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西班牙健康学童中产超广谱β-内酰胺酶肠杆菌科细菌的粪便携带情况。

Fecal carriage of extended-spectrum beta-lactamase-producing Enterobacterales in healthy Spanish schoolchildren.

作者信息

López-Siles Mireia, Moure Zaira, Muadica Aly Salimo, Sánchez Sergio, Cruces Raquel, Ávila Alicia, Lara Noelia, Köster Pamela Carolina, Dashti Alejandro, Oteo-Iglesias Jesús, Carmena David, McConnell Michael J

机构信息

Intrahospital Infections Unit, Reference and Research Laboratory in Resistance to Antibiotics and Infections Related to Healthcare, National Centre for Microbiology, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.

Serra Húnter Fellow, Microbiology of Intestinal Diseases, Biology Department, Universitat de Girona, Girona, Spain.

出版信息

Front Microbiol. 2023 Jun 9;14:1035291. doi: 10.3389/fmicb.2023.1035291. eCollection 2023.

Abstract

BACKGROUND

Extended-spectrum ß-lactamase-producing Enterobacterales (ESBL-E) are a serious threat among emerging antibiotic resistant bacteria. Particularly, the number of cases of ESBL-E infections reported in children has been increasing in recent years, and approved antibiotic treatments for this age group are limited. However, information regarding the prevalence of colonization in European children, risk factors associated with colonization, and the characteristics of the colonizing strains is scarce. The aims of this study were to determine the prevalence of ESBL-E colonization in fecal samples of apparently healthy schoolchildren, to identify lifestyle routines associated with colonization, and to characterize clonal relationships and mechanisms of resistance in ESBL-E isolates.

METHODS

A cohort of 887 healthy children (3-13  years old) from seven primary and secondary schools in the Madrid metropolitan area was recruited between April-June 2018, and sociodemographic information and daily habits were collected. Fecal samples were screened for ESBL-E carriage in selective medium. ESBL-E isolates were further characterized by assessing molecular epidemiology (PFGE and MLST), ESBL gene carriage, and antibiotic resistance profile. This information was analyzed in conjunction with the metadata of the participants in order to identify external factors associated with ESBL-E carriage.

RESULTS

Twenty four ESBL-E, all but one were detected in 23 children (prevalence: 2.6%; 95% CI: 1.6-3.6%). Of these, seven contained the allele, five the , five the , three the , three the , and one the . Significant clonal diversity was observed among the isolates that grouped into 22 distinct clusters (at <85% similarity of PFGE profile). ESBL-producing isolates belonged to 12 different STs, with ST10 (25%) and ST131 (17%) being the most frequent. Apart from ß-lactams, resistance to trimethoprim/sulfamethoxazole (46%), ciprofloxacin (33%), levofloxacin (33%), tobramycin (21%), and gentamicin (8%) were the most frequently detected.

CONCLUSION

The prevalence of ESBL-E in the studied cohort of children was lower than the average colonization rate previously detected in Europe for both children and adults. was the main ESBL-producing species detected and CTX-M were the most frequently identified ESBLs. High ST diversity suggests polyclonal dissemination. Compared to other STs, ST131 isolates were associated with resistance to various antimicrobials.

摘要

背景

产超广谱β-内酰胺酶肠杆菌科细菌(ESBL-E)是新出现的耐药菌中的严重威胁。特别是近年来,儿童中报告的ESBL-E感染病例数一直在增加,而针对该年龄组批准的抗生素治疗方法有限。然而,关于欧洲儿童定植率、与定植相关的危险因素以及定植菌株特征的信息却很少。本研究的目的是确定明显健康的学童粪便样本中ESBL-E定植的发生率,识别与定植相关的生活方式,以及表征ESBL-E分离株的克隆关系和耐药机制。

方法

2018年4月至6月期间,招募了来自马德里都会区7所中小学的887名健康儿童(3至13岁),并收集了社会人口统计学信息和日常习惯。在选择性培养基中筛查粪便样本中的ESBL-E携带情况。通过评估分子流行病学(PFGE和MLST)、ESBL基因携带情况和抗生素耐药谱,对ESBL-E分离株进行进一步表征。结合参与者的元数据对这些信息进行分析,以识别与ESBL-E携带相关的外部因素。

结果

在23名儿童中检测到24株ESBL-E,除1株外(发生率:2.6%;95%置信区间:1.6 - 3.6%)。其中,7株含有 等位基因,5株含有 ,5株含有 ,3株含有 ,3株含有 ,1株含有 。在聚为22个不同簇的分离株中观察到显著的克隆多样性(PFGE图谱相似度<85%)。产ESBL的 分离株属于12种不同的序列类型,其中ST10(25%)和ST131(17%)最为常见。除β-内酰胺类外,对甲氧苄啶/磺胺甲恶唑(46%)、环丙沙星(33%)、左氧氟沙星(33%)、妥布霉素(21%)和庆大霉素(8%)的耐药最为常见。

结论

在所研究的儿童队列中,ESBL-E的发生率低于欧洲先前检测到的儿童和成人的平均定植率。 是检测到的主要产ESBL菌种,CTX-M是最常鉴定出的ESBLs。高序列类型多样性表明多克隆传播。与其他序列类型相比,ST131分离株与对多种抗菌药物的耐药性相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4265/10288999/aac178603516/fmicb-14-1035291-g001.jpg

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