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1.
Methods Mol Biol ; 1954: 297-308, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30864141

RESUMO

The world is heading toward a dangerous post-antibiotic era where antibiotics fail to treat infections. Staphylococcus aureus is the leading cause of healthcare-associated infections worldwide, and an ever-increasing percentage of them are methicillin-resistant (MRSA). New strategies are urgently needed to combat this pathogen. Wall teichoic acids (WTA) in S. aureus are polyribitol phosphate polymers that play important roles in virulence and resistance to ß-lactam antibiotics. Here, we describe a high-throughput whole-cell screening platform for inhibitors targeting WTA biosynthesis. This platform takes advantage of the unique dispensability patterns of genes encoding WTA biosynthesis. We further describe follow-up dose-response assays to identify WTA inhibitors among the primary bioactives. WTA inhibitors offer an exciting opportunity for the development of novel antibacterial leads of unique mechanism in the fight against drug-resistant staphylococcal infections.


Assuntos
Antibacterianos/farmacologia , Ensaios de Triagem em Larga Escala/métodos , Testes de Sensibilidade Microbiana/métodos , Infecções Estafilocócicas/tratamento farmacológico , Staphylococcus aureus/efeitos dos fármacos , Ácidos Teicoicos/metabolismo , Vias Biossintéticas/efeitos dos fármacos , Parede Celular/efeitos dos fármacos , Parede Celular/genética , Parede Celular/metabolismo , Ensaios de Triagem em Larga Escala/economia , Humanos , Testes de Sensibilidade Microbiana/economia , Infecções Estafilocócicas/microbiologia , Staphylococcus aureus/genética , Staphylococcus aureus/metabolismo , Ácidos Teicoicos/genética
2.
Bioorg Med Chem ; 24(24): 6315-6319, 2016 12 15.
Artigo em Inglês | MEDLINE | ID: mdl-27713016

RESUMO

The rapid spread of antibiotic resistance has created a pressing need for the development of novel drug screening platforms. Herein, we report on the use of cell-based kinetic dose response curves for small molecule characterization in antibiotic discovery efforts. Kinetically monitoring bacterial growth at sub-inhibitory concentrations of antimicrobial small molecules generates unique dose response profiles. We show that clustering of profiles by growth characteristics can classify antibiotics by mechanism of action. Furthermore, changes in growth kinetics have the potential to offer insight into the mechanistic action of novel molecules and can be used to predict off-target effects generated through structure-activity relationship studies. Kinetic dose response also allows for detection of unstable compounds early in the lead development process. We propose that this kinetic approach is a rapid and cost-effective means to gather critical information on antimicrobial small molecules during the hit selection and lead development pipeline.


Assuntos
Antibacterianos/farmacologia , Bactérias/efeitos dos fármacos , Bibliotecas de Moléculas Pequenas/farmacologia , Antibacterianos/química , Antibacterianos/economia , Bactérias/citologia , Relação Dose-Resposta a Droga , Cinética , Testes de Sensibilidade Microbiana , Bibliotecas de Moléculas Pequenas/química , Bibliotecas de Moléculas Pequenas/economia
3.
Lancet Infect Dis ; 13(12): 1057-98, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24252483

RESUMO

The causes of antibiotic resistance are complex and include human behaviour at many levels of society; the consequences affect everybody in the world. Similarities with climate change are evident. Many efforts have been made to describe the many different facets of antibiotic resistance and the interventions needed to meet the challenge. However, coordinated action is largely absent, especially at the political level, both nationally and internationally. Antibiotics paved the way for unprecedented medical and societal developments, and are today indispensible in all health systems. Achievements in modern medicine, such as major surgery, organ transplantation, treatment of preterm babies, and cancer chemotherapy, which we today take for granted, would not be possible without access to effective treatment for bacterial infections. Within just a few years, we might be faced with dire setbacks, medically, socially, and economically, unless real and unprecedented global coordinated actions are immediately taken. Here, we describe the global situation of antibiotic resistance, its major causes and consequences, and identify key areas in which action is urgently needed.


Assuntos
Antibacterianos/administração & dosagem , Antibacterianos/efeitos adversos , Resistência Microbiana a Medicamentos , Animais , Infecções Bacterianas/tratamento farmacológico , Mudança Climática , Saúde Global , Necessidades e Demandas de Serviços de Saúde , Humanos
4.
Can J Microbiol ; 59(3): 153-6, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23540332

RESUMO

The United States GAIN (Generating Antibiotic Incentives Now) Act is a call to action for new antibiotic discovery and development that arises from a ground swell of concern over declining activity in this therapeutic area in the pharmaceutical sector. The GAIN Act aims to provide economic incentives for antibiotic drug discovery in the form of market exclusivity and accelerated drug approval processes. The legislation comes on the heels of nearly two decades of failure using the tools of modern drug discovery to find new antibiotic drugs. The lessons of failure are examined herein as are the prospects for a renewed effort in antibiotic drug discovery and development stimulated by new investments in both the public and private sector.


Assuntos
Antibacterianos , Descoberta de Drogas , Legislação de Medicamentos , Antibacterianos/economia , Aprovação de Drogas/economia , Aprovação de Drogas/legislação & jurisprudência , Descoberta de Drogas/economia , Descoberta de Drogas/legislação & jurisprudência , Descoberta de Drogas/tendências , Indústria Farmacêutica/economia , Indústria Farmacêutica/legislação & jurisprudência , Resistência Microbiana a Medicamentos , Humanos , Setor Privado/economia , Estados Unidos
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