Development of a 16S rRNA PCR-RFLP Assay for Bartonella identification: Applicability in the identification of species involved in human infections

Other authors

Universitat Politècnica de Catalunya. Departament d'Enginyeria Química

Universitat Politècnica de Catalunya. PSEP - Polimers Sintètics: Estructura i Propietats. Polimers Biodegradables

Publication date

2014

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 Mae III, Mse I, Sau96 I, Bsa AI, Drd I, Fok I, Bss HII, Bst UI, Alu I, Tsp DTI and Hph I which, according to a decision -making tree, faci litated 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


Peer Reviewed


Postprint (author's final draft)

Document Type

Article

Language

English

Publisher

Society of Exploration Geophysicists (SEG)

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Rights

http://creativecommons.org/licenses/by-nc-nd/3.0/es/

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E-prints [72986]