schematic of ODL antibiotic mechanism Credit: UIC/Yury Polikanov, et al
ODLs (yellow) bind to a site on the ribosome not used by other antibiotics. Location of this site is shown here relative to the sites of other known antibiotics, such as negamycin (green), tetracycline (dark blue), aminoglycoside antibiotic paromomycin (red) and streptomycin (light blue).

New class of antibiotics may combat drug resistance

Newly discovered antibiotic binds to ribosome and disrupts protein synthesis with bactericidal mechanism.

Researchers from the University of Illinois at Chicago (UIC) and Nosopharm, a biotechnology company based in Lyon, France, are part of an international team reporting on the discovery of a new class of antibiotics.

The antibiotic, first identified by Nosopharm, is unique and promising on two fronts: its unconventional source, and its distinct way of killing bacteria, both of which suggest that the compound may be effective at treating drug-resistant or hard-to-treat bacterial infections.

Called odilorhabdins (ODLs), the antibiotics are produced by symbiotic bacteria found in soil-dwelling nematode worms that colonize insects for food. The bacteria help kill the insect and, importantly, secrete the antibiotic to keep competing bacteria away. Until now, these nematode-associated bacteria and the antibiotics they make have been largely understudied, UIC said.

To identify the antibiotic, the Nosopharm research team screened 80 cultured strains of the bacteria for antimicrobial activity. They then isolated the active compounds, studied their chemical structures and engineered more potent derivatives.

The study, published in Molecular Cell, describes the new antibiotic and, for the first time, how it works.

UIC's Alexander Mankin and Yury Polikanov are corresponding authors on the study and led the research on the antibiotic's mechanism of action. They found that ODLs act on the ribosome — the molecular machine of individual cells that makes the proteins needed to function — of bacterial cells.

"Like many clinically useful antibiotics, ODLs work by targeting the ribosome," said Polikanov, assistant professor of biological sciences in the UIC College of Liberal Arts & Sciences. However, "ODLs are unique because they bind to a place on the ribosome that has never been used by other known antibiotics."

The UIC researchers, including graduate student Tanja Florin and postdoctoral research associate Malgorzata Dobosz-Bartoszek, also found that when bound to the ribosome, the antibiotic disrupts its ability to interpret and translate genetic code.

"When ODLs are introduced to the bacterial cells, they impact the reading ability of the ribosome and cause the ribosome to make mistakes when it creates new proteins," said Mankin, director of the Center for Biomolecular Sciences in the UIC College of Pharmacy. "This miscoding corrupts the cell with flawed proteins and causes the bacterial cell to die."

While many antibiotics can slow bacterial growth, Mankin said antibiotics that actually kill bacteria -- called bactericidal antibiotics -- are rare.

"The bactericidal mechanism of ODLs and the fact that they bind to a site on the ribosome not exploited by any known antibiotic are very strong indicators that ODLs have the potential to treat infections that are unresponsive to other antibiotics," said Mankin, who is also professor of medicinal chemistry and pharmacognosy.

In France, the Nosopharm researchers tested the ODL compounds against bacterial pathogens, including many known to develop resistance.

"We found that the ODL compounds cured mice infected with several pathogenic bacteria and demonstrated activity against both Gram-negative and Gram-positive pathogens, notably including carbapenem-resistant Enterobacteriacae (CRE)," said co-corresponding author Maxime Gualtieri, co-founder and chief scientific officer of Nosopharm.

CRE is a family of pathogens that have high levels of resistance to antibiotics. One study suggests that CRE, the common culprit in bloodstream and surgical site infections, contribute to death in up to 50% of patients who become infected.

The researchers said this study is a testament to the growing trend of international and cross-disciplinary collaboration that is needed to combat the growing and global threat of antibiotic resistance.

"In this case, the combined expertise of the industry, which has the resources to develop new compounds, and academia, which has the research and lab capabilities to understand how the compounds work, have enabled the development of this new class of antibiotics," Mankin said.

"The collaboration between multiple labs with diverse areas of expertise adds credibility to the research," Polikanov said.

While ODLs have yet to be thoroughly investigated for their therapeutic potential, the researchers said the study findings justify future research in this direction.

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