Human-environmental overlap of resistant Enterobacterales: genomic evidence linking coastal waters and community carriage of antimicrobial resistance in a low- and middle-income setting.

IF 3.9
Frontiers in antibiotics Pub Date : 2025-12-18 eCollection Date: 2025-01-01 DOI:10.3389/frabi.2025.1715797
Appiah-Korang Labi, Noah Obeng-Nkrumah, Abigail Sarpong, Lady Asantewah Boamah Adomako, Christian Owusu-Nyantakyi, Rachel Ama Adadziwa Akorful, Mary-Magdalene Osei, Beverly Egyir, Japheth Awuletey Opintan
{"title":"Human-environmental overlap of resistant Enterobacterales: genomic evidence linking coastal waters and community carriage of antimicrobial resistance in a low- and middle-income setting.","authors":"Appiah-Korang Labi, Noah Obeng-Nkrumah, Abigail Sarpong, Lady Asantewah Boamah Adomako, Christian Owusu-Nyantakyi, Rachel Ama Adadziwa Akorful, Mary-Magdalene Osei, Beverly Egyir, Japheth Awuletey Opintan","doi":"10.3389/frabi.2025.1715797","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Coastal waters contaminated by antimicrobial resistant hotspots may serve as reservoirs for third-generation cephalosporin resistant Enterobacterales (3GCR-E), extended-spectrum β-lactamase (ESBL)-producers, and carbapenem-resistant Enterobacterales (CRE), but their role in driving human carriage remains poorly understood.</p><p><strong>Aim: </strong>We investigated intestinal carriage of 3GCR-E, ESBL-producers, and CRE in coastal and inland communities in Accra, Ghana, and examined the genomic overlap between human and wastewater-derived CRE isolates.</p><p><strong>Methods: </strong>A comparative cross-sectional study was conducted from August 2023 to June 2024 with 800 participants (400 from coastal and 400 from inland communities). We cultured fecal samples from participants and water samples from lagoons and shorelines for 3GCR-E, ESBL-producers, and CRE. The CRE isolates from both human and wastewater were whole genome sequenced for comparison.</p><p><strong>Results: </strong>Overall, 53.6% (n=429/800) of participants carried 3GCR-E, with 43.6% being ESBL-producers and 1.5% being CRE, the latter restricted only to coastal residents. In the pooled analysis, inland residence was independently associated with reduced odds of 3GCR-E carriage (aOR 0.64, 95% CI 0.48-0.85; <i>p</i> = 0.001). For coastal participants, not swimming was protective against ESBL carriage (aOR 0.65, 95% CI 0.42-0.95; <i>p</i> = 0.030). All human and wastewater CRE isolates were <i>E. coli</i> and clustered in mixed-source phylogenetic clades (ST10, ST940) with >95% average nucleotide identity and pairwise SNP differences as low as 2-20. Both human and wastewater sources carried the identical carbapenemase gene <i>bla</i>OXA-181 on overlapping plasmid replicons, with 57-80% concordance across IncFIA, IncFIB (AP001918), IncX1, and Col440I.</p><p><strong>Conclusions: </strong>Our findings indicate a shared resistance gene pool between human and environmental sources, characterized by bidirectional CRE exchange but dominated by an environment-to-human transmission pathway. This underscores the urgent need for effective wastewater treatment and improved sanitation practices to reduce human exposure and curb the spread of antibiotic resistance.</p>","PeriodicalId":73065,"journal":{"name":"Frontiers in antibiotics","volume":"4 ","pages":"1715797"},"PeriodicalIF":3.9000,"publicationDate":"2025-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12756717/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in antibiotics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/frabi.2025.1715797","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Coastal waters contaminated by antimicrobial resistant hotspots may serve as reservoirs for third-generation cephalosporin resistant Enterobacterales (3GCR-E), extended-spectrum β-lactamase (ESBL)-producers, and carbapenem-resistant Enterobacterales (CRE), but their role in driving human carriage remains poorly understood.

