The changing epidemiology of carbapenemase-producing Klebsiella pneumoniae in Italy: toward polyclonal evolution with emergence of high-risk lineages

Abstract Background Previous studies showed that the epidemic of carbapenem-resistant Klebsiella pneumoniae (CR-KP) observed in Italy since 2010 was sustained mostly by strains of clonal group (CG) 258 producing KPC-type carbapenemases. In the framework of the National Antibiotic-Resistance Surveill...

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Veröffentlicht in:Journal of antimicrobial chemotherapy 2021-01, Vol.76 (2), p.355-361
Hauptverfasser: Di Pilato, Vincenzo, Errico, Giulia, Monaco, Monica, Giani, Tommaso, Del Grosso, Maria, Antonelli, Alberto, David, Sophia, Lindh, Erika, Camilli, Romina, Aanensen, David M, Rossolini, Gian Maria, Pantosti, Annalisa
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container_title Journal of antimicrobial chemotherapy
container_volume 76
creator Di Pilato, Vincenzo
Errico, Giulia
Monaco, Monica
Giani, Tommaso
Del Grosso, Maria
Antonelli, Alberto
David, Sophia
Lindh, Erika
Camilli, Romina
Aanensen, David M
Rossolini, Gian Maria
Pantosti, Annalisa
description Abstract Background Previous studies showed that the epidemic of carbapenem-resistant Klebsiella pneumoniae (CR-KP) observed in Italy since 2010 was sustained mostly by strains of clonal group (CG) 258 producing KPC-type carbapenemases. In the framework of the National Antibiotic-Resistance Surveillance (AR-ISS), a countrywide survey was conducted in 2016 to explore the evolution of the phenotypic and genotypic characteristics of CR-KP isolates. Methods From March to July 2016, hospital laboratories participating in AR-ISS were requested to provide consecutive, non-duplicated CR-KP (meropenem and/or imipenem MIC >1 mg/L) from invasive infections. Antibiotic susceptibility was determined according to EUCAST recommendations. A WGS approach was adopted to characterize the isolates by investigating phylogeny, resistome and virulome. Results Twenty-four laboratories provided 157 CR-KP isolates, of which 156 were confirmed as K. pneumoniae sensu stricto by WGS and found to carry at least one carbapenemase-encoding gene, corresponding in most cases (96.1%) to blaKPC. MLST- and SNP-based phylogeny revealed that 87.8% of the isolates clustered in four major lineages: CG258 (47.4%), with ST512 as the most common clone, CG307 (19.9%), ST101 (15.4%) and ST395 (5.1%). A close association was identified between lineages and antibiotic resistance phenotypes and genotypes, virulence traits and capsular types. Colistin resistance, mainly associated with mgrB mutations, was common in all major lineages except ST395. Conclusions This WGS-based survey showed that, although CG258 remained the most common CR-KP lineage in Italy, a polyclonal population has emerged with the spread of the new high-risk lineages CG307, ST101 and ST395, while KPC remained the most common carbapenemase.
doi_str_mv 10.1093/jac/dkaa431
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In the framework of the National Antibiotic-Resistance Surveillance (AR-ISS), a countrywide survey was conducted in 2016 to explore the evolution of the phenotypic and genotypic characteristics of CR-KP isolates. Methods From March to July 2016, hospital laboratories participating in AR-ISS were requested to provide consecutive, non-duplicated CR-KP (meropenem and/or imipenem MIC &gt;1 mg/L) from invasive infections. Antibiotic susceptibility was determined according to EUCAST recommendations. A WGS approach was adopted to characterize the isolates by investigating phylogeny, resistome and virulome. Results Twenty-four laboratories provided 157 CR-KP isolates, of which 156 were confirmed as K. pneumoniae sensu stricto by WGS and found to carry at least one carbapenemase-encoding gene, corresponding in most cases (96.1%) to blaKPC. MLST- and SNP-based phylogeny revealed that 87.8% of the isolates clustered in four major lineages: CG258 (47.4%), with ST512 as the most common clone, CG307 (19.9%), ST101 (15.4%) and ST395 (5.1%). A close association was identified between lineages and antibiotic resistance phenotypes and genotypes, virulence traits and capsular types. Colistin resistance, mainly associated with mgrB mutations, was common in all major lineages except ST395. Conclusions This WGS-based survey showed that, although CG258 remained the most common CR-KP lineage in Italy, a polyclonal population has emerged with the spread of the new high-risk lineages CG307, ST101 and ST395, while KPC remained the most common carbapenemase.