2017
DOI: 10.1371/journal.pone.0190075
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The impact of persistent bacterial bronchitis on the pulmonary microbiome of children

Abstract: IntroductionPersistent bacterial bronchitis (PBB) is a leading cause of chronic wet cough in young children. This study aimed to characterise the respiratory bacterial microbiota of healthy children and to assess the impact of the changes associated with the development of PBB.Blind, protected brushings were obtained from 20 healthy controls and 24 children with PBB, with an additional directed sample obtained from PBB patients. DNA was extracted, quantified using a 16S rRNA gene quantitative PCR assay prior t… Show more

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Cited by 33 publications
(51 citation statements)
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“…In 2017, a team of UK researchers compared protected brushing of 20 healthy controls and 24 children with PBB, finding that the microbiota of the latter was less different in terms of richness and evenness. Bacterial communities in children with PBB were dominated by Proteobacteria, and indicator species analysis showed that Haemophilus and Neisseria were significantly associated with the patient group ( 24 ). A more recent study found out that in BAL of children with PBB, one or more respiratory pathogens were detected.…”
Section: Etiopathogenesismentioning
confidence: 99%
“…In 2017, a team of UK researchers compared protected brushing of 20 healthy controls and 24 children with PBB, finding that the microbiota of the latter was less different in terms of richness and evenness. Bacterial communities in children with PBB were dominated by Proteobacteria, and indicator species analysis showed that Haemophilus and Neisseria were significantly associated with the patient group ( 24 ). A more recent study found out that in BAL of children with PBB, one or more respiratory pathogens were detected.…”
Section: Etiopathogenesismentioning
confidence: 99%
“…Total bacterial burden was measured using a SYBR green quantitative PCR assay using the primers 520F, and 820R, , targeting the V4 region of the 16S rRNA gene as described in Cuthbertson et al 2017[19]. All reactions were performed in triplicate and included standards and non-template controls on the ViiA 7 Real-time PCR system (Life Technologies, Paisley, UK) using SYBR Fast qPCR Master mix (KAPA Biosystems, Wilmington, MA, USA).…”
Section: Methodsmentioning
confidence: 99%
“…Community analysis was carried out using 16S rRNA gene sequencing. Custom dual barcoded fusion primers were used to target the previously quantified region of the 16S rRNA gene as previously described [19]. Each sequencing run contained a PCR negative control and a Mock community, consisting of 34 16S rRNA gene clones of known bacterial species in equal proportions.…”
Section: Methodsmentioning
confidence: 99%
“…DNA extraction was performed on throat swabs using the MPBio FastDNA TM spin kit for soil as per the manufacturer's instructions. Blank swabs were extracted and sequenced to control for any contamination as previously described [16].…”
Section: Dna Extractionmentioning
confidence: 99%