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<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Distribution of virulence associated genes in isolated
Escherichia coli from avian colibacillosis</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1</FirstPage>
			<LastPage>6</LastPage>
			<ELocationID EIdType="pii">32017</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32017</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Khatereh</FirstName>
					<LastName>Kafshdouzan</LastName>
<Affiliation>Department of Microbiology, Faculty of Veterinary Medicine, University of Semnan, Semnan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Taghi</FirstName>
					<LastName>Zahraei Salehi</LastName>
<Affiliation>Department of Microbiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Bahar</FirstName>
					<LastName>Nayeri</LastName>
<Affiliation>Department of Microbiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Omid</FirstName>
					<LastName>Madadgar</LastName>
<Affiliation>Department of Microbiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Shinji</FirstName>
					<LastName>Yamasaki</LastName>
<Affiliation>Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Osaka, Japan</Affiliation>

</Author>
<Author>
					<FirstName>Atsushi</FirstName>
					<LastName>Hinenoya</LastName>
<Affiliation>Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Osaka, Japan</Affiliation>

</Author>
<Author>
					<FirstName>Nouritomo</FirstName>
					<LastName>Yasuda</LastName>
<Affiliation>Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Osaka, Japan</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>03</Month>
					<Day>18</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND: Colibacillosis is one of the most prevalent&lt;br /&gt;diseases in the world that causes multimillion-dollar annual&lt;br /&gt;losses. OBJECTIVES: In order to evaluate molecular epidemiology&lt;br /&gt;of some virulence associated factors in Escherichia coli,&lt;br /&gt;isolated from poultry, the presence of iut A, iss, hly F, omp T, iro&lt;br /&gt;N, afa, sfa (S)and pap G (II) were investigated by multiplex PCR&lt;br /&gt;assay. METHODS: Two hundred thirty four Escherichia coli&lt;br /&gt;isolated from avian colibacillosis (APEC) and fifty four fecal E.&lt;br /&gt;coli isolates from the feces of apparently healthy birds (AFEC)&lt;br /&gt;were investigated for presence of some virulence associated&lt;br /&gt;genes by two panel of multiplex PCR. Statistical analysis was&lt;br /&gt;performed using |c&lt;br /&gt;2 test. the p-value was |£|0.05. RESULTS:&lt;br /&gt;Among 234 E. coli strains associated with colibacillosis and 54&lt;br /&gt;AFEC strains, 85% of isolates were positive for at least one of the&lt;br /&gt;virulence gene. The three most prevalent genes in E. coli isolated&lt;br /&gt;from colibacillosis were hly F (77.3%), omp T(73%) and iss&lt;br /&gt;(68.2%). Iut A, iro Nand pap G (II) were detected in 157 (67.4%),&lt;br /&gt;152 (65.2%) and 41(17.6%) respectively. None of isolates&lt;br /&gt;harbored sfa (s) and afa genes. Several combination patterns of&lt;br /&gt;virulence genes were detected. Combination of hly F, omp T&lt;br /&gt;(70.8%) was the most prevalent pattern. CONCLUSIONS: the&lt;br /&gt;prevalence of iss, hly F, omp T, iro N genes in APEC isolates was&lt;br /&gt;significantly more than AFEC strains and probably these genes&lt;br /&gt;play an important role in the pathogenesis of APEC strains.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Avian pathogenic Escherichia coli</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">multiplex PCR</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">virulent factors</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32017_8437796cc482a67e5069d1e45c2af869.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effects of mesenchymal stem cells with injectable scaffold on
cardiac function in myocardial infarction in Rabbit</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>7</FirstPage>
			<LastPage>13</LastPage>
			<ELocationID EIdType="pii">32018</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32018</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Nazanin</FirstName>
					<LastName>Jafari</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Mahdi</FirstName>
					<LastName>Dehghan</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-8825-9070</Identifier>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Abarkar</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, Islamic Azad University, Karaj Branch, Karaj, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Hejazi</LastName>
<Affiliation>Department of Animal Sciences, Faculty of Agriculture, Islamic Azad University, Khorramabad Branch,
Khorramabad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Pegah</FirstName>
					<LastName>Abbasnia</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Molazem</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Amir</FirstName>
