<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Journal of Fisheries Sciences</title>
<title_fa>مجله علوم شیلاتی ایران</title_fa>
<short_title>IJFS</short_title>
<subject>Agriculture</subject>
<web_url>http://jifro.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1562-2916</journal_id_issn>
<journal_id_issn_online>2322-5696</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.18869/acadpub.ijfs</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>1399</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2021</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<volume>20</volume>
<number>1</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>Research Article: Development of a co-agglutination method for detection of Aeromonas hydrophila as causative agent of motile Aeromonas septicemia (MAS) disease in gourami (Osphronemus goramy)</title>
	<subject_fa>fish disease</subject_fa>
	<subject>fish disease</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Orginal research papers</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;em&gt;Aeromonas hydrophila &lt;/em&gt;is an opportunistic pathogen causing high mortality and economic burden in freshwater fish farming. This study aims to develop a co-agglutination method for detecting and creating &lt;em&gt;Aeromonas hydrophila &lt;/em&gt;diagnostic rapidly. In this study, we injected rabbits (&amp;plusmn;2kg weight) with 1mL of &lt;em&gt;A. hydrophila&lt;/em&gt; antigen suspension 1.2 x 10&lt;sup&gt;9&lt;/sup&gt;cfu mL&lt;sup&gt;&amp;ndash;1&lt;/sup&gt; at one week intervals (three times, intra vena) respectively. The gouramis (15.48&amp;plusmn;0.55g-1 weight) were infected by &lt;em&gt;Aeromonas hydrophila, Aeromonas sobria&lt;/em&gt;, &lt;em&gt;Aeromonas salmonicida&lt;/em&gt;, &lt;em&gt;Streptococcus agalactiae&lt;/em&gt;, and &lt;em&gt;Pseudomonas aeruginosa&lt;/em&gt; separately with 0.1 mL fish&lt;sup&gt;&amp;ndash;1&lt;/sup&gt; and 10&lt;sup&gt;8&lt;/sup&gt; cfu mL&lt;sup&gt;&amp;ndash;1&lt;/sup&gt; bacterial cell suspensions. The antiserum was purified to couple with the &lt;em&gt;Staphylococcus aureus &lt;/em&gt;suspension protein A, in a 1:1 (v/v) ratio and used by the co-agglutination reagent. We compared this method with standard polymerase chain reaction (PCR) for &lt;em&gt;A. hydrophila &lt;/em&gt;detection. The rabbit antibody reaction occurred only against &lt;em&gt;A. hydrophila &lt;/em&gt;antigen showing specificity of the gourami tissue supernatant within 10-30 seconds. The sensitivity test had a detection limit of 10&lt;sup&gt;6&lt;/sup&gt; cfu mL&lt;sup&gt;&amp;ndash;1&lt;/sup&gt;. Comparison detection method with PCR showed that positive result of &lt;em&gt;A. hydrophila &lt;/em&gt;was located in 209 bp. Co-agglutination method could detect &lt;em&gt;A. hydrophila &lt;/em&gt;in the internal organ of fish at 12h after injection, but the PCR method could detect at one hour after injection. This research concluded that co-agglutination method could detect &lt;em&gt;A. hydrophila &lt;/em&gt;specifically, sensitively, rapidly and practically in laboratory and field examination.</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Aeromonas hydrophila, Diagnostic, Rapid, Co-agglutination Method.</keyword>
	<start_page>141</start_page>
	<end_page>156</end_page>
	<web_url>http://jifro.ir/browse.php?a_code=A-10-3103-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>M. </first_name>
	<middle_name></middle_name>
	<last_name>Dian Fitria </last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>dianfitria.manurung@gmail.com</email>
	<code>100319475328460039194</code>
	<orcid>100319475328460039194</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Bogor Agricultural University</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>S.</first_name>
	<middle_name></middle_name>
	<last_name>Sukenda</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>sukenda@ipb.ac.id</email>
	<code>100319475328460039195</code>
	<orcid>100319475328460039195</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Bogor Agricultural University</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>M.</first_name>
	<middle_name></middle_name>
	<last_name>Yuhana</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>yuhanamunti@gmail.com</email>
	<code>100319475328460039196</code>
	<orcid>100319475328460039196</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Bogor Agricultural University</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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