Emergence and spread of carbapenem-resistant Acinetobacter baumannii international clones II and III in Lima, Peru
Carbapenem-resistant Acinetobacter baumannii is the top-ranked pathogen in the World Health Organization priority list of antibiotic-resistant bacteria. It emerged as a global pathogen due to the successful expansion of a few epidemic lineages, or international clones (ICs), producing acquired class...
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creator | Levy-Blitchtein, Saúl Roca, Ignasi Plasencia-Rebata, Stefany Vicente-Taboada, William Velásquez-Pomar, Jorge Muñoz, Laura Moreno-Morales, Javier Pons, Maria J. del Valle-Mendoza, Juana Vila, Jordi |
description | Carbapenem-resistant Acinetobacter baumannii is the top-ranked pathogen in the World Health Organization priority list of antibiotic-resistant bacteria. It emerged as a global pathogen due to the successful expansion of a few epidemic lineages, or international clones (ICs), producing acquired class D carbapenemases (OXA-type). During the past decade, however, reports regarding IC-I isolates in Latin America are scarce and are non-existent for IC-II and IC-III isolates. This study evaluates the molecular mechanisms of carbapenem resistance and the epidemiology of 80 non-duplicate clinical samples of A. baumannii collected from February 2014 through April 2016 at two tertiary care hospitals in Lima. Almost all isolates were carbapenem-resistant (97.5%), and susceptibility only remained high for colistin (95%). Pulsed-field gel electrophoresis showed two main clusters spread between both hospitals: cluster D containing 51 isolates (63.8%) associated with sequence type 2 (ST2) and carrying OXA-72, and cluster F containing 13 isolates (16.3%) associated with ST79 and also carrying OXA-72. ST2 and ST79 were endemic in at least one of the hospitals. ST1 and ST3 OXA-23-producing isolates were also identified. They accounted for sporadic hospital isolates. Interestingly, two isolates carried the novel OXA-253 variant of OXA-143 together with an upstream novel insertion sequence (ISAba47). While the predominant A. baumannii lineages in Latin America are linked to ST79, ST25, ST15, and ST1 producing OXA-23 enzymes, we report the emergence of highly resistant ST2 (IC-II) isolates in Peru producing OXA-72 and the first identification of ST3 isolates (IC-III) in Latin America, both considered a serious threat to public health worldwide. |
doi_str_mv | 10.1038/s41426-018-0127-9 |
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It emerged as a global pathogen due to the successful expansion of a few epidemic lineages, or international clones (ICs), producing acquired class D carbapenemases (OXA-type). During the past decade, however, reports regarding IC-I isolates in Latin America are scarce and are non-existent for IC-II and IC-III isolates. This study evaluates the molecular mechanisms of carbapenem resistance and the epidemiology of 80 non-duplicate clinical samples of A. baumannii collected from February 2014 through April 2016 at two tertiary care hospitals in Lima. Almost all isolates were carbapenem-resistant (97.5%), and susceptibility only remained high for colistin (95%). Pulsed-field gel electrophoresis showed two main clusters spread between both hospitals: cluster D containing 51 isolates (63.8%) associated with sequence type 2 (ST2) and carrying OXA-72, and cluster F containing 13 isolates (16.3%) associated with ST79 and also carrying OXA-72. ST2 and ST79 were endemic in at least one of the hospitals. ST1 and ST3 OXA-23-producing isolates were also identified. They accounted for sporadic hospital isolates. Interestingly, two isolates carried the novel OXA-253 variant of OXA-143 together with an upstream novel insertion sequence (ISAba47). While the predominant A. baumannii lineages in Latin America are linked to ST79, ST25, ST15, and ST1 producing OXA-23 enzymes, we report the emergence of highly resistant ST2 (IC-II) isolates in Peru producing OXA-72 and the first identification of ST3 isolates (IC-III) in Latin America, both considered a serious threat to public health worldwide.</description><identifier>ISSN: 2222-1751</identifier><identifier>EISSN: 2222-1751</identifier><identifier>DOI: 10.1038/s41426-018-0127-9</identifier><identifier>PMID: 29970918</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Acinetobacter baumannii - classification ; Acinetobacter baumannii - drug effects ; Acinetobacter baumannii - genetics ; Acinetobacter baumannii - isolation & purification ; Acinetobacter Infections - epidemiology ; Acinetobacter Infections - microbiology ; Acinetobacter Infections - transmission ; Antibiotics ; beta-Lactam Resistance ; Carbapenems - pharmacology ; Communicable Diseases, Emerging - epidemiology ; Communicable Diseases, Emerging - microbiology ; Electrophoresis, Gel, Pulsed-Field ; Genes, Bacterial ; Humans ; Microbial Sensitivity Tests ; Multilocus Sequence Typing ; Pathogens ; Peru - epidemiology</subject><ispartof>Emerging microbes & infections, 2018-07, Vol.7 (1), p.1-9</ispartof><rights>The Author(s) 2018 2018</rights><rights>Copyright Nature Publishing Group Jul 2018</rights><rights>The Author(s) 2018. This work is licensed under the Creative Commons Attribution License https://creativecommons.org/licenses/by/4.0/ (the “License”). 