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荧光定量PCR检测巨细胞病毒感染的标本选择 被引量:8

Selection of cytomegalovirus infection samples detected by quantitative PCR
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摘要 目的优化检测标本,提高巨细胞病毒的阳性检出率,为临床诊断和治疗提供可靠依据。方法实时荧光定量PCR检测患者血、淋巴细胞和尿中的人巨细胞病毒DNA(HCMV-DNA),比较其阳性检出率。结果通过实时荧光定量PCR检测的572例患者标本中血浆标本300例,HCMV-DNA阳性45例,阳性率为15.0%;淋巴细胞标本176例,HCMV-DNA阳性30例,阳性率为17.0%;尿标本96例,HCMV-DNA阳性60例,阳性率为62.5%;45例患者配对检测血、尿标本HCMV-DNA,血HCMV-DNA阳性7例,阳性率15.6%,尿HCMV-DNA阳性率64.4%,采用χ2检验显示,血浆、淋巴细胞HCMV-DNA的检出率差异无统计学意义,而血和尿标本HCMV-DNA的检出率差异有统计学意义(P<0.05)。结论采用实时荧光定量PCR检测患者巨细胞病毒感染,以尿作为检测材料的阳性率高于淋巴细胞及血浆,可提高HCMV-DNA的阳性检出率。 OBJECTIVE To optimize the test samples,to improve the detection of CMV-positive rate and provide a reliable basis for clinical diagnosis and treatment.METHODS Blood,lymphocytes and urine human cytomegalovirus DNA(HCMV-DNA) were detected with real-time fluorescence quantitative PCR,and the positive rates were compared.RESULTS A total of 572 patients samples,blood samples of 476 cases,45 cases of plasma-positive,the positive rate was 15.0%;lymphocytes detected in 30 cases,the positive was 17.0%;urine samples of 96 cases,60 cases positive,the positive was 62.5%;of which 45 cases were also collected blood and urine samples were detected by fluorescence quantitative PCR,blood-positive and 7,the positive was 15.6%,urine-positive,the positive was 64.4%.X2 test showed the difference of lymphocytes detection rate of HCMV had no statistivally significance(P0.05),while the detection rates of blood and urine HCMV samples were significantly significant(P0.05).CONCLUSION Adopting real-time fluorescence quantitative PCR detection of cytomegalovirus infection and using urine testing materials as the positive rate in lymphocyte and plasma can increase the positive detection rate of HCMV.
出处 《中华医院感染学杂志》 CAS CSCD 北大核心 2011年第10期2149-2151,共3页 Chinese Journal of Nosocomiology
关键词 人巨细胞病毒 荧光定量聚合酶链反应 尿 HCMV Fluorescence quantitative PCR Urine
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  • 1余钟声,郑季彦,陈黎勤,尚世强,吴家波.婴儿人巨细胞病毒感染病原学和临床分析[J].中华传染病杂志,2006,24(5):333-337. 被引量:11
  • 2Chou S. Cytomegalovirus UL97 mutations in the era of ganciclovir and maribavir [J]. Rev Med Virol, 2008, 18 (4) :233-246.
  • 3吴素兰.PCR检测新生儿尿液人类巨细胞病毒DNA[J].临床检验杂志,1999,17(3):178.
  • 4Zhang S, Zhou S, Li L, et al. Mornitoring human cytomegalovirus infection with nested PCR comparision of positive rates in plasma and leukocytes and quantitative PCR [ J]. Viol J,2010,7:73.
  • 5Huygens A, Dauby N, Vermijlen D, et al. Immunity to cytomegalo- virus in early life[J]. Front Immunol, 2014, 5: 552.
  • 6Dollardl SC, Grosse SD, Ross DS. New estimates of the prevalence of neurological and sensory sequelae and mortality associated with congenital eytomegalovirus infeetion[ J]. Rev Med Virol, 2007, 17 (5) : 355 -363.
  • 7Lanzieri TM, Dollard SC, Josephson CD, et al. Breast milk- acquired eytomegalovirus infeetion and disease in VLBW and prema- ture infants[J]. Pediatrics, 2013, 131 (6) : e1937 -1945.
  • 8Vaziri S, Pezhman Z, Sayyad B, et al. Effieaey of valganeielovir and ganeielovir for eytomegalovirus disease in solid organ trans- plants: a meta-analysis[ J]. J Res Med Sci, 2014, 19(12) : 1185 - 1192.
  • 9Nozawa N,Koyano S,Yamamoto Y,et al.Real-time PCR assay using specimens on filter disks as a template for detection of cytomegalovirus in urine[J].J Clin Microbiol,2007,45(4):1305-1307.
  • 10Chou S.Cytomegalovirus UL97 mutations in the era of ganciclovir and maribavir[J].Rev Med Virol,2008,18(4):233-246.

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