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通过斑点印迹法和聚合酶链反应检测精液、尿液和尿道样本中的人乳头瘤病毒DNA。

Detection of HPV-DNA in semen, urine and urethral samples by dot blot and PCR.

作者信息

Astori G, Pipan C, Muffato G, Botta G A

机构信息

Istituto di Microbiologia, Facoltà di Medicina e Chirurgia, Università degli Studi di Udine, Italy.

出版信息

New Microbiol. 1995 Apr;18(2):143-9.

PMID:7603341
Abstract

Papillomavirus infection in women is associated with the development of carcinoma or squamous intraepithelial lesions (SIL). Limited information is available for men. Seventy asymptomatic male partners of HPV-DNA positive women were studied. Exfoliated cells collected using urethral swabs urine and semen were examined for HPV-DNA using Dot blot and PCR. On exfoliated cells collected using a urethral swab, 89% of the samples were inadequate on Dot blot, and 87% on PCR respectively. Using urine, 36% turned out to be inadequate on Dot blot, 21% on PCR. Using semen all of the 70 samples were satisfactory for both systems. Semen is thus the best material for analysis. The occurrence of HPV-DNA in urine in urine is less frequent than that in semen. Urethral swabs seem to represent the least reliable material. Carriage of human papillomaviruses is frequent in apparently healthy parternrs of HPV infected women.

摘要

女性乳头瘤病毒感染与癌或鳞状上皮内病变(SIL)的发生有关。关于男性的信息有限。对70名HPV-DNA阳性女性的无症状男性伴侣进行了研究。使用尿道拭子、尿液和精液收集脱落细胞,采用斑点印迹法和聚合酶链反应(PCR)检测HPV-DNA。在使用尿道拭子收集的脱落细胞上,斑点印迹法检测的样本中89%不合格,PCR检测的样本中87%不合格。使用尿液时,斑点印迹法检测有36%不合格,PCR检测有21%不合格。使用精液时,70个样本在两种检测系统中均令人满意。因此,精液是最佳分析材料。尿液中HPV-DNA的出现频率低于精液。尿道拭子似乎是最不可靠的材料。在HPV感染女性的明显健康伴侣中,人乳头瘤病毒携带情况很常见。

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