					<LastName>Tavakoli</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Rouh-allah</FirstName>
					<LastName>Mehdinavaz Aghdam</LastName>
<Affiliation>Nanotechnology Department, Engineering Research Institute, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Seyed Hosein</FirstName>
					<LastName>Ahmadi Tafti</LastName>
<Affiliation>Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Parviz</FirstName>
					<LastName>Tajik</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND: Bone marrow-derived mesenchymal cells&lt;br /&gt;can transdifferentiate into Cardiomyocyte cells and improve&lt;br /&gt;heart function after transplantation. Since biomaterials can&lt;br /&gt;improve the cell retention in the site, cell survival and differentiation,&lt;br /&gt;heart tissue engineering is now being explored as an&lt;br /&gt;applied solution to support cell-based therapies and increase&lt;br /&gt;their efficacy for myocardial diseases. Chitosan in combination&lt;br /&gt;with Glycerol Phosphate (GP) can produce a thermo sensitive&lt;br /&gt;material that in body temperature can form a jellylike material.&lt;br /&gt;OBJECTIVES:The aim of this study was to evaluate the effects of&lt;br /&gt;a combination of autologous undifferentiated bone marrow&lt;br /&gt;mesenchymal stem cells (MSCs) and injectable scaffold on cardiac&lt;br /&gt;function improvement in rabbits after inducing myocardial&lt;br /&gt;infarction. METHODS: The Left Anterior Descending (LAD)&lt;br /&gt;coronary artery was ligated by No. 6-0 polyamide suture&lt;br /&gt;material, and autologous MSCs with injectable scaffold were&lt;br /&gt;injected into the margins of the infarcted zone at the time of&lt;br /&gt;surgery. At 4 weeks after transplantation, the cardiac function&lt;br /&gt;and structure was detected using echocardiography. RESULTS:&lt;br /&gt;There was no significant difference among the three groups (MI&lt;br /&gt;only, MI Scaffold, and MI+Scaffold+MSCs) in the Echocardiographic&lt;br /&gt;parameters including, heart rate (HR), Ejection Fraction&lt;br /&gt;(EF), Fractional Shortening (FS), Left Ventricular Diameter&lt;br /&gt;(LVD) and Left Ventricular Parietal Wall Diameter (LVPW).&lt;br /&gt;CONCLUSIONS: A combination of autologous undifferentiated&lt;br /&gt;bone marrow MSCs and injectable scaffold made of Chitosan+&lt;br /&gt;Glycerol Phosphate in echocardiographic evaluation did not&lt;br /&gt;have a positive influence on achieving functional improvement.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Echocardiography</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">mesenchymal
stem cell</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Scaffold</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">ejection fraction</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">fractional shortening</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32018_79e1ddedcc421480fe1cdee3769a13ce.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>The mRNAexpression study on small amount of Theileria
annulata lymph node biopsy sample using SMART-cDNA
technology</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>15</FirstPage>
			<LastPage>22</LastPage>
			<ELocationID EIdType="pii">32019</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32019</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Nastaran</FirstName>
					<LastName>Sadr Shirazi</LastName>
<Affiliation>Department of Parasitology, Faculty of Veterinary Medicine, University of Tehran,Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Parviz</FirstName>
					<LastName>Shayan</LastName>
<Affiliation>Department of Parasitology, Faculty of Veterinary Medicine, University of Tehran,Tehran, Iran; Institute of Molecular Biological System Transfer (MBST), Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Berigiteh</FirstName>
					<LastName>Eckert</LastName>
<Affiliation>Institute of Molecular Biological System Transfer (MBST), Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Elaheh</FirstName>
					<LastName>Ebrahimzadeh</LastName>
<Affiliation>Department of Parasitology, Faculty of Veterinary Medicine, University of Tehran,Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Sedigheh</FirstName>
					<LastName>Jafari</LastName>
