Literature DB >> 22374855

RNA decay: a novel therapeutic target in bacteria.

Tess M Eidem1, Christelle M Roux, Paul M Dunman.   

Abstract

The need for novel antibiotics is greater now than perhaps any time since the pre-antibiotic era. Indeed, the recent collapse of most pharmaceutical antibacterial groups, combined with the emergence of hypervirulent and pan-antibiotic-resistant bacteria have, in effect, created a 'perfect storm' that has severely compromised infection treatment options and led to dramatic increases in the incidence and severity of bacterial infections. To put simply, it is imperative that we develop new classes of antibiotics for the therapeutic intervention of bacterial infections. In that regard, RNA degradation is an essential biological process that has not been exploited for antibiotic development. Herein we discuss the factors that govern bacterial RNA degradation, highlight members of this machinery that represent attractive antimicrobial drug development targets and describe the use of high-throughput screening as a means of developing antimicrobials that target these enzymes. Such agents would represent first-in-class antibiotics that would be less apt to inactivation by currently encountered enzymatic antibiotic-resistance determinants.
Copyright © 2012 John Wiley & Sons, Ltd.

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Year:  2012        PMID: 22374855      PMCID: PMC3331933          DOI: 10.1002/wrna.1110

Source DB:  PubMed          Journal:  Wiley Interdiscip Rev RNA        ISSN: 1757-7004            Impact factor:   9.957


  92 in total

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6.  Purification and some novel properties of Escherichia coli RNase II.

Authors:  R S Gupta; T Kasai; D Schlessinger
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Review 10.  The challenge of emerging and re-emerging infectious diseases.

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  13 in total

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Journal:  J Med Microbiol       Date:  2018-04-05       Impact factor: 2.472

2.  Both exo- and endo-nucleolytic activities of RNase J1 from Staphylococcus aureus are manganese dependent and active on triphosphorylated 5'-ends.

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4.  Small-molecule inhibitors of Staphylococcus aureus RnpA-mediated RNA turnover and tRNA processing.

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6.  Inhibition of ribosomal subunit synthesis in Escherichia coli by the vanadyl ribonucleoside complex.

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7.  The highly conserved bacterial RNase YbeY is essential in Vibrio cholerae, playing a critical role in virulence, stress regulation, and RNA processing.

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8.  Genome-wide analysis shows that RNase G plays a global role in the stability of mRNAs in Stenotrophomonas maltophilia.

Authors:  Alejandra Bernardini; José L Martínez
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9.  Identification of Small Molecule Inhibitors of Staphylococcus aureus RnpA.

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10.  Identification and analysis of novel small molecule inhibitors of RNase E: Implications for antibacterial targeting and regulation of RNase E.

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