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Purifying the Impure: Sequencing Metagenomes and Metatranscriptomes from Complex Animal-associated Samples
Published on: December 22, 2014
Pharyngeal Microenvironment Associated with Human Rhinovirus Infection in Children: Insights from Metatranscriptomic
Muhammad Noman1,2, Ying Li1,2,3,4, Jiaming Huang1,2
1State Key Laboratory of Virology and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Insights
Human rhinovirus (HRV) infections in children with acute low respiratory tract infections (ALRTIs) alter pharyngeal microbiome and host gene expression. HRV-positive children showed higher microbial diversity and distinct gene expression patterns, linked to antibiotic resistance genes.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Human rhinovirus (HRV) is a frequent cause of acute low respiratory tract infections (ALRTIs) in children.
- HRV infection significantly impacts host gene expression and the respiratory tract microbiome.
Purpose of the Study:
- To determine HRV prevalence in children with ALRTI in Wuhan.
- To investigate the interactions between HRV, host gene expression, and the pharyngeal microbiome.
Main Methods:
- Collected 1,790 samples from children with ALRTI and screened for HRV using qPCR and targeted next-generation sequencing (tNGS).
- Analyzed 47 HRV-positive, 29 healthy control, and 27 HRV-negative ALRTI samples using meta-transcriptomic sequencing.
- Compared microbiota dynamics, gene expression, and antimicrobial resistance genes (ARGs) between infected and healthy individuals.
Main Results:
- HRV prevalence was 13.8%, with HRV-A and HRV-C strains dominant.
- HRV-positive samples exhibited higher microbial diversity (Haemophilus, Neisseria, Streptococcus).
- Identified 22,321 differentially expressed genes (DEGs) linked to immune activation and cellular processes.
- ARGs were more prevalent in healthy individuals; significant concordance found between microbial composition and ARG profiles.
Conclusions:
- HRV infection induces distinct shifts in pharyngeal microbial communities and host transcriptional responses.
- Pharyngeal microbiome variations are closely associated with resistome composition.
Abstract:
Human rhinovirus (HRV) is one of the most common causes of acute low respiratory tract infections (ALRTIs) in children and adults resulting in significant alterations in host gene expression and respiratory tract microbiome composition. We sought to clarify HRV prevalence features in children in Wuhan, and investigate interactions between HRV and host in pharynx microenvironment. A total of 1,790 samples were collected from children with ALRTI between September 2021 and September 2023 and screened for HRV infections using qPCR and targeted next-generation sequencing (tNGS). Among all samples, 47 positive samples, 29 healthy control and 27 HRV-negative ALRTI samples were analyzed by meta-transcriptomic sequencing to compare the microbiota dynamics, gene expression and antimicrobial resistance genes (ARGs) profile of infected and healthy individuals. The analysis revealed an HRV positive rate of 13.8%, with HRV-A and HRV-C strains being more dominant than HRV-B in Wuhan. Microbial diversity was significantly higher in HRV-positive samples, with specific genera such as Haemophilus, Neisseria, and Streptococcus being more abundant. There were 22,321 differentially expressed genes (DEGs) identified in the HRV patients. Enrichment analysis showed that these DEGs were associated with alterations in host responses, including modulations in immune activation and cellular processes. The identified ARGs conferred resistance to 18 distinct classes of antibiotics, with these ARGs being more prevalent in healthy individuals compared to those infected with HRV. Procrustes analysis demonstrated significant concordance between pharyngeal microbial community composition and ARG profiles, while co-occurrence network analysis identified strong associations between Pseudomonadota and ARGs conferring resistance to multiple antibiotic classes. HRV infection was associated with distinct shifts in pharyngeal microbial communities and host transcriptional responses. Collectively, these findings suggest that variation in the pharyngeal microbiome is closely linked to variation in resistome composition.
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