<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>International Biological and Biomedical Journal</title>
<title_fa></title_fa>
<short_title>IBBJ</short_title>
<subject>Medical Sciences</subject>
<web_url>http://ibbj.org</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2423-4478</journal_id_issn>
<journal_id_issn_online></journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>7</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>2423</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1400</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2021</year>
	<month>4</month>
	<day>1</day>
</pubdate>
<volume>7</volume>
<number>1</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>Evaluation of Microscopy Sensitivity, Specificity in Detection of P. falciparum and P. vivax, Using Monoplex real-time PCR, Gezira, Sudan</title>
	<subject_fa>Infectious Disease</subject_fa>
	<subject>Infectious Disease</subject>
	<content_type_fa>Original Article</content_type_fa>
	<content_type>Original Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;strong&gt;Background:&lt;/strong&gt; Malaria is still account for 200 million cases annually. Microscopy is the gold standard technique for malaria parasites detection. PCR-based techniques can detect malaria infections with high sensitivity. The study aimed to evaluate the sensitivity of microscopy technique in the detection of &lt;em&gt;P. falciparum &lt;/em&gt;and&lt;em&gt; P. vivax&lt;/em&gt;, using monoplex real-time PCR&lt;em&gt;,&lt;/em&gt; Gezira State, Central Sudan.&lt;br&gt;
&lt;strong&gt;Methods: &lt;/strong&gt;Microscopic examination for the presence of malaria parasite was performed for 200 Giemsa blood smears. QIAamp DNA Mini Kit Qiagen, Germany, was used for parasite&amp;#39;s genomic DNA. Monoplex Real-time PCR was used for the identification and detection of &lt;em&gt;P. falciparum &lt;/em&gt;and&lt;em&gt; P. vivax &lt;/em&gt;malaria.&lt;br&gt;
&lt;strong&gt;Results: &lt;/strong&gt;71% of samples were positive for &lt;em&gt;P. falciparum&lt;/em&gt; by both microscopy and the &lt;em&gt;P. falciparum&lt;/em&gt; species-specific real-time PCR and 15% were negative by both. Out of the 40 negative samples by microscopy, 5% were found positive for &lt;em&gt;P. falciparum&lt;/em&gt; by &lt;em&gt;P. falciparum&lt;/em&gt; species-specific real-time PCR and 2.5% were positive for &lt;em&gt;P. vivax&lt;/em&gt; by &lt;em&gt;P. vivax&lt;/em&gt; species-specific real-time PCR. 18 samples that were found positive by microscopy for &lt;em&gt;P. falciparum&lt;/em&gt; were found negative by real-time PCR&lt;em&gt;, &lt;/em&gt;and were positive for&lt;em&gt; P. vivax &lt;/em&gt;by&lt;em&gt; P. vivax&lt;/em&gt; species-specific real-time PCR.&lt;br&gt;
&lt;strong&gt;Conclusions&lt;/strong&gt; There is concordance rate of 86% between microscopy and the species-specific real-time PCR. In malaria endemic areas, adoption of high quality control procedures for microscopy, as gold standard in accurate diagnosis and species differentiation, with well trained staff following WHO criteria is needed</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Real-time PCR, P. falciparum, P. vivax, malaria species differentiation, Central Sudan</keyword>
	<start_page>0</start_page>
	<end_page>0</end_page>
	<web_url>http://ibbj.org/browse.php?a_code=A-10-370-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Moahmed</first_name>
	<middle_name></middle_name>
	<last_name>Babiker</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>myab624@yahoo.co.uk</email>
	<code>10031947532846003965</code>
	<orcid>10031947532846003965</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Wad Medani College of Medical Sciences and Technology Gezira-Sudan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Bakri</first_name>
	<middle_name></middle_name>
	<last_name>Nour</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>bakrinour@hotmail.com</email>
	<code>10031947532846003966</code>
	<orcid>10031947532846003966</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Blue Nile National Institute for Communicable Diseases, University of Gezira, Sudan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Osman</first_name>
	<middle_name></middle_name>
	<last_name>Saeed</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>saeedosman82@yahoo.com</email>
	<code>10031947532846003967</code>
	<orcid>10031947532846003967</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Wad Medani College of Medical Sciences and Technology Gezira-Sudan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Adam</first_name>
	<middle_name></middle_name>
	<last_name>Abakar</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>adamd@uofg.edu.sd</email>
	<code>10031947532846003968</code>
	<orcid>10031947532846003968</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Faculty of Medical Laboratory Sciences University of Gezira, Sudan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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