Review

Six decades of lateral flow immunoassay: from determining metabolic markers to diagnosing COVID-19

  • Received: 05 July 2020 Accepted: 20 August 2020 Published: 26 August 2020
  • Technologies based on lateral flow immunoassay (LFIA), known in some countries of the world as immunochromatographic tests, have been successfully used for the last six decades in diagnostics of many diseases and conditions as they allow rapid detection of molecular ligands in biosubstrates. The popularity of these diagnostic platforms is constantly increasing in healthcare facilities, particularly those facing limited budgets and time, as well as in household use for individual health monitoring. The advantages of these low-cost devices over modern laboratory-based analyzers come from their availability, opportunity of rapid detection, and ease of use. The attractiveness of these portable diagnostic tools is associated primarily with their high analytical sensitivity and specificity, as well as with the easy visual readout of results. These qualities explain the growing popularity of LFIA in developing countries, when applied at small hospitals, in emergency situations where screening and monitoring health condition is crucially important, and as well as for self-testing of patients. These tools have passed the test of time, and now LFIA test systems are fully consistent with the world's modern concept of ‘point-of-care testing’, finding a wide range of applications not only in human medicine, but also in ecology, veterinary medicine, and agriculture. The extensive opportunities provided by LFIA contribute to the continuous development and improvement of this technology and to the creation of new-generation formats. This review will highlight the modern principles of design of the most widely used formats of test-systems for clinical laboratory diagnostics, summarize the main advantages and disadvantages of the method, as well as the current achievements and prospects of the LFIA technology. The latest innovations are aimed at improving the analytical performance of LFIA platforms for the diagnosis of bacterial and viral infections, including COVID-19.

    Citation: Boris G. Andryukov. Six decades of lateral flow immunoassay: from determining metabolic markers to diagnosing COVID-19[J]. AIMS Microbiology, 2020, 6(3): 280-304. doi: 10.3934/microbiol.2020018

    Related Papers:

  • Technologies based on lateral flow immunoassay (LFIA), known in some countries of the world as immunochromatographic tests, have been successfully used for the last six decades in diagnostics of many diseases and conditions as they allow rapid detection of molecular ligands in biosubstrates. The popularity of these diagnostic platforms is constantly increasing in healthcare facilities, particularly those facing limited budgets and time, as well as in household use for individual health monitoring. The advantages of these low-cost devices over modern laboratory-based analyzers come from their availability, opportunity of rapid detection, and ease of use. The attractiveness of these portable diagnostic tools is associated primarily with their high analytical sensitivity and specificity, as well as with the easy visual readout of results. These qualities explain the growing popularity of LFIA in developing countries, when applied at small hospitals, in emergency situations where screening and monitoring health condition is crucially important, and as well as for self-testing of patients. These tools have passed the test of time, and now LFIA test systems are fully consistent with the world's modern concept of ‘point-of-care testing’, finding a wide range of applications not only in human medicine, but also in ecology, veterinary medicine, and agriculture. The extensive opportunities provided by LFIA contribute to the continuous development and improvement of this technology and to the creation of new-generation formats. This review will highlight the modern principles of design of the most widely used formats of test-systems for clinical laboratory diagnostics, summarize the main advantages and disadvantages of the method, as well as the current achievements and prospects of the LFIA technology. The latest innovations are aimed at improving the analytical performance of LFIA platforms for the diagnosis of bacterial and viral infections, including COVID-19.


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    Funding of the study



    The study was supported by the ‘Far East’ Integrated Program of Basic Research, Far Eastern Branch, Russian Academy of Sciences, project no. 18-03-053.

    Conflict of interests



    The author declares that he has no conflict of interests.

    [1] Havelaar AH, Kirk MD, Torgerson PR, et al. (2010) World health organization global estimates and regional comparisons of the burden of foodborne disease in 2010. PLOS Med 12: e1001923. doi: 10.1371/journal.pmed.1001923
    [2] Byzova NA, Vinogradova SV, Porotikova EV, et al. (2018) Lateral flow immunoassay for rapid detection of grapevine leafroll-associated virus. Biosensors (Basel) 8: E111. doi: 10.3390/bios8040111
    [3] Anfossi L, Di Nardo F, Cavalera S, et al. (2018) Multiplex lateral flow immunoassay: an overview of strategies towards high-throughput point-of-need testing. Biosensors (Basel) 9: E2. doi: 10.3390/bios9010002
    [4] Kim H, Chung DR, Kang M (2019) A new point-of-care test for the diagnosis of infectious diseases based on multiplex lateral flow immunoassays. The Analyst 144: 2460-2466. doi: 10.1039/C8AN02295J
    [5] World Health Organization (2010) Global estimates and regional comparisons of the burden of foodborne disease in 2010. PLoS Med 12: e1001923.
