中华检验医学杂志
中華檢驗醫學雜誌
중화검험의학잡지
CHINESE JOURNAL OF LABORATORY MEDICINE
2014年
10期
763-766
,共4页
孙静娜%董威%赵帅%王国欣%刘泽世%张征
孫靜娜%董威%趙帥%王國訢%劉澤世%張徵
손정나%동위%조수%왕국흔%류택세%장정
鲍氏不动杆菌%抗药性, 多种, 细菌%碳酰氰化物间-氯苯基腙%表型%基因型
鮑氏不動桿菌%抗藥性, 多種, 細菌%碳酰氰化物間-氯苯基腙%錶型%基因型
포씨불동간균%항약성, 다충, 세균%탄선청화물간-록분기종%표형%기인형
Acinetobacter baumannii%Drug resistance,multiple,bacterial%Carbonyl cyanide m-chlorophenyl hydrazone%Phenotype%Genotype
目的:探讨多重耐药鲍曼不动杆菌外排泵表型和外排泵基因表达情况在耐药方面的作用。方法应用K-B法检测河北医科大学第一医院96株多重耐药鲍曼不动杆菌对15种抗菌药物的耐药情况,应用微量肉汤稀释法通过加入羰基氰氯苯腙( CCCP)泵抑制剂检测多重耐药鲍曼不动杆菌外排泵表型,并用PCR扩增进行外排泵蛋白基因的检测和测序。结果96株多重耐药鲍曼不动杆菌对喹诺酮类、头孢菌素类、氨基糖苷类、四环素类抗菌药物的耐药率为70.8%~94.8%。其中有34株外排泵表型阳性;外排泵表型阳性的34株鲍曼不动杆菌检测到 adeB、adeR、adeS、adeJ、adeE、adeM 基因分别有33株、32株、33株、33株、0株、33株,检出阳性率分别为97.06%、94.12%、97.06%、97.06%、0、97.06%;对adeB、adeR、adeS基因进行测序,经比对,所测序列与GenBank中序列同源性为100%。结论主动外排泵基因是鲍曼不动杆菌发生多重耐药的重要因素之一。
目的:探討多重耐藥鮑曼不動桿菌外排泵錶型和外排泵基因錶達情況在耐藥方麵的作用。方法應用K-B法檢測河北醫科大學第一醫院96株多重耐藥鮑曼不動桿菌對15種抗菌藥物的耐藥情況,應用微量肉湯稀釋法通過加入羰基氰氯苯腙( CCCP)泵抑製劑檢測多重耐藥鮑曼不動桿菌外排泵錶型,併用PCR擴增進行外排泵蛋白基因的檢測和測序。結果96株多重耐藥鮑曼不動桿菌對喹諾酮類、頭孢菌素類、氨基糖苷類、四環素類抗菌藥物的耐藥率為70.8%~94.8%。其中有34株外排泵錶型暘性;外排泵錶型暘性的34株鮑曼不動桿菌檢測到 adeB、adeR、adeS、adeJ、adeE、adeM 基因分彆有33株、32株、33株、33株、0株、33株,檢齣暘性率分彆為97.06%、94.12%、97.06%、97.06%、0、97.06%;對adeB、adeR、adeS基因進行測序,經比對,所測序列與GenBank中序列同源性為100%。結論主動外排泵基因是鮑曼不動桿菌髮生多重耐藥的重要因素之一。
목적:탐토다중내약포만불동간균외배빙표형화외배빙기인표체정황재내약방면적작용。방법응용K-B법검측하북의과대학제일의원96주다중내약포만불동간균대15충항균약물적내약정황,응용미량육탕희석법통과가입탄기청록분종( CCCP)빙억제제검측다중내약포만불동간균외배빙표형,병용PCR확증진행외배빙단백기인적검측화측서。결과96주다중내약포만불동간균대규낙동류、두포균소류、안기당감류、사배소류항균약물적내약솔위70.8%~94.8%。기중유34주외배빙표형양성;외배빙표형양성적34주포만불동간균검측도 adeB、adeR、adeS、adeJ、adeE、adeM 기인분별유33주、32주、33주、33주、0주、33주,검출양성솔분별위97.06%、94.12%、97.06%、97.06%、0、97.06%;대adeB、adeR、adeS기인진행측서,경비대,소측서렬여GenBank중서렬동원성위100%。결론주동외배빙기인시포만불동간균발생다중내약적중요인소지일。
Objective To expore multi-drug resistant Acinetobacter baumannii efflux pump phenotype and efflux pump gene expression in the resistant isolates. Methods Application of K-B method to detect 96 strains isolated from the First Hospital of Hebei Medical University multi-drug resistant Acinetobacter baumannii′ resistance to 15 kinds of antibacterial drugs, detecting multi-drug resistant Acinetobacter baumannii efflux pump phenotype with broth microdilution method by the addition of carbonyl cyanide chlorobenzene hydrazone ( CCCP) pump inhibitors,using PCR amplification and sequencing to study efflux pump protein gene sequence characteristics . Results The Acinetobacter baumannii resistance rate of 96 strains to quinolones, cephalosporins, aminoglycosides, tetracyclines were 70. 8%-94. 8%.There were 34 positive efflux pump phenotypes in 96 multi-drug resistant Acinetobacter baumannii strains, including 33 adeB strains, 32 adeR strains, 33 adeS strains, 33 adeJ strains,0 adeE strain,33 adeM strains, positive detection rate were 97. 06%, 94. 12%, 97. 06%, 97. 06%, 0, 97. 06%, respectively. By sequence comparison, adeB, adeR and adeS genes sequence homology was 100% in the GenBank. Conclusion Active efflux pump gene perturbation is one of the important factors in multi-drug resistant Acinetobacter baumannii.