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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>Shahid Bahonar University of Kerman and Iranian Biotechnology Society</PublisherName>
				<JournalTitle>Agricultural Biotechnology Journal</JournalTitle>
				<Issn>2228-6705</Issn>
				<Volume>15</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2023</Year>
					<Month>03</Month>
					<Day>21</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Investigation of Genetic Diversity in Fusarium of Elegans and Martiella-Ventricosum Sections related to Cucurbits using ISSR markers in Tehran province</ArticleTitle>
<VernacularTitle>Investigation of Genetic Diversity in Fusarium of Elegans and Martiella-Ventricosum Sections related to Cucurbits using ISSR markers in Tehran province</VernacularTitle>
			<FirstPage>125</FirstPage>
			<LastPage>144</LastPage>
			<ELocationID EIdType="pii">3704</ELocationID>
			
<ELocationID EIdType="doi">10.22103/jab.2023.19915.1418</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Forood Ali</FirstName>
					<LastName>Khazaee</LastName>
<Affiliation>Ph.D. Student, Department of Plant Protection, Faculty of Agriculture and Natural Resources, Lorestan University, Khorramabad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Mostafa</FirstName>
					<LastName>Darvishnia</LastName>
<Affiliation>Department of Plant Protection. Faculty of Agriculture, Lorestan University, Khorramabad , Iran</Affiliation>

</Author>
<Author>
					<FirstName>Eidi</FirstName>
					<LastName>Bazgir</LastName>
<Affiliation>Department of Plant Protection, Faculty of Agriculture, Lorestan University, Khorramabad , Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2022</Year>
					<Month>12</Month>
					<Day>11</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;Objective&lt;/strong&gt;
This research aimed to identify &lt;em&gt;Fusariums&lt;/em&gt; belonging to Elegans and &lt;em&gt;Martiella&lt;/em&gt;-&lt;em&gt;Ventricosum&lt;/em&gt; sections related to cucurbit plants in Tehran province and to evaluate the ability of ISSR markers to investigate the kinship relationships of these groups of &lt;em&gt;Fusariums&lt;/em&gt;.
 
&lt;strong&gt;Materials and methods&lt;/strong&gt;
In this research, five ISSR primers (AG)&lt;sub&gt;8&lt;/sub&gt;C, (AG)&lt;sub&gt;8&lt;/sub&gt;G, (AC)&lt;sub&gt;8&lt;/sub&gt;YA, (ATG)&lt;sub&gt;6&lt;/sub&gt; and BHB(GA)&lt;sub&gt;7&lt;/sub&gt; were selected. Fungal isolates identified based on morphological and microscopic characteristics. For ISSR markers, the statistics of polymorphism information content (PIC), Marker Index (MI) and Effective Multiplex Ratio (EMR) were calculated. Relationships and similarity between &lt;em&gt;Fusarium&lt;/em&gt; isolates were analyzed using NTSYS-PC V2.02.
 
&lt;strong&gt;Results&lt;/strong&gt;
Out of 96 &lt;em&gt;Fusarium&lt;/em&gt; isolates, 48 isolates were identified as &lt;em&gt;Fusarium solani&lt;/em&gt;, 25 isolates as &lt;em&gt;Fusarium oxysporum&lt;/em&gt; and 23 isolates as &lt;em&gt;Fusarium redolens&lt;/em&gt;. A total of 408 bands were obtained from ISSR amplifications. 130 different bands were produced, of which 83 were polymorphic and 47 were monomorphic. The size of PCR fragments produced varied from 273 to 2428 bp. The polymorphism percentage, ranged from the highest (73%) for (ATG)&lt;sub&gt;6&lt;/sub&gt; to the lowest (56%) for (AG)&lt;sub&gt;8&lt;/sub&gt;C. Primers (ATG)&lt;sub&gt;6&lt;/sub&gt; and BHB(GA)&lt;sub&gt;7&lt;/sub&gt; performed better in differentiation &lt;em&gt;Elegans&lt;/em&gt; and &lt;em&gt;Martiella&lt;/em&gt;-&lt;em&gt;Ventricosum&lt;/em&gt; sections from each other. Primers (AG)&lt;sub&gt;8&lt;/sub&gt;C with 26 gene loci, and BHB(GA)&lt;sub&gt;7&lt;/sub&gt; with 25 gene loci, produced the most bands in &lt;em&gt;Elegans&lt;/em&gt; isolates and &lt;em&gt;Martiella&lt;/em&gt;-&lt;em&gt;Ventricosum&lt;/em&gt; isolates, respectively.
 