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkaa431</identifier><identifier>PMID: 33188415</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><ispartof>Journal of antimicrobial chemotherapy, 2021-01, Vol.76 (2), p.355-361</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com. 2021</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c320t-907c4a732d36d87e28f1ff79e97b0cbc199cb7a06c3427d38f0b29b1769ad1813</citedby><cites>FETCH-LOGICAL-c320t-907c4a732d36d87e28f1ff79e97b0cbc199cb7a06c3427d38f0b29b1769ad1813</cites><orcidid>0000-0003-0295-6877 ; 0000-0002-5863-5805</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33188415$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Di Pilato, Vincenzo</creatorcontrib><creatorcontrib>Errico, Giulia</creatorcontrib><creatorcontrib>Monaco, Monica</creatorcontrib><creatorcontrib>Giani, Tommaso</creatorcontrib><creatorcontrib>Del Grosso, Maria</creatorcontrib><creatorcontrib>Antonelli, Alberto</creatorcontrib><creatorcontrib>David, Sophia</creatorcontrib><creatorcontrib>Lindh, Erika</creatorcontrib><creatorcontrib>Camilli, Romina</creatorcontrib><creatorcontrib>Aanensen, David M</creatorcontrib><creatorcontrib>Rossolini, Gian Maria</creatorcontrib><creatorcontrib>Pantosti, Annalisa</creatorcontrib><creatorcontrib>AR-ISS Laboratory Study Group on carbapenemase-producing Klebsiella pneumoniae</creatorcontrib><creatorcontrib>the AR-ISS Laboratory Study Group on carbapenemase-producing Klebsiella pneumoniae</creatorcontrib><title>The changing epidemiology of carbapenemase-producing Klebsiella pneumoniae in Italy: toward polyclonal evolution with emergence of high-risk lineages</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Abstract Background Previous studies showed that the epidemic of carbapenem-resistant Klebsiella pneumoniae (CR-KP) observed in Italy since 2010 was sustained mostly by strains of clonal group (CG) 258 producing KPC-type carbapenemases. In the framework of the National Antibiotic-Resistance Surveillance (AR-ISS), a countrywide survey was conducted in 2016 to explore the evolution of the phenotypic and genotypic characteristics of CR-KP isolates. Methods From March to July 2016, hospital laboratories participating in AR-ISS were requested to provide consecutive, non-duplicated CR-KP (meropenem and/or imipenem MIC &gt;1 mg/L) from invasive infections. Antibiotic susceptibility was determined according to EUCAST recommendations. A WGS approach was adopted to characterize the isolates by investigating phylogeny, resistome and virulome. Results Twenty-four laboratories provided 157 CR-KP isolates, of which 156 were confirmed as K. pneumoniae sensu stricto by WGS and found to carry at least one carbapenemase-encoding gene, corresponding in most cases (96.1%) to blaKPC. MLST- and SNP-based phylogeny revealed that 87.8% of the isolates clustered in four major lineages: CG258 (47.4%), with ST512 as the most common clone, CG307 (19.9%), ST101 (15.4%) and ST395 (5.1%). A close association was identified between lineages and antibiotic resistance phenotypes and genotypes, virulence traits and capsular types. Colistin resistance, mainly associated with mgrB mutations, was common in all major lineages except ST395. Conclusions This WGS-based survey showed that, although CG258 remained the most common CR-KP lineage in Italy, a polyclonal population has emerged with the spread of the new high-risk lineages CG307, ST101 and ST395, while KPC remained the most common carbapenemase.</description><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kU1P3DAURa0KVAboqvvKK4SEUuw4E8fsEOoHAokNrKMX-yUxOHZqJ6D5IfzfZjRTll29zdF5uvcS8pWz75wpcfkM-tK8ABSCfyIrXpQsy5niB2TFBFtnsliLI3Kc0jNjrFyX1WdyJASvqoKvV-T9sUeqe_Cd9R3F0RocbHCh29DQUg2xgRE9DpAwG2Mws95ydw6bZNE5oKPHeQjeAlLr6e0EbnNFp_AG0dAxuI12wYOj-BrcPNng6ZudeooDxg69xu2X3nZ9Fm16oc56hA7TKTlswSX8sr8n5Onnj8eb39n9w6_bm-v7TIucTZliUhcgRW5EaSqJedXytpUKlWyYbjRXSjcSWKlFkUsjqpY1uWq4LBUYXnFxQs533iXanxnTVA826W0uj2FOdb6UKcuCMbGgFztUx5BSxLYeox0gbmrO6u0O9bJDvd9hob_txXMzoPlg_xW_AGc7IMzjf01_AZtElOY</recordid><startdate>20210119</startdate><enddate>20210119</enddate><creator>Di Pilato, Vincenzo</creator><creator>Errico, Giulia</creator><creator>Monaco, Monica</creator><creator>Giani, Tommaso</creator><creator>Del Grosso, Maria</creator><creator>Antonelli, Alberto</creator><creator>David, Sophia</creator><creator>Lindh, Erika</creator><creator>Camilli, Romina</creator><creator>Aanensen, David M</creator><creator>Rossolini, Gian Maria</creator><creator>Pantosti, Annalisa</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0295-6877</orcidid><orcidid>https://orcid.org/0000-0002-5863-5805</orcidid></search><sort><creationdate>20210119</creationdate><title>The