Genomic Diversity of the <i>tet</i>(X)-Positive <i>Myroides</i> Species

The rapid spread of <i>tet</i>(X) genes capable of inactivating tigecycline represents a critical challenge to global public health. This study aims to explore the distribution, genetic diversity, and transferability of <i>tet</i>(X) genes in <i>Myroides</i>, a ge...

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Main Authors: Chong Chen, Taotao Wu, Jing Liu, Yilin Lv
Format: Article
Language:English
Published: MDPI AG 2025-05-01
Series:Microorganisms
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Online Access:https://www.mdpi.com/2076-2607/13/6/1180
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author Chong Chen
Taotao Wu
Jing Liu
Yilin Lv
author_facet Chong Chen
Taotao Wu
Jing Liu
Yilin Lv
author_sort Chong Chen
collection DOAJ
description The rapid spread of <i>tet</i>(X) genes capable of inactivating tigecycline represents a critical challenge to global public health. This study aims to explore the distribution, genetic diversity, and transferability of <i>tet</i>(X) genes in <i>Myroides</i>, a genus of Gram-negative bacteria increasingly implicated in multidrug-resistant (MDR) bacterial infections. From 2021 to 2024, 646 samples of chicken, sheep, soil, and water were randomly collected, yielding nine chicken-derived <i>tet</i>(X)-positive <i>Myroides</i> sp. strains in Shandong, China. All of them were MDR to tetracycline, ceftazidime, gentamicin, amikacin, colistin, ciprofloxacin, gatifloxacin, and trimethoprim-sulfamethoxazole, with elevated minimum inhibitory concentrations (MICs) for tigecycline, florfenicol, and macrolides, but exhibited susceptibility to meropenem (100%), ampicillin-sulbactam (66.7%), and cefotaxime (33.3%). A genomic analysis of the isolates and 86 public <i>tet</i>(X)-positive <i>Myroides</i> genomes revealed the widespread distribution of <i>tet</i>(X) and macrolide-inactivating <i>estT</i> genes across 12 <i>Myroides</i> species, including 7 novel species. Eight <i>tet</i>(X) and eight estT variants were identified, half of which were novel. The phylogenetic analysis highlighted interspecies transmission risks, with IS<i>CR2</i>-mediated transposons of <i>tet</i>(X6) and <i>estT-2</i> across <i>Myroides</i>, <i>Riemerella</i>, <i>Empedobacter</i>, <i>Providencia</i>, <i>Acinetobacter</i>, and <i>Proteus</i> species. These findings illuminate the genomic diversity driving antibiotic resistance in understudied bacterial taxa, with implications for global One Health strategies.
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spelling doaj-art-dd9136edabaa4f298bb98beb7819aa3a2025-08-20T02:20:59ZengMDPI AGMicroorganisms2076-26072025-05-01136118010.3390/microorganisms13061180Genomic Diversity of the <i>tet</i>(X)-Positive <i>Myroides</i> SpeciesChong Chen0Taotao Wu1Jing Liu2Yilin Lv3Joint International Research Laboratory of Agriculture and Agri-Product Safety, Institutes of Agricultural Science and Technology Development, Yangzhou University, Yangzhou 225009, ChinaJoint International Research Laboratory of Agriculture and Agri-Product Safety, Institutes of Agricultural Science and Technology Development, Yangzhou University, Yangzhou 225009, ChinaJoint International Research Laboratory of Agriculture and Agri-Product Safety, Institutes of Agricultural Science and Technology Development, Yangzhou University, Yangzhou 225009, ChinaJoint International Research Laboratory of Agriculture and Agri-Product Safety, Institutes of Agricultural Science and Technology Development, Yangzhou University, Yangzhou 225009, ChinaThe rapid spread of <i>tet</i>(X) genes capable of inactivating tigecycline represents a critical challenge to global public health. This study aims to explore the distribution, genetic diversity, and transferability of <i>tet</i>(X) genes in <i>Myroides</i>, a genus of Gram-negative bacteria increasingly implicated in multidrug-resistant (MDR) bacterial infections. From 2021 to 2024, 646 samples of chicken, sheep, soil, and water were randomly collected, yielding nine chicken-derived <i>tet</i>(X)-positive <i>Myroides</i> sp. strains in Shandong, China. All of them were MDR to tetracycline, ceftazidime, gentamicin, amikacin, colistin, ciprofloxacin, gatifloxacin, and trimethoprim-sulfamethoxazole, with elevated minimum inhibitory concentrations (MICs) for tigecycline, florfenicol, and macrolides, but exhibited susceptibility to meropenem (100%), ampicillin-sulbactam (66.7%), and cefotaxime (33.3%). A genomic analysis of the isolates and 86 public <i>tet</i>(X)-positive <i>Myroides</i> genomes revealed the widespread distribution of <i>tet</i>(X) and macrolide-inactivating <i>estT</i> genes across 12 <i>Myroides</i> species, including 7 novel species. Eight <i>tet</i>(X) and eight estT variants were identified, half of which were novel. The phylogenetic analysis highlighted interspecies transmission risks, with IS<i>CR2</i>-mediated transposons of <i>tet</i>(X6) and <i>estT-2</i> across <i>Myroides</i>, <i>Riemerella</i>, <i>Empedobacter</i>, <i>Providencia</i>, <i>Acinetobacter</i>, and <i>Proteus</i> species. These findings illuminate the genomic diversity driving antibiotic resistance in understudied bacterial taxa, with implications for global One Health strategies.https://www.mdpi.com/2076-2607/13/6/1180<i>Myroides</i> spp.tetracyclines<i>tet</i>(X)macrolides<i>estT</i>IS<i>CR2</i>
spellingShingle Chong Chen
Taotao Wu
Jing Liu
Yilin Lv
Genomic Diversity of the <i>tet</i>(X)-Positive <i>Myroides</i> Species
Microorganisms
<i>Myroides</i> spp.
tetracyclines
<i>tet</i>(X)
macrolides
<i>estT</i>
IS<i>CR2</i>
title Genomic Diversity of the <i>tet</i>(X)-Positive <i>Myroides</i> Species
title_full Genomic Diversity of the <i>tet</i>(X)-Positive <i>Myroides</i> Species
title_fullStr Genomic Diversity of the <i>tet</i>(X)-Positive <i>Myroides</i> Species
title_full_unstemmed Genomic Diversity of the <i>tet</i>(X)-Positive <i>Myroides</i> Species
title_short Genomic Diversity of the <i>tet</i>(X)-Positive <i>Myroides</i> Species
title_sort genomic diversity of the i tet i x positive i myroides i species
topic <i>Myroides</i> spp.
tetracyclines
<i>tet</i>(X)
macrolides
<i>estT</i>
IS<i>CR2</i>
url https://www.mdpi.com/2076-2607/13/6/1180
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AT taotaowu genomicdiversityoftheitetixpositiveimyroidesispecies
AT jingliu genomicdiversityoftheitetixpositiveimyroidesispecies
AT yilinlv genomicdiversityoftheitetixpositiveimyroidesispecies