您现在的位置: 首页> 研究主题> 氨基糖苷类修饰酶

氨基糖苷类修饰酶

氨基糖苷类修饰酶的相关文献在2004年到2019年内共计85篇,主要集中在基础医学、临床医学、药学 等领域,其中期刊论文79篇、会议论文6篇、专利文献228521篇;相关期刊43种,包括中华微生物学和免疫学杂志、实验与检验医学、检验医学等; 相关会议6种,包括第三届全国细菌耐药监测与临床专题学术会议、第七次全国临床微生物学术年会暨第三届两岸三地临床微生物与感染病学术论坛、2007年浙江省检验医学学术年会等;氨基糖苷类修饰酶的相关文献由227位作者贡献,包括糜祖煌、黄支密、单浩等。

氨基糖苷类修饰酶—发文量

期刊论文>

论文:79 占比:0.03%

会议论文>

论文:6 占比:0.00%

专利文献>

论文:228521 占比:99.96%

总计:228606篇

氨基糖苷类修饰酶—发文趋势图

氨基糖苷类修饰酶

-研究学者

  • 糜祖煌
  • 黄支密
  • 单浩
  • 秦玲
  • 仵蕾
  • 周军
  • 张馨琢
  • 杨海燕
  • 陆亚华
  • 陈榆
  • 期刊论文
  • 会议论文
  • 专利文献

搜索

排序:

