首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Loss of intrinsic aminoglycoside resistance in Acinetobacter haemolyticus as a result of three distinct types of alterations in the aac(6)-Ig gene including insertion of IS17.
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Loss of intrinsic aminoglycoside resistance in Acinetobacter haemolyticus as a result of three distinct types of alterations in the aac(6)-Ig gene including insertion of IS17.

机译:由于三种不同类型的aac(6)-Ig基因改变(包括插入IS17)导致溶血不动杆菌固有的氨基糖苷抗性丧失。

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摘要

The distribution of the aac(6')-Ig gene, encoding aminoglycoside 6'-N-acetyltransferase-Ig [AAC(6')-Ig], was studied in 96 Acinetobacter haemolyticus strains and 12 proteolytic Acinetobacter strains, including Acinetobacter genomospecies 6, 13, and 14 and 3 unnamed species assigned to this genomic group by DNA-DNA hybridization. This gene was detected by DNA-DNA hybridization in all 96 A. haemolyticus strains and by PCR in 95 strains but was not detected in strains of other species, indicating that it may be used to identify A. haemolyticus. Three A. haemolyticus strains were susceptible to tobramycin and did not produce an aminoglycoside 6'-N-acetylating activity, although they contained aac(6')-Ig-related sequences. An analysis of three susceptible A. haemolyticus strains indicated that aminoglycoside resistance was abolished by the following three distinct mechanisms: (i) a point mutation in aac(6')-Ig that led to a Met56-->Arg substitution, which was shown by analysis of a revertant to be responsible for the loss of resistance; (ii) a polythymine insertion that altered the reading frame; and (iii) insertion of IS17, a new member of the IS903 family. These observations indicated that AAC(6')-Ig is not essential for the viability of A. haemolyticus, although the aac(6')-Ig gene was detected in all members of this species.
机译:在96个溶血不动杆菌和12个蛋白水解不动杆菌(包括不动杆菌属)6个菌株中研究了编码氨基糖苷6'-N-乙酰基转移酶-Ig [AAC(6')-Ig]的aac(6')-Ig基因的分布。 ,13、14和3个通过DNA-DNA杂交分配给该基因组的未命名物种。在所有96个溶血曲霉菌株中通过DNA-DNA杂交检测了该基因,在95个菌株中通过PCR检测到该基因,但在其他物种的菌株中未检测到该基因,表明该基因可用于鉴定溶血曲霉。三个溶血曲霉菌株对妥布霉素敏感,尽管含有aac(6')-Ig相关序列,但不产生氨基糖苷6'-N-乙酰化活性。对三种易感溶血曲霉菌株的分析表明,氨基糖苷抗性通过以下三种不同的机制消除:(i)aac(6')-Ig中的点突变导致Met56-> Arg取代,这表明通过分析还原剂来引起电阻的损失; (ii)多聚胸腺嘧啶插入物改变了阅读框架; (iii)插入IS903家族的新成员IS17。这些观察结果表明,尽管在该物种的所有成员中都检测到了aac(6')-Ig基因,但AAC(6')-Ig对溶血曲霉的生存能力并不是必需的。

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