Single tube competitive PCR for quantitation of CMV DNA in the blood of HIV+ and solid organ transplant patients

被引:11
作者
Chatellard, P
Sahli, R
Iten, A
von Overbeck, J
Meylan, PRA [1 ]
机构
[1] CHU Vaudois, Inst Microbiol, CH-1011 Lausanne, Switzerland
[2] CHU Vaudois, Div Infect Dis, CH-1011 Lausanne, Switzerland
关键词
viral load; pathogenesis; prognostic marker; cytomegalovirus; CMV disease; preemptive treatment;
D O I
10.1016/S0166-0934(97)00087-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cytomegalovirus (CMV) infection is a major cause of morbidity and mortality in transplant and HIV-infected patients. However, CMV can also cause asymptomatic infection. An elevated blood viral load as assessed by various methods appears to be a predictor for symptomatic infections, and can be used to identify patients at the highest risk of developing CMV disease. We developed a single tube competitive quantitative PCR assay for CMV DNA, using as a competitor a plasmid carrying the target sequence for amplification with an internal deletion. The analysis of data from repeated extractions and amplifications of samples showed that the coefficient of variation of the assay was typically less than 20%. Clinical samples from 14 HIV-infected and 13 solid organ transplant patients were analyzed. Widely varying CMV DNA levels were found in leukocytes, with a positive correlation with the measure of infectivity in the leukocytes by quantitative culture on fibroblasts. The highest CMV DNA content in leukocytes was found in two patients with presumptive CMV disease. In HIV patients, the amount of DNA in leukocytes was much larger than in solid organ transplant recipients, when standardized for infectivity. Although based on a very limited number of patients, this observation probably points to a difference in the biology of CMV infection in these two categories of susceptible individuals. CMV DNA was also found in the plasma of some of the patients with a high CMV DNA leukocyte load. The present test should be useful for identifying patients at high risk of developing CMV disease, for monitoring therapeutic efficacy of antiviral regimens and to improve the understanding the pathogenesis of CMV infection. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:137 / 146
页数:10
相关论文
共 38 条
[1]   COMPARISON OF PLASMA PCR AND BRONCHOALVEOLAR LAVAGE FLUID CULTURE FOR DETECTION OF CYTOMEGALOVIRUS-INFECTION IN ADULT BONE-MARROW TRANSPLANT RECIPIENTS [J].
ASPIN, MM ;
GALLEZHAWKINS, GM ;
GIUGNI, TD ;
TEGTMEIER, B ;
LANG, DJ ;
SCHMIDT, GM ;
FORMAN, SJ ;
ZAIA, JA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (09) :2266-2269
[2]   Prognostic significance and risk factors of untreated cytomegalovirus viremia in liver transplant recipients [J].
Badley, AD ;
Patel, R ;
Portela, DF ;
Harmsen, WS ;
Smith, TF ;
Ilstrup, DM ;
Steers, JL ;
Wiesner, RH ;
Paya, CV .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (02) :446-449
[3]   QUANTITATIVE-ANALYSIS OF CYTOMEGALOVIRUS VIREMIA IN LUNG-TRANSPLANT RECIPIENTS [J].
BAILEY, TC ;
BULLER, RS ;
ETTINGER, NA ;
TRULOCK, EP ;
GAUDREAULTKEENER, M ;
LANGLOIS, TM ;
FORNOFF, JER ;
COOPER, JD ;
STORCH, GA .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (04) :1006-1010
[4]   Quantitation of cytomegalovirus DNA and characterization of viral gene expression in bronchoalveolar cells of infected patients with and without pneumonitis [J].
Boivin, G ;
Olson, CA ;
Quirk, MR ;
Kringstad, B ;
Hertz, MI ;
Jordan, MC .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (06) :1304-1312
[5]   EARLY DETECTION OF ACTIVE CYTOMEGALOVIRUS (CMV) INFECTION AFTER HEART AND KIDNEY-TRANSPLANTATION BY TESTING FOR IMMEDIATE EARLY ANTIGENEMIA AND INFLUENCE OF CELLULAR-IMMUNITY ON THE OCCURRENCE OF CMV INFECTION [J].
BOLAND, GJ ;
DEGAST, GC ;
HENE, RJ ;
JAMBROES, G ;
DONCKERWOLCKE, R ;
THE, TH ;
MUDDE, GC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (09) :2069-2075
[6]  
Bowen EF, 1996, AIDS, V10, P1515, DOI 10.1097/00002030-199611000-00009
[7]  
Bowen EF, 1996, AIDS, V10, pS37
[8]  
BRITT WJ, 1996, FIELDS VIROLOGY, P2493
[9]   ANALYSIS OF THE UL97 PHOSPHOTRANSFERASE CODING SEQUENCE IN CLINICAL CYTOMEGALOVIRUS ISOLATES AND IDENTIFICATION OF MUTATIONS CONFERRING GANCICLOVIR RESISTANCE [J].
CHOU, SW ;
ERICE, A ;
JORDAN, MC ;
VERCELLOTTI, GM ;
MICHELS, KR ;
TALARICO, CL ;
STANAT, SC ;
BIRON, KK .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (03) :576-583
[10]  
CLEMENTI M, 1997, GENET ANAL TECHNOL A, V11, P1