{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,18]],"date-time":"2026-09-18T09:42:21Z","timestamp":1789724541083,"version":"4.0.1"},"reference-count":36,"publisher":"SAGE Publications","issue":"6","license":[{"start":{"date-parts":[[2017,8,1]],"date-time":"2017-08-01T00:00:00Z","timestamp":1501545600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Journal of Investigative Medicine"],"published-print":{"date-parts":[[2017,8]]},"abstract":"<jats:sec>\n                    <jats:title>Rationale<\/jats:title>\n                    <jats:p>The nasopharyngeal (NP) microbiota of newborns and infants plays a key role in modulating airway inflammation and respiratory symptoms during viral infections. Premature (PM) birth modifies the early NP environment and is a major risk factor for severe viral respiratory infections. However, it is currently unknown if the NP microbiota of PM infants is altered relative to full-term (FT) individuals.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>To characterize the NP microbiota differences in preterm and FT infants during rhinovirus (RV) infection.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>We determined the NP microbiota of infants 6\u2005months to \u22642\u2005years of age born FT (n=6) or severely PM&lt;32\u2005weeks gestation (n=7). We compared microbiota composition in healthy NP samples and performed a longitudinal analysis during naturally occurring RV infections to contrast the microbiota dynamics in PM versus FT infants.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>We observed significant differences in the NP bacterial community of PM versus FT. NP from PM infants had higher within-group dissimilarity (heterogeneity) relative to FT infants. Bacterial composition of NP samples from PM infants showed increased Proteobacteria and decreased in Firmicutes. There were also differences in the major taxonomic groups identified, including Streptococcus, Moraxella, and Haemophilus. Longitudinal data showed that these prematurity-related microbiota features persisted during RV infection.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>PM is associated with NP microbiota changes beyond the neonatal stage. PM infants have an NP microbiota with high heterogeneity relative to FT infants. These prematurity-related microbiota features persisted during RV infection, suggesting that the NP microbiota of PM may play an important role in modulating airway inflammatory and immune responses in this vulnerable group.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1136\/jim-2017-000414","type":"journal-article","created":{"date-parts":[[2017,3,31]],"date-time":"2017-03-31T20:10:29Z","timestamp":1490991029000},"page":"984-990","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":18,"title":["Nasopharyngeal Microbiome in Premature Infants and Stability during Rhinovirus Infection"],"prefix":"10.1177","volume":"65","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-2843-6837","authenticated-orcid":false,"given":"Geovanny F","family":"Perez","sequence":"first","affiliation":[{"name":"Division of Pulmonary and Sleep Medicine, Children's National Health System, Washington, DC, USA"},{"name":"Department of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, USA"},{"name":"Department of Integrative Systems Biology, George Washington University, Washington, DC, USA"},{"name":"Center for Genetic Medicine Research, Children's National Health System, Washington, DC, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marcos","family":"P\u00e9rez-Losada","sequence":"additional","affiliation":[{"name":"Center for Genetic Medicine Research, Children's National Health System, Washington, DC, USA"},{"name":"Computational Biology Institute, George Washington University, Ashburn, Virginia, USA"},{"name":"CIBIO-InBIO, Centro de Investiga\u00e7\u00e3o em Biodiversidade e Recursos Gen\u00e9ticos, Universidade do Porto, Campus Agr\u00e1rio de Vair\u00e3o, Vair\u00e3o, Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Natalia","family":"Isaza","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, USA"},{"name":"Division of Neonatology, Children's National Medical Center, Washington, DC, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mary C","family":"Rose","sequence":"additional","affiliation":[{"name":"Division of Pulmonary and Sleep Medicine, Children's National Health System, Washington, DC, USA"},{"name":"Department of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, USA"},{"name":"Department of Integrative Systems Biology, George Washington University, Washington, DC, USA"},{"name":"Center for Genetic Medicine Research, Children's National Health System, Washington, DC, USA"},{"name":"Department of Biochemistry and Molecular Medicine, George Washington University, Washington, DC, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anamaris 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