Publication:
Molecular method for the characterization of Coxiella burnetii from clinical and environmental samples: variability of genotypes in Spain

dc.contributor.authorJado, Isabel
dc.contributor.authorCarranza-Rodríguez, Cristina
dc.contributor.authorBarandika, Jesús Félix
dc.contributor.authorToledo, Alvaro
dc.contributor.authorGarcia-Amil, Cristina
dc.contributor.authorSerrano, Beatriz
dc.contributor.authorBolaños, Margarita
dc.contributor.authorGil, Horacio
dc.contributor.authorEscudero, Raquel
dc.contributor.authorGarcía-Pérez, Ana L
dc.contributor.authorOlmeda, A Sonia
dc.contributor.authorAstobiza, Ianire
dc.contributor.authorLobo, Bruno
dc.contributor.authorRodriguez-Vargas, Manuela
dc.contributor.authorPérez-Arellano, José Luis
dc.contributor.authorLópez-Gatius, Fernando
dc.contributor.authorPascual-Velasco, Francisco
dc.contributor.authorCilla, Gustavo
dc.contributor.authorRodríguez, Noé F
dc.contributor.authorAnda, Pedro
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderGobierno de Canarias (España)
dc.contributor.funderBasque Government (España)
dc.contributor.funderInstituto Nacional de Investigación y Tecnología Agraria y Alimentaria (España)
dc.date.accessioned2019-02-07T11:29:37Z
dc.date.available2019-02-07T11:29:37Z
dc.date.issued2012-06-01
dc.description.abstractBACKGROUND: Coxiella burnetii is a highly clonal microorganism which is difficult to culture, requiring BSL3 conditions for its propagation. This leads to a scarce availability of isolates worldwide. On the other hand, published methods of characterization have delineated up to 8 different genomic groups and 36 genotypes. However, all these methodologies, with the exception of one that exhibited limited discriminatory power (3 genotypes), rely on performing between 10 and 20 PCR amplifications or sequencing long fragments of DNA, which make their direct application to clinical samples impracticable and leads to a scarce accessibility of data on the circulation of C. burnetii genotypes. RESULTS: To assess the variability of this organism in Spain, we have developed a novel method that consists of a multiplex (8 targets) PCR and hybridization with specific probes that reproduce the previous classification of this organism into 8 genomic groups, and up to 16 genotypes. It allows for a direct characterization from clinical and environmental samples in a single run, which will help in the study of the different genotypes circulating in wild and domestic cycles as well as from sporadic human cases and outbreaks. The method has been validated with reference isolates. A high variability of C. burnetii has been found in Spain among 90 samples tested, detecting 10 different genotypes, being those adaA negative associated with acute Q fever cases presenting as fever of intermediate duration with liver involvement and with chronic cases. Genotypes infecting humans are also found in sheep, goats, rats, wild boar and ticks, and the only genotype found in cattle has never been found among our clinical samples. CONCLUSIONS: This newly developed methodology has permitted to demonstrate that C. burnetii is highly variable in Spain. With the data presented here, cattle seem not to participate in the transmission of C. burnetii to humans in the samples studied, while sheep, goats, wild boar, rats and ticks share genotypes with the human population.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipGrant support for this work was from FIS PI10/00165, FUNCIS 26/03 from the Gobierno de Canarias “Diagnóstico directo de rickettsiosis prevalentes en nuestro medio (fiebre Q y tifus murino)”, from the “Departamento de Agricultura y Pesca, Gobierno Vasco” “Ensayo de control de la fiebre Q en la cabaña ovina lechera de la CAPV”, INIA FAU2006-00002-C04-01 to -04 “Ecología y control de la fiebre Q: Epidemiología molecular de Coxiella burnetii”, and AGL2010-21273-C03-01-GAN from CICYT “Interacciones-inmuno endocrinas materno-fetal y con Coxiella burnetii en vacas lecheras de alta producción”.es_ES
dc.format.number1es_ES
dc.format.page91es_ES
dc.format.volume12es_ES
dc.identifier.citationBMC Microbiol. 2012 Jun 1;12:91.es_ES
dc.identifier.doi10.1186/1471-2180-12-91es_ES
dc.identifier.issn1471-2180es_ES
dc.identifier.journalBMC microbiologyes_ES
dc.identifier.pubmedID22656068es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/7137
dc.language.isoenges_ES
dc.publisherBioMed Central (BMC)es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PI10/00165es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/FAU2006-00002-C04-01es_ES
dc.relation.publisherversionhttps://doi.org/10.1186/1471-2180-12-91es_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAnimalses_ES
dc.subject.meshCattlees_ES
dc.subject.meshCoxiella burnetiies_ES
dc.subject.meshGenetic Variationes_ES
dc.subject.meshGenotypees_ES
dc.subject.meshGoatses_ES
dc.subject.meshHumanses_ES
dc.subject.meshMolecular Epidemiologyes_ES
dc.subject.meshMultiplex Polymerase Chain Reactiones_ES
dc.subject.meshOligonucleotide Probeses_ES
dc.subject.meshQ Feveres_ES
dc.subject.meshRatses_ES
dc.subject.meshSheepes_ES
dc.subject.meshSpaines_ES
dc.subject.meshSus scrofaes_ES
dc.subject.meshTickses_ES
dc.subject.meshEnvironmental Microbiologyes_ES
dc.subject.meshMolecular Typinges_ES
dc.titleMolecular method for the characterization of Coxiella burnetii from clinical and environmental samples: variability of genotypes in Spaines_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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