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Genome-scale approach to study the genetic relatedness among Brucella melitensis strains

dc.contributor.authorPelerito, Ana
dc.contributor.authorNunes, Alexandra
dc.contributor.authorNúncio, Maria Sofia
dc.contributor.authorGomes, João Paulo
dc.date.accessioned2020-04-25T08:23:32Z
dc.date.available2020-04-25T08:23:32Z
dc.date.issued2020-03-09
dc.description.abstractBrucellosis is an important zoonotic disease that affects both humans and animals. To date, laboratory surveillance is still essentially based on the traditional MLVA-16 methodology and the associated epidemiological information is frequently scarce. Our goal was to contribute to the improvement of Brucella spp. surveillance through the implementation of a whole genome sequencing (WGS) approach. We created a curated ready-to-use species-specific wgMLST scheme enrolling a panel of 2656 targets (http://doi.org/10.5281/zenodo.3575026) and used this schema to perform a retrospective analysis of the genetic relatedness among B. melitensis strains causing human infection in Portugal (a country where brucellosis is an endemic disease) from 2010 to 2018. The strains showed a phylogenetic clustering within genotype II (25 out of 36) and IV (4 out of 36), and shared clades with strains isolated from countries with which Portugal has intense food trading, tourism and similar eating habits, such as Spain, Italy and Greece. In addition, our results point to the identification of strong associations between B. melitensis strains, likely underlying missed "outbreaks" as 22 out of the 36 strains showed genetic linkage with others. In fact, the applied gene-by-gene approach grouped these strains into six genetic clusters each one containing putative epidemiological links. Nevertheless, more studies will be needed in order to define the appropriate range of cut-offs (probable non-static cut-offs) that best illustrate the association between genetic linkage and epidemiological information and may serve as alerts for the health authorities. The release of this freely available and scalable schema contributes to the required technological transition for laboratorial surveillance of brucellosis and will facilitate the assessment of ongoing and future outbreaks in order to prevent the transmission spread.pt_PT
dc.description.sponsorshipThis work was supported by GenomePT (ref. POCI-01-0145-FEDER-022184) from Fundação para a Ciência e Tecnologia, Portugal.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPLoS One. 2020 Mar 9;15(3):e0229863. doi: 10.1371/journal.pone.0229863. eCollection 2020pt_PT
dc.identifier.doi10.1371/journal.pone.0229863pt_PT
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10400.18/6513
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherPublic Library of Sciencept_PT
dc.relation.publisherversionhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0229863pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectBrucellosispt_PT
dc.subjectZoonotic Diseasept_PT
dc.subjectBrucella spp.pt_PT
dc.subjectSurveillancept_PT
dc.subjectWhole Genome Sequencingpt_PT
dc.subjectInfecções Sistémicas e Zoonosespt_PT
dc.titleGenome-scale approach to study the genetic relatedness among Brucella melitensis strainspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue3pt_PT
oaire.citation.startPagee0229863pt_PT
oaire.citation.titlePLoS ONEpt_PT
oaire.citation.volume15pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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