A群链球菌毒力的遗传控制。3。质粒诱导的“关闭”——对某些致病特性的影响。

L. E. Ravdonikas, P. Christensen, L. Burova, K. Grabovskaya, L. Björck, C. Schalén, M. Svensson, A. Totolian
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引用次数: 5

摘要

最近,我们报道了将测定红霉素耐药性(Emr)的质粒pERL1偶联转移到A组链球菌中,可以触发抗吞噬活性、黏附性、不透明因子和结合免疫球蛋白Fc-parts和β 2-微球蛋白的能力的表达。在本研究中,溴化乙锭处理Emr转缀合物允许选择“治愈”的红霉素敏感(Ems)突变体。这一过程不影响上述特征的表达。然而,当质粒pERL1再次转移到两个这样的突变体时,获得的“次级”Emr转偶联子显示缺乏这些特性。因此,我们的实验证明了同一质粒pERL1对a群链球菌的一些主要致病特性具有“开启”和“关闭”作用。
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The genetic control of virulence in group A streptococci. III. Plasmid-induced "switch-off"--effect on some pathogenic properties.
Recently, we reported that conjugal transfer of plasmid pERL1, determining i.a. erythromycin resistance (Emr), into group A streptococci could trigger the expression of anti-phagocytic activity, adhesiveness, opacity factor and capacity to bind immunoglobulin Fc-parts and beta 2-microglobulin. In the present study, ethidium bromide treatment of Emr transconjugants allowed the selection of "cured", erythromycin sensitive (Ems) mutants. This procedure did not affect the expression of the abovementioned characteristics. However, when plasmid pERL1 was again transferred to two such mutants, the "secondary", Emr transconjugants obtained showed lack of each of these properties. Our experiments thus demonstrated a "switch-on" as well as a "switch-off" effect, exerted by the same plasmid, pERL1, on some major pathogenic properties of group A streptococci.
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The genetic control of virulence in group A streptococci. III. Plasmid-induced "switch-off"--effect on some pathogenic properties. The microscopic diagnosis of Pneumocystis carinii. An evaluation of the gram, the methylene blue, and the Ziehl-Neelsen procedures. The genetic control of virulence in group A streptococci. II. Trigger effect by plasmids on anti-phagocytic activity, opacity factor and IgG and IgA Fc-receptors. Investigation of Micrococcaceae in a department of cardiac surgery. Biochemical characterization and sensitivity patterns of strains isolated from patients, staff, and air. Evaluation of Minibact, a new system for rapid identification of Enterobacteriaceae. Comparison of Minibact, Micro-ID and API 20E with a conventional method as reference.
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