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Seasonal airway microbiome and transcriptome interactions promote childhood asthma exacerbations.
McCauley, Kathryn E; Flynn, Kaitlin; Calatroni, Agustin; DiMassa, Vincent; LaMere, Brandon; Fadrosh, Douglas W; Lynch, Kole V; Gill, Michelle A; Pongracic, Jacqueline A; Khurana Hershey, Gurjit K; Kercsmar, Carolyn M; Liu, Andrew H; Johnson, Christine C; Kim, Haejin; Kattan, Meyer; O'Connor, George T; Bacharier, Leonard B; Teach, Stephen J; Gergen, Peter J; Wheatley, Lisa M; Togias, Alkis; LeBeau, Petra; Presnell, Scott; Boushey, Homer A; Busse, William W; Gern, James E; Jackson, Daniel J; Altman, Matthew C; Lynch, Susan V.
Afiliação
  • McCauley KE; Department of Medicine, University of California, San Francisco, Calif.
  • Flynn K; Systems Immunology Program, Benaroya Research Institute, Seattle, Wash.
  • Calatroni A; Rho Inc, Chapel Hill, NC.
  • DiMassa V; Department of Medicine, University of California, San Francisco, Calif.
  • LaMere B; Department of Medicine, University of California, San Francisco, Calif.
  • Fadrosh DW; Department of Medicine, University of California, San Francisco, Calif.
  • Lynch KV; Department of Medicine, University of California, San Francisco, Calif.
  • Gill MA; Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Tex.
  • Pongracic JA; Ann Robert H. Lurie Children's Hospital of Chicago, Chicago, Ill.
  • Khurana Hershey GK; Cincinnati Children's Hospital, Cincinnati, Ohio.
  • Kercsmar CM; Cincinnati Children's Hospital, Cincinnati, Ohio.
  • Liu AH; Department of Allergy and Immunology, Children's Hospital Colorado, Unversity of Colorado School of Medicine, Aurora, Colo.
  • Johnson CC; Henry Ford Health System, Detroit, Mich.
  • Kim H; Henry Ford Health System, Detroit, Mich.
  • Kattan M; Columbia University College of Physicians and Surgeons, New York, NY.
  • O'Connor GT; Pulmonary Center, Department of Medicine, Boston University School of Medicine, Boston, Mass.
  • Bacharier LB; Division of Allergy, Immunology, and Pulmonary Medicine, Washington University, St Louis, Mo.
  • Teach SJ; Children's National Hospital, Washington, DC.
  • Gergen PJ; Division of Allergy, Immunology, and Transplantation, National Institute of Allergy and Infectious Diseases, Bethesda, Md.
  • Wheatley LM; Division of Allergy, Immunology, and Transplantation, National Institute of Allergy and Infectious Diseases, Bethesda, Md.
  • Togias A; Division of Allergy, Immunology, and Transplantation, National Institute of Allergy and Infectious Diseases, Bethesda, Md.
  • LeBeau P; Rho Inc, Chapel Hill, NC.
  • Presnell S; Systems Immunology Program, Benaroya Research Institute, Seattle, Wash.
  • Boushey HA; Department of Medicine, University of California, San Francisco, Calif.
  • Busse WW; University of Wisconsin School of Medicine and Public Health, Madison, Wisc.
  • Gern JE; University of Wisconsin School of Medicine and Public Health, Madison, Wisc.
  • Jackson DJ; University of Wisconsin School of Medicine and Public Health, Madison, Wisc.
  • Altman MC; Systems Immunology Program, Benaroya Research Institute, Seattle, Wash; Department of Allergy and Infectious Diseases, University of Washington, Seattle, Wash. Electronic address: maltman@benaroyaresearch.org.
  • Lynch SV; Department of Medicine, University of California, San Francisco, Calif. Electronic address: susan.lynch@ucsf.edu.
J Allergy Clin Immunol ; 150(1): 204-213, 2022 07.
Article em En | MEDLINE | ID: mdl-35149044
ABSTRACT

BACKGROUND:

Seasonal variation in respiratory illnesses and exacerbations in pediatric populations with asthma is well described, though whether upper airway microbes play season-specific roles in these events is unknown.

OBJECTIVE:

We hypothesized that nasal microbiota composition is seasonally dynamic and that discrete microbe-host interactions modify risk of asthma exacerbation in a season-specific manner.

METHODS:

Repeated nasal samples from children with exacerbation-prone asthma collected during periods of respiratory health (baseline; n = 181 samples) or first captured respiratory illness (n = 97) across all seasons, underwent bacterial (16S ribosomal RNA gene) and fungal (internal transcribed spacer region 2) biomarker sequencing. Virus detection was performed by multiplex PCR. Paired nasal transcriptome data were examined for seasonal dynamics and integrative analyses.

RESULTS:

Upper airway bacterial and fungal microbiota and rhinovirus detection exhibited significant seasonal dynamics. In seasonally adjusted analysis, variation in both baseline and respiratory illness microbiota related to subsequent exacerbation. Specifically, in the fall, when respiratory illness and exacerbation events were most frequent, several Moraxella and Haemophilus members were enriched both in virus-positive respiratory illnesses and those that progressed to exacerbations. The abundance of 2 discrete bacterial networks, characteristically comprising either Streptococcus or Staphylococcus, exhibited opposing interactions with an exacerbation-associated SMAD3 nasal epithelial transcriptional module to significantly increase the odds of subsequent exacerbation (odds ratio = 14.7, 95% confidence interval = 1.50-144, P = .02; odds ratio = 39.17, 95% confidence interval = 2.44-626, P = .008, respectively).

CONCLUSIONS:

Upper airway microbiomes covary with season and with seasonal trends in respiratory illnesses and asthma exacerbations. Seasonally adjusted analyses reveal specific bacteria-host interactions that significantly increase risk of asthma exacerbation in these children.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Viroses / Microbiota Limite: Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Viroses / Microbiota Limite: Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article