Cao Van, Lambert Thierry, Courvalin Patrice
Unité des Agents Antibactériens, Institut Pasteur, 75724 Paris Cedex 15, France.
Antimicrob Agents Chemother. 2002 May;46(5):1212-7. doi: 10.1128/AAC.46.5.1212-1217.2002.
The resistance of Klebsiella pneumoniae BM4493, isolated in Ho Chi Minh City, Vietnam, to cefotaxime and aztreonam was due to production of a novel beta-lactamase, CTX-M-17. The bla(CTX-M-17) gene was borne by 7,086-bp plasmid pIP843, which was entirely sequenced and which was found to belong to the ColE1 family. The 876-bp bla(CTX-M-17) gene differed from bla(CTX-M-14) by 2 nucleotides, which led to the single amino acid substitution Glu289-->Lys. bla(CTX-M-17) was flanked upstream by an ISEcp1-like element and downstream by an insertion sequence (IS) IS903 variant designated IS903-C. The transcriptional start site of bla(CTX-M-17) was located 109 nucleotides upstream from the initiation codon in the ISEcp1-like element, which also provided the promoter sequences. Plasmid pIP843, which was non-self-transferable and nonmobilizable, contained five open reading frames transcribed in the same orientation. Regions homologous to sequences coding for putative RNA II and RNA I transcripts, a rom gene, which is involved in initiation of replication, and a cer-like gene, which is responsible for the stability of ColE1-like plasmids, were identified. Consensus sequences for putative replication (oriV) and transfer (oriT) origins were present. Results of primer extension experiments indicated that ISEcp1 provides the promoter for expression of bla(CTX-M-17) and may contribute to dissemination of this gene.
从越南胡志明市分离出的肺炎克雷伯菌BM4493对头孢噻肟和氨曲南的耐药性是由于产生了一种新型β-内酰胺酶CTX-M-17。bla(CTX-M-17)基因由7086 bp的质粒pIP843携带,该质粒已被完全测序,发现属于ColE1家族。876 bp的bla(CTX-M-17)基因与bla(CTX-M-14)有2个核苷酸不同,导致单个氨基酸取代Glu289→Lys。bla(CTX-M-17)上游侧翼为ISEcp1样元件,下游侧翼为一个插入序列(IS) IS903变体,命名为IS903-C。bla(CTX-M-17)的转录起始位点位于ISEcp1样元件中起始密码子上游109个核苷酸处,该元件也提供启动子序列。非自我转移和不可移动的质粒pIP843包含5个同向转录的开放阅读框。鉴定出与推定的RNA II和RNA I转录本、参与复制起始的rom基因以及负责ColE1样质粒稳定性的cer样基因编码序列同源的区域。存在推定的复制(oriV)和转移(oriT)起始点的共有序列。引物延伸实验结果表明,ISEcp1为bla(CTX-M-17)的表达提供启动子,并可能有助于该基因的传播。