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  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2018-03-25</publicationDate>
    
        <volume>15</volume>
        <issue>1</issue>

 
    <startPage>119</startPage>
    <endPage>130</endPage>

	 
      <doi>10.13005/bbra/2614</doi>
        <publisherRecordId>29552</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Cultural, Anastomosis, and Universally Primed PCR Typing of Rhizoctonia Solani from Potato</title>

    <authors>
	 


      <author>
       <name>Mousa A. Alghuthaymi</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	

	

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Biology, Science and Humanities College, Alquwayiyah, Shaqra University, Saudi Arabia.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Forty two isolates of <em>Rhizoctonia solani </em>were recovered from potato in four agro-ecological regions of potato in Saudi Arabia were studied by using anastomosis typing, morphological characters, and molecular method. Almost of isolates sampled from potato cultures belonged to AG-1, AG-3, and AG-7.  RP1, RP2, RP3, and RP4 are bridging isolates, they might be classified into another anastomosis groups (AGs) or perhaps might be new anastomosis groups. Universally primed PCR (UP-PCR) fingerprinting was used to evaluate genetic diversity of<em> R.</em> <em>solani</em> AGs infecting potato and other hosts. The majority of the isolates representing various AGs were grouped together into different sub-clusters using all three primers. Molecular groups of the isolates did not correspond to agro-ecological regions or states and crops of the origin. In the current study, the UP-PCR markers could not identify and clearly differentiate the isolates of <em>R. solani</em>. There was no relationship between the geographic origin of the isolates and clustering of isolates based on the genetic diversity. Based on cultural characterization, anastomosis group typing and UP-PCR, no clear-cut conclusions about non-identified anastomosis groups from potato.</abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol15no1/cultural-anastomosis-and-universally-primed-pcr-typing-of-rhizoctonia-solani-from-potato/</fullTextUrl>



      <keywords language="eng">
        <keyword>Anastomosis Typing; Potato; <em>Thanatephorus Cucumeris</em>; Sclerotia; UP-PCR</keyword>
      </keywords>

  </record>
</records>