Quantitative duplex TaqMan real-time polymerase chain reaction for the assessment of the etiologic agent of epizootic bovine abortion
Epizootic bovine abortion (EBA), also commonly known as "foothill abortion," is a late-term abortion primarily in beef cattle with significant economic impacts in California, Nevada, and Oregon. The causative agent is a novel deltaproteobacterium (aoEBA) closely related to the order Myxoco...
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Veröffentlicht in: | Journal of veterinary diagnostic investigation 2011-11, Vol.23 (6), p.1153-1159 |
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creator | Brooks, Roxann S Blanchard, Myra T Anderson, Mark L Hall, Mark R Stott, Jeffery L |
description | Epizootic bovine abortion (EBA), also commonly known as "foothill abortion," is a late-term abortion primarily in beef cattle with significant economic impacts in California, Nevada, and Oregon. The causative agent is a novel deltaproteobacterium (aoEBA) closely related to the order Myxococcales and vectored by the soft-shelled tick Ornithodoros coriaceus. Historically, diagnosis has relied upon the pathologic examination of the fetus and the presence of elevated fetal serum immunoglobulins. Identification of the etiologic agent, a unique deltaproteobacterium, permitted the development of a quantitative duplex real-time polymerase chain reaction (qPCR) using a unique 90-bp sequence of aoEBA 16S ribosomal RNA gene in conjunction with an 88-bp sequence of the bovine beta-actin gene. Reaction efficiencies were 100.9% for the 16S aoEBA gene and 93.1% for the bovine beta-actin gene. Application of the duplex TaqMan to a set of aoEBA-infected fetal bovine necropsy tissues demonstrated the assay to be robust in quantitatively identifying the aoEBA bacteria and establishing host-tissue pathogen load. Consistent with previously reported immunohistochemical data, organized lymphoid tissue generally carried the heaviest bacterial load as compared to non-lymphoid tissue. The newly developed duplex TaqMan assay will facilitate diagnosis in difficult cases and provide an invaluable tool for delineating the pathogenesis of EBA. |
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The causative agent is a novel deltaproteobacterium (aoEBA) closely related to the order Myxococcales and vectored by the soft-shelled tick Ornithodoros coriaceus. Historically, diagnosis has relied upon the pathologic examination of the fetus and the presence of elevated fetal serum immunoglobulins. Identification of the etiologic agent, a unique deltaproteobacterium, permitted the development of a quantitative duplex real-time polymerase chain reaction (qPCR) using a unique 90-bp sequence of aoEBA 16S ribosomal RNA gene in conjunction with an 88-bp sequence of the bovine beta-actin gene. Reaction efficiencies were 100.9% for the 16S aoEBA gene and 93.1% for the bovine beta-actin gene. Application of the duplex TaqMan to a set of aoEBA-infected fetal bovine necropsy tissues demonstrated the assay to be robust in quantitatively identifying the aoEBA bacteria and establishing host-tissue pathogen load. Consistent with previously reported immunohistochemical data, organized lymphoid tissue generally carried the heaviest bacterial load as compared to non-lymphoid tissue. The newly developed duplex TaqMan assay will facilitate diagnosis in difficult cases and provide an invaluable tool for delineating the pathogenesis of EBA.</description><identifier>ISSN: 1040-6387</identifier><identifier>EISSN: 1943-4936</identifier><identifier>DOI: 10.1177/1040638711425573</identifier><identifier>PMID: 22362796</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Aborted Fetus - microbiology ; Abortion, Veterinary - microbiology ; actin ; Animals ; Antibodies, Bacterial ; bacteria ; beef cattle ; Cattle ; Deltaproteobacteria - genetics ; Deltaproteobacteria - isolation & purification ; economic impact ; Female ; fetus ; Gene Expression Regulation, Bacterial - physiology ; genes ; Immunoglobulin G ; Immunoglobulin M ; immunoglobulins ; immunohistochemistry ; microbial load ; Myxococcales ; necropsy ; Ornithodoros coriaceus ; pathogenesis ; pathogens ; quantitative polymerase chain reaction ; Real-Time Polymerase Chain Reaction - methods ; Real-Time Polymerase Chain Reaction - veterinary ; ribosomal RNA ; RNA, Ribosomal, 16S - genetics ; ticks</subject><ispartof>Journal of veterinary diagnostic investigation, 2011-11, Vol.23 (6), p.1153-1159</ispartof><rights>2011 