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ST2 and ST79 were endemic in at least one of the hospitals. ST1 and ST3 OXA-23-producing isolates were also identified. They accounted for sporadic hospital isolates. Interestingly, two isolates carried the novel OXA-253 variant of OXA-143 together with an upstream novel insertion sequence (ISAba47). While the predominant A. baumannii lineages in Latin America are linked to ST79, ST25, ST15, and ST1 producing OXA-23 enzymes, we report the emergence of highly resistant ST2 (IC-II) isolates in Peru producing OXA-72 and the first identification of ST3 isolates (IC-III) in Latin America, both considered a serious threat to public health worldwide.</description><subject>Acinetobacter baumannii - classification</subject><subject>Acinetobacter baumannii - drug effects</subject><subject>Acinetobacter baumannii - genetics</subject><subject>Acinetobacter baumannii - isolation & purification</subject><subject>Acinetobacter Infections - epidemiology</subject><subject>Acinetobacter Infections - microbiology</subject><subject>Acinetobacter Infections - transmission</subject><subject>Antibiotics</subject><subject>beta-Lactam Resistance</subject><subject>Carbapenems - pharmacology</subject><subject>Communicable Diseases, Emerging - epidemiology</subject><subject>Communicable Diseases, Emerging - microbiology</subject><subject>Electrophoresis, Gel, Pulsed-Field</subject><subject>Genes, Bacterial</subject><subject>Humans</subject><subject>Microbial Sensitivity Tests</subject><subject>Multilocus Sequence Typing</subject><subject>Pathogens</subject><subject>Peru - epidemiology</subject><issn>2222-1751</issn><issn>2222-1751</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kV1rFTEQhoMottT-AG8k4I0Xrib7kU1AhFKqHjigF3odJtlJTckmx2S30n9vTk8tVdCBZBLyzMtkXkKec_aGs06-LT3vW9EwLutqx0Y9IsdtjYaPA3_84HxETku5YjVGJmrRU3LUKjUyxeUxyRcz5kuMFinEiZZdRphoctRCNrDDiHOTsfiyQFzomfURl2TALpipgXWGGL2nPtZ7hMWnCIHakCIWutncSm5q9pFu_Qyv6RfM6zPyxEEoeHqXT8i3Dxdfzz81288fN-dn28b2nVzqboUYrB0NMOeENcYxroyUY29b6ME6oybHABnAyO0EfMBJSmUUSDFK7E7I-4PubjUzThbjkiHoXa6d5BudwOs_X6L_ri_TtRasY23bV4FXdwI5_VixLHr2xWIIEDGtRbd1nG2nmOQVffkXepXWOpFQqYELJiTr1H8pJjoh5XBL8QNlcyolo7tvmTO9t14frNfVer23Xu9rXjz8633Fb6Mr8O4A-OhSnuFnymHSC9yElF2GaH3R3b_1fwEvk76V</recordid><startdate>20180704</startdate><enddate>20180704</enddate><creator>Levy-Blitchtein, Saúl</creator><creator>Roca, Ignasi</creator><creator>Plasencia-Rebata, Stefany</creator><creator>Vicente-Taboada, William</creator><creator>Velásquez-Pomar, Jorge</creator><creator>Muñoz, Laura</creator><creator>Moreno-Morales, Javier</creator><creator>Pons, Maria J.</creator><creator>del Valle-Mendoza, Juana</creator><creator>Vila, Jordi</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><general>Nature Publishing Group UK</general><scope>0YH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1800-1576</orcidid></search><sort><creationdate>20180704</creationdate><title>Emergence and spread of carbapenem-resistant Acinetobacter baumannii international clones II and III in Lima, Peru</title><author>Levy-Blitchtein, Saúl ; 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It emerged as a global pathogen due to the successful expansion of a few epidemic lineages, or international clones (ICs), producing acquired class D carbapenemases (OXA-type). During the past decade, however, reports regarding IC-I isolates in Latin America are scarce and are non-existent for IC-II and IC-III isolates. This study evaluates the molecular mechanisms of carbapenem resistance and the epidemiology of 80 non-duplicate clinical samples of A. baumannii collected from February 2014 through April 2016 at two tertiary care hospitals in Lima. Almost all isolates were carbapenem-resistant (97.5%), and susceptibility only remained high for colistin (95%). Pulsed-field gel electrophoresis showed two main clusters spread between both hospitals: cluster D containing 51 isolates (63.8%) associated with sequence type 2 (ST2) and carrying OXA-72, and cluster F containing 13 isolates (16.3%) associated with ST79 and also carrying OXA-72. ST2 and ST79 were endemic in at least one of the hospitals. ST1 and ST3 OXA-23-producing isolates were also identified. They accounted for sporadic hospital isolates. Interestingly, two isolates carried the novel OXA-253 variant of OXA-143 together with an upstream novel insertion sequence (ISAba47). While the predominant A. baumannii lineages in Latin America are linked to ST79, ST25, ST15, and ST1 producing OXA-23 enzymes, we report the emergence of highly resistant ST2 (IC-II) isolates in Peru producing OXA-72 and the first identification of ST3 isolates (IC-III) in Latin America, both considered a serious threat to public health worldwide.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>29970918</pmid><doi>10.1038/s41426-018-0127-9</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1800-1576</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acinetobacter baumannii - classification Acinetobacter baumannii - drug effects Acinetobacter baumannii - genetics Acinetobacter baumannii - isolation & purification Acinetobacter Infections - epidemiology Acinetobacter Infections - microbiology Acinetobacter Infections - transmission Antibiotics beta-Lactam Resistance Carbapenems - pharmacology Communicable Diseases, Emerging - epidemiology Communicable Diseases, Emerging - microbiology Electrophoresis, Gel, Pulsed-Field Genes, Bacterial Humans Microbial Sensitivity Tests Multilocus Sequence Typing Pathogens Peru - epidemiology |
title | Emergence and spread of carbapenem-resistant Acinetobacter baumannii international clones II and III in Lima, Peru |
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