Co-localization of antibiotic resistance genes is widespread in the infant gut microbiome and associates with an immature gut microbial composition.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-05-10 DOI:10.1186/s40168-024-01800-5
Xuanji Li, Asker Brejnrod, Urvish Trivedi, Jakob Russel, Jonathan Thorsen, Shiraz A Shah, Gisle Alberg Vestergaard, Morten Arendt Rasmussen, Joseph Nesme, Hans Bisgaard, Jakob Stokholm, Søren Johannes Sørensen
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Abstract

Background: In environmental bacteria, the selective advantage of antibiotic resistance genes (ARGs) can be increased through co-localization with genes such as other ARGs, biocide resistance genes, metal resistance genes, and virulence genes (VGs). The gut microbiome of infants has been shown to contain numerous ARGs, however, co-localization related to ARGs is unknown during early life despite frequent exposures to biocides and metals from an early age.

Results: We conducted a comprehensive analysis of genetic co-localization of resistance genes in a cohort of 662 Danish children and examined the association between such co-localization and environmental factors as well as gut microbial maturation. Our study showed that co-localization of ARGs with other resistance and virulence genes is common in the early gut microbiome and is associated with gut bacteria that are indicative of low maturity. Statistical models showed that co-localization occurred mainly in the phylum Proteobacteria independent of high ARG content and contig length. We evaluated the stochasticity of co-localization occurrence using enrichment scores. The most common forms of co-localization involved tetracycline and fluoroquinolone resistance genes, and, on plasmids, co-localization predominantly occurred in the form of class 1 integrons. Antibiotic use caused a short-term increase in mobile ARGs, while non-mobile ARGs showed no significant change. Finally, we found that a high abundance of VGs was associated with low gut microbial maturity and that VGs showed even higher potential for mobility than ARGs.

Conclusions: We found that the phenomenon of co-localization between ARGs and other resistance and VGs was prevalent in the gut at the beginning of life. It reveals the diversity that sustains antibiotic resistance and therefore indirectly emphasizes the need to apply caution in the use of antimicrobial agents in clinical practice, animal husbandry, and daily life to mitigate the escalation of resistance. Video Abstract.

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抗生素耐药基因的共定位在婴儿肠道微生物组中很普遍,并且与未成熟的肠道微生物组成有关。
背景:在环境细菌中,抗生素抗性基因(ARGs)的选择优势可通过与其他ARGs、杀菌剂抗性基因、金属抗性基因和毒力基因(VGs)等基因共定位而增加。婴儿的肠道微生物组已被证明含有大量的 ARGs,然而,尽管婴儿从小就经常接触杀菌剂和金属,但其生命早期与 ARGs 相关的共定位情况尚不清楚:我们对 662 名丹麦儿童队列中抗性基因的基因共定位进行了全面分析,并研究了这种共定位与环境因素以及肠道微生物成熟之间的关联。我们的研究表明,ARGs 与其他抗性基因和毒力基因的共定位在早期肠道微生物组中很常见,并且与肠道细菌的低成熟度有关。统计模型显示,共定位主要发生在变形菌门,与高 ARG 含量和序列长度无关。我们使用富集分数评估了共定位发生的随机性。最常见的共定位形式涉及四环素和氟喹诺酮类抗性基因,在质粒上,共定位主要以 1 类整合子的形式出现。使用抗生素会导致短期内移动 ARGs 的增加,而非移动 ARGs 则无明显变化。最后,我们发现 VGs 的高丰度与肠道微生物的低成熟度有关,而且 VGs 比 ARGs 显示出更高的移动潜力:我们发现,ARGs 和其他抗药性与 VGs 之间的共定位现象在生命之初的肠道中十分普遍。它揭示了抗生素耐药性的多样性,因此间接强调了在临床实践、畜牧业和日常生活中谨慎使用抗菌药物以缓解耐药性升级的必要性。视频摘要
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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