tetano
Editor, Senior Moderator
BMC Infect Dis
. 2024 Dec 18;24(1):1417.
doi: 10.1186/s12879-024-10296-1. Rapid detection of SARS-CoV-2 RNA using a one-step fast multiplex RT-PCR coupled to lateral flow immunoassay
Insaf Bel Hadj Ali[SUP] #[/SUP][SUP] 1 [/SUP], Hejer Souguir[SUP] #[/SUP][SUP] 2 [/SUP], Mouna Melliti[SUP] 2 [/SUP], Mohamed Vall Taleb Mohamed[SUP] 2 [/SUP], Monia Ardhaoui[SUP] 2 [/SUP], Kaouther Ayouni[SUP] 3 4 [/SUP], Sondes Haddad-Boubaker[SUP] 3 4 [/SUP], Yusr Saadi Ben Aoun[SUP] 2 [/SUP], Henda Triki[SUP] 3 4 [/SUP], Ikram Guizani[SUP] 2 [/SUP]
Affiliations
Background: The COVID-19 has put emphasis on pivotal needs for diagnosis and surveillance worldwide, with the subsequent shortage of diagnostic reagents and kits. Therefore, it has become strategic for the countries to access diagnostics, expand testing capacity, and develop their own diagnostic capabilities and alternative rapid accurate nucleic acid diagnostics that are at lower costs. Here, we propose a visual SARS-CoV-2 detection using a one-step fast multiplex reverse transcription-PCR (RT-PCR) amplification coupled to lateral flow immunoassay detection on a PCRD device (Abingdon Health, UK).
Methods: We developed various simplex fast-PCRs for screening sets of primer pairs newly designed or selected from literature or from validated WHO diagnostics, targeting S, N, E, RdRp or ORF1ab genes. We retained primers showing specific and stable amplification to assess for their suitability for detection on PCRD. Thus, fast RT-PCR amplifications were performed using the retained primers. They were doubly labeled with Fam and Biotin or Dig and Biotin to allow visual detection of the labeled amplicons on the lateral flow immunoassay PCR Detection (PCRD) device, looking at lack of interaction of the labeled primers (or primer dimers) with the test-lines in negative or no RNA controls. We set up all the assays using RNAs isolated from patients' nasopharyngeal swabs. We used two simplex assays, targeting two different viral genomic regions (N and E) and showing specific detection on PCRD, to set up a one-step fast multiplex RT-PCR assay (where both differently labeled primer pairs were engaged) coupled to amplicons' detection on a PCRD device. We evaluated this novel assay on 50 SARS-CoV-2 positive and 50 SARS-CoV-2 negative samples and compared its performance to the results of the quantitative RT-PCR (RT-qPCR) assays used for diagnosing the patients, here considered as the standard tests.
Results: The new assay achieved a sensitivity of 88% (44/50) and a specificity of 98% (49/50). All patients who presented Ct values lower than 33 were positive for our assay. Except for one patient, those with Ct values above 33 returned negative results.
Conclusion: Our results have brought proof of principle on the usefulness of the one-step fast multiplex RT- PCR assay coupled to PCRD as a new assay for specific, sensitive, and rapid detection of SARS-CoV-2 without requiring costly laboratory equipment, and thus, at reduced costs in a format prone to be deployed when resources are limited. This assay offers a viable alternative for COVID-19 diagnosis or screening at points of need.
Keywords: E gene; N gene; Lateral flow immunoassay on PCRD; Molecular diagnosis; One-step fast multiplex RT-PCR; SARS-CoV-2.
. 2024 Dec 18;24(1):1417.
doi: 10.1186/s12879-024-10296-1. Rapid detection of SARS-CoV-2 RNA using a one-step fast multiplex RT-PCR coupled to lateral flow immunoassay
Insaf Bel Hadj Ali[SUP] #[/SUP][SUP] 1 [/SUP], Hejer Souguir[SUP] #[/SUP][SUP] 2 [/SUP], Mouna Melliti[SUP] 2 [/SUP], Mohamed Vall Taleb Mohamed[SUP] 2 [/SUP], Monia Ardhaoui[SUP] 2 [/SUP], Kaouther Ayouni[SUP] 3 4 [/SUP], Sondes Haddad-Boubaker[SUP] 3 4 [/SUP], Yusr Saadi Ben Aoun[SUP] 2 [/SUP], Henda Triki[SUP] 3 4 [/SUP], Ikram Guizani[SUP] 2 [/SUP]
Affiliations
- PMID: 39695471
- DOI: 10.1186/s12879-024-10296-1
Background: The COVID-19 has put emphasis on pivotal needs for diagnosis and surveillance worldwide, with the subsequent shortage of diagnostic reagents and kits. Therefore, it has become strategic for the countries to access diagnostics, expand testing capacity, and develop their own diagnostic capabilities and alternative rapid accurate nucleic acid diagnostics that are at lower costs. Here, we propose a visual SARS-CoV-2 detection using a one-step fast multiplex reverse transcription-PCR (RT-PCR) amplification coupled to lateral flow immunoassay detection on a PCRD device (Abingdon Health, UK).
Methods: We developed various simplex fast-PCRs for screening sets of primer pairs newly designed or selected from literature or from validated WHO diagnostics, targeting S, N, E, RdRp or ORF1ab genes. We retained primers showing specific and stable amplification to assess for their suitability for detection on PCRD. Thus, fast RT-PCR amplifications were performed using the retained primers. They were doubly labeled with Fam and Biotin or Dig and Biotin to allow visual detection of the labeled amplicons on the lateral flow immunoassay PCR Detection (PCRD) device, looking at lack of interaction of the labeled primers (or primer dimers) with the test-lines in negative or no RNA controls. We set up all the assays using RNAs isolated from patients' nasopharyngeal swabs. We used two simplex assays, targeting two different viral genomic regions (N and E) and showing specific detection on PCRD, to set up a one-step fast multiplex RT-PCR assay (where both differently labeled primer pairs were engaged) coupled to amplicons' detection on a PCRD device. We evaluated this novel assay on 50 SARS-CoV-2 positive and 50 SARS-CoV-2 negative samples and compared its performance to the results of the quantitative RT-PCR (RT-qPCR) assays used for diagnosing the patients, here considered as the standard tests.
Results: The new assay achieved a sensitivity of 88% (44/50) and a specificity of 98% (49/50). All patients who presented Ct values lower than 33 were positive for our assay. Except for one patient, those with Ct values above 33 returned negative results.
Conclusion: Our results have brought proof of principle on the usefulness of the one-step fast multiplex RT- PCR assay coupled to PCRD as a new assay for specific, sensitive, and rapid detection of SARS-CoV-2 without requiring costly laboratory equipment, and thus, at reduced costs in a format prone to be deployed when resources are limited. This assay offers a viable alternative for COVID-19 diagnosis or screening at points of need.
Keywords: E gene; N gene; Lateral flow immunoassay on PCRD; Molecular diagnosis; One-step fast multiplex RT-PCR; SARS-CoV-2.