An all-in-one assay based on CRISPR/Cas13a and a DNA circuit for rapid and ultrasensitive detection of Echovirus 11

被引:2
作者
Yang, Yixia [1 ]
Yi, Wenfu [2 ]
Gong, Feng [1 ]
Tan, Zhiyou [1 ]
Shan, Xiaoyun [1 ]
Qian, Jingjing [1 ]
Xie, Conghua [3 ,4 ]
Ji, Xinghu [1 ]
Zheng, Zhenhua [2 ]
He, Zhike [1 ,5 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
[3] Wuhan Univ, Zhongnan Hosp, Dept Radiat & Med Oncol, Hubei Key Lab Tumor Biol Behav, Wuhan 430071, Peoples R China
[4] Wuhan Univ, Zhongnan Hosp, Hubei Canc Clin Study Ctr, Wuhan 430071, Peoples R China
[5] Chinese Acad Med Sci, Wuhan Res Ctr Infect Dis & Canc, Wuhan 430071, Peoples R China
基金
中国国家自然科学基金;
关键词
Catalytic hairpin assembly; CRISPR/Cas13a; Echovirus RNA; One-pot detection; Hairpin probe; LINKED-IMMUNOSORBENT-ASSAY; MOLECULAR EPIDEMIOLOGY; DIAGNOSIS; DISEASE; ENTEROVIRUSES; CRISPR-CAS12A; EVOLUTION; SEROTYPE; STRAINS; EUROPE;
D O I
10.1016/j.snb.2023.133851
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Echovirus 11 (ECHO 11) is a positive-stranded RNA virus. The infections of ECHO 11 are associated with many clinical syndromes, thus the deployment of rapid point-of-care diagnostics is necessary. This study reported a new diagnostic assay based on All-In-One CRISPR/Cas13a and a DNA circuit (termed AIOC) for ECHO 11 detection. By combination of CRISPR/Cas13a and catalytic hairpin assembly (CHA) circuit in one-pot reaction, multiple handling steps and uncapping contamination could be effectively avoided. After recognition of target RNA, the activation of CRISPR/Cas13a induced the RNase activity of Cas13a to cleave hairpin probes, resulting in subsequent CHA amplification. This simplified assay was able to detect ECHO 11 RNA in the range of 500 x 10(-18) M to 5 x 10(-9) M for VP1 gene and 100 x 10(-18) M to 5 x 10(-9) M for RdRP gene. And the limit of detection was 152 x 10(-18) M and 24 x 10(-18) M, respectively. More importantly, the practicability of AIOC assay was validated by clinical ECHO samples. Taking together, the AIOC assay is rapid (similar to 30 min), isothermal (37 degrees C), ultrasensitive, specific, user-friendly and does not need the step of RNA reverse-transcription, making it an excellent detection performance in one-pot point-of-care assay.
引用
收藏
页数:8
相关论文
共 34 条
  • [1] C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector
    Abudayyeh, Omar O.
    Gootenberg, Jonathan S.
    Konermann, Silvana
    Joung, Julia
    Slaymaker, Ian M.
    Cox, David B. T.
    Shmakov, Sergey
    Makarova, Kira S.
    Semenova, Ekaterina
    Minakhin, Leonid
    Severinov, Konstantin
    Regev, Aviv
    Lander, Eric S.
    Koonin, Eugene V.
    Zhang, Feng
    [J]. SCIENCE, 2016, 353 (6299)
  • [2] Echovirus type 11: Outbreak of hand-foot-and-mouth disease in a Thai hospital nursery
    Apisarnthanarak, A
    Kitphati, R
    Pongsuwann, Y
    Tacharoenmueng, R
    Mundy, LM
    [J]. CLINICAL INFECTIOUS DISEASES, 2005, 41 (09) : 1361 - 1362
  • [3] CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity
    Chen, Janice S.
    Ma, Enbo
    Harrington, Lucas B.
    Da Costa, Maria
    Tian, Xinran
    Palefsky, Joel M.
    Doudna, Jennifer A.
    [J]. SCIENCE, 2018, 360 (6387) : 436 - +
  • [4] An RNA-based catalytic hairpin assembly circuit coupled with CRISPR-Cas12a for one-step detection of microRNAs
    Chen, Pinru
    Wang, Luying
    Qin, Peipei
    Yin, Bin-Cheng
    Ye, Bang-Ce
    [J]. BIOSENSORS & BIOELECTRONICS, 2022, 207
  • [5] Molecular comparison of echovirus 11 strains circulating in Europe during an epidemic of multisystem hemorrhagic disease of infants indicates that evolution generally occurs by recombination
    Chevaliez, S
    Szendröi, A
    Caro, V
    Balanant, J
    Guillot, S
    Berencsi, G
    Delpeyroux, F
    [J]. VIROLOGY, 2004, 325 (01) : 56 - 70
  • [6] RAPID DIAGNOSIS OF ECHOVIRUS TYPE-33 MENINGITIS BY SPECIFIC IGM DETECTION USING AN ENZYME LINKED IMMUNOSORBENT-ASSAY (ELISA)
    CHOMEL, JJ
    THOUVENOT, D
    FAYOL, V
    AYMARD, M
    [J]. JOURNAL OF VIROLOGICAL METHODS, 1985, 10 (01) : 11 - 19
  • [7] Two distinct RNase activities of CRISPR-C2c2 enable guide-RNA processing and RNA detection
    East-Seletsky, Alexandra
    O'Connell, Mitchell R.
    Knight, Spencer C.
    Burstein, David
    Cate, Jamie H. D.
    Tjian, Robert
    Doudna, Jennifer A.
    [J]. NATURE, 2016, 538 (7624) : 270 - +
  • [8] Prolonged Viral RNA Detection in the Central Nervous System of One-Week-Old Swiss Albino Mice following Coxsakievirus B4 and Echovirus 9 Infection
    El Hiar, Raida
    Hober, Didier
    Jaidane, Hela
    Sane, Famara
    Ben M'hadheb-Gharbi, Manel
    Caloone, Delphine
    Gharbi, Jawhar
    Aouni, Mahjoub
    [J]. INTERVIROLOGY, 2012, 55 (06) : 435 - 441
  • [9] Detection of negative and positive RNA strand of poliovirus Sabin 1 and echovirus E19 by a stem-loop reverse transcription PCR
    Fikatas, A.
    Dimitriou, T. G.
    Kyriakopoulou, Z.
    Moschonas, G. D.
    Amoutzias, G. D.
    Mossialos, D.
    Gartzonika, C.
    Levidiotou-Stefanou, S.
    Markoulatos, P.
    [J]. LETTERS IN APPLIED MICROBIOLOGY, 2017, 65 (03) : 234 - 240
  • [10] GONG CM, 1984, J VIROL METHODS, V9, P209, DOI 10.1016/0166-0934(84)90027-2