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Low-Level Tetracycline Resistance Gene tet(O)_3 in Campylobacter jejuni

Campylobacter (C.) spp. are the most important foodborne, bacterial, and zoonotic pathogens worldwide. Resistance monitoring of foodborne bacterial pathogens is an important tool to control antimicrobial resistance as a part of the “One Health” approach. The detection and functionality of new resist...

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Autores principales: Pacífico, Cátia, Wösten, Marc M. S. M., Hilbert, Friederike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044288/
https://www.ncbi.nlm.nih.gov/pubmed/36978293
http://dx.doi.org/10.3390/antibiotics12030426
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author Pacífico, Cátia
Wösten, Marc M. S. M.
Hilbert, Friederike
author_facet Pacífico, Cátia
Wösten, Marc M. S. M.
Hilbert, Friederike
author_sort Pacífico, Cátia
collection PubMed
description Campylobacter (C.) spp. are the most important foodborne, bacterial, and zoonotic pathogens worldwide. Resistance monitoring of foodborne bacterial pathogens is an important tool to control antimicrobial resistance as a part of the “One Health” approach. The detection and functionality of new resistance genes are of paramount importance in applying more effective screening methods based on whole genome sequencing (WGS). Most tetracycline-resistant C. spp. isolates harbor tet(O), a gene that encodes a ribosomal protection protein. Here we describe tet(O)_3, which has been identified in two food isolates of C. jejuni and is very similar to the tet(O) gene in Streptococcus pneumoniae, having a truncated promoter sequence. This gene confers resistance to tetracycline below 1 mg/L, which is the epidemiological cut-off value. We have analyzed the entire genome of these two isolates, together with a C. jejuni isolate found to have high-level resistance to tetracycline. In contrast to the highly resistant isolate, the promoter of tet(O)_3 is highly responsive to tetracycline, as observed by reverse transcription polymerase chain reaction (RT-PCR). In addition, the two isolates possess a CRISPR repeat, fluoroquinolone resistance due to the gyrA point mutation C257T, a β-lactamase resistance gene bla(OXA-184), a multidrug efflux pump CmeABC and its repressor CmeR, but no plasmid. Low-level antibiotic resistant C. jejuni might therefore have an advantage for surviving in non-host environments.
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spelling pubmed-100442882023-03-29 Low-Level Tetracycline Resistance Gene tet(O)_3 in Campylobacter jejuni Pacífico, Cátia Wösten, Marc M. S. M. Hilbert, Friederike Antibiotics (Basel) Article Campylobacter (C.) spp. are the most important foodborne, bacterial, and zoonotic pathogens worldwide. Resistance monitoring of foodborne bacterial pathogens is an important tool to control antimicrobial resistance as a part of the “One Health” approach. The detection and functionality of new resistance genes are of paramount importance in applying more effective screening methods based on whole genome sequencing (WGS). Most tetracycline-resistant C. spp. isolates harbor tet(O), a gene that encodes a ribosomal protection protein. Here we describe tet(O)_3, which has been identified in two food isolates of C. jejuni and is very similar to the tet(O) gene in Streptococcus pneumoniae, having a truncated promoter sequence. This gene confers resistance to tetracycline below 1 mg/L, which is the epidemiological cut-off value. We have analyzed the entire genome of these two isolates, together with a C. jejuni isolate found to have high-level resistance to tetracycline. In contrast to the highly resistant isolate, the promoter of tet(O)_3 is highly responsive to tetracycline, as observed by reverse transcription polymerase chain reaction (RT-PCR). In addition, the two isolates possess a CRISPR repeat, fluoroquinolone resistance due to the gyrA point mutation C257T, a β-lactamase resistance gene bla(OXA-184), a multidrug efflux pump CmeABC and its repressor CmeR, but no plasmid. Low-level antibiotic resistant C. jejuni might therefore have an advantage for surviving in non-host environments. MDPI 2023-02-21 /pmc/articles/PMC10044288/ /pubmed/36978293 http://dx.doi.org/10.3390/antibiotics12030426 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
Pacífico, Cátia
Wösten, Marc M. S. M.
Hilbert, Friederike
Low-Level Tetracycline Resistance Gene tet(O)_3 in Campylobacter jejuni
title Low-Level Tetracycline Resistance Gene tet(O)_3 in Campylobacter jejuni
title_full Low-Level Tetracycline Resistance Gene tet(O)_3 in Campylobacter jejuni
title_fullStr Low-Level Tetracycline Resistance Gene tet(O)_3 in Campylobacter jejuni
title_full_unstemmed Low-Level Tetracycline Resistance Gene tet(O)_3 in Campylobacter jejuni
title_short Low-Level Tetracycline Resistance Gene tet(O)_3 in Campylobacter jejuni
title_sort low-level tetracycline resistance gene tet(o)_3 in campylobacter jejuni
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044288/
https://www.ncbi.nlm.nih.gov/pubmed/36978293
http://dx.doi.org/10.3390/antibiotics12030426
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