Author:
Bhadriraju Sudha,Fadrosh Douglas W.,Shenoy Meera K.,Lin Din L.,Lynch Kole V.,McCauley Kathryn,Ferrand Rashida A.,Majonga Edith D.,McHugh Grace,Huang Laurence,Lynch Susan V.,Metcalfe John Z.
Abstract
AbstractChronic lung disease (CLD) is a common co-morbidity for HIV-positive children and adolescents on antiretroviral therapy (ART) in sub-Saharan Africa. In this population, distinct airway microbiota may differentially confer risk of CLD. In a cross-sectional study of 202 HIV-infected children aged 6–16 years in Harare, Zimbabwe, we determined the association of sputum microbiota composition (using 16S ribosomal RNA V4 gene region sequencing) with CLD defined using clinical, spirometric, or radiographic criteria. Forty-two percent of children were determined to have CLD according to our definition. Dirichlet multinomial mixtures identified four compositionally distinct sputum microbiota structures. Patients whose sputum microbiota was dominated by Haemophilus, Moraxella or Neisseria (HMN) were at 1.5 times higher risk of CLD than those with Streptococcus or Prevotella (SP)-dominated microbiota (RR = 1.48, p = 0.035). Cell-free products of HMN sputum microbiota induced features of epithelial disruption and inflammatory gene expression in vitro, indicating enhanced pathogenic potential of these CLD-associated microbiota. Thus, HIV-positive children harbor distinct sputum microbiota, with those dominated by Haemophilus, Moraxella or Neisseria associated with enhanced pathogenesis in vitro and clinical CLD.
Funder
National Heart, Lung, and Blood Institute
National Institute of Allergy and Infectious Diseases
Nina Ireland Program for Lung Health
Publisher
Springer Science and Business Media LLC
Cited by
9 articles.
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