    [6] Urusov AE, Zherdev AV, Dzantiev BB (2019) Towards lateral flow quantitative assays: detection approaches. Biosensors (Basel) 9: 89. doi: 10.3390/bios9030089
    [7] Cheng N, Song Y, Zeinhom MM, et al. (2017) Nanozyme-mediated dual immunoassay integrated with smartphone for use in simultaneous detection of pathogens. ACS Appl Mater Interfaces 9: 40671-40680. doi: 10.1021/acsami.7b12734
    [8] Zarei M (2018) Infectious pathogens meet point-of-care diagnostics. Biosens Bioelectron 106: 193-203. doi: 10.1016/j.bios.2018.02.007
    [9] Yalow RS, Berson SA (1960) Immunoassay of endogenous plasma insulin in man. J Clin Invest 39: 1157-1175. doi: 10.1172/JCI104130
    [10] Mak WC, Beni V, Turner APF (2016) Lateral-flow technology: From visual to instrumental. Trends Analyt Chem 79: 297-305. doi: 10.1016/j.trac.2015.10.017
    [11] McPartlin DA, O'Kennedy RJ (2014) Point-of-care diagnostics, a major opportunity for change in traditional diagnostic approaches: Potential and limitations. Expert Rev Mol Diagn 14: 979-998. doi: 10.1586/14737159.2014.960516
    [12] Fu X, Wen J, Li J, et al. (2019) Highly sensitive detection of prostate cancer specific PCA3 mimic DNA using SERS-based competitive lateral flow assay. Nanoscale 11: 15530-15536. doi: 10.1039/C9NR04864B
    [13] Zhao Y, Wang HR, Zhang PP, et al. (2016) Rapid multiplex detection of 10 foodborne pathogens with an up-converting phosphor technology-based 10-channel lateral flow assay. Sci Rep 6: 21342. doi: 10.1038/srep21342
    [14] Sastre P, Gallardo C, Monedero A, et al. (2016) Development of a novel lateral flow assay for detection of African swine fever in blood. BMC Vet Res 12: 206. doi: 10.1186/s12917-016-0831-4
    [15] Jones D, Glogowska M, Locock L, et al. (2016) Embedding new technologies in practice–a normalization process theory study of point of care testing. BMC Health Serv Res 16: 591. doi: 10.1186/s12913-016-1834-3
    [16] Kozel TR, Burnham-Marusich AR (2017) Point-of-care testing for infectious diseases: past, present, and future. J Clin Microb 55: 2313-2320. doi: 10.1128/JCM.00476-17
    [17] Kim C, Yoo YK, Han SI, et al. (2017) Battery operated preconcentration-assisted lateral flow assay. Lab Chip 17: 2451-2458. doi: 10.1039/C7LC00036G
    [18] Kim H, Chung DR, Kang M (2019) A new point-of-care test for the diagnosis of infectious diseases based on multiplex lateral flow immunoassays. Analyst 144: 2460-2466. doi: 10.1039/C8AN02295J
    [19] Gitonga LK, Boru WG, Kwena A, et al. (2017) Point of care testing evaluation of lateral flow immunoassay for diagnosis of cryptococcus meningitis in HIV-positive patients at an urban hospital in Nairobi, Kenya, 2017. BMC Res Notes 12: 797. doi: 10.1186/s13104-019-4829-4
    [20] Kumar S, Bhushan P, Krishna V, et al. (2018) Tapered lateral flow immunoassay-based point-of-care diagnostic device for ultrasensitive colorimetric detection of dengue NS1. Biomicrofluidics 12: 034104. doi: 10.1063/1.5035113
    [21] Anfossi L, Di Nardo F, Cavalera S, et al. (2018) Multiplex lateral flow immunoassay: an overview of strategies towards high-throughput point-of-need testing. Biosensors (Basel) 9: E2. doi: 10.3390/bios9010002
    [22] Banerjee R, Jaiswal A (2018) Recent advances in nanoparticle-based lateral flow immunoassay as a point-of-care diagnostic tool for infectious agents and diseases. Analyst 143: 1970-1996. doi: 10.1039/C8AN00307F
    [23] Safenkova IV, Panferov VG, Panferova NA, et al. (2019) Alarm lateral flow immunoassay for detection of the total infection caused by the five viruses. Talanta 95: 739-744. doi: 10.1016/j.talanta.2018.12.004
    [24] Zhao Y, Zhang Q, Meng Q, et al. (2017) Quantum dots-based lateral flow immunoassay combined with image analysis for semiquantitative detection of IgE antibody to mite. Int J Nanomedicine 12: 4805-4812. doi: 10.2147/IJN.S134539
    [25] Jørgensen CS, Uldum SA, Sørensen JF, et al. (2015) Evaluation of a new lateral flow test for detection of Streptococcus pneumoniae and Legionella pneumophila urinary antigen. J Microbiol Methods 116: 33-36. doi: 10.1016/j.mimet.2015.06.014
