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支原体种属特异性PCR引物的设计及对细胞培养物支原体的检测
引用本文:倪红霞,陈立梅,张雷. 支原体种属特异性PCR引物的设计及对细胞培养物支原体的检测[J]. 北华大学学报(自然科学版), 2007, 8(6): 510-512
作者姓名:倪红霞  陈立梅  张雷
作者单位:北华大学,基础医学院,吉林,吉林,132013;军事医学科学院兽医研究所,吉林,长春,130062
摘    要:目的快速全面检测感染细胞、疫苗等多种生物制品中的支原体.方法从多种支原体的16SrRNA核酸序列中选择了两段高度保守的核酸序列,作为支原体种属特异性引物,对标本进行检测.结果用这对种属特异性引物对已知阳性的50份标本进行检测,检测结果显示全部为阳性.应用于实践,检测了89份疫苗标本,阳性率为31.4%,而用常规培养法检测阳性率为12.3%.结论用该种属特异性引物检测支原体具有检测速度快、检测灵敏度高、特异性强等优点.

关 键 词:支原体种属特异性引物  支原体  疫苗  细胞培养物
文章编号:1009-4822(2007)06-0510-03
收稿时间:2007-08-05
修稿时间:2007-08-05

Species-specific PCR for Identification of Common Contaminant Mycoplasma in Cell Culture
NI HONG-Xia,CHEN Li-mei,ZHANG Lei. Species-specific PCR for Identification of Common Contaminant Mycoplasma in Cell Culture[J]. Journal of Beihua University(Natural Science), 2007, 8(6): 510-512
Authors:NI HONG-Xia  CHEN Li-mei  ZHANG Lei
Abstract:Objective To detect mycoplasma species mainly infected in cell cultures and vaccinum.Methods PCR primers were designed according to the published sequences of 16 s rRNA of Mycoplasma in genbank.Mycoplasma species were detected by species-specific PCR.Results To detect 50 samples by using species-specific PCR,the results are all positive.In practice,we detected 89 vaccinum samples by using species-specific PCR method and culture method,31.4% and 12.3% respectively showed the positive.Conclusion The species-specific PCR for mycoplasma could identify mycoplasma with high speed,sensitivity and specification in cell culture.
Keywords:Species-specific PCR  Mycoplasma  Vaccinum  Cell culture
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