Evidence map›Paper›PMID 37189465›Full record

ArticleDiagnostics (Basel, Switzerland)2023

Multiplex RT Real-Time PCR Based on Target Failure to Detect and Identify Different Variants of SARS-CoV-2: A Feasible Method That Can Be Applied in Clinical Laboratories.

Van Hung Pham, Huong Thien Pham, Mario G Balzanelli, Pietro Distratis, Rita Lazzaro, Quoc Viet Nguyen, Viet Quoc Tran, Duy Khanh Tran, Luan Duy Phan, Sang Minh Pham and 13 more

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 36% 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, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  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

23 authors at 4 institutions in 2 countries.

Van Hung PhamDepartment of Microbiology, Phan Chau Trinh University, Dien Ban 550000, Vietnam.
Huong Thien PhamInternational Research Institute of Gene and Immunology, Ho Chi Minh City 700000, Vietnam.
Mario G BalzanelliSET-118, Department of Pre-Hospital and Emergency, SG Giuseppe Moscati Hospital, 74010 Taranto, Italy.
Pietro DistratisSET-118, Department of Pre-Hospital and Emergency, SG Giuseppe Moscati Hospital, 74010 Taranto, Italy.
Rita LazzaroSET-118, Department of Pre-Hospital and Emergency, SG Giuseppe Moscati Hospital, 74010 Taranto, Italy.
Quoc Viet NguyenNam Khoa Co., Ltd., Ho Chi Minh City 700000, Vietnam.ORCID 0009-0006-3981-0897
Viet Quoc TranNam Khoa Co., Ltd., Ho Chi Minh City 700000, Vietnam.
Duy Khanh TranNam Khoa Co., Ltd., Ho Chi Minh City 700000, Vietnam.ORCID 0000-0001-8773-3933
Luan Duy PhanNam Khoa Co., Ltd., Ho Chi Minh City 700000, Vietnam.
Sang Minh PhamNam Khoa Co., Ltd., Ho Chi Minh City 700000, Vietnam.
Binh Thai PhamNam Khoa Co., Ltd., Ho Chi Minh City 700000, Vietnam.
Chien Vo DucNguyen Tri Phuong Hospital, Ho Chi Minh City 700000, Vietnam.
Ha Minh NguyenNguyen Tri Phuong Hospital, Ho Chi Minh City 700000, Vietnam.ORCID 0000-0001-5125-1828
Dung Ngoc Thi NguyenHCMC Society of Medicine, Ho Chi Minh City 700000, Vietnam.
Ngoc Van TranHCMC Society of Medicine, Ho Chi Minh City 700000, Vietnam.
Son Truong PhamNew South Wales Health, Sydney 2065, Australia.ORCID 0000-0002-4206-1747
Camelia QueckFaculty of Medicine and Health, The University of Sydney, Sydney 2006, Australia.
Kieu Diem Cao NguyenDepartment of Interdisciplinary Medicine, Section of Dentistry, Microbiology and Virology, School of Medicine, University of Bari "Aldo Moro", 70121 Bari, Italy.
Francesco InchingoloDepartment of Interdisciplinary Medicine, Section of Dentistry, Microbiology and Virology, School of Medicine, University of Bari "Aldo Moro", 70121 Bari, Italy.ORCID 0000-0003-3797-5883
Raffaele Del PreteDepartment of Interdisciplinary Medicine, Section of Dentistry, Microbiology and Virology, School of Medicine, University of Bari "Aldo Moro", 70121 Bari, Italy.
Nam Hai Dinh NguyenDepartment of Microbiology, Phan Chau Trinh University, Dien Ban 550000, Vietnam.
Luigi SantacroceDepartment of Interdisciplinary Medicine, Section of Dentistry, Microbiology and Virology, School of Medicine, University of Bari "Aldo Moro", 70121 Bari, Italy.ORCID 0000-0001-5671-8124
Ciro Gargiulo IsaccoDepartment of Interdisciplinary Medicine, Section of Dentistry, Microbiology and Virology, School of Medicine, University of Bari "Aldo Moro", 70121 Bari, Italy.
University of Bari Aldo Moro · ITAzienda Ospedaliera S.Giuseppe Moscati · ITNew South Wales Department of Health · AUThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Shortly after its emergence, Omicron and its sub-variants have quickly replaced the Delta variant during the current COVID-19 outbreaks in Vietnam and around the world. To enable the rapid and timely detection of existing and future variants for epidemiological surveillance and diagnostic applications, a robust, economical real-time PCR method that can specifically and sensitively detect and identify multiple different circulating variants is needed. The principle of target- failure (TF) real-time PCR is simple. If a target contains a deletion mutation, then there is a mismatch with the primer or probe, and the real-time PCR will fail to amplify the target. In this study, we designed and evaluated a novel multiplex RT real-time PCR (MPL RT-rPCR) based on the principle of target failure to detect and identify different variants of SARS-CoV-2 directly from the nasopharyngeal swabs collected from COVID-19 suspected cases. The primers and probes were designed based on the specific deletion mutations of current circulating variants. To evaluate the results from the MPL RT-rPCR, this study also designed nine pairs of primers for amplifying and sequencing of nine fragments from the S gene containing mutations of known variants. We demonstrated that (i) our MPL RT-rPCR was able to accurately detect multiple variants that existed in a single sample; (ii) the limit of detection of the MPL RT-rPCR in the detection of the variants ranged from 1 to 10 copies for Omicron BA.2 and BA.5, and from 10 to 100 copies for Delta, Omicron BA.1, recombination of BA.1 and BA.2, and BA.4; (iii) between January and September 2022, Omicron BA.1 emerged and co-existed with the Delta variant during the early period, both of which were rapidly replaced by Omicron BA.2, and this was followed by Omicron BA.5 as the dominant variant toward the later period. Our results showed that SARS-CoV-2 variants rapidly evolved within a short period of time, proving the importance of a robust, economical, and easy-to-access method not just for epidemiological surveillance but also for diagnoses around the world where SARS-CoV-2 variants remain the WHO's highest health concern. Our highly sensitive and specific MPL RT-rPCR is considered suitable for further implementation in many laboratories, especially in developing countries.

Indexed as

Delta variantmultiplex reverse transcriptase real-time PCROmicron variantSARS-CoV-2target-failure real-time PCR

Identifiers

PMID37189465
PMCPMC10137618
OpenAlexW4362699067

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.