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首页> 外文期刊>Journal of bacteriology >Refining the Application of Microbial Lipids as Tracers of Staphylococcus aureus Growth Rates in Cystic Fibrosis Sputum | Journal of Bacteriology
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Refining the Application of Microbial Lipids as Tracers of Staphylococcus aureus Growth Rates in Cystic Fibrosis Sputum | Journal of Bacteriology

机译:微生物脂质作为金黄色葡萄球菌生长速率示踪剂在囊性纤维化痰中的应用细菌学杂志

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Chronic lung infections in cystic fibrosis (CF) could be treated more effectively if the effects of antimicrobials on pathogens in situ were known. Here, we compared changes in the microbial community composition and pathogen growth rates in longitudinal studies of seven pediatric CF patients undergoing intravenous antibiotic administration during pulmonary exacerbations. The microbial community composition was determined by counting rRNA with NanoString DNA analysis, and growth rates were obtained by incubating CF sputum with heavy water and tracing incorporation of deuterium into two branched-chain (“anteiso”) fatty acids (a-C15:0 and a-C17:0) using gas chromatography-mass spectrometry (GC/MS). Prior to this study, both lipids were thought to be specific for Staphylococcaceae; hence, their isotopic enrichment was interpreted as a growth proxy for Staphylococcus aureus. Our experiments revealed, however, that Prevotella is also a relevant microbial producer of a-C17:0 fatty acid in some CF patients; thus, deuterium incorporation into these lipids is better interpreted as a more general pathogen growth rate proxy. Even accounting for a small nonmicrobial background source detected in some patient samples, a-C15:0 fatty acid still appears to be a relatively robust proxy for CF pathogens, revealing a median generation time of ~1.5 days, similar to prior observations. Contrary to our expectation, pathogen growth rates remained relatively stable throughout exacerbation treatment. We suggest two straightforward “best practices” for application of stable-isotope probing to CF sputum metabolites: (i) parallel determination of microbial community composition in CF sputum using culture-independent tools and (ii) assessing background levels of the diagnostic metabolite.
机译:如果已知抗生素对原发性病原体的作用,则可以更有效地治疗囊性纤维化(CF)中的慢性肺部感染。在这里,我们比较了纵向研究的七名小儿CF患者在肺部加重期间接受静脉内抗生素治疗的微生物群落组成和病原体生长速率的变化。通过用NanoString DNA分析对rRNA进行计数来确定微生物群落组成,并通过将CF痰与重水温育并追踪氘掺入两个支链(“ anteiso”)脂肪酸(a-C15:0和a-C17:0),使用气相色谱-质谱(GC / MS)。在这项研究之前,两种脂质都被认为对葡萄球菌具有特异性。因此,他们的同位素富集被解释为金黄色葡萄球菌的生长代用品。然而,我们的实验表明,普氏杆菌在某些CF患者中也是a-C17:0脂肪酸的相关微生物产生者;因此,将氘掺入到这些脂质中可以更好地解释为更一般的病原体生长速率替代物。即使考虑到在某些患者样本中检测到的少量非微生物本底源,α-C15:0脂肪酸似乎仍然是CF病原体的相对强大替代物,显示中位生成时间约为1.5天,与先前的观察结果相似。与我们的预期相反,在病情加重期间,病原体的增长率保持相对稳定。我们建议将稳定同位素探测应用于CF痰代谢物的两个简单的“最佳实践”:(i)使用不依赖培养物的工具平行测定CF痰中的微生物群落组成,以及(ii)评估诊断代谢物的背景水平。

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