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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>Tarbiat Modares University</PublisherName>
				<JournalTitle>Infection Epidemiology and Microbiology</JournalTitle>
				<Issn>2588-4107</Issn>
				<Volume>2</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2016</Year>
					<Month>01</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Evaluation of two different laboratory methods for the identification of Aeromonas spp. in stool sample of patients with diarrhea</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>18</FirstPage>
			<LastPage>21</LastPage>
			<ELocationID EIdType="pii">1693</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mina</FirstName>
					<LastName>Boustanshenas</LastName>
<Affiliation>Antimicrobial Resistance Research Center, Rasul-e-Akram Hospital, Iran University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Majid</FirstName>
					<LastName>Akbari</LastName>
<Affiliation>Department of Microbiology, School of Nursing and midwifery, Arak University of Medical Sciences, Arak, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Niloofar</FirstName>
					<LastName>Rezaie</LastName>
<Affiliation>Department of Bacteriology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Background: &lt;em&gt; Aeromonas&lt;/em&gt; spp. can cause diarrhea and various infections in humans. Access to rapid techniques with a high sensitivity and specificity is strongly needed for the identification of &lt;em&gt;Aeromonas&lt;/em&gt; species. The aim of this study was to evaluate two different methods including API 20E bacterial identification tests and the molecular detection using PCR primers specific for 16s-rRNA and 23S-rRNA genes sequences for identification of &lt;em&gt;Aeromonas&lt;/em&gt; spp. in stool samples from patients with diarrhea. Materials and Methods: One hundred stool samples from diarrheal patients were collected. All isolates were subjected toAPI 20 E strip tests and PCR using specific primers for identification of &lt;em&gt;Aeromonas&lt;/em&gt; spp. Results: The API 20E analysis identified 2 (2.2%) isolates as &lt;em&gt;Aeromonas&lt;/em&gt; spp. Molecular identification by aero-23S-rRNA gene confirmed the same 2 isolates as identified by the API 20E strips. Conclusion: Both API 20E system and PCR method using Aero 23S-rRNA primer were found to be accurate in identification of &lt;em&gt;Aeromona&lt;/em&gt;s spp. isolates with highconfidence.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">API bacterial identification</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Aeromonas spp</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">PCR</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://iem.modares.ac.ir/article_1693_b59a51a3c0bf9c5228fde841714f523a.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
