Quantification and viability assays of Toxoplasma gondii in commercial “Serrano” ham samples using magnetic capture real-time qPCR and bioassay techniques
“Serrano” ham is a typical pork product from the Mediterranean area, highly valued for its flavour. To make Serrano ham, pork undergoes a salting and a subsequent fermentation process known as curing. Certain pigs used for meat production are an important source of Toxoplasma gondii infection in hum...
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Veröffentlicht in: | Food microbiology 2015-04, Vol.46, p.107-113 |
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creator | Gomez-Samblas, M. Vílchez, S. Racero, J.C. Fuentes, M.V. Osuna, A. |
description | “Serrano” ham is a typical pork product from the Mediterranean area, highly valued for its flavour. To make Serrano ham, pork undergoes a salting and a subsequent fermentation process known as curing. Certain pigs used for meat production are an important source of Toxoplasma gondii infection in humans. We have developed a method for quantifying and assaying the viability of the T. gondii present in commercial Serrano ham samples. A magnetic capture method for the isolation of T. gondii DNA and a qRT-PCR were used to estimate the T. gondii burden in 475 commercial samples of “Serrano” ham in two presentation formats: ham pieces and sliced ham. The infectivity capacity of T. gondii in positive samples was assayed in mice. The global prevalence of T. gondii was 8.84%, ranging from 32.35% in one of the companies to 0% prevalence in three other companies. The infectivity assays revealed that only 4.84% of the positive samples were infective.
To the best of our knowledge this is the first report focussing on the prevalence of T. gondii in commercial “Serrano” ham. The method described here could be useful for producers to guarantee the safety of their products.
•We compare the infective Toxoplasma gondii burden in commercially cured “Serrano” ham.•qPCR was used for the analysis.•We used bioassays on mice to assess the infectivity of the tachyzoites in the ham. |
doi_str_mv | 10.1016/j.fm.2014.07.003 |
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To the best of our knowledge this is the first report focussing on the prevalence of T. gondii in commercial “Serrano” ham. The method described here could be useful for producers to guarantee the safety of their products.
•We compare the infective Toxoplasma gondii burden in commercially cured “Serrano” ham.•qPCR was used for the analysis.•We used bioassays on mice to assess the infectivity of the tachyzoites in the ham.</description><identifier>ISSN: 0740-0020</identifier><identifier>EISSN: 1095-9998</identifier><identifier>DOI: 10.1016/j.fm.2014.07.003</identifier><identifier>PMID: 25475273</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Bioassay ; Biological Assay - methods ; Commercial cured “Serrano Ham” ; DNA magnetic capture ; Food Contamination - analysis ; Humans ; Infectivity ; Magnetics ; Meat Products - economics ; Meat Products - parasitology ; Mice ; Mice, Inbred BALB C ; Quantitative real-time PCR ; Real-Time Polymerase Chain Reaction - instrumentation ; Real-Time Polymerase Chain Reaction - methods ; Spain ; Swine ; Toxoplasma - genetics ; Toxoplasma - growth & development ; Toxoplasma - isolation & purification ; Toxoplasma gondii ; Toxoplasmosis, Animal - parasitology</subject><ispartof>Food microbiology, 2015-04, Vol.46, p.107-113</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-cd521b0cbd50846e941e59ef8b6ba62c0de539e7b9daffb39928b4a880ed0c7f3</citedby><cites>FETCH-LOGICAL-c383t-cd521b0cbd50846e941e59ef8b6ba62c0de539e7b9daffb39928b4a880ed0c7f3</cites><orcidid>0000-0003-3729-4113 ; 0000-0003-4801-528X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fm.2014.07.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25475273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gomez-Samblas, M.</creatorcontrib><creatorcontrib>Vílchez, S.</creatorcontrib><creatorcontrib>Racero, J.C.</creatorcontrib><creatorcontrib>Fuentes, M.V.</creatorcontrib><creatorcontrib>Osuna, A.</creatorcontrib><title>Quantification and viability assays of Toxoplasma gondii in commercial “Serrano” ham samples using magnetic capture real-time qPCR and bioassay techniques</title><title>Food microbiology</title><addtitle>Food Microbiol</addtitle><description>“Serrano” ham is a typical pork product from the Mediterranean area, highly valued for its flavour. To make Serrano ham, pork undergoes a salting and a subsequent fermentation process known as curing. Certain pigs used for meat production are an important source of Toxoplasma gondii infection in humans. We have developed a method for quantifying and assaying the viability of the T. gondii present in commercial Serrano ham samples. A magnetic capture method for the isolation of T. gondii DNA and a qRT-PCR were used to estimate the T. gondii burden in 475 commercial samples of “Serrano” ham in two presentation formats: ham pieces and sliced ham. The infectivity capacity of T. gondii in positive samples was assayed in mice. The global prevalence of T. gondii was 8.84%, ranging from 32.35% in one of the companies to 0% prevalence in three other companies. The infectivity assays revealed that only 4.84% of the positive samples were infective.
