Клиническая микробиология и антимикробная химиотерапия (Oct 2019)
Antimicrobial resistance, carbapenemase production, and genotypes of nosocomial Acinetobacter spp. isolates in Russia: results of multicenter epidemiological study ”MARATHON 2015–2016”
- Shek E.A.,
- Sukhorukova M.V.,
- Edelstein M.V.,
- Skleenova E.Yu.,
- Ivanchik N.V.,
- Shajdullina E.R.,
- Kuzmenkov A.Yu.,
- Dekhnich A.V.,
- Kozlov R.S.,
- Semyonova N.V.,
- Slepakova S.A.,
- Shepotajlova N.V.,
- Strebkova V.V.,
- Rybina N.A.,
- Yaranceva N.Z.,
- Perevalova E.Yu.,
- Rozanova S.M.,
- Nagovicina S.G.,
- Moldovanu M.G.,
- Nasybullova Z.Z.,
- Arkhipenko M.V.,
- Shakhmuradyan R.M.,
- Nizhegorodceva I.A.,
- Varibrus E.V.,
- Aleksandrova I.A.,
- Lazareva A.V.,
- Kryzhanovskaya O.A.,
- Markelova N.N.,
- Chernyavskaya Yu.L.,
- Lebedeva E.V.,
- Kirillova G.Sh.,
- Bekker G.G.,
- Popova L.D.,
- Elokhina E.V.,
- Smol’kova Yu.E.,
- Zinov’ev D.Yu.,
- Ityaeva L.N.,
- Blinova G.Yu.,
- Zubareva N.A.,
- Vityazeva V.P.,
- Plaksina M.G.,
- Kucevalova O.Yu.,
- Panova N.I.,
- Suborova T.N.,
- Polukhina O.V.,
- Voroshilova T.M.,
- Churikova E.M.,
- Moskvitina E.N.,
- Krechikova O.I.,
- Petrova T.A.,
- Mart’yanova N.M.,
- Khokhlova K.O.,
- Gudkova L.V.,
- Bykonya S.A.,
- Khokhlyavina R.M.,
- Shpil’kina L.V.,
- Burasova E.G.,
- Khrebtovskaya V.A.,
- Molchanova I.V.,
- Zvonaryova O.V.,
- Kornilova P.A.,
- Kryanga V.G.,
- Portnyagina U.S.,
- Shamaeva S.Kh.,
- Popov D.A.,
- Vostrikova T.Yu.
Affiliations
- Shek E.A.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Sukhorukova M.V.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Edelstein M.V.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Skleenova E.Yu.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Ivanchik N.V.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Shajdullina E.R.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Kuzmenkov A.Yu.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Dekhnich A.V.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Kozlov R.S.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Semyonova N.V.
- Arkhangelsk Regional Clinical Hospital, Arkhangelsk, Russia
- Slepakova S.A.
- Amur Regional Children Clinical Hospital, Blagoveshchensk, Russia
- Shepotajlova N.V.
- Amur Regional Children Clinical Hospital, Blagoveshchensk, Russia
- Strebkova V.V.
- Voronezh City Clinical Emergency Care Hospital
- Rybina N.A.
- Voronezh City Clinical Emergency Care Hospital
- Yaranceva N.Z.
- Sverdlovsk Regional Clinical Psychiatric Hospital, Yekaterinburg, Russia
- Perevalova E.Yu.
- Clinical Diagnostic Center, Yekaterinburg, Russia
- Rozanova S.M.
- Clinical Diagnostic Center, Yekaterinburg, Russia
- Nagovicina S.G.
- City Clinical Hospital
- Moldovanu M.G.
- City Clinical Hospital
- Nasybullova Z.Z.
- Republican Clinical Hospital, Kazan, Russia
- Arkhipenko M.V.
- Research Institute – Regional Clinical Hospital
- Shakhmuradyan R.M.
- Research Institute – Regional Clinical Hospital
- Nizhegorodceva I.A.
- Regional Clinical Hospital
- Varibrus E.V.
- Regional Clinical Hospital
- Aleksandrova I.A.
- National Medical Research Center of Neurosurgery named after N.N. Burdenko, Moscow, Russia
- Lazareva A.V.
- National Medical Research Center for Children’s Health, Moscow, Russia
- Kryzhanovskaya O.A.
- National Medical Research Center for Children’s Health, Moscow, Russia
- Markelova N.N.
- Russian Scientific Center of Roentgenoradiology, Moscow, Russia
- Chernyavskaya Yu.L.
- Murmansk Regional Clinical Hospital named after P.A. Bayandin, Murmansk, Russia
- Lebedeva E.V.
- Murmansk Regional Clinical Hospital named after P.A. Bayandin, Murmansk, Russia
- Kirillova G.Sh.
- Emergency Care Hospital, Naberezhnye Chelny, Russia
- Bekker G.G.
- Clinical Hospital at the Novosibirsk-Main Station, Novosibirsk, Russia
- Popova L.D.
- Regional Clinical Hospital, Omsk, Russia
- Elokhina E.V.
- Regional Clinical Hospital, Omsk, Russia
- Smol’kova Yu.E.
- Clinical Hospital
- Zinov’ev D.Yu.
- Clinical Hospital
- Ityaeva L.N.
- Regional Oncology Dispensary, Penza, Russia
- Blinova G.Yu.
- Regional Oncology Dispensary, Penza, Russia
- Zubareva N.A.
- Perm State Medical University named after E.A. Wagner, Perm, Russia
- Vityazeva V.P.