    [26] Rohrman BA, Leautaud V, Molyneux E, et al. (2012) A lateral flow assay for quantitative detection of amplified HIV-1 RNA. PLoS One 7: e45611. doi: 10.1371/journal.pone.0045611
    [27] Boisen ML, Oottamasathien D, Jones AB, et al. (2015) Development of prototype filovirus recombinant antigen immunoassays. J Infect Dis 212: 359-367. doi: 10.1093/infdis/jiv353
    [28] Nielsen K, Yu WL, Kelly L, et al. (2008) Development of a lateral flow assay for rapid detection of bovine antibody to Anaplasma marginaleJ Immunoassay Immunochem 29: 10-18. doi: 10.1080/15321810701734693
    [29] Kamphee H, Chaiprasert A, Prammananan T, et al. (2015) Rapid molecular detection of multidrug-resistant tuberculosis by PCR-nucleic acid lateral flow immunoassay. PLos One 10: e0137791. doi: 10.1371/journal.pone.0137791
    [30] Helfmann J, Netz UJ (2015) Sensors in diagnostics and monitoring. Photonics Lasers Med 4: 36-42. doi: 10.1515/plm-2015-0012
    [31] You M, Lin M, Gong Y, et al. (2017) Household fluorescent lateral flow strip platform for sensitive and quantitative prognosis of heart failure using dual-color upconversion nanoparticles. ACS Nano 11: 6261-6270. doi: 10.1021/acsnano.7b02466
    [32] Pilavaki E, Demosthenous A (2017) Optimized Lateral Flow Immunoassay Reader for the Detection of Infectious Diseases in Developing Countries. Sensors (Basel) 17: E2673. doi: 10.3390/s17112673
    [33] Kim C, Yoo YK, Han SI, et al. (2017) Battery operated preconcentration-assisted lateral flow assay. Lab Chip 17: 2451-2458. doi: 10.1039/C7LC00036G
    [34] Naidoo N, Ghai M, Moodley K, et al. (2017) Modified RS-LAMP assay and use of lateral flow devices for rapid detection of Leifsonia xyli subsp. xyli. Lett Appl Microbiol 65: 496-503. doi: 10.1111/lam.12799
    [35] Xiao W, Huang C, Xu F, et al. (2018) A simple and compact smartphone-based device for the quantitative readout of colloidal gold lateral flow immunoassay strips. Sens Actuators B Chem 266: 63-70. doi: 10.1016/j.snb.2018.03.110
    [36] Nelis D, Bura L, Zhao Y, et al. (2019) The Efficiency of Color Space Channels to Quantify Color and Color Intensity Change in Liquids, pH Strips, and Lateral Flow Assays with Smartphones. Sensors (Basel) 19: E5104. doi: 10.3390/s19235104
    [37] Schwenke KU, Spiehl D, Krauße M, et al. (2019) Analysis of free chlorine in aqueous solution at very low concentration with lateral flow tests. Sci Rep 9: 17212. doi: 10.1038/s41598-019-53687-0
    [38] Borges M, Araújo J (2019) False-negative result of serum cryptococcal antigen lateral flow assay in an HIV-infected patient with culture-proven cryptococcaemia. Med Mycol Case Rep 26: 64-66. doi: 10.1016/j.mmcr.2019.10.009
    [39] Foysal KH, Seo SE, Kim MJ, et al. (2018) Analyte Quantity Detection from Lateral Flow Assay Using a Smartphone. Sensors (Basel) 19: E4812. doi: 10.3390/s19214812
    [40] Romeo A, Leunga T, Sánchez S (2016) Smart biosensors for multiplexed and fully integrated point-of-care diagnostics. Lab Chip 16: 1957-1961. doi: 10.1039/C6LC90046A
    [41] Lee S, Mehta S, Erickson D (2016) Two-Color Lateral Flow Assay for Multiplex Detection of Causative Agents Behind Acute Febrile Illnesses. Anal Chem 88: 8359-8363. doi: 10.1021/acs.analchem.6b01828
    [42] Yen CW, de Puig H, Tam JO, et al. (2015) Multicolored silver nanoparticles for multiplexed disease diagnostics: distinguishing dengue, yellow fever, and Ebola viruses. Lab Chip 5: 1638-1641. doi: 10.1039/C5LC00055F
    [43] Edwards KA, Korff R, Baeumner AJ (2017) Liposome-Enhanced Lateral-Flow Assays for Clinical Analyses. Methods Mol Biol 1571: 407-434. doi: 10.1007/978-1-4939-6848-0_25
    [44] Koczula K, Gallotta A (2016) Lateral flow assays. Essays Biochem 60: 111-120. doi: 10.1042/EBC20150012
    [45] Guo C, Zhong LL, Yi HL, et al. (2016) Clinical value of fluorescence lateral flow immunoassay in diagnosis of influenza A in children. Zhongguo Dang Dai Er Ke Za Zhi 18: 1272-1276.
