Molecular Characterization of Pseudomonas putida Group Isolates Carrying blaVIM-2 Disseminated in a University Hospital in Korea
Pseudomonas putida group are Gram-negative bacilli with polar flagellation, which are ubiquitous in the environment, although they are rarely involved in human infections. The aim of this study was to identify the dissemination of VIM-2–producing P. putida group in clinical isolates from a hospital...
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Veröffentlicht in: | Microbial drug resistance (Larchmont, N.Y.) N.Y.), 2018-06, Vol.24 (5), p.627-634 |
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creator | Hong, Jun Sung Yoon, Eun-Jeong Song, Wonkeun Seo, Yu Bin Shin, Saeam Park, Min-Jeong Jeong, Seok Hoon Lee, Kyungwon |
description | Pseudomonas putida
group are Gram-negative bacilli with polar flagellation, which are ubiquitous in the environment, although they are rarely involved in human infections. The aim of this study was to identify the dissemination of VIM-2–producing
P. putida
group in clinical isolates from a hospital in Korea. Thirteen strains were collected from 2014 to 2015 for the study. The isolates were recovered from urine cultures of both inpatients and outpatients at the hospital. Minimum inhibitory concentrations of antibiotics were determined by Etest. Carbapenemase genes were amplified by polymerase chain reaction and sequenced. Pulsed-field gel electrophoresis was performed for strain typing. Whole-genome sequencing was carried out randomly for two strains chosen from each year of the study to analyze the plasmid structure carrying the
bla
VIM-2
genes. The 13 isolates carried nine different class I integrons harboring VIM-2 and were resistant to meropenem and imipenem (minimum inhibitory concentrations, ≥32 μg/ml), thus exhibiting a multidrug-resistant phenotype. The
bla
VIM-2
gene was located on a plasmid in seven of the isolates and on the chromosome in six isolates. Each case of the
bla
VIM-2
gene was disseminated by clonal spread, horizontal transfer, and was mostly an occasional occurrence. In this study, we demonstrated that multidrug-resistant
P. putida
group carrying VIM-2 has reemerged in human specimens in Korea. |
doi_str_mv | 10.1089/mdr.2017.0257 |
format | Article |
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group are Gram-negative bacilli with polar flagellation, which are ubiquitous in the environment, although they are rarely involved in human infections. The aim of this study was to identify the dissemination of VIM-2–producing
P. putida
group in clinical isolates from a hospital in Korea. Thirteen strains were collected from 2014 to 2015 for the study. The isolates were recovered from urine cultures of both inpatients and outpatients at the hospital. Minimum inhibitory concentrations of antibiotics were determined by Etest. Carbapenemase genes were amplified by polymerase chain reaction and sequenced. Pulsed-field gel electrophoresis was performed for strain typing. Whole-genome sequencing was carried out randomly for two strains chosen from each year of the study to analyze the plasmid structure carrying the
bla
VIM-2
genes. The 13 isolates carried nine different class I integrons harboring VIM-2 and were resistant to meropenem and imipenem (minimum inhibitory concentrations, ≥32 μg/ml), thus exhibiting a multidrug-resistant phenotype. The
bla
VIM-2
gene was located on a plasmid in seven of the isolates and on the chromosome in six isolates. Each case of the
bla
VIM-2
gene was disseminated by clonal spread, horizontal transfer, and was mostly an occasional occurrence. In this study, we demonstrated that multidrug-resistant
P. putida
group carrying VIM-2 has reemerged in human specimens in Korea.</description><identifier>ISSN: 1076-6294</identifier><identifier>EISSN: 1931-8448</identifier><identifier>DOI: 10.1089/mdr.2017.0257</identifier><language>eng</language><publisher>New Rochelle: Mary Ann Liebert, Inc</publisher><subject>Antibiotics ; Bacilli ; Bacteria ; Carbapenemase ; Clinical isolates ; Deoxyribonucleic acid ; DNA ; Electrophoresis ; Epidemiology ; Gel electrophoresis ; Gene sequencing ; Genes ; Genomes ; Gram-negative bacilli ; Horizontal transfer ; Hospitals ; Hybridization ; Identification ; Imipenem ; Laboratories ; Medicine ; Meropenem ; Molecular chains ; Multidrug resistance ; Multilocus sequence typing ; Phenotypes ; Plasmids ; Polymerase chain reaction ; Pseudomonas ; Pseudomonas aeruginosa ; Pseudomonas putida ; Pulsed-field gel electrophoresis ; Research centers ; University colleges ; Urine</subject><ispartof>Microbial drug resistance (Larchmont, N.Y.), 2018-06, Vol.24 (5), p.627-634</ispartof><rights>2018, Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2018, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Hong, Jun Sung</creatorcontrib><creatorcontrib>Yoon, Eun-Jeong</creatorcontrib><creatorcontrib>Song, Wonkeun</creatorcontrib><creatorcontrib>Seo, Yu Bin</creatorcontrib><creatorcontrib>Shin, Saeam</creatorcontrib><creatorcontrib>Park, Min-Jeong</creatorcontrib><creatorcontrib>Jeong, Seok Hoon</creatorcontrib><creatorcontrib>Lee, Kyungwon</creatorcontrib><title>Molecular Characterization of Pseudomonas putida Group Isolates Carrying blaVIM-2 Disseminated in a University Hospital in Korea</title><title>Microbial drug resistance (Larchmont, N.Y.)</title><description>Pseudomonas putida
group are Gram-negative bacilli with polar flagellation, which are ubiquitous in the environment, although they are rarely involved in human infections. The aim of this study was to identify the dissemination of VIM-2–producing
P. putida
group in clinical isolates from a hospital in Korea. Thirteen strains were collected from 2014 to 2015 for the study. The isolates were recovered from urine cultures of both inpatients and outpatients at the hospital. Minimum inhibitory concentrations of antibiotics were determined by Etest. Carbapenemase genes were amplified by polymerase chain reaction and sequenced. Pulsed-field gel electrophoresis was performed for strain typing. Whole-genome sequencing was carried out randomly for two strains chosen from each year of the study to analyze the plasmid structure carrying the
bla
VIM-2
genes. The 13 isolates carried nine different class I integrons harboring VIM-2 and were resistant to meropenem and imipenem (minimum inhibitory concentrations, ≥32 μg/ml), thus exhibiting a multidrug-resistant phenotype. The
bla
VIM-2
gene was located on a plasmid in seven of the isolates and on the chromosome in six isolates. Each case of the
bla
VIM-2
gene was disseminated by clonal spread, horizontal transfer, and was mostly an occasional occurrence. In this study, we demonstrated that multidrug-resistant
P. putida
group carrying VIM-2 has reemerged in human specimens in Korea.</description><subject>Antibiotics</subject><subject>Bacilli</subject><subject>Bacteria</subject><subject>Carbapenemase</subject><subject>Clinical isolates</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Electrophoresis</subject><subject>Epidemiology</subject><subject>Gel electrophoresis</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Genomes</subject><subject>Gram-negative bacilli</subject><subject>Horizontal transfer</subject><subject>Hospitals</subject><subject>Hybridization</subject><subject>Identification</subject><subject>Imipenem</subject><subject>Laboratories</subject><subject>Medicine</subject><subject>Meropenem</subject><subject>Molecular chains</subject><subject>Multidrug resistance</subject><subject>Multilocus sequence typing</subject><subject>Phenotypes</subject><subject>Plasmids</subject><subject>Polymerase chain reaction</subject><subject>Pseudomonas</subject><subject>Pseudomonas aeruginosa</subject><subject>Pseudomonas putida</subject><subject>Pulsed-field gel electrophoresis</subject><subject>Research centers</subject><subject>University colleges</subject><subject>Urine</subject><issn>1076-6294</issn><issn>1931-8448</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkU1r3DAQhk1JIB_tMXdBLr14ow9Lto5l22SXJLSHbq9ibMmNgiy5khzYnvrTI5Oecpph3odhhqeqrgjeENzJm0nHDcWk3WDK2w_VOZGM1F3TdCelx62oBZXNWXWR0jPGmBPBzqt_j8GZYXEQ0fYJIgzZRPsXsg0ehRH9SGbRYQoeEpqXbDWguxiWGe1TcJBNQluI8Wj9b9Q7-LV_rCn6alMyk_Ul1sh6BOjg7YuJyeYj2oU02wxuDe5DNPCxOh3BJfPpf72sDrfffm539cP3u_32y0M9UYFzDUaC1N0oYAQOkrWsFbyTwzgywwgVjPMWdMm0FoPm5VHMgPZckr7HVGN2WX1-2zvH8GcxKavJpsE4B96EJSkiu6bllBJS0Ot36HNYoi_XKYobKbgoYKHYGzVBPIL3zprexKzmaNeJIlitVlSxolYrarXCXgHFfoIB</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Hong, Jun Sung</creator><creator>Yoon, Eun-Jeong</creator><creator>Song, 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Carrying blaVIM-2 Disseminated in a University Hospital in Korea</title><author>Hong, Jun Sung ; Yoon, Eun-Jeong ; Song, Wonkeun ; Seo, Yu Bin ; Shin, Saeam ; Park, Min-Jeong ; Jeong, Seok Hoon ; Lee, Kyungwon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-m260t-ae9a9d8f6afa5a937376589cff3e31263557adfa5dd6cd529403a2b591bb02d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antibiotics</topic><topic>Bacilli</topic><topic>Bacteria</topic><topic>Carbapenemase</topic><topic>Clinical isolates</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Electrophoresis</topic><topic>Epidemiology</topic><topic>Gel electrophoresis</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>Genomes</topic><topic>Gram-negative bacilli</topic><topic>Horizontal transfer</topic><topic>Hospitals</topic><topic>Hybridization</topic><topic>Identification</topic><topic>Imipenem</topic><topic>Laboratories</topic><topic>Medicine</topic><topic>Meropenem</topic><topic>Molecular chains</topic><topic>Multidrug resistance</topic><topic>Multilocus sequence typing</topic><topic>Phenotypes</topic><topic>Plasmids</topic><topic>Polymerase chain reaction</topic><topic>Pseudomonas</topic><topic>Pseudomonas aeruginosa</topic><topic>Pseudomonas putida</topic><topic>Pulsed-field gel electrophoresis</topic><topic>Research centers</topic><topic>University colleges</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hong, Jun Sung</creatorcontrib><creatorcontrib>Yoon, Eun-Jeong</creatorcontrib><creatorcontrib>Song, Wonkeun</creatorcontrib><creatorcontrib>Seo, Yu Bin</creatorcontrib><creatorcontrib>Shin, Saeam</creatorcontrib><creatorcontrib>Park, Min-Jeong</creatorcontrib><creatorcontrib>Jeong, Seok 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Eun-Jeong</au><au>Song, Wonkeun</au><au>Seo, Yu Bin</au><au>Shin, Saeam</au><au>Park, Min-Jeong</au><au>Jeong, Seok Hoon</au><au>Lee, Kyungwon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Characterization of Pseudomonas putida Group Isolates Carrying blaVIM-2 Disseminated in a University Hospital in Korea</atitle><jtitle>Microbial drug resistance (Larchmont, N.Y.)</jtitle><date>2018-06-01</date><risdate>2018</risdate><volume>24</volume><issue>5</issue><spage>627</spage><epage>634</epage><pages>627-634</pages><issn>1076-6294</issn><eissn>1931-8448</eissn><abstract>Pseudomonas putida
group are Gram-negative bacilli with polar flagellation, which are ubiquitous in the environment, although they are rarely involved in human infections. The aim of this study was to identify the dissemination of VIM-2–producing
P. putida
group in clinical isolates from a hospital in Korea. Thirteen strains were collected from 2014 to 2015 for the study. The isolates were recovered from urine cultures of both inpatients and outpatients at the hospital. Minimum inhibitory concentrations of antibiotics were determined by Etest. Carbapenemase genes were amplified by polymerase chain reaction and sequenced. Pulsed-field gel electrophoresis was performed for strain typing. Whole-genome sequencing was carried out randomly for two strains chosen from each year of the study to analyze the plasmid structure carrying the
bla
VIM-2
genes. The 13 isolates carried nine different class I integrons harboring VIM-2 and were resistant to meropenem and imipenem (minimum inhibitory concentrations, ≥32 μg/ml), thus exhibiting a multidrug-resistant phenotype. The
bla
VIM-2
gene was located on a plasmid in seven of the isolates and on the chromosome in six isolates. Each case of the
bla
VIM-2
gene was disseminated by clonal spread, horizontal transfer, and was mostly an occasional occurrence. In this study, we demonstrated that multidrug-resistant
P. putida
group carrying VIM-2 has reemerged in human specimens in Korea.</abstract><cop>New Rochelle</cop><pub>Mary Ann Liebert, Inc</pub><doi>10.1089/mdr.2017.0257</doi><tpages>8</tpages></addata></record> |
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source | Alma/SFX Local Collection |
subjects | Antibiotics Bacilli Bacteria Carbapenemase Clinical isolates Deoxyribonucleic acid DNA Electrophoresis Epidemiology Gel electrophoresis Gene sequencing Genes Genomes Gram-negative bacilli Horizontal transfer Hospitals Hybridization Identification Imipenem Laboratories Medicine Meropenem Molecular chains Multidrug resistance Multilocus sequence typing Phenotypes Plasmids Polymerase chain reaction Pseudomonas Pseudomonas aeruginosa Pseudomonas putida Pulsed-field gel electrophoresis Research centers University colleges Urine |
title | Molecular Characterization of Pseudomonas putida Group Isolates Carrying blaVIM-2 Disseminated in a University Hospital in Korea |
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