Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 May 13;8(5):731.
doi: 10.3390/microorganisms8050731.

Nasal Microbiota in RSV Bronchiolitis

Affiliations

Nasal Microbiota in RSV Bronchiolitis

Serena Schippa et al. Microorganisms. .

Abstract

Respiratory Syncytial Virus (RSV) is the leading cause of bronchiolitis, and the severity may be influenced by the bacterial ecosystem. Our aim was to analyze the nasal microbiota from 48 infants affected by bronchiolitis from RSV virus and 28 infants with bronchiolitis but negative for the virus. Results showed a significantly lower biodiversity in the RSV-positive group with respect to the RSV-negative group, a specific microbial profile associated with the RSV-positive group different from that observed in the negative group, and significant modifications in the relative abundance of taxa in the RSV-positive group, as well as in the RSV-A group, with respect to the negative group. Furthermore, microbial network analyses evidenced, in all studied groups, the presence of two predominant sub-networks characterized by peculiar inter- and intra-group correlation patterns as well as a general loss of connectivity among microbes in the RSV-positive group, particularly in the RSV-A group. Our results indicated that infants with more severe bronchiolitis disease, caused by RSV-A infection, present significant perturbations of both the nasal microbiota structure and the microbial relationships. Patients with a milder bronchiolitis course (RSV-B-infected and patients who have cleared the virus) presented less severe alterations.

Keywords: biodiversity; bronchiolitis; discriminant species; microbe interactions; microbial networks analyses; microbiota; respiratory syncytial virus; taxa abundance.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Analysis of microbial biodiversity. (a) Evaluation of Shannon index, Simpson index, and number of observed OTUs among groups. P values assessing statistical significance were also reported. (b) PCoA analysis performed for β diversity based on the Bray–Curtis measure of dissimilarity. For each principal coordinate, the percentage of variance explained is reported between parentheses.
Figure 2
Figure 2
Color-coded bar plot showing the average distribution of bacterial taxa at phylum, genus, and species level across different groups. Only taxa for which a mean relative abundance ≥0.5% was determined in at least one group are shown. Taxa are sorted in ascending order with respect to their mean relative abundance in the Vneg group.
Figure 3
Figure 3
Color-coded bar plot showing differential abundance analysis at genus and species levels performed by Mann–Whitney U tests. * p value ≤ 0.05.
Figure 4
Figure 4
Co-occurrence network analysis. Graphical representations of (a) virus-negative and (b) RSVpos networks, computed at species level performed on taxa with a mean relative abundance ≥0.5% in at least one group. The thickness of edges represents the level of association between taxa based on the SparCC score. The size of nodes is proportional to the number of edges departing from the node, indicating its degree of interaction.

References

    1. Piedra P.A., Mansbach J.M., Teach S.J., Sullivan A.F., Forgey T., Clark S., Espinola J.A., Camargo C.A. for the MARC-30 investigators prospective multicenter study of viral etiology and hospital length of stay in children with severe bronchiolitis. Arch. Pediatr. Adolesc. Med. 2012;166:700–706. doi: 10.1001/archpediatrics.2011.1669. - DOI - PMC - PubMed
    1. Midulla F., Nenna R., Scagnolari C., Petrarca L., Frassanito A., Viscido A., Arima S., Antonelli G., Pierangeli A. How respiratory syncytial virus genotypes influence the clinical course in infants hospitalized for bronchiolitis. J. Infect. Dis. 2018;219:526–534. doi: 10.1093/infdis/jiy496. - DOI - PubMed
    1. Biesbroek G., Tsivtsivadze E., Sanders E.A.M., Montijn R., Veenhoven R.H., Keijser B.J.F., Bogaert D. Early respiratory microbiota composition determines bacterial succession patterns and respiratory health in children. Am. J. Respir. Crit. Care Med. 2014;190:1283–1292. doi: 10.1164/rccm.201407-1240OC. - DOI - PubMed
    1. Teo S.M., Mok D., Pham K., Kusel M., Serralha M., Troy N., Holt B.J., Hales B.J., Walker M.L., Hollams E., et al. The infant nasopharyngeal microbiome impacts severity of lower respiratory infection and risk of asthma development. Cell Host Microbe. 2015;17:704–715. doi: 10.1016/j.chom.2015.03.008. - DOI - PMC - PubMed
    1. Hyde E.R., Petrosino J.F., Piedra P.A., Camargo C.A., Espinola J.A., Mansbach J.M. Nasopharyngeal proteobacteria are associated with viral etiology and acute wheezing in children with severe bronchiolitis. J. Allergy Clin. Immunol. 2013;133:1220–1222. doi: 10.1016/j.jaci.2013.10.049. - DOI - PMC - PubMed

LinkOut - more resources