American Association of Veterinary Laboratory Diagnosticians</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-d56a397e0e31941e7c88c51aefac3fcee0461cc4eb1cc2374b09dec8853dff7a3</citedby><cites>FETCH-LOGICAL-c402t-d56a397e0e31941e7c88c51aefac3fcee0461cc4eb1cc2374b09dec8853dff7a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1040638711425573$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1040638711425573$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,778,782,21806,27911,27912,43608,43609</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22362796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brooks, Roxann S</creatorcontrib><creatorcontrib>Blanchard, Myra T</creatorcontrib><creatorcontrib>Anderson, Mark L</creatorcontrib><creatorcontrib>Hall, Mark R</creatorcontrib><creatorcontrib>Stott, Jeffery L</creatorcontrib><title>Quantitative duplex TaqMan real-time polymerase chain reaction for the assessment of the etiologic agent of epizootic bovine abortion</title><title>Journal of veterinary diagnostic investigation</title><addtitle>J Vet Diagn Invest</addtitle><description>Epizootic bovine abortion (EBA), also commonly known as "foothill abortion," is a late-term abortion primarily in beef cattle with significant economic impacts in California, Nevada, and Oregon. The causative agent is a novel deltaproteobacterium (aoEBA) closely related to the order Myxococcales and vectored by the soft-shelled tick Ornithodoros coriaceus. Historically, diagnosis has relied upon the pathologic examination of the fetus and the presence of elevated fetal serum immunoglobulins. Identification of the etiologic agent, a unique deltaproteobacterium, permitted the development of a quantitative duplex real-time polymerase chain reaction (qPCR) using a unique 90-bp sequence of aoEBA 16S ribosomal RNA gene in conjunction with an 88-bp sequence of the bovine beta-actin gene. Reaction efficiencies were 100.9% for the 16S aoEBA gene and 93.1% for the bovine beta-actin gene. Application of the duplex TaqMan to a set of aoEBA-infected fetal bovine necropsy tissues demonstrated the assay to be robust in quantitatively identifying the aoEBA bacteria and establishing host-tissue pathogen load. Consistent with previously reported immunohistochemical data, organized lymphoid tissue generally carried the heaviest bacterial load as compared to non-lymphoid tissue. The newly developed duplex TaqMan assay will facilitate diagnosis in difficult cases and provide an invaluable tool for delineating the pathogenesis of EBA.</description><subject>Aborted Fetus - microbiology</subject><subject>Abortion, Veterinary - microbiology</subject><subject>actin</subject><subject>Animals</subject><subject>Antibodies, Bacterial</subject><subject>bacteria</subject><subject>beef cattle</subject><subject>Cattle</subject><subject>Deltaproteobacteria - genetics</subject><subject>Deltaproteobacteria - isolation & purification</subject><subject>economic impact</subject><subject>Female</subject><subject>fetus</subject><subject>Gene Expression Regulation, Bacterial - physiology</subject><subject>genes</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>immunoglobulins</subject><subject>immunohistochemistry</subject><subject>microbial load</subject><subject>Myxococcales</subject><subject>necropsy</subject><subject>Ornithodoros coriaceus</subject><subject>pathogenesis</subject><subject>pathogens</subject><subject>quantitative polymerase chain reaction</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Real-Time Polymerase Chain Reaction - veterinary</subject><subject>ribosomal RNA</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>ticks</subject><issn>1040-6387</issn><issn>1943-4936</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kL1vFDEQxS0EIiHQU4G7VAv-XN-WKAofUhBCJLU16x1fHO2uN7Y3Iun5v_HlDgoKGo_13m-eNI-Q15y949yY95wp1sqN4VwJrY18Qo55p2SjOtk-rf9qNzv_iLzI-YYxLbThz8mRELIVpmuPya_vK8wlFCjhDumwLiP-pJdw-xVmmhDGpoQJ6RLH-wkTZKTuGsKj5UqIM_Ux0XKNFHLGnCecC43-UcHqj3EbHIXtQcYlPMRYqtTHuzDXrT6mXcxL8szDmPHVYZ6Qq4_nl2efm4tvn76cfbhonGKiNINuQXYGGcp6JkfjNhunOaAHJ71DZKrlzins6yukUT3rBqyQloP3BuQJOd3nLinerpiLnUJ2OI4wY1yz7YTURncdqyTbky7FnBN6u6QwQbq3nNld9_bf7uvKm0P42k84_F34U3YFmj2QayP2Jq5prsf-L_DtnvcQLWxTyPbqh2BcMcaMEULL36kQmG0</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Brooks, Roxann S</creator><creator>Blanchard, Myra T</creator><creator>Anderson, Mark L</creator><creator>Hall, Mark R</creator><creator>Stott, Jeffery L</creator><general>SAGE