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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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. 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.</description><identifier>ISSN: 0022-0302</identifier><identifier>EISSN: 1525-3198</identifier><identifier>DOI: 10.3168/jds.2012-6124</identifier><identifier>PMID: 23587378</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>Journal of dairy science, 2013-06, Vol.96 (6), p.3611-3620</ispartof><rights>2013 American Dairy Science Association</rights><rights>Copyright © 2013 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-2ade7b88e6ad6502037fcb7835e2c2078749d18872f6d9827b16c84bda50693d3</citedby><cites>FETCH-LOGICAL-c404t-2ade7b88e6ad6502037fcb7835e2c2078749d18872f6d9827b16c84bda50693d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.3168/jds.2012-6124$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23587378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Perreten, Vincent</creatorcontrib><creatorcontrib>Endimiani, Andrea</creatorcontrib><creatorcontrib>Thomann, Andreas</creatorcontrib><creatorcontrib>Wipf, Juliette R.K.</creatorcontrib><creatorcontrib>Rossano, Alexandra</creatorcontrib><creatorcontrib>Bodmer, Michèle</creatorcontrib><creatorcontrib>Raemy, Andreas</creatorcontrib><creatorcontrib>Sannes-Lowery, Kristin A.</creatorcontrib><creatorcontrib>Ecker, David J.</creatorcontrib><creatorcontrib>Sampath, Rangarajan</creatorcontrib><creatorcontrib>Bonomo, Robert A.</creatorcontrib><title>Evaluation of PCR electrospray-ionization mass spectrometry for rapid molecular diagnosis of bovine mastitis</title><title>Journal of dairy science</title><addtitle>J Dairy Sci</addtitle><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.</description><subject>Animals</subject><subject>antibiotics</subject><subject>bacteria</subject><subject>Bacteria - genetics</subject><subject>Bacteria - isolation & purification</subject><subject>bovine mastitis</subject><subject>Cattle</subject><subject>cows</subject><subject>dairy cow</subject><subject>dairy industry</subject><subject>detection</subject><subject>diagnostic techniques</subject><subject>disease prevention</subject><subject>electrospray ionization mass spectrometry</subject><subject>Female</subject><subject>Fungi - isolation & purification</subject><subject>genes</subject><subject>mammary glands</subject><subject>Mastitis, Bovine - diagnosis</subject><subject>Mastitis, Bovine - microbiology</subject><subject>method</subject><subject>milk</subject><subject>Milk - microbiology</subject><subject>pathogens</subject><subject>polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Polymerase Chain Reaction - veterinary</subject><subject>screening</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><subject>Spectrometry, Mass, Electrospray Ionization - veterinary</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - genetics</subject><subject>Staphylococcus aureus - isolation & purification</subject><subject>yeasts</subject><subject>Yeasts - isolation & purification</subject><issn>0022-0302</issn><issn>1525-3198</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1v1DAURS1URIeWJds2SzYp_ohjZ1mNWkCqBIJ2bTn2S-UqiVO_ZKTh1-OQlh0bW_Y791o-hHxk9EqwWn9-8njFKeNlzXj1huyY5LIUrNEnZEcp5yUVlJ-S94hP-cg4le_IKRdSK6H0jvQ3B9svdg5xLGJX_Nj_LKAHN6eIU7LHMt-H39t4sIgFTn-HA8zpWHQxFclOwRdDzKGlt6nwwT6OEQOudW08hBHW5BzmgOfkbWd7hA8v-xl5uL25338t775_-ba_vitdRau55NaDarWG2vpaUk6F6lyrtJDAHadKq6rxTGvFu9o3mquW1U5XrbeS1o3w4ox82nqnFJ8XwNkMAR30vR0hLmiYkKLRtdA6o-WGuvxjTNCZKYXBpqNh1KyCTRZsVsFmFZz5i5fqpR3A_6NfjWbgcgM6G419TAHNw6-cl5SyvEqVCbURkBUcAiSDLsDowIeU5Rofw38e_wOLcpPn</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Perreten, Vincent</creator><creator>Endimiani, Andrea</creator><creator>Thomann, Andreas</creator><creator>Wipf, Juliette R.K.</creator><creator>Rossano, Alexandra</creator><creator>Bodmer, Michèle</creator><creator>Raemy, Andreas</creator><creator>Sannes-Lowery, Kristin A.</creator><creator>Ecker, David J.</creator><creator>Sampath, Rangarajan</creator><creator>Bonomo, Robert A.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130601</creationdate><title>Evaluation of PCR electrospray-ionization mass spectrometry for rapid molecular diagnosis of bovine mastitis</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-2ade7b88e6ad6502037fcb7835e2c2078749d18872f6d9827b16c84bda50693d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>antibiotics</topic><topic>bacteria</topic><topic>Bacteria - genetics</topic><topic>Bacteria - isolation & purification</topic><topic>bovine mastitis</topic><topic>Cattle</topic><topic>cows</topic><topic>dairy cow</topic><topic>dairy industry</topic><topic>detection</topic><topic>diagnostic techniques</topic><topic>disease prevention</topic><topic>electrospray ionization mass spectrometry</topic><topic>Female</topic><topic>Fungi - isolation & purification</topic><topic>genes</topic><topic>mammary glands</topic><topic>Mastitis, Bovine - diagnosis</topic><topic>Mastitis, Bovine - microbiology</topic><topic>method</topic><topic>milk</topic><topic>Milk - microbiology</topic><topic>pathogens</topic><topic>polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Polymerase Chain Reaction - veterinary</topic><topic>screening</topic><topic>Sensitivity and Specificity</topic><topic>Spectrometry, Mass, Electrospray Ionization - methods</topic><topic>Spectrometry, Mass, Electrospray Ionization - veterinary</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - genetics</topic><topic>Staphylococcus aureus - isolation & purification</topic><topic>yeasts</topic><topic>Yeasts - isolation & purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perreten, Vincent</creatorcontrib><creatorcontrib>Endimiani, Andrea</creatorcontrib><creatorcontrib>Thomann, Andreas</creatorcontrib><creatorcontrib>Wipf, Juliette R.K.</creatorcontrib><creatorcontrib>Rossano, Alexandra</creatorcontrib><creatorcontrib>Bodmer, Michèle</creatorcontrib><creatorcontrib>Raemy, Andreas</creatorcontrib><creatorcontrib>Sannes-Lowery, Kristin A.</creatorcontrib><creatorcontrib>Ecker, David J.</creatorcontrib><creatorcontrib>Sampath, Rangarajan</creatorcontrib><creatorcontrib>Bonomo, Robert A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dairy science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perreten, Vincent</au><au>Endimiani, Andrea</au><au>Thomann, Andreas</au><au>Wipf, Juliette R.K.</au><au>Rossano, Alexandra</au><au>Bodmer, Michèle</au><au>Raemy, Andreas</au><au>Sannes-Lowery, Kristin A.</au><au>Ecker, David J.</au><au>Sampath, Rangarajan</au><au>Bonomo, Robert A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of PCR electrospray-ionization mass spectrometry for rapid molecular diagnosis of bovine mastitis</atitle><jtitle>Journal of dairy science</jtitle><addtitle>J Dairy Sci</addtitle><date>2013-06-01</date><risdate>2013</risdate><volume>96</volume><issue>6</issue><spage>3611</spage><epage>3620</epage><pages>3611-3620</pages><issn>0022-0302</issn><eissn>1525-3198</eissn><abstract>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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23587378</pmid><doi>10.3168/jds.2012-6124</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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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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