Empowering the on-site detection of nucleic acids by integrating CRISPR and digital signal processing.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
25 Jul 2024
Historique:
received: 29 12 2023
accepted: 15 07 2024
medline: 26 7 2024
pubmed: 26 7 2024
entrez: 25 7 2024
Statut: epublish

Résumé

Addressing the global disparity in cancer care necessitates the development of rapid and affordable nucleic acid (NA) testing technologies. This need is particularly critical for cervical cancer, where molecular detection of human papillomavirus (HPV) has emerged as an accurate screening method. However, implementing this transition in low- and middle-income countries has been challenging due to the high costs and centralized facilities required for current NA tests. Here, we present CreDiT (CRISPR Enhanced Digital Testing) for on-site NA detection. The CreDiT platform integrates i) a one-pot CRISPR strategy that simultaneously amplifies both target NAs and analytical signals and ii) a robust fluorescent detection based on digital communication (encoding/decoding) technology. These features enable a rapid assay (<35 minutes) in a single streamlined workflow. We demonstrate the sensitive detection of cell-derived HPV DNA targets down to single copies and accurate identification of HPV types in clinical cervical brushing specimens (n = 121).

Identifiants

pubmed: 39054353
doi: 10.1038/s41467-024-50588-3
pii: 10.1038/s41467-024-50588-3
doi:

Substances chimiques

DNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6271

Subventions

Organisme : U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI)
ID : 5R25CA174650

Informations de copyright

© 2024. The Author(s).

