Better purification overcomes original renal toxicity concerns.
An old antibiotic could potentially offer much-needed protection against bacterial infections that are resistant to multiple drugs, reveals a recent study recently published in the journal PLOS Biology conducted by James Kirby and his team from Harvard Medical School, US. This discovery could present a new strategy to combat difficult-to-treat and potentially fatal infections.
Nourseothricin, a natural compound produced by a type of soil fungus, consists of multiple forms of a complex molecule known as streptothricin. When first discovered in the 1940s, this compound sparked great anticipation due to its strong efficacy against Gram-negative bacteria. These bacteria, notorious for their thick outer protective layer, are particularly resistant to other antibiotics.
But nourseothricin proved toxic to kidneys, and its development was dropped. However, the rise of antibiotic-resistant bacterial infections has spurred the search for new antibiotics, leading Kirby and colleagues to take another look at nourseothricin.
Early studies of nourseothricin suffered from incomplete purification of the streptothricins. More recent work has shown that the multiple forms have different toxicities with one, streptothricin-F, significantly less toxic, while remaining highly active against contemporary multidrug-resistant pathogens.
Here, the authors characterized the antibacterial action, renal toxicity, and mechanism of action of highly purified forms of two different streptothricins, D and F. The D form was more powerful than the F form against drug-resistant Enterobacterales and other bacterial
Reference: “Streptothricin F is a bactericidal antibiotic effective against highly drug-resistant gram-negative bacteria that interacts with the 30S subunit of the 70S ribosome” by Christopher E. Morgan, Yoon-Suk Kang, Alex B. Green, Kenneth P. Smith, Matthew G. Dowgiallo, Brandon C. Miller, Lucius Chiaraviglio, Katherine A. Truelson, Katelyn E. Zulauf, Shade Rodriguez, Anthony D. Kang, Roman Manetsch, Edward W. Yu and James E. Kirby, 16 May 2023, PLOS Biology.
DOI: 10.1371/journal.pbio.3002091