Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions
Mycoplasma pneumoniae (MPN) is a bacterial pathogen that primarily causes atypical pneumonia. It cannot synthesize certain essential lipids and therefore relies on the host for their acquisition to survive. MPN has been detected in increased amounts within ruptured atherosclerotic plaques. In this w...
| Autores: | , , , , , , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2025 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/421155 |
| Acceso en línea: | http://hdl.handle.net/10261/421155 https://api.elsevier.com/content/abstract/scopus_id/105025061980 |
| Access Level: | acceso abierto |
| Palabra clave: | Bacterial techniques and applications Cryoelectron microscopy Dyslipidaemias Lipoproteins |
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Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesionsVizarraga, DavidMarcos, MarinaRotllan, NoemiMartín, JesúsSantos, DavidCamacho, MercedesSoto, BegoñaVelasco-Reniu, LorenaGuerra, PabloPareja, FélixCollantes, MaríaWu, WanluRodríguez-Arce, IreneSerrano, LuisPiñol, JaumeFita, IgnacioEscolà-Gil, Joan CarlesBacterial techniques and applicationsCryoelectron microscopyDyslipidaemiasLipoproteinsMycoplasma pneumoniae (MPN) is a bacterial pathogen that primarily causes atypical pneumonia. It cannot synthesize certain essential lipids and therefore relies on the host for their acquisition to survive. MPN has been detected in increased amounts within ruptured atherosclerotic plaques. In this work, we show that the protein P116 facilitates cholesterol acquisition from LDL, HDL and various cell types. Targeting P116’s C-terminal domain with a monoclonal antibody inhibits cholesterol acquisition and bacterial growth in vitro. Phase contrast epifluorescence microscopy of human arteries reveals that this antibody blocks MPN binding to atherosclerotic lesions ex vivo. Additionally, an MPN chassis injected into hyperlipidemic female mice localizes to the liver and atherosclerotic plaques. Here, we report that P116 plays a role in extracting essential lipids from lipoproteins and host cells and regulates MPN localization to atheromatous plaques. The study highlights MPN’s potential as a tool for targeting atherosclerotic lesions and fatty liver.This work was partly funded by the Instituto de Salud Carlos III and FEDER “Una manera de hacer Europa” grant PI2300232 (to J.E.-G.). N.R. was funded by Agencia Estatal de Investigación (AEI/10.13039/501100011033 and CNS2023-144119) within the Subprograma Ramón y Cajal (RYC-201722879) and by MICINN-Spain grant PID2022-137186OB-I00. CIBERDEM is an Instituto de Salud Carlos III project. I.F. and J.P. were funded by MICINN-Spain grant PID2021-125632OB-C21 and PID2021-125632OB-C22. The authors acknowledge funding from Project, IU16-014045 (CRYO-TEM) from Generalitat de Catalunya, and by “ERDF A way of making Europe”, by the European Union.Peer reviewedSpringer NatureInstituto de Salud Carlos IIIEuropean CommissionAgencia Estatal de Investigación (España)Ministerio de Ciencia e Innovación (España)Generalitat de CatalunyaConsejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]202620262025info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501Publisher's versioninfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10261/421155https://api.elsevier.com/content/abstract/scopus_id/105025061980reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)Inglés#PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE#info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2022-137186OB-I00info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-125632OB-C21info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-125632OB-C22Download of the data available on the platform https://dataverse.csuc.cat/previewurl.xhtml?token=c28f573c-18ee-45f6-a3d8-323087d1342dhttps://doi.org/10.1038/s41467-025-66129-5Síinfo:eu-repo/semantics/openAccessoai:digital.csic.es:10261/4211552026-05-22T06:33:51Z |
| dc.title.none.fl_str_mv |
Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions |
| title |
Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions |
| spellingShingle |
Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions Vizarraga, David Bacterial techniques and applications Cryoelectron microscopy Dyslipidaemias Lipoproteins |
