Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial

Diagnostic differentiation between the ruminant pathogens Mycoplasma agalactiae and Mycoplasma bovis is known to be problematic when only conventional serological and biochemical tests are used. The main reason for this is that both agents share a considerable number of related proteins and common epitopes. DNA-based detection methods offer advantages in terms of specificity and sensitivity. However, there is an urgent need to compare currently used PCR assays because they target different genomic regions and, therefore, may perform differently. In the present work, five laboratories, which use PCR routinely, evaluated the specificity of four different PCR systems for M. agalactiae and three systems for M. bovis on a total of 41 strains of the two Mycoplasma species including six previously unidentified strains. As the vast majority of PCR examinations (97.1% of all tests) correctly identified the strains the specificity of all seven detection systems appears to be high. In four cases, incorrect identification by conventional diagnostic methods was rectified by PCR. Isolates from non-typical hosts, i.e. three M. bovis strains from small ruminants and two M. agalactiae strains from cattle, were characterised by sequencing the 16S and part of the 23S ribosomal RNA genes.

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Main Authors: Bashiruddin, John B., Frey, Joachim, Heldtander Königsson, Malin, Johansson, Karl-Erik, Hotzel, Helmut, Diller, Roland, De Santis, Paola, Botelho, Ana, Ayling, Roger D., Nicholas, Robin A.J., Thiaucourt, François, Sachse, Konrad
Format: article biblioteca
Language:eng
Subjects:L50 - Physiologie et biochimie animales, Mycoplasma bovis, Mycoplasma, biochimie, identification, Mycoplasma agalactiae, http://aims.fao.org/aos/agrovoc/c_27241, http://aims.fao.org/aos/agrovoc/c_5020, http://aims.fao.org/aos/agrovoc/c_910, http://aims.fao.org/aos/agrovoc/c_3791, http://aims.fao.org/aos/agrovoc/c_37782,
Online Access:http://agritrop.cirad.fr/525758/
http://agritrop.cirad.fr/525758/1/525758.pdf
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spelling dig-cirad-fr-5257582024-01-28T13:30:11Z http://agritrop.cirad.fr/525758/ http://agritrop.cirad.fr/525758/ Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial. Bashiruddin John B., Frey Joachim, Heldtander Königsson Malin, Johansson Karl-Erik, Hotzel Helmut, Diller Roland, De Santis Paola, Botelho Ana, Ayling Roger D., Nicholas Robin A.J., Thiaucourt François, Sachse Konrad. 2005. Veterinary Journal, 169 (2) : 268-275.https://doi.org/10.1016/j.tvjl.2004.01.018 <https://doi.org/10.1016/j.tvjl.2004.01.018> Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial Bashiruddin, John B. Frey, Joachim Heldtander Königsson, Malin Johansson, Karl-Erik Hotzel, Helmut Diller, Roland De Santis, Paola Botelho, Ana Ayling, Roger D. Nicholas, Robin A.J. Thiaucourt, François Sachse, Konrad eng 2005 Veterinary Journal L50 - Physiologie et biochimie animales Mycoplasma bovis Mycoplasma biochimie identification Mycoplasma agalactiae http://aims.fao.org/aos/agrovoc/c_27241 http://aims.fao.org/aos/agrovoc/c_5020 http://aims.fao.org/aos/agrovoc/c_910 http://aims.fao.org/aos/agrovoc/c_3791 http://aims.fao.org/aos/agrovoc/c_37782 Diagnostic differentiation between the ruminant pathogens Mycoplasma agalactiae and Mycoplasma bovis is known to be problematic when only conventional serological and biochemical tests are used. The main reason for this is that both agents share a considerable number of related proteins and common epitopes. DNA-based detection methods offer advantages in terms of specificity and sensitivity. However, there is an urgent need to compare currently used PCR assays because they target different genomic regions and, therefore, may perform differently. In the present work, five laboratories, which use PCR routinely, evaluated the specificity of four different PCR systems for M. agalactiae and three systems for M. bovis on a total of 41 strains of the two Mycoplasma species including six previously unidentified strains. As the vast majority of PCR examinations (97.1% of all tests) correctly identified the strains the specificity of all seven detection systems appears to be high. In four cases, incorrect identification by conventional diagnostic methods was rectified by PCR. Isolates from non-typical hosts, i.e. three M. bovis strains from small ruminants and two M. agalactiae strains from cattle, were characterised by sequencing the 16S and part of the 23S ribosomal RNA genes. article info:eu-repo/semantics/article Journal Article info:eu-repo/semantics/publishedVersion http://agritrop.cirad.fr/525758/1/525758.pdf text Cirad license info:eu-repo/semantics/restrictedAccess https://agritrop.cirad.fr/mention_legale.html https://doi.org/10.1016/j.tvjl.2004.01.018 10.1016/j.tvjl.2004.01.018 http://catalogue-bibliotheques.cirad.fr/cgi-bin/koha/opac-detail.pl?biblionumber=186120 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tvjl.2004.01.018 info:eu-repo/semantics/altIdentifier/purl/https://doi.org/10.1016/j.tvjl.2004.01.018
