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16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients

16S-based sequencing provides broader information on the respiratory microbial community than conventional culturing. However, it (often) lacks species- and strain-level information. To overcome this issue, we used 16S rRNA-based sequencing results from 246 nasopharyngeal samples obtained from 20 in...

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Autores principales: Kristensen, Maartje, de Koff, Emma M., Chu, Mei Ling, Groendijk, Simone, Tramper-Stranders, Gerdien A., de Winter-de Groot, Karin M., Janssens, Hettie M., Tiddens, Harm A., van Westreenen, Mireille, Sanders, Elisabeth A. M., Arets, Bert H. G. M., van der Ent, Cornelis K., Prevaes, Sabine M. P. J., Bogaert, Debby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269535/
https://www.ncbi.nlm.nih.gov/pubmed/37199622
http://dx.doi.org/10.1128/spectrum.04057-22
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author Kristensen, Maartje
de Koff, Emma M.
Chu, Mei Ling
Groendijk, Simone
Tramper-Stranders, Gerdien A.
de Winter-de Groot, Karin M.
Janssens, Hettie M.
Tiddens, Harm A.
van Westreenen, Mireille
Sanders, Elisabeth A. M.
Arets, Bert H. G. M.
van der Ent, Cornelis K.
Prevaes, Sabine M. P. J.
Bogaert, Debby
author_facet Kristensen, Maartje
de Koff, Emma M.
Chu, Mei Ling
Groendijk, Simone
Tramper-Stranders, Gerdien A.
de Winter-de Groot, Karin M.
Janssens, Hettie M.
Tiddens, Harm A.
van Westreenen, Mireille
Sanders, Elisabeth A. M.
Arets, Bert H. G. M.
van der Ent, Cornelis K.
Prevaes, Sabine M. P. J.
Bogaert, Debby
author_sort Kristensen, Maartje
collection PubMed
description 16S-based sequencing provides broader information on the respiratory microbial community than conventional culturing. However, it (often) lacks species- and strain-level information. To overcome this issue, we used 16S rRNA-based sequencing results from 246 nasopharyngeal samples obtained from 20 infants with cystic fibrosis (CF) and 43 healthy infants, which were all 0 to 6 months old, and compared them to both standard (blind) diagnostic culturing and a 16S-sequencing-informed “targeted” reculturing approach. Using routine culturing, we almost uniquely detected Moraxella catarrhalis, Staphylococcus aureus, and Haemophilus influenzae (42%, 38%, and 33% of samples, respectively). Using the targeted reculturing approach, we were able to reculture 47% of the top-5 operational taxonomical units (OTUs) in the sequencing profiles. In total, we identified 60 species from 30 genera with a median of 3 species per sample (range, 1 to 8). We also identified up to 10 species per identified genus. The success of reculturing the top-5 genera present from the sequencing profile depended on the genus. In the case of Corynebacterium being in the top 5, we recultured them in 79% of samples, whereas for Staphylococcus, this value was only 25%. The success of reculturing was also correlated with the relative abundance of those genera in the corresponding sequencing profile. In conclusion, revisiting samples using 16S-based sequencing profiles to guide a targeted culturing approach led to the detection of more potential pathogens per sample than conventional culturing and may therefore be useful in the identification and, consequently, treatment of bacteria considered relevant for the deterioration or exacerbation of disease in patients like those with CF. IMPORTANCE Early and effective treatment of pulmonary infections in cystic fibrosis is vital to prevent chronic lung damage. Although microbial diagnostics and treatment decisions are still based on conventional culture methods, research is gradually focusing more on microbiome and metagenomic-based approaches. This study compared the results of both methods and proposed a way to combine the best of both worlds. Many species can relatively easily be recultured based on the 16S-based sequencing profile, and it provides more in-depth information about the microbial composition of a sample than that obtained through routine (blind) diagnostic culturing. Still, well-known pathogens can be missed by both routine diagnostic culture methods as well as by targeted reculture methods, sometimes even when they are highly abundant, which may be a consequence of either sample storage conditions or antibiotic treatment at the time of sampling.
