El Aidy Sahar, Ramsteijn Anouschka S, Dini-Andreote Francisco, van Eijk Roel, Houwing Danielle J, Salles Joana F, Olivier Jocelien D A
Microbial Physiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of GroningenGroningen, Netherlands.
Neurobiology, Groningen Institute for Evolutionary Life Sciences, University of GroningenGroningen, Netherlands.
Front Cell Neurosci. 2017 Aug 3;11:222. doi: 10.3389/fncel.2017.00222. eCollection 2017.
The neurotransmitter serotonin (5-HT) plays a vital regulatory role in both the brain and gut. 5-HT is crucial for regulating mood in the brain as well as gastrointestinal motility and secretion peripherally. Alterations in 5-HT transmission have been linked to pathological symptoms in both intestinal and psychiatric disorders and selective 5-HT transporter (5-HTT) inhibitors, affecting the 5-HT system by blocking the 5-HT transporter (5-HTT) have been successfully used to treat CNS- and intestinal disorders. Humans that carry the short allele of the 5-HTT-linked polymorphic region (5-HTTLPR) are more vulnerable to adverse environmental stressors, in particular early life stress. Although, early life stress has been shown to alter the composition of the gut microbiota, it is not known whether a lower 5-HTT expression is also associated with an altered microbiome composition. To investigate this, male and female wild type (5-HTT), heterozygous (5-HTT), and knockout (5-HTT) 5-HT transporter rats were maternally separated for 6 h a day from postnatal day 2 till 15. On postnatal day 21, fecal samples were collected and the impact of 5-HTT genotype and maternal separation (MS) on the microbiome was analyzed using high-throughput sequencing of the bacterial 16S rRNA gene. MS showed a shift in the ratio between the two main bacterial phyla characterized by a decrease in and an increase in Firmicutes. Interestingly, the 5-HTT genotype caused a greater microbal dysbiosis (microbial imbalance) compared with MS. A significant difference in microbiota composition was found segregating 5-HTT apart from 5-HTT and 5-HTT rats. Moreover, exposure of rats with 5-HTT diminished expression to MS swayed the balance of their microbiota away from homeostasis to 'inflammatory' type microbiota characterized by higher abundance of members of the gut microbiome including , , and , all of which are previously reported to be associated with a state of intestinal inflammation, including inflammation associated with MS and brain disorders like multiple depressive disorders. Overall, our data show for the first time that altered expression of 5-HTT induces disruptions in male and female rat gut microbes and these 5-HTT genotype-related disruptions are augmented when combined with early life stress.
神经递质5-羟色胺(5-HT)在大脑和肠道中都起着至关重要的调节作用。5-HT对于调节大脑中的情绪以及外周的胃肠蠕动和分泌至关重要。5-HT传递的改变与肠道疾病和精神疾病的病理症状有关,而通过阻断5-羟色胺转运体(5-HTT)来影响5-HT系统的选择性5-羟色胺转运体(5-HTT)抑制剂已成功用于治疗中枢神经系统疾病和肠道疾病。携带5-羟色胺转运体相关多态性区域(5-HTTLPR)短等位基因的人更容易受到不良环境应激源的影响,尤其是早期生活压力。虽然早期生活压力已被证明会改变肠道微生物群的组成,但尚不清楚较低的5-HTT表达是否也与微生物群组成的改变有关。为了研究这一点,从出生后第2天到第15天,每天将雄性和雌性野生型(5-HTT)、杂合子(5-HTT)和敲除(5-HTT)5-羟色胺转运体大鼠与其母亲分开6小时。在出生后第21天,收集粪便样本,并使用细菌16S rRNA基因的高通量测序分析5-HTT基因型和母婴分离(MS)对微生物群的影响。母婴分离显示出两个主要细菌门之间比例的变化,其特征是拟杆菌门减少,厚壁菌门增加。有趣的是,与母婴分离相比,5-HTT基因型导致了更大的微生物群落失调(微生物失衡)。发现5-HTT大鼠与5-HTT和5-HTT大鼠在微生物群组成上存在显著差异。此外,5-HTT表达降低的大鼠暴露于母婴分离会使其微生物群的平衡从稳态转向“炎症性”微生物群,其特征是肠道微生物群成员丰度更高,包括拟杆菌属、双歧杆菌属和肠杆菌属,所有这些先前都被报道与肠道炎症状态有关,包括与母婴分离和诸如多发性抑郁症等脑部疾病相关的炎症。总体而言,我们的数据首次表明,5-HTT表达的改变会导致雄性和雌性大鼠肠道微生物的破坏,并且当与早期生活压力相结合时,这些与5-HTT基因型相关的破坏会加剧。