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鼠伤寒沙门氏菌中抗生素抗性决定因子的可逆易位

Reversible translocation of antibiotic resistance determinants in Salmonella ordonez.

作者信息

Roussel A, Carlier C, Gerbaud G, Chabbert Y A

出版信息

Mol Gen Genet. 1979 Jan 16;169(1):13-25. doi: 10.1007/BF00267540.

Abstract

Salmonella ordonez (BM 2000) codes for kanamycin (Km, aphA), ampicillin (Ap), streptomycin (SmSp:aadA and Sm:aphC), chloramphenicol (Cm), tetracycline (Tc) and sulfonamide (Su) resistances and for production of colicin Ib (Cib). Genetical analysis by incompatibility testing, conjugation, transformation and physical studies using electron microscopy, agarose gel electrophoresis, led us to associate the Km and Cib characters to a 98.7 kilobase (kb) IncI1 plasmid (pIP565), and the Sm (aphC) and Su determinants to a 8.3 kb plasmid (pIP605). The ApCmSmSp(aadA)SuTc determinants were not associated in BM2000 S. ordonez with a plasmid structure. Following conjugation of S. ordonez to E. coli, the ApCmSmSpSuTc determinants were found stably associated with a single plasmid structure (pIP173, 127.5 kb) belonging to IncI1 group. Agarose gel electrophoresis of plasmid DNA restriction endonuclease digests and electron microscopy heteroduplex analysis showed that the acquisition of the ApCmSmSpSuTc determinants resulted from the insertion into pIP565 of a 28.8 kb DNA sequence. This sequence coding for ApCmSmSpSuTu resistances in S. ordonez could be translocated either to pIP565 plasmid or to several IncI1 plasmids but never to plasmids belonging to IncW, IncP or IncFII, suggesting the existence of specific sequences on the IncI1 receptor plasmids. Moreover, R-determinants were translocated back "en bloc" from pIP173 to the chromosome of a susceptible S. ordanez. The results were consistent with the presence in BM2000 S. ordonez chromosomal DNA of an integrated translocatable sequence encoding ApCmSmSpSuTc resistances. Such a structural association could account for the stability of these resistances in the Salmonella ordonez serotype.

摘要

奥多涅斯沙门氏菌(BM 2000)编码卡那霉素(Km,aphA)、氨苄青霉素(Ap)、链霉素(SmSp:aadA和Sm:aphC)、氯霉素(Cm)、四环素(Tc)和磺胺类药物(Su)抗性,并产生大肠杆菌素Ib(Cib)。通过不相容性测试、接合、转化以及使用电子显微镜、琼脂糖凝胶电泳的物理研究进行的遗传分析,使我们将Km和Cib特性与一个98.7千碱基(kb)的IncI1质粒(pIP565)相关联,并将Sm(aphC)和Su决定簇与一个8.3 kb的质粒(pIP605)相关联。在BM2000奥多涅斯沙门氏菌中,ApCmSmSp(aadA)SuTc决定簇与质粒结构无关。在奥多涅斯沙门氏菌与大肠杆菌接合后,发现ApCmSmSpSuTc决定簇与一个属于IncI1组的单一质粒结构(pIP173,127.5 kb)稳定相关。质粒DNA限制性内切酶消化产物的琼脂糖凝胶电泳和电子显微镜异源双链分析表明,ApCmSmSpSuTc决定簇的获得是由于一个28.8 kb的DNA序列插入到pIP565中。该序列在奥多涅斯沙门氏菌中编码ApCmSmSpSuTu抗性,它可以转移到pIP565质粒或几个IncI1质粒上,但从未转移到属于IncW、IncP或IncFII的质粒上,这表明IncI1受体质粒上存在特定序列。此外,R决定簇从pIP173“整体”转移回一个敏感的奥多涅斯沙门氏菌的染色体上。这些结果与BM2000奥多涅斯沙门氏菌染色体DNA中存在一个编码ApCmSmSpSuTc抗性的整合可转移序列一致。这种结构关联可以解释这些抗性在奥多涅斯沙门氏菌血清型中的稳定性。

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