• Title of article

    Development of New Recombinant DgK Antigen for Diagnosis of Dirofilaria immitis Infections in Dogs Using ELISA Technique and Its Comparison to Molecular Methods

  • Author/Authors

    Solgi, Rahmat Department of Parasitology and Mycology - School of Medicine - Shiraz University of Medical Sciences, Shiraz, Iran , Sadjjadi, Mahmoud Department of Parasitology and Mycology - School of Medicine - Shiraz University of Medical Sciences, Shiraz, Iran , Mohebali, Mehdi Department of Medical Parasitology and Mycology - School of Public Health - Tehran University of Medical Sciences, Iran , Zarei, Zabihollah Department of Medical Parasitology and Mycology - School of Public Health - Tehran University of Medical Sciences, Iran , Golkar, Majid Molecular Parasitology Laboratory - Department of Parasitology - Pasteur Institute of Iran, Tehran, Iran , Raz, Abbasali Malaria and Vector Research Group (MVRG) - Biotechnology Research Center (BRC) - Pasteur Institute of Iran, Tehran, Iran

  • Pages
    7
  • From page
    283
  • To page
    289
  • Abstract
    Background: Dirofilaria immitis is a cosmopolitan zoonotic, vector-borne parasite of carnivorous animals causing dirofilariasis in human beings. Common commercial serodiagnostic tests for canine dirofilariasis usually lead to different results in their sensitivity and specificity. The present study reports development of recombinant DgK (rDgK) antigen of D. immitis for accurate immunodiagnosis of D. Immitis-infected dogs using indirect ELISA test. Methods: The rDgK coding sequence was successfully sequenced, codon optimized and cloned in pET-24a(+) expression vector and then expressed in Escherichia coli. The recombinant DgK was affinity purified using Ni²+- charged HiTrap chelating column, followed by testing in Western blotting and enzyme-linked immunosorbent assays (ELISA) with dog sera from a dirofilariasis endemic area. The performance of rDgK ELISA was evaluated using 60 sera collected from suspected dogs, while molecular technique was used as a reference test. Results: Sera from positive control D. immitis infection produced a strong IgG antibody response to rDgK both in ELISA and Western blotting tests. The sensitivity and specificity related to diagnostic potential of rDgK for ELISA were 92.5% and 87.5%, respectively. The results of rDgK ELISA showed a high agreement (0.764) with molecular identification. Conclusions: The findings revealed that the developed new rDgK antigen is sensitive and specific for immunodiagnosis of canine dirofilariasis using ELISA test.
  • Keywords
    Dirofilariasis , Dirofilaria immitis , Enzyme-linked immunosorbent assays , Proteins
  • Journal title
    Astroparticle Physics
  • Serial Year
    2018
  • Record number

    2482190