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Succession and persistence of microbial communities and antimicrobial resistance genes associated with International Space Station environmental surfaces

机译:与国际空间站环境表面相关的微生物群落和抗微生物抗性基因的连续和持久性

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摘要

Abstract Background The International Space Station (ISS) is an ideal test bed for studying the effects of microbial persistence and succession on a closed system during long space flight. Culture-based analyses, targeted gene-based amplicon sequencing (bacteriome, mycobiome, and resistome), and shotgun metagenomics approaches have previously been performed on ISS environmental sample sets using whole genome amplification (WGA). However, this is the first study reporting on the metagenomes sampled from ISS environmental surfaces without the use of WGA. Metagenome sequences generated from eight defined ISS environmental locations in three consecutive flights were analyzed to assess the succession and persistence of microbial communities, their antimicrobial resistance (AMR) profiles, and virulence properties. Metagenomic sequences were produced from the samples treated with propidium monoazide (PMA) to measure intact microorganisms. Results The intact microbial communities detected in Flight 1 and Flight 2 samples were significantly more similar to each other than to Flight 3 samples. Among 318 microbial species detected, 46 species constituting 18 genera were common in all flight samples. Risk group or biosafety level 2 microorganisms that persisted among all three flights were Acinetobacter baumannii, Haemophilus influenzae, Klebsiella pneumoniae, Salmonella enterica, Shigella sonnei, Staphylococcus aureus, Yersinia frederiksenii, and Aspergillus lentulus. Even though Rhodotorula and Pantoea dominated the ISS microbiome, Pantoea exhibited succession and persistence. K. pneumoniae persisted in one location (US Node 1) of all three flights and might have spread to six out of the eight locations sampled on Flight 3. The AMR signatures associated with β-lactam, cationic antimicrobial peptide, and vancomycin were detected. Prominent virulence factors were cobalt-zinc-cadmium resistance and multidrug-resistance efflux pumps. Conclusions There was an increase in AMR and virulence gene factors detected over the period sampled, and metagenome sequences of human pathogens persisted over time. Comparative analysis of the microbial compositions of ISS with Earth analogs revealed that the ISS environmental surfaces were different in microbial composition. Metagenomics coupled with PMA treatment would help future space missions to estimate problematic risk group microbial pathogens. Cataloging AMR/virulence characteristics, succession, accumulation, and persistence of microorganisms would facilitate the development of suitable countermeasures to reduce their presence in the closed built environment.
机译:摘要背景国际空间站(ISS)是一个理想的试验台,用于研究微生物持久性和连续在长太空飞行期间封闭系统的影响。以全基因组扩增(WGA)对ISS环境样品集进行了靶向基于基于基于基于基于基于基因的扩增子测序(细菌组,霉菌组和抵抗力)和霰弹枪偏霉菌方法。然而,这是第一研究从ISS环境表面取样而不使用WGA的研究报告。分析了从八个定义的ISS环境位置产生的偏见序列,分析了三次连续航班,以评估微生物社区的连续和持续性,其抗微生物抗性(AMR)型材和毒力特性。从用单氮化物(PMA)处理的样品中产生偏见序列以测量完整的微生物。结果在飞行1和飞行中检测到的完整微生物社区和2个样品中的彼此显着更类似于飞行3个样品。在318种微生物物种中,在所有飞行样本中,构成18个属的46种常见。所有三种航班中持续存在的风险群或生物安全级别2微生物是鲍曼,嗜血杆菌嗜血杆菌,肺炎,沙门氏菌,志贺氏菌,金黄色葡萄球菌,yersinia frederiksenii和曲霉属植物。尽管罗经罗拉和Pantoea在ISS Microbiome主导地位,但是Pantoea表现出连续和持久性。 K.肺炎仍然存在于所有三个航班的一个地点(美国节点1),并且可能已经将六个地方蔓延到八个地点3.检测到与β-内酰胺,阳离子抗微生物肽和万古霉素相关的AMR签名。突出的毒力因子是钴 - 锌 - 镉抗性和多药电阻的流出泵。结论在采样期间检测到的AMR和毒力基因因子增加,人病原体的偏见序列随着时间的推移而持续存在。具有地球模拟的ISS微生物组合物的比较分析表明,在微生物组合物中的ISS环境表面不同。与PMA治疗相结合的Metagenomics将有助于未来的空间任务来估算有问题的风险组微生物病原体。编目的AMR /毒力特征,继承,积累和持久性的微生物将有助于开发适当的对策,以减少其在封闭的环境中的存在。

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