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碳青霉烯类药物耐药肠杆菌科细菌传播机制的研究 被引量:6

The mechanism of the transmission of carbapenem-resistant Enterobacteriaceae
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摘要 目的研究大连医科大学附属一院2013-2014年期间收集的68株对碳青霉烯类药物耐药肠杆菌科细菌(CRE)的药敏结果、耐药基因携带情况及传播机制。方法采用WHONET 5.6软件分析菌株耐药情况;聚合酶链反应技术(PCR)检测KPC、IMP、VIM、ISCR1及ISCR1可变区;ERIC-PCR进行同源性分析。结果 2014年与2013年相比较,各类抗生素的耐药率差异虽没有统计学意义,但均有所升高,升高率大部分约为20%;68株CRE中,KPC阳性16株,占23.5%,IMP阳性2株,占2.9%,VIM阳性17株,占25.0%,ISCR1阳性37株,占54.4%,ISCR1可变区阳性21株,占30.9%;ERIC-PCR将45株碳青霉烯类耐药肺炎克雷菌分为4个型别(A^D):A型占64.5%,B型占13.3%,C型占8.9%,D型占13.3%;23株碳青霉烯类耐药大肠埃希菌分为3个型别(A^C):A型占60.9%,B型占30.4%,C型占8.7%。结论 ISCR1是耐药基因分子间水平传播的重要原因。 Objective To study the drug susceptibility,drug resistant genes and the mechanism of the transmission of 68 strains of carbapenem-resistant Enterobacteriaceae collected from 2013 to 2014in our hospital.Methods The drug resistance was analyzed by WHONET 5.6system;The KPC,IMP,VIM,ISCR1 and variable region of ISCR1 were identified by PCR.Enterobacterial repetitive intergenic consensus-PCR(ERIC-PCR)was performed to analyze the molecular epidemiology of the isolates.Results The rate of antibiotic resistance in 2014 increased by about 20% compared with that in 2013.Among the 68 strains of carbapenem-resistant Enterobacteriaceae,16 strains were KPC positive(23.5%),2strains were IMP positive(2.9%),17 strains were VIM positive(25.0%),37 strains were ISCR1positive(54.4%),and 21 strains were variable region of ISCR1positive(30.9%).45 strains of KPN(resistant to carbapenem)were identified by ERIC-PCR as belong to 4genotypes,among which type A accounted for 64.5%,type B 13.3%,type C 8.9%,and type D 13.3%.23 strains of ECO were identified as belong to 3genotypes,among which type A accounted for 60.9%,type B 30.4%,and type C8.7%.Conclusion ISCR1 is the main reason of molecular transmission of the drug-resistant gene.
出处 《中国微生态学杂志》 CAS CSCD 2016年第5期555-557,560,共4页 Chinese Journal of Microecology
关键词 碳青霉烯酶肠杆菌科细菌 基因 插入序列共同区域 Carbepenemases enterobacteriaceae Gene ISCR
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  • 1刘原,谭湘淑,韩新鹏.西安地区耐亚胺培南鲍曼不动杆菌的碳青霉烯酶及同源性研究[J].中国感染与化疗杂志,2009,9(1):37-41. 被引量:15
  • 2顾兵,童明庆,宁明哲,张小梅,沈翰,刘根焰.南京地区铜绿假单胞菌的整合子流行性调查[J].临床检验杂志,2006,24(2):118-121. 被引量:19
  • 3欧阳金鸣,康辉,王倩,邓宇欣.医院非发酵菌感染及耐药性分析[J].中国实验诊断学,2006,10(6):644-647. 被引量:8
  • 4张嵘,蔡加昌,周宏伟,陈功祥.对亚胺培南耐药粘质沙雷菌中质粒介导KPC-2型碳青霉烯酶的研究分析[J].中华微生物学和免疫学杂志,2007,27(8):734-738. 被引量:37
  • 5Toleman M A, Bennett P M, Walsh T R. ISCR elements:novel gene-capturing systems of the 21st century? [J]. Microbiol Mol Biol Rev,2006,70(2) :296.
  • 6Wolska K, Szweda P. A'comparative evaluation of PCR ribotyping and ERIC PCR for determining the diversity of clinical Pseudomonas aeruginosa isolates[J]. Pol J Microbiol, 2008,57 (2):157.
  • 7Alexandre P Zavascki C G C R. Multidrug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii: resistance mechanisms and implications for therapy[Z]. 2010.
  • 8Labbate M, Case R J, Stokes H W. The integron/gene cassette system : an active player in bacterial adaptation. [J]. Methods Mol Biol, 2009,532 : 103.
  • 9Lee M F,Peng C F,Hsu H J,et al. Use of inverse PCR for analysis of class 1 integrons carrying an unusual 3' conserved segment structure[J]. Antimicrob Agents Chemother, 2011,55 (2) : 943.
  • 10Kim S H, Lee B Y, Lau G W, et al. IscR modulates catalase A (KatA) activity,peroxide resistance and full virulence of Pseudomonas aeruginosa PA14. [J]. J Microbiol Bioteehnol, 2009, 19 (12) :1520.

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