Marine worm joins fight against superbugs
The humble marine sandworm may help in the hunt for a new class of antibiotics after University of Queensland researchers improved a molecule in the sand-dwelling animal which kills superbugs.
UQ’s Institute for Molecular Bioscience researcher Dr Alysha Elliott said the study assessed peptides inspired by natural antibiotics in sandworms to see if they could kill multi-drug resistant strains of bacteria.
“A Danish biotechnology company asked for our help to investigate a small peptide called arenicin-3 that they found in the marine sandworm Arenicola marina, which could kill Gram-negative bacteria — including strains resistant to last-resort antibiotics,” Dr Elliott said.
The marine worm has joined the fight against superbugs. Video: © Institute for Molecular Bioscience.
Arenicola marina, commonly known as the marine sandworm on the beach. Image: © Professor Matt Cooper/The University of Queensland.
Arenicola marina, commonly known as the marine sandworm on the beach. Image: © Professor Matt Cooper/The University of Queensland.
A close-up shot of the lugworm in the hand of Dr Elliott. Image: © Professor Matt Cooper/The University of Queensland.
A close-up shot of the lugworm in the hand of Dr Elliott. Image: © Professor Matt Cooper/The University of Queensland.
“Gram-negative bacteria have evolved to outsmart our current antibiotics, but natural antibiotics like the one found in the sandworm can penetrate the cell membrane of bacteria.”
Dr Elliott said Gram-negative bacteria were more difficult to kill due to an additional sophisticated line of defence in their membranes.
Arenicola marina, commonly known as the marine sandworm on the beach. Image: © Professor Matt Cooper/The University of Queensland.
UQ IMB scientists Dr Alysha Elliott and Dr Johnny Huang were part of the research team led by Professor Matt Cooper that tested arenicin-3 and new compounds inspired by the marine sandworm.
“While many of the initial compounds were remarkably active in killing the bacteria, they were toxic to human cells including red blood cells, and did not work well in the presence of lung surfactant,” Dr Huang said.
A close-up shot of the lugworm in the hand of Dr Elliott. Image: © Professor Matt Cooper/The University of Queensland.
“This would be an issue if we wanted to treat bacterial pneumonia where the infection is found in the lung.”
The researchers kept tweaking the structure of the peptide and succeeded in developing AA139 that could kill multi-drug resistant bacteria in many models of disease, with far fewer side effects.
A three structure of Arenicin - the peptide with antibiotic properties. Image: © Professor Matt Cooper/The University of Queensland.
A three structure of Arenicin - the peptide with antibiotic properties. Image: © Professor Matt Cooper/The University of Queensland.
“Our next challenge is to get this peptide to where the infections are found,” Dr Elliott said.
“Many bacterial infections are deep-seated, requiring penetration through tissue to reach them. This is a tough challenge for a peptide antibiotic, although there remains a dire unmet medical need for new antibiotics.”
This research was published in Nature Communications (DOI: -10.1038/s41467-020-16950-x) and was supported by the National Health and Medical Research Council.
Media contacts:
IMB Communications, communications@imb.uq.edu.au, +61 (0)4 0566 1856.
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