    [46] Berger P, Sturgeon C (2014) Pregnancy testing with hCG-future prospects. Trends Endocrinol. Metab 25: 637-648. doi: 10.1016/j.tem.2014.08.004
    [47] Lu F, Wang KH, Lin Y (2005) Rapid, quantitative and sensitive immunochromatographic assay based on stripping voltammetric detection of a metal ion label. Analyst 130: 1513-1517. doi: 10.1039/b507682j
    [48] Campbell JP, Heaney JL, Shemar M, et al. (2017) Development of a rapid and quantitative lateral flow assay for the simultaneous measurement of serum κ and λ immunoglobulin free light chains (FLC): inception of a new near-patient FLC screening tool. Clin Chem Lab Med 55: 424-434. doi: 10.1515/cclm-2016-0194
    [49] Pilavaki E, Demosthenous A (2017) Optimized lateral flow immunoassay reader for the detection of infectious diseases in developing countries. Sensors (Basel) 17: E2673. doi: 10.3390/s17112673
    [50] Hsieh HV, Dantzler JL, Weigl BH, et al. (2017) Analytical tools to improve optimization procedures for lateral flow assays. Diagnostics (Basel) 7: E29. doi: 10.3390/diagnostics7020029
    [51] Tran TV, Nguyen BV, Nguyen TTP, et al. (2019) Development of a highly sensitive magneto-enzyme lateral flow immunoassay for dengue NS1 detection. PeerJ 7: e7779. doi: 10.7717/peerj.7779
    [52] Chaterji S, Allen JC, Chow A, et al. (2011) Evaluation of the NS1 rapid test and the WHO dengue classification schemes for use as bedside diagnosis of acute dengue fever in adults. Am J Trop Med Hyg 84: 224-228. doi: 10.4269/ajtmh.2011.10-0316
    [53] Rong Z, Wang Q, Sun N, et al. (2019) Smartphone-based fluorescent lateral flow immunoassay platform for highly sensitive point-of-care detection of Zika virus nonstructural protein 1. Anal Chim Acta 1055: 140-147. doi: 10.1016/j.aca.2018.12.043
    [54] Kosasih H, Widjaja S, Surya E, et al. (2012) Evaluation of two IgM rapid immunochromatographic tests during circulation of Asian lineage chikungunya virus. Southeast Asian J Trop Med Public Health 43: 55-61.