年份

    • 张凡; 郭普; 张伦军; 郑晶; 郑照军; 徐元宏
    • 摘要: 目的 了解铜绿假单胞菌对氨基糖苷类抗生素耐药基因的分布情况.方法 收集临床分离的铜绿假单胞菌,采用仪器法和纸片扩散法(K-B法)进行药敏实验.筛选出对氨基糖苷类抗生素耐药的菌株,用PCR法检测16个氨基糖苷类修饰酶(AMEs)基因和5个16S rRNA甲基化酶基因的表达,进一步对阳性基因扩增产物进行测序验证.结果 54株菌中51 株AMEs基因阳性,检出率为94.4% ,28 株甲基化酶基因阳性,检出率为51.9% .共检出5 种AMEs基因:ant(3″) -Ⅰ、aac(3) -Ⅱc、ant(4′) -Ⅰa、aac(6′) -Ⅰb和ant ( 2″) - Ⅰa,阳性率分别为 66.7% 、 38.9% 、 31.5% 、31.5%和16.6% ;2种16S rRNA甲基化酶基因:rmtB和ar-mA,阳性率分别为29.6%和29.6% ,其余基因均未检出.测序结果与目的基因一致.结论 铜绿假单胞菌氨基糖苷类抗生素耐药的主要基因为ant(3″)-Ⅰ、aac(3)-Ⅱc、ant(4′) -Ⅰa、aac(6′)-Ⅰb和ant(2″)-Ⅰa以及rmtB, armA.%Objective To investigate the aminoglycoside antibiotic resistance gene distribution of Pseudomonas aeruginosa. Methods Pseudomonas aeruginosa was isolated and collected in clinic. Drug susceptibility test was performed by instrumental method and disk diffusion method ( K-B method) . Aminoglycoside antibiotic-resistant strains were screened, and the expression of 16 aminoglycoside modified enzyme( AMEs) genes and 5 16S rRNA methylase genes were detected by PCR,the positive gene amplification products were further verified by gene se-quencing. Results Among the 54 strains, 51 were positive for AMEs gene, with the detection rate of 94.4% ; 28 strains were positive for methylase gene, with the detection rate of 51.9% . Five kinds of AMEs gene were detec-ted, including ant(3″)-Ⅰ,aac (3)-Ⅱc, ant (4′)-Ⅰa, aac (6′)-Ⅰb and ant (2″)-Ⅰa, with the positive rate of 66.7% ,38.9% , 31.5% , 31.5% and 16.6% respectively; Two kinds of 16S rRNA methylase gene were detec-ted, including rmtB and armA, with the positive rate of 29.6% and 29.6% , respectively, no other gene was de-tected. The gene sequencing result was consistent with the target gene sequence. Conclusion The aminoglycoside resistance gene of Pseudomonas aeruginosa was detected with the 5 types of ant(3″)-Ⅰ, aac (3)-Ⅱc, ant (4′)-Ⅰa, aac (6ˊ)-Ⅰb, ant (2″) -Ⅰa, rmtB and armA, respectively.
    • 杨艳; 王厚照; 张玲
    • 摘要: The prevalence of aminoglycoside modifying enzymes and 16S rRNA methylase genes in multi-drug resist-ant Acinetobacter baumannii was studied .A total of 28 multi-drug resistant A.baumannii isolates were collected from Dec.2014 to Mar.2015 from patients in the ChengGong Hospital Affiliated to Xiamen University .Bacterial identifi-cation was performed by VITEK 2 Compact automatic bacterial identification system .Kirby-Bauer Diffusion Method was used to detect the drug resistance of antimicrobial drugs .The aminoglycoside modifying enzymes and 16S rRNA methylase genes were amplified by polymerase chain reaction ( PCR) .The results showed that the resistance rate of all the other measured drugs were all above 50%except for cefoperazone-sulbactam (21.4%).5 kinds of aminoglycoside modifying enzyme genes including aac(3)-I, aac(3)-II, aac (6′)-Ib, ant(3")-I,aph(3′)-I and one kind of 16S rRNA methylase gene armA were found in 28 strains of multi-drug resistant A .baumannii with the positive rates at 85.7%(24 strains), 7.14%(2 strains), 67.8%(19 strains), 92.9% (26 strains), 53.6% (15 strains) and 82.1%(23 strains) respectively.Therefore the genes of aminoglycoside modifying enzymes and 16S rRNA methylase were the major reasons for the resistance to aminoglycosides in multi-drug resistant A.baumannii.