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Intergeneric transfer of the conjugative tetracycline-resistance transposon Tn916 from Streptococcus faecalis to Staphylococcus aureus

机译:共轭四环素抗性转座子Tn916从粪链球菌向金黄色葡萄球菌的种间转移

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摘要

Three Streptococcus faecalis tetracycline-resistance conjugal plasmids carrying Tn916 were studied by using protoplast fusions, protoplast transformations, and membrane-filter matings between S. faecalis and Staphylococcus aureus. Two of these plasmids (pAD1: :Tn916 and pPD5: :Tn916)were capable of transfer to S. aureus by membrane-filter matings. These plasmids remained intact and expressed Tc(\u27r) in S. aureus. Further transfers by membrane-filter matings among strains of S. aureus occurred only with pAD1: :Tn916, which transferred into the restrictionless lytic group II S. aureus strain 879R4. The third plasmid, pPD1: :Tn916, could not be demonstrated to transfer from S. faecalis to S. aureus by membrane-filter matings, protoplast fusions, or protoplast transformations;Transposition of Tn916 from pAD1: :Tn916 to the chromosome of lytic group I S. aureus has been demonstrated. DNA hybridization profiles obtained frm Southern transfers showed that Tn916 inserted at various sites on the S. aureus chromosome. In two instances (S. aureus ISP823 and S. faecalis ISP871), two copies of Tn916 were shown to be present at separate chromosomal sites. Mapping data obtained by transformation showed that Tn916 chromosomal insertions occurred near ilv-129, tyrB282, ala-126, fus-149, and thrB-trpE. Identical results were obtained when biotinylated pAD1: :Tn916 and 32P-labelled pAD1: :Tn916 probes were used to detect Tn916-containing sequences in hybridization experiments;pAD1: :Tn916 and pPD5: :Tn916, when transformed into protoplasts of S. aureus, gave rise to transformants containing the streptococcal plasmid alone, the streptococcal plasmid plus pPQ12, or pPQ12 alone. pPQ12 is a 2.8-Mdal Tc(\u27r) plasmid in incompatibility group 3, and has the same restriction pattern and incompatibility grouping as pPQ3 and pSA0301, two representative naturally-occurring Tc(\u27r) plasmids of S. aureus. pPQ12 did not hybridize to pAD1: :Tn916 but did hybridize to several naturally occurring Tc(\u27r) plasmids of S. aureus as well as to lytic group I, II, and III S. aureus chromosomal DNA. It was concluded that pPQ12 is integrated in the S. aureus chromosome and does not express Tc(\u27r) from the chromosomal site.
机译:通过使用原生质体融合,原生质体转化以及粪肠球菌和金黄色葡萄球菌之间的膜滤器交配,研究了三种携带Tn916的粪链球菌四环素抗性结合质粒。这些质粒中的两个(pAD1 :: Tn916和pPD5 :: Tn916)能够通过膜滤器交配转移至金黄色葡萄球菌。这些质粒保持完整,并在金黄色葡萄球菌中表达Tc(\ u27r)。仅通过pAD1 :: Tn916,金黄色葡萄球菌菌株之间通过膜滤器交配进一步转移,而pAD1 :: Tn916则转移到无限制的溶血性II型金黄色葡萄球菌菌株879R4中。无法通过膜滤器交配,原生质体融合或原生质体转化证明第三种质粒pPD1 :: Tn916从粪链球菌转移到金黄色葡萄球菌; Tn916从pAD1 :: Tn916到易位组染色体的转座我已经证明了金黄色葡萄球菌。从Southern转移获得的DNA杂交图谱表明Tn916插入了金黄色葡萄球菌染色体的各个位点。在两种情况下(金黄色葡萄球菌ISP823和粪链球菌ISP871),Tn916的两个副本显示在单独的染色体位点。通过转化获得的作图数据显示Tn916染色体插入发生在ilv-129,tyrB282,ala-126,fus-149和thrB-trpE附近。当生物素化的pAD1 :: Tn916和32P标记的pAD1 :: Tn916探针在杂交实验中用于检测含Tn916的序列时,获得了相同的结果;当将pAD1 :: Tn916和pPD5 :: Tn916转化为金黄色葡萄球菌的原生质体时,产生仅包含链球菌质粒,链球菌质粒加pPQ12或仅pPQ12的转化子。 pPQ12是不相容性组3中的2.8-Mdal Tc(\ u27r)质粒,与金黄色葡萄球菌的两个天然存在的Tc(\ u27r)质粒pPQ3和pSA0301具有相同的限制模式和不相容性分组。 pPQ12不与pAD1 :: Tn916杂交,但与金黄色葡萄球菌的几种天然存在的Tc(\ u27r)质粒以及裂解的I,II和III金黄色葡萄球菌染色体DNA杂交。结论是pPQ12整合在金黄色葡萄球菌染色体中,并且不从染色体位点表达Tc(\ u27r)。

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  • 作者

    Jones, Joanne Marie;

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  • 年度 1985
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  • 原文格式 PDF
  • 正文语种 en
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