Lyte Joshua M, Koester Lucas R, Daniels Karrie M, Lyte Mark
Poultry Production and Product Safety Research, Agricultural Research Service, United States Department of Agriculture, Fayetteville, AR, United States.
Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA, United States.
Front Neurosci. 2022 Apr 12;16:827343. doi: 10.3389/fnins.2022.827343. eCollection 2022.
Although diet- and stress-induced perturbations in the microbiome (biotic and abiotic factors) associate with changes in host behavior via the microbiota-gut-brain axis, few mechanisms have been identified. The identification of causative pathways by which the microbiome influences host behavior therefore would benefit from the application of evidence-based conceptual frameworks. One such causal framework is microbial endocrinology which is the study of neuroendocrine axes as avenues of bi-directional neurochemical-based host-microbe crosstalk. As such, we investigated the relationship between diet- and stress-induced alterations in behavior, regional gut serotonergic response, and concomitant changes in the cecal and fecal bacterial populations of male and female mice. Our results demonstrate that sex is a dominant factor in determining compositional changes in the gut microbiome in response to stress and diet modifications. Intestinal serotonergic responses to stress were observed in both sexes but dietary modifications uniquely affected region-specific changes in males and females. Likewise, behavioral alterations diverged between male and female mice. Together, these results demonstrate distinct sex-dependent relationships between cecal and fecal bacterial taxa and behavioral- and serotonergic-responses to stress and diet. The present study demonstrates the importance of including both male and female sexes in the examination of the microbiota-gut-brain axis. As different microbial taxa were identified to associate with the behavioral and gut serotonergic responses of male and female mice, certain bacterial species may hold sex-dependent functional relevance for the host. Future investigations seeking to develop microbiome-based strategies to afford host stress resilience should include sex-based differences in the microbiome.
尽管饮食和压力引起的微生物群扰动(生物和非生物因素)通过微生物群-肠-脑轴与宿主行为的变化相关联,但已确定的机制很少。因此,通过基于证据的概念框架来确定微生物群影响宿主行为的因果途径将大有裨益。一种这样的因果框架是微生物内分泌学,它研究神经内分泌轴作为基于神经化学的宿主-微生物双向串扰的途径。因此,我们研究了饮食和压力引起的行为改变、肠道局部血清素能反应以及雄性和雌性小鼠盲肠和粪便细菌种群的相应变化之间的关系。我们的结果表明,性别是决定肠道微生物群组成变化以应对压力和饮食改变的主要因素。在两性中均观察到肠道对压力的血清素能反应,但饮食改变对雄性和雌性的区域特异性变化有独特影响。同样,雄性和雌性小鼠的行为改变也有所不同。总之,这些结果表明盲肠和粪便细菌分类群与对压力和饮食的行为及血清素能反应之间存在明显的性别依赖性关系。本研究证明了在检查微生物群-肠-脑轴时纳入雄性和雌性的重要性。由于已确定不同的微生物分类群与雄性和雌性小鼠的行为及肠道血清素能反应相关联,某些细菌物种可能对宿主具有性别依赖性的功能相关性。未来旨在开发基于微生物群的策略以提高宿主应激恢复力的研究应包括微生物群中的性别差异。