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Comparison and evaluation of four methods for extracting DNA from Giardia duodenalis cysts for PCR targeting the tpi gene

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Abstract

Giardia duodenalis is an intestinal flagellated protozoan and the common cause of gastrointestinal diseases in human. This parasite can be seen in two different forms in its life cycle including as cyst and trophozoite. Due to presence of resistant cyst wall, DNA extraction inhibitors along with artifact in stool specimens, this study was performed aiming to evaluate four methods for DNA extraction from G. duodenalis cysts. Seventy G. duodenalis positive stool specimens that were confirmed by light microscope were included in this study. All stool samples were concentrated using four layered discontinuous sucrose flotation technique (0.5, 0.75, 1, and 1.5 M) and single-layered sucrose solution (0.85 M). The isolated cysts were then subjected to DNA extraction by four methods. To remove the artifacts, the extracted DNA were evaluated by PCR. The results of the present study showed the high level of optical density (OD) in the method I (P < 0.01) with the following steps; Giardia cysts plus crushed cover glass were vortexed. Then, the samples were boiled and then followed by freeze–thaw cycles, yet this method yielded the lowest concentration. Furthermore, the highest concentration were observed in the method II (P <0.01) with the following steps; Giardia cysts plus crushed cover glass and TAE buffer were mixed and then shaken, followed by boiling. Based on the results of the present study, using crushed cover glass, boiling and freeze–thaw cycles can be effective in destruction of G. duodenalis cyst wall and have enough efficiency for extracting DNA from G. duodenalis cysts.

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References

  • Abbaszadegan MR et al (2007) Stool-based DNA testing, a new noninvasive method for colorectal cancer screening, the first report from Iran. World J Gastroenterol 13:1528–1533

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Amar CF, East C, Maclure E, McLauchlin J, Jenkins C, Duncanson P, Wareing DR (2004) Blinded application of microscopy, bacteriological culture, immunoassays and PCR to detect gastrointestinal pathogens from faecal samples of patients with community-acquired diarrhoea. Eur J Clin Microbiol Infect Dis 23:529–534. doi:10.1007/s10096-004-1149-x

    Article  CAS  PubMed  Google Scholar 

  • Babaei Z, Oormazdi H, Rezaie S, Rezaeian M, Razmjou E (2011) Giardia intestinalis: DNA extraction approaches to improve PCR results. Exp Parasitol 128:159–162. doi:10.1016/j.exppara.2011.02.001

    Article  CAS  PubMed  Google Scholar 

  • Blagg W, Schloegel EL, Mansour NS, Khalaf GI (1955) A new concentration technic for the demonstration of protozoa and helminth eggs in feces. Am J Trop Med Hyg 4:23–28

    CAS  PubMed  Google Scholar 

  • Caccio SM, Beck R, Lalle M, Marinculic A, Pozio E (2008) Multilocus genotyping of Giardia duodenalis reveals striking differences between assemblages A and B. Int J Parasitol 38:1523–1531. doi:10.1016/j.ijpara.2008.04.008

    Article  CAS  PubMed  Google Scholar 

  • Feng Y, Xiao L (2011) Zoonotic potential and molecular epidemiology of Giardia species and giardiasis. Clin Microbiol Rev 24:110–140. doi:10.1128/cmr.00033-10

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Gerwig GJ, van Kuik JA, Leeflang BR, Kamerling JP, Vliegenthart JF, Karr CD, Jarroll EL (2002) The Giardia intestinalis filamentous cyst wall contains a novel beta(1-3)-N-acetyl-D-galactosamine polymer: a structural and conformational study. Glycobiology 12:499–505

    Article  CAS  PubMed  Google Scholar 

  • Guy RA, Xiao C, Horgen PA (2004) Real-time PCR assay for detection and genotype differentiation of Giardia lamblia in stool specimens. J Clin Microbiol 42:3317–3320. doi:10.1128/jcm.42.7.3317-3320.2004

