학술논문

In Vivo Biosynthesis of Terpene Nucleosides Provides Unique Chemical Markers of Mycobacterium tuberculosis Infection
Document Type
article
Source
Cell Chemical Biology. 22(4)
Subject
Analytical Chemistry
Biological Sciences
Chemical Sciences
Rare Diseases
Emerging Infectious Diseases
Biotechnology
Infectious Diseases
Prevention
Tuberculosis
Vaccine Related
Aetiology
2.2 Factors relating to the physical environment
Infection
Good Health and Well Being
Animals
Bacterial Proteins
Chromatography
High Pressure Liquid
Isomerism
Lipids
Lung
Magnetic Resonance Spectroscopy
Mice
Mice
Inbred BALB C
Mycobacterium tuberculosis
Nucleosides
Polymorphism
Single Nucleotide
Spectrometry
Mass
Electrospray Ionization
Terpenes
Medicinal and Biomolecular Chemistry
Organic Chemistry
Biochemistry and Cell Biology
Biochemistry and cell biology
Medicinal and biomolecular chemistry
Language
Abstract
Although small molecules shed from pathogens are widely used to diagnose infection, such tests have not been widely implemented for tuberculosis. Here we show that the recently identified compound, 1-tuberculosinyladenosine (1-TbAd), accumulates to comprise >1% of all Mycobacterium tuberculosis lipid. In vitro and in vivo, two isomers of TbAd were detected that might serve as infection markers. Using mass spectrometry and nuclear magnetic resonance, we established the structure of the previously unknown molecule, N(6)-tuberculosinyladenosine (N(6)-TbAd). Its biosynthesis involves enzymatic production of 1-TbAd by Rv3378c followed by conversion to N(6)-TbAd via the Dimroth rearrangement. Intact biosynthetic genes are observed only within M. tuberculosis complex bacteria, and TbAd was not detected among other medically important pathogens, environmental bacteria, and vaccine strains. With no substantially similar known molecules in nature, the discovery and in vivo detection of two abundant terpene nucleosides support their development as specific diagnostic markers of tuberculosis.