<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<component xmlns="https://zibelinepub.com" version="1.0.2" type="journal" xml:lang="en">
<header>
<publicationMeta level="journal">
			<publisherInfo>
				<publisherName>Zibeline International Publishing</publisherName>
				<publisherLoc>Tropical Agrobiodiversity</publisherLoc>
			</publisherInfo>
			
			<doi origin="razipublishing" registered="yes">10.26480/trab.02.2024.106.109</doi>
			
			<issn type="online">2716-7046</issn>
			
			<titleGroup>
				<title type="subject" xml:lang="en" sort="Tropical Agrobiodiversity">Tropical Agrobiodiversity</title>
				<title type="title">PCR BASED DETECTION OF LATENTLY INFECTED POTATO WITH BROWN ROT PATHOGEN, RALSTONIA SOLANACEARUM</title>
			</titleGroup>
			
			<copyright ownership="publisher">Copyright © 2017 Zibeline International Publishing</copyright>
			
			<eventGroup>
				<event type="publication_date" date="31-07-2024"/>
			</eventGroup>
			
			<creators>
				<creator xml:id="mmh" creatorRole="editor">
					<personName>
						<editorNames>Md. Mokarram Hossain</editorNames>
					</personName>
				</creator>
				<creator xml:id="mri" creatorRole="editor">
					<personName>
						<editorNames>Md. Rashidul Islam</editorNames>
					</personName>
				</creator>
				<creator xml:id="rcd" creatorRole="editor">
					<personName>
						<editorNames>Ronzon Chandra Das</editorNames>
					</personName>
				</creator>
				<creator xml:id="mmh" creatorRole="editor">
					<personName>
						<editorNames>Md. Mahbubul Haque</editorNames>
					</personName>
				</creator>
				<creator xml:id="mdh" creatorRole="editor">
					<personName>
						<editorNames>Mohammad Delwar Hossain</editorNames>
					</personName>
				</creator>
				<creator xml:id="ftj" creatorRole="editor">
					<personName>
						<editorNames>Faria-Ter Jerin</editorNames>
					</personName>
				</creator>
			</creators>
			
</publicationMeta>

		<citation_keywords>
		    <keyword>PCR Detection, Brown rot pathogen, Management, Export quality, Potatoes</keyword>
		</citation_keywords>
			
		<citation_pdfformat>
		     <pdf_url>https://trab.org.my/archives/2trab2024/2trab2024-106-109.pdf</pdf_url>
	    </citation_pdfformat>
	   
	   <citation_XMLformat>
	         <xml_url>https://trab.org.my/xml/2trab2024/2trab2024-106-109.xml</xml_url>
	   </citation_XMLformat>
	   
	   <citation_volume>
	       <volume>5</volume>
	   </citation_volume>
	   
	   <citation_issue>
	        <issue>2</issue>
	   </citation_issue>
	   
	   <citation_pages>
	      <pages>106-109</pages>
	   </citation_pages>  
	   
	   <citation_fulltext_html>
	       <fulltext_html>https://trab.org.my/trab-02-2024-106-109</fulltext_html>
	    </citation_fulltext_html>
		
<abstractGroup>

			<abstract type="main" xml:lang="en">
			<title type="main">Summary</title>
			
					<p>Brown rot of potato is caused by a soil borne bacterium, Ralstonia solanacearum(Smith), a major limiting factor in the production of many crop plants around the world. An experiment was conducted to assess the status of brown rot disease in potatoes with the development of a rapid detection technique and approaches for production of brown rot free export quality potatoes to boost up potato export from Bangladesh. Survey results revealed a variation in latent infection (%) in tuber samples collected from six major growing areas viz. Dinajpur, Rangpur, Bogra, Joypurhat, Munshigonj and Comilla. The lowest (30%) latent infection was detected in tuber samples collected from Joypurhat as compared to Rangpur and Munshigonj in case of Asterix. However, in Diamant, the lowest (40%) latent infection was observed in Rangpur while 80% latent infection was recorded in Dinajpur and 88% was recorded in Munshigonj. Intriguingly, no latent infection was detected in Cardinal collected from Dinajpur while 40% latent infection was detected in samples from Joypurhat. However, 60% latent infection was detected in Granola which was collected from Dinajpur. The detection of R. solanacearum was reported in latently infected tubers by PCR using primers corresponding to 16SrDNA. In this study, PCR with primers PS-1 and PS-2 (16S rDNA) was used to detect R. solanacearum in latently infected tubers. An amplicon size corresponding to 553bp were obtained using enriched tuber extract as template. </p>
			</abstract>

</abstractGroup> 
			
			
			
</header>
	</component>
			