Visual single nucleotide polymorphism (SNP) detection for ALDH2 genotyping based on multiplex ligation probe amplification (MLPA) and lateral flow assay

被引:1
|
作者
Yin, Dan [1 ]
Li, Xiaolan [1 ]
Mai, Li [2 ]
Wang, Ruxin [3 ]
Tang, Sitian [1 ]
Hu, Liyi [1 ]
机构
[1] Peoples Hosp Chongqing Liangjiang New Area, Dept Lab Med, 199 Ren Xing Rd, Chongqing 401121, Peoples R China
[2] Chongqing Med Univ, Affiliated Hosp 2, Dept Lab Med, 74 LinJiang Rd, Chongqing 400010, Peoples R China
[3] Adm Affairs Management Ctr Chongqing Liangjiang Ne, 66 Jin Yu Ave, Chongqing 401120, Peoples R China
关键词
Single nucleotide polymorphism; Genotyping; ALDH2; gene; Multiplex ligation probe amplification; Lateral flow assay; GENE; MUTATION; DISEASE;
D O I
10.1016/j.microc.2023.109329
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Current techniques for single nucleotide polymorphism (SNP) detection require laborious experimental procedures, expensive and sophisticated instruments, as well as complex data analysis, which make it difficult to meet the demand for routine clinical laboratories or point of care testing (POCT). In this study, the authors propose a reliable and cost-effective method by integrating multiplex ligation probe amplification (MLPA) and gold nanoparticles (AuNPs)-based lateral flow assay (LFA) for visual detection of the ALDH2 gene rs671(G > A) polymorphism. The genotyping result can be easily observed with the naked eye within 5-10 min after loading the MLPA products on the LFA device. This system demonstrates high sensitivity with LOD down to 1 ng, meeting the requirement in clinical diagnostic. Furthermore, this method has been implemented in clinical practices to identify the genotypes of the ALDH2 gene. The results obtained from the MLPA-LFA, Sanger sequencing, and high-resolution melting (HRM) curve analysis demonstrate a perfect agreement rate of 100%. Compared to conventional genotyping assays, this system exhibits the following advantages, including visual interpretation of results, minimal requirements for sophisticated instruments and highly skilled technicians, time efficiency, as well as low cost with a price approximately at 5 dollars. We believe that the MLPA-LFA system is a robust and versatile method with the potential to detect other SNPs related to disease susceptibility and risk, as well as drug metabolism and therapeutic effects.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: Implications for molecular diagnosis
    Crompton, Danielle
    Rehal, Pauline K.
    MacPherson, Lesley
    Foster, Katharine
    Lunt, Peter
    Hughes, Imelda
    Brady, Angela F.
    Pike, Michael G.
    De Gressi, Susanna
    Morgan, Neil V.
    Hardy, Carol
    Smith, Matthew
    MacDonald, Fiona
    Maher, Eamonn R.
    Kurian, Manju A.
    MOLECULAR GENETICS AND METABOLISM, 2010, 100 (02) : 207 - 212
  • [42] Electrochemical genotyping and detection of single-nucleotide polymorphisms based on junction-probe containing 2′-deoxyinosine
    Zhang, Jing
    Wu, XiaoYan
    Chen, PingPing
    Lin, NingTing
    Chen, JingHua
    Chen, GuoNan
    Fu, FengFu
    CHEMICAL COMMUNICATIONS, 2010, 46 (37) : 6986 - 6988
  • [43] Visual simultaneous detection of single nucleotide polymorphism of tumor susceptibility gene and marker alpha-fetoprotein based on double-labeled colloidal gold probe with lateral flow strip biosensor
    Ma, Li-Hong
    Wang, Hai-Bo
    Zhang, Ting
    Xuan, Yang
    Li, Cheng
    Chen, Wei
    Liu, Bo
    Zhao, Yuan-Di
    SENSORS AND ACTUATORS B-CHEMICAL, 2019, 298
  • [44] COMPARISON OF MICROARRAY-BASED GENOMIC PROFILING AND MULTIPLEX LIGATION-DEPENDENT PROBE AMPLIFICATION (MLPA) FOR THE DETECTION OF CLINICALLY RELEVANT GENETIC LESIONS, INCLUDING IKZF1, IN ALL
    Stevens-Kroef, M.
    van Reijmersdal, S.
    Siepman, A.
    Pfundt, R.
    Croockewit, S.
    Kuiper, R.
    Simons, A.
    HAEMATOLOGICA, 2013, 98 : 393 - 394
  • [45] Loop-mediated isothermal amplification-based nucleic acid lateral flow assay for the specific and multiplex detection of genetic markers
    Kim, Seokhwan
    Kim, Jung Ho
    Kim, Seokjoon
    Park, Jung Soo
    Cha, Byung Seok
    Lee, Eun Sung
    Han, Jinjoo
    Shin, Jiye
    Jang, Youngjun
    Park, Ki Soo
    Analytica Chimica Acta, 2022, 1205
  • [46] Loop-mediated isothermal amplification-based nucleic acid lateral flow assay for the specific and multiplex detection of genetic markers
    Kim, Seokhwan
    Kim, Jung Ho
    Kim, Seokjoon
    Park, Jung Soo
    Cha, Byung Seok
    Lee, Eun Sung
    Han, Jinjoo
    Shin, Jiye
    Jang, Youngjun
    Park, Ki Soo
    ANALYTICA CHIMICA ACTA, 2022, 1205
  • [47] Development and Implementation of a Multiplex Single-Nucleotide Polymorphism Genotyping Assay for Detection of Virulence-Attenuating Mutations in the Listeria monocytogenes Virulence-Associated Gene inlA
    Van Stelten, A.
    Nightingale, K. K.
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (23) : 7365 - 7375
  • [48] Padlock probe-based rolling circle amplification lateral flow assay for point-of-need nucleic acid detection
    Jain, Sidhartha
    Dandy, David S.
    Geiss, Brian J.
    Henry, Charles S.
    ANALYST, 2021, 146 (13) : 4340 - 4347
  • [49] Direct Detection of Single Nucleotide Polymorphism (SNP) with Genomic DNA by the Ferrocenylnaphthalene Diimide-based Electrochemical Hybridization Assay (FND-EHA)
    Takahiko Nojima
    Kenichi Yamashita
    Atsuko Takagi
    Makoto Takagi
    Yasuyuki Ikeda
    Hiroki Kondo
    Shigeori Takenaka
    Analytical Sciences, 2003, 19 : 79 - 83
  • [50] Direct detection of single nucleotide polymorphism (SNP) with genomic DNA by the ferrocenylnaphthalene diimide-based electrochemical hybridization assay (FND-EHA)
    Nojima, T
    Yamashita, K
    Takagi, A
    Takagi, M
    Ikeda, Y
    Kondo, H
    Takenaka, S
    ANALYTICAL SCIENCES, 2003, 19 (01) : 79 - 83