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Inpankaew T et al (2014) Low risk for transmission of zoonotic Giardia duodenalis from dogs to humans in rural Cambodia. Parasit Vectors 7:412. doi:10.1186/1756-3305-7-412

    Article  PubMed  PubMed Central  Google Scholar 

  • Johnston SP, Ballard MM, Beach MJ, Causer L, Wilkins PP (2003) Evaluation of three commercial assays for detection of Giardia and Cryptosporidium organisms in fecal specimens. J Clin Microbiol 41:623–626

    Article  PubMed  PubMed Central  Google Scholar 

  • Lane S, Lloyd D (2002) Current trends in research into the waterborne parasite Giardia. Crit Rev Microbiol 28:123–147. doi:10.1080/1040-840291046713

    Article  PubMed  Google Scholar 

  • Machiels BM et al (2000) New protocol for DNA extraction of stool. Biotechniques 28:286–290

    CAS  PubMed  Google Scholar 

  • Nantavisai K, Mungthin M, Tan-ariya P, Rangsin R, Naaglor T, Leelayoova S (2007) Evaluation of the sensitivities of DNA extraction and PCR methods for detection of Giardia duodenalis in stool specimens. J Clin Microbiol 45:581–583. doi:10.1128/jcm.01823-06

    Article  CAS  PubMed  Google Scholar 

  • Pestehchian N, Rasekh H, Babaei Z, Yousefi HA, Eskandarian AA, Kazemi M, Akbari M (2012) Identification of genotypes of Giardia duodenalis human isolates in Isfahan, Iran, using polymerase chain reaction - Restriction Fragment Length polymorphism. Adv Biomed Res 1:84. doi:10.4103/2277-9175.105166

    Article  PubMed  PubMed Central  Google Scholar 

  • Pestechian N, Rasekh H, Rostami-Nejad M, Yousofi HA, Hosseini-Safa A (2014) Molecular identification of Giardia lamblia; is there any correlation between diarrhea and genotyping in Iranian population? Gastroenterol Hepatol Bed Bench 7:168–172

    PubMed  PubMed Central  Google Scholar 

  • Planelles D, Llopis F, Puig N, Montoro JA (1996) A new, fast, and simple DNA extraction method for HLA and VNTR genotyping by PCR amplification. J Clin Lab Anal 10:125–128. doi:10.1002/(sici)1098-2825(1996)10:3<125:aid-jcla2>3.0.co;2-a

    Article  CAS  PubMed  Google Scholar 

  • Rayani M, Zasmy Unyah N, Hatam G (2014) Molecular Identification of Giardia duodenalis Isolates from Fars Province, Iran. Iran J Parasitol 9:70–78

    CAS  PubMed  PubMed Central  Google Scholar 

  • Sam brooks J, Fritsch EF, Maniatist T (1989) Molecular cloning. A laboratory manual Cold Spring Harbor laboratory, New York

    Google Scholar 

  • World Health Organization (1996) The World health report, fighting disease, fostering development. Geneva

  • Zhang P, Liu Y, Alsarakibi M, Li J, Liu T, Li Y, Li G (2012) Application of HRM assays with EvaGreen dye for genotyping Giardia duodenalis zoonotic assemblages. Parasitol Res 111:2157–2163. doi:10.1007/s00436-012-3064-x

    Article  PubMed  Google Scholar 

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Acknowledgments

The authors would like to thank Vice-chancellor of Research and Technology, Isfahan University of Medical Sciences for the approval and financial support of this study and Infectious Disease and Tropical Medicine Research Center, Isfahan University of Medical Sciences for help and contribution.

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Correspondence to Nader Pestehchian.

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Sepahvand, A., Pestehchian, N., Yousefi, H.A. et al. Comparison and evaluation of four methods for extracting DNA from Giardia duodenalis cysts for PCR targeting the tpi gene. J Parasit Dis 41, 263–267 (2017). https://doi.org/10.1007/s12639-016-0790-5

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  • DOI: https://doi.org/10.1007/s12639-016-0790-5

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