Researchers at Johns Hopkins reported that they have laid the foundation to develop novel antibiotics that work against incurable, antibiotic-resistant bacteria like tuberculosis by targeting an enzyme essential to the production and integrity of bacterial cell walls.

       Their findings suggested that antibiotic drugs specifically targeting the recently discovered LD-transpeptidase enzyme, which is needed to build bacterial cell walls in some bacteria, could potentially cure many antibiotic-resistant infections.

       An additional implication of their research is that drugs targeting the enzyme could offer quicker, cheaper and more easily accessible treatment against tuberculosis, a disease that still kills more people worldwide than any other infection, according to the Centers for Disease Control and Prevention.

       Gyanu Lamichhane, Ph.D. associate professor of medicine at the Johns Hopkins University School of Medicine said that the complexity of TB treatment and growing prevalence of antibiotic resistance is a serious threat to public health. His team joined with the research team of Craig Townsend, Ph.D., the Alsoph H. Corwin Professor of Chemistry at The Johns Hopkins University's Krieger School of Arts and Sciences, to tackle this complex issue. Townsend said that their research offers steps toward the design of new antibiotics that attack a previously untargeted bacterial enzyme.

       At the root of their investigation, Lamichhane said that more than half of antibiotics prescribed today are of a class called beta-lactams, which work by interrupting the function of the DD-transpeptidase enzyme that creates bacterial cell walls. Without it, bacteria quickly die. However, in 2005, a team of researchers found a second wall-building enzyme, LD-transpeptidase, that allows bacteria like the ones that cause TB to survive antibiotic treatments. Hence they looked at the structure of LD-transpeptidase, thought about how it works and started making new compounds that could be used against it.

      Dr. Pankaj Kumar, postdoctoral fellow in infectious diseases at the Johns Hopkins University School of Medicine, began the research in the new study by extracting LD-transpeptidase from many species of bacteria and examining its detailed molecular structure with a sophisticated imaging system known as protein X-ray crystallography using the Advanced Photon Source at the Argonne National Laboratory in Chicago.

       By analyzing the enzyme's structure, Johns Hopkins researchers were able to design new compounds in the carbapenem group, a subclass of the beta-lactam antibiotics that bind to the LD-transpeptidase wall-building enzyme and stop its function.

       In live bacterial cultures, the carbapenems were shown by Lamichhane's and Townsend's groups to stop the enzyme's wall-building activity. The new compounds were even effective against the ESKAPE pathogens, a group of six bacterial species that the Centers for Disease Control and Prevention had identified as a threat because of their propensity for developing antibiotic resistance.

       Following these successes, Amit Kaushik, a postdoctoral fellow in infectious diseases at the Johns Hopkins University School of Medicine, tested two carbapenems in vivo against TB in mice infected with TB.

       Researchers infected mice with tuberculosis bacteria and separated them into different treatment groups. The rodent’s lungs were sampled periodically over a period of three weeks, and the results showed that even without use of classic TB antibiotic treatments, the new carbapenems, specifically biapenem, cured TB infection in mice.

       Townsend and Lamichhane said that the focus of their research is now on creating variations of their original compound those are designed to target specific bacteria. Many commonly prescribed antibiotics today work on a broad spectrum of bacterial species, meaning that in addition to killing off bad bacteria, they also destroy the friendly bacteria of our bodies that are needed to function normally and whose destruction can cause dangerous side effects. Lamichhane believes that the future of antibiotic treatments relies on good antimicrobial stewards and treats specific bacteria without affecting our body’s natural microbiome. Not only will this cut down on antibiotic side effects, but it will also slow the development of antibiotic resistance in the bacterial species not being targeted.

       The researchers are now in the process of initiating clinical trials to test the safety and efficacy of some of these new compounds.

       Antibiotic resistance has been an ever-present threat since the discovery of penicillin in 1928. Scientists and physicians have historically kept up with resistant bacteria through the frequent introduction of new antibiotic treatments. However, the research and development of antibiotics plummeted in the 1980s as other drugs became more profitable to produce. Because of the decreased incentive to invest in new antibiotics and the liberal use of antibiotics we already have, many bacterial species have quickly outpaced our ability to treat them. The Centers for Disease Control and Prevention estimates that annually, 2 million illnesses and 23,000 deaths are caused by antibiotic-resistant bacteria in the United States alone, and that 70 percent of hospital-acquired infections are now antibiotic-resistant.

Source: www.sciencedaily.com