Publications by authors named "Gerald J Larrouy-Maumus"

Article Synopsis
  • Colistin is a last-resort antibiotic that fights multi-drug-resistant Gram-negative bacteria by disrupting their cell membranes.
  • Resistance to colistin can occur through mutations or the acquisition of specific resistance genes, resulting in modifications to the bacteria's outer membrane.
  • Research indicates that colistin resistance primarily protects the inner membrane, allowing bacteria to survive, while also suggesting that permeabilizing the outer membrane can make these bacteria more susceptible to other antibiotics like rifampicin.
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The discovery of penicillin over 90 years ago and its subsequent uptake by healthcare systems around the world revolutionised global health. It marked the beginning of a golden age in antibiotic discovery with new antibiotics readily discovered from natural sources and refined into therapies that saved millions of lives. Towards the end of the last century, the rate of discovery slowed to a near standstill.

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Colistin is an antibiotic of last resort, but has poor efficacy and resistance is a growing problem. Whilst it is well established that colistin disrupts the bacterial outer membrane (OM) by selectively targeting lipopolysaccharide (LPS), it was unclear how this led to bacterial killing. We discovered that MCR-1 mediated colistin resistance in is due to modified LPS at the cytoplasmic rather than OM.

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The intestinal epithelial cells (IECs) that line the gut form a robust line of defense against ingested pathogens. We investigated the impact of infection with the enteric pathogen Citrobacter rodentium on mouse IEC metabolism using global proteomic and targeted metabolomics and lipidomics. The major signatures of the infection were upregulation of the sugar transporter Sglt4, aerobic glycolysis, and production of phosphocreatine, which mobilizes cytosolic energy.

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