<Affiliation>Department of Parasitology, Faculty of Veterinary Medicine, University of Tehran,Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>05</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND: A major issue in many gene expression&lt;br /&gt;studies utilizing small amount of biological materials is the&lt;br /&gt;limited quantity of RNApurified from clinical samples, which is&lt;br /&gt;often used for RT-PCR or standard Northern blot analysis.&lt;br /&gt;OBJECTIVES: The SMART cDNA synthesis method and subsequent&lt;br /&gt;SMART-cDNA-PCR technique was used to analyse 3&lt;br /&gt;genes in macroschizonts of Theileria annulata in small lymph&lt;br /&gt;node biopsy material. METHODS: The SMART-cDNA of TaSp&lt;br /&gt;gene was cloned in pTZ57R/T-vector and sequenced. We focused&lt;br /&gt;on genes encoding surface proteins TaSp, TaD and HSP70.&lt;br /&gt;RESULTS: Our results showed that SMART cDNA dependably&lt;br /&gt;reproduces the expression profile found in messenger RNA. The&lt;br /&gt;RT-SMART-PCR showed the amplification of the processed&lt;br /&gt;mRNAs. The sequencing analysis showed that the amplified&lt;br /&gt;cDNA was coded for TaSp protein in Theileria annulata.&lt;br /&gt;CONCLUSIONS: It was concluded that the SMART PCR&lt;br /&gt;technique is practical for amplification of complete sequence of&lt;br /&gt;mRNAs in the form of cDNAs, and therefore for gene expression&lt;br /&gt;studies if only small amounts of starting material are available.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Theileria annulata</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">SMART-cDNA</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">TaSp</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">TaD</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">HSP70</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32019_3e488d7a07aad80a635656ada23e1571.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Molecular characterization of non-structural gene of H9N2
subtype of avian influenza viruses isolated from broiler
chickens in Iran</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>23</FirstPage>
			<LastPage>34</LastPage>
			<ELocationID EIdType="pii">32020</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32020</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Hesam-aldin</FirstName>
					<LastName>Emadi Chashmi</LastName>
<Affiliation>Department of Poultry Diseases, Faculty of Veterinary Medicine University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mahdi</FirstName>
					<LastName>Vasfi Marandi</LastName>
<Affiliation>Department of Poultry Diseases, Faculty of Veterinary Medicine University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Hasan</FirstName>
					<LastName>Bozorgmehrifard</LastName>
<Affiliation>Department of Poultry Diseases, Faculty of Veterinary Medicine University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohsen</FirstName>
					<LastName>Bashashati</LastName>
<Affiliation>Department of Poultry Diseases, Faculty of Veterinary Medicine University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Abbas</FirstName>
					<LastName>Barin</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine University of Tehran, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>06</Month>
					<Day>05</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND: The H9N2 subtype of avian influenza&lt;br /&gt;viruses (AIVs) have spread in Asia and Middle East countries&lt;br /&gt;and have become a serious threat to poultry industry in Iran.&lt;br /&gt;OBJECTIVES:Characterization of genes of H9N2 subtype involving&lt;br /&gt;in pathogenicity and diagnosis are crucial in control of avian&lt;br /&gt;influenza outbreaks. The Nonstructural (NS) gene and its protein&lt;br /&gt;products (NS1 &amp; NS2) are important as diagnostic marker, life&lt;br /&gt;cycle and pathogenicity of AIVs. METHODS:The NS gene of five&lt;br /&gt;strains, isolated from 1998 to 2010, were completely sequenced&lt;br /&gt;and analyzed. RESULTS:All of the examined strains were composed&lt;br /&gt;of 890 nucleotides with 230 amino acids. In this regard, only&lt;br /&gt;two Iranian strains from GeneBank had 217 amino acids in NS1&lt;br /&gt;protein. All Iranian H9N2 strains subdivided into two distinct&lt;br /&gt;sublineages including I and II. Comparative analysis of NS genes&lt;br /&gt;of Iranian strains showed that since 2003, they might have&lt;br /&gt;originated from Pakistan H7N3 strains; whereas from 2008 they&lt;br /&gt;could be originated from Pakistan H9N2 strains. CONCLUSIONS:&lt;br /&gt;Although the low pathogenic H9N2 subtype has been permanently&lt;br /&gt;circulating from 1998 to the present in Iran, phylogenetic&lt;br /&gt;analysis of NS genes revealed that sublineage II has circulated&lt;br /&gt;more in poultry industry of Iran. These epidemio-logically&lt;br /&gt;variations could be related to vaccination pressure due to&lt;br /&gt;massive vaccination or NS gene reassortment in rural and&lt;br /&gt;backyard chickens.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Avian influenza virus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">H9N2 subtype</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">nonstructural gene</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Poultry</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32020_300b5d47321ba06e9c430a8ef76de3e7.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Characterization of Salmonella isolates from poultry
