Lybbert Andrew C, Williams Justin L, Raghuvanshi Ruma, Jones A Daniel, Quinn Robert A
Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48823, USA.
Department of Biology, University of Arkansas at Pine Bluff, Pine Bluff, AR 71601, USA.
Metabolites. 2020 Nov 5;10(11):445. doi: 10.3390/metabo10110445.
is a ubiquitous environmental bacterium that causes chronic infections of burn wounds and in the lungs of cystic fibrosis (CF) patients. Vital to its infection is a myriad of specialized metabolites that serve a variety of biological roles including quorum sensing, metal chelation and inhibition of other competing bacteria. This study employed newly available algorithms for searching individual tandem mass (MS/MS) spectra against the publicly available Global Natural Product Social Molecular Networking (GNPS) database to identify the chemical diversity of these compounds and their presence in environmental, laboratory and clinical samples. For initial characterization, the metabolomes of eight clinical isolates of were analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) and uploaded to GNPS for spectral searching. Quinolones, rhamnolipids, phenazines and siderophores were identified and characterized; including the discovery of modified forms of the iron chelator pyochelin. Quinolones were highly diverse with the three base forms quinolone signal 2-heptyl-3-hydroxy-4()-quinolone (PQS), 4-heptyl-4()-quinolone (HHQ) and 2-heptyl-4-quinolone--oxide (HQNO) having extensive variation in the length of their acyl chain from as small as 3 carbons to as large as 17. Rhamnolipids were limited to either one or two sugars with a limited set of fatty acyl chains, but the base lipid form without the rhamnose was also detected. These specialized metabolites were identified from diverse sources including ant-fungal mutualist dens, soil, plants, human teeth, feces, various lung mucus samples and cultured laboratory isolates. Their prevalence in fecal samples was particularly notable as is not known as a common colonizer of the human gut. The chemical diversity of the compounds identified, particularly the quinolones, demonstrates a broad spectrum of chemical properties within these the metabolite groups with likely significant impacts on their biological functions. Mining public data with GNPS enables a new approach to characterize the chemical diversity of biological organisms, which includes enabling the discovery of new chemistry from pathogenic bacteria.
是一种普遍存在的环境细菌,可导致烧伤创面慢性感染以及囊性纤维化(CF)患者肺部感染。对其感染至关重要的是大量特殊代谢产物,这些代谢产物发挥着多种生物学作用,包括群体感应、金属螯合以及抑制其他竞争性细菌。本研究采用新可用的算法,针对公开可用的全球天然产物社会分子网络(GNPS)数据库搜索单个串联质谱(MS/MS)谱图,以识别这些化合物的化学多样性及其在环境、实验室和临床样本中的存在情况。为进行初步表征,使用液相色谱 - 串联质谱(LC-MS/MS)分析了八种临床分离株的代谢组,并上传至GNPS进行谱图搜索。鉴定并表征了喹诺酮类、鼠李糖脂、吩嗪类和铁载体;包括发现了铁螯合剂绿脓菌素的修饰形式。喹诺酮类高度多样,三种基本形式喹诺酮信号2 - 庚基 - 3 - 羟基 - 4() - 喹诺酮(PQS)、4 - 庚基 - 4() - 喹诺酮(HHQ)和2 - 庚基 - 4 - 喹诺酮 - 氧化物(HQNO)的酰基链长度变化范围很大,从小至3个碳到大至17个碳。鼠李糖脂限于带有有限一组脂肪酰链的一种或两种糖,但也检测到了不含鼠李糖的基本脂质形式。这些特殊代谢产物从多种来源中被鉴定出来,包括抗真菌共生菌窝、土壤、植物、人类牙齿、粪便、各种肺黏液样本以及培养的实验室分离株。它们在粪便样本中的普遍存在尤为显著,因为并不被认为是人类肠道的常见定植菌。所鉴定化合物的化学多样性,尤其是喹诺酮类,表明这些代谢产物组内具有广泛的化学性质,可能对其生物学功能产生重大影响。利用GNPS挖掘公共数据能够采用一种新方法来表征生物有机体的化学多样性,其中包括能够从病原菌中发现新化学物质。