Publicador de contenidos

Resistencia antimicrobiana

Nuevos agentes contra bacilos gram-negativos

Nuevos enfoques para el diseño de agentes antibacterianos activos frente a bacilos gram-negativos multirresistentes

Duración
Jan 01, 2015 - Dec 31, 2018
Financiadores
Ministerio de Ciencia, Innovación y Universidades. Instituto de Salud Carlos III, Unión Europea. This project is co-funded by the Fondo Europeo de Desarrollo Regional (FEDER). “Una manera de hacer Europa”.

Currently a large partion of available antibiotics are not suitable for the treatment of multiresistant pathogens. Sometimes the choice of treatment is reduced to a single drug, such as colistin for P. aeruginosa and Acinetobacter. The lack of profitability has led to a decline in R+D for new antibiotics by the pharmaceutical industry. There is therefore a clear need for new antibacterial agents, mainly against multi-resistant Gram-negative bacilli.

The main objective of this project is the design of new antibacterial agents against P. aeruginosa, A. baumannii and K. pneumoniae by various approaches:

1. Characterization of potential inhibitors of efflux systems, we have found by docking, 50 compounds (from two libraries of compounds) that potentially can inhibit efflux pumps. These compounds will be characterized in detail.

2. To optimize peptides with activity against the organisms being studied. We have 18 antibacterial peptides with potential capacity and its stability and toxicity will be studied. Of those the three peptides with increased activity and stability and less toxicity, the "in vivo" activity will be investigated;

3. Characterization of two-component systems (TCS). By analysis "in silico" found 41 potential TCS in A. baumannii. The aim is to study its involvement in virulence and essentiality, in order to find possible inhibitors that would have antibacterial activity and antivirulencia; 

4. Design and study of the antibacterial activity of peptide-oligonucleotide and siderophore-oligonucleotide hybrids. Oligonucleotides inhibit mRNA expression of some essential genes, whereas either peptide or siderophor will be used as transport systems across the cell wall. Once designed these hybrids will be tested both "in vitro" and "in vivo".

Total funding

184,827.50 €

Project Code

PI14/00755

Nuestro equipo

ISGlobal team

  • Jordi Vila Estape
    Jordi Vila Estape

Otros proyectos

Ver proyectos pasados

COMBACTE

Combatiendo la Resistencia Bacteriana en Europa

GAMA

Development of Novel Gastrointestinal Biomarkers for Use in HIV Incidence Determination in a Sub-Saharan African Setting

COMBACTE-CARE

Combatting Bacterial Resistance in Europe - Carbapenem Resistance

MAMAH

Improving Maternal and Infant Health by reducing malaria risks in African women: evaluation of the safety and efficacy of dihydroartemisinin-piperaquine for intermittent preventive treatment of malaria in HIV-infected pregnant women

INTE-AFRICA

Integrating and decentralizing diabetes and hypertension services in Africa

ICARIA

Improving Care through Azithromycin Research for Infants in Africa

PreFIT

Predicting the Future: Incipient Tuberculosis

ANTICOV

Large Clinical Trial in Africa on the Treatment of Mild Cases of COVID-19

Stool4TB

Evaluating a new stool based qPCR for diagnosis of tuberculosis in children and people living with HIV

TB-RECONNECT

Reconnecting Transmission to Global Tuberculosis Control by Mapping Pathogen Transmission Events to Host Infection Status

SToolNIH

Quantifiable stool-based TB PCR to Improve Diagnostics and Treatment Monitoring

END-VOC

ENDing COVID-19 Variants Of concern through Cohort studies (END-VOC)

TwinAir

Digital Twins Enabled Indoor Air Quality Management for Healthy Living

ENDÈMIC

Community knowledge generation through scientific culture, urban ecology and art

EpiGen

Building Scalable Pathogen Genomic Epidemiology in Ethiopia

Hepatitis C Free Baleares

Eliminating hepatitis C on the Balearic Islands (Mallorca, Menorca and Ibiza): a study in governmental and non-governmental addiction service centres, a mobile methadone unit and a prison to test and link people who use drugs to HCV care.