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FosA3 emerging in clinical carbapenemase-producing C. freundii

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Author
Marchetti, Vittoria Mattioni
Venturelli, Irene
Cassetti, Tiziana
Meschiari, Marianna
Migliavacca, Roberta
Bitar, IbrahimORCiD Profile - 0000-0002-9117-3729WoS Profile - C-6589-2018Scopus Profile - 56241922600

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Publication date
2024
Published in
Frontiers in Cellular and Infection Microbiology
Volume / Issue
14 (06 August 2024)
ISBN / ISSN
ISSN: 2235-2988
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  • Faculty of Medicine in Pilsen

This publication has a published version with DOI 10.3389/fcimb.2024.1447933

Abstract
Fosfomycin (FOS) is an effective antibiotic against multidrug-resistant Enterobacterales, but its effectiveness is reducing. Little is known on the current prevalence of FosA enzymes in low-risk pathogens, such as Citrobacter freundii. The aim of the study was the molecular characterization of a carbapenemase- and FosA-producing C. freundii collected in Italy. AK867, collected in 2023, showed an XDR profile, retaining susceptibility only to colistin. AK867 showed a FOS MIC >128 mg/L by ADM. Based on WGS, AK867 belonged to ST116 and owned a wide resistome, including fosA3, blaKPC-2, and blaVIM-1. fosA3 was carried by a conjugative pKPC-CAV1312 plasmid of 320,480 bp, on a novel composite transposon (12,907 bp). FosA3 transposon shared similarities with other fosA3-harboring pKPC-CAV1312 plasmids among Citrobacter spp. We report the first case of FosA3 production in clinical carbapenemase-producing C. freundii ST116. The incidence of FosA3 enzymes is increasing among Enterobacterales, affecting even low-virulence pathogens, as C. freundii.
Keywords
fosfomycin, Citrobacter freundii, carbapenemases, fosfomycin resistance, fosA3 gene,
Permanent link
https://hdl.handle.net/20.500.14178/2666
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WOS:001294121200001
SCOPUS:2-s2.0-85201526679
PUBMED:39247055
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Full text of this result is licensed under: Creative Commons Uveďte původ 4.0 International

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