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Differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting

BACKGROUND: Staphylococcus aureus and beta-hemolytic streptococci (BHS) diseases disproportionately affect populations in middle/low-income countries. To assess if this disparity is reflected in colonization by these organisms, we compared their colonization frequency among children from different s...

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Autores principales: Neves, Felipe Piedade Gonçalves, Marlow, Mariel Asbury, Rezende-Pereira, Gabriel, Pinheiro, Marcos Gabriel, dos Santos, Allyne Fandino Martinez, de Fátima Nogueira de Freitas, Maria, Barros, Rosana Rocha, Aguiar-Alves, Fábio, Cardoso, Claudete Aparecida Araújo, Riley, Lee Woodland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540362/
https://www.ncbi.nlm.nih.gov/pubmed/31142269
http://dx.doi.org/10.1186/s12879-019-4104-2
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author Neves, Felipe Piedade Gonçalves
Marlow, Mariel Asbury
Rezende-Pereira, Gabriel
Pinheiro, Marcos Gabriel
dos Santos, Allyne Fandino Martinez
de Fátima Nogueira de Freitas, Maria
Barros, Rosana Rocha
Aguiar-Alves, Fábio
Cardoso, Claudete Aparecida Araújo
Riley, Lee Woodland
author_facet Neves, Felipe Piedade Gonçalves
Marlow, Mariel Asbury
Rezende-Pereira, Gabriel
Pinheiro, Marcos Gabriel
dos Santos, Allyne Fandino Martinez
de Fátima Nogueira de Freitas, Maria
Barros, Rosana Rocha
Aguiar-Alves, Fábio
Cardoso, Claudete Aparecida Araújo
Riley, Lee Woodland
author_sort Neves, Felipe Piedade Gonçalves
collection PubMed
description BACKGROUND: Staphylococcus aureus and beta-hemolytic streptococci (BHS) diseases disproportionately affect populations in middle/low-income countries. To assess if this disparity is reflected in colonization by these organisms, we compared their colonization frequency among children from different socioeconomic status (SES) communities in a city with high income inequality. METHODS: Between May–August 2014, we collected nasal and throat swabs to investigate S. aureus and BHS colonization among children who attended private and public pediatric clinics. Patients were classified as high SES, middle/low SES, and slum residents. We investigated the antimicrobial resistance profile, the SCCmec types and the presence of PVL genes among methicillin-resistant S. aureus (MRSA). We also examined the antimicrobial resistance profile and serogroups of BHS. RESULTS: Of 598 children, 221 (37%) were colonized with S. aureus, of which 49 (22%) were MRSA. MRSA colonization was higher in middle/low SES (n = 18; 14%) compared with high SES (n = 17; 6%) and slum (n = 14; 8%) residents (p = 0.01). All MRSA strains were susceptible to clindamycin, nitrofurantoin, and rifampin. The highest non-susceptibility frequency (42.9%) was observed to erythromycin. SCCmec type V was only found in isolates from high SES children; types I and II were found only in middle/low SES children. Ten (20%) MRSA isolates carried PVL genes. Twenty-four (4%) children were BHS carriers. All BHS (n = 8) found in high SES children and six (67%) isolates from slum patients belonged to group A. All group B streptococci were from middle/low SES children, corresponding to five (71%) of the seven BHS isolated in this group. BHS isolates were susceptible to all drugs tested. CONCLUSIONS: Children from different SES communities had distinct bacterial colonization profiles, including MRSA carriage. Public health officials/researchers should consider SES when assessing disease transmission and control measures.
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spelling pubmed-65403622019-06-03 Differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting Neves, Felipe Piedade Gonçalves Marlow, Mariel Asbury Rezende-Pereira, Gabriel Pinheiro, Marcos Gabriel dos Santos, Allyne Fandino Martinez de Fátima Nogueira de Freitas, Maria Barros, Rosana Rocha Aguiar-Alves, Fábio Cardoso, Claudete Aparecida Araújo Riley, Lee Woodland BMC Infect Dis Research Article BACKGROUND: Staphylococcus aureus and beta-hemolytic streptococci (BHS) diseases disproportionately affect populations in middle/low-income countries. To assess if this disparity is reflected in colonization by these organisms, we compared their colonization frequency among children from different socioeconomic status (SES) communities in a city with high income inequality. METHODS: Between May–August 2014, we collected nasal and throat swabs to investigate S. aureus and BHS colonization among children who attended private and public pediatric clinics. Patients were classified as high SES, middle/low SES, and slum residents. We investigated the antimicrobial resistance profile, the SCCmec types and the presence of PVL genes among methicillin-resistant S. aureus (MRSA). We also examined the antimicrobial resistance profile and serogroups of BHS. RESULTS: Of 598 children, 221 (37%) were colonized with S. aureus, of which 49 (22%) were MRSA. MRSA colonization was higher in middle/low SES (n = 18; 14%) compared with high SES (n = 17; 6%) and slum (n = 14; 8%) residents (p = 0.01). All MRSA strains were susceptible to clindamycin, nitrofurantoin, and rifampin. The highest non-susceptibility frequency (42.9%) was observed to erythromycin. SCCmec type V was only found in isolates from high SES children; types I and II were found only in middle/low SES children. Ten (20%) MRSA isolates carried PVL genes. Twenty-four (4%) children were BHS carriers. All BHS (n = 8) found in high SES children and six (67%) isolates from slum patients belonged to group A. All group B streptococci were from middle/low SES children, corresponding to five (71%) of the seven BHS isolated in this group. BHS isolates were susceptible to all drugs tested. CONCLUSIONS: Children from different SES communities had distinct bacterial colonization profiles, including MRSA carriage. Public health officials/researchers should consider SES when assessing disease transmission and control measures. BioMed Central 2019-05-29 /pmc/articles/PMC6540362/ /pubmed/31142269 http://dx.doi.org/10.1186/s12879-019-4104-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Neves, Felipe Piedade Gonçalves
Marlow, Mariel Asbury
Rezende-Pereira, Gabriel
Pinheiro, Marcos Gabriel
dos Santos, Allyne Fandino Martinez
de Fátima Nogueira de Freitas, Maria
Barros, Rosana Rocha
Aguiar-Alves, Fábio
Cardoso, Claudete Aparecida Araújo
Riley, Lee Woodland
Differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting
title Differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting
title_full Differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting
title_fullStr Differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting
title_full_unstemmed Differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting
title_short Differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting
title_sort differences in gram-positive bacterial colonization and antimicrobial resistance among children in a high income inequality setting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540362/
https://www.ncbi.nlm.nih.gov/pubmed/31142269
http://dx.doi.org/10.1186/s12879-019-4104-2
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