Key Laboratory of Biomechanics and Mechanobiology (Beihang University), Ministry of Education Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, 37 Xueyuan Road, Haidian District, Beijing 100083, China; International Joint Research Center of Aerospace Biotechnology & Medical Engineering, Beihang University, Beijing 100083, China.
School of Biological Science and Medical Engineering, Beihang University, Beijing 100191, China; 4+4 M D. Program, Chinese Academy of Medical Science & Peking Union Medical College, Beijing 100730, China.
Life Sci Space Res (Amst). 2023 Aug;38:29-38. doi: 10.1016/j.lssr.2023.04.005. Epub 2023 Apr 30.
Understanding the structural and antibiotic resistance changes of microbial communities in space environments is critical for identifying potential pathogens that may pose health risks to astronauts and for preventing and controlling microbial contamination. The research to date on microbes under simulated space factors has primarily been carried out on single bacterial species under the individual effects of microgravity or low-dose radiation. However, microgravity (MG) and low-dose ionizing radiation (LDIR) coexist in the actual spacecraft environment, and microorganisms coexist as communities in the spacecraft environment. Thus, the microbial response to the real changes present during space habitation has not been adequately explored. To address this knowledge gap, we compared the dynamics of community composition and antibiotic resistance of synthetic bacterial communities under simulated microgravit, low-dose ionizing radiation, and the conditions combined, as it occurs in spacecraft. To ensure representative bacteria were selected, we co-cultured of 12 bacterial strains isolated from spacecraft cleanrooms. We found that the weakened competition between communities increased the possibility of species coexistence, community diversity, and homogeneity. The number of Bacilli increased significantly, while different species under the combined conditions showed various changes in abundance compared to those under the individual conditions. The resistance of the synthetic community to penicillins increased significantly under low doses of ionizing radiation but did not change significantly under simulated microgravity or the combined conditions. The results of functional predictions revealed that antibiotic biosynthesis and resistance increased dramatically in the community under space environmental stress, which confirmed the results of the drug sensitivity assays. Our results show that combined space environmental factors exert different effects on the microbial community structure and antibiotic resistance, which provides new insights into our understanding of the mechanisms of evolution of microorganisms in spacecraft, and is relevant to effective microbial pollution prevention and control strategies.
了解空间环境中微生物群落的结构和抗生素耐药性变化对于识别可能对宇航员健康构成威胁的潜在病原体以及预防和控制微生物污染至关重要。迄今为止,在模拟空间因素下对微生物的研究主要是在微重力或低剂量辐射的单个作用下对单个细菌物种进行的。然而,微重力 (MG) 和低剂量电离辐射 (LDIR) 在实际航天器环境中共存,并且微生物在航天器环境中共存为群落。因此,微生物对太空居住期间实际变化的反应尚未得到充分探索。为了弥补这一知识空白,我们比较了模拟微重力、低剂量电离辐射和实际太空环境中组合条件下合成细菌群落的群落组成和抗生素耐药性的动态变化。为了确保选择有代表性的细菌,我们共培养了从航天器洁净室分离的 12 株细菌。我们发现,群落之间竞争的减弱增加了物种共存、群落多样性和同质性的可能性。芽孢杆菌的数量显著增加,而组合条件下的不同物种与单一条件下相比,丰度表现出不同的变化。在低剂量电离辐射下,合成群落对青霉素的抗性显著增加,但在模拟微重力或组合条件下没有显著变化。功能预测的结果表明,在空间环境应激下,群落中的抗生素生物合成和抗性显著增加,这证实了药敏试验的结果。我们的结果表明,联合空间环境因素对微生物群落结构和抗生素耐药性产生不同的影响,这为我们理解航天器中微生物进化的机制提供了新的见解,并与有效的微生物污染预防和控制策略相关。