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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2018-06-25</publicationDate>
    
        <volume>11</volume>
        <issue>2</issue>

 
    <startPage>951</startPage>
    <endPage>957</endPage>

	 
      <doi>10.13005/bpj/1453</doi>
        <publisherRecordId>20837</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Comparative Assessment of Sensitivity and Specificity of Rose Bengal Test and Modified In-House ELISA by using IS711 Taqman Real Time PCR Assay as a Gold Standard for the Diagnosis of Bovine Brucellosis</title>

    <authors>
	 


      <author>
       <name>Amira M. Zakaria</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	

	

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Biotechnology Research Institute, New campus Ismailia, Egypt.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Serological approaches such as Rose Bengal Test (RBT) and enzyme linked immunosorbent assay (ELISA) are common tests, however they are generally not sensitive or specific enough for diagnosis of <em>Brucella</em> because of cross-reactivity with different bacterial antigens. The work objected to evaluate the sensitivity and specificity of rose Bengal and  modified in-house ELISA using IS711 real time PCR as a gold test to detect <em>Brucella</em> in calves sera. Two hundred and thirty (n=230) blood samples were collected from (2-3) years asymptomatic male calves in two Egyptian abattoirs. Rose Bengal test (RBT) and modified in-house ELISA were applied to determine the seroprevalence of brucellosis in abattoirs animals while quantitative Taqman real-time PCRs (RT-PCR) were implemented for the identification of Brucella genus. The overall prevalence of brucellosis was (53.9 %), (75.2 %) and (79.1 %) as determined by ELISA,RBT and RT- PCR assays respectively. Regarding statistical analysis of the reported data and considering real time PCR the gold standard, the RBT recorded a sensitivity of (79.12%) and a specificity of (39.58 %) with an accuracy of (70.87%). While (83.24%) was reported as positive predictive value and (33.33 %) as a negative predictive value. The sensitivity and specificity of ELISA were (55.49%) and (52.08 %) respectively while the accuracy was (54.78%). Positive predictive value and negative predictive value for ELISA were determined as (81.45%) and (23.58 %) respectively. RBT can be routinely used for diagnosis of Brucella as cost effective , more sensitive and accurate test than ELISA However, real time PCR is highly recommend as gold test for identification and differentiation of bovine brucellosis.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol11no2/comparative-assessment-of-sensitivity-and-specificity-of-rose-bengal-test-and-modified-in-house-elisa-by-using-is711-taqman-real-time-pcr-assay-as-a-gold-standard-for-the-diagnosis-of-bovine-brucellos/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Brucellosis</keyword>
      

      
        <keyword> ELISA</keyword>
      

      
        <keyword> Rose Bengal Test</keyword>
      

      
        <keyword> Sensitivity</keyword>
      

      
        <keyword> Specificity</keyword>
      
</keywords>
  </record>
</records>