Cargando…

Dual spatially resolved transcriptomics for human host–pathogen colocalization studies in FFPE tissue sections

Technologies to study localized host–pathogen interactions are urgently needed. Here, we present a spatial transcriptomics approach to simultaneously capture host and pathogen transcriptome-wide spatial gene expression information from human formalin-fixed paraffin-embedded (FFPE) tissue sections at...

Descripción completa

Detalles Bibliográficos
Autores principales: Sounart, Hailey, Lázár, Enikő, Masarapu, Yuvarani, Wu, Jian, Várkonyi, Tibor, Glasz, Tibor, Kiss, András, Borgström, Erik, Hill, Andrew, Rezene, Sefanit, Gupta, Soham, Jurek, Aleksandra, Niesnerová, Anezka, Druid, Henrik, Bergmann, Olaf, Giacomello, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588020/
https://www.ncbi.nlm.nih.gov/pubmed/37858234
http://dx.doi.org/10.1186/s13059-023-03080-y
Descripción
Sumario:Technologies to study localized host–pathogen interactions are urgently needed. Here, we present a spatial transcriptomics approach to simultaneously capture host and pathogen transcriptome-wide spatial gene expression information from human formalin-fixed paraffin-embedded (FFPE) tissue sections at a near single-cell resolution. We demonstrate this methodology in lung samples from COVID-19 patients and validate our spatial detection of SARS-CoV-2 against RNAScope and in situ sequencing. Host–pathogen colocalization analysis identified putative modulators of SARS-CoV-2 infection in human lung cells. Our approach provides new insights into host response to pathogen infection through the simultaneous, unbiased detection of two transcriptomes in FFPE samples. \MENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-03080-y.