<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Biomedical Journal</title>
<title_fa>مجله بیومدیکال ایران</title_fa>
<short_title>IBJ</short_title>
<subject>Basic Sciences</subject>
<web_url>http://ibj.pasteur.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>1028-852X</journal_id_issn>
<journal_id_issn_online>2008-823X</journal_id_issn_online>
<journal_id_pii>-</journal_id_pii>
<journal_id_doi>10.61882/ibj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>-</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>-</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1397</year>
	<month>2</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2018</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<volume>22</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>Development of a DNA Aptamer for Screening Neisseria meningitidis Serogroup B by Cell SELEX</title>
	<subject_fa> Related Fields</subject_fa>
	<subject>Related Fields</subject>
	<content_type_fa>مقاله کامل</content_type_fa>
	<content_type>Full Length/Original Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;strong&gt;Background:&lt;/strong&gt; Artificial oligonucleotides like DNA or RNA aptamers can be used as biodiagnostic alternatives for antibodies to detect pathogens. Comparing to antibodies, artificial oligonucleotides are produced easily at lower costs and are more stable. &lt;em&gt;Neisseria meningitidis&lt;/em&gt;, the causative agent of meningitis, is responsible for about 1% of infections in an epidemic period. Specific DNA aptamers that bind to &lt;em&gt;N. meningitidis&lt;/em&gt; serogroup B were identified by whole-cell Systemic Evolution of Ligands by EXponential Enrichment (SELEX). &lt;strong&gt;Methods:&lt;/strong&gt; The SELEX begins with a library of labeled ssDNA molecules. After six rounds of selection and two rounds of counter-selection, 60 clones were obtained, of which the binding efficiency of 21 aptamers to the aforementioned bacterium was tested by flow cytometry. &lt;strong&gt;Results:&lt;/strong&gt; The aptamers K3 and K4 showed the highest affinity to &lt;em&gt;N. meningitidis&lt;/em&gt; serogroup B and no affinity to &lt;em&gt;N. meningitidis&lt;/em&gt; serogroups Y, A, and C, or to other meningitis causing bacteria. The dissociation constant (K&lt;sub&gt;d&lt;/sub&gt; value) for K3 and K4 were calculated as 28.3 &amp;plusmn; 8.9 pM and 39.1 &amp;plusmn; 8.6 pM, respectively. K3 aptamer with the lowest K&lt;sub&gt;d&lt;/sub&gt; was chosen as the main aptamer. K3 could detect &lt;em&gt;N. meningitidis&lt;/em&gt; in patients&amp;rsquo; cerebrospinal fluid (CSF) samples and in CSF from healthy volunteers inoculated with &lt;em&gt;N. meningitidis&lt;/em&gt; serogroup B (ATCC 13090)&amp;nbsp;at 200 and 100 CFU ml&lt;sup&gt;-1&lt;/sup&gt;, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; The findings suggest the application of the developed&amp;nbsp;aptamer in specific detection of &lt;em&gt;N. meningitidis&lt;/em&gt; serogroup B amongst a group of meningitis causing bacteria.&amp;nbsp;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Aptamer, Flow cytometry, Neisseria meningitidis, Serogroup</keyword>
	<start_page>193</start_page>
	<end_page>201</end_page>
	<web_url>http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-1-692&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Kimia</first_name>
	<middle_name></middle_name>
	<last_name>Mirzakhani</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>Yes
</coreauthor>
	<affiliation>Faculty of Medicine, Institute of Human Genetics, Friedrich-Schiller University, Jena, Germany</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Seyed Latif</first_name>
	<middle_name></middle_name>
	<last_name>Mousavi Gargari</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>Department of Biology, Shahed University, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Iraj</first_name>
	<middle_name></middle_name>
	<last_name>Rasooli</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>Department of Biology, Shahed University, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Samaneh</first_name>
	<middle_name></middle_name>
	<last_name>Rasoulinejad</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>Max Planck Institute for Polymer Research, Mainz, Germany</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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