sources in Iran</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>35</FirstPage>
			<LastPage>41</LastPage>
			<ELocationID EIdType="pii">32021</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32021</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Seyed Mostafa</FirstName>
					<LastName>Peighambari</LastName>
<Affiliation>Department of Avian Diseases, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0000-0001-9166-1303</Identifier>

</Author>
<Author>
					<FirstName>Ramin</FirstName>
					<LastName>Akbarian</LastName>
<Affiliation>Department of Avian Diseases, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Rima</FirstName>
					<LastName>Morshed</LastName>
<Affiliation>Veterinary and Agriculture Group, Ministry of Science, Research, and Technology, Iran Encyclopedia Compiling
Foundation, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Azam</FirstName>
					<LastName>Yazdani</LastName>
<Affiliation>Department of Avian Diseases, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>09</Month>
					<Day>24</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND: Salmonellosis is one of the most important&lt;br /&gt;zoonotic diseases throughout the world. OBJECTIVES: The&lt;br /&gt;purpose of this study was to characterize a large collection of&lt;br /&gt;Salmonella isolates from different poultry sources in Iran.&lt;br /&gt;METHODS: A total of 123 Salmonella isolates from different&lt;br /&gt;poultry sources were subjected to drug susceptibility test,&lt;br /&gt;hemolysin production, motility test, and plasmid profile (50&lt;br /&gt;isolates). RESULTS: Seventy-one resistance patterns were found&lt;br /&gt;to 29 antimicrobial agents among 123 Salmonella isolates, in&lt;br /&gt;which 81% of isolates were resistant to more than one&lt;br /&gt;antibacterial agent. The resistance patterns of 123 isolates to 10&lt;br /&gt;commonly used antibacterials in Iranian poultry industry were&lt;br /&gt;also quite variable and included 31 patterns. Four different&lt;br /&gt;plasmid patterns were found among 50 Salmonellaisolates. Fifty&lt;br /&gt;four percent of Salmonella isolates harbored one or three&lt;br /&gt;plasmids with approximate molecular size ranging from 2.3 to&lt;br /&gt;68 kb. No plasmid was detected in 46% of isolates. Aband of 68&lt;br /&gt;kb size was detected in all isolates that harbored plasmid. All&lt;br /&gt;isolates were motile but no isolate showed hemolysin&lt;br /&gt;production. CONCLUSIONS: The frequency of resistance to&lt;br /&gt;antibacterial agents among avian Salmonella isolates is a major&lt;br /&gt;public health concern.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Salmonella</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">drug susceptibility</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">plasmid profile</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Poultry</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32021_1c61cc2f7276f0b6dadc33d7e3a4f269.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Seroepidemiology and molecular detection of Brucella infection
in Iranian horses: Aprovincial study</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>43</FirstPage>
			<LastPage>49</LastPage>
			<ELocationID EIdType="pii">32022</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32022</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Khalil</FirstName>
					<LastName>Badiei</LastName>
<Affiliation>Department of Clinical Studies, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hasan</FirstName>
					<LastName>Sharifiyazdi</LastName>
<Affiliation>Department of Clinical Studies, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mehrdad</FirstName>
					<LastName>Pourjafar</LastName>
<Affiliation>Department of Clinical Studies, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohsen</FirstName>
					<LastName>Ghane</LastName>
<Affiliation>Department of Clinical Studies, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Seyyed Adol-Nabi</FirstName>
					<LastName>Hashemi</LastName>
<Affiliation>Department of Clinical Studies, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>22</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND: Brucellosis is a febrile zoonotic infection&lt;br /&gt;and has worldwide distribution among humans as well as&lt;br /&gt;animals. Although the seroprevalence of brucellosis in various&lt;br /&gt;animals has been described in Iran, there is only one report on&lt;br /&gt;equine brucellosis in the region. OBJECTIVES: This study was&lt;br /&gt;carried out to determine the seroprevalence of brucellosis in&lt;br /&gt;racing clubs and private horse owners in the south of Iran and risk&lt;br /&gt;factors associated with the disease in horses. METHODS: 312&lt;br /&gt;randomly selected equine serum samples were investigated for&lt;br /&gt;the presence of antibodies against Brucella genus, using slide&lt;br /&gt;agglutination