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Guidelines for the Isolation, Molecular Detection, and Characterization of Bartonella Species

Authors :
Ricardo Gutiérrez
Shimon Harrus
Muriel Vayssier-Taussat
Jean-Philippe Buffet
Biologie moléculaire et immunologie parasitaires et fongiques (BIPAR)
Laboratoire de santé animale, sites de Maisons-Alfort et de Dozulé
Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail (ANSES)-Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail (ANSES)-Institut National de la Recherche Agronomique (INRA)-École nationale vétérinaire d'Alfort (ENVA)-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
TD1303 COST Action
Israel Science Foundation [30/11]
École nationale vétérinaire - Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)-Laboratoire de santé animale, sites de Maisons-Alfort et de Dozulé
Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail (ANSES)-Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail (ANSES)-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Source :
Vector-Borne and Zoonotic Diseases, Vector-Borne and Zoonotic Diseases, Mary Ann Liebert, 2017, 17 (1), pp.42-50. ⟨10.1089/vbz.2016.1956⟩
Publication Year :
2017

Abstract

Bartonellae are fastidious, facultative, intracellular vector-borne bacteria distributed among mammalian reservoirs worldwide. The pathogenic potential of many Bartonella spp. has increased the interest in these bacteria and advanced their research. Isolation of Bartonella spp. is laborious using classical bacteriological methods and requires specific conditions and prolonged incubation periods. In contrast, molecular methods for detection of Bartonella DNA are considered as more practical and sensitive than the former. Among the molecular methods, the use of real-time PCR assays for primary screening of Bartonella spp., followed by several molecular confirmatory assays, using either conventional or real-time PCR, is recommended. Although primary isolation of Bartonella is a laborious task, we encourage its application to all PCR-positive samples as this is the most reliable proof for the presence of live bacteria. Moreover, a successful trial will enable a broader molecular characterization and speciation of isolated colonies. The present guideline gathers and summarizes recommendations, including advantages and limitations of isolation and molecular detection of Bartonella from mammalian and arthropod samples.

Details

ISSN :
15577759 and 15303667
Volume :
17
Issue :
1
Database :
OpenAIRE
Journal :
Vector borne and zoonotic diseases (Larchmont, N.Y.)
Accession number :
edsair.doi.dedup.....bbdfaeafc956b546e3bd0e0e9bf6d7cc
Full Text :
https://doi.org/10.1089/vbz.2016.1956⟩