To the best of our knowledge this is the first report focussing on the prevalence of T. gondii in commercial “Serrano” ham. The method described here could be useful for producers to guarantee the safety of their products.
•We compare the infective Toxoplasma gondii burden in commercially cured “Serrano” ham.•qPCR was used for the analysis.•We used bioassays on mice to assess the infectivity of the tachyzoites in the ham.</description><subject>Animals</subject><subject>Bioassay</subject><subject>Biological Assay - methods</subject><subject>Commercial cured “Serrano Ham”</subject><subject>DNA magnetic capture</subject><subject>Food Contamination - analysis</subject><subject>Humans</subject><subject>Infectivity</subject><subject>Magnetics</subject><subject>Meat Products - economics</subject><subject>Meat Products - parasitology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Quantitative real-time PCR</subject><subject>Real-Time Polymerase Chain Reaction - instrumentation</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Spain</subject><subject>Swine</subject><subject>Toxoplasma - genetics</subject><subject>Toxoplasma - growth & development</subject><subject>Toxoplasma - isolation & purification</subject><subject>Toxoplasma gondii</subject><subject>Toxoplasmosis, Animal - parasitology</subject><issn>0740-0020</issn><issn>1095-9998</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtv1EAQhC0EIkvgzgnNkYuXHj_H3NAqPKRIvMJ51B63N73yzDgzdsTe8kOAH5dfgjcbuCFx6stXVeqqJHkuYS1BVq92696uM5DFGuo1QP4gWUloyrRpGvUwWUFdQAqQwUnyJMYdgJRl3jxOTrKyqMuszlfJr88zuol7NjixdwJdJ64ZWx542guMEfdR-F5c-O9-HDBaFFvvOmbBThhvLQXDOIjbmx9fKQR0_vbmp7hEKyLacaAo5shuKyxuHU1shMFxmgOJQDikE1sSV582X-5yW_Z3gWIic-n4aqb4NHnU4xDp2f09Tb69PbvYvE_PP777sHlznppc5VNqujKTLZi2K0EVFTWFpLKhXrVVi1VmoKPlcarbpsO-b_OmyVRboFJAHZi6z0-Tl0ffMfhD7qQtR0PDgI78HLWsihqkUjL7DzQvslot7S4oHFETfIyBej0Gthj2WoI-DKh3urf6MKCGWi8DLpIX9-5za6n7K_iz2AK8PgK01HHNFHQ0TM5Qx4HMpDvP_3b_DRTfsEg</recordid><startdate>20150401</startdate><enddate>20150401</enddate><creator>Gomez-Samblas, M.</creator><creator>Vílchez, S.</creator><creator>Racero, J.C.</creator><creator>Fuentes, M.V.</creator><creator>Osuna, A.</creator><general>Elsevier Ltd</general><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><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0003-3729-4113</orcidid><orcidid>https://orcid.org/0000-0003-4801-528X</orcidid></search><sort><creationdate>20150401</creationdate><title>Quantification and viability assays of Toxoplasma gondii in commercial “Serrano” ham samples using magnetic capture real-time qPCR and bioassay techniques</title><author>Gomez-Samblas, M. ; Vílchez, S. ; Racero, J.C. ; Fuentes, M.V. ; Osuna, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-cd521b0cbd50846e941e59ef8b6ba62c0de539e7b9daffb39928b4a880ed0c7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Bioassay</topic><topic>Biological Assay - methods</topic><topic>Commercial cured “Serrano Ham”</topic><topic>DNA magnetic capture</topic><topic>Food Contamination - analysis</topic><topic>Humans</topic><topic>Infectivity</topic><topic>Magnetics</topic><topic>Meat Products - economics</topic><topic>Meat Products - parasitology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Quantitative real-time PCR</topic><topic>Real-Time Polymerase Chain Reaction - instrumentation</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Spain</topic><topic>Swine</topic><topic>Toxoplasma - genetics</topic><topic>Toxoplasma - growth & development</topic><topic>Toxoplasma - isolation & purification</topic><topic>Toxoplasma gondii</topic><topic>Toxoplasmosis, Animal - parasitology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomez-Samblas, M.