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http://hdl.handle.net/10553/132333
Título: | Targeting plasmid-encoded proteins that contain immunoglobulin-like domains to combat antimicrobial resistance | Autores/as: | Miró, Luïsa Prieto, Alejandro Margolles, Yago Bernabeu, Manuel Salguero, David Merino, Susana Tomas, Joan Corbera Sánchez, Juan Alberto Perez-Bosque, Anna Huttener, Mario Fernández, Luis Ángel Juarez, Antonio |
Clasificación UNESCO: | 240111 Patología animal 310905 Microbiología |
Palabras clave: | Enterica Infectious Disease Microbiology Mouse Salmonella, et al. |
Fecha de publicación: | 2024 | Publicación seriada: | eLife | Resumen: | Antimicrobial resistance (AMR) poses a significant threat to human health. Although vaccines have been developed to combat AMR, it has proven challenging to associate specific vaccine antigens with AMR. Bacterial plasmids play a crucial role in the transmission of AMR. Our recent research has identified a group of bacterial plasmids (specifically, IncHI plasmids) that encode large molecular mass proteins containing bacterial immunoglobulin-like domains. These proteins are found on the external surface of the bacterial cells, such as in the flagella or conjugative pili. In this study, we show that these proteins are antigenic and can protect mice from infection caused by an AMR Salmonella strain harboring one of these plasmids. Furthermore, we successfully generated nanobodies targeting these proteins, that were shown to interfere with the conjugative transfer of IncHI plasmids. Considering that these proteins are also encoded in other groups of plasmids, such as IncA/C and IncP2, targeting them could be a valuable strategy in combating AMR infections caused by bacteria harboring different groups of AMR plasmids. Since the selected antigens are directly linked to AMR itself, the protective effect extends beyond specific microorganisms to include all those carrying the corresponding resistance plasmids. | URI: | http://hdl.handle.net/10553/132333 | ISSN: | 2050-084X | DOI: | 10.7554/eLife.95328.3 | Fuente: | eLife[EISSN 2050-084X],v. 13, (Julio 2024) |
Colección: | Artículos |
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actualizado el 17-nov-2024
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