中华地方病学杂志
中華地方病學雜誌
중화지방병학잡지
Chinese Journal of Endemiology
2015年
5期
322-325
,共4页
刘芳%常子丽%李建云%王建军%王浩珲%胡艳红%武正华%马志东%范龙兴
劉芳%常子麗%李建雲%王建軍%王浩琿%鬍豔紅%武正華%馬誌東%範龍興
류방%상자려%리건운%왕건군%왕호혼%호염홍%무정화%마지동%범룡흥
鼠疫%基因扩增%DNA引物
鼠疫%基因擴增%DNA引物
서역%기인확증%DNA인물
Plague%Gene amplification%DNA primer
目的 确定内蒙古鼠疫自然疫源地8种啮齿类动物细胞色素C氧化酶亚基Ⅰ (CO Ⅰ)基因扩增的最佳引物.方法 在内蒙古锡林郭勒盟和乌兰察布市,采集8个鼠种的动物,提取基因组DNA,选择6对已报道的扩增鼠CO Ⅰ基因的引物(F1/R1、F2/R2、F3/R3、F4/R4、VF/VR、F6/R6),PCR扩增8个鼠种的CO Ⅰ基因,对扩增的产物进行测序,并对测序结果进行生物信息学分析和比较.结果 达乌尔黄鼠扩增CO Ⅰ基因的最佳引物为F3/R3,达乌尔鼠兔和蒙古兔尾鼠均为鸡尾酒引物VF/VR,大沙鼠、蒙古毛足鼠和布氏田鼠均为F6/R6,五趾跳鼠为F2/R2,子午沙鼠为F1/R1.8种啮齿动物的CO Ⅰ序列进行比对后,发现所有DNA条码都是物种所独有,每个物种都有各自的鉴别位点.结论 不同鼠种在扩增CO Ⅰ基因时需要相应种属特异性引物;扩增多种鼠种时,优先选择F6/R6引物或鸡尾酒引物,针对特殊鼠种可选择该鼠种特异引物进行扩增.
目的 確定內矇古鼠疫自然疫源地8種齧齒類動物細胞色素C氧化酶亞基Ⅰ (CO Ⅰ)基因擴增的最佳引物.方法 在內矇古錫林郭勒盟和烏蘭察佈市,採集8箇鼠種的動物,提取基因組DNA,選擇6對已報道的擴增鼠CO Ⅰ基因的引物(F1/R1、F2/R2、F3/R3、F4/R4、VF/VR、F6/R6),PCR擴增8箇鼠種的CO Ⅰ基因,對擴增的產物進行測序,併對測序結果進行生物信息學分析和比較.結果 達烏爾黃鼠擴增CO Ⅰ基因的最佳引物為F3/R3,達烏爾鼠兔和矇古兔尾鼠均為鷄尾酒引物VF/VR,大沙鼠、矇古毛足鼠和佈氏田鼠均為F6/R6,五趾跳鼠為F2/R2,子午沙鼠為F1/R1.8種齧齒動物的CO Ⅰ序列進行比對後,髮現所有DNA條碼都是物種所獨有,每箇物種都有各自的鑒彆位點.結論 不同鼠種在擴增CO Ⅰ基因時需要相應種屬特異性引物;擴增多種鼠種時,優先選擇F6/R6引物或鷄尾酒引物,針對特殊鼠種可選擇該鼠種特異引物進行擴增.
목적 학정내몽고서역자연역원지8충교치류동물세포색소C양화매아기Ⅰ (CO Ⅰ)기인확증적최가인물.방법 재내몽고석림곽륵맹화오란찰포시,채집8개서충적동물,제취기인조DNA,선택6대이보도적확증서CO Ⅰ기인적인물(F1/R1、F2/R2、F3/R3、F4/R4、VF/VR、F6/R6),PCR확증8개서충적CO Ⅰ기인,대확증적산물진행측서,병대측서결과진행생물신식학분석화비교.결과 체오이황서확증CO Ⅰ기인적최가인물위F3/R3,체오이서토화몽고토미서균위계미주인물VF/VR,대사서、몽고모족서화포씨전서균위F6/R6,오지도서위F2/R2,자오사서위F1/R1.8충교치동물적CO Ⅰ서렬진행비대후,발현소유DNA조마도시물충소독유,매개물충도유각자적감별위점.결론 불동서충재확증CO Ⅰ기인시수요상응충속특이성인물;확증다충서충시,우선선택F6/R6인물혹계미주인물,침대특수서충가선택해서충특이인물진행확증.
Objective To determine the optimal primers of cytochrome C oxidase subunit Ⅰ (CO Ⅰ) gene for 8 kinds of rodents in natural epidemic focus of plague in Inner Mongolia.Methods In Xilingol League and Wulanchabu City of Inner Mongolia,eight kinds of rodents were collected and DNA was extracted;six pairs of targeted primers (F1/R1,F2/R2,F3/R3,F4/R4,VFNR,F6/R6) were used to amplify the CO Ⅰ gene of the 8 species by PCR;PCR products were send to biotechnology company for sequencing,and bioinformatics analysis of the sequencing results was conducted.Results F3/R3 was the optimal CO Ⅰ gene primer for Spermophilus dauricus;cocktail primer (VFNR) was the optimal CO Ⅰ gene primer for Ochotona daurica and Lagurus przewalskii;F6/R6 was the optimal CO Ⅰ gene primer for Rhombomys opimus,Phodopus campbelli and Microtus brandti;F2/R2 was the optimal CO Ⅰ gene primer for Allactaga sibirica,and F1/R1 was the optimal CO Ⅰ gene primer for Meriones meridianus.CO Ⅰ gene sequences of the 8 kinds of rodents were compared;DNA barcoding was unique in each rodent and every rodent had differential point.Conclusions Different rodent needs its own species-specific primers for CO Ⅰ gene amplification.Upon amplification of different rodent,cocktail or F6/R6 primers are the first choices,and choose the species-specific primers for particular species to amplify.