Determination of Free DNA (cfDNA) by RT-qPCR in Individuals in Sperm Alterations

M. Mbaye, Hasnae Zekhnini, B. E. Khalfi, N. Louanjli, Mustafa Zakaria, Fatiha Elmellouli, A. Soukri
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Abstract

Previous studies have suggested that the presence of circulating nucleic acids (cell-free DNA) in seminal plasma may indicate disease states. However, the potential association between cell-free DNA (cfDNA) levels in seminal plasma and sperm fertility parameters has not yet been definitively determined. In this study, we will compare seminal free DNA levels between normozoospermic samples and those from different pathologies related to characteristic parameters of sperm quality (asthenozoospermia, azoospermia, teratozoospermia, oligozoospermia and a few samples with a high fragmentation index) in order to detect a potential association between free DNA levels in seminal plasma and these different pathologies of male fertility. The recovery of free DNA from our different samples was done with the MACHEREY-NAGEL NucleoSpin® kit. This kit allows isolation of DNA from cell-free biological fluids using rapid silica column procedures. The quantification of free DNA in our samples was performed by quantitative PCR (RT-qPCR). Our results showed a significant difference in the level of free seminal DNA between normozoospermic samples and oligozoosperimic, teratozoosperimic, azoosperimic samples and those with a high DNA fragmentation index. On the other hand, no significant difference in the level of seminal free DNA was noted between normozoospermic and asthenozoospermic samples. These results suggest that seminal free DNA may be an important biomarker in the assessment of human sperm fertility.
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RT-qPCR法测定精子变异个体游离DNA (cfDNA)
以前的研究表明,在精浆中循环核酸(无细胞DNA)的存在可能指示疾病状态。然而,精浆中游离DNA (cfDNA)水平与精子生育参数之间的潜在关联尚未明确确定。在本研究中,我们将比较正常精子样本和与精子质量特征参数相关的不同病理样本(弱精子症、无精子症、畸形精子症、少精子症和少数高碎片化指数样本)的精子游离DNA水平,以检测精子血浆中游离DNA水平与这些不同男性生育能力病理之间的潜在关联。使用MACHEREY-NAGEL NucleoSpin®试剂盒从不同样品中回收游离DNA。该试剂盒允许使用快速硅胶柱程序从无细胞生物液中分离DNA。我们的样品中游离DNA采用定量PCR (RT-qPCR)进行定量。我们的研究结果表明,正常精子样本与少精子、畸形精子、无精子样本和DNA片段化指数高的样本的游离精子DNA水平有显著差异。另一方面,正常精子和弱精子样本的精子游离DNA水平无显著差异。这些结果表明,精液游离DNA可能是评估人类精子生育能力的重要生物标志物。
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