Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/51343
Title: A specific PCR for the detection of Mycoplasma putrefaciens, one of the agents of the contagious agalactia syndrome of goats
Authors: Peyraud, A.
Woubit, S.
Poveda, JB 
De La Fe, C.
Mercier, P.
Thiaucourt, F.
Keywords: Ribosomal-Rna Genes
Caprine Mycoplasmosis
Mycoides Cluster
Sequence-Analysis
Phylogeny, et al
Issue Date: 2003
Publisher: 0890-8508
Journal: Molecular and Cellular Probes 
Abstract: Mycoplasma putrefaciens is listed as one of the etiologic agents of the contagious agalactia syndrome by the world organisation for animal health. This species has been characterized only recently, 1974, and the number of outbreaks caused by this microorganism so far is very scarce. It induces mastitis in infected goats although other symptoms such as arthritis in adults and septicaemia in kids are also frequently described. Up to now, the identification of M. putrefaciens relied on classical isolation and identification techniques which present a number of limitations. Specific primers for PCR have been designed based on sequence comparisons of the Arc B gene among the 'Mycoplasma mycoides cluster' and related species such as Mycoplasma cottewii and Mycoplasma yeatsii. Sequence alignments confirmed the taxonomic position of M. putrefaciens, which is related to the W. mycoides cluster' but also very close to M. yeatsii. The polymorphism observed amongst the different Arc B sequences allowed the determination of a primer pair yielding a specific amplification of a 316 bp-long DNA fragment by PCR. This PCR was validated in two different laboratories with a variety of mycoplasma strains isolated from goats. This new PCR technique will be very useful for a quicker determination of M. putrefaciens strains as well as a better understanding of the prevalence of M. putrefaciens infections. (C) 2003 Elsevier Ltd. All rights reserved.
URI: http://hdl.handle.net/10553/51343
ISSN: 0890-8508
DOI: 10.1016/j.mcp.2003.07.006
Source: Molecular And Cellular Probes[ISSN 0890-8508],v. 17 (6), p. 289-294
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