dc.creatorFarace, Pablo Daniel
dc.creatorMorsella, Claudia Graciela
dc.creatorCravero, Silvio Lorenzo Pedro
dc.creatorSioya, Bernardo Arturo
dc.creatorAmadio, Ariel
dc.creatorPaolicchi, Fernando
dc.creatorGioffre, Andrea
dc.date.accessioned2020-01-06T17:48:58Z
dc.date.accessioned2023-03-15T14:03:00Z
dc.date.available2020-01-06T17:48:58Z
dc.date.available2023-03-15T14:03:00Z
dc.date.created2020-01-06T17:48:58Z
dc.date.issued2019-11
dc.identifier2167-8359
dc.identifierhttps://doi.org/10.7717/peerj.7820
dc.identifierhttp://hdl.handle.net/20.500.12123/6617
dc.identifierhttps://peerj.com/articles/7820/
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/6209718
dc.description.abstractPhenotypic differences between Campylobacter fetus fetus and C. fetus venerealis subspecies allow the differential diagnosis of bovine genital campylobacteriosis. The hydrogensulfide production,for example,is atrait exclusive toC.fetus fetus and C. fetus venerealis biovar intermedius. This gas that can be biochemically tested can be produced from L-cysteine (L-Cys). Herein, we report a novel multiplex-PCR to differentiate C. fetus based on the evaluation of a deletion of an ATP-binding cassette-type L-Cys transporter that could be involved in hydrogen sulfide production, as previously described. A wet lab approach combined with an in silico whole genome data analysis showed complete agreement between this L-Cys transporter-PCR and the hydrogen sulfide production biochemical test. This multiplex-PCR may complement the tests currently employed for the differential diagnosis of C. fetus.
dc.languageeng
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourcePeerJ. 7 : e7820. (2019)
dc.subjectPCR
dc.subjectCampylobacteriosis
dc.subjectCampylobacter Fetus
dc.titleL-cysteine transporter-PCR to detect hydrogen sulfide-producing Campylobacter fetus
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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