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dc.contributor.authorKristensen, Maartje
dc.contributor.authorde Koff, Emma M
dc.contributor.authorChu, Mei Ling
dc.contributor.authorGroendijk, Simone
dc.contributor.authorTramper-Stranders, Gerdien A
dc.contributor.authorde Winter-de Groot, Karin M
dc.contributor.authorJanssens, Hettie M
dc.contributor.authorTiddens, Harm A
dc.contributor.authorvan Westreenen, Mireille
dc.contributor.authorSanders, Elisabeth A M
dc.contributor.authorArets, Bert H G M
dc.contributor.authorvan der Ent, Cornelis K
dc.contributor.authorPrevaes, Sabine M P J
dc.contributor.authorBogaert, Debby
dc.date.accessioned2023-05-22T09:56:43Z
dc.date.available2023-05-22T09:56:43Z
dc.date.issued2023-05-18
dc.identifier.pmid37199622
dc.identifier.doi10.1128/spectrum.04057-22
dc.identifier.urihttp://hdl.handle.net/10029/626705
dc.description.abstract16S-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.en_US
dc.language.isoenen_US
dc.subject16S rRNA sequencingen_US
dc.subjectbacterial cultureen_US
dc.subjectcystic fibrosisen_US
dc.subjectmicrobiomeen_US
dc.title16S rRNA-Based Microbiota Profiling Assists Conventional Culture Analysis of Airway Samples from Pediatric Cystic Fibrosis Patients.en_US
dc.typeArticleen_US
dc.identifier.eissn2165-0497
dc.identifier.journalMicrobiol Spectr 2023;e0405722en_US
dc.source.journaltitleMicrobiology spectrum
dc.source.beginpagee0405722
dc.source.endpage
dc.source.countryUnited States


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