%了解氨基糖苷类修饰酶、16 S rRNA甲基化酶基因在多重耐药鲍曼不动杆菌中的流行情况.收集2014年12月至2015年3月厦门大学附属成功医院住院患者临床分离的多重耐药鲍曼不动杆菌共28株,采用VIKET Compact 2全自动细菌鉴定系统进行细菌鉴定,应用纸片扩散法(K-B法)检测鲍曼不动杆菌对抗菌药物的耐药性,采用聚合酶链反应(PCR)法检测氨基糖苷类修饰酶、16S rRNA甲基化酶基因.结果显示,多重耐药鲍曼不动杆菌除对头孢哌酮/舒巴坦耐药率为21.4%外,对其他所测药物耐药率均>50%,本组28株多重耐药鲍曼不动杆菌共检出5种氨基糖苷类修饰酶基因aac(3)-Ⅰ、aac(3)-Ⅱ、aac(6′)-Ⅰb、ant(3")-Ⅰ、(3′)-Ⅰ和1种16S rRNA甲基化酶基因armA,阳性率分别为85.7%(24株)、7.14%(2株)、67.8%(19株)、92.9%(26株)、53.6%(15株)和82.1%(23株).氨基糖苷类修饰酶、16S rRNA甲基化酶耐药基因是多重耐药鲍曼不动杆菌对氨基糖苷类耐药的重要原因.
    • 吴海鹏; 林宁; 孙海平
    • 摘要: 目的:了解一组多药耐药克雷伯菌氨基糖苷类修饰酶基因和16SrRNA甲基化酶基因的存在状况.方法:收集南京医科大学附属淮安一院2013年2月至2015年3月病人标本中分离的多药耐药克雷伯菌属共20株,用分子鉴定法鉴定菌种,将15种氨基糖苷类修饰酶基因和6种16SrRNA甲基化酶基因使用聚合酶链反应(PCR)方法进行分析.结果:本组20株菌中19株为肺炎克雷伯菌,1株为变栖克雷伯菌.氨基糖苷类修饰酶基因或/和16SrRNA甲基化酶基因检出率达80.0%.其中aac (3)-Ⅱ、aac(6')-Ⅰb群、ant(3")-I、aph(3')-I、rmtB的检出分别为9株、12株、10株、5株、4株.并且在变栖克雷伯菌中发现了aac(6')-Ib-cr基因.结论:本组克雷伯菌对氨基糖苷类产生耐药,造成该结果的主要原因是其产4种氨基糖苷类修饰酶基因和1种16SrRNA甲基化酶基因.在变栖克雷伯菌中发现了aac(6')-Ⅰ b-cr基因是国内外首次报道.
    • 黄支密; 单浩; 夏守慧; 盛以泉; 杨海燕; 沈娟; 糜祖煌; 朱健铭
    • 摘要: 目的 了解临床分离的携带blaKPC-2型碳青霉烯酶基因泛耐药肺炎克雷伯菌中16S rRNA甲基化酶基因和氨基糖苷类修饰酶(AMEs)基因的分布.方法 在2008年11月~2009年7月从笔者医院住院患者中分离19株携带blaKPC-2型碳青霉烯酶基因泛耐药肺炎克雷伯菌,采用PCR及序列分析的方法分析6种16S rRNA甲基化酶基因(armA、rmtA、rmtB、rmtC、rmtD和npmA)和14种AMEs基因[ant(3″)-Ⅰ、ant(2″)-Ⅰ、ant(4′)-Ⅰ a/b、aadA4/5、aadA6/16、aac(3)-Ⅰ、aac (3)-Ⅱ、aac(3)-Ⅲ、aac(3)-Ⅳ、aac(6′)-Ⅰb、aac(6′)-Ⅱ、aph(3′)-Ⅰ、aph(3′)-Ⅱb和aph(3')-Ⅵa].结果 19株中,5种基因aac(3)-Ⅱ、aac(6′)-Ⅰb、aac(6′)-Ⅱ、ant(3″)-Ⅰ和aph(3′)-Ⅰ的阳性株数[阳性率(%)]分别为2(10.5%)、1(5.3%)、19(100.0%)、19(100.0%)和2(10.5%),其余15种基因均阴性;AMEs基因总阳性率为100.0% (19/19).对1株(6号菌株)aac(6′)-Ⅰb基因PCR阳性产物进行测序,证实为aac(6')-Ⅰb-cr双功能酶基因.结论 氨基糖苷类修饰酶基因aac(6′)-Ⅱ和ant(3″)-Ⅰ在携带blaKPc-2型碳青霉烯酶基因泛耐药肺炎克雷伯菌中广泛分布.
    • 王玉月; 史伟峰; 周军
    • 摘要: Objective To investigate the situation of acquired resistant genes against aminoglycosides in extensively drug-resistant (XDR)Acintobacter baumannii (AB)isolated from intensive care unit (ICU)patients.Methods Bacterial identification and susceptibility tests of AB were performed by phoenixTM-1 00 automatic bacterial identification and susceptibility analyzer,and the AB identification was confirmed by gyrA and parC gene amplification sequencing. For the 20 isolates of XDR-AB,1 0 aminoglycoside modifying enzyme genes,6 1 6S rRNA methylase genes and efflux pump adeB genes were detected by polymerase chain reaction(PCR)and verified and compared by DNA sequencing. Results Of the 20 isolates of XDR-AB,the detection rates of aac(3)-Ⅰ,aac(6′)-Ⅰb,ant(3″)-Ⅰ and aph(3′)-Ⅰgenes were 90.0%,30.0%,95.0% and 95.0%,respectively.However,aac(3)-Ⅱ,aac(6′)-Ⅰad,aac(6′)-Ⅱ,ant (2″)-Ⅰ,ant(4′)-Ⅰand aph(3′)-Ⅵa genes were not found.In addition,the armA 1 6S rRNA methylase gene and efflux pump adeB genes existed in all of the 20 isolates,and the detection rates were 1 00%.Conclusions All of the 20 isolates of XDR-AB carry not only armA and adeB genes but also a large amount of aac(3)-Ⅰ,ant(3″)-Ⅰand aph(3)-Ⅰgenes.It indicates that the high-level resistance to aminoglycosides in XDR-AB isolated from ICU may be associated with the resistant genes.%目的:了解重症监护病房(ICU)患者分离的广泛耐药(XDR)-鲍曼不动杆菌(AB)对氨基糖苷类药物获得性耐药基因情况。方法用phoenixTM-100全自动细菌鉴定药物敏感性分析仪对AB进行细菌鉴定和药物敏感性试验,gyrA和parC基因扩增测序确定AB。聚合酶链反应(PCR)测定20株XDR-AB的10种氨基糖苷类修饰酶基因、6种16S rRNA甲基化酶基因和外排泵adeB基因,并用DNA测序比对。结果20株XDR-AB中,氨基糖苷类修饰酶基因aac(3)-Ⅰ、aac(6′)-Ⅰb、ant(3″)-Ⅰ、aph(3′)-Ⅰ检出率分别为90.0%、30.0%、95.0%、95.0%,而aac(3)-Ⅱ、aac(6′)-Ⅰad、aac(6′)-Ⅱ、ant(2″)-Ⅰ、ant(4′)-Ⅰ及aph(3′)-Ⅵa基因均未检出。armA型16S rRNA甲基化酶基因和外排泵adeB基因检出率均为100%。结论20株XDR-AB均携带了armA和adeB基因,同时aac(3)-Ⅰ、ant(3″)-Ⅰ和aph(3)-Ⅰ检出率较高,提示ICU分离的XDR-AB对氨基糖苷类药物高水平耐药可能与携带的耐药基因有关。
