Evidence map›Paper›PMID 37626187›Full record

ArticleApplied microbiology and biotechnology2023

A Cas12a-based fluorescent microfluidic system for rapid on-site human papillomavirus diagnostics.

Baicheng Huang, Yufeng Lou, Zihan Zeng, Xingchi Kan, Xinping Shi, Yue Wu, Ling Guo, Muzhen Wang, Xingxu Huang, Xuemei Tian and 1 more

Abstract read
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In one paragraph

Article in Applied microbiology and biotechnology, 2023. 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
1.2field-weighted citation impact, top 20% 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, 8 citations in OpenAlex.

  1. Review
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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

11 authors at 5 institutions in 1 country.

Baicheng HuangZhejiang Laboratory, Hangzhou, China.
Yufeng LouDepartment of Laboratory Medicine, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zihan ZengZhejiang Laboratory, Hangzhou, China.
Xingchi KanZhejiang Laboratory, Hangzhou, China.
Xinping ShiDepartment of Laboratory Medicine, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Yue WuZhejiang Laboratory, Hangzhou, China.
Ling GuoZhejiang Laboratory, Hangzhou, China.
Muzhen WangSchool of Life Sciences, South China Normal University, Guangzhou, China.
Xingxu HuangZhejiang Laboratory, Hangzhou, China.
Xuemei TianSchool of Life Sciences, South China Normal University, Guangzhou, China. xmtian69@163.com.
Xinjie WangShenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, China. wangxinjie@caas.cn.ORCID http://orcid.org/0000-0002-1882-7845
Zhejiang Lab · CNSouth China Normal University · CNAgricultural Genomics Institute at Shenzhen · CNFirst Affiliated Hospital Zhejiang University · CNTongde Hospital of Zhejiang Province · CN

Funding

Key Research Project of Zhejiang Laboratory 2021PE0AC06National Natural Science Foundation of China 81772533National Natural Science Foundation of China 82002144Shanghai Municipal Science and Technology Commission 21N31900400
6 · The paper itself

Abstract

Persistent infection with human papillomavirus (HPV) is the leading cause of cervical cancer, and early diagnosis is crucial for clinical management. However, the easy and rapid on-site diagnostic for HPV genotyping remains challenging. Here, we develop a Cas12a-based fluorescent microfluidic detection system for diagnosing six HPV subtypes (HPV6, HPV11, HPV16, HPV18, HPV31, and HPV33). A panel of crRNAs and recombinase polymerase amplification (RPA) primers targeting the HPV L1 gene was screened for sensitive and specific detection. Furthermore, a one-pot RPA reaction was developed to amplify the six HPV subtypes without cross-reactivity. For on-site detection, we integrated the RPA-Cas12a detection into a microfluidic device, enabling the detection of processed clinical samples within 35 minutes. The assay was validated using 112 clinical swab samples and obtained consistent results with the qPCR assay, with a concordance rate of 99.1%. Overall, our diagnostic method offers a rapid, sensitive, and easy-to-use on-site assay for detecting HPV genotypes and holds promise for improving cervical cancer screening and prevention. KEY POINTS: • The Cas12a-based fluorescent microfluidic detection system for the diagnosis of six HPV subtypes. • A one-pot RPA reaction for amplifying the six HPV subtypes without cross-reactivity. • The RPA-Cas12a-microfluidic system provides results within 35 minutes for on-site detection.

Indexed as

Bacterial ProteinsCRISPR-Associated ProteinsEndodeoxyribonucleasesLab-On-A-Chip DevicesMicrofluidicsMolecular Diagnostic TechniquesPapillomaviridaePapillomavirus InfectionsFemaleFluorescenceGenotypeHuman Papillomavirus VirusesHumansNucleic Acid Amplification TechniquesRecombinasesSensitivity and SpecificityBacterial ProteinsCas12a proteinCRISPR-Associated ProteinsEndodeoxyribonucleasesRecombinasesCas12aDiagnosticHuman papillomavirusMicrofluidicsRecombinase polymerase amplification

Identifiers

PMID37626187
OpenAlexW4386188131

What OpenQuestion holds

Textmetadata
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.