhesins
Collagen
Extracellular matrix proteins
Fibronectin
Gram-negative bacteria
Laminin
Journal
Medical microbiology and immunology
ISSN: 1432-1831
Titre abrégé: Med Microbiol Immunol
Pays: Germany
ID NLM: 0314524
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
24
07
2019
accepted:
14
11
2019
pubmed:
1
12
2019
medline:
11
2
2021
entrez:
1
12
2019
Statut:
ppublish
Résumé
The capacity of pathogenic microorganisms to adhere to host cells and avoid clearance by the host immune system is the initial and most decisive step leading to infections. Bacteria have developed different strategies to attach to diverse host surface structures. One important strategy is the adhesion to extracellular matrix (ECM) proteins (e.g., collagen, fibronectin, laminin) that are highly abundant in connective tissue and basement membranes. Gram-negative bacteria express variable outer membrane proteins (adhesins) to attach to the host and to initiate the process of infection. Understanding the underlying molecular mechanisms of bacterial adhesion is a prerequisite for targeting this interaction by "anti-ligands" to prevent colonization or infection of the host. Future development of such "anti-ligands" (specifically interfering with bacteria-host matrix interactions) might result in the development of a new class of anti-infective drugs for the therapy of infections caused by multidrug-resistant Gram-negative bacteria. This review summarizes our current knowledge about the manifold interactions of adhesins expressed by Gram-negative bacteria with ECM proteins and the use of this information for the generation of novel therapeutic antivirulence strategies.
Identifiants
pubmed: 31784893
doi: 10.1007/s00430-019-00644-3
pii: 10.1007/s00430-019-00644-3
pmc: PMC7248048
doi:
Substances chimiques
Adhesins, Bacterial
0
Extracellular Matrix Proteins
0
Fibronectins
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
277-299Subventions
Organisme : H2020 European Research Council
ID : Marie Sklodowska-Curie Grant Agreement No 765042
Organisme : Deutsche Forschungsgemeinschaft
ID : DFG FOR 2251
Organisme : Robert Koch Institut, Berlin, Germany
ID : Bartonella consiliary laboratory
Organisme : Robert Koch Institut, Berlin, Germany
ID : 1369-354
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