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Characterization of Inflammatory Responses During Intranasal Colonization with Streptococcus pneumoniae
Published on: January 17, 2014
Characterization of Pneumococcal Colonization Dynamics and Antimicrobial Resistance Using Shotgun Metagenomic
Rendani I Manenzhe1, Felix S Dube1,2, Meredith Wright3
1Division of Medical Microbiology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Insights
Metagenomic sequencing of infant nasopharyngeal samples revealed a predominance of non-PCV13 pneumococcal serotypes and novel sequence types. This culture-independent method offers detailed insights into the infant microbiome and antimicrobial resistance patterns.
Area of Science:
- Microbiology
- Genomics
- Public Health
Background:
- Pneumococcal pneumonia remains a significant cause of infant mortality in low- and middle-income countries.
- Monitoring pneumococcal carriage is crucial for understanding vaccine impact, antimicrobial resistance, and disease ecology.
- Longitudinal studies in vaccinated infants are needed to track changes in pneumococcal colonization.
Purpose of the Study:
- To investigate pneumococcal carriage dynamics in PCV-13 vaccinated infants using longitudinal nasopharyngeal sampling.
- To explore strain-level colonization patterns and antimicrobial resistance determinants via whole metagenome shotgun sequencing.
- To evaluate metagenomic sequencing as a culture-independent method for microbiome analysis.
Main Methods:
- Collected nasopharyngeal samples bi-weekly from 137 infants for one year.
- Performed whole metagenome shotgun sequencing on 196 samples from 23 infants.
- Utilized in silico analysis for serotyping, multilocus sequence typing, and antimicrobial resistance gene detection.
Main Results:
- Metagenomic sequencing detected 22 pneumococcal serotypes, with 15B/15C and 16F being most common non-PCV13 serotypes.
- Identified 26 sequence types (STs), including four novel STs, and detected co-colonization in 15% of samples.
- Found mutations associated with cotrimoxazole and penicillin resistance, though correlation with phenotypic resistance was lower than expected.
Conclusions:
- Metagenomic sequencing is a valuable culture-independent tool for detailed analysis of the nasopharyngeal microbiome and its pneumococcal component.
- The study identified a predominance of non-PCV13 serotypes and novel STs in the vaccinated infant cohort.
- Detected numerous resistance genes and mutations, highlighting the need for further investigation into their correlation with phenotypic resistance.
Abstract:
Background: There remains a significant proportion of deaths due to pneumococcal pneumonia in infants from low- and middle-income countries despite the marginal global declines recorded in the past decade. Monitoring changes in pneumococcal carriage is key to understanding vaccination-induced shifts in the ecology of carriage, patterns of antimicrobial resistance, and impact on health. We longitudinally investigated pneumococcal carriage dynamics in PCV-13 vaccinated infants by collecting nasopharyngeal (NP) samples at 2-weekly intervals from birth through the first year of life from 137 infants. As a proof of concept, 196 NP samples were retrieved from a subset of 23 infants to explore strain-level pneumococcal colonization patterns and associated antimicrobial-resistance determinants. These were selected on the basis of changes in serotype and antibiogram over time. NP samples underwent short-term enrichment for streptococci prior to total nucleic acid extraction and whole metagenome shotgun sequencing (WMGS). Reads were assembled and aligned to pneumococcal reference genomes for the extraction of pneumococcal and non-pneumococcal bacterial reads. Pneumococcal contigs were aligned to the Antibiotic Resistance Gene-ANNOTation database of acquired AMR genes. In silico pneumococcal capsular and multilocus sequence typing were performed. Results: Of the 196 samples sequenced, 174 had corresponding positive cultures for pneumococci, of which, 152 were assigned an in silico serotype. Metagenomic sequencing detected a single pneumococcal serotype in 85% (129/152), and co-colonization in 15% (23/152) of the samples. Twenty-two different pneumococcal serotypes were identified, with 15B/15C and 16F being the most common non-PCV13 serotypes, while 23F and 19A were the most common PCV13 serotypes. Twenty-six different sequence types (STs), including four novel STs were identified in silico. Mutations in the folA and folP genes, associated with cotrimoxazole resistance, were detected in 89% (87/98) of cotrimoxazole-non-susceptible pneumococci, as well as in the pbp1a and pbp2x genes, in penicillin non-susceptible ST705215B/15C isolates. Conclusions: Metagenomic sequencing of NP samples is a valuable culture-independent technique for a detailed evaluation of the pneumococcal component and resistome of the NP microbiome. This method allowed for the detection of novel STs, as well as co-colonization, with a predominance of non-PCV13 serotypes in this cohort. Forty-eight resistance genes, as well as mutations associated with resistance were detected, but the correlation with phenotypic non-susceptibility was lower than expected.
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