- Children Republican Hospital, Petrozavodsk, Russia
- Plaksina M.G.
- Children Republican Hospital, Petrozavodsk, Russia
- Kucevalova O.Yu.
- Rostov Research Institute of Oncology, Rostov-on-Don, Russia
- Panova N.I.
- Rostov Research Institute of Oncology, Rostov-on-Don, Russia
- Suborova T.N.
- S.M. Kirov Military Medical Academy, Saint-Petersburg, Russia
- Polukhina O.V.
- Saint-Petersburg, Russia
- Voroshilova T.M.
- All-Russian Center of Emergency and Radiation Medicine named after A.M. Nikiforov, Saint-Petersburg, Russia
- Churikova E.M.
- All-Russian Center of Emergency and Radiation Medicine named after A.M. Nikiforov, Saint-Petersburg, Russia
- Moskvitina E.N.
- Siberian Federal Scientific Clinical Center, Seversk, Russia
- Krechikova O.I.
- Institute of Antimicrobial Chemotherapy, Smolensk, Russia
- Petrova T.A.
- Clinical Hospital
- Mart’yanova N.M.
- Tol’yatti City Clinical Hospital
- Khokhlova K.O.
- Tol’yatti City Clinical Hospital
- Gudkova L.V.
- Tomsk Regional Clinical Hospital, Tomsk, Russia
- Bykonya S.A.
- Tomsk Regional Clinical Hospital, Tomsk, Russia
- Khokhlyavina R.M.
- Regional Clinical Hospital
- Shpil’kina L.V.
- Regional Clinical Hospital
- Burasova E.G.
- Republican Clinical Hospital named after N.A. Semashko, Ulan-Ude, Russia
- Khrebtovskaya V.A.
- Republican Clinical Hospital named after N.A. Semashko, Ulan-Ude, Russia
- Molchanova I.V.
- Chelyabinsk Regional Clinical Hospital, Chelyabinsk, Russia
- Zvonaryova O.V.
- Chelyabinsk Regional Clinical Hospital, Chelyabinsk, Russia
- Kornilova P.A.
- Republican Hospital
- Kryanga V.G.
- Republican Hospital
- Portnyagina U.S.
- Republican Hospital
- Shamaeva S.Kh.
- Republican Hospital
- Popov D.A.
- A.N. Bakulev National Medical Research Center of Cardiovascular Surgery, Moscow, Russia
- Vostrikova T.Yu.
- A.N. Bakulev National Medical Research Center of Cardiovascular Surgery, Moscow, Russia
- DOI
- https://doi.org/10.36488/cmac.2019.2.171-180
- Journal volume & issue
-
Vol. 21,
no. 2
pp. 171 – 180
Abstract
Objective. Objectives. To assess the rates of antibiotic resistance and production of acquired carbapenemases in nosocomial strains of Acinetobacter spp., and to determine the genotypes and prevalence of “international high-risk clones” among nosocomial strains of Acinetobacter baumannii isolated in various regions of Russia within the “MARATHON 2015–2016” study. Materials and Methods. A total of 1005 non-duplicate nosocomial isolates of Acinetobacter spp., including 975 isolates of A. baumannii, collected in 44 hospitals from 25 cities in Russia in 2015– 2016 were studied. Species identification of isolates was performed by means of MALDI-TOF massspectrometry. Antimicrobial susceptibility was determined using broth microdilution method according to ISO 20776-1:2006 and interpreted using EUCAST MIC clinical breakpoints v.9.0. The presence of acquired carbapenemase genes of OXA-23, OXA-24/40, OXA-58, VIM, IMP, NDM, GES-2 and GES-5 groups was determined using real-time PCR. Genotyping of A. baumannii isolates was performed by analysis of selected single nucleotide polymorphisms in 10 chromosomal loci used for multi-locus sequence tying (MLST) of this species. Results. Acinetobacter spp. and A. baumannii comprised of 17.4% and 16.8% of all bacterial pathogens isolated within the “MARATHON 2015–2016” study. Resistance rates to carbapenems (imipenem and meropenem) were 77.4% and 77.1% of A. baumannii isolates, respectively. In 76.2% of A. baumannii isolates, the genes of acquired carbapenemases of molecular class D were detected, which belonged to the following groups: OXA-24/40 (57.5%), OXA-23 (18.4%) and OXA-58 (0.1%). Two isolates (0.2%) carried the genes of OXA-24/40- and OXA-23-like carbapenemases simultaneously. Most carbapenemaseproducing isolates belonged to the «international high-risk clones»: CC92/208OXF/CC2PAS (60.3%), CC944OXF/CC78PAS (25.4%) and CC109/231OXF/CC1PAS (11.6%). The vast majority of A. baumannii isolates exhibited resistance to ciprofloxacin (99.0%), amikacin (89.2%) and gentamicin (77.4%). The prevalence of resistance to tobramycin and trimethoprim/sulfamethoxazole was variable among strains of different genotypes. Colistin was the most active agent in vitro (0.9% of resistant isolates). Isolates of other Acinetobacter species were more susceptible to most antibiotics. However, two isolates of Acinetobacter ursingii and Acinetobacter baylyi carried the genes of NDM metallo-beta-lactamases. Conclusions. The results of this study indicate a very high prevalence of resistance to most antibiotics, including carbapenems, in nosocomial strains of Acinetobacter spp. This makes the selection of empiric antibiotic treatment extremely difficult and urges the need for regular local surveillance of resistance in every hospital.
Keywords