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土壤源细菌免疫对“双打击”应激模型中应激应对行为和认知表现的影响。

Effects of Immunization With the Soil-Derived Bacterium on Stress Coping Behaviors and Cognitive Performance in a "Two Hit" Stressor Model.

作者信息

Foxx Christine L, Heinze Jared D, González Antonio, Vargas Fernando, Baratta Michael V, Elsayed Ahmed I, Stewart Jessica R, Loupy Kelsey M, Arnold Mathew R, Flux M C, Sago Saydie A, Siebler Philip H, Milton Lauren N, Lieb Margaret W, Hassell James E, Smith David G, Lee Kyo A K, Appiah Sandra A, Schaefer Evan J, Panitchpakdi Morgan, Sikora Nicole C, Weldon Kelly C, Stamper Christopher E, Schmidt Dominic, Duggan David A, Mengesha Yosan M, Ogbaselassie Mikale, Nguyen Kadi T, Gates Chloe A, Schnabel K'loni, Tran Linh, Jones Joslynn D, Vitaterna Martha H, Turek Fred W, Fleshner Monika, Dorrestein Pieter C, Knight Rob, Wright Kenneth P, Lowry Christopher A

机构信息

Department of Integrative Physiology, University of Colorado Boulder, Boulder, CO, United States.

Center for Microbial Exploration, University of Colorado Boulder, Boulder, CO, United States.

出版信息

Front Physiol. 2021 Jan 5;11:524833. doi: 10.3389/fphys.2020.524833. eCollection 2020.

Abstract

Previous studies demonstrate that NCTC 11659 (), a soil-derived bacterium with anti-inflammatory and immunoregulatory properties, is a potentially useful countermeasure against negative outcomes to stressors. Here we used male C57BL/6NCrl mice to determine if repeated immunization with is an effective countermeasure in a "two hit" stress exposure model of chronic disruption of rhythms (CDR) followed by acute social defeat (SD). On day -28, mice received implants of biotelemetric recording devices to monitor 24-h rhythms of locomotor activity. Mice were subsequently treated with a heat-killed preparation of (0.1 mg, administered subcutaneously on days -21, -14, -7, and 27) or borate-buffered saline vehicle. Mice were then exposed to 8 consecutive weeks of either stable normal 12:12 h light:dark (LD) conditions or CDR, consisting of 12-h reversals of the LD cycle every 7 days (days 0-56). Finally, mice were exposed to either a 10-min SD or a home cage control condition on day 54. All mice were exposed to object location memory testing 24 h following SD. The gut microbiome and metabolome were assessed in fecal samples collected on days -1, 48, and 62 using 16S rRNA gene sequence and LC-MS/MS spectral data, respectively; the plasma metabolome was additionally measured on day 64. Among mice exposed to normal LD conditions, immunization with induced a shift toward a more proactive behavioral coping response to SD as measured by increases in scouting and avoiding an approaching male CD-1 aggressor, and decreases in submissive upright defensive postures. In the object location memory test, exposure to SD increased cognitive function in CDR mice previously immunized with . Immunization with stabilized the gut microbiome, attenuating CDR-induced reductions in alpha diversity and decreasing within-group measures of beta diversity. Immunization with also increased the relative abundance of 1-heptadecanoyl-sn-glycero-3-phosphocholine, a lysophospholipid, in plasma. Together, these data support the hypothesis that immunization with stabilizes the gut microbiome, induces a shift toward a more proactive response to stress exposure, and promotes stress resilience.

摘要

先前的研究表明,NCTC 11659(一种具有抗炎和免疫调节特性的土壤细菌)是应对应激源负面结果的一种潜在有效对策。在此,我们使用雄性C57BL/6NCrl小鼠来确定用NCTC 11659反复免疫在慢性节律紊乱(CDR)继以急性社会挫败(SD)的“两次打击”应激暴露模型中是否为一种有效对策。在第 -28天,小鼠植入生物遥测记录装置以监测24小时运动活动节律。随后,小鼠用热灭活的NCTC 11659制剂(0.1毫克,在第 -21、-14、-7和27天皮下注射)或硼酸盐缓冲盐水载体进行处理。然后,小鼠连续8周暴露于稳定的正常12:12小时光照:黑暗(LD)条件或CDR(每7天进行12小时的LD周期反转,第0 - 56天)。最后,在第54天,小鼠暴露于10分钟的SD或笼内对照条件。所有小鼠在SD后24小时接受物体位置记忆测试。分别使用16S rRNA基因序列和LC-MS/MS光谱数据评估在第 -1、48和62天收集的粪便样本中的肠道微生物组和代谢组;在第64天额外测量血浆代谢组。在暴露于正常LD条件的小鼠中,用NCTC 11659免疫诱导了对SD的行为应对反应向更主动的方向转变,表现为探索行为增加、避免接近的雄性CD-1攻击者以及顺从直立防御姿势减少。在物体位置记忆测试中,暴露于SD增加了先前用NCTC 11659免疫的CDR小鼠的认知功能。用NCTC 11659免疫稳定了肠道微生物组,减轻了CDR诱导的α多样性降低,并减少了组内β多样性测量值。用NCTC 11659免疫还增加了血浆中溶血磷脂1-十七烷酰-sn-甘油-3-磷酸胆碱的相对丰度。总之,这些数据支持以下假设:用NCTC 11659免疫可稳定肠道微生物组,诱导对应激暴露的反应向更主动的方向转变,并促进应激恢复力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5432/7813891/1779cde65232/fphys-11-524833-g001.jpg

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