|本期目录/Table of Contents|

[1]余艳玲,彭昊,冯世文,等.罗非鱼无乳链球菌环介导等温扩增(LAMP)检测技术的建立及应用[J].江苏农业科学,2019,47(13):200-203.
 Yu Yanling,et al.Establishment and application of real-time loop-mediated isothermal amplification techniques for detection of Streptococcus agalactiae in tilapia[J].Jiangsu Agricultural Sciences,2019,47(13):200-203.
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罗非鱼无乳链球菌环介导等温扩增(LAMP)
检测技术的建立及应用
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《江苏农业科学》[ISSN:1002-1302/CN:32-1214/S]

卷:
第47卷
期数:
2019年第13期
页码:
200-203
栏目:
畜牧兽医与水产蚕桑
出版日期:
2019-07-31

文章信息/Info

Title:
Establishment and application of real-time loop-mediated isothermal amplification techniques for detection of Streptococcus agalactiae in tilapia
作者:
余艳玲1 彭昊2 冯世文2 张永德1 罗洪林1 李军2
1.广西水产科学研究院/广西水产遗传育种与健康养殖重点实验室,广西南宁 530021;
2.广西兽医研究所/广西兽医生物技术重点实验室,广西南宁 530001
Author(s):
Yu Yanlinget al
关键词:
罗非鱼无乳链球菌(GBS)环介导等温扩增(LAMP)
Keywords:
-
分类号:
S917
DOI:
-
文献标志码:
A
摘要:
针对罗非鱼无乳链球菌Sip基因建立了LAMP检测方法,并对野外样本进行了无乳链球菌的调查研究。结果表明,目标Sip基因可在63 ℃ 40 min内被LAMP检测到,比PCR快约2 h,其DNA检测最低浓度为3.55×10-5 ng/μL,灵敏度比PCR高100倍,且对参考细菌无扩增。野外样品检测结果表明,运用LAMP检测技术对GBS的检出率为813%,比PCR高约20.0%。应用LAMP和PCR分别检测健康罗非鱼GBS检出率4.4%和2.2%,检测池塘水样品GBS检出率分别为10.0%和6.7%。
Abstract:
-

参考文献/References:

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备注/Memo

备注/Memo:
收稿日期:2018-04-08
基金项目:国家自然科学基金面上项目(编号:31372553);广西自然科学基金(编号:2015GXNSFAA139068)。
作者简介:余艳玲(1976—),女,陕西咸阳人,硕士,工程师,主要从事水产动物分子生物学研究。E-mail:yaeling@126.com。
通信作者:李军,副研究员,主要从事动物疫病防控与病原分子生物学研究工作。E-mail:jlee9981@163.com。
更新日期/Last Update: 2019-07-05