    [55] Escadafal C, Faye O, Sall AA, et al. (2014) Rapid molecular assays for the detection of yellow fever virus in low-resource settings. PLoS Negl Trop Dis 8: e2730. doi: 10.1371/journal.pntd.0002730
    [56] Wonderly B, Jones S, Gatton ML, et al. (2019) Comparative performance of four rapid Ebola antigen-detection lateral flow immunoassays during the 2014–2016 Ebola epidemic in West Africa. PLoS One 14: e0212113. doi: 10.1371/journal.pone.0212113
    [57] Si J, Li J, Zhang L, et al. (2019) A signal amplification system on a lateral flow immunoassay detecting for hepatitis e-antigen in human blood samples. J Med Virol 91: 1301-1306. doi: 10.1002/jmv.25452
    [58] Nakagiri I, Tasaka T, Okai M, et al. (2019) Screening for human immunodeficiency virus using a newly developed fourth generation lateral flow immunochromatography assay. J Virol Methods 274: 113746. doi: 10.1016/j.jviromet.2019.113746
    [59] Karaman E, Ilkit M, Kuşçu F (2019) Identification of Cryptococcus antigen in human immunodeficiency virus-positive Turkish patients by using the Dynamiker® lateral flow assay. Mycoses 62: 961-968. doi: 10.1111/myc.12969
    [60] Morioka K, Fukai K, Yosihda K, et al. (2015) Development and evaluation of a rapid antigen detection and serotyping lateral flow antigen detection system for foot-and-mouth disease virus. PLoS ONE 10: e0134931. doi: 10.1371/journal.pone.0134931
    [61] Wang C, Wang C, Wang X, et al. (2019) Magnetic SERS Strip for Sensitive and Simultaneous Detection of Respiratory Viruses. ACS Appl Mater Interfaces 11: 19495-19505. doi: 10.1021/acsami.9b03920
    [62] El-Tholoth M, Branavan M, Naveenathayalan A, et al. (2019) Recombinase polymerase amplification-nucleic acid lateral flow immunoassays for Newcastle disease virus and infectious bronchitis virus detection. Mol Biol Rep 46: 6391-6397. doi: 10.1007/s11033-019-05085-y
    [63] Huang YH, Yu KY, Huang SP, et al. (2020) Development of a Nucleic Acid Lateral Flow Immunoassay for the Detection of Human Polyomavirus BK. Diagnostics (Basel) 10: E403. doi: 10.3390/diagnostics10060403
    [64] Salminen T, Knuutila A, Barkoff AM, et al. (2018) A rapid lateral flow immunoassay for serological diagnosis of pertussis. Vaccine 36: 1429-1434. doi: 10.1016/j.vaccine.2018.01.064
    [65] Hwang J, Lee S, Choo J (2016) Application of a SERS-based lateral flow immunoassay strip for the rapid and sensitive detection of staphylococcal enterotoxin B. Nanoscale 8: 11418-11425. doi: 10.1039/C5NR07243C
    [66] Eryılmaz M, Acar Soykut E, Çetin D, et al. (2019) -based rapid assay for sensitive detection of Group A Streptococcus by evaluation of the swab sampling technique. Analyst 144: 3573-3580. doi: 10.1039/C9AN00173E
    [67] Prentice KW, DePalma L, Ramage JG, et al. (2019) Comprehensive Laboratory Evaluation of a Lateral Flow Assay for the Detection of Yersinia pestisHealth Secur 17: 439-453. doi: 10.1089/hs.2019.0094
    [68] Wang J, Katani R, Li L, et al. (2016) Rapid detection of Escherichia coli O157 and shiga toxins by lateral flow immunoassays. Toxins 8: 92. doi: 10.3390/toxins8040092
    [69] Wu Z (2019) Simultaneous detection of Listeria monocytogenes and Salmonella typhimurium by a SERS-Based lateral flow immunochromatographic assay. Food Anal Methods 12: 1086-1091. doi: 10.1007/s12161-019-01444-4
    [70] El-Shabrawi M, El-Aziz NA, El-Adly TZ, et al. (2018) Stool antigen detection versus 13C-urea breath test for non-invasive diagnosis of pediatric Helicobacter pylori infection in a limited resource setting. Arch Med Sci 14: 69-73. doi: 10.5114/aoms.2016.61031
    [71] Machiesky L, Côté O, Kirkegaard LH, et al. (2019) A rapid lateral flow immunoassay for identity testing of biotherapeutics. J Immunol Methods 474: 112666. doi: 10.1016/j.jim.2019.112666
    [72] Anfossi L, Di Nardo F, Cavalera S, et al. (2018) Multiplex Lateral Flow Immunoassay: An Overview of Strategies towards High-throughput Point-of-Need Testing. Biosensors (Basel) 9: 2. doi: 10.3390/bios9010002
    [73] Nouvellet P, Garske T, Mills HL, et al. (2015) The role of rapid diagnostics in managing Ebola epidemics. Nature 528: S109-S116. doi: 10.1038/nature16041
    [74] Hassan AHA, Bergua JF, Morales-Narváez E, et al. (2019) Validity of a single antibody-based lateral flow immunoassay depending on graphene oxide for highly sensitive determination of E. coli O157:H7 in minced beef and river water. Food Chem 297: 124965. doi: 10.1016/j.foodchem.2019.124965
    [75] Lai CC, Wang CY, Ko WC (2020) In vitro diagnostics of coronavirus disease 2019: Technologies and application. J Microbiol Immunol Infect .