</creatorcontrib><creatorcontrib>Vílchez, S.</creatorcontrib><creatorcontrib>Racero, J.C.</creatorcontrib><creatorcontrib>Fuentes, M.V.</creatorcontrib><creatorcontrib>Osuna, A.</creatorcontrib><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><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Food microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gomez-Samblas, M.</au><au>Vílchez, S.</au><au>Racero, J.C.</au><au>Fuentes, M.V.</au><au>Osuna, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification and viability assays of Toxoplasma gondii in commercial “Serrano” ham samples using magnetic capture real-time qPCR and bioassay techniques</atitle><jtitle>Food microbiology</jtitle><addtitle>Food Microbiol</addtitle><date>2015-04-01</date><risdate>2015</risdate><volume>46</volume><spage>107</spage><epage>113</epage><pages>107-113</pages><issn>0740-0020</issn><eissn>1095-9998</eissn><abstract>“Serrano” ham is a typical pork product from the Mediterranean area, highly valued for its flavour. To make Serrano ham, pork undergoes a salting and a subsequent fermentation process known as curing. Certain pigs used for meat production are an important source of Toxoplasma gondii infection in humans. We have developed a method for quantifying and assaying the viability of the T. gondii present in commercial Serrano ham samples. A magnetic capture method for the isolation of T. gondii DNA and a qRT-PCR were used to estimate the T. gondii burden in 475 commercial samples of “Serrano” ham in two presentation formats: ham pieces and sliced ham. The infectivity capacity of T. gondii in positive samples was assayed in mice. The global prevalence of T. gondii was 8.84%, ranging from 32.35% in one of the companies to 0% prevalence in three other companies. The infectivity assays revealed that only 4.84% of the positive samples were infective.
To the best of our knowledge this is the first report focussing on the prevalence of T. gondii in commercial “Serrano” ham. The method described here could be useful for producers to guarantee the safety of their products.
•We compare the infective Toxoplasma gondii burden in commercially cured “Serrano” ham.•qPCR was used for the analysis.•We used bioassays on mice to assess the infectivity of the tachyzoites in the ham.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25475273</pmid><doi>10.1016/j.fm.2014.07.003</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-3729-4113</orcidid><orcidid>https://orcid.org/0000-0003-4801-528X</orcidid></addata></record> |
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subjects | Animals Bioassay Biological Assay - methods Commercial cured “Serrano Ham” DNA magnetic capture Food Contamination - analysis Humans Infectivity Magnetics Meat Products - economics Meat Products - parasitology Mice Mice, Inbred BALB C Quantitative real-time PCR Real-Time Polymerase Chain Reaction - instrumentation Real-Time Polymerase Chain Reaction - methods Spain Swine Toxoplasma - genetics Toxoplasma - growth & development Toxoplasma - isolation & purification Toxoplasma gondii Toxoplasmosis, Animal - parasitology |
title | Quantification and viability assays of Toxoplasma gondii in commercial “Serrano” ham samples using magnetic capture real-time qPCR and bioassay techniques |
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