&lt;strong&gt;Conclusions&lt;/strong&gt;
The results of this research showed that there was a high genetic diversity among the investigated &lt;em&gt;Fusarium&lt;/em&gt; isolates and that the ISSR markers are efficient markers to reveal the molecular relationships between &lt;em&gt;Fusarium&lt;/em&gt; populations.</Abstract>
			<OtherAbstract Language="FA">&lt;strong&gt;Objective&lt;/strong&gt;
This research aimed to identify &lt;em&gt;Fusariums&lt;/em&gt; belonging to Elegans and &lt;em&gt;Martiella&lt;/em&gt;-&lt;em&gt;Ventricosum&lt;/em&gt; sections related to cucurbit plants in Tehran province and to evaluate the ability of ISSR markers to investigate the kinship relationships of these groups of &lt;em&gt;Fusariums&lt;/em&gt;.
 
&lt;strong&gt;Materials and methods&lt;/strong&gt;
In this research, five ISSR primers (AG)&lt;sub&gt;8&lt;/sub&gt;C, (AG)&lt;sub&gt;8&lt;/sub&gt;G, (AC)&lt;sub&gt;8&lt;/sub&gt;YA, (ATG)&lt;sub&gt;6&lt;/sub&gt; and BHB(GA)&lt;sub&gt;7&lt;/sub&gt; were selected. Fungal isolates identified based on morphological and microscopic characteristics. For ISSR markers, the statistics of polymorphism information content (PIC), Marker Index (MI) and Effective Multiplex Ratio (EMR) were calculated. Relationships and similarity between &lt;em&gt;Fusarium&lt;/em&gt; isolates were analyzed using NTSYS-PC V2.02.
 
&lt;strong&gt;Results&lt;/strong&gt;
Out of 96 &lt;em&gt;Fusarium&lt;/em&gt; isolates, 48 isolates were identified as &lt;em&gt;Fusarium solani&lt;/em&gt;, 25 isolates as &lt;em&gt;Fusarium oxysporum&lt;/em&gt; and 23 isolates as &lt;em&gt;Fusarium redolens&lt;/em&gt;. A total of 408 bands were obtained from ISSR amplifications. 130 different bands were produced, of which 83 were polymorphic and 47 were monomorphic. The size of PCR fragments produced varied from 273 to 2428 bp. The polymorphism percentage, ranged from the highest (73%) for (ATG)&lt;sub&gt;6&lt;/sub&gt; to the lowest (56%) for (AG)&lt;sub&gt;8&lt;/sub&gt;C. Primers (ATG)&lt;sub&gt;6&lt;/sub&gt; and BHB(GA)&lt;sub&gt;7&lt;/sub&gt; performed better in differentiation &lt;em&gt;Elegans&lt;/em&gt; and &lt;em&gt;Martiella&lt;/em&gt;-&lt;em&gt;Ventricosum&lt;/em&gt; sections from each other. Primers (AG)&lt;sub&gt;8&lt;/sub&gt;C with 26 gene loci, and BHB(GA)&lt;sub&gt;7&lt;/sub&gt; with 25 gene loci, produced the most bands in &lt;em&gt;Elegans&lt;/em&gt; isolates and &lt;em&gt;Martiella&lt;/em&gt;-&lt;em&gt;Ventricosum&lt;/em&gt; isolates, respectively.
 
&lt;strong&gt;Conclusions&lt;/strong&gt;
The results of this research showed that there was a high genetic diversity among the investigated &lt;em&gt;Fusarium&lt;/em&gt; isolates and that the ISSR markers are efficient markers to reveal the molecular relationships between &lt;em&gt;Fusarium&lt;/em&gt; populations.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Cucurbits</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Fusarium</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">ISSR marker</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Elegans</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Martiella- Ventricosum</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://jab.uk.ac.ir/article_3704_75f5ee39f8c24da05561257ed827f01c.pdf</ArchiveCopySource>
</Article>
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