Exploring the pangenome of Mycoplasma hyorhinis in search of potential virulence markers

dc.contributor.author
Obregon-Gutierrez, Pau
dc.contributor.author
Nogales, J.
dc.contributor.author
Gonzalez-Torres, C.
dc.contributor.author
Huerta Medina, Eva
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Rubio, A.
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Domingo, Mariano
dc.contributor.author
Segalés, Joaquim
dc.contributor.author
Kochanowski, Karl
dc.contributor.author
Perez-Pulido, A. J.
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Aragon, Virginia
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Correa-Fiz, Florencia
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Sibila, Marina
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Producció Animal
dc.date.issued
2025-12-31
dc.identifier.issn
2045-2322
dc.identifier.uri
http://hdl.handle.net/20.500.12327/5132
dc.description.abstract
Mycoplasma hyorhinis (homotypic synonym of Mesomycoplasma hyorhinis) is a pathobiont from the upper respiratory tract of pigs. Under unclear circumstances, it can disseminate systemically and cause disease. Although some studies have reported different infectious capabilities among strains, no factors have been directly linked to virulence. This study aimed to analyze the core and accessory genes of all available M. hyorhinis strains (pangenome) to identify potential virulence markers. We characterized the pangenome of 110 strains, including isolates from healthy (nasal cavity) and diseased (systemic organs, nasal cavity or lung) animals. Comparative analyses were performed according to the clinical background. Although most putative virulence genes were shared, we identified several genes absent in most health-associated strains related to DNA-processing mechanisms, including hsdM-hsdR restriction-modification system and various helicases. Furthermore, the particular analysis of variable lipoprotein (vlp) genes revealed a similar presence in all strains but higher number of repeats in region III of vlpF in strains isolated from systemic lesions. Genome-scale metabolic models were used to infer the metabolic capabilities of the strains, showing highly conserved predicted reactomes, including growth capabilities and auxotrophies. In conclusion, although all strains may carry genes enabling disease, nasal strains from healthy animals lacked some DNA-processing genes and showed distinct vlp patterns. Additional genomes, especially from strains isolated from healthy animals, would be needed to confirm these findings.
dc.description.sponsorship
This work was supported by the Spanish Ministry of Research and Innovation (projects PID2022-138657OB-I00/AEI/https://doi.org/10.13039/501100011033 and PDC2022-133904-I00/AEI/https://doi.org/10.13039/501100011033). POG is supported by a FPU (FPU19/02126/AEI/https://doi.org/10.13039/501100011033) fellowship from the Spanish Ministry of Science, Innovation and Universities. KK is supported by a Ramón y Cajal contract (RYC2021-033035-I/AEI/https://doi.org/10.13039/501100011033).
dc.format.extent
15
dc.language.iso
eng
dc.publisher
Nature Research
dc.relation.ispartof
Scientific Reports
dc.rights
Attribution 4.0 International
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.title
Exploring the pangenome of Mycoplasma hyorhinis in search of potential virulence markers
dc.type
info:eu-repo/semantics/article
dc.subject.udc
619
dc.description.version
info:eu-repo/semantics/publishedVersion
dc.embargo.terms
cap
dc.relation.projectID
MICINN/Programa Estatal para impulsar la investigación científico-técnica y su transferencia/PID2022-138657OB-I00/ES/CORE ESENCIAL DE LA MICROBIOTA NASAL Y SU USO PARA EL CONTROL DE LAS ENFERMEDADES RESPIRATORIAS PORCINAS/
dc.relation.projectID
MICINN/Programa Estatal para impulsar la investigación científico-técnica y su transferencia/PDC2022-133904-I00/ES/DESARROLLO DE UN TEST RAPIDO DE PRONOSTICO Y DIAGNOSTICO DE LA POLISEROSITIS PORCINA PARA SER REALIZADO EN GRANJA/
dc.relation.projectID
MICINN/Programa Estatal para desarrollar, atraer y retener talento/RYC2021-033035-I/ES/ /
dc.identifier.doi
https://doi.org/10.1038/s41598-025-31942-x
dc.rights.accessLevel
info:eu-repo/semantics/openAccess
dc.contributor.group
Sanitat Animal


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