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Characterization of Silver Resistance and Coexistence of sil Operon with Antibiotic Resistance Genes Among Gram-Negative Pathogens Isolated from Wound Samples by Using Whole-Genome Sequencing

PURPOSE: Due to the extensive consumption of silver-containing compound, silver resistance spreads among gram-negative pathogens and is regarded as a great public problem. In this study, we investigated silver resistance mechanisms and antibiotic resistance genes co-harbored with sil operon among gr...

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Autores principales: Wang, Haichen, Li, Jia, Min, Changhang, Xia, Fengjun, Tang, Mengli, Li, Jun, Hu, Yongmei, Zou, Mingxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982571/
https://www.ncbi.nlm.nih.gov/pubmed/35392367
http://dx.doi.org/10.2147/IDR.S358730
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author Wang, Haichen
Li, Jia
Min, Changhang
Xia, Fengjun
Tang, Mengli
Li, Jun
Hu, Yongmei
Zou, Mingxiang
author_facet Wang, Haichen
Li, Jia
Min, Changhang
Xia, Fengjun
Tang, Mengli
Li, Jun
Hu, Yongmei
Zou, Mingxiang
author_sort Wang, Haichen
collection PubMed
description PURPOSE: Due to the extensive consumption of silver-containing compound, silver resistance spreads among gram-negative pathogens and is regarded as a great public problem. In this study, we investigated silver resistance mechanisms and antibiotic resistance genes co-harbored with sil operon among gram-negative pathogens isolated from wound samples. METHODS: A total of 193 strains of gram-negative pathogens were collected from wound samples between 2018 and 2020 in Xiangya hospital. Silver resistance was obtained by broth microdilution method. The silver resistance mechanisms and the prevalence, genetic environments, and coexistence with antibiotic resistance genes of sil operon were investigated by polymerase chain reaction (PCR) and whole genome sequencing (WGS). RESULTS: Among 193 strains, nine strains (4.7%) were resistant to Ag(+) and assigned to the following species: Klebsiella pneumoniae (n = 5) and Enterobacter hormaechei (n = 4). WGS confirmed that 24 strains carried the entire sil operon, including the four Ag(+)-resistant E. hormaechei and 20 Ag(+)-susceptible strains, while PCR failed to detect some sil genes, especially silE, due to sequence variations. In seven strains, Tn7 transposon was identified in the upstream of sil operon. Spontaneous mutants resistant to Ag(+) were induced in 15 out of 20 Ag(+)-susceptible strains, including K. pneumoniae strains belonged to high-risk groups (ST11 and ST15). The sil-positive strains harbored various antibiotic resistance genes, including bla(ESBL) and bla(ApmC). WGS revealed that a single mutation in cusS gene and loss of major porins conferred silver resistance in the five K. pneumoniae strains. CONCLUSION: Our findings emphasize the cryptic silver resistance is prevalent among Enterobacteriaceae with sil operon or with the combination of cus operon and major porin loss and increase the understanding of the prevalence of sil operon with antibiotic resistance genes, especially bla(ESBL) and bla(ApmC).
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spelling pubmed-89825712022-04-06 Characterization of Silver Resistance and Coexistence of sil Operon with Antibiotic Resistance Genes Among Gram-Negative Pathogens Isolated from Wound Samples by Using Whole-Genome Sequencing Wang, Haichen Li, Jia Min, Changhang Xia, Fengjun Tang, Mengli Li, Jun Hu, Yongmei Zou, Mingxiang Infect Drug Resist Original Research PURPOSE: Due to the extensive consumption of silver-containing compound, silver resistance spreads among gram-negative pathogens and is regarded as a great public problem. In this study, we investigated silver resistance mechanisms and antibiotic resistance genes co-harbored with sil operon among gram-negative pathogens isolated from wound samples. METHODS: A total of 193 strains of gram-negative pathogens were collected from wound samples between 2018 and 2020 in Xiangya hospital. Silver resistance was obtained by broth microdilution method. The silver resistance mechanisms and the prevalence, genetic environments, and coexistence with antibiotic resistance genes of sil operon were investigated by polymerase chain reaction (PCR) and whole genome sequencing (WGS). RESULTS: Among 193 strains, nine strains (4.7%) were resistant to Ag(+) and assigned to the following species: Klebsiella pneumoniae (n = 5) and Enterobacter hormaechei (n = 4). WGS confirmed that 24 strains carried the entire sil operon, including the four Ag(+)-resistant E. hormaechei and 20 Ag(+)-susceptible strains, while PCR failed to detect some sil genes, especially silE, due to sequence variations. In seven strains, Tn7 transposon was identified in the upstream of sil operon. Spontaneous mutants resistant to Ag(+) were induced in 15 out of 20 Ag(+)-susceptible strains, including K. pneumoniae strains belonged to high-risk groups (ST11 and ST15). The sil-positive strains harbored various antibiotic resistance genes, including bla(ESBL) and bla(ApmC). WGS revealed that a single mutation in cusS gene and loss of major porins conferred silver resistance in the five K. pneumoniae strains. CONCLUSION: Our findings emphasize the cryptic silver resistance is prevalent among Enterobacteriaceae with sil operon or with the combination of cus operon and major porin loss and increase the understanding of the prevalence of sil operon with antibiotic resistance genes, especially bla(ESBL) and bla(ApmC). Dove 2022-03-31 /pmc/articles/PMC8982571/ /pubmed/35392367 http://dx.doi.org/10.2147/IDR.S358730 Text en © 2022 Wang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wang, Haichen
Li, Jia
Min, Changhang
Xia, Fengjun
Tang, Mengli
Li, Jun
Hu, Yongmei
Zou, Mingxiang
Characterization of Silver Resistance and Coexistence of sil Operon with Antibiotic Resistance Genes Among Gram-Negative Pathogens Isolated from Wound Samples by Using Whole-Genome Sequencing
title Characterization of Silver Resistance and Coexistence of sil Operon with Antibiotic Resistance Genes Among Gram-Negative Pathogens Isolated from Wound Samples by Using Whole-Genome Sequencing
title_full Characterization of Silver Resistance and Coexistence of sil Operon with Antibiotic Resistance Genes Among Gram-Negative Pathogens Isolated from Wound Samples by Using Whole-Genome Sequencing
title_fullStr Characterization of Silver Resistance and Coexistence of sil Operon with Antibiotic Resistance Genes Among Gram-Negative Pathogens Isolated from Wound Samples by Using Whole-Genome Sequencing
title_full_unstemmed Characterization of Silver Resistance and Coexistence of sil Operon with Antibiotic Resistance Genes Among Gram-Negative Pathogens Isolated from Wound Samples by Using Whole-Genome Sequencing
title_short Characterization of Silver Resistance and Coexistence of sil Operon with Antibiotic Resistance Genes Among Gram-Negative Pathogens Isolated from Wound Samples by Using Whole-Genome Sequencing
title_sort characterization of silver resistance and coexistence of sil operon with antibiotic resistance genes among gram-negative pathogens isolated from wound samples by using whole-genome sequencing
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982571/
https://www.ncbi.nlm.nih.gov/pubmed/35392367
http://dx.doi.org/10.2147/IDR.S358730
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