Références

Randall, T. C. & Ghebre, R. Challenges in prevention and care delivery for women with cervical cancer in sub-Saharan Africa. Front. Oncol. 6, 160 (2016).
doi: 10.3389/fonc.2016.00160 pubmed: 27446806 pmcid: 4923066
Montealegre, J. R. et al. Racial/ethnic differences in HPV 16/18 genotypes and integration status among women with a history of cytological abnormalities. Gynecol. Oncol. 148, 357–362 (2018).
doi: 10.1016/j.ygyno.2017.12.014 pubmed: 29276057
Islami, F., Fedewa, S. A. & Jemal, A. Trends in cervical cancer incidence rates by age, race/ethnicity, histological subtype, and stage at diagnosis in the United States. Prev. Med. 123, 316–323 (2019).
doi: 10.1016/j.ypmed.2019.04.010 pubmed: 31002830
Sankaranarayanan, R. et al. HPV screening for cervical cancer in rural India. N. Engl. J. Med. 360, 1385–1394 (2009).
doi: 10.1056/NEJMoa0808516 pubmed: 19339719
Castle, P. E. et al. Reliability of the Xpert HPV assay to detect high-risk human papillomavirus DNA in a colposcopy referral population. Am. J. Clin. Pathol 143, 126–133 (2015).
doi: 10.1309/AJCP4Q0NSDHWIZGU pubmed: 25511151
Zhang, J. et al. Effectiveness of high-risk human papillomavirus testing for cervical cancer screening in China: a multicenter, open-label, randomized clinical trial. JAMA Oncol. 7, 263–270 (2021).
doi: 10.1001/jamaoncol.2020.6575 pubmed: 33377903
Goel, A. et al. Visual inspection of the cervix with acetic acid for cervical intraepithelial lesions. Int. J. Gynaecol. Obstet. 88, 25–30 (2005).
doi: 10.1016/j.ijgo.2004.09.018 pubmed: 15617701
Hegde, D., Shetty, H., Shetty, P. K. & Rai, S. Diagnostic value of acetic acid comparing with conventional Pap smear in the detection of colposcopic biopsy-proved CIN. J. Cancer Res. Ther. 7, 454–458 (2011).
doi: 10.4103/0973-1482.92019 pubmed: 22269409
Lee, C. Y. et al. Development of integrated systems for on-site infection detection. Acc. Chem. Res. 54, 3991–4000 (2021).
doi: 10.1021/acs.accounts.1c00498 pubmed: 34677927 pmcid: 9099220
Aman, R., Mahas, A. & Mahfouz, M. Nucleic acid detection using CRISPR/Cas biosensing technologies. ACS Synth. Biol. 9, 1226–1233 (2020).
doi: 10.1021/acssynbio.9b00507 pubmed: 32159950
Kaminski, M. M., Abudayyeh, O. O., Gootenberg, J. S., Zhang, F. & Collins, J. J. CRISPR-based diagnostics. Nat. Biomed. Eng. 5, 643–656 (2021).
doi: 10.1038/s41551-021-00760-7 pubmed: 34272525
Grove, A. C. An introduction to Walsh functions and their applications. Int. J. Math. Educ. Sci. Technol. 14, 43–53 (1983).
doi: 10.1080/0020739830140107
Stoffer, D. S. Walsh-Fourier analysis and its statistical applications. J. Am. Stat. Assoc. 86, 461–479 (1991).
Wei, F. et al. Epidemiology of anal human papillomavirus infection and high-grade squamous intraepithelial lesions in 29,900 men according to HIV status, sexuality, and age: a collaborative pooled analysis of 64 studies. Lancet HIV 8, e531–e543 (2021).
doi: 10.1016/S2352-3018(21)00108-9 pubmed: 34339628 pmcid: 8408042
Marra, E., Lin, C. & Clifford, G. M. Type-specific anal human papillomavirus prevalence among men, according to sexual preference and HIV status: a systematic literature review and meta-analysis. J. Infect. Dis. 219, 590–598 (2019).
doi: 10.1093/infdis/jiy556 pubmed: 30239749
Ding, X. et al. Ultrasensitive and visual detection of SARS-CoV-2 using all-in-one dual CRISPR-Cas12a assay. Nat. Commun. 11, 4711 (2020).
doi: 10.1038/s41467-020-18575-6 pubmed: 32948757 pmcid: 7501862
Lee, C. Y. et al. Fluorescence polarization system for rapid COVID-19 diagnosis. Biosens. Bioelectron. 178, 113049 (2021).
doi: 10.1016/j.bios.2021.113049 pubmed: 33540323 pmcid: 7846465
Beauchamp, K. G. Applications of Walsh and Related Functions, with an Introduction to Sequency Theory (Academic Press, 1984).
Deb, A., Sen, S. K. & Datta, A. K. Walsh functions and their applications: a review. IETE Tech. Rev. 9, 238–252 (1992).
doi: 10.1080/02564602.1992.11438882
Ahmed, N. & Rao, K. R. Orthogonal Transforms for Digital Signal Processing (Springer Science & Business Media, 2012).
Beer, T. Walsh transforms. Am. J. Phys. 49, 466–472 (1981).
doi: 10.1119/1.12714
Chawla, P. & Singh, B. Role of Walsh Codes and pseudorandom noise sequences in CDMA. In 2014 IEEE International Conference on Industrial Engineering and Engineering Management (IEEE, 2014).
Ho, N. R. Y. et al. Visual and modular detection of pathogen nucleic acids with enzyme-DNA molecular complexes. Nat. Commun. 9, 3238 (2018).
doi: 10.1038/s41467-018-05733-0 pubmed: 30104566 pmcid: 6089962
Pathania, D. et al. Point-of-care cervical cancer screening using deep learning-based microholography. Theranostics 9, 8438–8447 (2019).
doi: 10.7150/thno.37187 pubmed: 31879529 pmcid: 6924258
Gustinucci, D. et al. Use of cytology, E6/E7 mRNA, and p16INK4a-Ki-67 to define the management of human papillomavirus (HPV)-positive women in cervical cancer screening. Am. J. Clin. Pathol. 145, 35–45 (2016).
doi: 10.1093/ajcp/aqv019 pubmed: 26712869
de Martel, C., Plummer, M., Vignat, J. & Franceschi, S. Worldwide burden of cancer attributable to HPV by site, country and HPV type. Int. J. Cancer 141, 664–670 (2017).
doi: 10.1002/ijc.30716 pubmed: 28369882 pmcid: 5520228
Lin, C., Franceschi, S. & Clifford, G. M. Human papillomavirus types from infection to cancer in the anus, according to sex and HIV status: a systematic review and meta-analysis. Lancet Infect. Dis. 18, 198–206 (2018).
