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泰国鸭中喹诺酮耐药性:gyrA、parC和qnr基因的突变分析。

Quinolone resistance in from Thai ducks: Mutation analysis of , and genes.

作者信息

Pathomchai-Umporn Chutima, Laopiem Sudtisa, Witoonsatian Kriangkrai, Kulprasetsri Sittinee, Panomwan Pun, Songserm Thaweesak, Sinwat Nuananong

机构信息

Department of Farm Resources and Production Medicine, Faculty of Veterinary Medicine, Kasetsart University, Kamphaeng Saen Campus, Nakhon Pathom, 73140 Thailand.

Department of Pathology, Faculty of Veterinary Medicine, Kasetsart University, Kamphaeng Saen Campus, Nakhon Pathom, 73140 Thailand.

出版信息

Vet World. 2025 Jul;18(7):1891-1898. doi: 10.14202/vetworld.2025.1891-1898. Epub 2025 Jul 11.

Abstract

BACKGROUND AND AIM

is a Gram-negative bacterium causing systemic infections in ducks, often treated with quinolones. However, increasing resistance to quinolones poses a threat to effective treatment, and the molecular mechanisms underlying this resistance remain inadequately understood in Thailand. This study aimed to determine the minimum inhibitory concentrations (MICs) of nalidixic acid, ciprofloxacin, and enrofloxacin; identify mutations in the quinolone resistance-determining regions of and ; and detect () genes in isolates from Thai ducks.

MATERIALS AND METHODS

A total of 37 clinical isolates of were collected from diseased ducks between 2021 and 2023. MICs were determined using the agar dilution method, following the guidelines of the Clinical and Laboratory Standards Institute. Polymerase chain reaction and Sanger sequencing were employed to detect mutations in and and to screen for genes (, , and ). Phylogenetic analysis of the gene was performed to assess the relatedness among isolates.

RESULTS

Nalidixic acid MICs ranged from 16 μg/mL to ≥128 μg/mL; ciprofloxacin from 1 μg/mL to 8 μg/mL; and enrofloxacin from 0.25 μg/mL to 4 μg/mL. All isolates had a single point mutation at codon 83 of , either C248T (Ser83Ile, n = 35) or C248G (Ser83Arg, n = 2). No mutations were observed in , and none of the genes were detected. Phylogenetic analysis grouped most Thai isolates into one major cluster, with a few aligning with Chinese strains and the American Type Culture Collection reference strain.

CONCLUSION

This study provides the first molecular evidence of quinolone resistance mechanisms in from ducks in Thailand. Resistance appears primarily associated with a single mutation at codon 83 of , while no mutations or genes were detected. These findings highlight the importance of ongoing resistance surveillance and prudent antimicrobial use. Despite limitations in sample size and gene scope, this study provides essential baseline data to inform treatment guidelines and supports the inclusion of monitoring in Thailand's national antimicrobial resistance action plan. Future research should explore additional resistance genes using advanced genomic tools.

摘要

背景与目的

[细菌名称]是一种革兰氏阴性菌,可导致鸭群发生全身性感染,常用喹诺酮类药物进行治疗。然而,对喹诺酮类药物的耐药性不断增加,对有效治疗构成了威胁,而在泰国,这种耐药性的分子机制仍未得到充分了解。本研究旨在确定萘啶酸、环丙沙星和恩诺沙星的最低抑菌浓度(MIC);鉴定[细菌名称]喹诺酮耐药决定区和[相关基因名称]的突变;并检测泰国鸭分离株中的[特定基因名称]基因。

材料与方法

2021年至2023年间,从患病鸭中总共收集了37株[细菌名称]临床分离株。按照临床和实验室标准协会的指南,采用琼脂稀释法测定MIC。采用聚合酶链反应和桑格测序法检测[相关基因名称]的突变,并筛选[特定基因名称]基因([具体基因名称1]、[具体基因名称2]和[具体基因名称3])。对[特定基因名称]基因进行系统发育分析,以评估分离株之间的相关性。

结果

萘啶酸的MIC范围为16μg/mL至≥128μg/mL;环丙沙星为1μg/mL至8μg/mL;恩诺沙星为0.25μg/mL至4μg/mL。所有分离株在[相关基因名称]的第83位密码子处均有一个单点突变,即C248T(Ser83Ile,n = 35)或C248G(Ser83Arg,n = 2)。在[相关基因名称]中未观察到突变,也未检测到任何[特定基因名称]基因。系统发育分析将大多数泰国分离株归为一个主要聚类,少数与中国菌株和美国模式培养物保藏中心参考菌株聚类在一起。

结论

本研究提供了泰国鸭源[细菌名称]喹诺酮耐药机制的首个分子证据。耐药性似乎主要与[相关基因名称]第83位密码子处的单个突变有关,而未检测到[相关基因名称]突变或[特定基因名称]基因。这些发现凸显了持续进行耐药性监测和谨慎使用抗菌药物的重要性。尽管样本量和基因范围存在局限性,但本研究提供了重要的基线数据,为制定治疗指南提供参考,并支持将[细菌名称]监测纳入泰国国家抗菌药物耐药行动计划。未来的研究应使用先进的基因组工具探索其他耐药基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c2a/12415127/0ad6882839d3/Vetworld-18-1891-g001.jpg

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