Gilbert Rachel, Tanenbaum Nicole, Bhattacharya Sharmila
NASA Postdoctoral Program, Universities Space Research Association, NASA Ames Research Center, Moffett Field, CA, USA.
Dept. of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Heliyon. 2022 May 4;8(5):e09379. doi: 10.1016/j.heliyon.2022.e09379. eCollection 2022 May.
While studies have shown an increase in pathogenicity in several microbes during spaceflight and after exposure to simulated microgravity, the mechanisms underlying these changes in phenotype are not understood across different pathogens, particularly in opportunistic pathogens. This study evaluates the mechanism for increased virulence of the opportunistic gram-negative bacterium, in simulated microgravity. Low-shear modeled microgravity (LSMMG) is used in ground-based studies to simulate the effects of microgravity as experienced in spaceflight. Our previous findings showed that there was a significant increase in mortality rates of the host when infected with either spaceflight or LSMMG treated . Here, we report that LSMMG increases asparagine uptake and synthesis in and that the increased host lethality induced by LSMMG bacteria grown in rich media can be recapitulated in minimal media by adding only aspartate and glutamine, the substrates of asparagine biosynthesis. Interestingly, increased bacterial growth rate alone is not sufficient to contribute to maximal host lethality, since the addition of aspartate to minimal media caused an LSMMG-specific increase in bacterial growth rate that is comparable to that induced by the combination of aspartate and glutamine, but this increase in growth does not cause an equivalent rate of host mortality. However, the addition of both aspartate and glutamine cause both an increase in host mortality and an overexpression of asparagine pathway genes in a LSMMG-dependent manner. We also report that L-asparaginase-mediated breakdown of asparagine is an effective countermeasure for the increased host mortality caused by LSMMG-treated bacteria. This investigation underscores the importance of the asparagine utilization pathway by helping uncover molecular mechanisms that underlie increased mortality rates of a model host infected with microgravity-treated and provides a potential mitigation strategy.
虽然研究表明,在太空飞行期间以及暴露于模拟微重力环境后,几种微生物的致病性有所增加,但不同病原体(尤其是机会致病菌)表型变化背后的机制尚不清楚。本研究评估了在模拟微重力环境下机会性革兰氏阴性菌毒力增加的机制。低剪切力模拟微重力(LSMMG)用于地面研究,以模拟太空飞行中所经历的微重力效应。我们之前的研究结果表明,用太空飞行或经LSMMG处理的[细菌名称未给出]感染宿主时,宿主死亡率显著增加。在此,我们报告LSMMG增加了[细菌名称未给出]中天冬酰胺的摄取和合成,并且在仅添加天冬酰胺生物合成底物天冬氨酸和谷氨酰胺的基本培养基中,能重现富含培养基中生长的LSMMG细菌诱导的宿主致死率增加。有趣的是,仅细菌生长速率增加不足以导致最大宿主致死率,因为向基本培养基中添加天冬氨酸会导致细菌生长速率出现LSMMG特异性增加,这与天冬氨酸和谷氨酰胺联合诱导的增加相当,但这种生长增加并未导致同等比例的宿主死亡率。然而,同时添加天冬氨酸和谷氨酰胺会导致宿主死亡率增加,并以LSMMG依赖的方式使天冬酰胺途径基因过度表达。我们还报告,L-天冬酰胺酶介导的天冬酰胺分解是对抗LSMMG处理细菌导致的宿主死亡率增加的有效对策。这项研究强调了天冬酰胺利用途径的重要性,有助于揭示感染微重力处理[细菌名称未给出]的模型宿主死亡率增加背后的分子机制,并提供了一种潜在的缓解策略。