Evidence map›Paper›PMID 35465708›Full record

ArticleJournal of clinical microbiology2022

Evaluation of a Rapid and Accessible Reverse Transcription-Quantitative PCR Approach for SARS-CoV-2 Variant of Concern Identification.

Priscilla S-W Yeung, Hannah Wang, Mamdouh Sibai, Daniel Solis, Fumiko Yamamoto, Naomi Iwai, Becky Jiang, Nathan Hammond, Bernadette Truong, Selamawit Bihon and 9 more

Abstract read
In one paragraph

Article in Journal of clinical microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Sierra SARS-CoV-2 sequence and antiviral resistance analysis program.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2022
    Article
  11. Outpatient human coronavirus associated conjunctivitis in India.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2022
    Article
  12. Article
  13. Article
  14. A robust, highly multiplexed mass spectrometry assay to identify SARS-CoV-2 variants.medRxiv : the preprint server for health sciences · 2022
    Article
  15. Heterologous immunity induced by 1Frontiers in immunology · 2022
    Review
  16. 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

19 authors.

Priscilla S-W Yeung *Department of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Hannah Wang *Department of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.ORCID 0000-0002-3712-9188
Mamdouh SibaiDepartment of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Daniel SolisDepartment of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Fumiko YamamotoDepartment of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Naomi IwaiClinical Virology Laboratory, Stanford Health Care, Stanford, California, USA.
Becky JiangClinical Virology Laboratory, Stanford Health Care, Stanford, California, USA.
Nathan HammondClinical Genomics Laboratory, Stanford Health Care, Stanford, California, USA.
Bernadette TruongClinical Virology Laboratory, Stanford Health Care, Stanford, California, USA.
Selamawit BihonClinical Virology Laboratory, Stanford Health Care, Stanford, California, USA.
Suzette SantosClinical Virology Laboratory, Stanford Health Care, Stanford, California, USA.
Marilyn MarClinical Virology Laboratory, Stanford Health Care, Stanford, California, USA.
Claire MaiClinical Genomics Laboratory, Stanford Health Care, Stanford, California, USA.
Kenji O MfuhClinical Virology Laboratory, Stanford Health Care, Stanford, California, USA.
Jacob A MillerDepartment of Radiation Oncology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
ChunHong HuangDepartment of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Malaya K SahooDepartment of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
James L ZehnderDepartment of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Benjamin A PinskyDepartment of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.ORCID 0000-0001-8751-4810

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to distinguish between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) is of ongoing interest due to differences in transmissibility, responses to vaccination, clinical prognosis, and therapy. Although detailed genetic characterization requires whole-genome sequencing (WGS), targeted nucleic acid amplification tests can serve a complementary role in clinical settings, as they are more rapid and accessible than sequencing in most laboratories. We designed and analytically validated a two-reaction multiplex reverse transcription-quantitative PCR (RT-qPCR) assay targeting spike protein mutations L452R, E484K, and N501Y in reaction 1 and del69-70, K417N, and T478K in reaction 2. This assay had 95 to 100% agreement with WGS for 502 upper respiratory tract swab samples collected between 26 April 2021 and 1 August 2021, consisting of 43 Alpha, 2 Beta, 20 Gamma, 378 Delta, and 59 non-VOC infections. Validation in a separate group of 230 WGS-confirmed Omicron variant samples collected in December 2021 and January 2022 demonstrated 100% agreement. This RT-qPCR-based approach can be implemented in clinical laboratories already performing SARS-CoV-2 nucleic acid amplification tests to assist in local epidemiological surveillance and clinical decision-making.

Indexed as

COVID-19SARS-CoV-2HumansMultiplex Polymerase Chain ReactionMutationReal-Time Polymerase Chain ReactionReverse TranscriptionSpike Glycoprotein, CoronavirusSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19OmicronSARS-CoV-2variant

Identifiers

PMID35465708
PMCPMC9119066

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.