{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T23:50:19Z","timestamp":1787010619603,"version":"build-2736575974"},"reference-count":31,"publisher":"Microbiology Society","issue":"9","license":[{"start":{"date-parts":[[2022,9,30]],"date-time":"2022-09-30T00:00:00Z","timestamp":1664496000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100001171","name":"Cancer Institute NSW","doi-asserted-by":"crossref","award":["15\/CDF\/1-11"],"award-info":[{"award-number":["15\/CDF\/1-11"]}],"id":[{"id":"10.13039\/501100001171","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100001773","name":"University of New South Wales","doi-asserted-by":"crossref","award":["Scientia fellowship"],"award-info":[{"award-number":["Scientia fellowship"]}],"id":[{"id":"10.13039\/501100001773","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100001171","name":"Cancer Institute NSW","doi-asserted-by":"crossref","award":["2019\/ECF1082"],"award-info":[{"award-number":["2019\/ECF1082"]}],"id":[{"id":"10.13039\/501100001171","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100001773","name":"University of New South Wales","doi-asserted-by":"crossref","award":["Scientia fellowship"],"award-info":[{"award-number":["Scientia fellowship"]}],"id":[{"id":"10.13039\/501100001773","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,9,30]]},"abstract":"<jats:p>\n                    Little is known of the relationships among paediatric upper gastrointestinal microbiotas, and the impact of medication use and disease on their diversity. Here, we investigated the diversity of three microbiotas in the upper gastrointestinal tract of paediatric patients in relation to each other and to host factors. Oral, oesophageal and gastric microbiotas from a prospective paediatric cohort (\n                    <jats:italic>n<\/jats:italic>\n                    =54) were profiled using the 16S rRNA gene and ITS2 amplicon sequencing. 16S rRNA gene amplicon sequencing of oesophageal biopsies from a retrospective paediatric cohort (\n                    <jats:italic>n<\/jats:italic>\n                    =96) and shotgun metagenomics data from oesophageal brushings (\n                    <jats:italic>n<\/jats:italic>\n                    =88) were employed for genomic signature validation. Bacterial diversity and composition showed substantial differences across oral, oesophageal and gastric fluid samples that were not replicated for fungi, and the presence of reflux led to increased homogeneity in the bacterial component of these three microbiotas. The oral and oesophageal microbiotas were associated with age, sex, history of oesophageal atresia and presence of oesophageal metaplasia, with the latter characterized by\n                    <jats:italic>\n                      <jats:named-content content-type=\"genus\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.8042\" xlink:type=\"simple\">Prevotella<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    enrichment. Proton pump inhibitor use was associated with increased oral bacterial richness in the gastric fluid, and this correlated with increased levels of gastric pro-inflammatory cytokines. Profiling of oesophageal biopsies from a retrospective paediatric cohort confirmed an increased\n                    <jats:italic>\n                      <jats:named-content content-type=\"genus\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.8042\" xlink:type=\"simple\">Prevotella<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    prevalence in samples with metaplasia. Analysis of metagenome-derived oesophageal\n                    <jats:italic>\n                      <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.8043\" xlink:type=\"simple\">Prevotella melaninogenica<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    genomes identified strain-specific features that were significantly increased in prevalence in samples with metaplasia.\n                    <jats:italic>\n                      <jats:named-content content-type=\"genus\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.8042\" xlink:type=\"simple\">Prevotella<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    enrichment is a signature associated with paediatric oesophageal metaplasia, and proton pump inhibitor use substantially alters the paediatric gastric microenvironment.\n                  <\/jats:p>","DOI":"10.1099\/mgen.0.000870","type":"journal-article","created":{"date-parts":[[2022,9,15]],"date-time":"2022-09-15T11:16:45Z","timestamp":1663240605000},"source":"Crossref","is-referenced-by-count":4,"title":["Changes to the upper gastrointestinal microbiotas of children with reflux oesophagitis and oesophageal metaplasia"],"prefix":"10.1099","volume":"8","author":[{"given":"Laurence D. W.","family":"Luu","sequence":"first","affiliation":[{"name":"School of Biotechnology and Biomolecular Sciences, UNSW Sydney, NSW 2052, Australia"},{"name":"School of Medical Sciences, UNSW Sydney, NSW 2052, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harveen","family":"Singh","sequence":"additional","affiliation":[{"name":"Department of Pediatric Gastroenterology, Sydney Children\u2019s Hospital, Randwick, NSW 2031, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Natalia","family":"Casta\u00f1o-Rodr\u00edguez","sequence":"additional","affiliation":[{"name":"School of Biotechnology and Biomolecular Sciences, UNSW Sydney, NSW 2052, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Steven T.","family":"Leach","sequence":"additional","affiliation":[{"name":"School of Women\u2019s and Children\u2019s Health, UNSW Sydney, NSW 2052, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stephen M.","family":"Riordan","sequence":"additional","affiliation":[{"name":"Gastrointestinal and Liver Unit, The Prince of Wales Hospital, Randwick, NSW 2031, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nicodemus","family":"Tedla","sequence":"additional","affiliation":[{"name":"School of Medical Sciences, UNSW Sydney, NSW 2052, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Usha","family":"Krishnan","sequence":"additional","affiliation":[{"name":"School of Women\u2019s and Children\u2019s Health, UNSW Sydney, NSW 2052, Australia"},{"name":"Department of Pediatric Gastroenterology, Sydney Children\u2019s Hospital, Randwick, NSW 2031, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4017-1077","authenticated-orcid":false,"given":"Nadeem 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