Microbiome-X, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, China.
Shandong University, State Key Laboratory of Microbial Technology, Qingdao, China.
mSphere. 2024 Jan 30;9(1):e0060823. doi: 10.1128/msphere.00608-23. Epub 2023 Dec 19.
Transposons, plasmids, bacteriophages, and other mobile genetic elements facilitate horizontal gene transfer in the gut microbiota, allowing some pathogenic bacteria to acquire antibiotic resistance genes (ARGs). Currently, the relationship between specific ARGs and specific transposons in the comprehensive infant gut microbiome has not been elucidated. In this study, ARGs and transposons were annotated from the Unified Human Gastrointestinal Genome (UHGG) and the Early-Life Gut Genomes (ELGG). Association rules mining was used to explore the association between specific ARGs and specific transposons in UHGG, and the robustness of the association rules was validated using the external database in ELGG. Our results suggested that ARGs and transposons were more likely to be relevant in infant gut microbiota compared to adult gut microbiota, and nine robust association rules were identified, among which , , and played important roles in this association phenomenon. The emphasis of this study is to investigate the synergistic transfer of specific ARGs and specific transposons in the infant gut microbiota, which can contribute to the study of microbial pathogenesis and the ARG dissemination dynamics.IMPORTANCEThe transfer of transposons carrying antibiotic resistance genes (ARGs) among microorganisms accelerates antibiotic resistance dissemination among infant gut microbiota. Nonetheless, it is unclear what the relationship between specific ARGs and specific transposons within the infant gut microbiota. , , and were identified as key players in the nine robust association rules we discovered. Meanwhile, we found that infant gut microorganisms were more susceptible to horizontal gene transfer events about specific ARGs and specific transposons than adult gut microorganisms. These discoveries could enhance the understanding of microbial pathogenesis and the ARG dissemination dynamics within the infant gut microbiota.
转座子、质粒、噬菌体和其他移动遗传元件促进了肠道微生物群的水平基因转移,使一些致病菌能够获得抗生素耐药基因(ARGs)。目前,特定 ARGs 与综合婴儿肠道微生物组中特定转座子之间的关系尚未阐明。在这项研究中,从统一人类胃肠道基因组(UHGG)和早期生命肠道基因组(ELGG)中注释了 ARGs 和转座子。使用关联规则挖掘来探索 UHGG 中特定 ARGs 和特定转座子之间的关联,并使用 ELGG 中的外部数据库验证关联规则的稳健性。我们的结果表明,与成人肠道微生物组相比,婴儿肠道微生物组中 ARGs 和转座子更有可能相关,并且确定了九条稳健的关联规则,其中 、 和 在这种关联现象中起着重要作用。本研究的重点是研究婴儿肠道微生物组中特定 ARGs 和特定转座子的协同转移,这有助于研究微生物发病机制和 ARG 传播动态。
重要性:携带抗生素耐药基因(ARGs)的转座子在微生物之间的转移加速了婴儿肠道微生物组中抗生素耐药性的传播。然而,目前尚不清楚婴儿肠道微生物组中特定 ARGs 和特定转座子之间的关系。在我们发现的九条稳健关联规则中, 、 和 被确定为关键参与者。同时,我们发现婴儿肠道微生物比成人肠道微生物更容易受到特定 ARGs 和特定转座子的水平基因转移事件的影响。这些发现可以增强对婴儿肠道微生物组中微生物发病机制和 ARG 传播动态的理解。