    [76] Askim JR, Suslick KS (2015) Hand-held reader for colorimetric sensor arrays. Anal. Chem 87: 7810-7816. doi: 10.1021/acs.analchem.5b01499
    [77] Liu J, Geng Z, Fan Z, et al. (2019) Point-of-care testing based on smartphone: The current state-of-the-art (2017–2018). Biosens Bioelectron 132: 17-37. doi: 10.1016/j.bios.2019.01.068
    [78] You M, Lin M, Gong Y, et al. (2017) Household fluorescent lateral flow strip platform for sensitive and quantitative prognosis of heart failure using dual-color upconversion nanoparticles. ACS Nano 11: 6261-6270. doi: 10.1021/acsnano.7b02466
    [79] Xiao W, Huang C, Xu F, et al. (2018) A simple and compact smartphone-based device for the quantitative readout of colloidal gold lateral flow immunoassay strips. Sens Actuators B Chem 266: 63-70. doi: 10.1016/j.snb.2018.03.110
    [80] Saisin L, Amarit R, Somboonkaew A, et al. (2020) Significant sensitivity improvement for camera-based lateral flow immunoassay readers. Sensors 18: 4026. doi: 10.3390/s18114026
    [81] Nsabimana AP, Uzabakiriho B, Kagabo DM, et al. (2018) Bringing Real-Time Geospatial Precision to HIV Surveillance Through Smartphones: Feasibility Study. JMIR Public Health Surveill 4: e11203. doi: 10.2196/11203
    [82] Gong Y, Zheng Y, Jin B, et al. (2019) A portable and universal upcon version nanoparticle-based lateral flow assay platform for point-of-care testing. Talanta 201: 126-133. doi: 10.1016/j.talanta.2019.03.105
    [83] Petrosillo N, Viceconte G, Ergonul O, et al. (2020) COVID-19, SARS and MERS: are they closely related? Clin Microbiol Infect 26: 729-734. doi: 10.1016/j.cmi.2020.03.026
    [84] Pfefferle S, Reucher S, Nörz D, et al. (2020) Evaluation of a quantitative RT-PCR assay for the detection of the emerging coronavirus SARS-CoV-2 using a high throughput system. Euro Surveill 25: 2000152. doi: 10.2807/1560-7917.ES.2020.25.9.2000152
    [85] Chu DKW, Pan Y, Cheng SMS, et al. (2020) Molecular diagnosis of a novel Coronavirus (2019-nCoV) causing an outbreak of pneumonia. Clin Chem 66: 549-555. doi: 10.1093/clinchem/hvaa029
    [86] Jo S, Kim S, Shin DH, et al. (2020) Inhibition of SARS-CoV 3CL protease by flavonoids. J Enzyme Inhib Med Chem 35: 145-151. doi: 10.1080/14756366.2019.1690480
    [87] Yip CC, Ho CC, Chan JF, et al. (2020) Development of a Novel, Genome Subtraction-Derived, SARS-CoV-2-Specific COVID-19-nsp2 Real-Time RT-PCR Assay and Its Evaluation Using Clinical Specimens. Int J Mol Sci 21: 2574. doi: 10.3390/ijms21072574
    [88] Wu JL, Tseng WP, Lin CH, et al. (2020) Four point-of-care lateral flow immunoassays for diagnosis of COVID-19 and for assessing dynamics of antibody responses to SARS-CoV-2. J Infect .
    [89] Lu F, Wang KH, Lin Y (2005) Rapid, quantitative and sensitive immunochromatographic assay based on stripping voltammetric detection of a metal ion label. Analyst 130: 1513-1517. doi: 10.1039/b507682j
    [90] Zhang Y, Kong H, Liu X, et al. (2018) Quantum dot-based lateral-flow immunoassay for rapid detection of rhein using specific egg yolk antibodies. Artif Cells Nanomed Biotechnol 46: 1685-1693.
    [91] Liu Y, Gayle AA, Wilder-Smith A, et al. (2020) The reproductive number of COVID-19 is higher compared to SARS coronavirus. J Travel Med 27: taaa021. doi: 10.1093/jtm/taaa021
    [92] Chen Y, Chan KH, Hong C, et al. (2016) A highly specific rapid antigen detection assay for on-site diagnosis of MERS. J Infect 73: 82-84. doi: 10.1016/j.jinf.2016.04.014
    [93] Bhadra S, Jiang YS, Kumar MR, et al. (2015) Real-time sequence-validated loop-mediated isothermal amplification assays for detection of Middle East respiratory syndrome coronavirus (MERS-CoV). PLoS One 10: e0123126. doi: 10.1371/journal.pone.0123126
    [94] Pallesen J, Wang N, Corbett KS, et al. (2017) Immunogenicity and structures of a rationally designed prefusion MERS-CoV spike antigen. Proc Natl Acad Sci USA 114: E7348-E7357. doi: 10.1073/pnas.1707304114
    [95] Malik YS, Sircar S, Bhat S, et al. (2020) Emerging novel coronavirus (2019-nCoV)-current scenario, evolutionary perspective based on genome analysis and recent developments. Vet Q 40: 68-76. doi: 10.1080/01652176.2020.1727993
    [96] Corman VM, Landt O, Kaiser M, et al. (2020) Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Euro Surveill 25: 2000045.
