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机会性病原体细菌群落的无标记分子成像

Label-free molecular imaging of bacterial communities of the opportunistic pathogen .

作者信息

Baig Nameera, Polisetti Sneha, Morales-Soto Nydia, Dunham Sage J B, Sweedler Jonathan V, Shrout Joshua D, Bohn Paul W

机构信息

Department of Chemistry & Biochemistry and Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, IN 46556, USA.

Department of Civil and Environmental Engineering and Earth Sciences and Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556, USA.

出版信息

Proc SPIE Int Soc Opt Eng. 2016 Aug-Sep;9930. doi: 10.1117/12.2236695. Epub 2016 Sep 27.

Abstract

Biofilms, such as those formed by the opportunistic human pathogen are complex, matrix enclosed, and surface-associated communities of cells. Bacteria that are part of a biofilm community are much more resistant to antibiotics and the host immune response than their free-floating counterparts. biofilms are associated with persistent and chronic infections in diseases such as cystic fibrosis and HIV-AIDS. P. aeruginosa synthesizes and secretes signaling molecules such as the Pseudomonas quinolone signal (PQS) which are implicated in quorum sensing (QS), where bacteria regulate gene expression based on population density. Processes such as biofilms formation and virulence are regulated by QS. This manuscript describes the powerful molecular imaging capabilities of confocal Raman microscopy (CRM) and surface enhanced Raman spectroscopy (SERS) in conjunction with multivariate statistical tools such as principal component analysis (PCA) for studying the spatiotemporal distribution of signaling molecules, secondary metabolites and virulence factors in biofilm communities of . Our observations reveal that the laboratory strain PAO1C synthesizes and secretes 2-alkyl-4-hydroxyquinoline N-oxides and 2-alkyl-4-hydroxyquinolones in high abundance, while the isogenic acyl homoserine lactone QS-deficient mutant (I) strain produces predominantly 2-alkyl-quinolones during biofilm formation. This study underscores the use of CRM, along with traditional biological tools such as genetics, for studying the behavior of microbial communities at the molecular level.

摘要

生物膜,例如由机会性人类病原体形成的生物膜,是复杂的、被基质包裹的、与表面相关的细胞群落。作为生物膜群落一部分的细菌比其自由漂浮的同类细菌对抗生素和宿主免疫反应的抵抗力要强得多。生物膜与诸如囊性纤维化和艾滋病毒/艾滋病等疾病中的持续性和慢性感染有关。铜绿假单胞菌合成并分泌信号分子,如假单胞菌喹诺酮信号(PQS),这些信号分子与群体感应(QS)有关,在群体感应中细菌根据种群密度调节基因表达。生物膜形成和毒力等过程受群体感应调节。本手稿描述了共聚焦拉曼显微镜(CRM)和表面增强拉曼光谱(SERS)结合主成分分析(PCA)等多元统计工具在研究铜绿假单胞菌生物膜群落中信号分子、次生代谢产物和毒力因子的时空分布方面的强大分子成像能力。我们的观察结果表明,实验室菌株PAO1C大量合成并分泌2-烷基-4-羟基喹啉N-氧化物和2-烷基-4-羟基喹诺酮,而等基因酰基高丝氨酸内酯群体感应缺陷突变体(I)菌株在生物膜形成过程中主要产生2-烷基喹诺酮。这项研究强调了使用CRM以及遗传学等传统生物学工具在分子水平上研究微生物群落行为的重要性。

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