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Here, the effects of antibiotic-induced microbiota alteration on experimental cerebral malaria (ECM) were examined.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Male C57BL\/6N mice that were administered drinking water containing a four-antibiotic cocktail, ampicillin, neomycin, metronidazole and vancomycin, from 2\u00a0weeks before\n                      <jats:italic>P. berghei<\/jats:italic>\n                      ANKA (PbA) infection were used for the experiments. Disease progression, blood\u2013brain barrier (BBB) integrity, immune responses, and gut microbiota composition were evaluated.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Approximately 80% of mice with modified gut microbiota avoided ECM and showed reduced BBB disruption and lymphocyte infiltration into the brain. 16S rRNA gene sequencing revealed specific bacterial species that contributed to either the protection or pathogenesis of ECM. The mono-colonization of germ-free mice revealed that distinct bacterial species could attenuate or exacerbate ECM symptoms, independent of antibiotic effects.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>The findings highlight that distinct gut microbial populations can modulate host susceptibility or resistance to ECM, underscoring the important influence of the intestinal microbiota on infectious disease outcomes. This work broadens the understanding of host\u2012microbe interactions and may inform new strategies for managing cerebral malaria through microbiota modulation.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1186\/s41182-026-00947-1","type":"journal-article","created":{"date-parts":[[2026,4,16]],"date-time":"2026-04-16T18:47:58Z","timestamp":1776365278000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Gut microbiota bidirectionally influences protection and severity in cerebral malaria in mice"],"prefix":"10.1186","volume":"54","author":[{"given":"Tomoyo","family":"Taniguchi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eiji","family":"Miyauchi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Reika","family":"Kawabata-Iwakawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masahiko","family":"Nishiyama","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rika","family":"Umemiya-Shirafuji","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiromu","family":"Toma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nobuo","family":"Sasaki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hajime","family":"Hisaeda","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Haruyoshi","family":"Tomita","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiroshi","family":"Ohno","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hidehiro","family":"Kishimoto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiroshi","family":"Suzuki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2026,4,16]]},"reference":[{"key":"947_CR1","unstructured":"World Health Organization. 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