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AmpC酶与革兰阴性菌的耐药特征 被引量:24

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出处 《中华微生物学和免疫学杂志》 CAS CSCD 北大核心 2001年第S1期18-20,共3页 Chinese Journal of Microbiology and Immunology
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参考文献16

  • 1徐英春,张小江,陈民钧,王清涛,张秀珍,许淑珍,周贵民.肠杆菌属的耐药调查及抗感染用药探讨[J].中华医院感染学杂志,2001,11(3):230-232. 被引量:80
  • 2吴伟元,陈民钧.阴沟肠杆菌ampD基因突变与去阻遏持续高产AmpC酶[J].中国抗感染化疗杂志,2001,1(2):65-69. 被引量:37
  • 3SandersCC,BradfordPA,EhrhardtAF ,etal.Penicillin bindingpro teinsandinductionofAmpCβ lactamase. AntimicrobsAgentsChemoth er . 1997
  • 4BauernfeindA,ChongY,KyungwonL.Plasmid encodedAmpCβ lacta mases:howfarhavewegone10yearsafterthediscovery?. JYonseiMed ical . 1998
  • 5Sanders CC.Chromosomal cephalosporinases responsible for multiple resistance to newer β-lactam antibiotics. Annual Review of Microbiology . 1987
  • 6Lister PD,Gardner VM,Sanders CC.Clavulanate induces expression of the Pseudomonas aeruginosa AmpC cephalosporinase at phiologically relevant concentrations and antagonizes the antibacterial activity of ticarcillin. Antimicrobial Agents and Chemotherapy . 1999
  • 7Maiti S N,Phillips O A,Micetich R G,et al.Beta-lactamase inhibitors: agents to overcome bacterial resistance. Current Medicinal Chemistry . 1998
  • 8Bauernfeind A,Stemplinger I,Jungwirth R,et al.Characterization of the plasmidic Beta-lactamase CMY-2 , which is responsible for cephamycin resistance. Antimicrobial Agents and Chemotherapy . 1996
  • 9Tuomanen E,Lindquist S,Sande S,et al.Coordinate regulation of Betalactamase induction and peptidoglycan composition by the amp operant. Science . 1991
  • 10Bennett PM,Ian Chop RA.Molecular basis of β-Lactamase induction in bacteria. Antimicrobial Agents and Chemotherapy . 1993

二级参考文献11

  • 1Liu P Y F,J Antimicrob Chemother,1992年,30卷,429页
  • 2Wiedemann B, Dietz H, Pfeifle D. Induction of β-lactamase in Enterobacter cloacae[J]. Clin Infect Dis, 1998, 27(Suppl 1): S42-47.
  • 3Ehrhardt AF, Sanders CC, Romero JR et al. Sequencing and analysis of four new Enterobacter ampD alleles[J]. Antimicrob Agents Chemother, 1996, 40(8): 1953-1956.
  • 4Stapleton P, Shannon K, Phillips I. DNA sequence differences of ampD mutants of Citrobacter freundii[J]. Antimicrob Agents Chemother, 1995, 39(11): 2494-2498.
  • 5Matthew M, Harris AM, Marshall MJ, et al. The use of analytical isoelectric focusing for detection and identification of β-lactamases[J]. J Gen Microbiol, 1975, 88:169-178.
  • 6Stapleton P, Shannon K, Phillips I. The ability of β-lactamse antibitics to select mutants with derepressed β-lactamase synthesis from Citrobacter freundii[J]. J Antimicrobial Chemother, 1995, 36:483-496.
  • 7Kopp U, Wiedemann B, Lindquist S et al. Sequences of wild-type and mutant ampD genes of Citrobacter freundii and Enterobacter cloacae[J]. Antimicrob Agents Chemother, 1993, 37(2): 224-228.
  • 8Bennett PM, Chopra I. Molecular basis of β-lactamase induction in bacteria[J]. Antimicrob Agents Chemother, 1993, 37(2): 153-158.
  • 9Korfmann G, Sanders CC, Moland ES. Alterd phenotypes associated with ampD mutations in E. cloacae[J]. Antimicrob Agents Chemother, 1991, 35(2): 358-364.
  • 10肖征,吴坚,赵莉萍.对1055株病原菌抗生素耐药特性的分析[J].中华医院感染学杂志,1998,8(2):117-118. 被引量:67

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二级引证文献153

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