Randegger C C, Hächler H
Institute of Medical Microbiology, University of Zürich, PO Box, CH-8028 Zürich, Switzerland.
J Antimicrob Chemother. 2001 May;47(5):547-54. doi: 10.1093/jac/47.5.547.
Three amino acid substitutions, Met-69-->Ile, Arg-244-->Ser and/or Asn-276-->Asp, mediate inhibitor resistance (IR) in TEM beta-lactamases. They were introduced in all possible combinations at homologous positions into either SHV-1 or the respective extended-spectrum beta-lactamases (ESBLs), SHV-2 or SHV-5. Susceptibility testing of the resulting set of seven variants of each parental strain, all in an isogenic background, was performed. The phenotypes of the constructions revealed that most substitutions resulted in reduced resistance to most tested single beta-lactam formulations. This decrease over-compensated for the expected increase in inhibitor resistance, so that most mutants showed no rise in resistance to inhibitor/beta-lactam combinations, although increases of MICs from one- to 43-fold compared with the respective parental strains were also measured. Combination of several IR-determining substitutions impaired both phenotypes in the carrier strains even more. None of the 14 mutants derived from the ESBLs, SHV-2 and SHV-5, showed a clinically relevant combined ESBL-IR phenotype. These findings indicate that the SHV beta-lactamase does not benefit proportionally from simultaneous substitution of residues relevant for the ESBL and the IR phenotype.
三种氨基酸替换,即甲硫氨酸-69→异亮氨酸、精氨酸-244→丝氨酸和/或天冬酰胺-276→天冬氨酸,介导TEMβ-内酰胺酶的抑制剂抗性(IR)。它们以所有可能的组合在同源位置引入到SHV-1或相应的超广谱β-内酰胺酶(ESBLs),即SHV-2或SHV-5中。对每个亲本菌株的七个变体的所得集合进行了药敏试验,所有变体均处于同基因背景中。构建体的表型显示,大多数替换导致对大多数测试的单一β-内酰胺制剂的抗性降低。这种降低过度补偿了预期的抑制剂抗性增加,因此大多数突变体对抑制剂/β-内酰胺组合的抗性没有增加,尽管与各自的亲本菌株相比,最小抑菌浓度(MIC)也有1至43倍的增加。几种IR决定替换的组合对携带菌株的两种表型的损害更大。来自ESBLs、SHV-2和SHV-5的14个突变体中,没有一个表现出临床相关的ESBL-IR联合表型。这些发现表明,SHVβ-内酰胺酶不会因同时替换与ESBL和IR表型相关的残基而按比例受益。