中华临床感染病杂志
中華臨床感染病雜誌
중화림상감염병잡지
CHINESE JOURNAL OF CLINICAL INFECTIOUS DISEASES
2010年
3期
142-144,165
,共4页
沈晓强%周华%季淑娟%魏泽庆%徐俭朴%俞云松%李兰娟
瀋曉彊%週華%季淑娟%魏澤慶%徐儉樸%俞雲鬆%李蘭娟
침효강%주화%계숙연%위택경%서검박%유운송%리란연
β-内酰胺酶类%基因%16S%rRNA甲基化酶%抗药性%质粒
β-內酰胺酶類%基因%16S%rRNA甲基化酶%抗藥性%質粒
β-내선알매류%기인%16S%rRNA갑기화매%항약성%질립
Beta-lactamases%Gene%16S rRNA methylase%Drug resistance%Plasmid
目的 研究产超广谱β-内酰胺酶(ESBLs)肠杆菌科细菌中16S rRNA甲基化酶基因的分布及传播机制.方法 采用PCR扩增、序列分析确定16S rRNA甲基化酶基因和ESBLs基因,Etest 法检测17种抗菌药物的最小抑菌浓度(MIC),并通过接合试验、质粒抽提等方法对耐药基因的传播机制进行研究.结果 447株产ESBLs菌株中筛选到1株产armA型16S rRNA甲基化酶的产酸克雷伯菌(ZJ157),并在该菌株中同时检出CTX-M-15型ESBLs和TEM-1型β-内酰胺酶基因;该菌株对氨基糖苷类、环丙沙星及大部分β-内酰胺类抗菌药物耐药,但对碳青霉烯类、多黏菌素E和替加环素敏感;对阿米卡星及β-内酰胺类抗菌药物的耐药性可以通过接合试验传递给受体菌,且PCR扩增证实接合子的armA、CTX-M-15及TEM-1基因均为阳性.质粒抽提发现原始菌和接合子均有1个约55 kb的质粒.结论 在产酸克雷伯菌中检出armA型16S rRNA甲基化酶基因.介导氨基糖苷类抗菌药物高水平耐药的armA基因可以与CTX-M-15及TEM-1基因同时经质粒传递,协同介导菌株的多药耐药.
目的 研究產超廣譜β-內酰胺酶(ESBLs)腸桿菌科細菌中16S rRNA甲基化酶基因的分佈及傳播機製.方法 採用PCR擴增、序列分析確定16S rRNA甲基化酶基因和ESBLs基因,Etest 法檢測17種抗菌藥物的最小抑菌濃度(MIC),併通過接閤試驗、質粒抽提等方法對耐藥基因的傳播機製進行研究.結果 447株產ESBLs菌株中篩選到1株產armA型16S rRNA甲基化酶的產痠剋雷伯菌(ZJ157),併在該菌株中同時檢齣CTX-M-15型ESBLs和TEM-1型β-內酰胺酶基因;該菌株對氨基糖苷類、環丙沙星及大部分β-內酰胺類抗菌藥物耐藥,但對碳青黴烯類、多黏菌素E和替加環素敏感;對阿米卡星及β-內酰胺類抗菌藥物的耐藥性可以通過接閤試驗傳遞給受體菌,且PCR擴增證實接閤子的armA、CTX-M-15及TEM-1基因均為暘性.質粒抽提髮現原始菌和接閤子均有1箇約55 kb的質粒.結論 在產痠剋雷伯菌中檢齣armA型16S rRNA甲基化酶基因.介導氨基糖苷類抗菌藥物高水平耐藥的armA基因可以與CTX-M-15及TEM-1基因同時經質粒傳遞,協同介導菌株的多藥耐藥.
목적 연구산초엄보β-내선알매(ESBLs)장간균과세균중16S rRNA갑기화매기인적분포급전파궤제.방법 채용PCR확증、서렬분석학정16S rRNA갑기화매기인화ESBLs기인,Etest 법검측17충항균약물적최소억균농도(MIC),병통과접합시험、질립추제등방법대내약기인적전파궤제진행연구.결과 447주산ESBLs균주중사선도1주산armA형16S rRNA갑기화매적산산극뢰백균(ZJ157),병재해균주중동시검출CTX-M-15형ESBLs화TEM-1형β-내선알매기인;해균주대안기당감류、배병사성급대부분β-내선알류항균약물내약,단대탄청매희류、다점균소E화체가배소민감;대아미잡성급β-내선알류항균약물적내약성가이통과접합시험전체급수체균,차PCR확증증실접합자적armA、CTX-M-15급TEM-1기인균위양성.질립추제발현원시균화접합자균유1개약55 kb적질립.결론 재산산극뢰백균중검출armA형16S rRNA갑기화매기인.개도안기당감류항균약물고수평내약적armA기인가이여CTX-M-15급TEM-1기인동시경질립전체,협동개도균주적다약내약.
Objective To investigate the prevalence and dissemination mechanism of 16S rRNA methylase genes in extended-spectrum beta-lactamases(ESBLs)-producing Enterobacteriaceae in China.Methods PCR amplification and DNA sequencing were used for screening and identifing 16S rRNA methylase genes and ESBLs genes.Minimal inhibitory concentrations(MICs)of the antimicrobial agents were detected by Etest.Conjugation and plasmid extract were performed to study dissemination mechanism of 16S rRNA methylase genes and ESBLs genes.Results Only one strain.Klebsiella oxytoca strain ZJ157 was screened as positive for armA gene from 447 ESBLs-producing isolates,which also contained CTX-M-15 and TEM-1 genes.It was resistant to aminoglycesides,ciprofloxacin,and most β-lactams,except carbapenems,polymyxin E and tigecyeline.Resistance to amikacin and β-lactams was transferred to a recipient Escherichia coli 600 by conjugation experiment.arntA.CTX-M-15 and TEM-1 genes were detected in the transconjugant.A plasmid about 55 kb was extracted from Klebsiella oxytoca ZJl57 and the transconjugant.Conclusions A 16S rRNA methylase gene armA was detected in an isolate of Klebsiella oxytoca.armA,CTX-M-15 and TEM-1 genes can be co-transferred in the same plasmid leading to multi-drug resistance.