<?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>12</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<volume>23</volume>
<number>2</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>Comparison of OmpA Gene-Targeted Real-Time PCR 
with the Conventional Culture Method for Detection of 
Acinetobacter baumanii in Pneumonic BALB/c Mice</title>
	<subject_fa> Related Fields</subject_fa>
	<subject>Related Fields</subject>
	<content_type_fa>مقاله کوتاه</content_type_fa>
	<content_type>Short Communication</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Acinetobacter baumannii &lt;/em&gt;is an important pathogen in health care and is responsible for severe nosocomial and community-acquired pneumonia. To design novel therapeutic agents, a mouse model for &lt;em&gt;A. baumannii &lt;/em&gt;pneumonia is essential. &lt;strong&gt;Methods:&lt;/strong&gt; We described a mouse model of &lt;em&gt;A. baumannii &lt;/em&gt;using clinical and 19606R standard strains for developing a quantitative real-time PCR (qRT-PCR) for rapid identification of &lt;em&gt;A. baumannii&lt;/em&gt; infection from lung tissues of BALB/c mice. &lt;strong&gt;Results:&lt;/strong&gt; To infect the mice, three doses of bacteria (0.5 &amp;times; 10&lt;sup&gt;8&lt;/sup&gt;, 1 &amp;times; 10&lt;sup&gt;8&lt;/sup&gt;, and 1.5 &amp;times; 10&lt;sup&gt;8&lt;/sup&gt; cfu/ml) were used. Lung tissues were cultured and compared with &lt;em&gt;ompA &lt;/em&gt;gene. Clinical isolates had better positive results at day three with the highest dose than 19606 strain either in culture (4 versus 3) or in qRT-PCR (5 versus 4). However, qRT-PCR detection was 100%, the specificity was 70%, and the positive predictive value was 27%. &lt;strong&gt;Conclusion:&lt;/strong&gt; The qRT-PCR detection of &lt;em&gt;A. baumannii &lt;/em&gt;in the BALB/c mice model has a higher sensitivity than the culture method.&amp;nbsp;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Acinetobacter baumanii, OmpA, qRT-PCR Pneumonia, BALB/c mice</keyword>
	<start_page>159</start_page>
	<end_page>164</end_page>
	<web_url>http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-1-770&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Niloofar </first_name>
	<middle_name></middle_name>
	<last_name>Hassannejad</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>0000-0002-7930-807X</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Cell Biology, Science and Research branch, Islamic Azad University, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Abbas</first_name>
	<middle_name></middle_name>
	<last_name>Bahador</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>0000-0001-5308-7208</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Microbiology, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Nasim</first_name>
	<middle_name></middle_name>
	<last_name>Hayati Rudbari</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>0000-0002-5942-5770</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Cell Biology, Science and Research branch, Islamic Azad University, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mohammad Hossein</first_name>
	<middle_name></middle_name>
	<last_name>Modarressi</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>0000-0002-8203-5674</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Medical Genetics, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Kazem </first_name>
	<middle_name></middle_name>
	<last_name>Parivar</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>0000-0002-7235-2852</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Dept. of Cell Biology, Science and Research branch, Islamic Azad University, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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