CRISPR/Cas-Based Biosensor As a New Age Detection Method for Pathogenic Bacteria

被引:36
作者
Chakraborty, Joydeep [1 ]
Chaudhary, Anis Ahmad [2 ]
Khan, Salah-Ud-Din [3 ]
Rudayni, Hassan Ahmad [2 ]
Rahaman, Sayed Modinur [1 ]
Sarkar, Hironmoy [1 ]
机构
[1] Raiganj Univ, Dept Microbiol, Raiganj 733134, W Bengal, India
[2] Imam Mohammad Ibn Saud Islamic Univ IMSIU, Coll Sci, Dept Biol, Riyadh 11623, Saudi Arabia
[3] Imam Mohammad Ibn Saud Islamic Univ IMSIU, Coll Med, Dept Biochem, Riyadh 11623, Saudi Arabia
关键词
RESISTANT STAPHYLOCOCCUS-AUREUS; NUCLEIC-ACID DETECTION; ESCHERICHIA-COLI O157H7; METHICILLIN-RESISTANT; LISTERIA-MONOCYTOGENES; ISOTHERMAL AMPLIFICATION; DNA; FOOD; IDENTIFICATION; INFECTIONS;
D O I
10.1021/acsomega.2c04513
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Methods enabling rapid and on-site detection of pathogenic bacteria are a prerequisite for public health assurance, medical diagnostics, ensuring food safety and security, and research. Many current bacteria detection technologies are inconvenient and time-consuming, making them unsuitable for field detection. New technology based on the CRISPR/Cas system has the potential to fill the existing gaps in detection. The clustered regularly interspaced short palindromic repeats (CRISPR) system is a part of the bacterial adaptive immune system to protect them from intruding bacteriophages. The immunological memory is saved by the CRISPR array of bacteria in the form of short DNA sequences (spacers) from invading viruses and incorporated with the CRISPR DNA repeats. Cas proteins are responsible for triggering and initiating the adaptive immune function of CRISPR/Cas systems. In advanced biological research, the CRISPR/Cas system has emerged as a significant tool from genome editing to pathogen detection. By considering its sensitivity and specificity, this system can become one of the leading detection methods for targeting DNA/RNA. This technique is well applied in virus detection like Dengue, ZIKA, SARS-CoV-2, etc., but for bacterial detection, this CRISPR/Cas system is limited to only a few organisms to date. In this review, we have discussed the different techniques based on the CRISPR/Cas system that have been developed for the detection of various pathogenic bacteria like L. monocytogenes, M. tuberculosis, Methicillin-resistant S. aureus, Salmonella, E. coli, P. aeruginosa, and A. baumannii.
引用
收藏
页码:39562 / 39573
页数:12
相关论文
共 89 条
[1]   CRISPR-based rapid and ultra-sensitive diagnostic test for Mycobacterium tuberculosis [J].
Ai, Jing-Wen ;
Zhou, Xian ;
Xu, Teng ;
Yang, Minling ;
Chen, Yuanyuan ;
He, Gui-Qing ;
Pan, Ningp ;
Cai, Yuwei ;
Li, Yongjun ;
Wang, Xiaorui ;
Su, Hang ;
Wang, Ting ;
Zeng, Weiqi ;
Zhang, Wen-Hong .
EMERGING MICROBES & INFECTIONS, 2019, 8 (01) :1361-1369
[2]   Direct detection of Listeria monocytogenes from milk by magnetic based DNA isolation and PCR [J].
Amagliani, G ;
Brandi, G ;
Omiccioli, E ;
Casiere, A ;
Bruce, IJ ;
Magnani, M .
FOOD MICROBIOLOGY, 2004, 21 (05) :597-603
[3]   CRISPR provides acquired resistance against viruses in prokaryotes [J].
Barrangou, Rodolphe ;
Fremaux, Christophe ;
Deveau, Helene ;
Richards, Melissa ;
Boyaval, Patrick ;
Moineau, Sylvain ;
Romero, Dennis A. ;
Horvath, Philippe .
SCIENCE, 2007, 315 (5819) :1709-1712
[4]   Recent and emerging innovations in Salmonella detection: a food and environmental perspective [J].
Bell, Rebecca L. ;
Jarvis, Karen G. ;
Ottesen, Andrea R. ;
McFarland, Melinda A. ;
Brown, Eric W. .
MICROBIAL BIOTECHNOLOGY, 2016, 9 (03) :279-292
[5]   Serious Infections Caused by Methicillin-Resistant Staphylococcus aureus [J].
Boucher, Helen ;
Miller, Loren G. ;
Razonable, Raymund R. .
CLINICAL INFECTIOUS DISEASES, 2010, 51 :S183-S197
[6]   Diagnosis of Ebola Virus Disease: Past, Present, and Future [J].
Broadhurst, M. Jana ;
Brooks, Tim J. G. ;
Pollock, Nira R. .
CLINICAL MICROBIOLOGY REVIEWS, 2016, 29 (04) :773-793
[7]   CRISPR-Cas12-based detection of SARS-CoV-2 [J].
Broughton, James P. ;
Deng, Xianding ;
Yu, Guixia ;
Fasching, Clare L. ;
Servellita, Venice ;
Singh, Jasmeet ;
Miao, Xin ;
Streithorst, Jessica A. ;
Granados, Andrea ;
Sotomayor-Gonzalez, Alicia ;
Zorn, Kelsey ;
Gopez, Allan ;
Hsu, Elaine ;
Gu, Wei ;
Miller, Steve ;
Pan, Chao-Yang ;
Guevara, Hugo ;
Wadford, Debra A. ;
Chen, Janice S. ;
Chiu, Charles Y. .
NATURE BIOTECHNOLOGY, 2020, 38 (07) :870-+
[8]   Antibacterial activity of extracellular compounds produced by a Pseudomonas strain against methicillin-resistant Staphylococcus aureus (MRSA) strains [J].
Cardozo, Viviane F. ;
Oliveira, Admilton G. ;
Nishio, Erick K. ;
Perugini, Marcia R. E. ;
Andrade, Celia G. T. J. ;
Silveira, Wanderley D. ;
Duran, Nelson ;
Andrade, Galdino ;
Kobayashi, Renata K. T. ;
Nakazato, Gerson .
ANNALS OF CLINICAL MICROBIOLOGY AND ANTIMICROBIALS, 2013, 12
[9]   Cas6 is an endoribonuclease that generates guide RNAs for invader defense in prokaryotes [J].
Carte, Jason ;
Wang, Ruiying ;
Li, Hong ;
Terns, Rebecca M. ;
Terns, Michael P. .
GENES & DEVELOPMENT, 2008, 22 (24) :3489-3496
[10]   CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity [J].
Chen, Janice S. ;
Ma, Enbo ;
Harrington, Lucas B. ;
Da Costa, Maria ;
Tian, Xinran ;
Palefsky, Joel M. ;
Doudna, Jennifer A. .
SCIENCE, 2018, 360 (6387) :436-+