Digoxigenin 탐식자를 이용한 혈청내 B형간염 바이러스 DNA의 검출

Title
Digoxigenin 탐식자를 이용한 혈청내 B형간염 바이러스 DNA의 검출
Other Titles
Detection of Hepatitis B virus DNA in Serum by Digoxigenin Labeled DNA Probe
Authors
김수희백원기서민호김재룡신동학Su Hee KimWon Ki BaekMin Ho SuhJae Ryong KimDong Hak Shin
Keimyung Author(s)
신동학; 백원기; 서민호; 김재룡
Department
Dept. of Family Medicine (가정의학); Dept. of Microbiology (미생물학); Dept. of Laboratory Medicine (진단검사의학)
Keywords
Hepatitis B virus; Dot blot hybridization
Issue Date
1993
Publisher
School of Medicine
Citation
대한미생물학회 The Korean Society For Microblology, Vol.28(4) : 303-311, 1993
Abstract
To estimate the clinical efficiency of digoxigenin (DIG) labeled DNA probe for the detection of hepatitis B virus (HBV) DNA, 149 HBs Ag positive and 15 normal serum samples were tested by DNA dot blot hybridization using 32P-dCTP-labeled HBV DNA probe and DIG-dUTP-labeled HBV DNA probe. Serological markers were tested by ELISA. The sensitivity of 32P-dCTP-labeled HBV DNA probe in detecting HBV DNA was 0.5μg, that of DIG-dUTP-labeled HBV DNA probe labeled by random primed labeling method was 4μg, and the sensitivity of DIG-dUTP-labeled HBV DNA probe labeled by polymerase chain reaction (PCE) was 0.5μg Expire time of 32P-dCTP-labeled HBV DNA probe was within a week, that of DIG-dUTP-labeled HBV DNA probe labeled by random primed labeling method was 4 to 6 months, and that of DIG- dUTP-labeled HBV DNA probe labeled by PCR was 2 to 4 weeks. Time needed for autoradiography was 24-48 hours, but in the case of DIG-labeled probe, visualization of the result needed only 6 hours. The relationship between serum HBV DNA positivity by DIG-labeled probe and serological markers positivity was evaluated. Twenty-seven(79.4%) of 34 patients positive for both HBs Ag and HBs Ag were positive for HBV DNA compared with 25(21.7%) of 115 HBs Ag positive but HBs Ag negative individuals. There was a statistically significant correlation between the positivity of HBV DNA in serum and the presence or absence of HBe Ag. None of the 15 HBs Ag and HBe Ag negative individuals tested was positive for HBV DNA. But the detection rate of HBV DNA in the cases of HBe Ag negative was as high as 21.7%(25/115), so we concluded that dot blot hybridization technic using DIG-labeled HBV DNA probe could be very efficiently applied for both diagnosing HBV infection and evaluating the infectivity of the HBs Ag positive sera.
URI
http://kumel.medlib.dsmc.or.kr/handle/2015.oak/23322
ISSN
0253-3162
Appears in Collections:
1. 연구논문 > 1. School of Medicine (의과대학) > Dept. of Family Medicine (가정의학)
1. 연구논문 > 1. School of Medicine (의과대학) > Dept. of Microbiology (미생물학)
1. 연구논문 > 1. School of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학)
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