<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Journal of Food Quality and Hazards Control</title>
<title_fa>مجله کیفیت و کنترل مخاطرات مواد غذایی</title_fa>
<short_title>J. Food Qual. Hazards Control</short_title>
<subject>Medical Sciences</subject>
<web_url>http://jfqhc.ssu.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2345-685X</journal_id_issn>
<journal_id_issn_online>2345-6825</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>10.29252/jfqhc</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1397</year>
	<month>6</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2018</year>
	<month>9</month>
	<day>1</day>
</pubdate>
<volume>5</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Potential Use of DNA Aptamer-Magnetic Bead Separation-PCR  Assay for Salmonella Detection in Food

</title>
	<subject_fa>تخصصي</subject_fa>
	<subject>Special</subject>
	<content_type_fa>Original article</content_type_fa>
	<content_type>Original article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;&lt;span style=&quot;font-size:14px;&quot;&gt;&lt;span style=&quot;font-family:times new roman;&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Salmonella&lt;/em&gt; is one of the most common food-borne pathogens that can cause illness. In this study, the sensitivity and the specificity of Aptamer-Magnetic bead Separation-Polymerase Chain Reaction (AMS-PCR) method were determined for&lt;em&gt; Salmonella&lt;/em&gt; spp. detection.&lt;br&gt;
&lt;strong&gt;Methods:&lt;/strong&gt; Different concentrations of &lt;em&gt;Salmonella enterica&lt;/em&gt; were mixed with streptavidin-magnetic beads coated with biotinylated DNA aptamer. The bound bacteria were eluted and tested with PCR targeting the &lt;em&gt;inv&lt;/em&gt;A gene of &lt;em&gt;Salmonella&lt;/em&gt;. Ten different serovars of &lt;em&gt;Salmonella enterica&lt;/em&gt; and four non-&lt;em&gt;Salmonella&lt;/em&gt; were tested to determine the specificity of the DNA aptamer. For field application, 14 different food samples were tested and compared with the culture method.&lt;br&gt;
&lt;strong&gt;Results:&lt;/strong&gt; The limit of detection of AMS-PCR method was 10&lt;sup&gt;2&lt;/sup&gt; CFU/ml which was 10 times more sensitive than conventional PCR without AMS (10&lt;sup&gt;3&lt;/sup&gt; CFU/ml). The AMS-PCR assay showed high specificity as it detected ten different serovars of &lt;em&gt;Salmonella enterica&lt;/em&gt; with no cross-reactivity with other food-borne pathogens. AMS-PCR reduced the analytical duration from 6 to 7 h instead of 4 days by the culture method.&lt;br&gt;
&lt;strong&gt;Conclusion:&lt;/strong&gt; In comparison with the culture method, AMS helped to improve the upstream sample preparation in reducing the pre-enrichment and enrichment times. So, it seems that combining AMS with PCR is cost-effective and time-saving. In addition, it is highly specific for monitoring of &lt;em&gt;Salmonella&lt;/em&gt; spp. in food chain.&lt;br&gt;
&lt;br&gt;
&lt;br&gt;
&lt;strong&gt;DOI:&lt;/strong&gt; 10.29252/jfqhc.5.3.94&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Salmonella, Aptamers, Nucleotide, Polymerase Chain Reaction, Food Safety </keyword>
	<start_page>94</start_page>
	<end_page>101</end_page>
	<web_url>http://jfqhc.ssu.ac.ir/browse.php?a_code=A-10-637-2&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>A.N. </first_name>
	<middle_name></middle_name>
	<last_name>Zifruddin</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Institute of Biological Sciences, Faculty of Sciences, University of Malaya, 50603 Kuala Lumpur, Malaysia</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>K.L. </first_name>
	<middle_name></middle_name>
	<last_name>Thong</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>thongkl@um.edu.my</email>
	<code></code>
	<orcid></orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Institute of Biological Sciences, Faculty of Sciences, University of Malaya, 50603 Kuala Lumpur, Malaysia</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
