Rapid and Sensitive Detection of Vibrio vulnificus Using CRISPR/Cas12a Combined With a Recombinase-Aided Amplification Assay

被引:50
作者
Xiao, Xingxing [1 ]
Lin, Ziqin [1 ]
Huang, Xianhui [1 ]
Lu, Jinfang [1 ]
Zhou, Yan [1 ]
Zheng, Laibao [1 ]
Lou, Yongliang [1 ]
机构
[1] Wenzhou Med Univ, Sch Lab Med & Life Sci, Wenzhou Key Lab Sanit Microbiol, Minist Educ,Key Lab Lab Med, Wenzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Vibrio vulnificus; recombinase-aided amplification assay; CRISPR; Cas12a; early diagnosis; on-site detection; ISOTHERMAL AMPLIFICATION; IDENTIFICATION; OYSTERS; INFECTIONS;
D O I
10.3389/fmicb.2021.767315
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Vibrio vulnificus is an important zoonotic and aquatic pathogen and can cause vibriosis in humans and aquatic animals (especially farmed fish and shrimp species). Rapid and sensitive detection methods for V. vulnificus are still required to diagnose human vibriosis early and reduce aquaculture losses. Herein, we developed a rapid and sensitive diagnostic method comprising a recombinase-aided amplification (RAA) assay and the CRISPR/Cas12a system (named RAA-CRISPR/Cas12a) to detect V. vulnificus. The RAA-CRISPR/Cas12a method allows rapid and sensitive detection of V. vulnificus in 40 min without a sophisticated instrument, and the limit of detection is two copies of V. vulnificus genomic DNA per reaction. Meanwhile, the method shows satisfactory specificity toward non-target bacteria and high accuracy in the spiked blood, stool, and shrimp samples. Therefore, our proposed rapid and sensitive V. vulnificus detection method, RAA-CRISPR/Cas12a, has great potential for early diagnosis of human vibriosis and on-site V. vulnificus detection in aquaculture and food safety control.
引用
收藏
页数:10
相关论文
共 43 条
[1]   Miniaturized isothermal nucleic acid amplification, a review [J].
Asiello, Peter J. ;
Baeumner, Antje J. .
LAB ON A CHIP, 2011, 11 (08) :1420-1430
[2]   Vibrio spp. infections [J].
Baker-Austin, Craig ;
Oliver, James D. ;
Alamo, Munirul ;
Ali, Afsar ;
Waldor, Matthew K. ;
Qadri, Firdausi ;
Martinez-Urtaza, Jaime .
NATURE REVIEWS DISEASE PRIMERS, 2018, 4 :1-19
[3]   Vibrio vulnificus: new insights into a deadly opportunistic pathogen [J].
Baker-Austin, Craig ;
Oliver, James D. .
ENVIRONMENTAL MICROBIOLOGY, 2018, 20 (02) :423-430
[4]  
Baker-Austin C, 2013, NAT CLIM CHANGE, V3, P73, DOI [10.1038/nclimate1628, 10.1038/NCLIMATE1628]
[5]   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-+
[6]   Real-time PCR analysis of Vibrio vulnificus from oysters [J].
Campbell, MS ;
Wright, AC .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (12) :7137-7144
[7]   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-+
[8]   Field-Effect Biosensors for On-Site Detection: Recent Advances and Promising Targets [J].
Choi, Jaebin ;
Seong, Tae Wha ;
Jeun, Minhong ;
Lee, Kwan Hyi .
ADVANCED HEALTHCARE MATERIALS, 2017, 6 (20)
[9]   VIBRIO-VULNIFICUS INFECTION IN TAIWAN - REPORT OF 28 CASES AND REVIEW OF CLINICAL MANIFESTATIONS AND TREATMENT [J].
CHUANG, YC ;
YUAN, CY ;
LIU, CY ;
LAN, CK ;
HUANG, AHM .
CLINICAL INFECTIOUS DISEASES, 1992, 15 (02) :271-276
[10]   Good guide, bad guide: spacer sequence-dependent cleavage efficiency of Cas12a [J].
Creutzburg, Sjoerd ;
Wu, Wen Y. ;
Mohanraju, Prarthana ;
Swartjes, Thomas ;
Alkan, Ferhat ;
Gorodkin, Jan ;
Staals, Raymond H. J. ;
van der Oost, John .
NUCLEIC ACIDS RESEARCH, 2020, 48 (06) :3228-3243