    [97] Wu A, Peng Y, Huang B, et al. (2020) Genome Composition and Divergence of the Novel Coronavirus (2019-nCoV) Originating in China. Cell Host Microbe 27: 325-328. doi: 10.1016/j.chom.2020.02.001
    [98] Chen Z, Zhang Z, Zhai X, et al. (2020) Rapid and sensitive detection of anti-SARS-CoV-2 IgG, using lanthanide-doped nanoparticles-based lateral flow immunoassay. Anal Chem 92: 7226-7231. doi: 10.1021/acs.analchem.0c00784
    [99] Li YC, Bai WZ, Hashikawa T (2020) The neuroinvasive potential of SARS-CoV2 may play a role in the respiratory failure of COVID-19 patients. J Med Virol 92: 552-555. doi: 10.1002/jmv.25728
    [100] Huang WE, Lim B, Hsu CC, et al. (2020) RT-LAMP for rapid diagnosis of coronavirus SARS-CoV-2. Microb Biotechnol 13: 950-961. doi: 10.1111/1751-7915.13586
    [101] Nguyen T, Duong Bang D, Wolff A (2020) Novel Coronavirus Disease (COVID-19): paving the road for rapid detection and point-of-care ciagnostics. Micromachines (Basel) 11: 306. doi: 10.3390/mi11030306
    [102] Kashir J, Yaqinuddin A (2020) Loop mediated isothermal amplification (LAMP) assays as a rapid diagnostic for COVID-19. Med Hypotheses 141: 109786. doi: 10.1016/j.mehy.2020.109786
    [103] Koch T, Dahlke C, Fathi A, et al. (2020) Safety and immunogenicity of a modified vaccinia virus Ankara vector vaccine candidate for Middle East respiratory syndrome: an open-label, phase 1 trial. Lancet Infect Dis 20: 827-838. doi: 10.1016/S1473-3099(20)30248-6
    [104] Zhu FC, Li YH, Guan XH, et al. (2020) Safety, tolerability, and immunogenicity of a recombinant adenovirus type-5 vectored COVID-19 vaccine: a dose-escalation, open-label, non-randomised, first-in-human trial. Lancet 395: 1845-1854. doi: 10.1016/S0140-6736(20)31208-3
    [105] Alkan F, Ozkul A, Bilge-Dagalp S, et al. (2011) The detection and genetic characterization based on the S1 gene region of BCoVs from respiratory and enteric infections in Turkey. Transbound Emerg Dis 58: 179-185. doi: 10.1111/j.1865-1682.2010.01194.x
    [106] Pradhan SK, Kamble NM, Pillai AS, et al. (2014) Recombinant nucleocapsid protein based single serum dilution ELISA for the detection of antibodies to infectious bronchitis virus in poultry. J Virol Methods 209: 1-6. doi: 10.1016/j.jviromet.2014.08.015
    [107] Montesinos I, Gruson D, Kabamba B, et al. (2020) Evaluation of two automated and three rapid lateral flow immunoassays for the detection of anti-SARS-CoV-2 antibodies. J Clin Virol 128: 104413. doi: 10.1016/j.jcv.2020.104413
    [108] Deeks JJ, Dinnes J, Takwoingi Y, et al. (2020) Antibody tests for identification of current and past infection with SARS-CoV-2. Cochrane Database Syst Rev 6: CD013652.
    [109] Wen T, Huang C, Shi FJ, et al. (2020) Development of a lateral flow immunoassay strip for rapid detection of IgG antibody against SARS-CoV-2 virus. Analyst 10: 1039.
    [110] Wang Y, Hou Y, Li H, et al. (2019) A SERS-based lateral flow assay for the stroke biomarker S100-β. Mikrochim Acta 186: 548. doi: 10.1007/s00604-019-3634-z
    [111] Nicol T, Lefeuvre C, Serri O, et al. (2020) Assessment of SARS-CoV-2 serological tests for the diagnosis of COVID-19 through the evaluation of three immunoassays: Two automated immunoassays (Euroimmun and Abbott) and one rapid lateral flow immunoassay (NG Biotech). J Clin Virol 129: 104511. doi: 10.1016/j.jcv.2020.104511
    [112] (2020)  Johns Hopkins University Health Safety Center official website. Available from: https://www.centerforhealthsecurity.org/resources/COVID-19/serology/Serology-based-tests-for-COVID-19.html.
