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

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...

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Main Authors: Regina E. Abotsi, Mark P. Nicol, Grace McHugh, Victoria Simms, Andrea M. Rehman, Charmaine Barthus, Slindile Mbhele, Brewster W. Moyo, Lucky G. Ngwira, Hilda Mujuru, Beauty Makamure, Justin Mayini, Jon Ø. Odland, Rashida A. Ferrand, Felix S. Dube
Format: Article
Language:English
Published: BMC 2021-02-01
Series:BMC Infectious Diseases
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Online Access:https://doi.org/10.1186/s12879-021-05904-3
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author Regina E. Abotsi
Mark P. Nicol
Grace McHugh
Victoria Simms
Andrea M. Rehman
Charmaine Barthus
Slindile Mbhele
Brewster W. Moyo
Lucky G. Ngwira
Hilda Mujuru
Beauty Makamure
Justin Mayini
Jon Ø. Odland
Rashida A. Ferrand
Felix S. Dube
author_facet Regina E. Abotsi
Mark P. Nicol
Grace McHugh
Victoria Simms
Andrea M. Rehman
Charmaine Barthus
Slindile Mbhele
Brewster W. Moyo
Lucky G. Ngwira
Hilda Mujuru
Beauty Makamure
Justin Mayini
Jon Ø. Odland
Rashida A. Ferrand
Felix S. Dube
author_sort Regina E. Abotsi
collection DOAJ
description 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.
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spelling doaj.art-8eaea3006f434a2ba36b9fd84dd8cfa82022-12-21T22:21:17ZengBMCBMC Infectious Diseases1471-23342021-02-0121111710.1186/s12879-021-05904-3Prevalence and antimicrobial resistance profiles of respiratory microbial flora in African children with HIV-associated chronic lung diseaseRegina E. Abotsi0Mark P. Nicol1Grace McHugh2Victoria Simms3Andrea M. Rehman4Charmaine Barthus5Slindile Mbhele6Brewster W. Moyo7Lucky G. Ngwira8Hilda Mujuru9Beauty Makamure10Justin Mayini11Jon Ø. Odland12Rashida A. Ferrand13Felix S. Dube14Department of Molecular and Cell Biology & Institute of Infectious Diseases and Molecular Medicine, University of Cape TownDivision of Infection and Immunity, School of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Western AustraliaBiomedical Research and Training InstituteMRC International Statistics & Epidemiology Group, London School of Hygiene and Tropical MedicineMRC International Statistics & Epidemiology Group, London School of Hygiene and Tropical MedicineDivision of Medical Microbiology, University of Cape TownDivision of Medical Microbiology, University of Cape TownMalawi-Liverpool Wellcome Trust Clinical Research ProgrammeMalawi-Liverpool Wellcome Trust Clinical Research ProgrammeDepartment of Paediatrics, University of ZimbabweBiomedical Research and Training InstituteBiomedical Research and Training InstituteDepartment of Community Medicine, University of TromsøBiomedical Research and Training InstituteDepartment of Molecular and Cell Biology & Institute of Infectious Diseases and Molecular Medicine, University of Cape TownAbstract 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.https://doi.org/10.1186/s12879-021-05904-3Streptococcus pneumoniaeStaphylococcus aureusMoraxella catarrhalisHaemophilus influenzaeAntibiotic resistanceChildren
spellingShingle Regina E. Abotsi
Mark P. Nicol
Grace McHugh
Victoria Simms
Andrea M. Rehman
Charmaine Barthus
Slindile Mbhele
Brewster W. Moyo
Lucky G. Ngwira
Hilda Mujuru
Beauty Makamure
Justin Mayini
Jon Ø. Odland
Rashida A. Ferrand
Felix S. Dube
Prevalence and antimicrobial resistance profiles of respiratory microbial flora in African children with HIV-associated chronic lung disease
BMC Infectious Diseases
Streptococcus pneumoniae
Staphylococcus aureus
Moraxella catarrhalis
Haemophilus influenzae
Antibiotic resistance
Children
title Prevalence and antimicrobial resistance profiles of respiratory microbial flora in African children with HIV-associated chronic lung disease
title_full Prevalence and antimicrobial resistance profiles of respiratory microbial flora in African children with HIV-associated chronic lung disease
title_fullStr Prevalence and antimicrobial resistance profiles of respiratory microbial flora in African children with HIV-associated chronic lung disease
title_full_unstemmed Prevalence and antimicrobial resistance profiles of respiratory microbial flora in African children with HIV-associated chronic lung disease
title_short Prevalence and antimicrobial resistance profiles of respiratory microbial flora in African children with HIV-associated chronic lung disease
title_sort prevalence and antimicrobial resistance profiles of respiratory microbial flora in african children with hiv associated chronic lung disease
topic Streptococcus pneumoniae
Staphylococcus aureus
Moraxella catarrhalis
Haemophilus influenzae
Antibiotic resistance
Children
url https://doi.org/10.1186/s12879-021-05904-3
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