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Identification of a novel aminoglycoside O-nucleotidyltransferase AadA33 in Providencia vermicola

A novel chromosome-encoded aminoglycoside O-nucleotidyltransferase AadA33 was identified in Providencia vermicola strain P13. The AadA33 shares the highest amino acid identity of 51.28% with the function characterized AadA31. Antibiotic susceptibility testing and enzyme kinetics analysis revealed th...

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Autores principales: Feng, Chunlin, Gao, Mengdi, Jiang, Weiyan, Shi, Weina, Li, Anqi, Liu, Shuang, Zhang, Lei, Zhang, Xueya, Li, Qiaoling, Lin, Hailong, Lu, Junwan, Li, Kewei, Zhang, Hailin, Hu, Yunliang, Bao, Qiyu, Lin, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513248/
https://www.ncbi.nlm.nih.gov/pubmed/36177473
http://dx.doi.org/10.3389/fmicb.2022.990739
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author Feng, Chunlin
Gao, Mengdi
Jiang, Weiyan
Shi, Weina
Li, Anqi
Liu, Shuang
Zhang, Lei
Zhang, Xueya
Li, Qiaoling
Lin, Hailong
Lu, Junwan
Li, Kewei
Zhang, Hailin
Hu, Yunliang
Bao, Qiyu
Lin, Xi
author_facet Feng, Chunlin
Gao, Mengdi
Jiang, Weiyan
Shi, Weina
Li, Anqi
Liu, Shuang
Zhang, Lei
Zhang, Xueya
Li, Qiaoling
Lin, Hailong
Lu, Junwan
Li, Kewei
Zhang, Hailin
Hu, Yunliang
Bao, Qiyu
Lin, Xi
author_sort Feng, Chunlin
collection PubMed
description A novel chromosome-encoded aminoglycoside O-nucleotidyltransferase AadA33 was identified in Providencia vermicola strain P13. The AadA33 shares the highest amino acid identity of 51.28% with the function characterized AadA31. Antibiotic susceptibility testing and enzyme kinetics analysis revealed that the function of AadA33 is to mediate spectinomycin and streptomycin resistance. The recombinant strain harboring aadA33 (pUCP20-aadA33/Escherichia coli DH5α) displayed >256- and 128-fold increases in the minimum inhibitory concentration levels to spectinomycin and streptomycin, respectively, compared with the control strains pUCP20/DH5α. Enzyme kinetic parameters manifested the substrate of AadA33 including spectinomycin and streptomycin, with k(cat)/K(m) of 3.28 × 10(4) (M(−1) s(−1)) and 3.37 × 10(4) (M(−1) s(−1)), respectively. Bioinformatics analysis revealed its structural mechanism of antimicrobial resistance, genetic context, and phylogenetic relationship with other aminoglycoside O-nucleotidyltransferases. This study of AadA33 contributed to understanding the function and resistance mechanism of aminoglycoside O-nucleotidyltransferase.
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spelling pubmed-95132482022-09-28 Identification of a novel aminoglycoside O-nucleotidyltransferase AadA33 in Providencia vermicola Feng, Chunlin Gao, Mengdi Jiang, Weiyan Shi, Weina Li, Anqi Liu, Shuang Zhang, Lei Zhang, Xueya Li, Qiaoling Lin, Hailong Lu, Junwan Li, Kewei Zhang, Hailin Hu, Yunliang Bao, Qiyu Lin, Xi Front Microbiol Microbiology A novel chromosome-encoded aminoglycoside O-nucleotidyltransferase AadA33 was identified in Providencia vermicola strain P13. The AadA33 shares the highest amino acid identity of 51.28% with the function characterized AadA31. Antibiotic susceptibility testing and enzyme kinetics analysis revealed that the function of AadA33 is to mediate spectinomycin and streptomycin resistance. The recombinant strain harboring aadA33 (pUCP20-aadA33/Escherichia coli DH5α) displayed >256- and 128-fold increases in the minimum inhibitory concentration levels to spectinomycin and streptomycin, respectively, compared with the control strains pUCP20/DH5α. Enzyme kinetic parameters manifested the substrate of AadA33 including spectinomycin and streptomycin, with k(cat)/K(m) of 3.28 × 10(4) (M(−1) s(−1)) and 3.37 × 10(4) (M(−1) s(−1)), respectively. Bioinformatics analysis revealed its structural mechanism of antimicrobial resistance, genetic context, and phylogenetic relationship with other aminoglycoside O-nucleotidyltransferases. This study of AadA33 contributed to understanding the function and resistance mechanism of aminoglycoside O-nucleotidyltransferase. Frontiers Media S.A. 2022-09-13 /pmc/articles/PMC9513248/ /pubmed/36177473 http://dx.doi.org/10.3389/fmicb.2022.990739 Text en Copyright © 2022 Feng, Gao, Jiang, Shi, Li, Liu, Zhang, Zhang, Li, Lin, Lu, Li, Zhang, Hu, Bao and Lin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Feng, Chunlin
Gao, Mengdi
Jiang, Weiyan
Shi, Weina
Li, Anqi
Liu, Shuang
Zhang, Lei
Zhang, Xueya
Li, Qiaoling
Lin, Hailong
Lu, Junwan
Li, Kewei
Zhang, Hailin
Hu, Yunliang
Bao, Qiyu
Lin, Xi
Identification of a novel aminoglycoside O-nucleotidyltransferase AadA33 in Providencia vermicola
title Identification of a novel aminoglycoside O-nucleotidyltransferase AadA33 in Providencia vermicola
title_full Identification of a novel aminoglycoside O-nucleotidyltransferase AadA33 in Providencia vermicola
title_fullStr Identification of a novel aminoglycoside O-nucleotidyltransferase AadA33 in Providencia vermicola
title_full_unstemmed Identification of a novel aminoglycoside O-nucleotidyltransferase AadA33 in Providencia vermicola
title_short Identification of a novel aminoglycoside O-nucleotidyltransferase AadA33 in Providencia vermicola
title_sort identification of a novel aminoglycoside o-nucleotidyltransferase aada33 in providencia vermicola
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513248/
https://www.ncbi.nlm.nih.gov/pubmed/36177473
http://dx.doi.org/10.3389/fmicb.2022.990739
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