    [113] (2020)  Cellex Ltd. official website. Cellex qSARS-CoV-2 IgG/IgM Rapid Test. Available from: https://cellexcovid.com.
    [114] (2020)  ChemBio Ltd. official website. DPP® COVID-19 IgM/IgG System. Available from: http://chembio.com.
    [115] (2020)  Hardy diagnostics official website. Anti-SARS-CoV-2 Rapid Test. Available from: https://hardydiagnostics.com/sars-cov-2.
    [116] (2020)  Healgen Scientific LLC official website. COVID-19 Antibody Rapid Detection Kit. Available from: https://www.healgen.com/if-respiratory-covid-19.
    [117] (2020)  Hangzhou Biotest Biotech Co., Ltd official website. RightSign™ COVID-19 IgM/IgG Rapid Test Kit. Available from: https://www.healgen.com/if-respiratory-covid-19.
    [118] (2020)  Biohit Healthcare (Heifei) Co. Ltd. official website. Biohit SARS-CoV-2 IgM/IgG Antibody Test Kit. Available from: https://www.fda.gov/media/139283/download.
    [119] (2020)  Hangzhou Laihe Biotech Co., Ltd official website. Novel Coronavirus (2019-nCoV) IgM/IgG Antibody Combo Test Kit. Available from: https://www.fda.gov/media/139410/download.
    [120] (2020)  Aytu Biosciences/Orient Gene Biotech official website. The COVID-19 IgG/IgM Point-of-Care Rapid Test. Available from: https://stocknewsnow.com/companynews/5035338834942348/ AYTU/101843.
    [121] Sajid M, Kawde AN, Daud M (2015) Designs, formats and applications of lateral flow assay: A literature review. J Saudi Chem Soc 19: 689-705. doi: 10.1016/j.jscs.2014.09.001
    [122] Choi JR, Hu J, Gong Y, et al. (2016) An integrated lateral flow assay for effective DNA amplification and detection at the point of care. Analyst 141: 2930-2939. doi: 10.1039/C5AN02532J
    [123] Kamphee H, Chaiprasert A, Prammananan T, et al. (2015) Rapid molecular detection of multidrug-resistant tuberculosis by PCR-nucleic acid lateral flow immunoassay. PLoS One 10: e0137791. doi: 10.1371/journal.pone.0137791
    [124] Huang YH, Yu KY, Huang SP, et al. (2020) Development of a Nucleic Acid Lateral Flow Immunoassay for the Detection of Human Polyomavirus BK. Diagnostics (Basel) 10: 403. doi: 10.3390/diagnostics10060403
    [125] Mens PF, de Bes HM, Sondo P, et al. (2012) Direct blood PCR in combination with nucleic acid lateral flow immunoassay for detection of Plasmodium species in settings where malaria is endemic. J Clin Microbiol 50: 3520-3525. doi: 10.1128/JCM.01426-12
    [126] Pecchia S, Da Lio D (2018) Development of a rapid PCR-Nucleic Acid Lateral Flow Immunoassay (PCR-NALFIA) based on rDNA IGS sequence analysis for the detection of Macrophomina phaseolina in soil. J Microbiol Methods 151: 118-128. doi: 10.1016/j.mimet.2018.06.010
    [127] Moers AP, Hallett RL, Burrow R, et al. (2015) Detection of single-nucleotide polymorphisms in Plasmodium falciparum by PCR primer extension and lateral flow immunoassay. Antimicrob Agents Chemother 59: 365-371. doi: 10.1128/AAC.03395-14
    [128] Roth JM, Sawa P, Omweri G, et al. (2018) Molecular Detection of Residual Parasitemia after Pyronaridine-Artesunate or Artemether-Lumefantrine Treatment of Uncomplicated Plasmodium falciparum Malaria in Kenyan Children. Am J Trop Med Hyg 99: 970-977. doi: 10.4269/ajtmh.18-0233
    [129] Rule GS, Montagna RA, Durst RA (1996) Rapid method for visual identification of specific DNA sequences based on DNA-tagged liposomes. Clinical Chemistry 42: 1206-1209. doi: 10.1093/clinchem/42.8.1206
    [130] Jauset-Rubio M, Svobodová M, Mairal T, et al. (2016) Ultrasensitive, rapid and inexpensive detection of DNA using paper based lateral flow assay. Sci Rep 6: 37732. doi: 10.1038/srep37732
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