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1
In vitro susceptibilities of Pseudomonas pseudomallei to 27 antimicrobial agents.类鼻疽杆菌对27种抗菌药物的体外敏感性
Antimicrob Agents Chemother. 1990 Oct;34(10):2027-9. doi: 10.1128/AAC.34.10.2027.
2
Pseudomonas pseudomallei, a common pathogen in Thailand that is resistant to the bactericidal effects of many antibiotics.类鼻疽杆菌，泰国一种常见的病原体，对许多抗生素的杀菌作用具有抗性。
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In vitro activities of the newer beta-lactam and quinolone antimicrobial agents against Pseudomonas pseudomallei.新型β-内酰胺类和喹诺酮类抗菌药物对类鼻疽杆菌的体外活性
Antimicrob Agents Chemother. 1988 Sep;32(9):1435-6. doi: 10.1128/AAC.32.9.1435.
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[Comparative studies on activities of antimicrobial agents against causative organisms isolated from urinary tract infections (1992). I. Susceptibility distribution].[1992年抗微生物剂对从尿路感染分离出的病原体的活性比较研究。I. 敏感性分布]
Jpn J Antibiot. 1995 Nov;48(11):1627-57.
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The antimicrobial susceptibility of Pseudomonas pseudomallei. Emergence of resistance in vitro and during treatment.类鼻疽杆菌的抗菌药敏性。体外及治疗过程中耐药性的出现。
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6
Susceptibility of Pseudomonas pseudomallei to new beta-lactam and aminoglycoside antibiotics.类鼻疽假单胞菌对新型β-内酰胺类和氨基糖苷类抗生素的敏感性
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In vitro activity of meropenem against ciprofloxacin-resistant enterobacteriaceae and Pseudomonas aeruginosa.美罗培南对耐环丙沙星肠杆菌科细菌和铜绿假单胞菌的体外活性。
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In vitro susceptibility pattern of cephalosporin-resistant Gram-negative bacteria.耐头孢菌素革兰氏阴性菌的体外药敏模式
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[Comparative studies on activities of antimicrobial agents against causative organisms isolated from urinary tract infections (1993). I. Susceptibility distribution].[1993年抗菌药物对从尿路感染分离出的病原体的活性比较研究。I. 敏感性分布]
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[Comparative studies on activities of antimicrobial agents against causative organisms isolated from patients with urinary tract infections (1994). I. Susceptibility distribution].[1994年抗微生物药物对从尿路感染患者分离出的病原体的活性比较研究。I. 敏感性分布]
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引用本文的文献

1
Genetic control of weight loss during pneumonic Burkholderia pseudomallei infection.肺炎型类鼻疽伯克霍尔德菌感染期间体重减轻的遗传控制。
Pathog Dis. 2014 Jul;71(2):249-64. doi: 10.1111/2049-632X.12172. Epub 2014 Apr 22.
2
Clinical features and laboratory diagnosis of infection with the potential bioterrorism agents burkholderia mallei and burkholderia pseudomallei.潜在生物恐怖主义病原体鼻疽伯克霍尔德菌和类鼻疽伯克霍尔德菌感染的临床特征与实验室诊断
Int J Biomed Sci. 2007 Sep;3(3):144-52.
3
Melioidosis: epidemiology, pathophysiology, and management.类鼻疽病：流行病学、病理生理学及管理
Clin Microbiol Rev. 2005 Apr;18(2):383-416. doi: 10.1128/CMR.18.2.383-416.2005.
4
Outcomes of patients with melioidosis treated with meropenem.用美罗培南治疗类鼻疽患者的结果。
Antimicrob Agents Chemother. 2004 May;48(5):1763-5. doi: 10.1128/AAC.48.5.1763-1765.2004.

