A cell-based Papain-like Protease (PLpro) activity assay for rapid detection of active SARS-CoV-2 infections and antivirals

被引:0
|
作者
Jimenez-Campos, Anahi G. [1 ]
Maestas, Lucas I. [1 ]
Velappan, Nileena [2 ]
Beck, Brian [3 ]
Ye, Chunyan [4 ,5 ]
Wernsing, Keith [6 ]
Mata-Solis, Yaniksa [6 ]
Bruno, William J. [7 ]
Bussmann, Silas C. [1 ]
Bradfute, Steven [4 ,5 ]
Baca, Justin T. [1 ]
Rininsland, Frauke H. [6 ]
机构
[1] Univ New Mexico, Dept Emergency Med, Hlth Sci Ctr, Albuquerque, NM USA
[2] Los Alamos Natl Lab, Los Alamos, NM USA
[3] Microbiologics, St Cloud, MN USA
[4] Univ New Mexico, Hlth Sci Ctr, Ctr Global Hlth, Albuquerque, NM USA
[5] Univ New Mexico, Dept Internal Med, Albuquerque, NM USA
[6] Mesa Photon, Santa Fe, NM 87505 USA
[7] SciTransTech, Santa Fe, NM USA
来源
PLOS ONE | 2024年 / 19卷 / 12期
关键词
RESPIRATORY SYNDROME CORONAVIRUS; CYCLE THRESHOLD VALUES; PURIFICATION; COVID-19; RNA;
D O I
10.1371/journal.pone.0309305
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its variants are a continuous threat to human life. An urgent need remains for simple and fast tests that reliably detect active infections with SARS-CoV-2 and its variants in the early stage of infection. Here we introduce a simple and rapid activity-based diagnostic (ABDx) test that identifies SARS-CoV-2 infections by measuring the activity of a viral enzyme, Papain-Like protease (PLpro). The test system consists of a peptide that fluoresces when cleaved by SARS PLpro that is active in crude, unprocessed lysates from human tongue scrapes and saliva. Test results are obtained in 30 minutes or less using widely available fluorescence plate readers, or a battery-operated portable instrument for on-site testing. Proof-of-concept was obtained in a study on clinical specimens collected from patients with COVID-19 like symptoms who tested positive (n = 10) or negative (n = 10) with LIAT RT-PCR using nasal mid turbinate swabs. When saliva from these patients was tested with in-house endpoint RT-PCR, 17 were positive and only 5 specimens were negative, of which 2 became positive when tested 5 days later. PLpro activity correlated in 17 of these cases (3 out of 3 negatives and 14 out of 16 positives, with one invalid specimen). Despite the small number of samples, the agreement was significant (p value = 0.01). Two false negatives were detected, one from a sample with a late Ct value of 35 in diagnostic RT-PCR, indicating that an active infection was no longer present. The PLpro assay is easily scalable and expected to detect all viable SARS-CoV-2 variants, making it attractive as a screening and surveillance tool. Additionally, we show feasibility of the platform as a new homogeneous phenotypic assay for rapid screening of SARS-CoV-2 antiviral drugs and neutralizing antibodies.
引用
收藏
页数:35
相关论文
共 50 条
  • [41] Potential Inhibitors Targeting Papain-Like Protease of SARS-CoV-2: Two Birds With One Stone
    Jiang, Haihai
    Yang, Peiyao
    Zhang, Jin
    FRONTIERS IN CHEMISTRY, 2022, 10
  • [42] Deubiquitinating activity of SARS-CoV-2 papain-like protease does not influence virus replication or innate immune responses in vivo
    van Huizen, Mariska
    Bloeme-ter Horst, Jonna R.
    de Gruyter, Heidi L. M.
    Geurink, Paul P.
    van Noort, Gerbrand J. van der Heden
    Knaap, Robert C. M.
    Nelemans, Tessa
    Ogando, Natacha S.
    Leijs, Anouk A.
    Urakova, Nadya
    Mark, Brian L.
    Snijder, Eric J.
