Hedreyda C T, Krause D C
Department of Microbiology, University of Georgia, Athens 30602, USA.
Infect Immun. 1995 Sep;63(9):3479-83. doi: 10.1128/iai.63.9.3479-3483.1995.
Transposon mutagenesis was used to analyze Mycoplasma pneumoniae cytadherence. Mycoplasmas were electroporated with Tn4001, and transformants were identified by antibiotic selection using gentamicin. The resulting colonies were screened for hemadsorption (HA) as an indicator for cytadherence. Six HA- colonies from independent transformations were isolated, filter cloned, and characterized in more detail. Southern hybridization analysis revealed that all six transposon insertions mapped to the same 252-kbp ApaI fragment and 19.5-kbp XhoI fragment. More detailed analysis localized the insertion to two adjacent EcoRI fragments. This site is distinct from the locus containing the genes for the high-molecular weight cytadherence-accessory proteins HMW1 and HMW3, and yet these proteins were absent from the protein profiles of all six transformants. To determine if transposon insertion was responsible for the HA- phenotype, reversion frequencies of the transformants were assessed after passage in the presence of antibiotic selection. In contrast to a spontaneously arising HMW-deficient variant, which reverted to an HA+ phenotype readily, no HA+ revertants were identified for any of the six transformants. These observations suggest that a potential regulatory locus that may be important in the expression of the HMW cytadherence-accessory proteins has been identified.
转座子诱变被用于分析肺炎支原体的细胞黏附。用Tn4001对支原体进行电穿孔,通过使用庆大霉素进行抗生素筛选来鉴定转化体。对所得菌落进行血吸附(HA)筛选,作为细胞黏附的指标。从独立转化中分离出6个HA-菌落,进行滤膜克隆并更详细地进行表征。Southern杂交分析表明,所有6个转座子插入都定位在同一个252-kbp的ApaI片段和19.5-kbp的XhoI片段上。更详细的分析将插入定位到两个相邻的EcoRI片段。该位点与包含高分子量细胞黏附辅助蛋白HMW1和HMW3基因的位点不同,然而所有6个转化体的蛋白质谱中都没有这些蛋白质。为了确定转座子插入是否导致了HA-表型,在抗生素选择存在的情况下传代后评估转化体的回复频率。与自发产生的HMW缺陷变体容易回复到HA+表型不同,6个转化体中没有一个被鉴定出有HA+回复体。这些观察结果表明,已鉴定出一个可能在HMW细胞黏附辅助蛋白表达中起重要作用的潜在调控位点。