Literature DB >> 11728875

Exploiting genomics to discover new antibiotics.

D McDevitt1, M Rosenberg.   

Abstract

There is an urgent need to develop new classes of antibiotics to tackle the increase in resistance in many common bacterial pathogens. One strategy to develop new antibiotics is to identify and exploit new molecular targets and this strategy is being driven by the wealth of new genome sequence information now available. Additionally, new technologies have been developed to validate new antibacterial targets, for example, new technologies have been developed to enable rapid determination of whether a gene is essential and to assess the transcription status of a putative target during infection. As a result, many novel validated targets have now been identified and for some, appropriate high-throughput screens against diverse compound collections have been carried out. Novel antibiotic leads are emerging from these genomics-derived targeted screens and the challenge now is to optimize and develop these leads to become part of the next generation of antibiotics.

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Year:  2001        PMID: 11728875     DOI: 10.1016/s0966-842x(01)02235-1

Source DB:  PubMed          Journal:  Trends Microbiol        ISSN: 0966-842X            Impact factor:   17.079


  17 in total

1.  Identification of 113 conserved essential genes using a high-throughput gene disruption system in Streptococcus pneumoniae.

Authors:  Jane A Thanassi; Sandra L Hartman-Neumann; Thomas J Dougherty; Brian A Dougherty; Michael J Pucci
Journal:  Nucleic Acids Res       Date:  2002-07-15       Impact factor: 16.971

Review 2.  Antimicrobial resistance: the example of Staphylococcus aureus.

Authors:  Franklin D Lowy
Journal:  J Clin Invest       Date:  2003-05       Impact factor: 14.808

3.  Evaluating the suitability of essential genes as targets for antibiotic screening assays using proteomics.

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Journal:  Protein Cell       Date:  2012-01       Impact factor: 14.870

4.  Targeting antibacterial agents by using drug-carrying filamentous bacteriophages.

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Journal:  Antimicrob Agents Chemother       Date:  2006-06       Impact factor: 5.191

Review 5.  Novel approaches to developing new antibiotics for bacterial infections.

Authors:  A R M Coates; Y Hu
Journal:  Br J Pharmacol       Date:  2007-08-20       Impact factor: 8.739

6.  Staphylococcus aureus cell wall stress stimulon gene-lacZ fusion strains: potential for use in screening for cell wall-active antimicrobials.

Authors:  Rebecca Steidl; Stacy Pearson; Robert E Stephenson; Nagender Ledala; Sutthirat Sitthisak; Brian J Wilkinson; Radheshyam K Jayaswal
Journal:  Antimicrob Agents Chemother       Date:  2008-06-09       Impact factor: 5.191

7.  Substrate recognition by β-ketoacyl-ACP synthases.

Authors:  Janine G Borgaro; Andrew Chang; Carl A Machutta; Xujie Zhang; Peter J Tonge
Journal:  Biochemistry       Date:  2011-11-17       Impact factor: 3.162

8.  Complexes of bacterial nicotinate mononucleotide adenylyltransferase with inhibitors: implication for structure-based drug design and improvement.

Authors:  Nian Huang; Rohit Kolhatkar; Yvonne Eyobo; Leonardo Sorci; Irina Rodionova; Andrei L Osterman; Alexander D Mackerell; Hong Zhang
Journal:  J Med Chem       Date:  2010-07-22       Impact factor: 7.446

9.  Targeting NAD biosynthesis in bacterial pathogens: Structure-based development of inhibitors of nicotinate mononucleotide adenylyltransferase NadD.

Authors:  Leonardo Sorci; Yongping Pan; Yvonne Eyobo; Irina Rodionova; Nian Huang; Oleg Kurnasov; Shijun Zhong; Alexander D MacKerell; Hong Zhang; Andrei L Osterman
Journal:  Chem Biol       Date:  2009-08-28

10.  Rhomboid homologs in mycobacteria: insights from phylogeny and genomic analysis.

Authors:  David P Kateete; Moses Okee; Fred A Katabazi; Alfred Okeng; Jeniffer Asiimwe; Henry W Boom; Kathleen D Eisenach; Moses L Joloba
Journal:  BMC Microbiol       Date:  2010-10-29       Impact factor: 3.605

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