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接触多西环素会增加老年人群中携带广泛肠道抗菌药物耐药决定因素的风险。

Exposure to doxycycline increases risk of carrying a broad range of enteric antimicrobial resistance determinants in an elderly cohort.

机构信息

Microbiome and Host Health Program, South Australian Health and Medical Research Institute, Adelaide, SA, Australia; Infection and Immunity, Flinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.

Microbiome and Host Health Program, South Australian Health and Medical Research Institute, Adelaide, SA, Australia; SA Pathology, SA Health, Adelaide, SA, Australia.

出版信息

J Infect. 2024 Oct;89(4):106243. doi: 10.1016/j.jinf.2024.106243. Epub 2024 Aug 12.

Abstract

OBJECTIVES

High rates of antibiotic prescription in residential aged care are likely to promote enteric carriage of antibiotic-resistant pathogens and increase the risk of antibiotic treatment failure. Despite their importance, relationships between antibiotic exposures and patterns of enteric resistance carriage in this population remain poorly understood.

METHODS

We conducted a cross-sectional metagenomic cohort analysis of stool samples from residents of five long-term aged-care facilities in South Australia. Taxonomic composition was determined, and enteric carriage of antibiotic resistance genes (ARGs) was identified and quantified against the Comprehensive Antibiotic Resistance Database. Both the detection and abundance of stool taxa and ARGs were related to antibiotic exposures up to 12 months prior. Factors associated with the abundance of ARGs of high clinical concern were identified.

RESULTS

Stool samples were provided by 164 participants (median age: 88 years, IQR 81-93; 72% female). Sixty-one percent (n = 100) of participants were prescribed antibiotics at least once in the prior 12 months (median prescriptions: 4, range: 1-52), most commonly a penicillin (n = 55, 33.5%), cephalosporin (n = 53, 32.3%), diaminopyrimidine (trimethoprim) (n = 36, 22%), or tetracycline (doxycycline) (n = 21, 12.8%). More than 1100 unique ARGs, conferring resistance to 38 antibiotic classes, were identified, including 20 ARGs of high clinical concern. Multivariate logistic regression showed doxycycline exposure to be the greatest risk factor for high ARG abundance (adjusted odds ratio [aOR]=14.8, q<0.001) and a significant contributor to inter-class selection, particularly for ARGs relating to penicillins (aOR=3.1, q=0.0004) and cephalosporins (aOR=3.4, q=0.003). High enteric ARG abundance was associated with the number of separate antibiotic exposures (aOR: 6.4, q<0.001), exposures within the prior 30 days (aOR: 4.6, q=0.008) and prior 30-100 days (aOR: 2.6, q=0.008), high duration of antibiotic exposure (aOR: 7.9, q<0.001), and exposure to 3 or more antibiotic classes (aOR: 7.4, q<0.001). Carriage of one or more ARGs of high clinical concern was identified in 99% of participants (n = 162, median: 3, IQR: 2-4), involving 11 ARGs conferring resistance to aminoglycosides, four to beta-lactams, one to glycopeptides, three to fluoroquinolones, and one to oxazolidinones. Carriage of ARGs of high clinical concern was positively associated with exposure to doxycycline (aminoglycoside, fluoroquinolone, and oxazolidinone ARGs) and trimethoprim (fluoroquinolone and beta-lactam ARGs). Analysis of doxycycline impact on microbiota composition suggested that observed resistome changes arose principally through direct ARG selection, rather than through the antibiotic depletion of sensitive bacterial populations.

CONCLUSIONS

The gut microbiome of aged care residents is a major reservoir of antibiotic resistance. As a critical antibiotic in medical practice, a comprehensive understanding of the impact of doxycycline exposure on the gut resistome is paramount for informed antibiotic use, particularly in an evolving landscape of prophylactic applications. Near-universal asymptomatic carriage of clinically critical resistance determinants is highly concerning and reinforces the urgent need for improved management of antibiotic use in long-term aged care.

摘要

目的

在养老院居住的人群中,抗生素处方率较高可能会促进肠道携带耐药病原体,并增加抗生素治疗失败的风险。尽管其重要性,但人们对该人群中抗生素暴露与肠道耐药菌携带模式之间的关系仍知之甚少。

方法

我们对南澳大利亚州五家长期养老院的居民的粪便样本进行了横断面宏基因组队列分析。确定了分类组成,并针对综合抗生素耐药数据库鉴定和量化了肠道携带抗生素耐药基因(ARGs)。粪便分类和 ARGs 的检出和丰度均与 12 个月前的抗生素暴露有关。确定了与高临床关注的 ARGs 丰度相关的因素。

结果

164 名参与者(中位年龄:88 岁,IQR 81-93;72%为女性)提供了粪便样本。61%(n=100)的参与者在过去 12 个月内至少接受过一次抗生素治疗(中位数处方:4,范围:1-52),最常见的是青霉素(n=55,33.5%)、头孢菌素(n=53,32.3%)、二氨基嘧啶(甲氧苄啶)(n=36,22%)或四环素(多西环素)(n=21,12.8%)。鉴定出超过 1100 种独特的 ARGs,可赋予 38 种抗生素类别的耐药性,包括 20 种高临床关注的 ARGs。多变量逻辑回归显示,多西环素暴露是高 ARG 丰度的最大危险因素(调整后的优势比[aOR]=14.8,q<0.001),并且是类间选择的重要因素,特别是与青霉素(aOR=3.1,q=0.0004)和头孢菌素(aOR=3.4,q=0.003)相关的 ARGs。高肠道 ARG 丰度与单独抗生素暴露的数量有关(aOR:6.4,q<0.001)、在过去 30 天内的暴露(aOR:4.6,q=0.008)和过去 30-100 天内的暴露(aOR:2.6,q=0.008)、抗生素暴露的持续时间较长(aOR:7.9,q<0.001)和暴露于 3 种或更多种抗生素类别(aOR:7.4,q<0.001)。在 99%的参与者(n=162,中位数:3,IQR:2-4)中鉴定出携带一种或多种高临床关注的 ARGs,涉及 11 种赋予氨基糖苷类耐药性的 ARGs、4 种赋予β-内酰胺类耐药性的 ARGs、1 种赋予糖肽类耐药性的 ARGs、3 种赋予氟喹诺酮类耐药性的 ARGs和 1 种赋予唑烷酮类耐药性的 ARGs。携带高临床关注的 ARGs 与多西环素(氨基糖苷类、氟喹诺酮类和唑烷酮类 ARGs)和甲氧苄啶(氟喹诺酮类和β-内酰胺类 ARGs)暴露呈正相关。多西环素对抗生素组影响的分析表明,观察到的耐药组变化主要是通过直接的 ARG 选择产生的,而不是通过抗生素耗尽敏感细菌种群产生的。

结论

养老院居民的肠道微生物组是抗生素耐药性的主要储存库。多西环素作为一种重要的抗生素,全面了解其暴露对肠道耐药组的影响对于合理使用抗生素至关重要,特别是在预防性应用的不断发展的背景下。普遍存在的无症状携带临床重要耐药决定因素的情况令人高度关注,并强调迫切需要改善长期养老院的抗生素使用管理。

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