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Detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical DNA chip

Bovine mastitis causes significant economic losses in the dairy industry. Effective prevention of bovine mastitis requires an understanding of the infection status of a pathogenic microorganism in a herd that has not yet shown clinical signs of mastitis and appropriate treatment specific for the pat...

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Autores principales: KAWAI, Kazuhiro, INADA, Mika, ITO, Keiko, HASHIMOTO, Koji, NIKAIDO, Masaru, HATA, Eiji, KATSUDA, Ken, KIKU, Yoshio, TAGAWA, Yuichi, HAYASHI, Tomohito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745174/
https://www.ncbi.nlm.nih.gov/pubmed/29093278
http://dx.doi.org/10.1292/jvms.17-0263
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author KAWAI, Kazuhiro
INADA, Mika
ITO, Keiko
HASHIMOTO, Koji
NIKAIDO, Masaru
HATA, Eiji
KATSUDA, Ken
KIKU, Yoshio
TAGAWA, Yuichi
HAYASHI, Tomohito
author_facet KAWAI, Kazuhiro
INADA, Mika
ITO, Keiko
HASHIMOTO, Koji
NIKAIDO, Masaru
HATA, Eiji
KATSUDA, Ken
KIKU, Yoshio
TAGAWA, Yuichi
HAYASHI, Tomohito
author_sort KAWAI, Kazuhiro
collection PubMed
description Bovine mastitis causes significant economic losses in the dairy industry. Effective prevention of bovine mastitis requires an understanding of the infection status of a pathogenic microorganism in a herd that has not yet shown clinical signs of mastitis and appropriate treatment specific for the pathogenic microorganism. However, bacterial identification by culture has drawbacks in that the sensitivity may be low and the procedure can be complex. In this study, we developed a genetic detection method to identify mastitis pathogens using a simple and highly sensitive electrochemical DNA chip which can specifically detect bacterial DNA in milk specimens. First, we selected microorganisms belonging to 12 families and/or genera associated with mastitis for which testing should be performed. Next, we optimized the conditions for amplifying microorganism DNA by loop-mediated isothermal amplification (LAMP) using 32 primers and the use of a DNA chip capable of measuring all pathogens simultaneously. Sample detection could be completed in just a few hours using this method. Comparison of the results obtained with our DNA chip method and those obtained by bacterial culture verified that when the culture method was set to 100%, the total positive concordance rate of the DNA chip was 85.0% and the total negative concordance rate was 86.9%. Furthermore, the proposed method allows both rapid and highly sensitive detection of mastitis pathogens. We believe that this method will contribute to the development of an effective mastitis control program.
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spelling pubmed-57451742018-01-05 Detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical DNA chip KAWAI, Kazuhiro INADA, Mika ITO, Keiko HASHIMOTO, Koji NIKAIDO, Masaru HATA, Eiji KATSUDA, Ken KIKU, Yoshio TAGAWA, Yuichi HAYASHI, Tomohito J Vet Med Sci Bacteriology Bovine mastitis causes significant economic losses in the dairy industry. Effective prevention of bovine mastitis requires an understanding of the infection status of a pathogenic microorganism in a herd that has not yet shown clinical signs of mastitis and appropriate treatment specific for the pathogenic microorganism. However, bacterial identification by culture has drawbacks in that the sensitivity may be low and the procedure can be complex. In this study, we developed a genetic detection method to identify mastitis pathogens using a simple and highly sensitive electrochemical DNA chip which can specifically detect bacterial DNA in milk specimens. First, we selected microorganisms belonging to 12 families and/or genera associated with mastitis for which testing should be performed. Next, we optimized the conditions for amplifying microorganism DNA by loop-mediated isothermal amplification (LAMP) using 32 primers and the use of a DNA chip capable of measuring all pathogens simultaneously. Sample detection could be completed in just a few hours using this method. Comparison of the results obtained with our DNA chip method and those obtained by bacterial culture verified that when the culture method was set to 100%, the total positive concordance rate of the DNA chip was 85.0% and the total negative concordance rate was 86.9%. Furthermore, the proposed method allows both rapid and highly sensitive detection of mastitis pathogens. We believe that this method will contribute to the development of an effective mastitis control program. The Japanese Society of Veterinary Science 2017-11-01 2017-12 /pmc/articles/PMC5745174/ /pubmed/29093278 http://dx.doi.org/10.1292/jvms.17-0263 Text en ©2017 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Bacteriology
KAWAI, Kazuhiro
INADA, Mika
ITO, Keiko
HASHIMOTO, Koji
NIKAIDO, Masaru
HATA, Eiji
KATSUDA, Ken
KIKU, Yoshio
TAGAWA, Yuichi
HAYASHI, Tomohito
Detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical DNA chip
title Detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical DNA chip
title_full Detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical DNA chip
title_fullStr Detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical DNA chip
title_full_unstemmed Detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical DNA chip
title_short Detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical DNA chip
title_sort detection of bovine mastitis pathogens by loop-mediated isothermal amplification and an electrochemical dna chip
topic Bacteriology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745174/
https://www.ncbi.nlm.nih.gov/pubmed/29093278
http://dx.doi.org/10.1292/jvms.17-0263
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