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spelling pubmed-102695352023-06-16 16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients Kristensen, Maartje de Koff, Emma M. Chu, Mei Ling Groendijk, Simone Tramper-Stranders, Gerdien A. de Winter-de Groot, Karin M. Janssens, Hettie M. Tiddens, Harm A. van Westreenen, Mireille Sanders, Elisabeth A. M. Arets, Bert H. G. M. van der Ent, Cornelis K. Prevaes, Sabine M. P. J. Bogaert, Debby Microbiol Spectr Research Article 16S-based sequencing provides broader information on the respiratory microbial community than conventional culturing. However, it (often) lacks species- and strain-level information. To overcome this issue, we used 16S rRNA-based sequencing results from 246 nasopharyngeal samples obtained from 20 infants with cystic fibrosis (CF) and 43 healthy infants, which were all 0 to 6 months old, and compared them to both standard (blind) diagnostic culturing and a 16S-sequencing-informed “targeted” reculturing approach. Using routine culturing, we almost uniquely detected Moraxella catarrhalis, Staphylococcus aureus, and Haemophilus influenzae (42%, 38%, and 33% of samples, respectively). Using the targeted reculturing approach, we were able to reculture 47% of the top-5 operational taxonomical units (OTUs) in the sequencing profiles. In total, we identified 60 species from 30 genera with a median of 3 species per sample (range, 1 to 8). We also identified up to 10 species per identified genus. The success of reculturing the top-5 genera present from the sequencing profile depended on the genus. In the case of Corynebacterium being in the top 5, we recultured them in 79% of samples, whereas for Staphylococcus, this value was only 25%. The success of reculturing was also correlated with the relative abundance of those genera in the corresponding sequencing profile. In conclusion, revisiting samples using 16S-based sequencing profiles to guide a targeted culturing approach led to the detection of more potential pathogens per sample than conventional culturing and may therefore be useful in the identification and, consequently, treatment of bacteria considered relevant for the deterioration or exacerbation of disease in patients like those with CF. IMPORTANCE Early and effective treatment of pulmonary infections in cystic fibrosis is vital to prevent chronic lung damage. Although microbial diagnostics and treatment decisions are still based on conventional culture methods, research is gradually focusing more on microbiome and metagenomic-based approaches. This study compared the results of both methods and proposed a way to combine the best of both worlds. Many species can relatively easily be recultured based on the 16S-based sequencing profile, and it provides more in-depth information about the microbial composition of a sample than that obtained through routine (blind) diagnostic culturing. Still, well-known pathogens can be missed by both routine diagnostic culture methods as well as by targeted reculture methods, sometimes even when they are highly abundant, which may be a consequence of either sample storage conditions or antibiotic treatment at the time of sampling. American Society for Microbiology 2023-05-18 /pmc/articles/PMC10269535/ /pubmed/37199622 http://dx.doi.org/10.1128/spectrum.04057-22 Text en Copyright © 2023 Kristensen et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Kristensen, Maartje
de Koff, Emma M.
Chu, Mei Ling
Groendijk, Simone
Tramper-Stranders, Gerdien A.
de Winter-de Groot, Karin M.
Janssens, Hettie M.
Tiddens, Harm A.
van Westreenen, Mireille
Sanders, Elisabeth A. M.
Arets, Bert H. G. M.
van der Ent, Cornelis K.
Prevaes, Sabine M. P. J.
Bogaert, Debby
16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients
title 16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients
title_full 16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients
title_fullStr 16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients
title_full_unstemmed 16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients
title_short 16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients
title_sort 16s rrna-based microbiota profiling assists conventional culture analysis of airway samples from pediatric cystic fibrosis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269535/
https://www.ncbi.nlm.nih.gov/pubmed/37199622
http://dx.doi.org/10.1128/spectrum.04057-22
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