Test combination to detect latent Leishmania infection: A prevalence study in a newly endemic area for L. infantum, northeastern Italy

Abstract

Background Most people infected with Leishmania remain asymptomatic, which is a common element that may promote the resurgence of clinically evident leishmaniasis in individuals with impaired cell-mediated immune responses. Unfortunately, there is no universally accepted assay to identify asymptomatic infection. This cross-sectional study focuses on the employment of three methods targeting different features of the parasitic infection to be used in combination for the screening of latent leishmaniasis in a newly endemic area of northeastern Italy. Methodology/principle findings The selected methods included highly sensitive Real-Time PCR for detection of parasitic kinetoplast (k)DNA in peripheral blood, Western Blot (WB) for detection of specific IgG, and Whole Blood stimulation Assay (WBA) to evaluate the anti-leishmanial T-cell response by quantifying the production of IL-2 after stimulation of patients’ blood with Leishmania specific antigens. Among 145 individuals, living in a municipality of the Bologna province, northeastern Italy, recruited and screened for Leishmania infection, 23 subjects tested positive (15.9%) to one or more tests. Positive serology was the most common marker of latent leishmaniasis (15/145, 10%), followed by the detection of specific cell-mediated response (12/145, 8%), while only few individuals (6/145, 4%) harbored parasitic DNA in the blood. Conclusions/significance Combining different tests substantially increased the yield of positivity in detecting latent Leishmania infection. The test combination that we employed in this study appears to be effective to accurately identify latent leishmaniasis in an endemic area.

Demographic characteristics and prevalence of asymptomatic Leishmania donovani infection in migrant workers working in an endemic area in Northwest Ethiopia

“…And indeed, our results show that almost half of PCR-positive individuals reverted to being PCR negative at T2. Furthermore, as shown by others ( 70 – 73 ), there was poor agreement between DAT and PCR tests. At T2, 16 FC were tested by both PCR and DAT, and only 2 were positive for the presence of parasite DNA in the blood, as well as anti- Leishmania antibodies.…”

Demographic characteristics and prevalence of asymptomaticLeishmania donovaniinfection in migrant workers working in an endemic area in Northwest Ethiopia

“…And indeed, our results show that almost half of PCRpositive individuals reverted to being PCR negative at T2. Furthermore, as shown by others (71)(72)(73)(74), there was poor agreement between DAT and PCR tests. At T2, 16 FC were tested by both PCR and DAT, and only 2 were positive for the presence of parasite DNA in the blood, as well as anti-Leishmania antibodies.…”