首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Analysis of the complete nucleotide sequence of an Actinobacillus pleuropneumoniae streptomycin-sulfonamide resistance plasmid, pMS260
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Analysis of the complete nucleotide sequence of an Actinobacillus pleuropneumoniae streptomycin-sulfonamide resistance plasmid, pMS260

机译:胸膜肺炎放线杆菌链霉素-磺酰胺耐药质粒pMS260的完整核苷酸序列分析

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pMS260 is an 8.1-kb non-conjugative but mobilizable plasmid that was isolated from Actinobacillus pleuropneumoniae and encodes streptomycin (SM) and sulfonamide (SA) resistances. The analysis of the complete nucleotide sequence of the plasmid revealed a high degree of similarity between pMS260 and the broad-host-range IncQ family plasmids. pMS260 had a single copy of an origin of vegetative replication (oriV). This sequence was identical to a functional oriV of the IncQ-like plasmid plE1130 that had been exogenously isolated from piggery manure. However, pMS260 did not carry the second IncQ plasmid RSF1010-like oriV region present in pIE1130. A pIE1130-identical transfer origin was also found in pMS260. In addition, the deduced amino acid sequences from 10 open reading frames identified in pMS260 were entirely or nearly identical to those from genes for the replication, mobilization, and SM-SA resistance of pIE1130, indicating that pMS260 belongs to the IncQ-1 gamma subgroup. pMS260 is physically indistinguishable from pIE1130 apart from two DNA regions that contain the chloramphenicol and kanamycin resistance genes (catIII and aphI, respectively) and the second oriV-like region of pIE1130. The codon bias analysis of each gene of pIE1130 and the presence of potential recombination sites in the sulII-strA intergenic regions suggest that pIE1130 seems to have acquired the catIII and aphI genes more recently than the other genes of plE1130. Therefore, pMS260 may be the ancestor of plE1130. Information regarding the broad-host-range replicon of pMS260 will be useful in the development of genetic systems for a wide range of bacteria including A. pleuropneumoniae. (C) 2003 Elsevier Inc. All rights reserved. [References: 20]
机译:pMS260是一个8.1 kb非共轭但可动员的质粒,该质粒从胸膜肺炎放线杆菌中分离,编码链霉素(SM)和磺酰胺(SA)耐药性。对该质粒完整核苷酸序列的分析表明,pMS260与宽宿主范围的IncQ家族质粒之间具有高度相似性。 pMS260具有营养复制原点(oriV)的单个副本。该序列与已经从猪粪中外源分离的IncQ样质粒pIE1130的功能oriV相同。然而,pMS260没有携带pIE1130中存在的第二个IncQ质粒RSF1010样oriV区。在pMS260中也发现了pIE1130相同的转移起点。此外,从pMS260中鉴定的10个开放阅读框推导的氨基酸序列与pIE1130的复制,动员和SM-SA抗性基因完全相同或几乎相同,表明pMS260属于IncQ-1γ亚组。除了两个含有氯霉素和卡那霉素抗性基因(分别为catIII和aphI)的DNA区域以及pIE1130的第二个oriV样区域之外,pMS260与pIE1130在物理上没有区别。对pIE1130的每个基因的密码子偏倚分析以及sulII-strA基因间区域中潜在重组位点的存在表明,pIE1130似乎比plE1130的其他基因更早地获得了catIII和aphI基因。因此,pMS260可能是plE1130的祖先。有关pMS260的广泛宿主复制子的信息将有助于开发包括胸膜肺炎链球菌在内的多种细菌的遗传系统。 (C)2003 Elsevier Inc.保留所有权利。 [参考:20]

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