DOI QR코드

DOI QR Code

Development of a diagnostic method for human enteric Adenovirus-41 with rapid, specific and high sensitivity using the loop-mediated isothermal amplification assay

  • Lee, Jin-Young (Department of Microbiology, College of Natural Sciences, Dankook University) ;
  • Rho, Jae Young (Department of Microbiology, College of Natural Sciences, Dankook University)
  • Received : 2020.01.08
  • Accepted : 2020.08.24
  • Published : 2020.09.01

Abstract

Human enteric Adenovirus 41 (HueAdV-41) is a major waterborne virus that causes human gastroenteritis and is classified as a viral group I double-strand DNA virus, Adenoviridae. HueAdV-41 has been detected with the polymerase chain reaction (PCR) in various samples such as ground water. However, the PCR-based diagnostic method has problems such as reaction time, sensitivity, and specificity. Thus, the loop-mediated isothermal amplification (LAMP) assay has emerged as an excellent method for field applications. In this study, we developed a LAMP system that can rapidly detect HueAdV-41 with high specificity and sensitivity. HueAdV-41 specific LAMP primer sets were tested through a specific, non-specific selection and sensitivity test for three prepared LAMP primer sets, of which only one primer set and optimum reaction temperature were selected. The developed LAMP primer set condition was confirmed as 63℃, and the sensitivity was 1 copy. In addition, to confirm the system, a LAMP positive reaction was developed with the restriction enzyme Taq I (T/GCC). The developed method in this study was more specific, rapid (typically within 2 - 3 hours), and highly sensitive than that of the conventional PCR method. To evaluate and verify the developed LAMP assay, an artificial infection test was done with five cDNAs from groundwater samples, and the results were compared to those of the conventional PCR method. We expect the developed LAMP primer set will be used to diagnose HueAdV-41 from various samples.