by Rose Bengal plate test (RBPT), serum agglutination&lt;br /&gt;test (SAT) and 2-mercaptoethanol (2-ME) test, using&lt;br /&gt;whole cell antigen. PCR assay was also used for detection of&lt;br /&gt;clinically suspected cases. RESULTS: Most seropositive horses&lt;br /&gt;in this study were asymptomatic. The true seroprevalence of&lt;br /&gt;brucellosis was found to be 9.9, 8 and 7% by RBPT, SAT and 2-&lt;br /&gt;mercaptoethanol tests, respectively. All horses with history of&lt;br /&gt;clinical signs (3.2% of all samples) had RBPT, SAT and 2-&lt;br /&gt;mercaptoethanol positive results. It was also revealed that age,&lt;br /&gt;sex and a history of contact with ruminants had no effect on&lt;br /&gt;acquiring the infection in positive cases. In the PCR, one of the&lt;br /&gt;three horses with fistula withers produced amplicon of 450 bp&lt;br /&gt;fragment of wbo sequences specific to Brucella spp. field strain.&lt;br /&gt;CONCLUSIONS: This study showed the seroprevalence of&lt;br /&gt;brucellosis in horses of Fars province and it was indicated that&lt;br /&gt;the PCR assay may be helpful in detection of clinically suspected&lt;br /&gt;horses.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Horse</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Brucella infection</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">PCR</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32022_94ce46da136eceef48aa41cbb54a299e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>An outbreak of abortion in Afshari sheep with probable
involvement of Campylobacter fetus</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>51</FirstPage>
			<LastPage>56</LastPage>
			<ELocationID EIdType="pii">32023</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32023</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Masoumeh</FirstName>
					<LastName>Saleh</LastName>
<Affiliation>Department of Animal Sciences, Faculty of Agriculture, University of Zanjan, Zanjan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Taher</FirstName>
					<LastName>Harkinezhad</LastName>
<Affiliation>Department of Animal Sciences, Faculty of Agriculture, University of Zanjan, Zanjan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Marefat</LastName>
<Affiliation>Department of Plant Protection, Faculty of Agriculture, University of Zanjan, Zanjan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Vahid</FirstName>
					<LastName>Salmani</LastName>
<Affiliation>Department of Animal Sciences, Faculty of Agriculture, University of Zanjan, Zanjan, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>09</Month>
					<Day>26</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND:Abortion is one of the most important factors&lt;br /&gt;reducing lambing rate and consequently profitability of sheep&lt;br /&gt;farms. In addition to financial losses, it is also important from a&lt;br /&gt;zoonotic point of view. OBJECTIVES: The aim of this study was&lt;br /&gt;to investigate bacterial abortifacient agents in an outbreak of&lt;br /&gt;abortion occurring in Afshari sheep in the northwest of Zanjan&lt;br /&gt;province. METHODS:Vaginal swab samples were collected from&lt;br /&gt;217 Afshari ewes (129 samples were taken from aborted ewes, 3&lt;br /&gt;samples from ewes with crippled and deformed lambs, and 85&lt;br /&gt;samples from animals that had given birth to healthy lambs) from&lt;br /&gt;reported flocks involved in outbreak. Swabs were examined by&lt;br /&gt;PCR assay to detect DNAfrom Coxiella burnetii, Chlamydophila&lt;br /&gt;abortus, Salmonella enterica, Yersinia enterocolitica, Campylobacter&lt;br /&gt;fetus, Brucella ovis and Leptospira interrogans. RESULTS:&lt;br /&gt;Based on the results, only DNA of Campylobacter was detected&lt;br /&gt;in the samples. A 266 bp fragment specific for Campylobacter&lt;br /&gt;was amplified from 51.52% and 34.12% samples belonging to&lt;br /&gt;aborted and non-aborted ewes, respectively. CONCLUSIONS:&lt;br /&gt;Significant presence of the bacterium in aborted ewes (p&lt;0.001)&lt;br /&gt;compared to the non-aborted groups with odd ratio of 3,&lt;br /&gt;emphasizes that Campylobacter could be involved in the&lt;br /&gt;outbreak of the abortion. Considering the importance of the&lt;br /&gt;disease, prophylactic measures are needed to reduce the disease.&lt;br /&gt;However, further investigations are required to determine the&lt;br /&gt;impact of this bacterium in prevalence of abortion in sheep in&lt;br /&gt;other areas.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">PCR</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Campylobacter</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">abortion</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">afshari ewes</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32023_fb8844e18687f293377ccc49056ff4c5.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Comparison of immunochromatographic rapid test with
