Evaluation of PCR electrospray-ionization mass spectrometry for rapid molecular diagnosis of bovine mastitis

Bovine mastitis, an inflammatory disease of the mammary gland, is one of the most costly diseases affecting the dairy industry. The treatment and prevention of this disease is linked heavily to the use of antibiotics in agriculture and early detection of the primary pathogen is essential to control...

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Veröffentlicht in:Journal of dairy science 2013-06, Vol.96 (6), p.3611-3620
Hauptverfasser: Perreten, Vincent, Endimiani, Andrea, Thomann, Andreas, Wipf, Juliette R.K., Rossano, Alexandra, Bodmer, Michèle, Raemy, Andreas, Sannes-Lowery, Kristin A., Ecker, David J., Sampath, Rangarajan, Bonomo, Robert A.
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container_end_page 3620
container_issue 6
container_start_page 3611
container_title Journal of dairy science
container_volume 96
creator Perreten, Vincent
Endimiani, Andrea
Thomann, Andreas
Wipf, Juliette R.K.
Rossano, Alexandra
Bodmer, Michèle
Raemy, Andreas
Sannes-Lowery, Kristin A.
Ecker, David J.
Sampath, Rangarajan
Bonomo, Robert A.
description Bovine mastitis, an inflammatory disease of the mammary gland, is one of the most costly diseases affecting the dairy industry. The treatment and prevention of this disease is linked heavily to the use of antibiotics in agriculture and early detection of the primary pathogen is essential to control the disease. Milk samples (n=67) from cows suffering from mastitis were analyzed for the presence of pathogens using PCR electrospray-ionization mass spectrometry (PCR/ESI-MS) and were compared with standard culture diagnostic methods. Concurrent identification of the primary mastitis pathogens was obtained for 64% of the tested milk samples, whereas divergent results were obtained for 27% of the samples. The PCR/ESI-MS failed to identify some of the primary pathogens in 18% of the samples, but identified other pathogens as well as microorganisms in samples that were negative by culture. The PCR/ESI-MS identified bacteria to the species level as well as yeasts and molds in samples that contained a mixed bacterial culture (9%). The sensitivity of the PCR/ESI-MS for the most common pathogens ranged from 57.1 to 100% and the specificity ranged from 69.8 to 100% using culture as gold standard. The PCR/ESI-MS also revealed the presence of the methicillin-resistant gene mecA in 16.2% of the milk samples, which correlated with the simultaneous detection of staphylococci including Staphylococcus aureus. We demonstrated that PCR/ESI-MS, a more rapid diagnostic platform compared with bacterial culture, has the significant potential to serve as an important screening method in the diagnosis of bovine clinical mastitis and has the capacity to be used in infection control programs for both subclinical and clinical disease.
doi_str_mv 10.3168/jds.2012-6124
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The treatment and prevention of this disease is linked heavily to the use of antibiotics in agriculture and early detection of the primary pathogen is essential to control the disease. Milk samples (n=67) from cows suffering from mastitis were analyzed for the presence of pathogens using PCR electrospray-ionization mass spectrometry (PCR/ESI-MS) and were compared with standard culture diagnostic methods. Concurrent identification of the primary mastitis pathogens was obtained for 64% of the tested milk samples, whereas divergent results were obtained for 27% of the samples. The PCR/ESI-MS failed to identify some of the primary pathogens in 18% of the samples, but identified other pathogens as well as microorganisms in samples that were negative by culture. The PCR/ESI-MS identified bacteria to the species level as well as yeasts and molds in samples that contained a mixed bacterial culture (9%). The sensitivity of the PCR/ESI-MS for the most common pathogens ranged from 57.1 to 100% and the specificity ranged from 69.8 to 100% using culture as gold standard. The PCR/ESI-MS also revealed the presence of the methicillin-resistant gene mecA in 16.2% of the milk samples, which correlated with the simultaneous detection of staphylococci including Staphylococcus aureus. 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The sensitivity of the PCR/ESI-MS for the most common pathogens ranged from 57.1 to 100% and the specificity ranged from 69.8 to 100% using culture as gold standard. The PCR/ESI-MS also revealed the presence of the methicillin-resistant gene mecA in 16.2% of the milk samples, which correlated with the simultaneous detection of staphylococci including Staphylococcus aureus. 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subjects Animals
antibiotics
bacteria
Bacteria - genetics
Bacteria - isolation & purification
bovine mastitis
Cattle
cows
dairy cow
dairy industry
detection
diagnostic techniques
disease prevention
electrospray ionization mass spectrometry
Female
Fungi - isolation & purification
genes
mammary glands
Mastitis, Bovine - diagnosis
Mastitis, Bovine - microbiology
method
milk
Milk - microbiology
pathogens
polymerase chain reaction
Polymerase Chain Reaction - methods
Polymerase Chain Reaction - veterinary
screening
Sensitivity and Specificity
Spectrometry, Mass, Electrospray Ionization - methods
Spectrometry, Mass, Electrospray Ionization - veterinary
Staphylococcus aureus
Staphylococcus aureus - genetics
Staphylococcus aureus - isolation & purification
yeasts
Yeasts - isolation & purification
title Evaluation of PCR electrospray-ionization mass spectrometry for rapid molecular diagnosis of bovine mastitis
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