changing epidemiology of carbapenemase-producing Klebsiella pneumoniae in Italy: toward polyclonal evolution with emergence of high-risk lineages</title><author>Di Pilato, Vincenzo ; Errico, Giulia ; Monaco, Monica ; Giani, Tommaso ; Del Grosso, Maria ; Antonelli, Alberto ; David, Sophia ; Lindh, Erika ; Camilli, Romina ; Aanensen, David M ; Rossolini, Gian Maria ; Pantosti, Annalisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c320t-907c4a732d36d87e28f1ff79e97b0cbc199cb7a06c3427d38f0b29b1769ad1813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Di Pilato, Vincenzo</creatorcontrib><creatorcontrib>Errico, Giulia</creatorcontrib><creatorcontrib>Monaco, Monica</creatorcontrib><creatorcontrib>Giani, Tommaso</creatorcontrib><creatorcontrib>Del Grosso, Maria</creatorcontrib><creatorcontrib>Antonelli, Alberto</creatorcontrib><creatorcontrib>David, Sophia</creatorcontrib><creatorcontrib>Lindh, Erika</creatorcontrib><creatorcontrib>Camilli, Romina</creatorcontrib><creatorcontrib>Aanensen, David M</creatorcontrib><creatorcontrib>Rossolini, Gian Maria</creatorcontrib><creatorcontrib>Pantosti, Annalisa</creatorcontrib><creatorcontrib>AR-ISS Laboratory Study Group on carbapenemase-producing Klebsiella pneumoniae</creatorcontrib><creatorcontrib>the AR-ISS Laboratory Study Group on carbapenemase-producing Klebsiella pneumoniae</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Di Pilato, Vincenzo</au><au>Errico, Giulia</au><au>Monaco, Monica</au><au>Giani, Tommaso</au><au>Del Grosso, Maria</au><au>Antonelli, Alberto</au><au>David, Sophia</au><au>Lindh, Erika</au><au>Camilli, Romina</au><au>Aanensen, David M</au><au>Rossolini, Gian Maria</au><au>Pantosti, Annalisa</au><aucorp>AR-ISS Laboratory Study Group on carbapenemase-producing Klebsiella pneumoniae</aucorp><aucorp>the AR-ISS Laboratory Study Group on carbapenemase-producing Klebsiella pneumoniae</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The changing epidemiology of carbapenemase-producing Klebsiella pneumoniae in Italy: toward polyclonal evolution with emergence of high-risk lineages</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2021-01-19</date><risdate>2021</risdate><volume>76</volume><issue>2</issue><spage>355</spage><epage>361</epage><pages>355-361</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>Abstract Background Previous studies showed that the epidemic of carbapenem-resistant Klebsiella pneumoniae (CR-KP) observed in Italy since 2010 was sustained mostly by strains of clonal group (CG) 258 producing KPC-type carbapenemases. In the framework of the National Antibiotic-Resistance Surveillance (AR-ISS), a countrywide survey was conducted in 2016 to explore the evolution of the phenotypic and genotypic characteristics of CR-KP isolates. Methods From March to July 2016, hospital laboratories participating in AR-ISS were requested to provide consecutive, non-duplicated CR-KP (meropenem and/or imipenem MIC &gt;1 mg/L) from invasive infections. Antibiotic susceptibility was determined according to EUCAST recommendations. A WGS approach was adopted to characterize the isolates by investigating phylogeny, resistome and virulome. Results Twenty-four laboratories provided 157 CR-KP isolates, of which 156 were confirmed as K. pneumoniae sensu stricto by WGS and found to carry at least one carbapenemase-encoding gene, corresponding in most cases (96.1%) to blaKPC. MLST- and SNP-based phylogeny revealed that 87.8% of the isolates clustered in four major lineages: CG258 (47.4%), with ST512 as the most common clone, CG307 (19.9%), ST101 (15.4%) and ST395 (5.1%). A close association was identified between lineages and antibiotic resistance phenotypes and genotypes, virulence traits and capsular types. Colistin resistance, mainly associated with mgrB mutations, was common in all major lineages except ST395. Conclusions This WGS-based survey showed that, although CG258 remained the most common CR-KP lineage in Italy, a polyclonal population has emerged with the spread of the new high-risk lineages CG307, ST101 and ST395, while KPC remained the most common carbapenemase.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>33188415</pmid><doi>10.1093/jac/dkaa431</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-0295-6877</orcidid><orcidid>https://orcid.org/0000-0002-5863-5805</orcidid></addata></record>
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title The changing epidemiology of carbapenemase-producing Klebsiella pneumoniae in Italy: toward polyclonal evolution with emergence of high-risk lineages
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