Author
Listed:
- Fereshteh Bayat
(McMaster University, Hamilton)
- Arwa Hilal
(McMaster University, Hamilton)
- Mathura Thirugnanasampanthar
(McMaster University, Hamilton)
- Denise Tremblay
(Faculté des sciences et de génie, Université Laval
Université Laval
Université Laval)
- Carlos D. M. Filipe
(McMaster University, Hamilton)
- Sylvain Moineau
(Faculté des sciences et de génie, Université Laval
Université Laval
Université Laval)
- Tohid F. Didar
(McMaster University, Hamilton
McMaster University, Hamilton
McMaster University, Hamilton)
- Zeinab Hosseinidoust
(McMaster University, Hamilton
McMaster University, Hamilton
McMaster University, Hamilton
McMaster University, Hamilton)
Abstract
As bacteriophages continue to gain regulatory approval for personalized human therapy against antibiotic-resistant infections, there is a need for transformative technologies for rapid target identification through multiple, large, decentralized therapeutic phages biobanks. Here, we design a high throughput phage screening platform comprised of a portable library of individual shelf-stable, ready-to-use phages, in all-inclusive solid tablets. Each tablet encapsulates one phage along with luciferin and luciferase enzyme stabilized in a sugar matrix comprised of pullulan and trehalose capable of directly detecting phage-mediated adenosine triphosphate (ATP) release through ATP bioluminescence reaction upon bacterial cell burst. The tablet composition also enhances desiccation tolerance of all components, which should allow easier and cheaper international transportation of phages and as a result, increased accessibility to therapeutic phages. We demonstrate high throughput screening by identifying target phages for select multidrug-resistant clinical isolates of Pseudomonas aeruginosa, Salmonella enterica, Escherichia coli, and Staphylococcus aureus with targets identified within 30-120 min.
Suggested Citation
Fereshteh Bayat & Arwa Hilal & Mathura Thirugnanasampanthar & Denise Tremblay & Carlos D. M. Filipe & Sylvain Moineau & Tohid F. Didar & Zeinab Hosseinidoust, 2024.
"High throughput platform technology for rapid target identification in personalized phage therapy,"
Nature Communications, Nature, vol. 15(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49710-2
DOI: 10.1038/s41467-024-49710-2
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49710-2. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.