<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19(1)</volume><submitter>Saralahti AK</submitter><funding>Competitive State Research Financing of the Expert Responsibility area of Tampere University Hospital</funding><funding>Tampereen Tuberkuloosisäätiö</funding><funding>Suomalainen Konkordia-liitto</funding><funding>Sigrid Juséliuksen Säätiö</funding><funding>Suomen Kulttuurirahasto</funding><funding>Oskar Öflunds Stiftelse</funding><funding>Competitive State Research Financing of the Expert Responsibility Area of Oulu University Hospital</funding><funding>Tampereen kaupungin tiederahasto</funding><funding>The University of Tampere Foundation</funding><funding>Väinö ja Laina Kiven Säätiö</funding><funding>The Doctoral Programme in Medicine and Life Sciences, Tampere University</funding><funding>Emil Aaltosen Säätiö</funding><funding>Suomen Tuberkuloosin Vastustamisyhdistyksen Säätiö</funding><funding>Maud Kuistilan Muistosäätiö</funding><funding>Pirkanmaan Rahasto</funding><pubmed_abstract>Streptococcus pneumoniae (pneumococcus) is one of the most frequent causes of pneumonia, sepsis and meningitis in humans, and an important cause of mortality among children and the elderly. We have previously reported the suitability of the zebrafish (Danio rerio) larval model for the study of the host-pathogen interactions in pneumococcal infection. In the present study, we characterized the zebrafish innate immune response to pneumococcus in detail through a whole-genome level transcriptome analysis and revealed a well-conserved response to this human pathogen in challenged larvae. In addition, to gain understanding of the genetic factors associated with the increased risk for severe pneumococcal infection in humans, we carried out a medium-scale forward genetic screen in zebrafish. In t</pubmed_abstract><journal>PLoS genetics</journal><pagination>e1010586</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9858863</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Characterization of the innate immune response to Streptococcus pneumoniae infection in zebrafish.</pubmed_title><pmcid>PMC9858863</pmcid><pubmed_authors>Junno M</pubmed_authors><pubmed_authors>Rounioja S</pubmed_authors><pubmed_authors>Saralahti AK</pubmed_authors><pubmed_authors>Rantapero T</pubmed_authors><pubmed_authors>Kaasinen M</pubmed_authors><pubmed_authors>Nykter M</pubmed_authors><pubmed_authors>Parikka M</pubmed_authors><pubmed_authors>Harjula SE</pubmed_authors><pubmed_authors>Uusi-Makela MIE</pubmed_authors><pubmed_authors>Lohi O</pubmed_authors><pubmed_authors>Ramet M</pubmed_authors><pubmed_authors>Piippo H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of the innate immune response to Streptococcus pneumoniae infection in zebrafish.</name><description>Streptococcus pneumoniae (pneumococcus) is one of the most frequent causes of pneumonia, sepsis and meningitis in humans, and an important cause of mortality among children and the elderly. We have previously reported the suitability of the zebrafish (Danio rerio) larval model for the study of the host-pathogen interactions in pneumococcal infection. In the present study, we characterized the zebrafish innate immune response to pneumococcus in detail through a whole-genome level transcriptome analysis and revealed a well-conserved response to this human pathogen in challenged larvae. In addition, to gain understanding of the genetic factors associated with the increased risk for severe pneumococcal infection in humans, we carried out a medium-scale forward genetic screen in zebrafish. In t</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-05-27T22:45:03.226Z</modification><creation>2025-02-19T04:46:01.719Z</creation></dates><accession>S-EPMC9858863</accession><cross_references><pubmed>36622851</pubmed><doi>10.1371/journal.pgen.1010586</doi></cross_references></HashMap>