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[多重耐药性对N-甲酰亚胺硫霉素及6种对照物质对铜绿假单胞菌和4种肠杆菌科细菌的最低抑菌浓度的影响]

[Effect of multiresistance on the minimal inhibitory concentration of N-formimidoyl thienamycin and 6 comparing substances against P. aeruginosa and 4 Enterobacteriaceae species].

作者信息

Schröter G, Schrettenbrunner A, Strenzel I

出版信息

Zentralbl Bakteriol Mikrobiol Hyg A Med Mikrobiol Infekt Parasitol. 1983 Feb;253(4):531-43.

PMID:6407236
Abstract

The minimal inhibitory concentrations (MICs) of multiresistant strains of P. aeruginosa and four species of Enterobacteriaceae were compared with those of more sensitive ones in N-f-thienamycin and six other antibiotics. The greatest difference between these two differently resistant bacterial populations was found in cefoperazone and the beta-lactamase-instable piperacillin. The latter was used for comparison purposes. The activity of cefsulodin was distinctly reduced in multiresistant strains of P. aeruginosa. Cefotaxime and lamoxactam displayed slightly elevated MICs in multiresistant strains. In N-f-thienamycin a significant difference between the multiresistant and the more sensitive population could not be verified (p greater than 0.05). In this regard it resembles fosfomycin. beta-lactam antibiotics could be ranked by means of correlation analysis of their MICs. Using piperacillin as a reference antibiotic the following order of succession could be arranged according to correlation coefficients in P. aeruginosa: cefoperazone, cefsulodin, lamoxactam, cefotaxime and N-f-thienamycin. For the Enterobacteriaceae species some antibiotics could not be evaluated in this test. Moreover, it was recognized that there was an obvious correlation between the activities of lamoxactam and cefotaxime in P. aeruginosa (r = 0.81) and E. coli (r = 0.80). A correlation was also observed between those of cefsulodin and cefoperazone in P. aeruginosa (r = 0.75). Lower correlation coefficients were seen in N-f-thienamycin with cefoperazone, piperacillin and cefsulodin in P. aeruginosa and with cefoperazone in Klebsiella spec.. Notwithstanding, strains resistant to cefsulodin and cefoperazone were inhibited by concentrations less than or equal to 8 micrograms/ml of N-f-thienamycin. These results showed that in N-f-thienamycin, cefotaxime and lamoxactam multiresistance has only a minimal influence on the MICs of the species of Enterobacteriaceae examined. For therapeutic considerations concerning multiresistance the small differences recognized among these three antibiotics might be without significance. However, N-f-thienamycin was distinctly more active in multiresistant strains of P. aeruginosa than the other beta-lactam antibiotics tested.

摘要

比较了铜绿假单胞菌多耐药菌株及四种肠杆菌科细菌对N - f - 噻烯霉素和其他六种抗生素的最低抑菌浓度(MIC),并与更敏感菌株进行对比。这两类耐药性不同的细菌群体之间,头孢哌酮和对β - 内酰胺酶不稳定的哌拉西林差异最大。使用后者作比较。在铜绿假单胞菌多耐药菌株中,舒噻孢霉素的活性明显降低。头孢噻肟和拉氧头孢在多耐药菌株中的MIC略有升高。在N - f - 噻烯霉素中,多耐药群体和更敏感群体之间未证实有显著差异(p>0.05)。在这方面它类似于磷霉素。β - 内酰胺类抗生素可通过对其MIC的相关分析进行排序。以哌拉西林作为参照抗生素,在铜绿假单胞菌中,根据相关系数可排列出如下顺序:头孢哌酮、舒噻孢霉素、拉氧头孢、头孢噻肟和N - f - 噻烯霉素。对于肠杆菌科细菌,部分抗生素在本试验中无法评估。此外,还认识到拉氧头孢和头孢噻肟在铜绿假单胞菌(r = 0.81)和大肠杆菌(r = 0.80)中的活性之间存在明显相关性。在铜绿假单胞菌中,舒噻孢霉素和头孢哌酮的活性之间也观察到相关性(r = 0.75)。在铜绿假单胞菌中,N - f - 噻烯霉素与头孢哌酮、哌拉西林和舒噻孢霉素以及在克雷伯菌属中与头孢哌酮的相关系数较低。尽管如此,对舒噻孢霉素和头孢哌酮耐药的菌株被浓度小于或等于8微克/毫升的N - f - 噻烯霉素所抑制。这些结果表明,对于所检测的肠杆菌科细菌,N - f - 噻烯霉素、头孢噻肟和拉氧头孢中的多耐药性对MIC的影响极小。对于多耐药性的治疗考虑,这三种抗生素之间所识别出的微小差异可能并无意义。然而,在铜绿假单胞菌多耐药菌株中,N - f - 噻烯霉素比所测试的其他β - 内酰胺类抗生素活性明显更高。

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