Publications</general><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>20111101</creationdate><title>Quantitative duplex TaqMan real-time polymerase chain reaction for the assessment of the etiologic agent of epizootic bovine abortion</title><author>Brooks, Roxann S ; Blanchard, Myra T ; Anderson, Mark L ; Hall, Mark R ; Stott, Jeffery L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-d56a397e0e31941e7c88c51aefac3fcee0461cc4eb1cc2374b09dec8853dff7a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aborted Fetus - microbiology</topic><topic>Abortion, Veterinary - microbiology</topic><topic>actin</topic><topic>Animals</topic><topic>Antibodies, Bacterial</topic><topic>bacteria</topic><topic>beef cattle</topic><topic>Cattle</topic><topic>Deltaproteobacteria - genetics</topic><topic>Deltaproteobacteria - isolation & purification</topic><topic>economic impact</topic><topic>Female</topic><topic>fetus</topic><topic>Gene Expression Regulation, Bacterial - physiology</topic><topic>genes</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin M</topic><topic>immunoglobulins</topic><topic>immunohistochemistry</topic><topic>microbial load</topic><topic>Myxococcales</topic><topic>necropsy</topic><topic>Ornithodoros coriaceus</topic><topic>pathogenesis</topic><topic>pathogens</topic><topic>quantitative polymerase chain reaction</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Real-Time Polymerase Chain Reaction - veterinary</topic><topic>ribosomal RNA</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>ticks</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brooks, Roxann S</creatorcontrib><creatorcontrib>Blanchard, Myra T</creatorcontrib><creatorcontrib>Anderson, Mark L</creatorcontrib><creatorcontrib>Hall, Mark R</creatorcontrib><creatorcontrib>Stott, Jeffery L</creatorcontrib><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 veterinary diagnostic investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brooks, Roxann S</au><au>Blanchard, Myra T</au><au>Anderson, Mark L</au><au>Hall, Mark R</au><au>Stott, Jeffery L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative duplex TaqMan real-time polymerase chain reaction for the assessment of the etiologic agent of epizootic bovine abortion</atitle><jtitle>Journal of veterinary diagnostic investigation</jtitle><addtitle>J Vet Diagn Invest</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>23</volume><issue>6</issue><spage>1153</spage><epage>1159</epage><pages>1153-1159</pages><issn>1040-6387</issn><eissn>1943-4936</eissn><abstract>Epizootic bovine abortion (EBA), also commonly known as "foothill abortion," is a late-term abortion primarily in beef cattle with significant economic impacts in California, Nevada, and Oregon. The causative agent is a novel deltaproteobacterium (aoEBA) closely related to the order Myxococcales and vectored by the soft-shelled tick Ornithodoros coriaceus. Historically, diagnosis has relied upon the pathologic examination of the fetus and the presence of elevated fetal serum immunoglobulins. Identification of the etiologic agent, a unique deltaproteobacterium, permitted the development of a quantitative duplex real-time polymerase chain reaction (qPCR) using a unique 90-bp sequence of aoEBA 16S ribosomal RNA gene in conjunction with an 88-bp sequence of the bovine beta-actin gene. Reaction efficiencies were 100.9% for the 16S aoEBA gene and 93.1% for the bovine beta-actin gene. Application of the duplex TaqMan to a set of aoEBA-infected fetal bovine necropsy tissues demonstrated the assay to be robust in quantitatively identifying the aoEBA bacteria and establishing host-tissue pathogen load. 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subjects | Aborted Fetus - microbiology Abortion, Veterinary - microbiology actin Animals Antibodies, Bacterial bacteria beef cattle Cattle Deltaproteobacteria - genetics Deltaproteobacteria - isolation & purification economic impact Female fetus Gene Expression Regulation, Bacterial - physiology genes Immunoglobulin G Immunoglobulin M immunoglobulins immunohistochemistry microbial load Myxococcales necropsy Ornithodoros coriaceus pathogenesis pathogens quantitative polymerase chain reaction Real-Time Polymerase Chain Reaction - methods Real-Time Polymerase Chain Reaction - veterinary ribosomal RNA RNA, Ribosomal, 16S - genetics ticks |
title | Quantitative duplex TaqMan real-time polymerase chain reaction for the assessment of the etiologic agent of epizootic bovine abortion |
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