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Mosaic plasmids and mosaic replicons: evolutionary lessons from the analysis of genetic diversity in IncFII-related replicons.嵌合质粒和嵌合复制子:来自IncFII相关复制子遗传多样性分析的进化启示
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Plasmid copy number control: an ever-growing story.质粒拷贝数控制:一个不断发展的故事。
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Food-related illness and death in the United States.美国与食物相关的疾病和死亡情况。
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Complete DNA sequence and structural analysis of the enteropathogenic Escherichia coli adherence factor plasmid.肠致病性大肠杆菌黏附因子质粒的完整DNA序列及结构分析
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Characterization of IS1541-like elements in Yersinia enterocolitica and Yersinia pseudotuberculosis.小肠结肠炎耶尔森菌和假结核耶尔森菌中类IS1541元件的特征分析
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小肠结肠炎耶尔森菌0:8血清型低钙反应质粒的完整DNA序列揭示了一种新的与毒力质粒相关的复制子。

Complete DNA sequence of Yersinia enterocolitica serotype 0:8 low-calcium-response plasmid reveals a new virulence plasmid-associated replicon.

作者信息

Snellings N J, Popek M, Lindler L E

机构信息

Department of Bacterial Diseases, Division of Communicable Diseases and Immunology, Walter Reed Army Institute of Research, Silver Spring, Maryland 20910-7500, USA.

出版信息

Infect Immun. 2001 Jul;69(7):4627-38. doi: 10.1128/IAI.69.7.4627-4638.2001.

DOI:10.1128/IAI.69.7.4627-4638.2001
PMID:11402007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC98540/
Abstract

The complete nucleotide sequence and organization of the Yersinia enterocolitica serotype 0:8 low-calcium-response (LCR) plasmid, pYVe8081, were determined. The 67,720-bp plasmid encoded all the genes known to be part of the LCR stimulon except for ylpA. Eight of 13 intact open reading frames of unknown function identified in pYVe8081 had homologues in Yersinia pestis plasmid pCD1 or in Y. enterocolitica serotype 0:9 plasmid pYVe227. A region of approximately 17 kbp showed no DNA identity to pCD1 or pYVe227 and contained six potential new genes, a possible new replicon, and two intact insertion sequence (IS) elements. One intact IS element, ISYen1, was a new IS belonging to the IS256 family. Several vestigial IS elements appeared different from the IS distribution seen in the other LCR plasmids. The RepA proteins encoded by Y. enterocolitica serotype 0:8 pYVeWA and pYVe8081 were identical. The putative pYVe8081 replicon showed significant homology to the IncL/M replicon of pMU407.1 but was only distantly related to the replicons of pCD1 and pYVe227. In contrast, the putative partitioning genes of pYVe8081 showed 97% DNA identity to the spy/sopABC loci of pCD1 and pYVe227. Sequence analysis suggests that Yersinia LCR plasmids are from a common ancestor but that Y. enterocolitica serotype 0:8 plasmid replicons may have evolved independently via cointegrate formation following a transposition event. The change in replicon structure is predicted to change the incompatibility properties of Y. enterocolitica serotype 0:8 plasmids from those of Y. enterocolitica serotype 0:9 and Y. pestis LCR plasmids.

摘要

测定了小肠结肠炎耶尔森菌0:8血清型低钙应答(LCR)质粒pYVe8081的完整核苷酸序列和结构。该67720碱基对的质粒编码了已知为LCR刺激子一部分的所有基因,但ylpA除外。在pYVe8081中鉴定出的13个功能未知的完整开放阅读框中有8个在鼠疫耶尔森菌质粒pCD1或小肠结肠炎耶尔森菌0:9血清型质粒pYVe227中有同源物。一个约17kbp的区域与pCD1或pYVe227没有DNA同源性,包含6个潜在的新基因、一个可能的新复制子和两个完整的插入序列(IS)元件。一个完整的IS元件ISYen1是属于IS256家族的一个新IS。几个残留的IS元件似乎与其他LCR质粒中的IS分布不同。小肠结肠炎耶尔森菌0:8血清型pYVeWA和pYVe8081编码的RepA蛋白是相同的。推测的pYVe8081复制子与pMU407.1的IncL/M复制子有显著同源性,但与pCD1和pYVe227的复制子只有远缘关系。相比之下,pYVe8081的推测分区基因与pCD1和pYVe227的spy/sopABC位点有97%的DNA同源性。序列分析表明,耶尔森菌LCR质粒来自一个共同祖先,但小肠结肠炎耶尔森菌0:8血清型质粒复制子可能在一次转座事件后通过共整合形成而独立进化。复制子结构的变化预计会改变小肠结肠炎耶尔森菌0:8血清型质粒与小肠结肠炎耶尔森菌0:9血清型和鼠疫耶尔森菌LCR质粒的不相容特性。