国际医学寄生虫病杂志
國際醫學寄生蟲病雜誌
국제의학기생충병잡지
INTERNATIONAL JOURNAL OF MEDICAL PARASITIC DISEASES
2010年
3期
145-147
,共3页
卢潍媛%袁忠英%沈玉娟%尹建海%曹建平
盧濰媛%袁忠英%瀋玉娟%尹建海%曹建平
로유원%원충영%침옥연%윤건해%조건평
环介导等温扩增法%蓝氏贾第鞭毛虫%安氏隐孢子虫
環介導等溫擴增法%藍氏賈第鞭毛蟲%安氏隱孢子蟲
배개도등온확증법%람씨가제편모충%안씨은포자충
Loop-mediated isothermal amplification%Giardia lamblia%Cryptosporidium andersoni
目的 建立应用环介导等温扩增技术(loop-mediated isothermal amplification,LAMP)检测蓝氏贾第鞭毛虫的方法. 方法 体外培养蓝氏贾第鞭毛虫滋养体,提取DNA.根据GenBank显示的贾第虫序列及环介导等温扩增技术的原理,设计4条贾第虫特异引物,利用LAMP检测蓝氏贾第鞭毛虫DNA,以隐孢子虫卵囊DNA、疟原虫DNA为对照,并将不含病原体DNA的纯水作为阴性对照.LAMP产物经SYBR green I显色后观察结果,绿色为阳性,棕色为阴性;对LAMP产物进行琼脂糖凝胶电泳分析,观察其特征条带的情况. 结果 蓝氏贾第鞭毛虫DNA检测管经显色后呈绿色,隐孢子虫卵囊DNA、疟原虫DNA及水阴性对照管呈棕色.含有蓝氏贾第鞭毛虫DNA的LAMP产物经电泳后呈LAMP特征性梯状条带,安氏隐孢子虫DNA、恶性疟原虫DNA及阴性对照水无扩增产物. 结论 成功建立了检测蓝氏贾第鞭毛虫的LAMP方法.
目的 建立應用環介導等溫擴增技術(loop-mediated isothermal amplification,LAMP)檢測藍氏賈第鞭毛蟲的方法. 方法 體外培養藍氏賈第鞭毛蟲滋養體,提取DNA.根據GenBank顯示的賈第蟲序列及環介導等溫擴增技術的原理,設計4條賈第蟲特異引物,利用LAMP檢測藍氏賈第鞭毛蟲DNA,以隱孢子蟲卵囊DNA、瘧原蟲DNA為對照,併將不含病原體DNA的純水作為陰性對照.LAMP產物經SYBR green I顯色後觀察結果,綠色為暘性,棕色為陰性;對LAMP產物進行瓊脂糖凝膠電泳分析,觀察其特徵條帶的情況. 結果 藍氏賈第鞭毛蟲DNA檢測管經顯色後呈綠色,隱孢子蟲卵囊DNA、瘧原蟲DNA及水陰性對照管呈棕色.含有藍氏賈第鞭毛蟲DNA的LAMP產物經電泳後呈LAMP特徵性梯狀條帶,安氏隱孢子蟲DNA、噁性瘧原蟲DNA及陰性對照水無擴增產物. 結論 成功建立瞭檢測藍氏賈第鞭毛蟲的LAMP方法.
목적 건립응용배개도등온확증기술(loop-mediated isothermal amplification,LAMP)검측람씨가제편모충적방법. 방법 체외배양람씨가제편모충자양체,제취DNA.근거GenBank현시적가제충서렬급배개도등온확증기술적원리,설계4조가제충특이인물,이용LAMP검측람씨가제편모충DNA,이은포자충란낭DNA、학원충DNA위대조,병장불함병원체DNA적순수작위음성대조.LAMP산물경SYBR green I현색후관찰결과,록색위양성,종색위음성;대LAMP산물진행경지당응효전영분석,관찰기특정조대적정황. 결과 람씨가제편모충DNA검측관경현색후정록색,은포자충란낭DNA、학원충DNA급수음성대조관정종색.함유람씨가제편모충DNA적LAMP산물경전영후정LAMP특정성제상조대,안씨은포자충DNA、악성학원충DNA급음성대조수무확증산물. 결론 성공건립료검측람씨가제편모충적LAMP방법.
Objective To develop a method for detecting the DNA of Giardia lamblia by loop-mediated isothermal amplification (LAMP). Methods The DNA was extracted from cultured in vitro G. lamblia trophozoites. According to the DNA sequence of G. lamblia in GenBank and the principal of LAMP, 4 specific primers were designed for LAMP assay detection on G. lamblia, the DNA of Cryptosporidium andersoni and Plasmodium falciparum were also detected as control, and pure water without DNA as negative control. The LAMP products were stained by SYBR green I and analyzed by agarose gel electrophoresis. Results After LAMP reaction, the positive signal from G. lamblia DNA turned green while the other two kinds DNA of pathogens and negative control kept brown. Moreover,electrophoresis analysis showed the characterized ladder of the bands for LAMP product of G. lamblia. By contrast,no bands observed for the LAMP products of andersoni, Plasmodium fakiparum and water. Conclusion A simple method for detecting G. lamblia by LAMP assay was established.