Aim: We investigated intestinal carriage of 3GCR-E, ESBL-producers, and CRE in coastal and inland communities in Accra, Ghana, and examined the genomic overlap between human and wastewater-derived CRE isolates.

Methods: A comparative cross-sectional study was conducted from August 2023 to June 2024 with 800 participants (400 from coastal and 400 from inland communities). We cultured fecal samples from participants and water samples from lagoons and shorelines for 3GCR-E, ESBL-producers, and CRE. The CRE isolates from both human and wastewater were whole genome sequenced for comparison.

Results: Overall, 53.6% (n=429/800) of participants carried 3GCR-E, with 43.6% being ESBL-producers and 1.5% being CRE, the latter restricted only to coastal residents. In the pooled analysis, inland residence was independently associated with reduced odds of 3GCR-E carriage (aOR 0.64, 95% CI 0.48-0.85; p = 0.001). For coastal participants, not swimming was protective against ESBL carriage (aOR 0.65, 95% CI 0.42-0.95; p = 0.030). All human and wastewater CRE isolates were E. coli and clustered in mixed-source phylogenetic clades (ST10, ST940) with >95% average nucleotide identity and pairwise SNP differences as low as 2-20. Both human and wastewater sources carried the identical carbapenemase gene blaOXA-181 on overlapping plasmid replicons, with 57-80% concordance across IncFIA, IncFIB (AP001918), IncX1, and Col440I.

Conclusions: Our findings indicate a shared resistance gene pool between human and environmental sources, characterized by bidirectional CRE exchange but dominated by an environment-to-human transmission pathway. This underscores the urgent need for effective wastewater treatment and improved sanitation practices to reduce human exposure and curb the spread of antibiotic resistance.

Abstract Image

Abstract Image

Abstract Image

耐药肠杆菌的人-环境重叠:在低收入和中等收入环境中将沿海水域和社区携带抗微生物药物耐药性联系起来的基因组证据。
背景:受耐药热点污染的沿海水域可能是第三代头孢菌素耐药肠杆菌(3GCR-E)、广谱β-内酰胺酶(ESBL)产生菌和碳青霉烯耐药肠杆菌(CRE)的宿主,但它们在驱动人类运输中的作用尚不清楚。目的:我们调查了加纳阿克拉沿海和内陆社区3GCR-E、esbl生产者和CRE的肠道携带情况,并检查了人类和废水来源的CRE分离株之间的基因组重叠。方法:于2023年8月至2024年6月对800名参与者(沿海社区400人,内陆社区400人)进行比较横断面研究。我们培养了来自参与者的粪便样本和来自泻湖和海岸线的水样,用于3GCR-E、esbl生产者和CRE。对从人体和废水中分离的CRE进行全基因组测序进行比较。结果:总体而言,53.6% (n=429/800)的参与者携带3GCR-E,其中43.6%为esbl生产者,1.5%为CRE,后者仅限于沿海居民。在汇总分析中,内陆居住与3GCR-E携带几率降低独立相关(aOR 0.64, 95% CI 0.48-0.85; p = 0.001)。对于沿海地区的参与者,不游泳对ESBL携带有保护作用(aOR 0.65, 95% CI 0.42-0.95; p = 0.030)。所有人类和废水CRE分离株均为大肠杆菌,聚集在混合源系统发育分支(ST10, ST940)中,平均核苷酸同源性为bb0 95%,成对SNP差异低至2-20。人类和废水源在重叠的质粒复制子上携带相同的碳青霉烯酶基因blaOXA-181,在IncFIA、IncFIB (AP001918)、IncX1和Col440I中具有57-80%的一致性。结论:我们的研究结果表明,人类和环境来源之间存在一个共享的抗性基因库,其特征是CRE双向交换,但以环境-人传播途径为主。这突出表明迫切需要进行有效的废水处理和改善卫生习惯,以减少人类接触并遏制抗生素耐药性的传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书