The discovery, published today in Nature Communications by researchers from La Trobe University and the University of Queensland, provides details on how proteins in the outer membrane of bacteria — the bacteria’s ‘superglue’ — are able to stick to and populate parts of the human body.
This new information paves the way for the development of innovative treatments for preventing and curing infections, in what could be a significant step forward for new anti-microbial development.
The study focused on UpaB — the superglue protein of a pathogen known to cause urinary tract infections within 50 per cent of women within their lifetime.
Similar proteins are found in the outer membrane of other pathogens responsible for infections ranging from life-threatening food poisoning to whooping cough, meningitis, typhus fever and chlamydia.
Lead researcher at La Trobe University, Dr Begoña Heras, said the study provides unprecedented fundamental science that could inform future solutions to the world health crisis in antibiotic resistance.
“The knowledge we now have on this bacteria’s protein gives us the ability to block the bacteria sticking to different parts of the human body,” said Dr Heras.
“Antibiotic resistance is an urgent, global problem and this information gives us an important opportunity to develop new anti-microbial treatments. Naturally, this is the next step for this research.”
La Trobe researcher Dr Jason Paxman added that there is a flip-side to these bacterial proteins in that they could be harnessed for good.
“There is nothing like these bacterial proteins in modern medicine; bacteria have had thousands of years to develop these adhesive proteins,” Dr Paxman explained.
“These findings could open up new opportunities such as delivering targeted therapies to parts of the human body, which could even help in the fight against cancer down the line.”
Materials provided by La Trobe University. Note: Content may be edited for style and length.
- Jason J. Paxman, Alvin W. Lo, Matthew J. Sullivan, Santosh Panjikar, Michael Kuiper, Andrew E. Whitten, Geqing Wang, Chi-Hao Luan, Danilo G. Moriel, Lendl Tan, Kate M. Peters, Minh-Duy Phan, Christine L. Gee, Glen C. Ulett, Mark A. Schembri, Begoña Heras. Unique structural features of a bacterial autotransporter adhesin suggest mechanisms for interaction with host macromolecules. Nature Communications, 2019; 10 (1) DOI: 10.1038/s41467-019-09814-6