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| Content Provider | PubMed Central |
|---|---|
| Author | Swanepoel, Conrad C. Loots, Du Toit |
| Copyright Year | 2014 |
| Abstract | Tuberculosis (TB), caused by Mycobacterium tuberculosis, is a fatal infectious disease, resulting in 1.4 million deaths globally per annum. Over the past three decades, genomic studies have been conducted in an attempt to elucidate the functionality of the genome of the pathogen. However, many aspects of this complex genome remain largely unexplored, as approaches like genomics, proteomics, and transcriptomics have failed to characterize them successfully. In turn, metabolomics, which is relatively new to the “omics” revolution, has shown great potential for investigating biological systems or their modifications. Furthermore, when these data are interpreted in combination with previously acquired genomics, proteomics and transcriptomics data, using what is termed a systems biology approach, a more holistic understanding of these systems can be achieved. In this review we discuss how metabolomics has contributed so far to characterizing TB, with emphasis on the resulting improved elucidation of M. tuberculosis in terms of (1) metabolism, (2) growth and replication, (3) pathogenicity, and (4) drug resistance, from the perspective of systems biology. |
| Related Links | http://dx.doi.org/10.1155/2014/124218 |
| Starting Page | 124218 |
| File Format | |
| ISSN | 02780240 |
| e-ISSN | 18758630 |
| Journal | Disease Markers |
| Volume Number | 2014 |
| Language | English |
| Publisher | Hindawi Publishing Corporation |
| Publisher Date | 2014-01-01 |
| Access Restriction | Open |
| Rights Holder | Hindawi Publishing Corporation |
| Subject Keyword | Clinical Biochemistry Genetics Molecular Biology Biochemistry, medical Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Biochemistry (medical) Genetics Clinical Biochemistry Molecular Biology |
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