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Main Authors: Yu, Yan, Zhang, Runzhi, Pan, Wei, Sheng, Xinyi, Chen, Susu, Wang, Junjun, Lu, Junwan, Bao, Qiyu, Hu, Yunliang, Jiang, Pengfei, Huang, Dawei
Format: Artículo científico
Language:en
Published: Frontiers in microbiology 2024
Online Access:https://pubmed.ncbi.nlm.nih.gov/39726966/
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author Yu, Yan
Zhang, Runzhi
Pan, Wei
Sheng, Xinyi
Chen, Susu
Wang, Junjun
Lu, Junwan
Bao, Qiyu
Hu, Yunliang
Jiang, Pengfei
Huang, Dawei
author_facet Yu, Yan
Zhang, Runzhi
Pan, Wei
Sheng, Xinyi
Chen, Susu
Wang, Junjun
Lu, Junwan
Bao, Qiyu
Hu, Yunliang
Jiang, Pengfei
Huang, Dawei
Yu, Yan
Zhang, Runzhi
Pan, Wei
Sheng, Xinyi
Chen, Susu
Wang, Junjun
Lu, Junwan
Bao, Qiyu
Hu, Yunliang
Jiang, Pengfei
Huang, Dawei
collection PubMed - marine biology
contents Identification and characterization of a novel chromosome-encoded aminoglycoside -nucleotidyltransferase gene, in sp. TYF-12 isolated from the marine fish intestine. Yu, Yan Zhang, Runzhi Pan, Wei Sheng, Xinyi Chen, Susu Wang, Junjun Lu, Junwan Bao, Qiyu Hu, Yunliang Jiang, Pengfei Huang, Dawei The mechanisms underlying the resistance of the genus to aminoglycosides are complex, which poses a challenge for the efficient treatment of infectious diseases caused by these pathogens. To help clinicians treat infections more effectively, a more comprehensive understanding of antibiotic resistance mechanisms is urgently needed. Plates were streaked to isolate bacteria from the intestinal contents of fish. The standard agar dilution method was used to determine the minimum inhibitory concentrations (MICs) of the antimicrobial agents. Molecular cloning was carried out to study the function of the novel antibiotic inactivation gene The kinetic parameters of ANT(9)Id were measured by a SpectraMax multifunctional microplate reader. Whole-genome sequencing and bioinformatic analysis were conducted to elucidate the sequence structure and evolutionary relationships of similar genes. The novel aminoglycoside -nucleotidyltransferase gene was encoded on the chromosome of a species-unclassified isolate designated sp. TYF-12, which was isolated from the intestine of a marine fish. Among the 11 aminoglycosides tested, was resistant to only spectinomycin. The MIC of spectinomycin for the recombinant strain carrying (pUCP20-/DH5α) increased 64-fold compared with that of the control strain (pUCP20/DH5ɑ). ANT(9)Id shares the highest amino acid (aa) identity of 46.70% with the known drug resistance enzyme ANT(9)-Ic. Consistent with the MIC results, ANT(9)Id showed high affinity and catalytic efficiency for spectinomycin, with a of 8.94 ± 2.50 μM and a / of 26.15 μM·s. This novel resistance gene and its close homologs are conserved in strains from various sources, including some of clinical significance. No mobile genetic elements (MGEs) surrounding the (-like) genes were identified. This work revealed and characterized a novel spectinomycin resistance gene, , along with its biological features. Identifying novel resistance genes in pathogens can assist in rational medication use and the identification of additional antimicrobial resistance mechanisms in microbial populations.
format Artículo científico
id pubmed_39726966
institution PubMed
language en
publishDate 2024
publisher Frontiers in microbiology
record_format pubmed
spellingShingle Identification and characterization of a novel chromosome-encoded aminoglycoside -nucleotidyltransferase gene, in sp. TYF-12 isolated from the marine fish intestine.
Yu, Yan
Zhang, Runzhi
Pan, Wei
Sheng, Xinyi
Chen, Susu
Wang, Junjun
Lu, Junwan
Bao, Qiyu
Hu, Yunliang
Jiang, Pengfei
Huang, Dawei
Identification and characterization of a novel chromosome-encoded aminoglycoside -nucleotidyltransferase gene, in sp. TYF-12 isolated from the marine fish intestine. Yu, Yan Zhang, Runzhi Pan, Wei Sheng, Xinyi Chen, Susu Wang, Junjun Lu, Junwan Bao, Qiyu Hu, Yunliang Jiang, Pengfei Huang, Dawei The mechanisms underlying the resistance of the genus to aminoglycosides are complex, which poses a challenge for the efficient treatment of infectious diseases caused by these pathogens. To help clinicians treat infections more effectively, a more comprehensive understanding of antibiotic resistance mechanisms is urgently needed. Plates were streaked to isolate bacteria from the intestinal contents of fish. The standard agar dilution method was used to determine the minimum inhibitory concentrations (MICs) of the antimicrobial agents. Molecular cloning was carried out to study the function of the novel antibiotic inactivation gene The kinetic parameters of ANT(9)Id were measured by a SpectraMax multifunctional microplate reader. Whole-genome sequencing and bioinformatic analysis were conducted to elucidate the sequence structure and evolutionary relationships of similar genes. The novel aminoglycoside -nucleotidyltransferase gene was encoded on the chromosome of a species-unclassified isolate designated sp. TYF-12, which was isolated from the intestine of a marine fish. Among the 11 aminoglycosides tested, was resistant to only spectinomycin. The MIC of spectinomycin for the recombinant strain carrying (pUCP20-/DH5α) increased 64-fold compared with that of the control strain (pUCP20/DH5ɑ). ANT(9)Id shares the highest amino acid (aa) identity of 46.70% with the known drug resistance enzyme ANT(9)-Ic. Consistent with the MIC results, ANT(9)Id showed high affinity and catalytic efficiency for spectinomycin, with a of 8.94 ± 2.50 μM and a / of 26.15 μM·s. This novel resistance gene and its close homologs are conserved in strains from various sources, including some of clinical significance. No mobile genetic elements (MGEs) surrounding the (-like) genes were identified. This work revealed and characterized a novel spectinomycin resistance gene, , along with its biological features. Identifying novel resistance genes in pathogens can assist in rational medication use and the identification of additional antimicrobial resistance mechanisms in microbial populations.
title Identification and characterization of a novel chromosome-encoded aminoglycoside -nucleotidyltransferase gene, in sp. TYF-12 isolated from the marine fish intestine.
url https://pubmed.ncbi.nlm.nih.gov/39726966/