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1.
PLoS One ; 6(3): e18095, 2011 Mar 29.
Artigo em Inglês | MEDLINE | ID: mdl-21479232

RESUMO

Human papillomaviruses (HPV) may cause sexually transmitted disease. High-risk types of HPV are involved in the development of cervical cell dysplasia, whereas low-risk types may cause genital condyloma. Despite the association between HPV and cancer, donor sperm need not be tested for HPV according to European regulations. Consequently, the potential health risk of HPV transmission by donor bank sperm has not been elucidated, nor is it known how HPV is associated with sperm. The presence of 35 types of HPV was examined on DNA from semen samples of 188 Danish sperm donors using a sensitive HPV array. To examine whether HPV was associated with the sperm, in situ hybridization were performed with HPV-6, HPV-16 and -18, and HPV-31-specific probes. The prevalence of HPV-positive sperm donors was 16.0% and in 66.7% of these individuals high-risk types of HPV were detected. In 5.3% of sperm donors, two or more HPV types were detected. Among all identified HPV types, 61.9% were high-risk types. In situ hybridization experiments identified HPV genomes particularly protruding from the equatorial segment and the tail of the sperm. Semen samples from more than one in seven healthy Danish donors contain HPV, most of them of high-risk types binding to the equatorial segment of the sperm cell. Most HPV-positive sperm showed decreased staining with DAPI, indicative of reduced content of DNA. Our data demonstrate that oncogenic HPV types are frequent in men.


Assuntos
Papillomaviridae/isolamento & purificação , Espermatozoides/virologia , Doadores de Tecidos , Adolescente , Adulto , Sondas de DNA , Dinamarca , Humanos , Hibridização in Situ Fluorescente , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Papillomaviridae/classificação , Espermatozoides/citologia , Adulto Jovem
2.
Fertil Steril ; 82(5): 1463-5, 2004 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-15533383

RESUMO

History was taken systematically for 100 azoospermic, nonvasectomized men referred consecutively to a Danish fertility clinic. The men were examined by ultrasound, and their blood samples were analyzed for karyotype, Y microdeletions, and cystic fibrosis transmembrane conductance regulator gene mutations. In 29% of patients, the condition could be explained by genetic abnormalities; in 22%, by diseases or external influence; and in 27%, by former cryptorchidism. The azoospermic condition remained unexplained in only 22%.


Assuntos
Oligospermia/etiologia , Criptorquidismo/complicações , Regulador de Condutância Transmembrana em Fibrose Cística/genética , Humanos , Masculino , Mutação , Oligospermia/diagnóstico por imagem , Oligospermia/genética , Oligospermia/patologia , Ultrassonografia , Ducto Deferente/anormalidades
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