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首页> 外文期刊>Applied and Environmental Microbiology >Vesicle-Mediated Transfer of Virulence Genes fromEscherichia coli O157:H7 to Other Enteric Bacteria
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Vesicle-Mediated Transfer of Virulence Genes fromEscherichia coli O157:H7 to Other Enteric Bacteria

机译:囊泡介导的毒力基因从大肠杆菌O157:H7转移至其他肠道细菌

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摘要

Membrane vesicles are released from the surfaces of many gram-negative bacteria during growth. Vesicles consist of proteins, lipopolysaccharide, phospholipids, RNA, and DNA. Results of the present study demonstrate that membrane vesicles isolated from the food-borne pathogen Escherichia coli O157:H7 facilitate the transfer of genes, which are then expressed by recipient Salmonella enterica serovar Enteritidis or E. coli JM109. Electron micrographs of purified DNA from E. coli O157:H7 vesicles showed large rosette-like structures, linear DNA fragments, and small open-circle plasmids. PCR analysis of vesicle DNA demonstrated the presence of specific genes from host and recombinant plasmids (hly, L7095, mobA, andgfp), chromosomal DNA (uidA andeaeA), and phage DNA (stx1 andstx2). The results of PCR and the Vero cell assay demonstrate that genetic material, including virulence genes, is transferred to recipient bacteria and subsequently expressed. The cytotoxicity of the transformed enteric bacteria was sixfold higher than that of the parent isolate (E. coli JM109). Utilization of the nonhost plasmid (pGFP) permitted the evaluation of transformation efficiency (ca. 103 transformants μg of DNA?1) and demonstrated that vesicles can deliver antibiotic resistance. Transformed E. coli JM109 cells were resistant to ampicillin and fluoresced a brilliant green. The role vesicles play in genetic exchange between different species in the environment or host has yet to be defined.
机译:生长期间,膜囊泡从许多革兰氏阴性细菌的表面释放出来。囊泡由蛋白质,脂多糖,磷脂,RNA和DNA组成。本研究结果表明,从食源性病原体大肠杆菌O157:H7中分离出的膜囊泡可促进基因的转移,然后由受体肠炎沙门氏菌血清肠炎沙门氏菌或大肠杆菌JM109表达。从大肠杆菌O157:H7囊泡纯化得到的DNA的电子显微照片显示出大的玫瑰花状结构,线性DNA片段和小的空心质粒。囊泡DNA的PCR分析表明存在来自宿主和重组质粒(hly,L7095,mobA和gfp),染色体DNA(uidA andeaeA)和噬菌体DNA(stx1和stx2)的特定基因。 PCR和Vero细胞测定的结果表明,遗传物质(包括毒力基因)已转移到受体细菌中并随后表达。转化的肠细菌的细胞毒性比亲本分离株(大肠杆菌JM109)高六倍。利用非宿主质粒(pGFP)可以评估转化效率(约103个转化子μgDNA?1),并证明囊泡可以提供抗生素抗性。转化的大肠杆菌JM109细胞对氨苄西林具有抗性,并发出亮绿色荧光。囊泡在环境或宿主中不同物种之间的遗传交换中所扮演的角色尚未确定。

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