Indirect ELISA with Recombinant GP5 for Detecting Antibodies to Porcine Reproductive and Respiratory Syndrome Virus
	    		
		   		
		   			
		   		
	    	
    	 
    	10.1007/s12250-011-3154-9
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Yan CHEN
			        		
			        		;
		        		
		        		
		        		
			        		Hong TIAN
			        		
			        		;
		        		
		        		
		        		
			        		Jianhui HE
			        		
			        		;
		        		
		        		
		        		
			        		Jinyin WU
			        		
			        		;
		        		
		        		
		        		
			        		Youjun SHANG
			        		
			        		;
		        		
		        		
		        		
			        		Xiangtao LIU
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Porcine reproductive and respiratory syndromevirus(PRRSV);
			        		
			        		
			        		
				        		GP5 protein;
			        		
			        		
			        		
				        		Indirect ELISA
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Virologica Sinica
	            		
	            		 2011;26(1):61-66
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Porcine reproductive and respiratory syndrome is caused by the PRRS virus(PRRSV), which has six structural proteins(GP2, GP3, GP4, GP5, M and N). GP5 and N protein are important targets for serological detection by enzyme-linked immunosorbent assay(ELISA)and other methods. Toward this goal, we developed an indirect ELISA with recombinant GP5 antigens and this method was validated by comparison to the LSI PRRSV-Ab ELISA kit. The results indicated that the optimal concentration of coated recombinant antigen was 0.2 μg/well for a serum dilution of 1:40. The rate of agreement with the LSI PRRSV-Ab kit was 88.7%(266/300). These results support the potential use of recombinant GP5 as an antigen for indirect ELISA to detect PRRSV antibodies in pigs.