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首页> 外文期刊>Journal of Clinical Microbiology >Stability of Hepatitis C Virus, HIV, and Hepatitis B Virus Nucleic Acids in Plasma Samples after Long-Term Storage at ?20oC and ?70oC
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Stability of Hepatitis C Virus, HIV, and Hepatitis B Virus Nucleic Acids in Plasma Samples after Long-Term Storage at ?20oC and ?70oC

机译:长期保存在?20oC和?70oC后血浆样品中的丙型肝炎病毒,HIV和乙型肝炎病毒核酸的稳定性

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The storage of biological samples may affect detection of viral nucleic acid, yet the stability of viral nucleic acid at standard laboratory storage temperatures (?70°C and ?20°C) has not been comprehensively assessed. Deterioration of viral RNA and DNA during storage may affect the detection of viruses, thus leading to an increased likelihood of false-negative results on diagnostic testing. The viral loads of 99 hepatitis C virus (HCV), 41 HIV, and 101 hepatitis B virus (HBV) patient samples were measured before and after storage at ?20°C and ?70°C for up to 9.1 years using Versant branched DNA assays, Cobas Monitor assays, and/or AmpliPrep/AmpliScreen assays. Clinical samples stored at ?20°C for up to 1.2 years and at ?70°C for up to 9 years showed a statistically significant difference from baseline with respect to HCV RNA titer, although this difference was not greater than 0.5 log10 unit. The concentration of HIV RNA in clinical samples stored at ?20°C for 2.3 years and at ?70°C for up to 9.1 years did not differ significantly from the baseline viral load. HBV DNA-positive clinical samples stored at ?20°C for up to 5 years and at ?70°C for up to 4 years differed significantly in viral load. In all studies, however, the loss of viral load of HCV, HIV, or HBV in clinical samples tested after storage at ?20°C and ?70°C for up to 9 years ranged from 0.01 to 0.35 log10 IU/ml and did not exceed 0.5 log10, which is the estimated intra-assay variation for molecular tests. Hence, the loss was considered of minimal clinical impact and adequate for the detection of HCV, HIV-1, and HBV nucleic acids using nucleic acid assays for the assessment of the infectious risk of cell, blood, and tissue donors.
机译:生物样品的储存可能会影响病毒核酸的检测,但尚未全面评估病毒核酸在标准实验室储存温度(约70°C和约20°C)下的稳定性。储存过程中病毒RNA和DNA的恶化可能会影响病毒的检测,从而导致诊断测试中出现假阴性结果的可能性增加。使用Versant分支DNA在99°C和70°C下储存9.1年前后,测量99例丙型肝炎病毒(HCV),41例HIV和101例乙型肝炎病毒的病毒载量。检测,Cobas Monitor检测和/或AmpliPrep / AmpliScreen检测。在-20°C下最多可保存1.2年和在70℃下最多可保存9年的临床样品显示,相对于HCV RNA滴度,与基线相比具有统计学上的显着差异,尽管该差异不大于0.5 log 10 单元。在?20°C储存2.3年和在70°C储存长达9.1年的临床样品中HIV RNA的浓度与基线病毒载量没有显着差异。 HBV DNA阳性临床样品在?20°C下保存长达5年和在?70°C下保存长达4年的病毒载量存在显着差异。但是,在所有研究中,在?20°C和?70°C下存储长达9年后测试的临床样品中HCV,HIV或HBV病毒载量的损失范围为0.01至0.35 log 10 < / sub> IU / ml,且不超过0.5 log 10 ,这是分子检测的估计批内含量差异。因此,该损失被认为对临床的影响最小,并且足以通过使用核酸测定法评估细胞,血液和组织供体的感染风险来检测HCV,HIV-1和HBV核酸。

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