molecular method in diagnosis of canine parvovirus</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>57</FirstPage>
			<LastPage>61</LastPage>
			<ELocationID EIdType="pii">32024</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32024</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Shahab-aldin</FirstName>
					<LastName>Mohyedini</LastName>
<Affiliation>Department of Internal Medicine, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Shahram</FirstName>
					<LastName>Jamshidi</LastName>
<Affiliation>Department of Internal Medicine, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Sima</FirstName>
					<LastName>Rafati</LastName>
<Affiliation>Molecullar Immunology and Vaccine Research Laboratory, Pasteur Institute of Iran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Gholam Reza</FirstName>
					<LastName>Nikbakht Boroujeni</LastName>
<Affiliation>Department of Microbiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Abdolali</FirstName>
					<LastName>Malmasi</LastName>
<Affiliation>Department of Internal Medicine, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Yasaman</FirstName>
					<LastName>Taslimi</LastName>
<Affiliation>Molecullar Immunology and Vaccine Research Laboratory, Pasteur Institute of Iran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hesam-aldin</FirstName>
					<LastName>Akbarein</LastName>
<Affiliation>Department of Food Hygiene and Quality Control, Faculty of Veterinary Medicine, University of Tehran,
Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>09</Month>
					<Day>05</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND: Canine parvovirus (CPV) infection is one of&lt;br /&gt;the most common causes of infectious gastroenteritis in dogs and&lt;br /&gt;is a highly contagious, often fatal disease. The original virus&lt;br /&gt;(CPV type 2) has had some mutations since its emergence and&lt;br /&gt;new variants (CPV-2a, 2b and 2c) have been reported from many&lt;br /&gt;countries all around the world. Early diagnosis and treatment can&lt;br /&gt;profoundly affect the disease outcome. OBJECTIVES:To compare&lt;br /&gt;the ability of Immunochromatographic (IC) test to detect CPV&lt;br /&gt;infection in 50 PCR positive samples (n=50) with regard to virus&lt;br /&gt;strains. METHODS: 50 rectal swabs (n=50) were prepared from&lt;br /&gt;suspicious dogs and subjected to PCR and IC test respectively.&lt;br /&gt;RESULTS: The sensitivity of IC test in PCR positive samples was&lt;br /&gt;84% (42 out of 50 samples) and the positive predictive value of&lt;br /&gt;the test was 100%. Using PCR, CPV strains in our study were 2a&lt;br /&gt;(18/50, 36%) and 2b (32/50, 64%) with the predominance of 2b&lt;br /&gt;strain. IC test was also able to diagnose 15/18 (83.3%) of CPV-&lt;br /&gt;2a and 27/32 (84.3%) CPV-2b strain positive samples, which&lt;br /&gt;means IC test can detect CPV infections caused by both virus&lt;br /&gt;strains (2a and 2b), without significant difference. CONCLUSIONS:&lt;br /&gt;This study shows that IC test results are relatively reliable for&lt;br /&gt;diagnosing CPVinfection in daily veterinary practice and the test&lt;br /&gt;is able to diagnose both CPV-2a and CPV-2b which are prevalent&lt;br /&gt;strains in Iran.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">canine parvovirus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">detection methods</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">PCR</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">immunochromatography</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32024_674aafe016c520e2e20d036ec268ac53.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Histological study of cartilaginous cells in the body of penis in
one-humped camel (camelus dromedarius)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>63</FirstPage>
			<LastPage>67</LastPage>
			<ELocationID EIdType="pii">32025</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32025</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mohammad Hasan</FirstName>
					<LastName>Yousefi</LastName>
<Affiliation>Department of Basic Sciences, Faculty of Veterinary Medicine, Semnan University, Semnan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Hasan</FirstName>
					<LastName>Gilanpour</LastName>
<Affiliation>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad Reza</FirstName>
					<LastName>Salimi-Bejestani</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Semnan University, Semnan, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>09</Month>
					<Day>10</Day>
				</PubDate>
			</History>