    • 张侠家; 徐元宏
    • 摘要: 耐氨基糖苷类高水平肠球菌(HLAR)是医院感染的重要病原菌,氨基糖苷类修饰酶(AME)是肠球菌对氨基糖苷类高水平耐药的主要机制,其中N-乙酰转移酶(AAC)、O-核苷转移酶(ANT)和O-磷酶转移酶(APH)是参与耐药基因表达的主要氨基糖苷类修饰酶类.现就氨基糖苷类修饰酶的耐药基因及其耐药基因的传播进行临床研究,从而为减少医院HLAR感染的发生提供分子生物学依据.
    • 赵书平; 包健; 姜梅杰
    • 摘要: 目的:调查氨基糖苷类修饰酶基因(AMES)和16S rRNA甲基化酶基因在院内不同时间分离的多重耐药鲍曼不动杆菌中的存在情况。方法采用PCR法检测aac(3)-Ⅰ、aac(3)-Ⅱ、aac (3)-Ⅲ、aac(3)-Ⅳ、aac(6′)-Ⅰ、aac(6′)-Ⅱ、aph(3′)-Ⅵ、ant(3″)-Ⅰ、ant(2″)-Ⅰ和16S rRNA甲基化酶基因在临床不同时间分离的88株多重耐药鲍曼不动杆菌中的存在情况。结果2010年6月至2011年6月临床分离的46株多重耐药鲍曼不动杆菌中,41株(89.1%)含ant(3″)-Ⅰ基因,33株(71.7%)含aac(3)-Ⅰ基因,2株(4.3%)含aac(3)-Ⅱ基因,1株(2.2%)含aac(6′)-Ⅱ基因,1株(2.2%)含aph(3′)-Ⅵ基因,40株(87%)含armA基因。2012年12月至2013年1月本院临床分离的42株多重耐药鲍曼不动杆菌中,41株(97.7%)含ant(3″)-Ⅰ基因,34株(81%)含aac(3)-Ⅰ基因,7株(16.7%)含aac(6′)-Ⅰ基因,16株(38.1%)含armA基因。结论院内不同时间分离的多重耐药鲍曼不动杆菌ant(3″)-Ⅰ、aac(3)-Ⅰ和armA基因检出率一直很高,对其氨基糖苷类耐药与AMES和16S rRNA甲基化酶基因有关。%Objective To investigate the prevalence of genes encoding aminoglycoside modifying enzymes and 16S rRNA methylases in multi-drug resistant Acinetobacter baumannii isolated in hospital at different times. Methods The genes of aac (3)-Ⅰ, aac (3)-Ⅱ, aac (3)-Ⅲ, aac (3)-Ⅳ, aac (6′)-Ⅰ, aac (6′)-Ⅱ, aph (3′)-Ⅵ, ant (3″)-Ⅰ, ant (2″)-Ⅰand 16S rRNA methylases in the samples of 88 multi-drug resistant Acinetobacter baumannii stains isolated at different times were analyzed by polymerase chain reaction (PCR). Results Among the 46 multi-drug resistant Acinetobacter baumannii stains collected from June 2010 to June 2011, aminoglycoside modifying enzymes gene ant (3″)-Ⅰwas found in 41 strains (89.1%), aac (3)-Ⅰwas identified in 33 strains (71.7%), aac (3)-Ⅱ in 2 strains (4.3%), aac (6′)-Ⅱ in 1 strain (2.2%), aph (3′)-Ⅵ in 1 strain (2.2%), and 40 strains (87.0%) carried armA gene. Among the 42 multi-drug resistant Acinetobacter baumannii stains collected from December 2012 to January 2013, aminoglycoside modifying enzymes gene ant (3″)-Ⅰwas found in 41 strains (97.7%), aac (3)-Ⅰwas identified in 34 strains (81.0%), aac(6′)-Ⅰ in 7 strains (16.7%), and 16 strains (38.1%) carried armA gene. Conclusions The detection rate of the genes as ant (3″)-Ⅰ, aac (3)-Ⅰand armA has been high in multi-drug resistant Acinetobacter baumannii isolated in hospital at different times, and the aminoglycoside resistance of them is closed with the genes encoding aminoglycoside modifying enzymes and 16S rRNA methylases.
    • 周佳琦; 卢佳睿; 徐花; 韩放; 孙延波
    • 摘要: 目的:分析长春地区部分医院革兰阴性杆菌氨基糖苷类修饰酶基因的分布和类型,为抗生素的合理应用提供依据.方法:通过琼脂稀释法筛选出阿米卡星与庆大霉素的耐药菌株,采用聚合酶链式反应及序列分析的方法检测耐药菌株所携带的氨基糖苷类修饰酶基因类型.结果:69株革兰阴性杆菌对阿米卡星与庆大霉素的耐药率分别为44.9%和87.0%,其中63株(91.3%)检出氨基糖苷类修饰酶基因,基因类型包括aac(3)-Ⅰ、aac(3)-Ⅱ、aac(6')-Ⅰb、ant(3")-Ⅰ和ant(2")-Ⅰ,阳性率分别为4.3%、81.2%、43.5%、33.3%和13.0%;而aac(6')-Ⅱ基因为阴性.结论:本地区革兰阴性杆菌氨基糖苷类修饰酶基因主要以aac(3)-Ⅰ、aac(3)-Ⅱ、aac(6')-Ⅰb、ant(3")-Ⅰ和ant(2")-Ⅰ5种类型存在,其中以aac(3)-Ⅱ型氨基糖苷类修饰酶基因最为常见.合理应用氨基糖苷类抗生素对于降低细菌的耐药性具有重要意义.
  • 查看更多

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号