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Prevalence and antimicrobial resistance profiles of respiratory microbial flora in African children with HIV-associated chronic lung disease

  • Regina E. Abotsi
  • , Mark P. Nicol
  • , Grace McHugh
  • , Victoria Simms
  • , Andrea M. Rehman
  • , Charmaine Barthus
  • , Slindile Mbhele
  • , Brewster W. Moyo
  • , Lucky Gift Chiwiya Ngwira
  • , Hilda Mujuru
  • , Beauty Makamure
  • , Justin Mayini
  • , Jon Odland
  • , Rashida A. Ferrand
  • , Felix S. Dube
  • University of Cape Town
  • University of Health and Allied Sciences
  • University of Western Australia
  • Biomedical Research and Training Institute
  • Medical Research Council
  • Malawi-Liverpool-Wellcome Trust Clinical Research Programme
  • University of Zimbabwe
  • University of Tromsø – The Arctic University of Norway
  • Higher School of Economics
  • University of Pretoria
  • London School of Hygiene and Tropical Medicine

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)

Abstract

Abstract: Background: HIV-associated chronic lung disease (CLD) is common among children living with HIV (CLWH) in sub-Saharan Africa, including those on antiretroviral therapy (ART). However, the pathogenesis of CLD and its possible association with microbial determinants remain poorly understood. We investigated the prevalence, and antibiotic susceptibility of Streptococcus pneumoniae (SP), Staphylococcus aureus (SA), Haemophilus influenzae (HI), and Moraxella catarrhalis (MC) among CLWH (established on ART) who had CLD (CLD+), or not (CLD-) in Zimbabwe and Malawi. Methods: Nasopharyngeal swabs (NP) and sputa were collected from CLD+ CLWH (defined as forced-expiratory volume per second z-score < − 1 without reversibility post-bronchodilation with salbutamol), at enrolment as part of a randomised, placebo-controlled trial of azithromycin (BREATHE trial - NCT02426112), and from age- and sex-matched CLD- CLWH. Samples were cultured, and antibiotic susceptibility testing was conducted using disk diffusion. Risk factors for bacterial carriage were identified using questionnaires and analysed using multivariate logistic regression. Results: A total of 410 participants (336 CLD+, 74 CLD-) were enrolled (median age, 15 years [IQR = 13–18]). SP and MC carriage in NP were higher in CLD+ than in CLD- children: 46% (154/336) vs. 26% (19/74), p = 0.008; and 14% (49/336) vs. 3% (2/74), p = 0.012, respectively. SP isolates from the NP of CLD+ children were more likely to be non-susceptible to penicillin than those from CLD- children (36% [53/144] vs 11% [2/18], p = 0.036). Methicillin-resistant SA was uncommon [4% (7/195)]. In multivariate analysis, key factors associated with NP bacterial carriage included having CLD (SP: adjusted odds ratio (aOR) 2 [95% CI 1.1–3.9]), younger age (SP: aOR 3.2 [1.8–5.8]), viral load suppression (SP: aOR 0.6 [0.4–1.0], SA: 0.5 [0.3–0.9]), stunting (SP: aOR 1.6 [1.1–2.6]) and male sex (SA: aOR 1.7 [1.0–2.9]). Sputum bacterial carriage was similar in both groups (50%) and was associated with Zimbabwean site (SP: aOR 3.1 [1.4–7.3], SA: 2.1 [1.1–4.2]), being on ART for a longer period (SP: aOR 0.3 [0.1–0.8]), and hot compared to rainy season (SP: aOR 2.3 [1.2–4.4]). Conclusions: CLD+ CLWH were more likely to be colonised by MC and SP, including penicillin-non-susceptible SP strains, than CLD- CLWH. The role of these bacteria in CLD pathogenesis, including the risk of acute exacerbations, should be further studied.

Original languageEnglish
Article number216
Pages (from-to)216
JournalBMC Infectious Diseases
Volume21
Issue number1
DOIs
Publication statusPublished - 25 Feb 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Antibiotic resistance
  • Children
  • Chronic lung disease
  • Haemophilus influenzae
  • HIV
  • Moraxella catarrhalis
  • Staphylococcus aureus
  • Streptococcus pneumoniae

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