<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Journal of Virology</title>
<title_fa>مجله ویروس شناسی ایران</title_fa>
<short_title>Iran J Virol</short_title>
<subject>Medical Sciences</subject>
<web_url>http://journal.isv.org.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1735-5680</journal_id_issn>
<journal_id_issn_online>2588-5030</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.21859/isv</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1394</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2015</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<volume>9</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Screening Cydia pomonella granulovirus (CpGV) isolates via comparative bioassays</title>
	<subject_fa>تخصصي</subject_fa>
	<subject>Special</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Original article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div&gt;
&lt;p&gt;&lt;strong&gt;Abstract&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Background and Aims:&lt;/strong&gt; The &lt;em&gt;Cydia pomonella&lt;/em&gt; granulovirus (CpGV) is a baculovirus and very effective biological control agent against apple pest, codling moth, &lt;em&gt;Cydia pomonella&lt;/em&gt; L. especially for healthy organic apple production and protection.&amp;nbsp; Not only, screening of CpGV isolates via biochemical variation, but also their biological variation is practically necessary.&amp;nbsp; However, the bioassay methods and biological activity parameters, such as LC50, LD50 and LT50 are different, sensitive and usually time and expense consuming; the right chosen method of bioassay can show differences and variation for applied screening purposes.&amp;nbsp; &lt;strong&gt;Materials and Methods:&lt;/strong&gt; In this study, an appropriate double bioassay method have been successfully set to express biological variation of CpGV isolates on neonate larvae under laboratory conditions (26&amp;plusmn;0.2 ˚C, RH: 60%&amp;plusmn;2, 16:8 L: D).&amp;nbsp; The diet incorporation bioassays (LC50) with&amp;nbsp; 0 to 16000 occlusion bodies/ml usually determine the rate of larval mortality on 7th day.&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Results:&lt;/strong&gt; The LC50 of CpGV isolates were evaluated 4454 to 2277 occlusion bodies (OBs) per ml of artificial diet.&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;Tthat show the double bioassay method have been successfully set and comparable with other results that can enhance biocontrol of codling moth especially in organic apple orchards.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;&lt;/div&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>codling moth, Cydia pomonella granulovirus, bioassay.</keyword>
	<start_page>1</start_page>
	<end_page>5</end_page>
	<web_url>http://journal.isv.org.ir/browse.php?a_code=A-10-76-5&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name></first_name>
	<middle_name></middle_name>
	<last_name></last_name>
	<suffix></suffix>
	<first_name_fa>M</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>Rezapanah</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>m.rezapanah@areeo.ac.ir</email>
	<code>10031947532846003161</code>
	<orcid>10031947532846003161</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Insect Virology Lab., Biological Control Dept., Iranian Research Institute of Plant Protection (IRIPP), Agricultural Research Education and Extension Organization (AREEO),Tehran, Iran</affiliation>
	<affiliation_fa>Insect Virology Lab., Biological Control Dept., Iranian Research Institute of Plant Protection (IRIPP), Agricultural Research Education and Extension Organization (AREEO),Tehran, Iran</affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
