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2
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3
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4
Comparative antibacterial activities of new beta-lactam antibiotics against Pseudomonas aeruginosa.新型β-内酰胺类抗生素对铜绿假单胞菌的抗菌活性比较
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Comparative in vitro study in new cephalosporins.新型头孢菌素的体外比较研究。
Antimicrob Agents Chemother. 1981 Aug;20(2):226-30. doi: 10.1128/AAC.20.2.226.
2
beta-Lactamase activity in human pus.人脓液中的β-内酰胺酶活性
J Infect Dis. 1980 Oct;142(4):594-601. doi: 10.1093/infdis/142.4.594.
3
Selection of variants of Pseudomonas aeruginosa resistant of Beta-lactam antibiotics.耐β-内酰胺类抗生素铜绿假单胞菌变体的筛选
Infection. 1980;8(2):73-80. doi: 10.1007/BF01639151.
4
Staphylococcal beta-lactamase and efficacy of beta-lactam antibiotics: in vitro and in vivo evaluation.葡萄球菌β-内酰胺酶与β-内酰胺类抗生素的疗效:体外和体内评估
J Infect Dis. 1983 Jun;147(6):1078-89. doi: 10.1093/infdis/147.6.1078.
5
A turbidimetric study of the responses of selected strains of Pseudomonas aeruginosa to eight antipseudomonal beta-lactam antibiotics.对铜绿假单胞菌选定菌株对八种抗假单胞菌β-内酰胺抗生素反应的比浊法研究。
J Infect Dis. 1982 Jan;145(1):110-7. doi: 10.1093/infdis/145.1.110.
6
Mode of action of ceftazidime: affinity for the penicillin-binding proteins of Escherichia coli K12, Pseudomonas aeruginosa and Staphylococcus aureus.头孢他啶的作用方式:对大肠杆菌K12、铜绿假单胞菌和金黄色葡萄球菌青霉素结合蛋白的亲和力。
J Antimicrob Chemother. 1983 Aug;12(2):119-26. doi: 10.1093/jac/12.2.119.
7
Emergence of resistance during therapy with the newer beta-lactam antibiotics: role of inducible beta-lactamases and implications for the future.新型β-内酰胺类抗生素治疗期间耐药性的出现:诱导性β-内酰胺酶的作用及对未来的影响。
Rev Infect Dis. 1983 Jul-Aug;5(4):639-48. doi: 10.1093/clinids/5.4.639.
8
Mechanisms of bacterial resistance to antimicrobial agents, with particular reference to cefotaxime and other beta-lactam compounds.细菌对抗菌药物的耐药机制,特别涉及头孢噻肟及其他β-内酰胺类化合物。
Rev Infect Dis. 1982 Sep-Oct;4 Suppl:S288-99. doi: 10.1093/clinids/4.supplement_2.s288.
9
Influence of inoculum size on activity of cefoperazone, cefotaxime, moxalactam, piperacillin, and N-formimidoyl thienamycin (MK0787) against Pseudomonas aeruginosa.接种量对头孢哌酮、头孢噻肟、拉氧头孢、哌拉西林及N-甲酰亚胺硫霉素(MK0787)抗铜绿假单胞菌活性的影响。
Antimicrob Agents Chemother. 1980 Dec;18(6):893-6. doi: 10.1128/AAC.18.6.893.
10
Third-generation cephalosporins in the treatment of pneumonia due to Pseudomonas aeruginosa in guinea pigs.第三代头孢菌素治疗豚鼠铜绿假单胞菌所致肺炎
J Infect Dis. 1982 Oct;146(4):567. doi: 10.1093/infdis/146.4.567.

新型β-内酰胺类抗生素对铜绿假单胞菌的接种物效应

Inoculum effect of new beta-lactam antibiotics on Pseudomonas aeruginosa.

作者信息

Eng R H, Smith S M, Cherubin C

出版信息

Antimicrob Agents Chemother. 1984 Jul;26(1):42-7. doi: 10.1128/AAC.26.1.42.

DOI:10.1128/AAC.26.1.42
PMID:6433787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC179914/
Abstract

The degree of the inoculum effect shown by the new beta-lactam antibiotics with Pseudomonas aeruginosa was investigated, and the antibiotics were divided into three groups based upon the observations. The group 1 antibiotics (cefotaxime, moxalactam, cefoperazone, azlocillin, piperacillin, and aztreonam) demonstrated a large inoculum effect, were poorly bactericidal, produced aberrant, elongated bacilli, and did not inhibit the increase in turbidity of high inocula during an 18-h incubation. The group 2 antibiotics (ceftazidime and ticarcillin) were slowly bactericidal, caused minimal formation of aberrant, elongated bacilli, and slowly decreased the turbidity of high inocula. The group 3 antibiotics (imipenem and gentamicin) were bactericidal, did not cause the formation of elongated bacilli, and decreased the turbidity of high inocula rapidly. Data are presented which suggest that the inoculum effect seen with the group 1 beta-lactam antibiotics is related to (i) the poor intrinsic antibactericidal activity of these antibiotics for P. aeruginosa at the inocula tested and (ii) failure of these antibiotics to inhibit the formation of aberrant and filamentous bacilli, which can result in increased bacterial mass and turbidity.

摘要

研究了新型β-内酰胺类抗生素对铜绿假单胞菌的接种物效应程度,并根据观察结果将这些抗生素分为三组。第1组抗生素(头孢噻肟、拉氧头孢、头孢哌酮、阿洛西林、哌拉西林和氨曲南)表现出较大的接种物效应,杀菌能力差,产生异常的细长杆菌,并且在18小时培养期间不能抑制高接种量菌液的浊度增加。第2组抗生素(头孢他啶和替卡西林)杀菌作用缓慢,导致异常细长杆菌的形成最少,并且缓慢降低高接种量菌液的浊度。第3组抗生素(亚胺培南和庆大霉素)具有杀菌作用,不会导致细长杆菌的形成,并且能迅速降低高接种量菌液的浊度。所呈现的数据表明,第1组β-内酰胺类抗生素的接种物效应与以下因素有关:(i)在测试接种量下,这些抗生素对铜绿假单胞菌的固有杀菌活性较差;(ii)这些抗生素未能抑制异常和丝状杆菌的形成,这可能导致细菌量增加和浊度升高。