Galley J D, Rajasekera T A, Bennouna D J, Batabyal A, Verosky B, Woodke S, Stokes J, Brown A K, Murthy S, Kopec R E, Gur T L
Department of Psychiatry and Behavioral Health, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.
Institute for Behavioral Medicine Research, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.
Benef Microbes. 2024 Nov 27;16(3):293-310. doi: 10.1163/18762891-bja00047.
Prenatal stress (PNS) has widespread effects on offspring, including aberrant immune development and behavioural deficits. The microbiome is a mediator of the dissemination of stress effects to the offspring through immunomodulation and metabolite production. Metabolites derived from the mother and their gut microbiota pass to the foetus and can affect immune and nervous development. Stress affects the abundance of such metabolites, including the tryptophan (Trp) pathway, which are involved in immune and nervous system function. We hypothesized that the PNS is associated with dysregulation of Trp metabolism. We further posited that treatment with a Trp-metaboliser Parasutterella excrementihominis would abrogate PNS-associated deleterious effects on offspring development. To test this hypothesis, pregnant mice were exposed to restraint stress and administered P. excrementihominis (Dam n = 3-9; Offspring n = 5-10). PNS increased maternal gut Trp and both maternal and offspring inflammation. P. excrementihominis treatment reduced the PNS-induced excess pool of maternal gut Trp. Some PNS effects on foetal neuroinflammation were reduced in severity due to handling effects from bacterial gavage. However, P. excrementihominis was anti-inflammatory in dam and offspring and anxiolytic in offspring of Pe-treated dams. These data illustrate that elevated Trp levels are associated PNS and its downstream deleterious offspring inflammatory and behavioural outcomes while P. excrementihominis, a Trp-metabolizer, can ameliorate these effects and improve offspring outcomes.
产前应激(PNS)对后代具有广泛影响,包括异常的免疫发育和行为缺陷。微生物群是应激效应通过免疫调节和代谢产物生成向后代传播的介质。源自母体及其肠道微生物群的代谢产物会传递给胎儿,并可影响免疫和神经发育。应激会影响此类代谢产物的丰度,包括参与免疫和神经系统功能的色氨酸(Trp)途径。我们假设PNS与Trp代谢失调有关。我们进一步推测,用Trp代谢菌人粪便副萨特氏菌进行治疗将消除PNS对后代发育的有害影响。为了验证这一假设,将怀孕小鼠暴露于束缚应激下,并给予人粪便副萨特氏菌(母鼠n = 3 - 9;后代n = 5 - 10)。PNS增加了母体肠道中的Trp以及母体和后代的炎症。人粪便副萨特氏菌治疗减少了PNS诱导的母体肠道Trp过量蓄积。由于灌胃细菌的操作影响,PNS对胎儿神经炎症的一些影响在严重程度上有所降低。然而,人粪便副萨特氏菌在母鼠和后代中具有抗炎作用,并且在接受该菌治疗的母鼠的后代中具有抗焦虑作用。这些数据表明,Trp水平升高与PNS及其下游对后代有害的炎症和行为结果相关,而Trp代谢菌人粪便副萨特氏菌可以改善这些影响并改善后代结局。