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聚合酶链反应-酶切分型鉴定广州地区环境水源军团菌
引用本文:赵利伟,胡朝晖,宣瑞红,刘洋敏,朱庆义,王娟,詹晓勇. 聚合酶链反应-酶切分型鉴定广州地区环境水源军团菌[J]. 微生物学报, 2010, 50(11): 1532-1536
作者姓名:赵利伟  胡朝晖  宣瑞红  刘洋敏  朱庆义  王娟  詹晓勇
作者单位:广州金域医学检验中心,广州,510330
基金项目:国家标准化委员会资助项目(20081021-T-361);“十一五”国家科技重大专项课题(2008ZX10004-005)
摘    要:【目的】探讨聚合酶链反应-酶切分型在快速鉴定环境水源军团菌方面的应用价值,并了解广州地区环境水源军团菌的分布状况。【方法】对广州地区采集的44份环境水样,作军团菌分离培养,再对分离菌株进行16Sr DNA PCR-酶切分型鉴定、16S rDNA基因测序和mip基因测序鉴定。【结果】在广州地区环境水源分离的112株军团菌,经聚合酶链反应-酶切分型鉴定、16S rDNA基因测序和mip基因测序鉴定,检出嗜肺军团菌66株,非嗜肺军团菌46株,其中菲氏军团菌20株,戈氏军团菌17株,橡树岭军团菌7株,长滩军团菌2株。【结论】聚合酶链反应-酶切分型检测环境水源军团菌是一种简便、快速、特异的鉴定方法;在广州地区环境水源中普遍存在军团菌,主要是嗜肺军团菌,其次是菲氏军团菌,戈氏军团菌,橡树岭军团菌和长滩军团菌。

关 键 词:关键词:军团菌;环境水源;聚合酶链反应-酶切分型;基因测序
收稿时间:2010-04-10
修稿时间:2010-08-12

Identification of Legionella isolates from environmental water by using PCR combined with enzymatic digestion analysis
Liwei Zhao,Chaohui Hu,Ruihong Xuan,Yangmin Liu,Qingyi Zhu,Juan Wang and Xiaoyong Zhan. Identification of Legionella isolates from environmental water by using PCR combined with enzymatic digestion analysis[J]. Acta microbiologica Sinica, 2010, 50(11): 1532-1536
Authors:Liwei Zhao  Chaohui Hu  Ruihong Xuan  Yangmin Liu  Qingyi Zhu  Juan Wang  Xiaoyong Zhan
Affiliation:Guangzhou Kingmed Center for Clinical Laboratory, Guangzhou 510330, China;Guangzhou Kingmed Center for Clinical Laboratory, Guangzhou 510330, China;Guangzhou Kingmed Center for Clinical Laboratory, Guangzhou 510330, China;Guangzhou Kingmed Center for Clinical Laboratory, Guangzhou 510330, China;Guangzhou Kingmed Center for Clinical Laboratory, Guangzhou 510330, China;Guangzhou Kingmed Center for Clinical Laboratory, Guangzhou 510330, China;Guangzhou Kingmed Center for Clinical Laboratory, Guangzhou 510330, China
Abstract:Abstract: [Objective] To evaluate polymerase chain reaction (PCR) combined with enzymatic digestion for identification of Legionella, and distribution of Legionella in environmental water systems in Guangzhou. [Methods] Forty-four water samples collected in Guangzhou were cultivated for Legionella were identified by PCR-enzymatic digestion, 16S rDNA and mip gene sequencing analysis. [Results] Sixty-six strains of Legionella pneumophila and 46 Non-L. pneumophila were identified by PCR-enzymatic digestion and sequencing analysis. Forty-six strains of Non-L. pneumophila included 20 strains of L. feeilei, 17 L. gormanii, 7 L. oakridgensis and 2 L. longbeachae. [Conclusion] PCR combined with enzymatic digestion is a simple, rapid, and specific method for the identification of Legionella. L. pneumophila was distributed widely, followed by L. feeilei, L. gormanii, L. oakridgensis and L. longbeachae, in environmental water in Guangzhou area.
Keywords:Keywords: Legionella   Environmental water   PCR combined with enzymatic digestion   Gene sequencing
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