Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections
Descripción del Articulo
Abstract We designed a 16S rRNA gene PCR-RFLP scheme to identify all currently described Bartonella spp. The 16S rRNA genes of all Bartonella spp. were in-silico analyzed in order to design a RFLP technique able to discriminate among different species. The restriction enzymes selected were MaeIII, M...
| Autores: | , , , , , , , , , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2014 |
| Institución: | Universidad Peruana de Ciencias Aplicadas |
| Repositorio: | UPC-Institucional |
| Lenguaje: | inglés |
| OAI Identifier: | oai:repositorioacademico.upc.edu.pe:10757/322342 |
| Enlace del recurso: | http://hdl.handle.net/10757/322342 |
| Nivel de acceso: | acceso abierto |
| Materia: | Bartonella PCR-RFLP 16s rRNA Gene Identification |
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| dc.title.es_PE.fl_str_mv |
Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections |
| title |
Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections |
| spellingShingle |
Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections Del Valle, Luis J. Bartonella PCR-RFLP 16s rRNA Gene Identification |
| title_short |
Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections |
| title_full |
Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections |
| title_fullStr |
Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections |
| title_full_unstemmed |
Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections |
| title_sort |
Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infections |
| author |
Del Valle, Luis J. |
| author_facet |
Del Valle, Luis J. Jaramillo, Michael L. Talledo, Miguel Pons, Maria J. Flores, Lidia Quispe, Ruth L. Ramírez, Pablo García de la Guarda, Ruth Alvarado, Débora Espinoza-Culupú, Abraham Del Valle Mendoza, Juana Vargas, Martha Ruíz, Joaquim |
| author_role |
author |
| author2 |
Jaramillo, Michael L. Talledo, Miguel Pons, Maria J. Flores, Lidia Quispe, Ruth L. Ramírez, Pablo García de la Guarda, Ruth Alvarado, Débora Espinoza-Culupú, Abraham Del Valle Mendoza, Juana Vargas, Martha Ruíz, Joaquim |
| author2_role |
author author author author author author author author author author author author |
| dc.contributor.author.fl_str_mv |
Del Valle, Luis J. Jaramillo, Michael L. Talledo, Miguel Pons, Maria J. Flores, Lidia Quispe, Ruth L. Ramírez, Pablo García de la Guarda, Ruth Alvarado, Débora Espinoza-Culupú, Abraham Del Valle Mendoza, Juana Vargas, Martha Ruíz, Joaquim |
| dc.subject.es_PE.fl_str_mv |
Bartonella PCR-RFLP 16s rRNA Gene Identification |
| topic |
Bartonella PCR-RFLP 16s rRNA Gene Identification |
| description |
Abstract We designed a 16S rRNA gene PCR-RFLP scheme to identify all currently described Bartonella spp. The 16S rRNA genes of all Bartonella spp. were in-silico analyzed in order to design a RFLP technique able to discriminate among different species. The restriction enzymes selected were MaeIII, MseI, Sau96I, BsaAI, DrdI, FokI, BssHII, BstUI, AluI, TspDTI and HphI which, according to a decision-making tree, facilitated the differentiation of all the currently described species of Bartonella.The technique was experimentally tested in different species of Bartonella, including human pathogenic B. bacilliformis and B. henselae with a 100% of concordance with the in-silico predicted patterns.This novel RFLP assay could be used to identify both human and non-human pathogenic Bartonella in diagnostic, phylogenetic and epidemiologic studies. |
| publishDate |
2014 |
| dc.date.accessioned.none.fl_str_mv |
2014-07-03T03:09:59Z |
| dc.date.available.none.fl_str_mv |
2014-07-03T03:09:59Z |
| dc.date.issued.fl_str_mv |
2014-07-02 |
| dc.type.es_PE.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.issn.none.fl_str_mv |
2331-6721 |
| dc.identifier.doi.none.fl_str_mv |
10.13189/ujmr.2014.020102 |
| dc.identifier.uri.es_PE.fl_str_mv |
http://hdl.handle.net/10757/322342 |
| dc.identifier.eissn.none.fl_str_mv |
2331-673X |
| dc.identifier.journal.es_PE.fl_str_mv |
Universal Journal of Microbiology Research |
| identifier_str_mv |
2331-6721 10.13189/ujmr.2014.020102 2331-673X Universal Journal of Microbiology Research |
| url |
http://hdl.handle.net/10757/322342 |
| dc.language.iso.es_PE.fl_str_mv |
eng |
| language |
eng |
| dc.relation.url.es_PE.fl_str_mv |
http://www.hrpub.org/download/20131215/UJMR2-10201796.pdf |
| dc.rights.es_PE.fl_str_mv |
info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.format.es_PE.fl_str_mv |
application/pdf |
| dc.publisher.es_PE.fl_str_mv |
Horizon Research Publishing |
