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从坦桑尼亚疑似尿路感染患者的尿液、粪便、动物及环境中分离出的产超广谱β-内酰胺酶菌株对环丙沙星和庆大霉素的等位基因分布及表型耐药性

Allele distribution and phenotypic resistance to ciprofloxacin and gentamicin among extended-spectrum β-lactamase-producing isolated from the urine, stool, animals, and environments of patients with presumptive urinary tract infection in Tanzania.

作者信息

Mwakyoma Adam A, Kidenya Benson R, Minja Caroline A, Mushi Martha F, Sandeman Alison, Sabiti Wilber, Holden Mathew T G, Mshana Stephen E

机构信息

Department of Biochemistry and Molecular Biology, Catholic University of Health and Allied Sciences, Mwanza, Tanzania.

Department of Clinical Microbiology, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.

出版信息

Front Antibiot. 2023 Jun 5;2:1164016. doi: 10.3389/frabi.2023.1164016. eCollection 2023.

Abstract

BACKGROUND

Additional antimicrobial resistance to extended-spectrum β-lactamase (ESBL)-producing exhausts treatment options. We investigated allele distribution and resistance to ciprofloxacin and gentamicin among ESBL-producing isolates from the urine, stool, animals, and environments of presumptive urinary tract infection (UTI) patients, in order to gain a crucial insight toward devising prevention and control measures and treatment guidelines.

METHODS

Archived ESBL-producing isolates from the urine, stool, animals, and surrounding environments of presumptive UTI patients were retrieved. Antimicrobial susceptibility profiles for ciprofloxacin and gentamicin were done followed by multiplex Polymerase chain reaction (PCR) for , , and , to determine ESBL allele distribution. Data were analyzed using STATA version 17.

RESULTS

A total of 472 confirmed ESBL-producing isolates from Mwanza 243 (51.5%), Kilimanjaro 143 (30.3%), and Mbeya 86 (18.2%) were analyzed. Of these, 75 (15.9%) were from urine, 199 (42.2%) from stool, 58 (12.3%) from rectal/cloaca swabs of animals, and 140 (29.7%) from surrounding environments. Out of the 472 ESBL-producing , 98.9% (467) had at least one ESBL allele. The most frequent allele was , which was detected in 88.1% (416/472) of isolates, followed by the allele, which was detected in 51.5% (243/472) of isolates. A total of 40.7% (192/472) of isolates harbored dual  +  alleles and only 0.2% (1/472) of isolates had dual  +  alleles, whereas 2.3% (11/472) of isolates had a combination of all three alleles (  +   +  ). None of the isolates harbored a combination of  +  only. Resistance to ciprofloxacin and gentamicin was observed in 70.8% (334/472) and 46.0% (217/472) of isolates, respectively. There was a significant difference in the distribution of resistance to ciprofloxacin as well as gentamicin among ESBL-producing isolated from various sources (-value < 0.001 and 0.002, respectively).

CONCLUSION

Almost all ESBL-producing isolates carry , , and either alone or in combination, with the most common allele being The resistance to ciprofloxacin and gentamicin, which are frontline antibiotics for UTIs among ESBL-producing , is high. This implies the need to continually revise the local guidelines used for optimal empirical therapy for UTIs, and for continual research and surveillance using one health approach.

摘要

背景

对产超广谱β-内酰胺酶(ESBL)菌株产生额外的抗菌耐药性会耗尽治疗选择。我们调查了产ESBL菌株在疑似尿路感染(UTI)患者的尿液、粪便、动物及环境中的等位基因分布以及对环丙沙星和庆大霉素的耐药性,以便为制定预防控制措施和治疗指南提供关键见解。

方法

检索存档的来自疑似UTI患者尿液、粪便、动物及周围环境的产ESBL菌株。进行环丙沙星和庆大霉素的药敏试验,随后进行针对 、 和 的多重聚合酶链反应(PCR),以确定ESBL等位基因分布。使用STATA 17版分析数据。

结果

共分析了来自姆万扎的243株(51.5%)、乞力马扎罗的143株(30.3%)和姆贝亚的86株(18.2%)确诊产ESBL菌株。其中,75株(15.9%)来自尿液,199株(42.2%)来自粪便,58株(12.3%)来自动物的直肠/泄殖腔拭子,140株(29.7%)来自周围环境。在472株产ESBL菌株中,98.9%(467株)至少有一个ESBL等位基因。最常见的等位基因是 ,在88.1%(416/472)的菌株中检测到,其次是 等位基因,在51.5%(243/472)的菌株中检测到。共有40.7%(192/472)的菌株携带双 + 等位基因,仅0.2%(1/472)的菌株有双 + 等位基因,而2.3%(11/472)的菌株具有所有三个等位基因的组合( + + )。没有菌株仅携带 + 的组合。分别在70.8%(334/472)和46.0%(217/472)的菌株中观察到对环丙沙星和庆大霉素的耐药性。从不同来源分离的产ESBL菌株对环丙沙星和庆大霉素的耐药性分布存在显著差异( 值分别<0.001和0.002)。

结论

几乎所有产ESBL菌株单独或组合携带 、 和 ,最常见的等位基因是 。产ESBL菌株中作为UTI一线抗生素的环丙沙星和庆大霉素耐药率很高。这意味着需要不断修订用于UTI最佳经验性治疗的当地指南,并采用“同一健康”方法持续进行研究和监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88cc/11732152/e707d63f639a/frabi-02-1164016-g001.jpg

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