本文引用的文献

1
Transduction of linked genetic characters of the host by bacteriophage P1.噬菌体P1对宿主连锁遗传性状的转导
Virology. 1955 Jul;1(2):190-206. doi: 10.1016/0042-6822(55)90016-7.
2
Meliodosis.类鼻疽病
Med J Aust. 1980 Apr 5;1(7):314-6.
3
In vitro activity of various cephalosporins against Pseudomonas pseudomallei.多种头孢菌素对类鼻疽假单胞菌的体外活性。
J Infect Dis. 1984 Nov;150(5):779-80. doi: 10.1093/infdis/150.5.779.
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The pseudomallei group: a review.类鼻疽杆菌属：综述
J Infect Dis. 1971 Dec;124(6):598-606. doi: 10.1093/infdis/124.6.598.
5
Comparison of a new cephalosporin, BMY 28142, with other broad-spectrum beta-lactam antibiotics.新型头孢菌素BMY 28142与其他广谱β-内酰胺类抗生素的比较。
Antimicrob Agents Chemother. 1985 Feb;27(2):207-16. doi: 10.1128/AAC.27.2.207.
6
In vitro activity against aerobic and anaerobic gram-positive and gram-negative bacteria and beta-lactamase stability of RS-533, a novel carbapenem.新型碳青霉烯类药物RS-533对需氧和厌氧革兰氏阳性及革兰氏阴性菌的体外活性及β-内酰胺酶稳定性
Antimicrob Agents Chemother. 1986 Dec;30(6):828-34. doi: 10.1128/AAC.30.6.828.
7
Comparative antibacterial activities of temafloxacin hydrochloride (A-62254) and two reference fluoroquinolones.盐酸替马沙星（A-62254）与两种氟喹诺酮类对照品的抗菌活性比较
Antimicrob Agents Chemother. 1987 Nov;31(11):1768-74. doi: 10.1128/AAC.31.11.1768.
8
Activities of five new fluoroquinolones against Pseudomonas pseudomallei.五种新型氟喹诺酮类药物对类鼻疽杆菌的活性。
Antimicrob Agents Chemother. 1988 Jun;32(6):928-9. doi: 10.1128/AAC.32.6.928.
9
Aspects of chemistry in the development of the 4-quinolone antibacterial agents.4-喹诺酮类抗菌药物研发中的化学相关方面。
Rev Infect Dis. 1988 Jan-Feb;10 Suppl 1:S2-9.
10
Susceptibility of Pseudomonas pseudomallei to new beta-lactam and aminoglycoside antibiotics.类鼻疽假单胞菌对新型β-内酰胺类和氨基糖苷类抗生素的敏感性
J Antimicrob Chemother. 1988 Feb;21(2):171-5. doi: 10.1093/jac/21.2.171.

类鼻疽杆菌对27种抗菌药物的体外敏感性

In vitro susceptibilities of Pseudomonas pseudomallei to 27 antimicrobial agents.

作者信息

Yamamoto T, Naigowit P, Dejsirilert S, Chiewsilp D, Kondo E, Yokota T, Kanai K

机构信息

Department of Bacteriology, School of Medicine, Juntendo University, Tokyo, Japan.

出版信息

Antimicrob Agents Chemother. 1990 Oct;34(10):2027-9. doi: 10.1128/AAC.34.10.2027.

DOI:10.1128/AAC.34.10.2027
PMID:2291671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC171985/
Abstract

Clinical isolates of Pseudomonas pseudomallei isolated in Thailand from 1981 to 1989 were tested for their in vitro susceptibilities to 27 antimicrobial agents, including older and newer quinolones, broad-spectrum cephems, carbapenems, monobactams, penicillins, tetracyclines, chloramphenicol, rifamycin, sulfamethoxazole, trimethoprim, and fosfomycin. Tosufloxacin, meropenem, CS-533, and minocycline were active against P. pseudomallei at levels comparable to or even greater than those of antimicrobial agents tested in previous studies, such as ciprofloxacin, ceftazidime, imipenem, carumonam, and piperacillin. Drug-resistant P. pseudomallei was found in only 1% of the isolates. The drug-resistant P. pseudomallei isolates displayed a unique pattern of susceptibility to the above-listed drugs.

摘要

对1981年至1989年在泰国分离出的类鼻疽假单胞菌临床分离株进行了检测，以测定它们对27种抗菌药物的体外敏感性，这些抗菌药物包括较老的和较新的喹诺酮类、广谱头孢菌素、碳青霉烯类、单环β-内酰胺类、青霉素类、四环素类、氯霉素、利福霉素、磺胺甲恶唑、甲氧苄啶和磷霉素。托氟沙星、美罗培南、CS-533和米诺环素对类鼻疽假单胞菌的活性与之前研究中测试的抗菌药物（如环丙沙星、头孢他啶、亚胺培南、卡芦莫南和哌拉西林）相当，甚至更高。仅在1%的分离株中发现了耐药类鼻疽假单胞菌。耐药类鼻疽假单胞菌分离株对上述药物呈现出独特的敏感性模式。