Optimization of urinary sample preparation process for real-time PCR detection of BK virus 
	    		
		   		
		   			 
		   		
	    	
    	 
    	10.3724/SP.J.1008.2010.00438
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Chun-Lan LIN
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		
		        		
		        		
		        		
    Author Information Author Information
 
			        		
			        		
			        			1. Department of Biochemistry
 
 
- Publication Type:Journal Article
- Keywords:
        			
	        			
	        				
	        				
			        		
				        		BK virus;
			        		
			        		
			        		
				        		Real-time PCR;
			        		
			        		
			        		
				        		Urine;
			        		
			        		
			        		
				        		Viral load
			        		
			        		
	        			
        			
        		
- From:
	            		
	            			Academic Journal of Second Military Medical University
	            		
	            		 2010;31(4):438-441
	            	
            	
- CountryChina
- Language:Chinese
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		        	Abstract:
			       	
			       		
				        
				        	 Objective: To develop an effective preparation method to improve the sensitivity and accuracy of real-time PCR in detection of BK virus's (BKV's) load in urine samples. Methods: A total of 24 samples documented as positive probes in primary detection were enrolled in this study. The candidate samples were prepared by 4 different approaches: unprocessed urine, BKV's DNA extracted from urine, 1:10 diluted urine, and 1:100 diluted urine; and then they were subjected to real-time PCR examination to obtain the viral load. The data obtained were analyzed by SPSS 11.0. Results: The four different preparation processes for urinary specimens had significant impact on detection results of real-time PCR. Three samples were negative in the unprocessed urine group and 66.7% of its samples had the lowest viral loads compared with the other three groups. Two samples in the 1:100 diluted urine group were negative and 79.2% of its samples had the highest viral loads, but its median load was similar to that of the 1:10 group. Viral gene was detected in all samples in the DNA extraction group and 1:10 diluted urine group, but the loss of the target gene was more severe in the DNA extraction group. Conclusion: The 1:10 diluted urine is better for real-time PCR detection of BKV's load, as it lose less viral gene and is more efficient, easy to perform and economical.