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Detection of human immunodeficiency virus-1 RNA and DNA by extractive and in situ PCR in unprocessed semen and seminal fractions isolated by semen-washing procedure.

机译:通过提取和原位PCR检测未处理的精液中的人类免疫缺陷病毒-1 RNA和DNA,并通过精液洗涤程序分离出精液。

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BACKGROUND: To determine the presence of human immunodeficiency virus-1 (HIV-1) viral RNA/DNA in whole semen, in properly isolated seminal fractions and in spermatozoa after swim-up, by extractive nested PCR and to compare the detection of HIV DNA by in situ PCR (IS-PCR) with the results of nested PCR. METHODS: We tested HIV-1 RNA and DNA by nested PCR in semen and in seminal fractions from 55 patients. Non-spermatic cells and spermatozoa pellet fractions from 10 HIV-1-positive and five HIV-1-negative men were tested for proviral DNA by IS-PCR. RESULTS: All samples of spermatozoa recovered after sperm washing were free of HIV RNA. HIV RNA tested positive in seven (13%) seminal plasma samples and only in two (4.2%) whole semen of these same samples. Of the seven seminal plasma samples testing positive for HIV RNA, four men had elevated blood viral load and three an undetectable viraemia. HIV DNA by IS-PCR turned positive in three of five samples in semen of HIV-noninfected men. CONCLUSION: HIV RNA/DNA detection in the semen of HIV-infected men proves the efficacy of sperm washing with swim-up of spermatozoa. It is recommended that nested PCR be conducted on purified seminal compartments. IS-PCR is inadequate for detecting HIV in semen.
机译:背景:通过提取巢式PCR来确定人精液中,正确分离的精液片段和游泳后精子中人类免疫缺陷病毒-1(HIV-1)病毒RNA / DNA的存在,并通过巢式提取PCR进行比较,并比较HIV DNA的检测通过原位PCR(IS-PCR)和嵌套PCR的结果。方法:我们通过巢式PCR检测了55例患者精液和精液中的HIV-1 RNA和DNA。通过IS-PCR检测了来自10名HIV-1阳性和5名HIV-1阴性的男性的非精细胞和精子沉淀级分的原病毒DNA。结果:精子清洗后回收的所有精子样本均不含HIV RNA。 HIV RNA在七个(13%)精浆样本中检测为阳性,而在这些相​​同样本中仅两个(4.2%)全精液中检测为阳性。在七个检测到的HIV RNA阳性的精浆样本中,有四名男子血液病毒载量升高,三名未检测到病毒血症。通过IS-PCR检测的HIV DNA在未感染HIV的男性精液中的五个样本中有三个呈阳性。结论:在感染了艾滋病毒的男性精液中检测HIV RNA / DNA证明了用精子游走可以清洗精子。建议在纯化的精巢区进行巢式PCR。 IS-PCR不足以检测精液中的HIV。

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