institution CIRAD FR
collection DSpace
country Francia
countrycode FR
component Bibliográfico
access En linea
databasecode dig-cirad-fr
tag biblioteca
region Europa del Oeste
libraryname Biblioteca del CIRAD Francia
language eng
topic L50 - Physiologie et biochimie animales
Mycoplasma bovis
Mycoplasma
biochimie
identification
Mycoplasma agalactiae
http://aims.fao.org/aos/agrovoc/c_27241
http://aims.fao.org/aos/agrovoc/c_5020
http://aims.fao.org/aos/agrovoc/c_910
http://aims.fao.org/aos/agrovoc/c_3791
http://aims.fao.org/aos/agrovoc/c_37782
L50 - Physiologie et biochimie animales
Mycoplasma bovis
Mycoplasma
biochimie
identification
Mycoplasma agalactiae
http://aims.fao.org/aos/agrovoc/c_27241
http://aims.fao.org/aos/agrovoc/c_5020
http://aims.fao.org/aos/agrovoc/c_910
http://aims.fao.org/aos/agrovoc/c_3791
http://aims.fao.org/aos/agrovoc/c_37782
spellingShingle L50 - Physiologie et biochimie animales
Mycoplasma bovis
Mycoplasma
biochimie
identification
Mycoplasma agalactiae
http://aims.fao.org/aos/agrovoc/c_27241
http://aims.fao.org/aos/agrovoc/c_5020
http://aims.fao.org/aos/agrovoc/c_910
http://aims.fao.org/aos/agrovoc/c_3791
http://aims.fao.org/aos/agrovoc/c_37782
L50 - Physiologie et biochimie animales
Mycoplasma bovis
Mycoplasma
biochimie
identification
Mycoplasma agalactiae
http://aims.fao.org/aos/agrovoc/c_27241
http://aims.fao.org/aos/agrovoc/c_5020
http://aims.fao.org/aos/agrovoc/c_910
http://aims.fao.org/aos/agrovoc/c_3791
http://aims.fao.org/aos/agrovoc/c_37782
Bashiruddin, John B.
Frey, Joachim
Heldtander Königsson, Malin
Johansson, Karl-Erik
Hotzel, Helmut
Diller, Roland
De Santis, Paola
Botelho, Ana
Ayling, Roger D.
Nicholas, Robin A.J.
Thiaucourt, François
Sachse, Konrad
Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial
description Diagnostic differentiation between the ruminant pathogens Mycoplasma agalactiae and Mycoplasma bovis is known to be problematic when only conventional serological and biochemical tests are used. The main reason for this is that both agents share a considerable number of related proteins and common epitopes. DNA-based detection methods offer advantages in terms of specificity and sensitivity. However, there is an urgent need to compare currently used PCR assays because they target different genomic regions and, therefore, may perform differently. In the present work, five laboratories, which use PCR routinely, evaluated the specificity of four different PCR systems for M. agalactiae and three systems for M. bovis on a total of 41 strains of the two Mycoplasma species including six previously unidentified strains. As the vast majority of PCR examinations (97.1% of all tests) correctly identified the strains the specificity of all seven detection systems appears to be high. In four cases, incorrect identification by conventional diagnostic methods was rectified by PCR. Isolates from non-typical hosts, i.e. three M. bovis strains from small ruminants and two M. agalactiae strains from cattle, were characterised by sequencing the 16S and part of the 23S ribosomal RNA genes.
format article
topic_facet L50 - Physiologie et biochimie animales
Mycoplasma bovis
Mycoplasma
biochimie
identification
Mycoplasma agalactiae
http://aims.fao.org/aos/agrovoc/c_27241
http://aims.fao.org/aos/agrovoc/c_5020
http://aims.fao.org/aos/agrovoc/c_910
http://aims.fao.org/aos/agrovoc/c_3791
http://aims.fao.org/aos/agrovoc/c_37782
author Bashiruddin, John B.
Frey, Joachim
Heldtander Königsson, Malin
Johansson, Karl-Erik
Hotzel, Helmut
Diller, Roland
De Santis, Paola
Botelho, Ana
Ayling, Roger D.
Nicholas, Robin A.J.
Thiaucourt, François
Sachse, Konrad
author_facet Bashiruddin, John B.
Frey, Joachim
Heldtander Königsson, Malin
Johansson, Karl-Erik
Hotzel, Helmut
Diller, Roland
De Santis, Paola
Botelho, Ana
Ayling, Roger D.
Nicholas, Robin A.J.
Thiaucourt, François
Sachse, Konrad
author_sort Bashiruddin, John B.
title Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial
title_short Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial
title_full Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial
title_fullStr Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial
title_full_unstemmed Evaluation of PCR systems for the identification and differentiation of Mycoplasma agalactiae and Mycoplasma bovis: a collaborative trial
title_sort evaluation of pcr systems for the identification and differentiation of mycoplasma agalactiae and mycoplasma bovis: a collaborative trial
url http://agritrop.cirad.fr/525758/
http://agritrop.cirad.fr/525758/1/525758.pdf
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