Université Clermont-Auvergne, INRAE, MEDIS, Clermont-Ferrand, France.
Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Microbiol Spectr. 2023 Jun 15;11(3):e0466722. doi: 10.1128/spectrum.04667-22. Epub 2023 Mar 30.
Metagenome analyses of the human microbiome suggest that horizontal gene transfer (HGT) is frequent in these rich and complex microbial communities. However, so far, only a few HGT studies have been conducted . In this work, three different systems mimicking the physiological conditions encountered in the human digestive tract were tested, including (i) the TNO gastro-Intestinal tract Model 1 (TIM-1) system (for the upper part of the intestine), (ii) the ARtificial COLon (ARCOL) system (to mimic the colon), and (iii) a mouse model. To increase the likelihood of transfer by conjugation of the integrative and conjugative element studied in the artificial digestive systems, bacteria were entrapped in alginate, agar, and chitosan beads before being placed in the different gut compartments. The number of transconjugants detected decreased, while the complexity of the ecosystem increased (many clones in TIM-1 but only one clone in ARCOL). No clone was obtained in a natural digestive environment (germfree mouse model). In the human gut, the richness and diversity of the bacterial community would offer more opportunities for HGT events to occur. In addition, several factors (SOS-inducing agents, microbiota-derived factors) that potentially increase HGT efficiency were not tested here. Even if HGT events are rare, expansion of the transconjugant clones can happen if ecological success is fostered by selecting conditions or by events that destabilize the microbial community. The human gut microbiota plays a key role in maintaining normal host physiology and health, but its homeostasis is fragile. During their transit in the gastrointestinal tract, bacteria conveyed by food can exchange genes with resident bacteria. New traits acquired by HGT (e.g., new catabolic properties, bacteriocins, antibiotic resistance) can impact the gut microbial composition and metabolic potential. We showed here that TIM-1, a system mimicking the upper digestive tract, is a useful tool to evaluate HGT events in conditions closer to the physiological ones. Another important fact pointed out in this work is that Enterococcus faecalis is a good candidate for foreign gene acquisition. Due to its high ability to colonize the gut and acquire mobile genetic elements, this commensal bacterium could serve as an intermediate for HGT in the human gut.
人类微生物组的宏基因组分析表明,水平基因转移(HGT)在这些丰富而复杂的微生物群落中很频繁。然而,到目前为止,只有少数 HGT 研究已经进行。在这项工作中,我们测试了三种不同的系统,这些系统模拟了人类消化道中遇到的生理条件,包括(i)TNO 胃肠道模型 1(TIM-1)系统(用于上肠道),(ii)人工结肠(ARCOL)系统(模拟结肠),和(iii)小鼠模型。为了增加通过整合和共轭元件进行接合转移的可能性,在将细菌困在藻酸盐、琼脂和壳聚糖珠中之前,将其放置在不同的肠道隔室中。检测到的转导子数量减少,而生态系统的复杂性增加(在 TIM-1 中有许多克隆,但在 ARCOL 中只有一个克隆)。在自然消化环境(无菌小鼠模型)中未获得克隆。在人类肠道中,细菌群落的丰富度和多样性将为 HGT 事件的发生提供更多机会。此外,这里没有测试可能增加 HGT 效率的几个因素(SOS 诱导剂、微生物群衍生因子)。即使 HGT 事件很少,如果生态成功通过选择条件或通过破坏微生物群落的事件来促进,转导子克隆的扩展也可能发生。人类肠道微生物群在维持正常宿主生理学和健康方面起着关键作用,但它的内稳态很脆弱。在胃肠道中运输过程中,食物携带的细菌可以与常驻细菌交换基因。通过 HGT 获得的新特征(例如,新的代谢特性、细菌素、抗生素抗性)会影响肠道微生物群落组成和代谢潜力。我们在这里表明,TIM-1 是一种模拟上消化道的系统,是评估更接近生理条件下 HGT 事件的有用工具。这项工作中指出的另一个重要事实是,粪肠球菌是获得外源基因的良好候选者。由于其定植肠道和获得移动遗传元件的能力很高,这种共生菌可以作为人类肠道中 HGT 的中间媒介。