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温和噬菌体Aa phi 23介导放线共生放线杆菌菌株间抗生素抗性标记的转导

Transduction of antibiotic resistance markers among Actinobacillus actinomycetemcomitans strains by temperate bacteriophages Aa phi 23.

作者信息

Willi K, Sandmeier H, Kulik E M, Meyer J

机构信息

Institute of Preventive Dentistry and Oral Microbiology, University of Basel, Switzerland.

出版信息

Cell Mol Life Sci. 1997 Dec;53(11-12):904-10. doi: 10.1007/s000180050109.

Abstract

Actinobacillus actinomycetemcomitans (Aa) strain ST1 carries the tetracycline (Tc) resistance transposon Tn916 and the Aa phi ST1 prophage, which is closely related to temperate bacteriophage Aa phi 23. High titre phage preparations were obtained from this strain by mitomycin C induction and were used to transduce the TcR determinant to the TcS recipient strains ZIB1001 and ZIB1015 (MIC 2 micrograms Tc/ml). TcR transductants (MIC > or = 32 micrograms Tc/ml) were detected at frequencies of 3 x 10(-6) to 5 x 10(-8) per pfu. All TcR transductants examined contained the entire Tn916 inserted at several different locations within the Aa genome. They appear to have resulted from generalized transduction. In addition both bacteriophages, Aa phi 23 and Aa phi ST1, were capable of transducing the chloramphenicol (Cm) resistance marker of plasmid pKT210 (transduction frequencies of 2 x 10(-5) to 3 x 10(-7) per pfu) to the recipient strain ZIB1001 (MIC 8 micrograms Cm/ml). Eleven CmR ZIB1001 transductants (MIC > or = 100 micrograms Cm/ml) studied carried a plasmid indistinguishable from pKT210 by restriction analyses. In view of the high prevalence of this phage family, and the increasing use of tetracycline in periodontitis therapy, these findings may have clinical importance.

摘要

伴放线放线杆菌(Aa)菌株ST1携带四环素(Tc)抗性转座子Tn916和Aa phi ST1原噬菌体,该原噬菌体与温和噬菌体Aa phi 23密切相关。通过丝裂霉素C诱导从该菌株获得了高滴度的噬菌体制剂,并用于将TcR决定簇转导至TcS受体菌株ZIB1001和ZIB1015(MIC为2微克Tc/毫升)。以每噬菌斑形成单位(pfu)3×10^(-6)至5×10^(-8)的频率检测到TcR转导子(MIC≥32微克Tc/毫升)。所有检测的TcR转导子都含有完整插入Aa基因组内几个不同位置的Tn916。它们似乎是由普遍性转导产生的。此外,噬菌体Aa phi 23和Aa phi ST1都能够将质粒pKT210的氯霉素(Cm)抗性标记(每pfu的转导频率为2×10^(-5)至3×10^(-7))转导至受体菌株ZIB1001(MIC为8微克Cm/毫升)。通过限制性分析研究的11个CmR ZIB1001转导子(MIC≥100微克Cm/毫升)携带的质粒与pKT210无法区分。鉴于该噬菌体家族的高流行率以及四环素在牙周炎治疗中的使用增加,这些发现可能具有临床重要性。

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