Buu-Hoï A, Horodniceanu T
J Bacteriol. 1980 Jul;143(1):313-20. doi: 10.1128/jb.143.1.313-320.1980.
Two antibiotic-resistant isolates of Streptococcus pneumoniae were investigated for conjugative transfer of their drug resistance markers into streptococcal (groups B and D) and pneumococcal (encapsulated and non-encapsulataed) recipients. Of these, 7 wild-type donor pneumococci transferred all their resistance markers (except Pc [penicillin], Su [sulfonamide], and Tp [trimethoprim]) into group D Streptococcus and non-encapsulated S. pneumoniae recipients at a low frequency (10(-5) to 10(-6)). The resistance markers transferred were Tc (tetracycline); Tc and Cm (chloramphenicol); Tc and MLS (macrolides, lincosamides, and streptogramin B); Tc, MLS, Km (kanamycin), and Cm. The transconjugants obtained retransferred their resistance markers into appropriate streptococcal or pneumococcal recipients or both. The resistance markers of streptococcal transconjugants could not be cured by chemical agents. All attempts to detect extra-chromosomal deoxyribonucleic acid from pneumococcal or streptococcal transconjugants were unsuccessful. The molecular weight of a streptococcal conjugative R plasmid (pIP501) was investigated after transfer into the non-encapsulated S. pneumoniae recipient and was found to be similar to that of the wild-type group B Streptococcus host (20 x 10(6)).
对两株肺炎链球菌的抗生素抗性分离株进行了研究,以检测其耐药性标记向链球菌(B组和D组)和肺炎球菌(有荚膜和无荚膜)受体的接合转移。其中,7株野生型供体肺炎球菌将其所有耐药性标记(除青霉素(Pc)、磺胺类药物(Su)和甲氧苄啶(Tp)外)以低频率(10⁻⁵至10⁻⁶)转移至D组链球菌和无荚膜肺炎链球菌受体。转移的耐药性标记有四环素(Tc);四环素和氯霉素(Cm);四环素和大环内酯类、林可酰胺类及链阳菌素B(MLS);四环素、MLS、卡那霉素(Km)和氯霉素。获得的转接合子将其耐药性标记重新转移至合适的链球菌或肺炎球菌受体,或两者均可。化学试剂无法消除链球菌转接合子的耐药性标记。所有从肺炎球菌或链球菌转接合子中检测染色体外脱氧核糖核酸的尝试均未成功。将链球菌接合性R质粒(pIP501)转移至无荚膜肺炎链球菌受体后,对其分子量进行了研究,发现其与野生型B组链球菌宿主的分子量相似(20×10⁶)。