    Myeni, Sebenzile K.
    Kikkert, Marjolein
    PLOS PATHOGENS, 2024, 20 (03) : 1 - 31
  • [43] Insights for Future Pharmacology: Exploring Phytochemicals as Potential Inhibitors Targeting SARS-CoV-2 Papain-like Protease
    Jabeen, Jawaria
    Ahmed, Nabeel
    Shahzad, Zunaira
    Shahid, Maida
    Ahmad, Taseer
    FUTURE PHARMACOLOGY, 2024, 4 (03): : 510 - 540
  • [44] SARS-CoV-2 papain-like protease plays multiple roles in regulating cellular proteins in the endoplasmic reticulum
    Yang, Mei
    Mariano, Jennifer
    Su, Rebecca
    Smith, Christopher E.
    Das, Sudipto
    Gill, Catherine
    Andresson, Thorkell
    Loncarek, Jadranka
    Tsai, Yien Che
    Weissman, Allan M.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2023, 299 (12)
  • [45] An ISG15-Based High-Throughput Screening Assay for Identification and Characterization of SARS-CoV-2 Inhibitors Targeting Papain-like Protease
    Samrat, Subodh Kumar
    Kumar, Prashant
    Liu, Yuchen
    Chen, Ke
    Lee, Hyun
    Li, Zhong
    Chen, Yin
    Li, Hongmin
    VIRUSES-BASEL, 2024, 16 (08):
  • [46] Inhibitors of Deubiquitinating Enzymes Interfere with the SARS-CoV-2 Papain-like Protease and Block Virus Replication In Vitro
    Grosse, Maximilian
    Setz, Christian
    Rauch, Pia
    Auth, Janina
    Morokutti-Kurz, Martina
    Temchura, Vladimir
    Schubert, Ulrich
    VIRUSES-BASEL, 2022, 14 (07):
  • [47] Naphthalen-1-ylethanamine-containing small molecule inhibitors of the papain-like protease of SARS-CoV-2
    Shinohara, Kouki
    Kobayakawa, Takuya
    Tsuji, Kohei
    Takamatsu, Yuki
    Mitsuya, Hiroaki
    Tamamura, Hirokazu
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2024, 280
  • [48] Identification of ebselen and its analogues as potent covalent inhibitors of papain-like protease from SARS-CoV-2
    Weglarz-Tomczak, Ewelina
    Tomczak, Jakub M.
    Talma, Michal
    Burda-Grabowska, Malgorzata
    Giurg, Miroslaw
    Brul, Stanley
    SCIENTIFIC REPORTS, 2021, 11 (01)
  • [49] Mutational profiling of SARS-CoV-2 papain-like protease reveals requirements for function, structure, and drug escape
    Wu, Xinyu
    Go, Margareta
    Nguyen, Julie V.
    Kuchel, Nathan W.
    Lu, Bernadine G. C.
    Zeglinski, Kathleen
    Lowes, Kym N.
    Calleja, Dale J.
    Mitchell, Jeffrey P.
    Lessene, Guillaume
    Komander, David
    Call, Matthew E.
    Call, Melissa J.
    NATURE COMMUNICATIONS, 2024, 15 (01)
  • [50] Structure of papain-like protease from SARS-CoV-2 and its complexes with non-covalent inhibitors
    Osipiuk, Jerzy
    Azizi, Saara-Anne
    Dvorkin, Steve
    Endres, Michael
    Jedrzejczak, Robert
    Jones, Krysten A.
    Kang, Soowon
    Kathayat, Rahul S.
    Kim, Youngchang
    Lisnyak, Vladislav G.
    Maki, Samantha L.
    Nicolaescu, Vlad
    Taylor, Cooper A.
    Tesar, Christine
    Zhang, Yu-An
    Zhou, Zhiyao
    Randall, Glenn
    Michalska, Karolina
    Snyder, Scott A.
    Dickinson, Bryan C.
    Joachimiak, Andrzej
    NATURE COMMUNICATIONS, 2021, 12 (01)