J D Galley, T A Rajasekera, D J Bennouna, A Batabyal, B Verosky, S Woodke, J Stokes, A K Brown, S Murthy, R E Kopec, T L Gur
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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.</p>","PeriodicalId":8834,"journal":{"name":"Beneficial microbes","volume":" ","pages":"1-18"},"PeriodicalIF":3.0000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multifactorial effects of probiotic Parasutterella excrementihominis on gestational inflammation, offspring behaviour and prenatal-stress induced disruptions in tryptophan metabolism.\",\"authors\":\"J D Galley, T A Rajasekera, D J Bennouna, A Batabyal, B Verosky, S Woodke, J Stokes, A K Brown, S Murthy, R E Kopec, T L Gur\",\"doi\":\"10.1163/18762891-bja00047\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Prenatal stress (PNS) has widespread effects on offspring, including aberrant immune development and behavioural deficits. 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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. 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引用次数: 0
摘要
产前应激(PNS)对后代有广泛的影响,包括异常免疫发育和行为缺陷。微生物组是通过免疫调节和代谢物产生向后代传播应激效应的中介。来自母亲及其肠道微生物群的代谢物传递给胎儿,并可影响免疫和神经发育。压力会影响这些代谢物的丰度,包括与免疫和神经系统功能有关的色氨酸(Trp)途径。我们假设PNS与色氨酸代谢失调有关。我们进一步假设,用一种trp代谢物处理粪人Parasutterella exmentihominis可以消除pns相关的对后代发育的有害影响。为了验证这一假设,将怀孕小鼠暴露于约束应激并给予粪人疟原虫(Dam n = 3-9;子代n = 5-10)。PNS增加母体肠道Trp和母体和子代炎症。粪便假单胞菌治疗减少了pns诱导的母体肠道Trp的过量池。由于细菌灌胃的处理作用,PNS对胎儿神经炎症的影响程度有所降低。然而,粪人假单胞菌对小鼠及其后代具有抗炎作用,对pe处理的小鼠后代具有抗焦虑作用。这些数据表明,色氨酸水平升高与PNS及其下游有害后代的炎症和行为结果有关,而粪便卟啉卟啉卟啉代谢物可以改善这些影响并改善后代的预后。
Multifactorial effects of probiotic Parasutterella excrementihominis on gestational inflammation, offspring behaviour and prenatal-stress induced disruptions in tryptophan metabolism.
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.
期刊介绍:
Beneficial Microbes is a peer-reviewed scientific journal with a specific area of focus: the promotion of the science of microbes beneficial to the health and wellbeing of man and animal. The journal contains original research papers and critical reviews in all areas dealing with beneficial microbes in both the small and large intestine, together with opinions, a calendar of forthcoming beneficial microbes-related events and book reviews. The journal takes a multidisciplinary approach and focuses on a broad spectrum of issues, including safety aspects of pro- & prebiotics, regulatory aspects, mechanisms of action, health benefits for the host, optimal production processes, screening methods, (meta)genomics, proteomics and metabolomics, host and bacterial physiology, application, and role in health and disease in man and animal. Beneficial Microbes is intended to serve the needs of researchers and professionals from the scientific community and industry, as well as those of policy makers and regulators.
The journal will have five major sections:
* Food, nutrition and health
* Animal nutrition
* Processing and application
* Regulatory & safety aspects
* Medical & health applications
In these sections, topics dealt with by Beneficial Microbes include:
* Worldwide safety and regulatory issues
* Human and animal nutrition and health effects
* Latest discoveries in mechanistic studies and screening methods to unravel mode of action
* Host physiology related to allergy, inflammation, obesity, etc.
* Trends in application of (meta)genomics, proteomics and metabolomics
* New developments in how processing optimizes pro- & prebiotics for application
* Bacterial physiology related to health benefits