doi: 10.1016/S1473-3099(17)30653-9 pubmed: 29158102 pmcid: 5805865
Zhao, Y. et al. Integrating CRISPR-Cas12a into a microfluidic dual-droplet device enables simultaneous detection of HPV16 and HPV18. Anal. Chem. 95, 3476–3485 (2023).
doi: 10.1021/acs.analchem.2c05320 pubmed: 36724385
Xu, Z. et al. Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification. Nat. Commun. 13, 6480 (2022).
doi: 10.1038/s41467-022-34086-y pubmed: 36309521 pmcid: 9617605
Zhou, H. et al. Coupling CRISPR/Cas12a and recombinase polymerase amplification on a stand-alone microfluidics platform for fast and parallel nucleic acid detection. Anal. Chem. 95, 3379–3389 (2023).
doi: 10.1021/acs.analchem.2c04713 pubmed: 36735954
Xue, Y. et al. PddCas: a polydisperse droplet digital CRISPR/Cas-based assay for the rapid and ultrasensitive amplification-free detection of viral DNA/RNA. Anal. Chem. 95, 966–975 (2023).
pubmed: 36584292
Tang, Y. et al. CLIPON: a CRISPR-enabled strategy that turns commercial pregnancy test strips into general point-of-need test devices. Angew. Chem. Int. Ed. Engl. 61, e202115907 (2022).
doi: 10.1002/anie.202115907 pubmed: 35064613
McCredie, M. R. et al. Natural history of cervical neoplasia and risk of invasive cancer in women with cervical intraepithelial neoplasia 3: a retrospective cohort study. Lancet Oncol. 9, 425–434 (2008).
doi: 10.1016/S1470-2045(08)70103-7 pubmed: 18407790
Ogilvie, G. S. et al. HPV for cervical cancer screening (HPV FOCAL): complete round 1 results of a randomized trial comparing HPV-based primary screening to liquid-based cytology for cervical cancer. Int. J. Cancer 140, 440–448 (2017).
doi: 10.1002/ijc.30454 pubmed: 27685757
Ogilvie, G. S. et al. Effect of screening with primary cervical HPV testing vs cytology testing on high-grade cervical intraepithelial neoplasia at 48 months: the HPV FOCAL randomized clinical trial. JAMA 320, 43–52 (2018).
doi: 10.1001/jama.2018.7464 pubmed: 29971397 pmcid: 6583046
Abreu, A. L., Souza, R. P., Gimenes, F. & Consolaro, M. E. A review of methods for detect human Papillomavirus infection. Virol. J. 9, 262 (2012).
doi: 10.1186/1743-422X-9-262 pubmed: 23131123 pmcid: 3507852
Arbyn, M. et al. Accuracy of human papillomavirus testing on self-collected versus clinician-collected samples: a meta-analysis. Lancet Oncol. 15, 172–183 (2014).
doi: 10.1016/S1470-2045(13)70570-9 pubmed: 24433684
Kelly, R. S. et al. HPV testing as a triage for borderline or mild dyskaryosis on cervical cytology: results from the Sentinel Sites study. Br. J. Cancer 105, 983–988 (2011).
doi: 10.1038/bjc.2011.326 pubmed: 21897395 pmcid: 3185942
Ragin, C. et al. Prevalence of HPV infection in racial-ethnic subgroups of head and neck cancer patients. Carcinogenesis 38, 218–229 (2017).
doi: 10.1093/carcin/bgw203 pubmed: 28025390
Vidal, A. C. et al. HPV genotypes and cervical intraepithelial neoplasia in a multiethnic cohort in the southeastern USA. Cancer Causes Control 25, 1055–1062 (2014).
doi: 10.1007/s10552-014-0406-2 pubmed: 24928693 pmcid: 4082644
Gootenberg, J. S. et al. Multiplexed and portable nucleic acid detection platform with Cas13, Cas12a, and Csm6. Science 360, 439–444 (2018).
doi: 10.1126/science.aaq0179 pubmed: 29449508 pmcid: 5961727
Jiao, C. et al. Noncanonical crRNAs derived from host transcripts enable multiplexable RNA detection by Cas9. Science 372, 941–948 (2021).
doi: 10.1126/science.abe7106 pubmed: 33906967 pmcid: 8224270
Lee, C. et al. Empowering the on-site detection of nucleic acids by integrating CRISPR and digital signal processing. Zenodo https://doi.org/10.5281/zenodo.12675606 (2024).

Auteurs

Chang Yeol Lee (CY)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA.
Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Bionanotechnology Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.

Hyunho Kim (H)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA.
Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Ismail Degani (I)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA.
Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA, USA.

Hanna Lee (H)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA.

Angel Sandoval (A)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA.

Yoonho Nam (Y)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA.
Department of Chemical and Biomolecular Engineering (BK21 Four), Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, Republic of Korea.

Madeleine Pascavis (M)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA.
CaNCURE program, College of Science, Northeastern University, Boston, MA, USA.

Hyun Gyu Park (HG)

Department of Chemical and Biomolecular Engineering (BK21 Four), Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, Republic of Korea.

Thomas Randall (T)

Department of Obstetrics and Gynecology, Massachusetts General Hospital, Boston, MA, USA.

Amy Ly (A)

Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Cesar M Castro (CM)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA. Castro.Cesar@mgh.harvard.edu.
Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. Castro.Cesar@mgh.harvard.edu.

Hakho Lee (H)

Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA. hlee@mgh.harvard.edu.
Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. hlee@mgh.harvard.edu.

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