Evidence map›Paper›PMID 38668234›Full record

ArticlePathogens (Basel, Switzerland)2024

Whole-Genome Sequencing and Mutation Analyses of SARS-CoV-2 Isolates from Indonesia.

Sukma Oktavianthi, Aksar Chair Lages, Rinaldy Kusuma, Tri Shinta Kurniasih, Hidayat Trimarsanto, Febi Andriani, David Rustandi, Tandry Meriyanti, Irawan Yusuf, Safarina G Malik and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

1 citing paper in PubMed, 9 citations in OpenAlex.

  1. Comprehensive Review on Viral RNA Extraction Strategies for Enhanced Molecular Diagnostics.Interdisciplinary perspectives on infectious diseases · 2025
    Review
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 2 institutions in 2 countries.

Sukma OktavianthiMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.ORCID 0000-0002-5600-8111
Aksar Chair LagesMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.
Rinaldy KusumaMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.
Tri Shinta KurniasihMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.
Hidayat TrimarsantoEijkman Institute for Molecular Biology, Jakarta 10430, Indonesia.
Febi AndrianiMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.
David RustandiSiloam Hospital Lippo Village, Tangerang 15810, Indonesia.
Tandry MeriyantiSiloam Hospital Lippo Village, Tangerang 15810, Indonesia.
Irawan YusufMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.
Safarina G MalikMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.
Juandy JoMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.ORCID 0000-0002-5366-7605
Ivet SuriapranataMochtar Riady Institute for Nanotechnology, Tangerang 15810, Indonesia.
Eijkman Institute for Molecular Biology · IDPelita Harapan University · ID

Funding

Research and Innovation Consortium Program 2021 from the Ministry of Research and Technology/National Research and Innovation Agency, Republic of Indonesia N/AYayasan Mochtar Riady Nanotechnology Institute N/A
6 · The paper itself

Abstract

The SARS-CoV-2 infection that caused the COVID-19 pandemic has become a significant public health concern. New variants with distinct mutations have emerged, potentially impacting its infectivity, immune evasion capacity, and vaccine response. A whole-genome sequencing study of 292 SARS-CoV-2 isolates collected from selected regions of Indonesia between January and October 2021 was performed to identify the distribution of SARS-CoV-2 variants and common mutations in Indonesia. During January-April 2021, Indonesian lineages B.1.466.2 and B.1.470 dominated, but from May 2021, Delta's AY.23 lineage outcompeted them. An analysis of 7515 published sequences from January 2021 to June 2022 revealed a decline in Delta in November 2021, followed by the emergence of Omicron variants in December 2021. We identified C241T (5'UTR), P314L (NSP12b), F106F (NSP3), and D614G (Spike) mutations in all sequences. The other common substitutions included P681R (76.4%) and T478K (60%) in Spike, D377Y in Nucleocapsid (61%), and I82T in Membrane (60%) proteins. Breakthrough infection and prolonged viral shedding cases were associated with Delta variants carrying the Spike T19R, G142D, L452R, T478K, D614G, P681R, D950N, and V1264L mutations. The dynamic of SARS-CoV-2 variants in Indonesia highlights the importance of continuous genomic surveillance in monitoring and identifying potential strains leading to disease outbreaks.

Indexed as

COVID-19Genome, ViralMutationSARS-CoV-2Whole Genome SequencingHumansIndonesiaPhylogenySpike Glycoprotein, CoronavirusSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2genomic surveillancemutationSARS-CoV-2whole-genome sequencing

Identifiers

PMID38668234
PMCPMC11053823
OpenAlexW4393148295

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.