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Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk

BACKGROUND: Laboratory diagnostic techniques able to detect Mycoplasma agalactiae are essential in contagious agalactia in dairy goats. This study was designed: 1) to determine the detection limits of PCR and culture in goat milk samples, 2) to examine the effects of experimental conditions includin...

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Autores principales: Tatay-Dualde, J., Sánchez, A., Prats-van der Ham, M., Gómez-Martín, A., Paterna, A., Corrales, J.C., de la Fe, C., Contreras, A., Amores, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562104/
https://www.ncbi.nlm.nih.gov/pubmed/26351565
http://dx.doi.org/10.1186/s13620-015-0049-y
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author Tatay-Dualde, J.
Sánchez, A.
Prats-van der Ham, M.
Gómez-Martín, A.
Paterna, A.
Corrales, J.C.
de la Fe, C.
Contreras, A.
Amores, J.
author_facet Tatay-Dualde, J.
Sánchez, A.
Prats-van der Ham, M.
Gómez-Martín, A.
Paterna, A.
Corrales, J.C.
de la Fe, C.
Contreras, A.
Amores, J.
author_sort Tatay-Dualde, J.
collection PubMed
description BACKGROUND: Laboratory diagnostic techniques able to detect Mycoplasma agalactiae are essential in contagious agalactia in dairy goats. This study was designed: 1) to determine the detection limits of PCR and culture in goat milk samples, 2) to examine the effects of experimental conditions including the DNA extraction method, PCR technique and storage conditions (fresh versus frozen stored milk samples) on these methods and 3), to establish agreement between PCR and culture techniques using milk samples from goats with mastitis in commercial dairy herds. The study was conducted both on artificially inoculated and field samples. RESULTS: Our findings indicate that culture is able to detect M. agalactiae in goat milk at lower concentrations than PCR. Qualitative detection of M.agalactiae by culture and PCR was not affected by sample freezing, though the DNA extraction method used significantly affected the results of the different PCR protocols. When clinical samples were used, both techniques showed good agreement. CONCLUSIONS: The results from this study indicate that both culture and PCR are able to detect M. agalactiae in clinical goat mastitis samples. However, in bulk tank milk samples with presumably lower M. agalactiae concentrations, culture is recommended within the first 24 h of sample collection due to its lower limit of detection. To improve the diagnostic sensitivity of PCR in milk samples, there is a need to increase the efficiency of extracting DNA from milk samples using protocols including a previous step of enzymatic digestion.
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spelling pubmed-45621042015-09-09 Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk Tatay-Dualde, J. Sánchez, A. Prats-van der Ham, M. Gómez-Martín, A. Paterna, A. Corrales, J.C. de la Fe, C. Contreras, A. Amores, J. Ir Vet J Research BACKGROUND: Laboratory diagnostic techniques able to detect Mycoplasma agalactiae are essential in contagious agalactia in dairy goats. This study was designed: 1) to determine the detection limits of PCR and culture in goat milk samples, 2) to examine the effects of experimental conditions including the DNA extraction method, PCR technique and storage conditions (fresh versus frozen stored milk samples) on these methods and 3), to establish agreement between PCR and culture techniques using milk samples from goats with mastitis in commercial dairy herds. The study was conducted both on artificially inoculated and field samples. RESULTS: Our findings indicate that culture is able to detect M. agalactiae in goat milk at lower concentrations than PCR. Qualitative detection of M.agalactiae by culture and PCR was not affected by sample freezing, though the DNA extraction method used significantly affected the results of the different PCR protocols. When clinical samples were used, both techniques showed good agreement. CONCLUSIONS: The results from this study indicate that both culture and PCR are able to detect M. agalactiae in clinical goat mastitis samples. However, in bulk tank milk samples with presumably lower M. agalactiae concentrations, culture is recommended within the first 24 h of sample collection due to its lower limit of detection. To improve the diagnostic sensitivity of PCR in milk samples, there is a need to increase the efficiency of extracting DNA from milk samples using protocols including a previous step of enzymatic digestion. BioMed Central 2015-09-07 /pmc/articles/PMC4562104/ /pubmed/26351565 http://dx.doi.org/10.1186/s13620-015-0049-y Text en © Tatay-Dualde et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Tatay-Dualde, J.
Sánchez, A.
Prats-van der Ham, M.
Gómez-Martín, A.
Paterna, A.
Corrales, J.C.
de la Fe, C.
Contreras, A.
Amores, J.
Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk
title Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk
title_full Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk
title_fullStr Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk
title_full_unstemmed Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk
title_short Sensitivity of two methods to detect Mycoplasma agalactiae in goat milk
title_sort sensitivity of two methods to detect mycoplasma agalactiae in goat milk
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562104/
https://www.ncbi.nlm.nih.gov/pubmed/26351565
http://dx.doi.org/10.1186/s13620-015-0049-y
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