<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran Press</PublisherName>
				<JournalTitle>Journal of Veterinary Research</JournalTitle>
				<Issn>2008-2525</Issn>
				<Volume>76</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2021</Year>
					<Month>03</Month>
					<Day>21</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Molecular Discrimination of Different Types of Trypanosoma Evansi in One-Humped Camels (Camelus dromedarius) in Sistan-va-Baluchestan Province, Iran</ArticleTitle>
<VernacularTitle>Molecular Discrimination of Different Types of Trypanosoma Evansi in One-Humped Camels (Camelus dromedarius) in Sistan-va-Baluchestan Province, Iran</VernacularTitle>
			<FirstPage>8</FirstPage>
			<LastPage>13</LastPage>
			<ELocationID EIdType="pii">81630</ELocationID>
			
<ELocationID EIdType="doi">10.22059/jvr.2020.275071.2901</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Fereshte</FirstName>
					<LastName>Mirshekar</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Yakhchali</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Fariborz</FirstName>
					<LastName>Shariati-Sharifi</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Parasitology Division, ZabolUniversity, Zabol, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2020</Year>
					<Month>08</Month>
					<Day>31</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND: Trypanosomosis is a blood parasitic disease with veterinary and cosmopolitan importance due to &lt;em&gt;Trypanosoma evansi &lt;/em&gt;(Kinetoplastida: Trypanosomatidae) type A in camels, cattle, buffaloes, and equine and type B in camels. &lt;br /&gt;OBJECTIVES: We conducted the present study to discriminate &lt;em&gt;Trypanosoma evansi&lt;/em&gt; type A and B infection in one-humped camels (&lt;em&gt;Camelus dromedarius&lt;/em&gt;) in Sistan-va-Baluchestan Province, south eastern Iran. &lt;br /&gt;METHODS: A total number of 369 blood samples were randomly taken from jugular &lt;em&gt;vein&lt;/em&gt; of the examined one-humped camels from different parts of the region. Genomic DNA was extracted and polymerase chain reaction (PCR) was performed to amplify 205bp-fragment-length and 436bp-fragment-length of RoTat 1.2 VSG gene (&lt;em&gt;T. evansi&lt;/em&gt; type A) and Minicircle gene (&lt;em&gt;T. evansi&lt;/em&gt; type B), respectively. &lt;br /&gt;RESULTS: Molecular findings revealed that all the infected camels were affected by &lt;em&gt;T. evansi&lt;/em&gt; type A. &lt;br /&gt;CONCLUSIONS: Based on the results of the current study, we could conclude that the cause of infection in the examined camels of the region, like other parts of the world, was &lt;em&gt;T. evansi&lt;/em&gt; type A.</Abstract>
			<OtherAbstract Language="FA">BACKGROUND: Trypanosomosis is a blood parasitic disease with veterinary and cosmopolitan importance due to &lt;em&gt;Trypanosoma evansi &lt;/em&gt;(Kinetoplastida: Trypanosomatidae) type A in camels, cattle, buffaloes, and equine and type B in camels. &lt;br /&gt;OBJECTIVES: We conducted the present study to discriminate &lt;em&gt;Trypanosoma evansi&lt;/em&gt; type A and B infection in one-humped camels (&lt;em&gt;Camelus dromedarius&lt;/em&gt;) in Sistan-va-Baluchestan Province, south eastern Iran. &lt;br /&gt;METHODS: A total number of 369 blood samples were randomly taken from jugular &lt;em&gt;vein&lt;/em&gt; of the examined one-humped camels from different parts of the region. Genomic DNA was extracted and polymerase chain reaction (PCR) was performed to amplify 205bp-fragment-length and 436bp-fragment-length of RoTat 1.2 VSG gene (&lt;em&gt;T. evansi&lt;/em&gt; type A) and Minicircle gene (&lt;em&gt;T. evansi&lt;/em&gt; type B), respectively. &lt;br /&gt;RESULTS: Molecular findings revealed that all the infected camels were affected by &lt;em&gt;T. evansi&lt;/em&gt; type A. &lt;br /&gt;CONCLUSIONS: Based on the results of the current study, we could conclude that the cause of infection in the examined camels of the region, like other parts of the world, was &lt;em&gt;T. evansi&lt;/em&gt; type A.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Prevalence</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Trypanosoma evansi type A</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Camel</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Camelus dromedarius</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">PCR</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://jvr.ut.ac.ir/article_81630_a986eebac261692bad69d7a74a87e43c.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
