Value of two PCR methods for the diagnosis of canine visceral leishmaniasis and the detection of asymptomatic carriers

Parasitology. 2002 Sep;125(Pt 3):197-207. doi: 10.1017/s0031182002002081.

Abstract

The value of 2 PCR methods, targeting genomic and kinetoplast minicircle DNA respectively, was investigated for both diagnosis and prevalence studies of canine visceral leishmaniasis (CVL). The first method (R) was 5000-fold less sensitive than the second (method KRV). Both were tested for diagnosis of CVL in 44 sick dogs with confirmed disease using different biological samples. Method R was highly efficient when using invasive samples, but the use of method KRV proved necessary for a 100% sensitive diagnosis using peripheral blood. This method was applied to peripheral blood and skin samples in 263 dogs during a mass survey in the Cévennes focus. PCR was compared to serology and all results were analysed according to clinical status. The 'CVL-infection' prevalence was found to be 79.8% by PCR compared with 29.6% by serology: 89.4% of symptomatic and 65.2% of asymptomatic dogs harboured parasites in peripheral blood. This study confirms the high prevalence of asymptomatic carriers of Leishmania. In total, for the diagnosis of CVL in sick dogs, method R is recommended in view of its 100% positive predictive value (compared with 30% for method KRV). A strategy best adapted for prevalence surveys might combine serology and highly sensitive PCR on peripheral blood.

Publication types

  • Comparative Study
  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier State / diagnosis*
  • Carrier State / parasitology*
  • DNA, Kinetoplast / analysis
  • DNA, Kinetoplast / genetics
  • DNA, Protozoan / analysis
  • DNA, Protozoan / genetics
  • Dog Diseases / diagnosis*
  • Dog Diseases / parasitology*
  • Dogs
  • France
  • Leishmania infantum / genetics
  • Leishmania infantum / isolation & purification
  • Leishmaniasis, Visceral / diagnosis*
  • Leishmaniasis, Visceral / veterinary*
  • Polymerase Chain Reaction / methods*
  • Prevalence
  • Sensitivity and Specificity

Substances

  • DNA, Kinetoplast
  • DNA, Protozoan