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Non typable-Haemophilus influenzae biofilm formation and acute otitis media
BACKGROUND: Non-typable Haemophilus influenzae (NT-Hi) infection is frequently associated with acute otitis media (AOM) treatment failure, recurrence or chronic otitis media. Persistence of otopathogens in a biofilm-structured community was implicated in these situations. Here, we compared biofilm p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223365/ https://www.ncbi.nlm.nih.gov/pubmed/25037572 http://dx.doi.org/10.1186/1471-2334-14-400 |
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author | Mizrahi, Assaf Cohen, Robert Varon, Emmanuelle Bonacorsi, Stephane Bechet, Stephane Poyart, Claire Levy, Corinne Raymond, Josette |
author_facet | Mizrahi, Assaf Cohen, Robert Varon, Emmanuelle Bonacorsi, Stephane Bechet, Stephane Poyart, Claire Levy, Corinne Raymond, Josette |
author_sort | Mizrahi, Assaf |
collection | PubMed |
description | BACKGROUND: Non-typable Haemophilus influenzae (NT-Hi) infection is frequently associated with acute otitis media (AOM) treatment failure, recurrence or chronic otitis media. Persistence of otopathogens in a biofilm-structured community was implicated in these situations. Here, we compared biofilm production by H. influenzae strains obtained by culture of middle ear fluid (MEF) from children with AOM treatment failure and by strains isolated from nasopharyngeal (NP) samples from healthy children or those with AOM (first episode or recurrence). We aimed to evaluate an association of clinical signs and in vitro biofilm formation and establish risk factors of carrying a biofilm-producing strain. METHODS: We used a modification of the microtiter plate assay with crystal violet staining to compare biofilm production by 216 H. influenzae strains: 41 in MEF from children with AOM treatment failure (group MEF), 43 in NP samples from healthy children (NP group 1), 88 in NP samples from children with a first AOM episode (NP group 2, n = 43) or recurrent (NP group 3, n = 45) and 44 in NP samples from children with AOM associated with conjunctivitis (NP group 4). RESULTS: At all, 106/216 (49%) H. influenzae strains produced biofilm as did 26/43 (60.5%) in NP samples from healthy children. Biofilm production in MEF samples and NP samples did not significantly differ (40.5% vs 60.5%, 55.8%, 56.8% and 31.1% for NP groups 1, 2, 3 and 4, respectively). On multivariate analysis, only presence of conjunctivitis was significantly associated with low biofilm production (OR = 0.3, CI [0.16-0.60], p = 0.001). The ampicillin resistance of H. influenzae produced by penicillin-binding protein modification was significantly associated with low biofilm production (p = 0.029). CONCLUSION: We found no association of biofilm production and AOM treatment failure or recurrence. Biofilm production was low from H. influenzae strains associated with conjunctivitis-otitis syndrome and from strains with modified penicillin-binding protein. |
format | Online Article Text |
id | pubmed-4223365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42233652014-11-08 Non typable-Haemophilus influenzae biofilm formation and acute otitis media Mizrahi, Assaf Cohen, Robert Varon, Emmanuelle Bonacorsi, Stephane Bechet, Stephane Poyart, Claire Levy, Corinne Raymond, Josette BMC Infect Dis Research Article BACKGROUND: Non-typable Haemophilus influenzae (NT-Hi) infection is frequently associated with acute otitis media (AOM) treatment failure, recurrence or chronic otitis media. Persistence of otopathogens in a biofilm-structured community was implicated in these situations. Here, we compared biofilm production by H. influenzae strains obtained by culture of middle ear fluid (MEF) from children with AOM treatment failure and by strains isolated from nasopharyngeal (NP) samples from healthy children or those with AOM (first episode or recurrence). We aimed to evaluate an association of clinical signs and in vitro biofilm formation and establish risk factors of carrying a biofilm-producing strain. METHODS: We used a modification of the microtiter plate assay with crystal violet staining to compare biofilm production by 216 H. influenzae strains: 41 in MEF from children with AOM treatment failure (group MEF), 43 in NP samples from healthy children (NP group 1), 88 in NP samples from children with a first AOM episode (NP group 2, n = 43) or recurrent (NP group 3, n = 45) and 44 in NP samples from children with AOM associated with conjunctivitis (NP group 4). RESULTS: At all, 106/216 (49%) H. influenzae strains produced biofilm as did 26/43 (60.5%) in NP samples from healthy children. Biofilm production in MEF samples and NP samples did not significantly differ (40.5% vs 60.5%, 55.8%, 56.8% and 31.1% for NP groups 1, 2, 3 and 4, respectively). On multivariate analysis, only presence of conjunctivitis was significantly associated with low biofilm production (OR = 0.3, CI [0.16-0.60], p = 0.001). The ampicillin resistance of H. influenzae produced by penicillin-binding protein modification was significantly associated with low biofilm production (p = 0.029). CONCLUSION: We found no association of biofilm production and AOM treatment failure or recurrence. Biofilm production was low from H. influenzae strains associated with conjunctivitis-otitis syndrome and from strains with modified penicillin-binding protein. BioMed Central 2014-07-19 /pmc/articles/PMC4223365/ /pubmed/25037572 http://dx.doi.org/10.1186/1471-2334-14-400 Text en Copyright © 2014 Mizrahi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Mizrahi, Assaf Cohen, Robert Varon, Emmanuelle Bonacorsi, Stephane Bechet, Stephane Poyart, Claire Levy, Corinne Raymond, Josette Non typable-Haemophilus influenzae biofilm formation and acute otitis media |
title | Non typable-Haemophilus influenzae biofilm formation and acute otitis media |
title_full | Non typable-Haemophilus influenzae biofilm formation and acute otitis media |
title_fullStr | Non typable-Haemophilus influenzae biofilm formation and acute otitis media |
title_full_unstemmed | Non typable-Haemophilus influenzae biofilm formation and acute otitis media |
title_short | Non typable-Haemophilus influenzae biofilm formation and acute otitis media |
title_sort | non typable-haemophilus influenzae biofilm formation and acute otitis media |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223365/ https://www.ncbi.nlm.nih.gov/pubmed/25037572 http://dx.doi.org/10.1186/1471-2334-14-400 |
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