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从海洋鱼类肠道分离出的sp. TYF-12中一个新的染色体编码氨基糖苷-核苷酸转移酶基因的鉴定与表征。

Identification and characterization of a novel chromosome-encoded aminoglycoside -nucleotidyltransferase gene, in sp. TYF-12 isolated from the marine fish intestine.

作者信息

Yu Yan, Zhang Runzhi, Pan Wei, Sheng Xinyi, Chen Susu, Wang Junjun, Lu Junwan, Bao Qiyu, Hu Yunliang, Jiang Pengfei, Huang Dawei

机构信息

Institute of Biomedical Informatics/School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.

Institute of Molecular Virology and Immunology, Department of Microbiology and Immunology, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, China.

出版信息

Front Microbiol. 2024 Dec 12;15:1475172. doi: 10.3389/fmicb.2024.1475172. eCollection 2024.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

该属对氨基糖苷类抗生素产生耐药性的机制复杂,这给有效治疗由这些病原体引起的传染病带来了挑战。为帮助临床医生更有效地治疗感染,迫切需要更全面地了解抗生素耐药机制。

方法

将平板划线以从鱼的肠道内容物中分离细菌。采用标准琼脂稀释法测定抗菌剂的最低抑菌浓度(MIC)。进行分子克隆以研究新型抗生素失活基因的功能。通过SpectraMax多功能微孔板读数仪测量ANT(9)Id的动力学参数。进行全基因组测序和生物信息学分析以阐明相似基因的序列结构和进化关系。

结果

新型氨基糖苷 - 核苷酸转移酶基因在一株未分类的菌株sp. TYF - 12的染色体上编码,该菌株从海鱼肠道中分离得到。在所测试的11种氨基糖苷类抗生素中,该菌株仅对壮观霉素耐药。携带(pUCP20 - /DH5α)的重组菌株对壮观霉素的MIC与对照菌株(pUCP20/DH5ɑ)相比增加了64倍。ANT(9)Id与已知耐药酶ANT(9) - Ic的氨基酸(aa)同一性最高,为46.70%。与MIC结果一致,ANT(9)Id对壮观霉素表现出高亲和力和催化效率, 为8.94±2.50 μM, / 为26.15 μM·s。这种新型耐药基因及其紧密同源物在来自各种来源的菌株中保守,包括一些具有临床意义的菌株。未发现( - 样)基因周围的移动遗传元件(MGE)。

结论

这项工作揭示并表征了一个新型壮观霉素耐药基因 及其生物学特性。在病原体中鉴定新型耐药基因有助于合理用药以及识别微生物群体中其他的抗菌耐药机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8caa/11669914/3ce6f4e7d084/fmicb-15-1475172-g001.jpg

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