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从生发酵香肠中分离出的粪肠球菌接合型多耐药质粒pRE25的分子结构与进化

Molecular structure and evolution of the conjugative multiresistance plasmid pRE25 of Enterococcus faecalis isolated from a raw-fermented sausage.

作者信息

Teuber Michael, Schwarz Franziska, Perreten Vincent

机构信息

Laboratory of Food Microbiology, ETH Zurich, Zurich CH-8092, Switzerland.

出版信息

Int J Food Microbiol. 2003 Dec 1;88(2-3):325-9. doi: 10.1016/s0168-1605(03)00195-8.

Abstract

Plasmid pRE25 from Enterococcus faecalis transfers resistances against kanamycin, neomycin, streptomycin, clindamycin, lincomycin, azithromycin, clarithromycin, erythromycin, roxithromycin, tylosin, chloramphenicol, and nourseothricin sulfate by conjugation in vitro to E. faecalis JH2-2, Lactococcus lactis Bu2, and Listeria innocua L19. Its nucleotide sequence of 50237 base pairs represents the largest, fully sequenced conjugative multiresistance plasmid of enterococci (Plasmid 46 (2001) 170). The gene for chloramphenicol resistance (cat) was identified as an acetyltransferase identical to the one of plasmid pIP501 of Streptococcus agalactiae. Erythromycin resistance is due to a 23S ribosomal RNA methyl transferase, again as found in pIP501 (ermB). The aminoglycoside resistance genes are packed in tandem as in transposon Tn5405 of Staphylococcus aureus: an aminoglycoside 6-adenyltransferase, a streptothricin acetyl transferase, and an aminoglycoside phosphotransferase.). Identical resistance genes are known from pathogens like Streptococcus pyogenes, S. agalactiae, S. aureus, Campylobacter coli, Clostridium perfringens, and Clostridium difficile. pRE25 is composed of a 30.5-kbp segment almost identical to pIP501. Of the 15 genes involved in conjugative transfer, 10 codes for putative transmembrane proteins (e.g. trsB, traC, trsF, trsJ, and trsL). The enterococcal part is joined into the pIP501 part by insertion elements IS1216V of E. faecium Tn1545 (three copies), and homologs of IS1062 (E. faecalis) and IS1485 (E. faecium). pRE25 demonstrates that enterococci from fermented food do participate in the molecular communication between Gram-positive and Gram-negative bacteria of the human and animal microflora.

摘要

粪肠球菌的质粒pRE25通过体外接合作用,将对卡那霉素、新霉素、链霉素、克林霉素、林可霉素、阿奇霉素、克拉霉素、红霉素、罗红霉素、泰乐菌素、氯霉素和硫酸诺尔斯菌素的抗性转移至粪肠球菌JH2-2、乳酸乳球菌Bu2和无害李斯特菌L19。其50237个碱基对的核苷酸序列代表了粪肠球菌中已完全测序的最大的接合型多抗性质粒(《质粒》46(2001)170)。氯霉素抗性基因(cat)被鉴定为一种乙酰转移酶,与无乳链球菌的质粒pIP501中的乙酰转移酶相同。红霉素抗性是由一种23S核糖体RNA甲基转移酶引起的,同样也存在于pIP501中(ermB)。氨基糖苷类抗性基因像金黄色葡萄球菌的转座子Tn5405那样串联排列:一种氨基糖苷6-腺苷转移酶、一种链丝菌素乙酰转移酶和一种氨基糖苷磷酸转移酶。化脓性链球菌、无乳链球菌、金黄色葡萄球菌、大肠弯曲菌、产气荚膜梭菌和艰难梭菌等病原体中也存在相同的抗性基因。pRE25由一个与pIP501几乎相同的30.5千碱基对片段组成。在参与接合转移的15个基因中,有10个编码推定的跨膜蛋白(如trsB、traC、trsF、trsJ和trsL)。粪肠球菌部分通过粪肠球菌Tn1545的插入元件IS1216V(三个拷贝)以及IS1062(粪肠球菌)和IS1485(屎肠球菌)的同源物连接到pIP501部分。pRE25表明来自发酵食品的粪肠球菌确实参与了人和动物微生物群中革兰氏阳性菌和革兰氏阴性菌之间的分子交流。

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