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In this study, outbred pregnant CD1 mice with semi allogeneic fetuses were infected with transgenic\n                  <jats:italic>Plasmodium berghei<\/jats:italic>\n                  or mock-inoculated by mosquito bite at either embryonic day (E) 6 (first trimester-equivalent) or 10 (second trimester- equivalent) and compared with non-pregnant females.\n                  <jats:italic>P. berghei<\/jats:italic>\n                  -infected mosquitoes had greater biting avidity for E10 dams than uninfected mosquitoes, which was not apparent for E6 dams nor non-pregnant females. Infected E10 dams had greater numbers of parasites than E6 dams in the uterus and spleen, but not in the blood or liver. While parasites were found in placentas, no parasites were present in fetuses. Maternal infection at E6 caused greater maternal morbidity, with greater rates of fetal reabsorption and stillbirths than at E10. Infection at E10 caused adverse offspring outcomes, including growth restriction. To identify possible mechanisms of adverse offspring outcomes, E10 dams were euthanized during peak parasitemia (8 days post infection), and outcomes were compared with mock-infected dams.\n                  <jats:italic>P. berghei<\/jats:italic>\n                  caused significant systemic maternal immune activation with elevated circulating lymphocytes, eosinophils, and neutrophils and splenic cytokine concentrations.\n                  <jats:italic>P. berghei<\/jats:italic>\n                  infection at E10 increased corticosterone and decreased progesterone concentrations, which could contribute to adverse perinatal outcomes through immunomodulation. There were limited changes in the maternal fecal microbiome after\n                  <jats:italic>P. berghei<\/jats:italic>\n                  infection. Mosquito bite infection of outbred dams with\n                  <jats:italic>P. berghei<\/jats:italic>\n                  causes placental malaria and provides a novel, tractable model to investigate therapeutic treatments.\n                <\/jats:p>","DOI":"10.1101\/2025.01.15.633265","type":"posted-content","created":{"date-parts":[[2025,1,16]],"date-time":"2025-01-16T04:30:16Z","timestamp":1737001816000},"source":"Crossref","is-referenced-by-count":0,"title":["Multi-System Dysregulation in Placental Malaria Contributes to Adverse Perinatal Outcomes in Mice"],"prefix":"10.64898","author":[{"given":"Phebe","family":"Ekregbesi","sequence":"first","affiliation":[{"name":"W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Brittany","family":"Seibert","sequence":"additional","affiliation":[{"name":"W. 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