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Multi-excitation raman spectroscopy complements whole genome sequencing for rapid detection of bacterial infection and resistance in WHO priority pathogens

Multi-excitation raman spectroscopy complements whole genome sequencing for rapid detection of bacterial infection and resistance in WHO priority pathogens
Multi-excitation raman spectroscopy complements whole genome sequencing for rapid detection of bacterial infection and resistance in WHO priority pathogens
Current methods for diagnosing acute and complex infections mostly rely on culture-based methods and, for biofilms, fluorescence in-situ hybridization. These techniques are labor-intensive and can take 2-4 days to return a test result, especially considering an extra culturing step required for the antibiotic susceptibility testing (AST). This places a significant burden on healthcare providers, delaying treatment and leading to adverse patient outcomes. Here, we report the complementary use of our newly developed multi-excitation Raman spectroscopy (ME-RS) method with whole-genome sequencing (WGS). Four WHO priority pathogens are AST phenotyped and their antimicrobial resistance (AMR) profile determined by WGS. On application of ME-RS method we find high correlation with the WGS characterization. Highly accurate classification based on the species (98.93%), wild-type/non-wild type (99.45%), and presence or absence of thick peptidoglycan layers in cell walls (100%), as well as at the individual strain level (99.29%). These results clearly demonstrate the potential of ME-RS as a rapid and first-stage tool for species, resistance and strain-level classification which can be followed up by WGS for confirmation. Such a workflow can facilitate efficient antimicrobial stewardship to handle and prevent the spread of AMR.
Lister, Adam
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Avershina, Ekaterina
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Devitt, George
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Hanrahan, Niall
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Highmore, Callum
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Webb, Jeremy
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Muller, Fredrik
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Mahajan, Sumeet
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Norway, Department of Biotechnology Inland Norway University of Applied
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Ahamed, Shaikh Rafi
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Lister, Adam
7a3153da-d63b-4cb9-9048-38f372dd26c7
Avershina, Ekaterina
fd44dafe-430e-4df3-8ed6-432af310db0e
Devitt, George
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Hanrahan, Niall
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Highmore, Callum
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Webb, Jeremy
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Muller, Fredrik
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Mahajan, Sumeet
b131f40a-479e-4432-b662-19d60d4069e9
Norway, Department of Biotechnology Inland Norway University of Applied
a8a296dd-d67c-4b3a-9e97-be49a27819d5
Ahamed, Shaikh Rafi
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Lister, Adam, Avershina, Ekaterina, Devitt, George, Hanrahan, Niall, Highmore, Callum, Webb, Jeremy, Muller, Fredrik, Mahajan, Sumeet, Norway, Department of Biotechnology Inland Norway University of Applied and Ahamed, Shaikh Rafi (2022) Multi-excitation raman spectroscopy complements whole genome sequencing for rapid detection of bacterial infection and resistance in WHO priority pathogens. bioRxiv. (doi:10.1101/2022.02.08.479540).

Record type: Article

Abstract

Current methods for diagnosing acute and complex infections mostly rely on culture-based methods and, for biofilms, fluorescence in-situ hybridization. These techniques are labor-intensive and can take 2-4 days to return a test result, especially considering an extra culturing step required for the antibiotic susceptibility testing (AST). This places a significant burden on healthcare providers, delaying treatment and leading to adverse patient outcomes. Here, we report the complementary use of our newly developed multi-excitation Raman spectroscopy (ME-RS) method with whole-genome sequencing (WGS). Four WHO priority pathogens are AST phenotyped and their antimicrobial resistance (AMR) profile determined by WGS. On application of ME-RS method we find high correlation with the WGS characterization. Highly accurate classification based on the species (98.93%), wild-type/non-wild type (99.45%), and presence or absence of thick peptidoglycan layers in cell walls (100%), as well as at the individual strain level (99.29%). These results clearly demonstrate the potential of ME-RS as a rapid and first-stage tool for species, resistance and strain-level classification which can be followed up by WGS for confirmation. Such a workflow can facilitate efficient antimicrobial stewardship to handle and prevent the spread of AMR.

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2022.02.08.479540v1.full - Author's Original
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e-pub ahead of print date: 8 February 2022
Published date: 8 February 2022

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Local EPrints ID: 457458
URI: http://eprints.soton.ac.uk/id/eprint/457458
PURE UUID: cc61d83c-095e-43cc-9035-9ea2ec321f9c
ORCID for George Devitt: ORCID iD orcid.org/0000-0001-7179-4459
ORCID for Niall Hanrahan: ORCID iD orcid.org/0000-0002-3596-7049
ORCID for Jeremy Webb: ORCID iD orcid.org/0000-0003-2068-8589
ORCID for Sumeet Mahajan: ORCID iD orcid.org/0000-0001-8923-6666

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Date deposited: 09 Jun 2022 16:34
Last modified: 17 Mar 2024 04:06

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Contributors

Author: Adam Lister
Author: Ekaterina Avershina
Author: George Devitt ORCID iD
Author: Niall Hanrahan ORCID iD
Author: Callum Highmore
Author: Jeremy Webb ORCID iD
Author: Fredrik Muller
Author: Sumeet Mahajan ORCID iD
Author: Department of Biotechnology Inland Norway University of Applied Norway
Author: Shaikh Rafi Ahamed

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