#AntibioticResistance is a growing problem for #Streptococcal infections. @motile_microbe &co show that disrupting fermentation with #Fomepizole increases sensitivity of S. pneumoniae to #antibiotics, incl in vivo #pneumonia model validation #PLOSBiology https://plos.io/3mYWTwx
Targeting NAD+ regeneration enhances antibiotic susceptibility of Streptococcus pneumoniae during invasive disease

Antibiotic resistance is a increasingly important problem for Streptococcus pneumoniae infections. This study shows that blocking fermentation and disrupting redox balance increases the sensitivity of this bacterium to antibiotics, including validation in vivo using a pneumonia model with antibiotic resistant pneumococci.

#AntibioticResistance is a growing problem for #Streptococcal infections. @motile_microbe &co show that disrupting fermentation with #Fomepizole increases sensitivity of S. pneumoniae to #antibiotics, incl in vivo #pneumonia model validation #PLOSBiology https://plos.io/3mYWTwx
Targeting NAD+ regeneration enhances antibiotic susceptibility of Streptococcus pneumoniae during invasive disease

Antibiotic resistance is a increasingly important problem for Streptococcus pneumoniae infections. This study shows that blocking fermentation and disrupting redox balance increases the sensitivity of this bacterium to antibiotics, including validation in vivo using a pneumonia model with antibiotic resistant pneumococci.

#AntibioticResistance is a growing problem for #Streptococcal infections. @motile_microbe &co show that disrupting fermentation with #Fomepizole increases sensitivity of S. pneumoniae to #antibiotics, incl in vivo #pneumonia model validation #PLOSBiology https://plos.io/3mYWTwx
Targeting NAD+ regeneration enhances antibiotic susceptibility of Streptococcus pneumoniae during invasive disease

Antibiotic resistance is a increasingly important problem for Streptococcus pneumoniae infections. This study shows that blocking fermentation and disrupting redox balance increases the sensitivity of this bacterium to antibiotics, including validation in vivo using a pneumonia model with antibiotic resistant pneumococci.