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首页> 外文期刊>Journal of bacteriology >Leptospira species categorized by arbitrarily primed polymerase chain reaction (PCR) and by mapped restriction polymorphisms in PCR-amplified rRNA genes.
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Leptospira species categorized by arbitrarily primed polymerase chain reaction (PCR) and by mapped restriction polymorphisms in PCR-amplified rRNA genes.

机译:钩端螺旋体物种通过任意引发的聚合酶链反应(PCR)和PCR扩增的rRNA基因中的定位限制性多态性进行分类。

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Reference strains from 48 selected serovars representing eight species of Leptospira were examined by two polymerase chain reaction (PCR)-based strategies. First, mapped restriction site polymorphisms (MRSP) were examined in PCR products from portions of rrs (16S rRNA gene) and rrl (23S rRNA gene). Twenty MRSP and 2 length polymorphisms were used to group reference strains into 16 MRSP profiles. Species assignments were consistent with those obtained by a second method, genomic fingerprinting with arbitrarily primed PCR, in which strains within a species were characterized by many shared arbitrarily primed PCR products. The results of both of these methods were in general agreement with those of previous studies that used DNA-DNA relatedness and confirmed the high level of divergence among the recognized species of Leptospira. However, Leptospira meyeri serovar ranarum and evansi strains were indistinguishable from some strains of Leptospira interrogans sensu stricto. Intervening sequences of about 485 to 740 bp were located near base 1230 in rrl of some strains.
机译:通过两种基于聚合酶链反应(PCR)的策略检查了来自代表48种钩端螺旋体的48个选定血清型的参考菌株。首先,在来自rrs(16S rRNA基因)和rrl(23S rRNA基因)部分的PCR产物中检查了定位限制性位点多态性(MRSP)。使用20个MRSP和2个长度多态性将参考菌株分组为16个MRSP谱。物种分配与通过第二种方法(通过任意引发的PCR进行的基因组指纹分析)获得的物种分配一致,其中物种内的菌株通过许多共享的任意引发的PCR产物进行表征。这两种方法的结果与以前使用DNA-DNA相关性的研究大体一致,并证实了公认的钩端螺旋体物种之间存在高度差异。然而,Meyeri serovar ranarum和evansi菌株与某些问号钩端螺旋体菌株之间没有区别。在一些菌株的rrl中,大约485至740bp的插入序列位于碱基1230附近。

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