Evidence map›Paper›PMID 40261064›Full record

ArticlemSystems2025

Longitudinal dynamics of the nasopharyngeal microbiome in response to SARS-CoV-2 Omicron variant and HIV infection in Kenyan women and their children.

Ayla Žuštra, Victoria R Leonard, LaRinda A Holland, James C Hu, Tianchen Mu, Steven C Holland, Lily I Wu, Emily R Begnel, Ednah Ojee, Bhavna H Chohan and 7 more

Abstract read
In one paragraph

Article in mSystems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Ayla ŽuštraSchool of Life Sciences, Arizona State University, Tempe, Arizona, USA.ORCID 0009-0007-9357-9785
Victoria R LeonardCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
LaRinda A HollandCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
James C HuCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Tianchen MuCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Steven C HollandCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Lily I WuCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Emily R BegnelDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Ednah OjeeDepartment of Paediatrics and Child Health, University of Nairobi, Nairobi, Kenya.
Bhavna H ChohanDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Barbra A RichardsonDepartment of Global Health, University of Washington, Seattle, Washington, USA.
John KinuthiaDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Dalton WamalwaDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Jennifer SlykerDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Dara A LehmanDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Soren GanttDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Centre de Recherche du CHU St-Justine, Montréal, Québec, Canada.
Efrem S LimSchool of Life Sciences, Arizona State University, Tempe, Arizona, USA.ORCID 0000-0002-3397-9310

Funding

The effect of cytomegalovirus, inflammation, and immune activation on neurodevelopment in children exposed to maternal HIV infectionP01HD107669 · NICHD · UNIVERSITY OF WASHINGTON · PI Grace C. John-Stewart, John Kinuthia · 2022 to 2026
$8.8M
Maternal-infant Virome Transmission: the role of HIV and Antiretroviral TherapyR01HD092311 · NICHD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEHMAN, DARA ANN · 2017 to 2021
$3.9M
CDC HHS BAA 75D30121C11084CIHR 390237CIHR 447944NICHD NIH HHS P01 HD107669NICHD NIH HHS R01 HD092311NIH HHS R01HD092311
6 · The paper itself

Abstract

The nasopharynx and its microbiota are implicated in respiratory health and disease. The interplay between viral infection and the nasopharyngeal microbiome is an area of increased interest. The impact of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the etiological agent of the coronavirus disease 2019 pandemic, on the nasopharyngeal microbiome among individuals living with HIV is not fully characterized. Here, we describe the nasopharyngeal microbiome before, during, and after SARS-CoV-2 infection in a longitudinal cohort of Kenyan women (21 living with HIV and 14 HIV-uninfected) and their children (18 HIV-exposed, uninfected and 7 HIV-unexposed, uninfected) between September 2021 and March 2022. We show using genomic epidemiology that mother and child dyads were infected with the same strain of the SARS-CoV-2 Omicron variant that spread rapidly across Kenya. We used metagenomic sequencing to characterize the nasopharyngeal microbiome of 20 women and children infected with SARS-CoV-2, six children negative for SARS-CoV-2 but experiencing respiratory symptoms, and 34 timepoint-matched SARS-CoV-2-negative mothers and children. Since individuals were sampled longitudinally before and after SARS-CoV-2 infection, we could characterize the short- (within a week of infection) and longer- (average of 38 days post-infection) term impact of SARS-CoV-2 infection on the nasopharyngeal microbiome. We found that mothers and children had significantly different microbiome composition and bacterial load ( IMPORTANCE: The nasopharyngeal microbiome plays an important role in human health. The degree of impact that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has on the nasopharyngeal microbiome varies among studies and may be influenced by diverse SARS-CoV-2 variants and variations in the microbiome between individuals. Our results show that the nasopharyngeal microbiome was not altered substantially by SARS-CoV-2 infection nor by HIV infection in mothers or HIV exposure in children. Our findings highlight the resilience of the nasopharyngeal microbiome after SARS-CoV-2 infection. These findings advance our understanding of the nasopharyngeal microbiome and its interactions with viral infections.

Indexed as

COVID-19HIV InfectionsMicrobiotaNasopharynxSARS-CoV-2AdultChildChild, PreschoolFemaleHumansInfantKenyaLongitudinal StudiesMaleCOVID-19genomic epidemiologyhuman immunodeficiency viruslongitudinalmother-infantnasopharyngeal microbiomeSARS-CoV-2

Identifiers

PMID40261064
PMCPMC12090742

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.