AI Article Synopsis

  • - The 2001 anthrax attacks highlighted the risks of bioterrorism, leading to the need for improved treatments and diagnostic methods for biological threats.
  • - Researchers conducted flux balance analyses on the metabolic networks of three key bioterrorism bacteria (Bacillus anthracis, Francisella tularensis, Yersinia pestis) and identified several metabolic enzymes as potential drug targets.
  • - Nine enzymes related to common metabolic pathways were found across these bacteria, suggesting that a mix of targeted antibiotics could create effective treatments against these high-risk bioterrorism agents.

Article Abstract

The 2001 anthrax mail attacks in the United States demonstrated the potential threat of bioterrorism, hence driving the need to develop sophisticated treatment and diagnostic protocols to counter biological warfare. Here, by performing flux balance analyses on the fully-annotated metabolic networks of multiple, whole genome-sequenced bacterial strains, we have identified a large number of metabolic enzymes as potential drug targets for each of the three Category A-designated bioterrorism agents including Bacillus anthracis, Francisella tularensis and Yersinia pestis. Nine metabolic enzymes- belonging to the coenzyme A, folate, phosphatidyl-ethanolamine and nucleic acid pathways common to all strains across the three distinct genera were identified as targets. Antimicrobial agents against some of these enzymes are available. Thus, a combination of cross species-specific antibiotics and common antimicrobials against shared targets may represent a useful combinatorial therapeutic approach against all Category A bioterrorism agents.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893172PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0085195PLOS

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