Comparative PCR-based diagnosis for the detection of Leishmania infantum in naturally infected dogs

Acta Trop. 2020 Jul:207:105495. doi: 10.1016/j.actatropica.2020.105495. Epub 2020 Apr 17.

Abstract

The applicability of molecular biology/PCR for canine visceral leishmaniasis diagnosis presents challenges, mainly due to the diversity of targets described. The objectives of this study were to compare the sensitivities and reliability of five targets (kDNA/120, kDNA/145, ITS1, hsp70/234 and hsp70/1300) in four different tissue samples (bone marrow, popliteal lymph node, skin and conjunctival swab). Sixty-five dogs (32 males and 33 females) naturally infected with Leishmania infantum and ten dogs without infection were examined. Dogs were characterized by serological and parasitological methods. The parasitological test was considered the gold standard for analysis. All tests presented high specificity 100% (95% CI 0.72-1), and variable sensitivity. The targets kDNA/145, ITS1, kDNA/120, hsp70/234 and hsp70/1300 detected 100% (65/65), 93.4% (61/65), 92.3% (60/65), 84.61% (55/65) and 72.3% (77/65) of positive animals respectively. The performance of PCR methods was analyzed in two different scenarios. The highest sensitivity value identified in all scenarios studied was kDNA/145. Our results suggest that popliteal lymph node and conjunctival swab samples, besides being less invasive collections, represent a good substratum for PCR-based diagnosis, and the target kDNA/145 is the best choice for detecting L. infantum DNA in naturally infected dogs.

Keywords: Canine visceral leishmaniasis; Leishmaniainfantum; Molecular diagnosis.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • DNA, Kinetoplast / genetics
  • Dog Diseases / diagnosis*
  • Dogs / parasitology*
  • Female
  • Leishmania infantum / genetics
  • Leishmania infantum / isolation & purification*
  • Leishmaniasis, Visceral / veterinary*
  • Male
  • Polymerase Chain Reaction / methods*

Substances

  • DNA, Kinetoplast