Literature DB >> 17606362

A PCR for the detection of mycoplasmas belonging to the Mycoplasma mycoides cluster: application to the diagnosis of contagious agalactia.

S Woubit1, L Manso-Silván, S Lorenzon, P Gaurivaud, F Poumarat, M-P Pellet, V P Singh, F Thiaucourt.   

Abstract

Contagious agalactia is a mycoplasmal infection caused by Mycoplasma agalactiae, Mycoplasma mycoides subsp. mycoides LC, M. mycoides subsp. capri, Mycoplasma capricolum subsp. capricolum and Mycoplasma putrefaciens. Identification of the causative organisms is usually performed by isolation and classical biochemical and serological tests, though this is a lengthy and cumbersome process for mycoplasmas. Specific PCR assays have been developed for the identification of Mycoplasma agalactiae and M. putrefaciens. For members of the M. mycoides cluster existing PCR tests are based on the amplification of highly conserved genes coding for ribosomal proteins, hence a possibility of cross-reactions. The gene glk, coding for a glucokinase, that is found in this cluster is very distantly related to any other bacterial glucokinase described so far. It was therefore chosen as target to design a new PCR test. The validation was performed independently in three laboratories in France and India using over 100 mycoplasma strains of various geographical origins. All strains belonging to the M. mycoides cluster were detected by amplification of the expected PCR product (428 bp) while no amplification was obtained from M. agalactiae strains. Our results demonstrate the universality of this PCR in spite of the great heterogeneity found within this cluster. This new tool may be of great help for the implementation of control measures directed towards contagious agalactia.

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Year:  2007        PMID: 17606362     DOI: 10.1016/j.mcp.2007.05.008

Source DB:  PubMed          Journal:  Mol Cell Probes        ISSN: 0890-8508            Impact factor:   2.365


  5 in total

1.  Mycoplasma agalactiae p40 Gene, a novel marker for diagnosis of contagious agalactia in sheep by real-time PCR: assessment of analytical performance and in-house validation using naturally contaminated milk samples.

Authors:  Katarína Oravcová; Lorena López-Enríquez; David Rodríguez-Lázaro; Marta Hernández
Journal:  J Clin Microbiol       Date:  2008-11-19       Impact factor: 5.948

2.  Suppression-subtractive hybridization as a strategy to identify taxon-specific sequences within the Mycoplasma mycoides Cluster: design and validation of an M. capricolum subsp. capricolum-specific PCR assay.

Authors:  Laure Maigre; Christine Citti; Marc Marenda; François Poumarat; Florence Tardy
Journal:  J Clin Microbiol       Date:  2008-01-30       Impact factor: 5.948

3.  Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cells.

Authors:  Reza Tabatabaei-Qomi; Mohsen Sheykh-Hasan; Hoda Fazaely; Naser Kalhor; Mahdieh Ghiasi
Journal:  Iran J Microbiol       Date:  2014-08

4.  Antimicrobial susceptibility and multilocus sequence typing of Mycoplasma capricolum subsp. capricolum.

Authors:  Juan Tatay-Dualde; Miranda Prats-van der Ham; Christian de la Fe; Ana Paterna; Antonio Sánchez; Juan Carlos Corrales; Antonio Contreras; Sebastiana Tola; Ángel Gómez-Martin
Journal:  PLoS One       Date:  2017-03-27       Impact factor: 3.240

5.  A survey of Mycoplasma agalactiae in dairy sheep farms in Spain.

Authors:  Jaime Ariza-Miguel; David Rodríguez-Lázaro; Marta Hernández
Journal:  BMC Vet Res       Date:  2012-09-24       Impact factor: 2.741

  5 in total

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