New MRSA Treatment Drug Developed, Structural Flexibility Identified as Key
Hiroyoshi Matsumura, Professor of College of Life Sciences
at Ritsumeikan University, teamed with Junso Fujita, a third year Ph. D.
student of Graduate School of Engineering at Osaka University, Daniel
S. Pilch, Associate Professor at Rutgers University and other
researchers, developed a drug effective against methicillin-resistant
Staphylococcus aureus (MRSA), a strain of bacteria that developed
resistance to antibiotics. The findings have been recently published on
ACS Chemical Biology, an online comprehensive scientific journal.
MRSA is a strain of bacterium that has developed resistance to
antibiotic drugs because of antibiotics overuse. Due to this
characteristic, treatment of MRSA infection relies on immune systems of
patients. Therefore, the infection is known to become especially severe
when a patient with a weakened immune system is affected.
Previously, the research group developed a new therapeutic
drug against MRSA infection that binds Filamentous temperature-sensitive
protein Z (FtsZ), a cell division protein in MRSA. When the drug binds
FtsZ, its function is weakened, resulting in inhibiting MRSA
proliferation. If MRSA cannot proliferate, it is killed. Experiments
conducted on mice showed that the drug was highly effective, but when
used continually, MRSA developed resistance on it as well.
Given this situation, this research developed a second drug that can
treat MRSA that developed resistance to the first drug. In addition, the
research explained why the first drug became ineffective and the second
drug became effective, and identified “structural flexibility of the
drug” as the key factor.
Since the research revealed the process of resistance development in
MRSA as well as its countermeasures, development of more drugs effective
against MRSA infection can be expected.
The research was jointly conducted by Ritsumeikan University, Osaka University, and Rutgers University.