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阴沟肠杆菌感染治疗期间对头孢他啶耐药性的出现。

Emergence of resistance to ceftazidime during therapy for Enterobacter cloacae infections.

作者信息

Quinn J P, DiVincenzo C A, Foster J

出版信息

J Infect Dis. 1987 May;155(5):942-7. doi: 10.1093/infdis/155.5.942.

Abstract

The mechanism of resistance to ceftazidime in two clinical isolates of Enterobacter cloacae that emerged during therapy with broad-spectrum beta-lactam antibiotics was studied. Both isolates acquired broad resistance to advanced-spectrum beta-lactam drugs other than imipenem. Biotyping confirmed strain identity in both cases, and no new plasmids were detected in the resistant isolates. Both resistant isolates produced beta-lactamase constitutively. Slow but definite hydrolysis of ceftazidime was demonstrated by using purified beta-lactamase in a spectrophotometric assay. Further evidence that beta-lactamase is responsible for resistance in these organisms was provided by the demonstration that cefoxitin, a potent inducer of beta-lactamase, antagonized the activity of ceftazidime against these isolates. This antagonism could be prevented by inhibition of derepression of beta-lactamase with clindamycin. Clindamycin also prevented regrowth of ceftazidime-treated cells in time-kill studies and markedly reduced production of beta-lactamase in induced cultures at concentrations as low as 2 micrograms/ml.

摘要

对在使用广谱β-内酰胺抗生素治疗期间出现的两株阴沟肠杆菌临床分离株对头孢他啶的耐药机制进行了研究。这两株分离株对除亚胺培南外的超广谱β-内酰胺类药物均获得了广泛耐药性。生物分型在两例中均确认了菌株同一性,且在耐药分离株中未检测到新的质粒。两株耐药分离株均组成性产生β-内酰胺酶。通过在分光光度法测定中使用纯化的β-内酰胺酶,证实了头孢他啶的缓慢但明确的水解。通过证明头孢西丁(一种强力的β-内酰胺酶诱导剂)拮抗头孢他啶对这些分离株的活性,进一步证明了β-内酰胺酶是这些生物体耐药的原因。这种拮抗作用可通过用克林霉素抑制β-内酰胺酶的去阻遏来预防。在时间-杀菌研究中,克林霉素还可防止头孢他啶处理的细胞再生长,并且在低至2微克/毫升的浓度下,可显著降低诱导培养物中β-内酰胺酶的产生。

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