» Articles » PMID: 26571305

Rhinovirus Detection in Symptomatic and Asymptomatic Children: Value of Host Transcriptome Analysis

Abstract

Rationale: Rhinoviruses (RVs) are a major cause of symptomatic respiratory tract infection in all age groups. However, RVs can frequently be detected in asymptomatic individuals.

Objectives: To evaluate the ability of host transcriptional profiling to differentiate between symptomatic RV infection and incidental detection in children.

Methods: Previously healthy children younger than 2 years old (n = 151) were enrolled at four study sites and classified into four clinical groups: RV- healthy control subjects (n = 37), RV+ asymptomatic subjects (n = 14), RV+ outpatients (n = 30), and RV+ inpatients (n = 70). Host responses were analyzed using whole-blood RNA transcriptional profiles.

Measurements And Main Results: RV infection induced a robust transcriptional signature, which was validated in three independent cohorts and by quantitative real-time polymerase chain reaction with high prediction accuracy. The immune profile of symptomatic RV infection was characterized by overexpression of innate immunity and underexpression of adaptive immunity genes, whereas negligible changes were observed in asymptomatic RV+ subjects. Unsupervised hierarchical clustering identified two main clusters of subjects. The first included 93% of healthy control subjects and 100% of asymptomatic RV+ subjects, and the second comprised 98% of RV+ inpatients and 88% of RV+ outpatients. Genomic scores of healthy control subjects and asymptomatic RV+ children were similar and significantly lower than those of RV+ inpatients and outpatients (P < 0.0001).

Conclusions: Symptomatic RV infection induced a robust and reproducible transcriptional signature, whereas identification of RV in asymptomatic children was not associated with significant systemic transcriptional immune responses. Transcriptional profiling represents a useful tool to discriminate between active infection and incidental virus detection.

Citing Articles

International multi-cohort analysis identifies novel framework for quantifying immune dysregulation in critical illness: results of the SUBSPACE consortium.

Moore A, Zheng H, Ganesan A, Hasin-Brumshtein Y, Maddali M, Levitt J bioRxiv. 2024; .

PMID: 39605502 PMC: 11601436. DOI: 10.1101/2024.11.12.623298.


Epigenetic training of human bronchial epithelium cells by repeated rhinovirus infections.

Risha M, Reddy K, Nemani S, Jakwerth C, Schmidt-Weber C, Bahmer T Allergy. 2024; 79(12):3385-3400.

PMID: 39513674 PMC: 11657021. DOI: 10.1111/all.16388.


A T-Cell-Derived 3-Gene Signature Distinguishes SARS-CoV-2 from Common Respiratory Viruses.

Li Y, Tao X, Ye S, Tai Q, You Y, Huang X Viruses. 2024; 16(7).

PMID: 39066192 PMC: 11281602. DOI: 10.3390/v16071029.


Systems immunology of transcriptional responses to viral infection identifies conserved antiviral pathways across macaques and humans.

Ratnasiri K, Zheng H, Toh J, Yao Z, Duran V, Donato M Cell Rep. 2024; 43(2):113706.

PMID: 38294906 PMC: 10915397. DOI: 10.1016/j.celrep.2024.113706.


Virome Data Explorer: A web resource to longitudinally explore respiratory viral infections, their interactions with other pathogens and host transcriptomic changes in over 100 people.

Galanti M, Patino-Galindo J, Filip I, Morita H, Galianese A, Youssef M PLoS Biol. 2024; 22(1):e3002089.

PMID: 38236818 PMC: 10796020. DOI: 10.1371/journal.pbio.3002089.


References
1.
Zhai Y, Franco L, Atmar R, Quarles J, Arden N, Bucasas K . Host Transcriptional Response to Influenza and Other Acute Respiratory Viral Infections--A Prospective Cohort Study. PLoS Pathog. 2015; 11(6):e1004869. PMC: 4466531. DOI: 10.1371/journal.ppat.1004869. View

2.
Suarez N, Bunsow E, Falsey A, Walsh E, Mejias A, Ramilo O . Superiority of transcriptional profiling over procalcitonin for distinguishing bacterial from viral lower respiratory tract infections in hospitalized adults. J Infect Dis. 2015; 212(2):213-22. PMC: 4565998. DOI: 10.1093/infdis/jiv047. View

3.
Jartti T, Hasegawa K, Mansbach J, Piedra P, Camargo Jr C . Rhinovirus-induced bronchiolitis: Lack of association between virus genomic load and short-term outcomes. J Allergy Clin Immunol. 2015; 136(2):509-12.e11. PMC: 7173288. DOI: 10.1016/j.jaci.2015.02.021. View

4.
van Benten I, Koopman L, Niesters B, Hop W, van Middelkoop B, De Waal L . Predominance of rhinovirus in the nose of symptomatic and asymptomatic infants. Pediatr Allergy Immunol. 2003; 14(5):363-70. PMC: 7168036. DOI: 10.1034/j.1399-3038.2003.00064.x. View

5.
Levandowski R, Ou D, JACKSON G . Acute-phase decrease of T lymphocyte subsets in rhinovirus infection. J Infect Dis. 1986; 153(4):743-8. DOI: 10.1093/infdis/153.4.743. View