<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE341nnn/GSE341918/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Mus musculus</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE341918</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Dual host-pathogen screening of the lung during severe influenza using spatial transcriptomics</name><description>Here, we assessed whether spatially-resolved capture of polyadenylated mRNA permitted simultaneous screening of host and viral responses in situ. Fresh-frozen lung samples from mice infected with H1N1 influenza A strain, PR8, were processed via genome-wide, spatial transcriptomics (ST) at 10 μm resolution. To determine if specific cell-types were detectable within the ST data, we first performed cellular deconvolution using publicly available, single-cell RNA-seq data of immune and non-immune cells from PR8-infected lungs. This revealed expected structures such as rings of epithelial cells lining airways, and at day 10 post-infection (p.i.) unexpected structures dominated by B cells. We next screened ST data alone for groups of genes displaying similar spatial expression patterns. This again identified at day 10 p.i. cellular aggregates enriched for genes associated with B cell biology. Mapping these gene signatures to a B cell transcriptomic atlas suggested plasmablasts had emerged early in the lung, which was confirmed by flow cytometry. Finally, by mapping ST data to the influenza A genome, we observed widespread expression of all ten viral transcripts across samples at day 4 but not day 10 p.i., consistent with viral clearance. Cellular deconvolution analysis at day 4 p.i. revealed proportions of every detected cell-type harboured viral transcripts, suggesting indiscriminate infection across the specific area of tissue examined. Subsequent whole-section immunohistochemical assessment further supported the phenomenon of localised indiscriminate infection, with these areas found adjacent to minimally-infected zones. Thus, spatial screening of mRNA in tissues can simultaneously inform upon viral pathogenesis and host responses to infection.</description><dates><publication>2026/09/15</publication></dates><accession>GSE341918</accession><cross_references><GSM>GSM9920044</GSM><GSM>GSM9920043</GSM><GSM>GSM9920042</GSM><GSM>GSM9920041</GSM><GPL>30172</GPL><GSE>341918</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>