Evidence map›Paper›PMID 35760384›Full record

ArticleInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2022

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

Miftahul Faridl, Karlina Mellyani, Karimatu Khoirunnisa, Popi Septiani, Ernawati Arifin Giri-Rachman, Husna Nugrahapraja, Ema Rahmawati, Cut Nur Cinthia Alamanda, Ryan Bayusantika Ristandi, Rifky Walujayati Rachman and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Miftahul FaridlSchool of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.
Karlina MellyaniSchool of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.
Karimatu KhoirunnisaSchool of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.
Popi SeptianiSchool of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.
Ernawati Arifin Giri-RachmanSchool of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.
Husna NugrahaprajaSchool of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia.
Ema RahmawatiWest Java Health Laboratory, Bandung, West Java, Indonesia.
Cut Nur Cinthia AlamandaWest Java Health Laboratory, Bandung, West Java, Indonesia.
Ryan Bayusantika RistandiWest Java Health Laboratory, Bandung, West Java, Indonesia.
Rifky Walujayati RachmanWest Java Health Laboratory, Bandung, West Java, Indonesia.
Rini RobianiWest Java Health Laboratory, Bandung, West Java, Indonesia.
Azzania FibrianiSchool of Life Sciences and Technology, Bandung Institute of Technology, Bandung, West Java, Indonesia. Electronic address: afibriani@sith.itb.ac.id.
Bandung Institute of Technology · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe 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.

methodsA 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.

resultsBoth 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.

conclusionA 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.

Indexed as

CoinfectionCOVID-19HumansNasopharynxRNA, ViralSARS-CoV-2Sequence AnalysisSequence Analysis, RNARNA, ViralCOVID-19Differential gene expressionGene ontologySARS-CoV-2Transcriptomics

Identifiers

PMID35760384
PMCPMC9233886
OpenAlexW4283519889

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.