Evidence map›Paper›PMID 36319880›Full record

ArticleBiotechnology letters2022

A gold nanoparticles-based lateral flow assay utilizing baculovirus expressed recombinant nucleocapsid and receptor binding domain proteins for serodetection of IgG and IgM against SARS-CoV-2.

Reda Salem, Amany M Elshamy, Noha Kamel, Soha Younes, Ohoud M Marie, Fatma R Waly, Alaa A El-Kholy, Wael Elmenofy

Open access · hybridAbstract read
In one paragraph

Article in Biotechnology letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

8 authors at 4 institutions in 1 country.

Reda SalemAgricultural Genetic Engineering Research Institute (AGERI), ARC, Giza, 12619, Egypt.ORCID https://orcid.org/0000-0001-8579-0328
Amany M ElshamyMedical Laboratory Science Department, High Technology Institute of Applied Health Sciences, Badr Academy, Badr City, Cairo, Egypt.
Noha KamelClinical Pathology Department, Faculty of Medicine, Suez Canal University, 4.5 K, Ring Road, Ismailia, 41511, Egypt. noha_mohamed@med.suez.edu.eg.ORCID http://orcid.org/0000-0002-8990-2312
Soha YounesClinical Pathology Department, Faculty of Medicine, Suez Canal University, 4.5 K, Ring Road, Ismailia, 41511, Egypt.
Ohoud M MarieChemistry Department, Faculty of Science, Suez Canal University, Ismailia, 41516, Egypt.
Fatma R WalyAgricultural Genetic Engineering Research Institute (AGERI), ARC, Giza, 12619, Egypt.
Alaa A El-KholyVeterinary Sera and Vaccines Research Institute (VSVRI), ARC, Abbassia, P.O. Box # 131, Cairo, 11381, Egypt.
Wael ElmenofyAgricultural Genetic Engineering Research Institute (AGERI), ARC, Giza, 12619, Egypt.
Agricultural Genetic Engineering Research Institute · EGSuez Canal University · EGBadr University in Cairo · EGVeterinary Serum and Vaccine Research Institute · EG

Funding

Science, technology and innovation funding authority 43798
6 · The paper itself

Abstract

Serological assays for SARS-CoV-2 are being utilized at an exponential rate for surveillance programs. This enterprise was designed to develop and validate a qualitative immunochromatographic test, via the Lateral Flow Assay (LFA), for detection of immunoglobulins M and G (IgM and IgG) against both nucleocapsid (N) and the receptor-binding domain (RBD) of the spike protein of SARS-CoV-2. Both targeted proteins were cloned and expressed in baculovirus expression system utilizing insect cells Sf9. The recombinant RBD and N proteins were purified and conjugated with gold nanoparticles (AuNPs) to set up the coating antigens pad. Both anti-human IgG and IgM were dispensed on nitrocellulose membrane to capture human antibodies in serum samples. A home-made dispensing system was developed to draw identical test and control lines. The validity of the developed LFA was verified by testing serum samples from 103 convalescent COVID-19 patients who were PCR positive for SARS-CoV-2 along with 28 control serum samples. The developed strips showed distinctive bands for IgM and IgG of both proteins (RBD and N) in positive samples. The sensitivity of RBD-based LFA was 70.9% and 39.8% for IgG and IgM, respectively, with a specificity of 100% for both. The N-based LFA exhibited a sensitivity of 73.8% and 35.9% for IgG and IgM, respectively, while its specificity was 75% and 100% for IgG and IgM, respectively. Our developed LFA could afford a tool for surveillance programs in low-resource countries. Moreover, it might be functional for rapid and inexpensive monitoring of the anti-SARS-CoV-2 antibodies in the sera of vaccinated individuals.

Indexed as

COVID-19Metal NanoparticlesBaculoviridaeCarrier ProteinsGoldHumansImmunoglobulin GImmunoglobulin MNucleocapsidSARS-CoV-2Spike Glycoprotein, CoronavirusCarrier ProteinsGoldImmunoglobulin GImmunoglobulin MSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19Lateral flow assayNucleocapsidRBDSARS-CoV-2

Identifiers

PMID36319880
PMCPMC9628349
OpenAlexW4308042261

What OpenQuestion holds

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LicenceCC BY
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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.