中国奶牛
中國奶牛
중국내우
CHINA DAIRY CATTLE
2014年
16期
13-16
,共4页
王姗姗%马瑛%马梦婷%廉德平%高庆华
王姍姍%馬瑛%馬夢婷%廉德平%高慶華
왕산산%마영%마몽정%렴덕평%고경화
奶牛%不孕%抗精子抗体%宫颈黏液%间接ELISA
奶牛%不孕%抗精子抗體%宮頸黏液%間接ELISA
내우%불잉%항정자항체%궁경점액%간접ELISA
Dairy cows%Infertility%Anti-sperm antibody%Cervical mucus%Indirect ELISA
为建立检测奶牛宫颈黏液ASA免疫不孕的间接ELISA方法,以精子膜蛋白为包被抗原,进行奶牛宫颈黏液ASA的间接ELISA的优化试验。对27头ASA阳性不孕和29头ASA阳性可孕奶牛进行了间接ELISA检测标准的确定试验;对137头奶牛的宫颈黏液ASA免疫不孕进行间接ELISA临床检测。奶牛宫颈黏液ASA的间接ELISA优化条件为:抗原包被量为5μg/mL,宫颈黏液稀释度为1:5,宫颈黏液反应时间1h,二抗反应时间1.5h;奶牛宫颈黏液ASA免疫不孕检测的判定标准为:当样品OD490nm值大于0.513时判定为ASA阳性免疫不孕,当样品OD490nm值小于0.410时可孕,当样品OD490nm值介于0.410~0.513时为ASA阳性疑似,重复试验的变异系数均小于10%。对临床137份宫颈黏液样品进行检测,发现13头ASA阳性免疫不孕奶牛都不能受孕,而98头阴性结果牛中有89头怀孕。结果表明,间接ELISA可以有效检测奶牛宫颈黏液ASA免疫不孕。
為建立檢測奶牛宮頸黏液ASA免疫不孕的間接ELISA方法,以精子膜蛋白為包被抗原,進行奶牛宮頸黏液ASA的間接ELISA的優化試驗。對27頭ASA暘性不孕和29頭ASA暘性可孕奶牛進行瞭間接ELISA檢測標準的確定試驗;對137頭奶牛的宮頸黏液ASA免疫不孕進行間接ELISA臨床檢測。奶牛宮頸黏液ASA的間接ELISA優化條件為:抗原包被量為5μg/mL,宮頸黏液稀釋度為1:5,宮頸黏液反應時間1h,二抗反應時間1.5h;奶牛宮頸黏液ASA免疫不孕檢測的判定標準為:噹樣品OD490nm值大于0.513時判定為ASA暘性免疫不孕,噹樣品OD490nm值小于0.410時可孕,噹樣品OD490nm值介于0.410~0.513時為ASA暘性疑似,重複試驗的變異繫數均小于10%。對臨床137份宮頸黏液樣品進行檢測,髮現13頭ASA暘性免疫不孕奶牛都不能受孕,而98頭陰性結果牛中有89頭懷孕。結果錶明,間接ELISA可以有效檢測奶牛宮頸黏液ASA免疫不孕。
위건립검측내우궁경점액ASA면역불잉적간접ELISA방법,이정자막단백위포피항원,진행내우궁경점액ASA적간접ELISA적우화시험。대27두ASA양성불잉화29두ASA양성가잉내우진행료간접ELISA검측표준적학정시험;대137두내우적궁경점액ASA면역불잉진행간접ELISA림상검측。내우궁경점액ASA적간접ELISA우화조건위:항원포피량위5μg/mL,궁경점액희석도위1:5,궁경점액반응시간1h,이항반응시간1.5h;내우궁경점액ASA면역불잉검측적판정표준위:당양품OD490nm치대우0.513시판정위ASA양성면역불잉,당양품OD490nm치소우0.410시가잉,당양품OD490nm치개우0.410~0.513시위ASA양성의사,중복시험적변이계수균소우10%。대림상137빈궁경점액양품진행검측,발현13두ASA양성면역불잉내우도불능수잉,이98두음성결과우중유89두부잉。결과표명,간접ELISA가이유효검측내우궁경점액ASA면역불잉。
In order to establish an indirect ELISA method for detection of cervical mucus ASA immune infertility in dairy cows, this study was conducted using sperm membrane protein as coating antigen, and the optimization of indirect ELISA for dairy ASA of cervical mucus was tested. Totally 27 ASA positive infertile cows and 29 ASA positive pregnant cows were tested to determine indirect ELISA detection standard. The cervical mucus ASA from the 137 cows was detected using the indirect ELISA respectively. It was the indirect ELISA optimization condition for cervical mucus ASA in dairy cows that antigen coated amount was 5μg/mL, cervical mucus dilution was 1:5, cervical mucus reaction time was 1h, and reaction time of the enzyme-labeled second antibody was 1.5h. The criteria for cervical mucus ASA immune infertility in dairy cows was that the OD490nm values higher than 0.513 were determined as ASA positive immune infertility for the indirect ELISA and lower than 0.410 as negative fertility, and the OD490nmvaluesbetween0.410and0.513weredeterminedasASApositivesuspectedcases.Thecoefifcient of variation for the method was less than 10% in the repeated trials. The results of the 137 clinical samples of cervical mucus showed that the 13 ASA positive immune infertile cows could not conceive, and there were the 89 pregnancies among the 98 dairy cows with negative results. It can be concluded that the indirect ELISA was an effective method on investigation of ASA in cervical mucus of immune infertility dairy cows.