Elimination of negative feedback in TLR signalling allows rapid and hypersensitive detection of microbial contaminants.

Seumen, Clovis H T; Tomasiunaite, Urte; Legler, Daniel F; Hauck, Christof R (2021). Elimination of negative feedback in TLR signalling allows rapid and hypersensitive detection of microbial contaminants. Scientific reports, 11(1), p. 24414. Springer Nature 10.1038/s41598-021-03618-9

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The exquisite specificity of Toll-like receptors (TLRs) to sense microbial molecular signatures is used as a powerful tool to pinpoint microbial contaminants. Various cellular systems, from native human blood cells to transfected cell lines exploit TLRs as pyrogen detectors in biological preparations. However, slow cellular responses and limited sensitivity have hampered the replacement of animal-based tests such as the rabbit pyrogen test or lipopolysaccharide detection by Limulus amoebocyte lysate. Here, we report a novel human cell-based approach to boost detection of microbial contaminants by TLR-expressing cells. By genetic and pharmacologic elimination of negative control circuits, TLR-initiated cellular responses to bacterial molecular patterns were accelerated and significantly elevated. Combining depletion of protein phosphatase PP2ACA and pharmacological inhibition of PP1 in the optimized reporter cells further enhanced the sensitivity to allow detection of bacterial lipoprotein at 30 picogram/ml. Such next-generation cellular monitoring is poised to replace animal-based testing for microbial contaminants.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > Theodor Kocher Institute

UniBE Contributor:

Legler, Daniel

Subjects:

600 Technology > 610 Medicine & health

ISSN:

2045-2322

Publisher:

Springer Nature

Language:

English

Submitter:

Andrea Stettler

Date Deposited:

10 Feb 2023 09:12

Last Modified:

10 Feb 2023 23:27

Publisher DOI:

10.1038/s41598-021-03618-9

PubMed ID:

34952917

BORIS DOI:

10.48350/178608

URI:

https://boris.unibe.ch/id/eprint/178608

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