首页> 美国卫生研究院文献>Canadian Journal of Comparative Medicine >Plasmid transfer and plasmid-mediated genetic exchange in Brucella abortus.
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Plasmid transfer and plasmid-mediated genetic exchange in Brucella abortus.

机译:流产布鲁氏菌中的质粒转移和质粒介导的遗传交换。

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摘要

Naturally-occurring plasmids and gene transfer mechanisms have not yet been reported in brucellae. Here we show that Brucella abortus is capable of maintaining and transferring the broad-host-range plasmids pTH10 (IncP), pSa (IncW) and R751 (IncP), and describe pTH10-mediated transfer of B. abortus chromosomal genes to Escherichia coli. All three plasmids transferred by conjugation from E. coli to B. abortus S19, and from B. abortus S19 to B. abortus 292 (biovar 4). They were stably maintained with no effect on biotyping characteristics. Plasmid pTH10 is a Tn1-containing derivative of RP4. It confers temperature-sensitive resistance to kanamycin, tetracycline and ampicillin to E. coli, but its tetracycline resistance and temperature sensitivity were poorly expressed in B. abortus. Plasmids pTH10 and pSa both transferred from B. abortus to E. coli DP50, a strain that is auxotrophic for diaminopimelic acid (DAP) Plasmid pTH10 (but not pSa) mobilized Brucella chromosomal gene(s) for DAP synthesis to DP50, yielding non-DAP-requiring (NDR) transconjugants. Neither plasmid transferred the NDR marker from their original E. coli host strains, nor did pTH10 transfer it from NDR transconjugants. Escherichia coli NDR transconjugant EP8.11 was cured of pTH10 by passage at the nonpermissive temperature, but retained the NDR marker and the Tn1-encoded resistance to ampicillin, indicating Tn1-mediated integration of Brucella chromosomal DNA into the E. coli chromosome.
机译:布鲁氏菌病尚未报道天然存在的质粒和基因转移机制。在这里,我们显示流产布鲁氏菌能够维持和转移宿主范围广泛的质粒pTH10(IncP),pSa(IncW)和R751(IncP),并描述pTH10介导的流产布鲁氏菌染色体基因向大肠杆菌的转移。所有三种质粒通过缀合从大肠杆菌转移到流产双歧杆菌S19,并且从流产双歧杆菌S19转移到流产双歧杆菌292(biovar 4)。它们被稳定地保持,对生物型特征没有影响。质粒pTH10是RP4的含Tn1的衍生物。它赋予对卡那霉素,四环素和氨苄青霉素对大肠杆菌具有温度敏感性,但在流产芽孢杆菌中其四环素抗性和温度敏感性均较差。质粒pTH10和pSa都从流产双歧杆菌转移到大肠杆菌DP50中,该菌株对二氨基庚二酸(DAP)是营养缺陷的菌株质粒pTH10(而非pSa)将布鲁氏菌的染色体基因动员用于DAP合成,从而产生DP50。需要DAP(NDR)的转导结合剂。质粒既不从其原始大肠杆菌宿主菌株中转移NDR标记,也没有pTH10从NDR转导结合体中转移它。大肠杆菌NDR转导结合体EP8.11通过在非允许温度下通过而治愈了pTH10,但保留了NDR标记和Tn1编码的氨苄青霉素抗性,表明Tn1介导的布鲁氏菌染色体DNA整合到大肠杆菌染色体中。

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