Keywords

References

  1. Allard A, Albinsson B, Wadell G. 2001. Rapid typing of human adenoviruses by a general PCR combined with restriction endonuclease analysis. Journal of Clinical Microbiology 39:498-505. https://doi.org/10.1128/JCM.39.2.498-505.2001
  2. Banerjee A, De P, Manna B, Chawla-sarkar M. 2017. Molecular characterization of enteric adenovirus genotypes 40 and 41 identified in children with acute gastroenteritis in Kolkata, India during 2013-2014. Journal of Medical Virology 89:606-614. https://doi.org/10.1002/jmv.24672
  3. Berk AJ. 2013. Adenoviridae. In Fields virology (6th) edited by Knipe DM, Howley PM. pp. 1704-1731. Lippincott Williams & Wikins, Philadelphia, PA, USA.
  4. Cheong S, Lee C, Song SW, Choi WC, Lee CH, Kim SJ. 2009. Enteric viruses in raw vegetables and groundwater used for irrigation in South Korea. Applied and Environmental Microbiology 75:7745-7751. https://doi.org/10.1128/AEM.01629-09
  5. Cho KB. 2018. Construction of improved PCR primer set for the detection of human enteric adenovirus 41. Biomedical Science Letters 24:230-238. [in Korean] https://doi.org/10.15616/BSL.2018.24.3.230
  6. Choi S, Jiang SC. 2005. Real-Time PCR quantification of human adenovirus in urban rivers indicates genome prevalence but Low Infectivity. Applied and Environmental Microbiology 71:7426-7433. https://doi.org/10.1128/AEM.71.11.7426-7433.2005
  7. Echavarria M, Forman M, Ticehurst J, Dumler JS, Charache P. 1998. PCR method for detection of adenovirus in urine of healthy and human immunodeficiency virus-infected individuals. Journal of Clinical Microbiology 36:3323-3326. https://doi.org/10.1128/JCM.36.11.3323-3326.1998
  8. Ferreyra LJ, Giordano MO, Martinez LC, Barril PA, Masachessi G, Isa MB, Poma R, Rajal V, Biganzoil P, Nates SV, Pavan JV. 2015. Tracking novel adenovirus in environmental and human clinical samples: No evidence of endemic human adenovirus type 58 circulation in Cordoba city, Argentina. Epidemiology Infect 28:1-5.
  9. Filho EP, da Costa Faria NR, Fialho AM, de Assis RS, Almeida MMS, Rocha M, Galvao M, dos Santos FB, Barreto ML, Leite JPG. 2007. Adenoviruses associated with acute gastroenteritis in hospitalized and community children up to 5 years old in Rio de Janeiro and Salvador, Brazil. Journal of Medical Microbiology 56:313-319. https://doi.org/10.1099/jmm.0.46685-0
  10. Ha TH. 2018. The latest trend in isothermal amplification. BioChip Letters 13:10-14. [in Korean]
  11. Hong SH, Heo MS. 2015. Development of loop-mediated isothermal amplification (LAMP) for Detection of Vibrio alginolyticus. Journal of Life Science 25:903-909. [in Korean] https://doi.org/10.5352/JLS.2015.25.8.903
  12. Jothikumar N, Cromeans TL, Hill VR, Lu X, Sobesey M, Erdman D. 2005. Quantitative real-time PCR assays for detection of human adenoviruses and identification of serotypes 40 and 41. Applied and Environmental Microbiology 71:3131-3136. https://doi.org/10.1128/AEM.71.6.3131-3136.2005
  13. Kim J, Kim HS, Kim HS, Kim JS, Song W, Lee KM, Lee S, Park KU, Lee W, Hong YJ. 2014. Evaluation of an immunochromatographic assay for the rapid and simultaneous detection of rotavirus and adenovirus in stool samples. Annals of Laboratory Medicine 34:216-222. https://doi.org/10.3343/alm.2014.34.3.216
  14. Kim JS, Lee SK, Ko DH, Hyun J, Kim HS, Song W, Kim HS. 2017. Associations of adenovirus genotypes in Korean acute gastroenteritis patients with respiratory symptoms and intussusception. BioMed Research International 2017:1-6.
  15. Lee JY, Kim JH, Rho JY. 2019. Development of rapid and specific detection for the human Aichivirus A using the loopmediated isothermal amplification from water samples. Indian Journal of Microbiology 59:375-378. https://doi.org/10.1007/s12088-019-00803-3
  16. Lee JY, Rho JY. 2018. Primer set for loop-mediated isothermal amplification reaction for detecting human enteric adenovirus 41, and use thereof. Korean Patent 10-2018-0173040. [in Korean]
  17. Lee JY, Rho JY. 2020. Development of diagnostic method for human Astrovirus with rapid, specific and high sensitivity using loop-mediated isothermal amplification method. Korean Journal of Agricultural Science 47:173-182. [in Korean]
  18. NIER (National Institute of Environmental Research). 2017. National institute of environmental research notice No. 2017-50. NIER, Incheon, Korea. [in Korean]
  19. Notomi T, Okayama H, Masubuchi H, Yoneawa T, Watanabe K, Amino N, Hase T. 2000. Loop-mediated isothermal amplification of DNA. Nucleic Acids Research 28:e63. https://doi.org/10.1093/nar/28.12.e63
  20. Papafragkou E, Plante M, Mattison K, Bidawid S, Karthikeyan K, Farber JM, Jaykus LA. 2008. Rapid and sensitive detection of hepatitis A virus in representative food matrices. Journal of Virological Methods 147:177-187. https://doi.org/10.1016/j.jviromet.2007.08.024
  21. Raboni SM, Damasio GA, Ferreira CEO, Pereira LA, Nogueira MB, Vidal LR, Cruz CR, Almeida SM. 2014. Acute gastroenteritis and enteric viruses in hospitalised children in southern Brazil: Aetiology, seasonality and clinical outcomes. Memorias do Instituto Oswaldo Cruz 109:428-435. https://doi.org/10.1590/0074-0276140066
  22. Reis TAV, Assis ASF, do Valle DA, Barletta VH, de Carvalho IP, Rose TL, Portes SAR, Leite JPG, Silva MLR. 2016. The role of human adenoviruses type 41 in acute diarrheal disease in Minas Gerais after rotavirus vaccination. Brazilian Journal of Microbiology 47:243-250. https://doi.org/10.1016/j.bjm.2015.11.011
  23. Schneider L, Blakely H, Tripathi A. 2019. Mathematical model to reduce loop mediated isothermal amplification (LAMP) false-positive diagnosis. Electrophoresis 40:2706-2717. https://doi.org/10.1002/elps.201900167
  24. Steele M, Odumeru J. 2004. Irrigation water as source of foodborne pathogens on fruit and vegetables. Journal of Food Protection 67:2839-2849. https://doi.org/10.4315/0362-028X-67.12.2839
  25. Wieczorek M, Krzysztoszek A, Witek A. 2015. Species-specific identification of human adenoviruses in sewage. Polish Journal of Microbiology 64:23-28. https://doi.org/10.33073/pjm-2015-003
  26. Ziros PG, Kokkinos PA, Allard A, Vantarakis A. 2015. Development and evaluation of a loop-mediated isothermal amplification assay for the detection of adenovirus 40 and 41. Food and Environmental Virology 7:276-285. https://doi.org/10.1007/s12560-015-9182-8