睾丸器官型培养中活动精子和生精细胞中巨细胞病毒的检测。

Victor A Naumenko, Yurii A Tyulenev, Sergei A Yakovenko, Lubov' F Kurilo, Ludmila V Shileyko, Aleksander S Segal, Larisa E Zavalishina, Regina R Klimova, Anton S Tsibizov, Sergei V Alkhovskii, Alla A Kushch
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引用次数: 34

摘要

背景:人类巨细胞病毒(HCMV)在男性生殖道的存在提示其通过精子垂直传播并发展为潜在危险的胎儿感染。本研究的目的是评估HCMV在男性生殖细胞内定位的可能性,并检查病毒对人类精子发生的影响。方法:对91例不育男性和47例可育男性的精液样本进行分析。采用实时PCR、快速培养法和原位PCR检测HCMV。采用人睾丸器官型培养和定量核学分析研究了病毒对精子发生的影响。采用单克隆抗体免疫染色和感染器官型培养物的超微结构分析,研究了HCMV在未成熟生殖细胞和精子中的定位。结果:在12.3%的活动精子样本中检测到病毒DNA,而在2.9%的不育和可育男性中仅检测到感染活性,组间差异无统计学意义。原位PCR结果显示,两组感染细胞的平均百分比为1.5%(0.25% ~ 15%),可作为评价HCMV传播风险的标准。在感染hcmv的器官型培养中,第4天在精子中鉴定出病毒抗原,第8天在精原细胞和精母细胞中鉴定出病毒抗原,第14天在精子中鉴定出病毒抗原。电镜观察了生殖细胞的空衣壳和满衣壳及病毒粒子。引入培养前取细胞数为100%。第14天,感染培养的精原细胞占36.8%,精母细胞占18.7%,圆形精母细胞占27.6%,细长精母细胞占42.5%;与未感染培养的82.2%、51.5%、70.4%、65.7%相比,差异均有统计学意义(p < 0.05)。精子的数量和活力没有变化。结论:HCMV可在男性生殖细胞中检测到,包括精子样本和睾丸器官型培养。该病毒可感染未成熟的生殖细胞,这些生殖细胞发育为携带hcmv的成熟精子。未成熟生殖细胞数量的大量减少表明HCMV产生直接的配子毒性作用,并可能导致男性不育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Detection of human cytomegalovirus in motile spermatozoa and spermatogenic cells in testis organotypic culture.

Detection of human cytomegalovirus in motile spermatozoa and spermatogenic cells in testis organotypic culture.

Detection of human cytomegalovirus in motile spermatozoa and spermatogenic cells in testis organotypic culture.

Background: The presence of human cytomegalovirus (HCMV) in male genital tract suggests its vertical transmission with spermatozoa and the development of a potentially dangerous fetal infection. The objective of the present study was to evaluate the possibility of intracellular HCMV localization in male germ cells and to examine the effect of the virus on human spermatogenesis.

Methods: Semen samples from 91 infertile and 47 fertile men were analyzed. HCMV was detected by real time PCR, rapid culture method and PCR in situ. Human testis organotypic culture and quantitative karyological analysis were used to investigate viral effects on spermatogenesis. Localization of HCMV in immature germ cells and spermatozoa was studied by immunostaining with monoclonal antibodies and ultrastructural analysis of infected organotypic culture.

Results: Viral DNA was detected in 12.3% samples of motile spermatozoa, while infectious activity only in 2.9% infertile and fertile men without statistically significant intergroup difference. According to PCR in situ, the mean percentage of infected cell in both groups was 1.5% (0.25%-15%), which can serve as a criterion for evaluating the risk of HCMV transmission. In HCMV-infected organotypic culture viral antigens were identified in spermatides on day 4, in spermatogonia and spermatocytes on day 8, and in spermatozoa on day 14. Empty and full capsides and virions were visualized in germ cells by electron microscopy. The number of cells before introduction in culture was taken for 100%. On day 14 infected culture contained 36.8% spermatogonia, 18.7% spermatocytes, 27.6% round spermatides and 42.5% elongated spermatides; in comparison with 82.2%, 51.5%, 70.4% and 65.7% in uninfected culture, respectively (all p < 0.05). There were no changes in the number and viability of spermatozoa.

Conclusions: HCMV was detected in male germ cells, both in sperm samples and in testis organotypic culture. The virus may infect immature germ cells which develop to mature HCMV-carrying spermatozoa. A considerable decrease in the number of immature germ cells indicates that HCMV produces a direct gametotoxic effect and can contribute to male infertility.

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