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Self-Transmissible Mercury Resistance Plasmids with Gene-Mobilizing Capacity in Soil Bacterial Populations: Influence of Wheat Roots and Mercury Addition

机译:在土壤细菌种群中具有基因动员能力的自传递抗汞质粒:小麦根和汞添加的影响

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摘要

A set of mercury resistance plasmids was obtained from wheat rhizosphere soil amended or not amended with mercuric chloride via exogenous plasmid isolation by using Pseudomonas fluorescens R2f, Pseudomonas putida UWC1, and Enterobacter cloacae BE1 as recipient strains. The isolation frequencies were highest from soil amended with high levels of mercury, and the isolation frequencies from unamended soil were low. With P. putida UWC1 as the recipient, the isolation frequency was significantly enhanced in wheat rhizosphere compared to bulk soil. Twenty transconjugants were analyzed per recipient strain. All of the transconjugants contained plasmids which were between 40 and 50 kb long. Eight selected plasmids were distributed among five groups, as shown by restriction digestion coupled with a similarity matrix analysis. However, all of the plasmids formed a tight group, as judged by hybridization with two whole-plasmid probes and comparisons with other plasmids in dot blot hybridization analyses. The results of replicon typing and broad-host-range incompatibility (Inc) group-specific PCR suggested that the plasmid isolates were not related to any previously described Inc group. Although resistance to copper, resistance to streptomycin, and/or resistance to chloramphenicol was found in several plasmids, catabolic sequences were generally not identified. One plasmid, pEC10, transferred into a variety of bacteria belonging to the β and γ subdivisions of the class Proteobacteria and mobilized as well as retromobilized the IncQ plasmid pSUP104. A PCR method for detection of pEC10-like replicons was used, in conjunction with other methods, to monitor pEC10-homologous sequences in mercury-polluted and unpolluted soils. The presence of mercury enhanced the prevalence of pEC10-like replicons in soil and rhizosphere bacterial populations.
机译:使用荧光假单胞菌R2f,恶臭假单胞菌UWC1和阴沟肠杆菌BE1作为受体菌株,通过外源分离从小麦根际土壤中获得了一套抗汞质粒,该质粒经过氯化汞的修饰或未修饰。从含汞量高的土壤中分离出来的频率最高,而从未经改性的土壤中分离出来的频率低。与普通土壤相比,以恶臭假单胞菌UWC1为受体,小麦根际的隔离频率显着提高。每个受体菌株分析二十个转导结合体。所有转导结合体均包含长度为40至50 kb的质粒。如限制性酶切消化和相似性矩阵分析所示,将八个选择的质粒分布在五个组中。然而,通过与两种全质粒探针的杂交以及在斑点印迹杂交分析中与其他质粒的比较判断,所有质粒均形成一个紧密的基团。复制子分型和广泛宿主不相容性(Inc)组特异性PCR的结果表明,质粒分离物与任何先前描述的Inc组均不相关。尽管在几个质粒中发现了对铜的抗性,对链霉素的抗性和/或对氯霉素的抗性,但通常未鉴定出分解代谢序列。一种质粒pEC10转移到属于变形杆菌类β和γ子的多种细菌中,并动员和重新动员了IncQ质粒pSUP104。一种用于检测pEC10样复制子的PCR方法与其他方法一起用于监测汞污染和未污染土壤中的pEC10同源序列。汞的存在增强了土壤和根际细菌种群中pEC10样复制子的流行。

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