Evidence map›Paper›PMID 39724215›Full record

ArticlePloS one2024

A cell-based Papain-like Protease (PLpro) activity assay for rapid detection of active SARS-CoV-2 infections and antivirals.

Anahi G Jimenez-Campos, Lucas I Maestas, Nileena Velappan, Brian Beck, Chunyan Ye, Keith Wernsing, Yaniksa Mata-Solis, William J Bruno, Silas C Bussmann, Steven Bradfute and 2 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Anahi G Jimenez-CamposUniversity of New Mexico Health Sciences Center, Department of Emergency Medicine, Albuquerque, New Mexico, United States of America.
Lucas I MaestasUniversity of New Mexico Health Sciences Center, Department of Emergency Medicine, Albuquerque, New Mexico, United States of America.
Nileena VelappanLos Alamos National Laboratory, Los Alamos, NM, United States of America.
Brian BeckMicroBiologics, St. Cloud, MN, United States of America.
Chunyan YeHealth Science Center, Center for Global Health and Department of Internal Medicine, University of New Mexico, Albuquerque, New Mexico, United States of America.
Keith WernsingMesa Photonics, Santa Fe, NM, United States of America.
Yaniksa Mata-SolisMesa Photonics, Santa Fe, NM, United States of America.
William J BrunoSciTransTech, Santa Fe, NM, United States of America.
Silas C BussmannUniversity of New Mexico Health Sciences Center, Department of Emergency Medicine, Albuquerque, New Mexico, United States of America.ORCID 0000-0001-9740-4260
Steven BradfuteHealth Science Center, Center for Global Health and Department of Internal Medicine, University of New Mexico, Albuquerque, New Mexico, United States of America.
Justin T BacaUniversity of New Mexico Health Sciences Center, Department of Emergency Medicine, Albuquerque, New Mexico, United States of America.ORCID 0000-0002-9335-5200
Frauke H RininslandMesa Photonics, Santa Fe, NM, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its variants are a continuous threat to human life. An urgent need remains for simple and fast tests that reliably detect active infections with SARS-CoV-2 and its variants in the early stage of infection. Here we introduce a simple and rapid activity-based diagnostic (ABDx) test that identifies SARS-CoV-2 infections by measuring the activity of a viral enzyme, Papain-Like protease (PLpro). The test system consists of a peptide that fluoresces when cleaved by SARS PLpro that is active in crude, unprocessed lysates from human tongue scrapes and saliva. Test results are obtained in 30 minutes or less using widely available fluorescence plate readers, or a battery-operated portable instrument for on-site testing. Proof-of-concept was obtained in a study on clinical specimens collected from patients with COVID-19 like symptoms who tested positive (n = 10) or negative (n = 10) with LIAT RT-PCR using nasal mid turbinate swabs. When saliva from these patients was tested with in-house endpoint RT-PCR, 17 were positive and only 5 specimens were negative, of which 2 became positive when tested 5 days later. PLpro activity correlated in 17 of these cases (3 out of 3 negatives and 14 out of 16 positives, with one invalid specimen). Despite the small number of samples, the agreement was significant (p value = 0.01). Two false negatives were detected, one from a sample with a late Ct value of 35 in diagnostic RT-PCR, indicating that an active infection was no longer present. The PLpro assay is easily scalable and expected to detect all viable SARS-CoV-2 variants, making it attractive as a screening and surveillance tool. Additionally, we show feasibility of the platform as a new homogeneous phenotypic assay for rapid screening of SARS-CoV-2 antiviral drugs and neutralizing antibodies.

Indexed as

Antiviral AgentsCOVID-19SARS-CoV-2Coronavirus Papain-Like ProteasesHumansSalivaAntiviral AgentsCoronavirus Papain-Like Proteasespapain-like protease, SARS-CoV-2

Identifiers

PMID39724215
PMCPMC11670956

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.