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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Nucleotide sequence and transfer properties of two novel types of Actinobacillus pleuropneumoniae plasmids carrying the tetracycline resistance gene tet(H).
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Nucleotide sequence and transfer properties of two novel types of Actinobacillus pleuropneumoniae plasmids carrying the tetracycline resistance gene tet(H).

机译:带有四环素抗性基因tet(H)的两种新型胸膜肺炎放线杆菌细菌质粒的核苷酸序列和转移特性。

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OBJECTIVES: To analyse the sequence and transfer properties of two tetracycline resistance plasmids found in clinical isolates of Actinobacillus pleuropneumoniae in order to assess their role in the spread of tetracycline resistance. METHODS: The plasmids designated p9956 and p12494 were purified from A. pleuropneumoniae and completely sequenced. The transfer properties of both plasmids were evaluated by electroporation and/or conjugation into Pasteurella multocida and Escherichia coli. RESULTS: Both plasmids showed a modular structure consisting of three regions involved in mobilization, tetracycline resistance or replication. The mobilization regions included the mobA gene, encoding a relaxase, a protein involved in plasmid transfer. The tetracycline resistance regions were closely related and consisted of the tet(H) gene and its repressor gene tetR. The tetracycline resistance phenotype was transferred successfully to P. multocida and in the case of p9956 also to E. coli by electroporation of the plasmids. Moreover, plasmid p9956 could be mobilized in E. coli with the assistance of RP4 conjugal transfer functions. CONCLUSIONS: For the first time, the complete sequences of two tet(H)-carrying plasmids from A. pleuropneumoniae were determined. These two plasmids differed from one another and from known tet(H)-carrying plasmids from Pasteurella or Mannheimia spp. Structural analysis confirmed that these plasmids consisted of segments that have been previously detected in members of the families Pasteurellaceae and Enterobacteriaceae.
机译:目的:分析胸膜肺炎放线杆菌临床分离物中发现的两个四环素抗性质粒的序列和转移特性,以评估它们在四环素抗性传播中的作用。方法:从胸膜肺炎链球菌中纯化出命名为p9956和p12494的质粒,并进行完整测序。通过电穿孔和/或缀合到多杀巴斯德氏菌和大肠杆菌中来评估两种质粒的转移特性。结果:两个质粒均显示出模块结构,该模块结构由涉及动员,四环素抗性或复制的三个区域组成。动员区域包括mobA基因,该基因编码松弛酶,一种参与质粒转移的蛋白质。四环素抗性区域密切相关,由tet(H)基因及其阻遏基因tetR组成。通过对质粒进行电穿孔,将四环素抗性表型成功转移至多杀性巴氏杆菌,对于p9956,也成功转移至大肠杆菌。此外,质粒p9956可借助RP4结合转移功能在大肠杆菌中动员。结论:首次确定了胸膜肺炎链球菌的两个携带tet(H)的质粒的完整序列。这两个质粒彼此不同,与巴斯德氏菌或曼海姆氏菌属已知的携带tet(H)的质粒不同。结构分析证实,这些质粒由先前在巴斯德杆菌科和肠杆菌科的成员中检测到的区段组成。

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