中国医师杂志
中國醫師雜誌
중국의사잡지
JOURNAL OF CHINESE PHYSICIAN
2008年
12期
1610-1613
,共4页
谢小毛%黄开淑%李文华%陈红娟%张文权%胡兰英
謝小毛%黃開淑%李文華%陳紅娟%張文權%鬍蘭英
사소모%황개숙%리문화%진홍연%장문권%호란영
不育,男(雄)性%解脲支原体%基因型
不育,男(雄)性%解脲支原體%基因型
불육,남(웅)성%해뇨지원체%기인형
Infertility,male%Ureaplasm urealyticum%Genotype
目的 了解继发不育男性患者泌尿生殖系解脲脲原体(UU)的感染状况.方法 对572例男性继发不育患者取尿道和前列腺分泌物标本进行培养,采用聚合酶链反应(PCR)和基因型分型技术,时其泌尿道生殖系UU进行生物变种和基因型分型鉴定,分析其结果.结果 572例男性继发不育患者,UU培养阳性278例(48.6%);PCR基因扩增检测UU-DNA阳性311例(54.4%).其中生物变种(biovar)1和生物变种2分别为212例(37.1%)和99例(17.3%);基因分型结果:生物变种1血清变种(serovar)1、3/14、6分别为71例(12.4%)、98例(17.2%)、43例(7.5%).生物变种2亚型(subtype)1、2、3分别为32例(5.6%)、51例(8.9%)、16例(2.8%).结论 UU感染是男性继发不育的重要危险因素,MBA多带抗原基因与16S-rRNA基因和尿素酶基因分型鉴定具有简便,快速,敏感,特异之优点.
目的 瞭解繼髮不育男性患者泌尿生殖繫解脲脲原體(UU)的感染狀況.方法 對572例男性繼髮不育患者取尿道和前列腺分泌物標本進行培養,採用聚閤酶鏈反應(PCR)和基因型分型技術,時其泌尿道生殖繫UU進行生物變種和基因型分型鑒定,分析其結果.結果 572例男性繼髮不育患者,UU培養暘性278例(48.6%);PCR基因擴增檢測UU-DNA暘性311例(54.4%).其中生物變種(biovar)1和生物變種2分彆為212例(37.1%)和99例(17.3%);基因分型結果:生物變種1血清變種(serovar)1、3/14、6分彆為71例(12.4%)、98例(17.2%)、43例(7.5%).生物變種2亞型(subtype)1、2、3分彆為32例(5.6%)、51例(8.9%)、16例(2.8%).結論 UU感染是男性繼髮不育的重要危險因素,MBA多帶抗原基因與16S-rRNA基因和尿素酶基因分型鑒定具有簡便,快速,敏感,特異之優點.
목적 료해계발불육남성환자비뇨생식계해뇨뇨원체(UU)적감염상황.방법 대572례남성계발불육환자취뇨도화전렬선분비물표본진행배양,채용취합매련반응(PCR)화기인형분형기술,시기비뇨도생식계UU진행생물변충화기인형분형감정,분석기결과.결과 572례남성계발불육환자,UU배양양성278례(48.6%);PCR기인확증검측UU-DNA양성311례(54.4%).기중생물변충(biovar)1화생물변충2분별위212례(37.1%)화99례(17.3%);기인분형결과:생물변충1혈청변충(serovar)1、3/14、6분별위71례(12.4%)、98례(17.2%)、43례(7.5%).생물변충2아형(subtype)1、2、3분별위32례(5.6%)、51례(8.9%)、16례(2.8%).결론 UU감염시남성계발불육적중요위험인소,MBA다대항원기인여16S-rRNA기인화뇨소매기인분형감정구유간편,쾌속,민감,특이지우점.
Objective To understand the infection of ureaplasma urealyticum in genitourinary of secondary infertility of male and ex-plore the relationship between the genotype of individual ureaplasma species and genitourinary infection of them . Methods Based on the multiple-banded antigen genes (MBA) of ureaplasma urealyticum, 10 pairs of oligonueleotide primers targeting the 5'ends of the MBA genes were designed to identify the MBA genes of U. parvum and U. ureaplasma by PCR-based genotyping system. The 10 pairs of oligonucleotide primers could distinguish the two biovars and 14 serovars of U. ureaplasma. Results A total of 278 (48.6%) positive ureaplasma culture were obtained from 572 patients attending our clinic of reproductive medical eenter. These methods were used to identify and genotype U. ureaplasma in 311 (54.4%) of 572 patients with genitourinary infection among them U. parvum (biovar 1) was detected in 37.1% and U. ureaplasma (biovar 2) in 17.8%. serovar 1 was in 12.4%, serovars3/14 in 17.1% serovar 6 in 7.5%; subtype 1 of biovar 2 was in 5.6%, subtype 2 in 8.9% and subtype 3 in 2.8%, respectively. Conclusion The PCR-based genotyping system will facilitate future stud-ies of relationship between individual Ureaplasma species or subtypes in genitourinary of secondary infertility of male. The methods described here are relatively rapid, practicable, and specific for the detection species identification and subtyping of Ureaplasma species.