Author

S. L. Fletcher

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Microbiology· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Assay:bulk RNA-seq· 1 Research Focus:drug response / drug discovery· 1 Organism:fungi (other)· 1 Organism:human· 1 Assay:metagenomics· 1 Assay:proteomics· 1

Frequent Co-Authors

C. Tait-Burkard· 3 shared A. Daniels· 2 shared M. O'Shea· 2 shared N. Craig· 2 shared A. Hardas· 1 shared A. J. Hanton· 1 shared A. Kratzel· 1 shared A. Malbon· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersMicrobiology

C. Tait-Burkard

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Emergence and spread of feline infectious peritonitis due to a highly pathogenic canine/feline recombinant coronavirus

C. Atippa, A. S. Warr, D. Epaminondas, M. O'Shea, A. J. Hanton, S. L. Fletcher, A. Malbon, M. Lyraki, R. Hammond, A. Hardas, A. Zanti, S. Loukaidou, M. Gentil, D. Gunn-Moore, S. Mazeri, C. Tait-Burkard

This study reports the emergence of a highly pathogenic FCoV-CCoV recombinant causing a rapidly spreading FIP outbreak in Cyprus, with evidence of direct transmission and potential receptor binding changes.

bioRxiv · Nov 8, 2023 · PreprintMicrobiology

One for all - Human kidney Caki-1 cells are highly susceptible to infection with corona- and other respiratory viruses

A. Daniels, S. L. Fletcher, H. E. M. Kerr, A. Kratzel, N. Kriplani, N. Craig, C. J. Hastie, P. Davies, P. Digard, V. Thiel, C. Tait-Burkard

This paper identifies Caki-1 human kidney cells as a highly susceptible model for studying multiple respiratory viruses, including coronaviruses and influenza, offering a versatile platform for cross-virus comparison.

bioRxiv · Oct 25, 2022 · PreprintMicrobiology

Direct lysis RT-qPCR of SARS-CoV-2 in cell culture supernatant allows for fast and accurate quantification of virus, opening a vast array of applications

N. Craig, S. L. Fletcher, A. Daniels, C. Newman, M. O'Shea, A. Warr, C. Tait-Burkard

This paper introduces a direct lysis RT-qPCR method for fast, accurate, and cost-effective quantification of SARS-CoV-2 in cell culture supernatant, enabling high-throughput applications.

bioRxiv · Nov 30, 2021 · PreprintMicrobiology