		<Abstract>BACKGROUND:Several investigations showed cartilaginous&lt;br /&gt;cells in fibrous tissue of the free part of the penis in one humped&lt;br /&gt;camel. OBJECTIVES: The aim of this study was accurate assessment&lt;br /&gt;of existence of cartilaginous cells in penis shaft of onehumped&lt;br /&gt;camel. METHODS: Six camel penises from matured&lt;br /&gt;camels more than 3 years-old were collected from an abattoir.&lt;br /&gt;Different specimens were prepared from each penis and kept in&lt;br /&gt;10% formalin container for fixation. After passing different&lt;br /&gt;stages of histotechnique methods, several slides were prepared&lt;br /&gt;from each specimen, stained with Haematoxylin Eosin and&lt;br /&gt;studied. RESULTS: Results showed that the majority of cartilaginous&lt;br /&gt;cells were inside the collagen fibers of tunica albuginea and&lt;br /&gt;around corpus cavernosum and corpus spongiosum of penis and&lt;br /&gt;their distributions were dissimilar in different parts of the penis&lt;br /&gt;shaft. This survey further showed that in penis shaft length, the&lt;br /&gt;majority of cartilaginous cells were inside tunica albuginea,&lt;br /&gt;which is surrounded by corpus spongiosum and particularly, the&lt;br /&gt;ventral surface of urethra. CONCLUSIONS: The number of&lt;br /&gt;cartilaginous cells decreased gradually from distal extremity&lt;br /&gt;towards the proximal extremity of the body of the penis and&lt;br /&gt;increased gradually from external layer of tunica albuginea&lt;br /&gt;towards the internal layer of tunica albuginea and centre of&lt;br /&gt;corpus cavernosum penis. Existence of cartilaginous cells inside&lt;br /&gt;the leaf tissue of the penis was seen with aging and puberty.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Camel</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Histology</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">penis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cartilage</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32025_31835449d44e4a1765f47b52436a628e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Medicine</JournalTitle>
				<Issn>2251-8894</Issn>
				<Volume>7</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Probable occurrence of black leg in a sucker dairy calf: the
necessity of providing sufficient maternal antibody in endemic
regions</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>69</FirstPage>
			<LastPage>72</LastPage>
			<ELocationID EIdType="pii">32026</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijvm.2013.32026</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Javad</FirstName>
					<LastName>Tajik</LastName>
<Affiliation>Department of Clinical Sciences, School of Veterinary Medicine, Shahid Bahonar University of Kerman,
Kerman, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Aziz Allah</FirstName>
					<LastName>Khodakaram Tafti</LastName>
<Affiliation>Department of Patobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Abdollah</FirstName>
					<LastName>Derakhshandeh</LastName>
<Affiliation>Department of Patobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Tahmineh</FirstName>
					<LastName>Tajik</LastName>
<Affiliation>Department of Patobiology, School of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>07</Month>
					<Day>24</Day>
				</PubDate>
			</History>
		<Abstract>Black leg has been reported in a variety of animals, but is of&lt;br /&gt;the most importance in cattle and sheep. A20 days old Holstein&lt;br /&gt;dairy calf was examined because of anorexia and lameness from&lt;br /&gt;2 days ago. The calf was depressed, tachypneic, tachycardic, and&lt;br /&gt;had a body temperature of 38.5ºC. Both hind limbs proximal to&lt;br /&gt;the tarsal joint were markedly swollen, firm and painful. No&lt;br /&gt;crepitation was noted on palpation. The calf had bruxism, stiffness&lt;br /&gt;of gait and unwillingness to move. At necropsy, massive&lt;br /&gt;necrosis of thigh muscles which caused dark discolorated tissue&lt;br /&gt;with metallic sheen, large amount of thin sanguineous exuda and&lt;br /&gt;abundant gas bubbles were evident in the underlying tissues.&lt;br /&gt;Histopathologic examination revealed extensive degeneration&lt;br /&gt;and coagulative necrosis of muscle fibers and supported a&lt;br /&gt;diagnosis of black leg. No vaccination against Clostridium&lt;br /&gt;chauvoei was applied in the herd and the calf did not receive&lt;br /&gt;notable maternal antibody. Providing sufficient maternal&lt;br /&gt;antibody or early vaccination of the susceptible newborn calves&lt;br /&gt;should be considered in the endemic regions.</Abstract>
			<OtherAbstract Language="FA"></OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">black leg</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">sucker calf</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Dairy</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">maternal antibody</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">endemic regions</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvm.ut.ac.ir/article_32026_18bab4326d2417c4f9e602a06f007552.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