| dc.source.es_PE.fl_str_mv |
Universidad Peruana de Ciencias Aplicadas (UPC) Repositorio Académico - UPC |
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reponame:UPC-Institucional instname:Universidad Peruana de Ciencias Aplicadas instacron:UPC |
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Universidad Peruana de Ciencias Aplicadas |
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UPC |
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UPC |
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UPC-Institucional |
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UPC-Institucional |
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Del Valle, Luis J.Jaramillo, Michael L.Talledo, MiguelPons, Maria J.Flores, LidiaQuispe, Ruth L.Ramírez, PabloGarcía de la Guarda, RuthAlvarado, DéboraEspinoza-Culupú, AbrahamDel Valle Mendoza, JuanaVargas, MarthaRuíz, Joaquim2014-07-03T03:09:59Z2014-07-03T03:09:59Z2014-07-022331-672110.13189/ujmr.2014.020102http://hdl.handle.net/10757/3223422331-673XUniversal Journal of Microbiology ResearchAbstract We designed a 16S rRNA gene PCR-RFLP scheme to identify all currently described Bartonella spp. The 16S rRNA genes of all Bartonella spp. were in-silico analyzed in order to design a RFLP technique able to discriminate among different species. The restriction enzymes selected were MaeIII, MseI, Sau96I, BsaAI, DrdI, FokI, BssHII, BstUI, AluI, TspDTI and HphI which, according to a decision-making tree, facilitated the differentiation of all the currently described species of Bartonella.The technique was experimentally tested in different species of Bartonella, including human pathogenic B. bacilliformis and B. henselae with a 100% of concordance with the in-silico predicted patterns.This novel RFLP assay could be used to identify both human and non-human pathogenic Bartonella in diagnostic, phylogenetic and epidemiologic studies.application/pdfengHorizon Research Publishinghttp://www.hrpub.org/download/20131215/UJMR2-10201796.pdfinfo:eu-repo/semantics/openAccessUniversidad Peruana de Ciencias Aplicadas (UPC)Repositorio Académico - UPCreponame:UPC-Institucionalinstname:Universidad Peruana de Ciencias Aplicadasinstacron:UPCBartonella90e0ceed-7293-48e8-b9d9-26175db1be23600PCR-RFLPb895831f-cb9e-4773-8584-18da7ff3794860016s rRNA Geneea496d83-c5a5-46fc-a681-c8cb24826db8600Identificationdf27fafe-5121-4570-b31b-5831e172ddcd600Development of a 16S rRNA PCR-RFLP Assay for Bartonella Identification: Applicability in the Identification of Species Involved in Human Infectionsinfo:eu-repo/semantics/article2018-06-15T10:46:04ZAbstract We designed a 16S rRNA gene PCR-RFLP scheme to identify all currently described Bartonella spp. The 16S rRNA genes of all Bartonella spp. were in-silico analyzed in order to design a RFLP technique able to discriminate among different species. The restriction enzymes selected were MaeIII, MseI, Sau96I, BsaAI, DrdI, FokI, BssHII, BstUI, AluI, TspDTI and HphI which, according to a decision-making tree, facilitated the differentiation of all the currently described species of Bartonella.The technique was experimentally tested in different species of Bartonella, including human pathogenic B. bacilliformis and B. henselae with a 100% of concordance with the in-silico predicted patterns.This novel RFLP assay could be used to identify both human and non-human pathogenic Bartonella in diagnostic, phylogenetic and epidemiologic studies.ORIGINALJuana del Valle_UJMR2-10201796.pdfJuana del Valle_UJMR2-10201796.pdfapplication/pdf758669https://repositorioacademico.upc.edu.pe/bitstream/10757/322342/1/Juana%20del%20Valle_UJMR2-10201796.pdf32dd2cbb744d811796986ebc04a1db60MD51trueLICENSElicense.txtlicense.txttext/plain; charset=utf-81659https://repositorioacademico.upc.edu.pe/bitstream/10757/322342/2/license.txt1ed8f33c5404431ad7aabc05080746c5MD52falseTEXTJuana del Valle_UJMR2-10201796.pdf.txtJuana del Valle_UJMR2-10201796.pdf.txtExtracted Texttext/plain29895https://repositorioacademico.upc.edu.pe/bitstream/10757/322342/3/Juana%20del%20Valle_UJMR2-10201796.pdf.txt56e08b7491e0635dbb6507d79652c160MD53falseTHUMBNAILJuana del Valle_UJMR2-10201796.pdf.jpgJuana del Valle_UJMR2-10201796.pdf.jpgGenerated Thumbnailimage/jpeg106105https://repositorioacademico.upc.edu.pe/bitstream/10757/322342/4/Juana%20del%20Valle_UJMR2-10201796.pdf.jpg9af13411267f66daa7520f1d8f561d52MD54false10757/322342oai:repositorioacademico.upc.edu.pe:10757/3223422019-08-30 08:00:40.333Repositorio académico upcupc@openrepository.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 |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).