Trinh S, Haggoud A, Reysset G, Sebald M
Unité des Anaérobies, Institut Pasteur, Paris, France.
Microbiology (Reading). 1995 Apr;141 ( Pt 4):927-35. doi: 10.1099/13500872-141-4-927.
The genetic organization of two different 5-nitroimidazole (5-Ni) resistance genes was investigated: nimC and nimD from Bacteroides plasmids pIP419 and pIP421, respectively. The nimC gene (492 bp) and the nimD gene (495 bp) directed the synthesis of polypeptides with deduced molecular masses of 18.37 kDa and 18.48 kDa, respectively. The predicted proteins showed 67-83% identity and 78-91% similarity with the products of two other nimA and nimB genes previously described and could be derived from a common ancestral gene. An insertion sequence element (IS1170) was identified upstream of the nimC gene. IS1170 is 1604 bp in length and is flanked by imperfect inverted repeats (15 bp). IS1170 is similar to the Bacteroides insertion sequence element IS942 with an identity of 70% at the nucleotide level. The single copy of IS1170 present on plasmid pIP419 is integrated 24 bp upstream of the initiation codon of nimC. Similar genetic organization was found on plasmid pIP421. One copy of another insertion sequence (IS1169) was found 4 bp upstream of the first ATG codon of the nimD gene. This element (1325 bp) shows a strong homology at the nucleotide level (70% identity) with IS1186 and IS1168 found to be associated with the Bacteroides carbapenem resistance gene cfiA, and the 5-Nirgenes nimA and nimB, respectively. There is strong evidence that, as in the case of the cfiA gene, the transcription of the four nim genes so far studied is directed by outward-oriented promoters, carried on the right ends of the different insertion sequence elements.
对两个不同的5-硝基咪唑(5-Ni)抗性基因的遗传结构进行了研究:分别来自拟杆菌属质粒pIP419和pIP421的nimC和nimD。nimC基因(492 bp)和nimD基因(495 bp)分别指导合成推导分子量为18.37 kDa和18.48 kDa的多肽。预测的蛋白质与先前描述的另外两个nimA和nimB基因的产物具有67-83%的同一性和78-91%的相似性,可能源自一个共同的祖先基因。在nimC基因上游鉴定出一个插入序列元件(IS1170)。IS1170长度为1604 bp,两侧为不完美的反向重复序列(15 bp)。IS1170与拟杆菌属插入序列元件IS942相似,在核苷酸水平上具有70%的同一性。存在于质粒pIP419上的单拷贝IS1170整合在nimC起始密码子上游24 bp处。在质粒pIP421上发现了类似的遗传结构。在nimD基因的第一个ATG密码子上游4 bp处发现了另一个插入序列(IS1169)的一个拷贝。该元件(1325 bp)在核苷酸水平上与分别与拟杆菌属碳青霉烯抗性基因cfiA以及5-Nir基因nimA和nimB相关的IS1186和IS1168具有很强的同源性(70%同一性)。有强有力的证据表明,与cfiA基因的情况一样,迄今为止研究的四个nim基因的转录由位于不同插入序列元件右端的外向型启动子指导。