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肠杆菌科中附加体介导的耐药性转移。III. 耐药因子的转导

Episome-mediated transfer of drug resistance in Enterobacteriaceae. III. Transduotion of resistance factors.

作者信息

WATANABE T, FUKASAWA T

出版信息

J Bacteriol. 1961 Aug;82(2):202-9. doi: 10.1128/jb.82.2.202-209.1961.

Abstract

Watanabe, Tsutomu (Keio University, Tokyo, Japan), and Toshio Fukasawa. Episome-mediated transfer of drug resistance in Enterobacteriaceae. III. Transduction of resistance factors. J. Bacteriol. 82:202-209. 1961.-Transmissible multiple drug resistance of Enterobacteriaceae, which includes resistance to streptomycin (SM), chloramphenicol (CM), tetracycline (TC), and sulfonamide (Su), was found to be transduced in the systems of Salmonella typhimurium strain LT-2 with phage P-22 and Escherichia coli strain K-12 with phage P1kc. No linked chromosomal markers to the resistance factors have so far been found in the substrains of K-12. The transductants of K-12 were all found to be able to transfer their resistance factors by conjugation, whereas a majority of those of LT-2 could not transfer their resistance factors by conjugation. The resistance factors were segregated rarely in K-12 and consistently in LT-2. Defective resistance factors could be transferred by conjugation to the transductants of LT-2. The transductants thus made resistant to the four drugs were able to transfer only the resistance factors which had been introduced by conjugation and none of those which had been transduced. The patterns of segregation of the resistance factors by transduction suggested that they are located in the following sequence; Su-----Sm-----Cm-----Tc, and they were assumed to be carried by an episome "resistance transfer factor" which is considered to be located at the distal end of Tc.

摘要

渡边勉(日本东京庆应义塾大学)和深泽敏夫。肠杆菌科中附加体介导的耐药性转移。III. 耐药因子的转导。《细菌学杂志》82:202 - 209。1961年。——发现肠杆菌科的可传递多重耐药性,包括对链霉素(SM)、氯霉素(CM)、四环素(TC)和磺胺类药物(Su)的耐药性,在鼠伤寒沙门氏菌LT - 2菌株与噬菌体P - 22以及大肠杆菌K - 12菌株与噬菌体P1kc的系统中可被转导。到目前为止,在K - 12的亚菌株中尚未发现与耐药因子连锁的染色体标记。发现K - 12的转导子都能够通过接合转移其耐药因子,而LT - 2的大多数转导子则不能通过接合转移其耐药因子。耐药因子在K - 12中很少分离,而在LT - 2中则持续分离。有缺陷的耐药因子可通过接合转移到LT - 2的转导子中。由此对这四种药物产生耐药性的转导子只能转移通过接合引入的耐药因子,而不能转移通过转导引入的任何耐药因子。通过转导产生的耐药因子的分离模式表明它们按以下顺序定位:Su-----Sm-----Cm-----Tc,并且假定它们由一个附加体“耐药转移因子”携带,该附加体被认为位于Tc的远端。

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