Su C J, Dallo S F, Baseman J B
Department of Microbiology, University of Texas Health Science Center, San Antonio 78284-7758.
J Clin Microbiol. 1990 Jul;28(7):1538-40. doi: 10.1128/jcm.28.7.1538-1540.1990.
Restriction enzyme fingerprinting of genomic DNA and Southern blots probed with subclones of the Mycoplasma pneumoniae cytadhesin P1 gene were used to characterize clinical isolates of M. pneumoniae. On the basis of the examination of 29 individual M. pneumoniae isolates, two distinct groups were established. Group 1, which displayed a 12-kilobase band following DNA digestion with HindIII, consisted of strain M129-B16 and three others obtained in the state of Washington during the 1960s. The remaining M. pneumoniae strains belonged to group 2, which lacked the 12-kilobase band and included samples from the 1940s, 1970s, and 1980s. This category also included the only M. pneumoniae strain isolated from the synovial fluid of an arthritic patient.
利用基因组DNA的限制性酶切指纹图谱以及用肺炎支原体细胞黏附素P1基因亚克隆进行探针杂交的Southern印迹法来鉴定肺炎支原体的临床分离株。基于对29株肺炎支原体分离株的检测,确定了两个不同的组。第1组在用HindIII消化DNA后显示出一条12千碱基的条带,由菌株M129 - B16和20世纪60年代在华盛顿州获得的其他三株菌株组成。其余的肺炎支原体菌株属于第2组,该组缺乏12千碱基的条带,包括20世纪40年代、70年代和80年代的样本。这一组还包括从一名关节炎患者滑液中分离出的唯一一株肺炎支原体菌株。