| title_short |
Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions |
| title_full |
Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions |
| title_fullStr |
Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions |
| title_full_unstemmed |
Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions |
| title_sort |
Sources of essential lipids for Mycoplasma pneumoniae via P116 to target liver and atherosclerotic lesions |
| dc.creator.none.fl_str_mv |
Vizarraga, David Marcos, Marina Rotllan, Noemi Martín, Jesús Santos, David Camacho, Mercedes Soto, Begoña Velasco-Reniu, Lorena Guerra, Pablo Pareja, Félix Collantes, María Wu, Wanlu Rodríguez-Arce, Irene Serrano, Luis Piñol, Jaume Fita, Ignacio Escolà-Gil, Joan Carles |
| author |
Vizarraga, David |
| author_facet |
Vizarraga, David Marcos, Marina Rotllan, Noemi Martín, Jesús Santos, David Camacho, Mercedes Soto, Begoña Velasco-Reniu, Lorena Guerra, Pablo Pareja, Félix Collantes, María Wu, Wanlu Rodríguez-Arce, Irene Serrano, Luis Piñol, Jaume Fita, Ignacio Escolà-Gil, Joan Carles |
| author_role |
author |
| author2 |
Marcos, Marina Rotllan, Noemi Martín, Jesús Santos, David Camacho, Mercedes Soto, Begoña Velasco-Reniu, Lorena Guerra, Pablo Pareja, Félix Collantes, María Wu, Wanlu Rodríguez-Arce, Irene Serrano, Luis Piñol, Jaume Fita, Ignacio Escolà-Gil, Joan Carles |
| author2_role |
author author author author author author author author author author author author author author author author |
| dc.contributor.none.fl_str_mv |
Instituto de Salud Carlos III European Commission Agencia Estatal de Investigación (España) Ministerio de Ciencia e Innovación (España) Generalitat de Catalunya Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] |
| dc.subject.none.fl_str_mv |
Bacterial techniques and applications Cryoelectron microscopy Dyslipidaemias Lipoproteins |
| topic |
Bacterial techniques and applications Cryoelectron microscopy Dyslipidaemias Lipoproteins |
| description |
Mycoplasma pneumoniae (MPN) is a bacterial pathogen that primarily causes atypical pneumonia. It cannot synthesize certain essential lipids and therefore relies on the host for their acquisition to survive. MPN has been detected in increased amounts within ruptured atherosclerotic plaques. In this work, we show that the protein P116 facilitates cholesterol acquisition from LDL, HDL and various cell types. Targeting P116’s C-terminal domain with a monoclonal antibody inhibits cholesterol acquisition and bacterial growth in vitro. Phase contrast epifluorescence microscopy of human arteries reveals that this antibody blocks MPN binding to atherosclerotic lesions ex vivo. Additionally, an MPN chassis injected into hyperlipidemic female mice localizes to the liver and atherosclerotic plaques. Here, we report that P116 plays a role in extracting essential lipids from lipoproteins and host cells and regulates MPN localization to atheromatous plaques. The study highlights MPN’s potential as a tool for targeting atherosclerotic lesions and fatty liver. |
| publishDate |
2025 |
| dc.date.none.fl_str_mv |
2025 2026 2026 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article http://purl.org/coar/resource_type/c_6501 Publisher's version info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
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http://hdl.handle.net/10261/421155 https://api.elsevier.com/content/abstract/scopus_id/105025061980 |
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http://hdl.handle.net/10261/421155 https://api.elsevier.com/content/abstract/scopus_id/105025061980 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
#PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2022-137186OB-I00 info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-125632OB-C21 info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-125632OB-C22 Download of the data available on the platform https://dataverse.csuc.cat/previewurl.xhtml?token=c28f573c-18ee-45f6-a3d8-323087d1342d https://doi.org/10.1038/s41467-025-66129-5 Sí |
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Springer Nature |
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Springer Nature |
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