The Biodesign Institute, Center for Infectious Diseases and Vaccinology, Arizona State University, 1001 S. McAllister Avenue, Tempe, AZ 85287, UDA.
Appl Environ Microbiol. 2011 Feb;77(4):1221-30. doi: 10.1128/AEM.01582-10. Epub 2010 Dec 17.
Assessing bacterial behavior in microgravity is important for risk assessment and prevention of infectious diseases during spaceflight missions. Furthermore, this research field allows the unveiling of novel connections between low-fluid-shear regions encountered by pathogens during their natural infection process and bacterial virulence. This study is the first to characterize the spaceflight-induced global transcriptional and proteomic responses of Pseudomonas aeruginosa, an opportunistic pathogen that is present in the space habitat. P. aeruginosa responded to spaceflight conditions through differential regulation of 167 genes and 28 proteins, with Hfq as a global transcriptional regulator. Since Hfq was also differentially regulated in spaceflight-grown Salmonella enterica serovar Typhimurium, Hfq represents the first spaceflight-induced regulator acting across bacterial species. The major P. aeruginosa virulence-related genes induced in spaceflight were the lecA and lecB lectin genes and the gene for rhamnosyltransferase (rhlA), which is involved in rhamnolipid production. The transcriptional response of spaceflight-grown P. aeruginosa was compared with our previous data for this organism grown in microgravity analogue conditions using the rotating wall vessel (RWV) bioreactor. Interesting similarities were observed, including, among others, similarities with regard to Hfq regulation and oxygen metabolism. While RWV-grown P. aeruginosa mainly induced genes involved in microaerophilic metabolism, P. aeruginosa cultured in spaceflight presumably adopted an anaerobic mode of growth, in which denitrification was most prominent. Whether the observed changes in pathogenesis-related gene expression in response to spaceflight culture could lead to an alteration of virulence in P. aeruginosa remains to be determined and will be important for infectious disease risk assessment and prevention, both during spaceflight missions and for the general public.
评估细菌在微重力环境下的行为对于评估航天任务期间传染病的风险和预防至关重要。此外,这一研究领域揭示了病原体在其自然感染过程中遇到的低液流剪切区域与细菌毒力之间的新联系。本研究首次对机会性病原体铜绿假单胞菌在太空飞行条件下的全球转录组和蛋白质组反应进行了特征描述,该病原体存在于太空栖息地中。铜绿假单胞菌通过调节 167 个基因和 28 种蛋白质来应对太空飞行条件,其中 Hfq 是一个全局转录调节因子。由于 Hfq 在太空飞行中生长的沙门氏菌肠炎血清型 Typhimurium 中也受到差异调节,因此 Hfq 代表了第一个跨细菌物种作用的太空飞行诱导调节因子。在太空飞行中诱导的铜绿假单胞菌主要与毒力相关的基因是 lecA 和 lecB 凝集素基因以及参与鼠李糖脂产生的 rhamnosyltransferase(rhlA)基因。将太空飞行中生长的铜绿假单胞菌的转录反应与我们之前使用旋转壁式生物反应器(RWV)生物反应器在微重力模拟条件下生长的该生物体的数据进行了比较。观察到了有趣的相似之处,包括 Hfq 调节和氧气代谢的相似之处。虽然 RWV 中生长的铜绿假单胞菌主要诱导参与微需氧代谢的基因,但在太空飞行中培养的铜绿假单胞菌可能采用了无氧生长模式,其中反硝化作用最为明显。由于太空飞行培养引起的与发病机制相关的基因表达变化是否会导致铜绿假单胞菌毒力的改变仍有待确定,这对于评估航天任务期间和一般公众的传染病风险和预防都很重要。