RNA sequence analysis of nasopharyngeal swabs from asymptomatic and mildly symptomatic patients with COVID-19.


Journal

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
ISSN: 1878-3511
Titre abrégé: Int J Infect Dis
Pays: Canada
ID NLM: 9610933

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 29 12 2021
revised: 24 05 2022
accepted: 21 06 2022
pubmed: 28 6 2022
medline: 9 9 2022
entrez: 27 6 2022
Statut: ppublish

Résumé

The characterization of asymptomatic and mildly symptomatic patients with COVID-19 by observing changes in gene expression profile and possible bacterial coinfection is relevant to be investigated. We aimed to identify transcriptomic and coinfection profiles in both groups of patients. A ribonucleic acid (RNA) sequence analysis on nasopharyngeal swabs were performed using a shotgun sequencing pipeline. Differential gene analysis, viral genome assembly, and metagenomics analysis were further performed using the retrieved data. Both groups of patients underwent a cilia modification and mRNA splicing. Modulations in macroautophagy, epigenetics, and cell cycle processes were observed specifically in the asymptomatic group. Modulation in the RNA transport was found specifically in the mildly symptomatic group. The mildly symptomatic group showed modulation in the RNA transport and upregulation of autophagy regulator genes and genes in the complement system. No link between viral variants and disease severity was found. Microbiome analysis revealed the elevation of Streptococcus pneumoniae and Veillonella parvula proportion in symptomatic patients. A reduction in the autophagy influx and modification in the epigenetic profile might be involved in halting the disease progression. A global dysregulation of RNA processing and translation might cause more severe outcomes in symptomatic individuals. Coinfection by opportunistic microflora should be taken into account when assessing the possible outcome of SARS-CoV-2 infection.

Identifiants

pubmed: 35760384
pii: S1201-9712(22)00368-X
doi: 10.1016/j.ijid.2022.06.035
pmc: PMC9233886
pii:
doi:

Substances chimiques

RNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

449-460

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have no competing interests to declare.

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Auteurs

Miftahul Faridl (M)

School of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.

Karlina Mellyani (K)

School of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.

Karimatu Khoirunnisa (K)

School of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.

Popi Septiani (P)

School of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.

Ernawati Arifin Giri-Rachman (EA)

School of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.

Husna Nugrahapraja (H)

School of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.

Ema Rahmawati (E)

West Java Health Laboratory, Bandung, West Java, Indonesia.

Cut Nur Cinthia Alamanda (CNC)

West Java Health Laboratory, Bandung, West Java, Indonesia.

Ryan Bayusantika Ristandi (RB)

West Java Health Laboratory, Bandung, West Java, Indonesia.

Rifky Walujayati Rachman (RW)

West Java Health Laboratory, Bandung, West Java, Indonesia.

Rini Robiani (R)

West Java Health Laboratory, Bandung, West Java, Indonesia.

Azzania Fibriani (A)

School of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia. Electronic address: afibriani@sith.itb.ac.id.

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