Crowdsourcing friendly bacteria helps superbug cause infection
Antimicrobial resistant pathogens crowdsource friendly bacteria to survive in immune cells and cause disease, a new study by the University of Sheffield has revealed.
Scientists have discovered the human pathogen Staphylococcus aureus (S.aureus), uses benign bacteria present in the skin to initiate infection.
Known commonly as its infamous antimicrobial resistant form MRSA (meticillin-resistant Staphylococcus aureus), the ground-breaking research discovered that by using the other bacteria present on the skin, the pathogen can survive the mechanisms our immune system deploys to destroy it.
The findings, published today (16 July 2018) in Nature Microbiology, give scientists a new insight into the mechanisms of the so-called superbug, which is hard to treat due to its resistance to several widely used antibiotics.
Professor Simon Foster, Director of Research and Innovation in the Faculty of Science and Professor of Molecular Microbiology within our department at the University of Sheffield is lead author of the study. He said: “The remarkable discovery that S.aureus uses the presence of the otherwise benign members of the human skin microflora to augment disease, changes our understanding of how pathogens can elude our defences and initiate infection.
“We harbour a vast array of bacteria as microflora in our guts and on our skin so understanding this combination of pathogen, native microflora and host provides new avenues for approaches to prevent and treat infection.
“A lot of people have been trying to develop a vaccine against the potentially life-threatening virus for a number of years without success. This study has shown how a potentially fatal disease like MRSA gains access to our bodies and how the organisms are able to survive inside immune cells – phagocytes.”
The pioneering five-year project was led by the Florey Institute at the University of Sheffield in collaboration with an international team of scientists from Canada, Holland, Sweden and the UK.
Professor Foster added: “All infectious disease starts from an environment of mixed bacteria and other material so this might have much wider ramifications.
“The study has important implications for disease because with our work we can drop the infectious dose by over 1,000 fold. Importantly, S. aureus is not a dominant member of our bacterial flora and so this study can explain how relatively few pathogenic bacteria can crowdsource from the other organisms present on our skin to allow it to set an infection that may ultimately prove fatal. It alters the way that we view how infection occurs, the way it should be studied and sets the scene for how it might be tackled.
The Florey Institute at the University of Sheffield is addressing one of the world’s biggest biomedical challenges – infectious disease.
Set within the context of emerging antibiotic resistance, the institute studies the complex interaction between pathogens and their host.
By working together with collaborative partners from the Department of Molecular Biology and Biotechnology, across the university and beyond, the Florey Institute is ‘bridging the gap’ between science and patient care to tackle this global threat to human healthcare.
The Department of Molecular Biology and Biotechnology is focussed on studying DNA, RNA and proteins, and how they affect biological function. Researchers work on topics from genomics and nucleic acids to plants and photosynthesis, with the aim of addressing the major global challenges of food security, antimicrobial resistance and an aging population. Many of our scientists are following in the footsteps of Sir Hans Krebs, the department’s first Professor of Biochemistry, who was awarded the Nobel Prize in Physiology or Medicine in 1953.
Read the paper: Human skin commensals augment Staphylococcus aureus pathogenesis
Learn more: The Florey Institute