Tally F P, Snydman D R, Shimell M J, Malamy M H
J Bacteriol. 1982 Aug;151(2):686-91. doi: 10.1128/jb.151.2.686-691.1982.
Bacteroides fragilis TMP10, which is clindamycin-erythromycin resistant (Clnr) and tetracycline resistant (Tetr), contains several plasmids and is capable of transferring drug resistance markers to suitable recipients. We were able to separate a 14.6-kilobase self-transmissible Clnr plasmid, pBFTM10, from the other plasmids of TMP10 in a tetracycline-sensitive recipient strain, B. fragilis TM4000. All Clnr transconjugants acquired an unaltered pBFTM10 and became plasmid donor strains. Transfer is proposed to occur by conjugation since it required to cell-to-cell contact of filter matings and was insensitive to DNase, but sensitive to chloroform treatment of donor cells. The efficiency of transfer of pBFTM10 in a Tets background (TM4003) was not affected by pretreatment of donor cells with clindamycin. A spontaneously occurring Clns derivative, pBFTM10 delta 1, suffered a deletion of DNA, which included a 4.4-kilobase EcoRI fragment. A complex interaction between the autonomous plasmid pBFTM10 and a tetracycline transfer element also present in strain TMP10 was observed since pretreatment of this donor with tetracycline or clindamycin resulted in a marked increase in transfer of both tetracycline and clindamycin resistance.
脆弱拟杆菌TMP10对克林霉素和红霉素耐药(Clnr)且对四环素耐药(Tetr),含有多个质粒,能够将耐药标记转移至合适的受体菌。我们能够在四环素敏感的受体菌株脆弱拟杆菌TM4000中,从TMP10的其他质粒中分离出一个14.6千碱基的可自我转移的Clnr质粒pBFTM10。所有Clnr转接合子都获得了未改变的pBFTM10并成为质粒供体菌株。推测转移是通过接合作用发生的,因为这需要滤膜交配时细胞与细胞的接触,并且对DNA对DNA酶不敏感,但对供体细胞的氯仿处理敏感。在Tets背景(TM4003)中,pBFTM10的转移效率不受用克林霉素预处理供体细胞的影响。一个自发产生的Clns衍生物pBFTM10 delta 1发生了DNA缺失,其中包括一个4.4千碱基的EcoRI片段。由于用四环素或克林霉素预处理该供体导致四环素和克林霉素耐药性的转移显著增加,因此观察到自主质粒pBFTM10与TMP10菌株中也存在的四环素转移元件之间存在复杂的相互作用。