圣彼得堡和俄罗斯联邦其他一些地区产碳青霉烯酶革兰氏阴性菌的流行和耐药性

Q4 Medicine Antibiotiki i Khimioterapiya Pub Date : 2016-01-01
I V Lazareva, V A Ageevets, T A Ershova, L P Zueva, A E Goncharov, M G Darina, Yu S Svetlichnaya, A N Uskov, S V Sidorenko
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引用次数: 0

摘要

产生碳青霉烯酶的革兰氏阴性菌可水解大多数内酰胺类,包括碳青霉烯类,对全球卫生保健系统构成威胁。已知碳青霉烯酶的数量在不断增加,但广泛分布的只有四种类型:ndm型、kpc型、oxa -48型和vim型。圣彼得堡医院产碳青霉烯酶克雷伯肺炎菌的感染率为9.2% (ndm型为5.9%,oxa -48型为1.4%,ndm型+ oxa -48型为1.9%)。2011-2016年,莫斯科、叶卡捷琳堡、沃洛格达、摩尔曼斯克、库尔干、克拉斯诺亚尔斯克、伊热夫斯克、克拉斯诺达尔和彼尔姆医院共检出碳青霉烯酶产生菌281株,分别来自感染或定植患者(肺炎克雷菌247株、不动杆菌29株、阴沟肠杆菌2株、粘结沙雷菌1株、大肠埃希菌1株和mirabifis变形杆菌1株)。产碳青霉烯酶的肺炎克雷伯菌具有相当大的遗传多样性,ndm型产碳青霉烯酶的菌株分别有8个,kpc型- 3个,oxa -48型-4个不同的序列型(STs)。检测到全球优势遗传系的代表,克隆群258 (CG258),以及一些不太常见的遗传系(ST147, ST273, ST307和ST377)。肺炎克雷伯菌具有较高的交叉耐药频率和不同类群对抗生素的相关耐药特征。头孢菌素类和氟喹诺酮类药物耐药率达100%。ndm型碳青霉烯酶对氨基糖苷类药物的耐药率超过90%,kpc型碳青霉烯酶对阿米卡星和庆大霉素的耐药率分别为66%和93%,OXA-48型碳青霉烯酶对氨基糖苷类药物的耐药率更低(分别为50%和73%)。大约80%的ndm型、90%的kpc型和只有60%的oxa -48型碳青霉烯酶产生者对亚胺培南和美罗培南表现出高水平的耐药性。对替加环素的耐药频率在6.7% ~ 14.8%之间,对多粘菌素的耐药频率在4.2% ~ 20%之间。产碳青霉烯酶的OXA-40型和oxa -23型不动杆菌仅对多粘菌素敏感。显然,碳青霉烯酶引起的感染的抗菌治疗的可能性是有限的。
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Prevalence and Antibiotic Resistance of Carbapenemase-Producing Gram-Negative Bacteria in Saint Petersburg and Some Other Regions of the Russian Federation.

Carbapenemase-producing gramnegative bacteria, which hydrolyze most offi-lactams, including carbapenems, is of global health care system threat. The number of the known carbapenemases is constantly increasing, however only four types are widely distributed: NDM-type, KPC-type, OXA-48-type and VIM-type. The frequency of carbapenemase-producing Klebsiellapneumoniae in hospitals of Saint Petersburg reached 9.2% (5.9% for NDM-type, 1.4% for OXA-48-type, 1.9% for NDM-type + OXA-48-type). Carbapenemase producers were also detected in hospitals of Moscow, Yekaterinburg, Vologda, Murmansk, Kurgan, Krasnoyarsk, Izhevsk, Krasnodar and Perm. In total 281 carbapenemase producers were recorded within 2011-2016, which were isolated from infected or colonized patients (K.pneumoniae - 247 isolates, Acinetobacter spp - 29 isolates, Enterobacter cloacae - 2 isolates, Serratia marcescens - 1 isolate, Escherichia coli - 1 isolate and Proteus mirabifis - 1 isolate). The carbapenemase-producing K.pneumoniae isolates were distinguished by considerable genetic diversity, the NDM-type carbapenemase-producers belonged to eight, KPC-type - to three and OXA-48-type - to four different sequence-types (STs) respectively. The representatives of the globally dominant genetic line, Clonal Group 258 (CG258), and also a number of the less common lines (ST147, ST273, ST307 and ST377) were detected. The K.pneumoniae strains were distinguished by a high frequency of cross-resistance and the associated resistance to antibiotics of different groups. The frequency of resistance to cephalosporins and fluoroquinolones reached 100%. Among the NDM-type carbapenemase producers the frequency of resistance to aminoglycosides exceeded 90%, among the KPC-type carbapenemase producers the frequency of resistance corresponded to 66% for amikacin and 93% for gentamicin, among the OXA-48 type carbapenemase producers the frequency of resistance was even lower (50% and 73% respectively). Approximately 80% of the NDM-type, 90% of the KPC-type and only 60% of the OXA-48-type carbapenemase producers showed a high level of resistance to imipenem and meropenem. The frequency of resistance to tigecycline varied within 6.7% to 14.8% and the frequency of resistance to polymyxin was within 4.2% to 20%. The OXA-40- and OXA-23-types carbapenemase-producing Acinetobacter spp. remained susceptible only to polymyxin. It is obvious that the possibility of antibacterial therapy of infections caused by carbapenemases producers is limited.

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来源期刊
Antibiotiki i Khimioterapiya
Antibiotiki i Khimioterapiya Medicine-Infectious Diseases
CiteScore
0.80
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0.00%
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46
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