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Genomics Insight into cfr-Mediated Linezolid-Resistant LA-MRSA in Italian Pig Holdings
The cfr genes encode for a 23S rRNA methyltransferase, conferring a multiresistance phenotype to phenicol, lincosamide, oxazolidinone, pleuromutilin, and streptogramin A antibiotics. These genes have been described in staphylococci, including methicillin-resistant Staphylococcus aureus (MRSA). In th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044604/ https://www.ncbi.nlm.nih.gov/pubmed/36978397 http://dx.doi.org/10.3390/antibiotics12030530 |
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author | Iurescia, Manuela Diaconu, Elena Lavinia Alba, Patricia Feltrin, Fabiola Buccella, Carmela Onorati, Roberta Giacomi, Angelo Caprioli, Andrea Franco, Alessia Battisti, Antonio Carfora, Virginia |
author_facet | Iurescia, Manuela Diaconu, Elena Lavinia Alba, Patricia Feltrin, Fabiola Buccella, Carmela Onorati, Roberta Giacomi, Angelo Caprioli, Andrea Franco, Alessia Battisti, Antonio Carfora, Virginia |
author_sort | Iurescia, Manuela |
collection | PubMed |
description | The cfr genes encode for a 23S rRNA methyltransferase, conferring a multiresistance phenotype to phenicol, lincosamide, oxazolidinone, pleuromutilin, and streptogramin A antibiotics. These genes have been described in staphylococci, including methicillin-resistant Staphylococcus aureus (MRSA). In this study, we retrospectively performed an in-depth genomic characterisation of three cfr-positive, multidrug-resistant (MDR) livestock-associated (LA) MRSA clonal complexes (CCs) 1 and 398 detected in different Italian pig holdings (2008–2011) during population studies on Italian livestock (2008–2014). We used a combined Illumina and Oxford Nanopore Technologies (ONT) whole genome sequencing (WGS) approach on two isolates (the 2008 CC1 and the 2010 CC398 isolates, but not the 2011 CC1 isolate). Interestingly, the three isolates presented different cfr variants, with only one displaying a linezolid-resistant phenotype. In isolate 2008 CC1, the cfr gene was identified within a Tn558 composite transposon-like structure flanked by IS elements located on a novel 44,826 bp plasmid. This represents the first report of CC1 LA-MRSA harbouring the cfr gene in its functional variant. Differently, cfr was chromosomally located in isolate 2010 CC398. Our findings have significant public health implications, confirm the need for the continuous genomic surveillance of cfr-positive zoonotic LA-MRSA, and backdate cfr presence in LA-MRSA from Italian pigs to at least 2008. |
format | Online Article Text |
id | pubmed-10044604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100446042023-03-29 Genomics Insight into cfr-Mediated Linezolid-Resistant LA-MRSA in Italian Pig Holdings Iurescia, Manuela Diaconu, Elena Lavinia Alba, Patricia Feltrin, Fabiola Buccella, Carmela Onorati, Roberta Giacomi, Angelo Caprioli, Andrea Franco, Alessia Battisti, Antonio Carfora, Virginia Antibiotics (Basel) Article The cfr genes encode for a 23S rRNA methyltransferase, conferring a multiresistance phenotype to phenicol, lincosamide, oxazolidinone, pleuromutilin, and streptogramin A antibiotics. These genes have been described in staphylococci, including methicillin-resistant Staphylococcus aureus (MRSA). In this study, we retrospectively performed an in-depth genomic characterisation of three cfr-positive, multidrug-resistant (MDR) livestock-associated (LA) MRSA clonal complexes (CCs) 1 and 398 detected in different Italian pig holdings (2008–2011) during population studies on Italian livestock (2008–2014). We used a combined Illumina and Oxford Nanopore Technologies (ONT) whole genome sequencing (WGS) approach on two isolates (the 2008 CC1 and the 2010 CC398 isolates, but not the 2011 CC1 isolate). Interestingly, the three isolates presented different cfr variants, with only one displaying a linezolid-resistant phenotype. In isolate 2008 CC1, the cfr gene was identified within a Tn558 composite transposon-like structure flanked by IS elements located on a novel 44,826 bp plasmid. This represents the first report of CC1 LA-MRSA harbouring the cfr gene in its functional variant. Differently, cfr was chromosomally located in isolate 2010 CC398. Our findings have significant public health implications, confirm the need for the continuous genomic surveillance of cfr-positive zoonotic LA-MRSA, and backdate cfr presence in LA-MRSA from Italian pigs to at least 2008. MDPI 2023-03-07 /pmc/articles/PMC10044604/ /pubmed/36978397 http://dx.doi.org/10.3390/antibiotics12030530 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Iurescia, Manuela Diaconu, Elena Lavinia Alba, Patricia Feltrin, Fabiola Buccella, Carmela Onorati, Roberta Giacomi, Angelo Caprioli, Andrea Franco, Alessia Battisti, Antonio Carfora, Virginia Genomics Insight into cfr-Mediated Linezolid-Resistant LA-MRSA in Italian Pig Holdings |
title | Genomics Insight into cfr-Mediated Linezolid-Resistant LA-MRSA in Italian Pig Holdings |
title_full | Genomics Insight into cfr-Mediated Linezolid-Resistant LA-MRSA in Italian Pig Holdings |
title_fullStr | Genomics Insight into cfr-Mediated Linezolid-Resistant LA-MRSA in Italian Pig Holdings |
title_full_unstemmed | Genomics Insight into cfr-Mediated Linezolid-Resistant LA-MRSA in Italian Pig Holdings |
title_short | Genomics Insight into cfr-Mediated Linezolid-Resistant LA-MRSA in Italian Pig Holdings |
title_sort | genomics insight into cfr-mediated linezolid-resistant la-mrsa in italian pig holdings |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044604/ https://www.ncbi.nlm.nih.gov/pubmed/36978397 http://dx.doi.org/10.3390/antibiotics12030530 |
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