Abe K, Konomi N
Department of Pathology, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo 162-8640, Japan.
J Clin Microbiol. 1998 Oct;36(10):3070-2. doi: 10.1128/JCM.36.10.3070-3072.1998.
To overcome the instability of viral RNA, we carried out hepatitis C virus (HCV) RNA detection in dried serum spotted onto filter paper. The spotted serum samples were stored at room temperature and then processed for PCR assay at intervals of 1, 2, 3, and 4 weeks. The results showed that serum HCV RNA is stable in a dried condition, as it was detectable in spotted serum samples stored for 4 weeks at room temperature. Furthermore, although the HCV RNA titer showed an approximately 10-fold reduction in virus yield in dried serum stored at room temperature for 4 weeks, the PCR results of frozen serum samples and dried serum samples matched completely. This storage method facilitates transport and analysis by nucleic acid amplification techniques even when freezing conditions are not available.
为克服病毒RNA的不稳定性,我们对点样于滤纸上的干燥血清进行了丙型肝炎病毒(HCV)RNA检测。点样后的血清样本在室温下储存,然后分别在1周、2周、3周和4周的间隔时间进行PCR检测。结果显示,血清HCV RNA在干燥状态下是稳定的,因为在室温下储存4周的点样血清样本中仍可检测到。此外,尽管室温下储存4周的干燥血清中HCV RNA滴度显示病毒产量约降低了10倍,但冷冻血清样本和干燥血清样本的PCR结果完全匹配。即使在无法进行冷冻的情况下,这种储存方法也便于通过核酸扩增技术进行运输和分析。