RT-LAMP in SARS-CoV-2 detection: point to improve primer designing and decrease molecular diagnosis pitfalls.

CT scan Data mining RT-LAMP RT-qPCR SARS-CoV-2 detection

Journal

Expert review of molecular diagnostics
ISSN: 1744-8352
Titre abrégé: Expert Rev Mol Diagn
Pays: England
ID NLM: 101120777

Informations de publication

Date de publication:
31 Oct 2022
Historique:
pubmed: 19 10 2022
medline: 19 10 2022
entrez: 18 10 2022
Statut: aheadofprint

Résumé

Due to the high transmission rate of SARS-CoV-2, diagnostic tests have become tools for identifying patients. The key points were the virus genomes survey to design RT-LAMP primers; comparing the sensitivity and specificity of RT-LAMP and RT-qPCR; and determining the relationship among clinical symptoms, CT scan, RT-qPCR, and RT-LAMP results. This cohort study included 444 symptomatic patients. The specificity and sensitivity of RT-LAMP were assayed. The five statistical models, simultaneously, by RapidMiner to find the best method for detecting the virus were done through the correlation between the clinical symptoms, RT-LAMP, RT-qPCR, and CT scan results. The chi-square test by SPSS 26.0 was used to calculate kappa agreement. The virus genome was detected in all the positive samples (198) by RT-qPCR and RT-LAMP. In addition, 246 samples were negative by RT-qPCR, while 88 were positive by RT-LAMP. Data mining analysis indicated that there were most associations between the RT-LAMP and CT scan data compared to RT-qPCR and CT scan data. RT-LAMP could detect SARS-CoV-2 with great simplicity, speed, and cheapness. Therefore, it is logical to screen, a large number of patients by RT-LAMP, and then RT-qPCR can be used on the limited samples.

Sections du résumé

BACKGROUND UNASSIGNED
Due to the high transmission rate of SARS-CoV-2, diagnostic tests have become tools for identifying patients. The key points were the virus genomes survey to design RT-LAMP primers; comparing the sensitivity and specificity of RT-LAMP and RT-qPCR; and determining the relationship among clinical symptoms, CT scan, RT-qPCR, and RT-LAMP results.
METHODS UNASSIGNED
This cohort study included 444 symptomatic patients. The specificity and sensitivity of RT-LAMP were assayed. The five statistical models, simultaneously, by RapidMiner to find the best method for detecting the virus were done through the correlation between the clinical symptoms, RT-LAMP, RT-qPCR, and CT scan results. The chi-square test by SPSS 26.0 was used to calculate kappa agreement.
RESULTS UNASSIGNED
The virus genome was detected in all the positive samples (198) by RT-qPCR and RT-LAMP. In addition, 246 samples were negative by RT-qPCR, while 88 were positive by RT-LAMP. Data mining analysis indicated that there were most associations between the RT-LAMP and CT scan data compared to RT-qPCR and CT scan data.
CONCLUSIONS UNASSIGNED
RT-LAMP could detect SARS-CoV-2 with great simplicity, speed, and cheapness. Therefore, it is logical to screen, a large number of patients by RT-LAMP, and then RT-qPCR can be used on the limited samples.

Identifiants

pubmed: 36254603
doi: 10.1080/14737159.2022.2136991
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-9

Auteurs

Hossein Teimouri (H)

Laboratory Sciences Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

Maryam Rahimi (M)

Department of Horticulture, University of Zabol, Zabol, Iran.

Mahdeih Taheri (M)

Department of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.

Alijan Tabarraei (A)

Department of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.

Majid Shahbazi (M)

Medical Cellular and Molecular Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

Shahriar Omidvar (S)

Department of Biotechnology, Vision Daru Farmod, Tehran, Iran.

Naeme Javid (N)

Department of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.

Abdolreza Fazel (A)

Cancer Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

Mohammad Reza Honarvar (MR)

Nutrition Science, Health Management and Social Development Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

Gholamreza Roshandel (G)

Golestan Research Center of Gastroenterology and Hepatology, Golestan University of Medical Sciences, Gorgan, Iran.

Nafiseh Abdollahi (N)

Golestan Rheumatology Research Center, Golestan University of Medical Science, Gorgan, Iran.

Ahad Yamchi (A)

Department of Biotechnology, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran.

Hadi Razavi Nikoo (H)

Laboratory Sciences Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Department of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Infectious Diseases Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

Classifications MeSH