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Interplay between Klebsiella pneumoniae producing KPC-31 and KPC-3 under treatment with high dosage meropenem: a case report
The objective was to study ceftazidime-avibactam resistant and susceptible Klebsiella pneumoniae isolated from a patient admitted to the Policlinico Umberto I of Rome for SARS-CoV2. Data on the evolution of patient’s conditions, antimicrobial therapies, and microbiological data were collected. Whole...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8731190/ https://www.ncbi.nlm.nih.gov/pubmed/34988712 http://dx.doi.org/10.1007/s10096-021-04388-y |
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author | Arcari, Gabriele Oliva, Alessandra Sacco, Federica Di Lella, Federica Maria Raponi, Giammarco Tomolillo, Dario Curtolo, Ambrogio Venditti, Mario Carattoli, Alessandra |
author_facet | Arcari, Gabriele Oliva, Alessandra Sacco, Federica Di Lella, Federica Maria Raponi, Giammarco Tomolillo, Dario Curtolo, Ambrogio Venditti, Mario Carattoli, Alessandra |
author_sort | Arcari, Gabriele |
collection | PubMed |
description | The objective was to study ceftazidime-avibactam resistant and susceptible Klebsiella pneumoniae isolated from a patient admitted to the Policlinico Umberto I of Rome for SARS-CoV2. Data on the evolution of patient’s conditions, antimicrobial therapies, and microbiological data were collected. Whole-genome sequencing performed by Illumina and Nanopore sequencing methods were used to type the strains. During the hospitalization, a SARS-CoV2-infected patient was colonized by a KPC-producing K. pneumoniae strain and empirically treated with ceftazidime-avibactam (CZA) when presenting spiking fever symptoms. Successively, ST2502 CZA-resistant strain producing the KPC-31 variant gave a pulmonary infection to the patient. The infection was treated with high doses of meropenem. The KPC-31-producing strain disappeared but the patient remained colonized by a KPC-3-producing K. pneumoniae strain. An interplay between highly conserved KPC-31- and KPC-3-producing ST2502 strains occurred in the SARS-CoV2 patient during the hospitalization, selected by CZA and carbapenem treatments, respectively. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10096-021-04388-y. |
format | Online Article Text |
id | pubmed-8731190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-87311902022-01-06 Interplay between Klebsiella pneumoniae producing KPC-31 and KPC-3 under treatment with high dosage meropenem: a case report Arcari, Gabriele Oliva, Alessandra Sacco, Federica Di Lella, Federica Maria Raponi, Giammarco Tomolillo, Dario Curtolo, Ambrogio Venditti, Mario Carattoli, Alessandra Eur J Clin Microbiol Infect Dis Brief Report The objective was to study ceftazidime-avibactam resistant and susceptible Klebsiella pneumoniae isolated from a patient admitted to the Policlinico Umberto I of Rome for SARS-CoV2. Data on the evolution of patient’s conditions, antimicrobial therapies, and microbiological data were collected. Whole-genome sequencing performed by Illumina and Nanopore sequencing methods were used to type the strains. During the hospitalization, a SARS-CoV2-infected patient was colonized by a KPC-producing K. pneumoniae strain and empirically treated with ceftazidime-avibactam (CZA) when presenting spiking fever symptoms. Successively, ST2502 CZA-resistant strain producing the KPC-31 variant gave a pulmonary infection to the patient. The infection was treated with high doses of meropenem. The KPC-31-producing strain disappeared but the patient remained colonized by a KPC-3-producing K. pneumoniae strain. An interplay between highly conserved KPC-31- and KPC-3-producing ST2502 strains occurred in the SARS-CoV2 patient during the hospitalization, selected by CZA and carbapenem treatments, respectively. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10096-021-04388-y. Springer Berlin Heidelberg 2022-01-06 2022 /pmc/articles/PMC8731190/ /pubmed/34988712 http://dx.doi.org/10.1007/s10096-021-04388-y Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Brief Report Arcari, Gabriele Oliva, Alessandra Sacco, Federica Di Lella, Federica Maria Raponi, Giammarco Tomolillo, Dario Curtolo, Ambrogio Venditti, Mario Carattoli, Alessandra Interplay between Klebsiella pneumoniae producing KPC-31 and KPC-3 under treatment with high dosage meropenem: a case report |
title | Interplay between Klebsiella pneumoniae producing KPC-31 and KPC-3 under treatment with high dosage meropenem: a case report |
title_full | Interplay between Klebsiella pneumoniae producing KPC-31 and KPC-3 under treatment with high dosage meropenem: a case report |
title_fullStr | Interplay between Klebsiella pneumoniae producing KPC-31 and KPC-3 under treatment with high dosage meropenem: a case report |
title_full_unstemmed | Interplay between Klebsiella pneumoniae producing KPC-31 and KPC-3 under treatment with high dosage meropenem: a case report |
title_short | Interplay between Klebsiella pneumoniae producing KPC-31 and KPC-3 under treatment with high dosage meropenem: a case report |
title_sort | interplay between klebsiella pneumoniae producing kpc-31 and kpc-3 under treatment with high dosage meropenem: a case report |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8731190/ https://www.ncbi.nlm.nih.gov/pubmed/34988712 http://dx.doi.org/10.1007/s10096-021-04388-y |
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