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Heterogeneity of the streptokinase gene in group A streptococci.

机译:A组链球菌中链激酶基因的异质性。

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A molecular epidemiological study was conducted to determine the distribution of the streptokinase gene in group A streptococcal strains of different M types and in other streptococcal species. Plasmid pNC1, containing only the internal coding sequence of the streptokinase gene from group C streptococcal strain H46A, was used as a DNA probe in colony and Southern hybridization experiments. Only the pathogenic group A, C, and G streptococci contained a streptokinase gene; 12 other Lancefield group strains did not. A total of 134 group A strains, including 61 M types and 6 T types, were tested. Although only 62% (83 of 134) of the strains tested showed positive streptokinase activity by the casein-plasminogen overlay assay, all strains contained the streptokinase gene as evidenced by strong hybridization with the pNC1 probe. Southern blot DNA hybridizations were carried out with 101 strains of group A streptococci. The restriction enzymes HindIII and HaeIII were used to digest the genomic DNA. Six hybridization patterns were observed after HindIII digestion. Double hybridization bands appeared in all of the patterns, which indicated the existence of a highly conserved HindIII site. More complex hybridization results were obtained after HaeIII digestion. Twelve hybridization patterns were observed; three were characterized by a single hybridization band, and nine were characterized by double bands. Variations in hybridization patterns were observed in strains of both the same and different serotypes. The overall results at the gene level indicate that there is considerable heterogeneity among the streptokinases of group A streptococci, consistent with previous findings of immunological and chemical differences among streptokinases of group A streptococci.
机译:进行了分子流行病学研究,以确定链激酶基因在不同M型A组链球菌菌株和其他链球菌物种中的分布。仅含有来自C组链球菌菌株H46A的链激酶基因的内部编码序列的质粒pNC1在集落和Southern杂交实验中用作DNA探针。仅致病性A,C和G组链球菌含有链激酶基因; Lancefield组的其他12种菌株则没有。总共测试了134个A组菌株,包括61 M型和6 T型。尽管通过酪蛋白-纤溶酶原覆盖测定法仅测试的菌株中有62%(134个菌株中的83个)显示出正的链激酶活性,但所有菌株均含有链激酶基因,这是通过与pNC1探针的强杂交证明的。用101株A组链球菌进行Southern印迹DNA杂交。限制性内切酶HindIII和HaeIII用于消化基因组DNA。 HindIII消化后观察到六个杂交模式。在所有模式中均出现双杂交带,这表明存在高度保守的HindIII位点。 HaeIII消化后获得更复杂的杂交结果。观察到十二种杂交模式; 3个具有一个杂交带,9个具有双带。在相同和不同血清型的菌株中均观察到杂交模式的变化。在基因水平上的总体结果表明,A组链球菌之间的链激酶之间存在相当大的异质性,这与先前A组链球菌之间的免疫学和化学差异的发现一致。

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