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NpmC – a novel A1408 16S rRNA methyltransferase in the gut of humans and animals

dc.contributor.authorMatamoros, Bosco R.
dc.contributor.authorSerna Bernaldo, Carlos
dc.contributor.authorWedel, Emilia
dc.contributor.authorMontero Serra, Natalia
dc.contributor.authorKirpekar, Finn
dc.contributor.authorGonzález Zorn, Bruno
dc.date.accessioned2024-12-19T14:18:29Z
dc.date.available2024-12-19T14:18:29Z
dc.date.issued2025
dc.description.abstractNpmA and NpmB are 16S rRNA methyltransferases that act on residue A1408 and confer high-level resistance to almost all aminoglycosides; however, these methyltransferases are rarely reported. A novel gene, npmC, was identified after analysisng all world-wide available metagenomic projects in a One Health context. This gene has a high level of similarity (91.5%) with npmA and up to 92.7% similarity at amino acidic level. The protein encoded by this gene presents the conserved motifs required for A1408 methylation. npmC was synthesized and its expression in Escherichia coli resulted in a high level of resistance to 4,5-disubstituted 2-deoxystreptamine (2-DOS) and 4-monosubstituted 2-DOS aminoglycosides, as well as moderate resistance to 4,6-disusbstituted 2-DOS aminoglycosides, including the last resort aminoglycoside, plazomicin. Methylation at residue A1408 was confirmed by mass spectrometry assays. Analysis of the npmC gene background revealed that its genetic context was associated with different insertion sequences that could mobilise the gene. Similarities in the genetic context between npmC and npmA indicate that they share a common ancestor. The immediate genetic context of this methyltransferase indicates a high relationship to the Eubacteriales order. This finding reveals the dark matter of the microbiome as a potential source of novel resistance genes, expands the list of the true pan-aminoglycoside 16S rRNA methyltransferases, which threaten the usefulness and development of next-generation aminoglycosides.
dc.description.departmentDepto. de Sanidad Animal
dc.description.facultyCentro de Vigilancia Sanitaria Veterinaria (VISAVET)
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.sponsorshipEuropean Commission
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades (España)
dc.description.sponsorshipNovo Nordisk Foundation
dc.description.statuspub
dc.identifier.citationMatamoros, B. R., Serna, C., Wedel, E., Montero, N., Kirpekar, F., & Gonzalez-Zorn, B. (2024). NpmC - a novel A1408 16S rRNA methyltransferase in the gut of humans and animals. International journal of antimicrobial agents, 65(1), 107382. Advance online publication. https://doi.org/10.1016/j.ijantimicag.2024.107382
dc.identifier.doi10.1016/j.ijantimicag.2024.107382
dc.identifier.essn1872-7913
dc.identifier.issn0924-8579
dc.identifier.officialurlhttps://doi.org/10.1016/j.ijantimicag.2024.107382
dc.identifier.pmid39522830
dc.identifier.urihttps://hdl.handle.net/20.500.14352/113056
dc.issue.number1
dc.journal.titleInternational Journal of Antimicrobial Agents
dc.language.isoeng
dc.page.final6
dc.page.initial1
dc.publisherElsevier
dc.relation.projectIDMCIN/AEI/10.13039/501100011033
dc.relation.projectID773830
dc.relation.projectIDPLEC2023-010275
dc.relation.projectIDNNF20OC0061575
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu636.09
dc.subject.keywordAntimicrobial resistance
dc.subject.keywordAminoglycoside
dc.subject.keyword16S rRNA methyltransferase
dc.subject.keywordMetagenomics
dc.subject.keywordGut microbiome
dc.subject.ucmVeterinaria
dc.subject.unesco3109 Ciencias Veterinarias
dc.titleNpmC – a novel A1408 16S rRNA methyltransferase in the gut of humans and animals
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number65
dspace.entity.typePublication
relation.isAuthorOfPublicationcaa0a4b8-95b6-47df-9550-dd5b64795c01
relation.isAuthorOfPublication226746a8-2306-4c65-b577-0e87145953c2
relation.isAuthorOfPublicationabbfe61a-3e58-4cfb-85fc-d2e2ec46b0a3
relation.isAuthorOfPublication.latestForDiscoverycaa0a4b8-95b6-47df-9550-dd5b64795c01

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