H2020Individual fellowship2015–2017

AND · Antibacterial (Nano)medicines Development

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2015-04-01 → 2017-03-31
EU contribution
€165,599
Participants
1
Scheme
MSCA-IF-EF-ST

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Results in brief

Antibacterial (Nano)medicines Development

The discovery of antibiotics in the 1950s saved millions of lives from once deadly diseases and opened possibilities for medical interventions such as organ transplants or cancer treatment, that would not be possible due to risk of life-threatening infections. However, the overuse and misuse of antibiotics has promoted the development and spread of antimicrobial resistance (AMR), including antibiotic resistance. The growing problem of AMR threatens health security, and damages trade and economies. The evolution of resistant strains is a natural phenomenon that happens when microorganisms are exposed to antimicrobial drugs, and resistant traits are transferred between microorganisms through horizontal gene transfer mechanisms. Efforts to reduce the inappropriate use of antibiotics in humans and animals, improve infection control strategies and promote international cooperation will help to reduce the spread of AMR. However, research on new prevention and therapeutic strategies for bacterial infections is also urgently needed to address the lack of new drugs entering the market in the past 30 years. This was the focus of the research performed within the project “Antibacterial (Nano)medicines Development”, AND-659121. The specific objectives of the project were to identify a lead-candidate for the development of a novel broad-spectrum antibacterial (nano)medicine by improving the pharmacological properties and Gram-negative membrane permeability of previously identified bacterial histidine kinase inhibitors (HKIs). Histidine kinases (HKs) are a component of the bacterial two-component systems (TCSs), major signalling systems in bacteria.

Data: CORDIS, © European Union

Project objective

Despite the investment of billions of euros, there has been an inexorable decline in the discovery of new antibiotics over the last decades. In this individual fellowship (IF) application we propose a strategy to develop bacterial histidine-kinase (HK) inhibitors targeted at the catalytic and ATP-biding domain (CA) as novel broad-spectrum antibacterial (nano)medicines. Furthermore, putative mechanism of resistance to HK inhibitors and known antibiotics will be studied and novel antibacterial drug targets will be identified by using transposon insertion mutant libraries (Tn-libraries) to identify mutations involved in intrinsic resistance to antibiotics and/or leading to increased sensitivity to existing antibiotics in multi-drug resistant (MDR) strains.

Original text from CORDIS.

Participants

  • WAGENINGEN UNIVERSITY · WageningenCoordinatorNetherlands

Links

Data: CORDIS, © European Union