Abstract

In leishmaniasis caused by Leishmania infantum, the dog acts as the main reservoir for the disease. Non-invasive sampling for Leishmania detection is pivotal for rapid and affordable diagnosis. Recently, the use of conjunctival swab (CS) has been evaluated as a non-invasive sampling technique for quantitative real-time PCR (qPCR). However, few investigations have been made on the applicability of CS qPCR in particular cases such as dogs with borderline IFAT titres, suspected disease relapse with comorbidity and therapy monitoring. The aims of this study were i) to confirm the efficacy of CS, comparing these samples to buffy coat (BC) samples, as effective non-invasive samples for Leishmania quantitative detection by qPCR and ii) to verify the usefulness of qPCR compared to conventional laboratory and clinical parameters to assist in therapeutic decision making regarding dogs with complex clinical cases. Eighty dogs were divided into 4 groups based on their IFAT titres and clinical histories. Two qPCR assays were performed both on CS raw lysates and on purified DNA from BC samples. The assays were then compared. Z tests for difference of proportion, with Bonferroni correction, were carried out to evaluate the qPCR results. Logistic regression with backward stepwise elimination was performed to detect the subset of haematochemical variables significantly associated with PCR positivity. The qPCR performed on CS samples showed better sensitivity (87%) and specificity (96%) than assays carried out using BC samples, regardless of the primers used. The haematochemical parameters haemoglobin and globulins were found to be significantly associated with qPCR positivity. Pearson correlations between Leishmania k DNA load in CS and body condition scores or IFAT titres were calculated in dogs with new leishmaniasis diagnoses. The Leishmania k DNA load in CS correlated moderately with IFAT titres (R = 0.59) but a very weak correlation (R = 0.37) with body condition score (BCS) was found. The applicability of CS for Leishmania detection in dogs was confirmed, revealing the usefulness of raw lysates for quantitative purposes. Moreover, the qPCR was found to be particularly useful in cases lacking a clear clinical diagnosis, where the haematochemical values cannot be predictive.

Highlights

  • In leishmaniasis caused by Leishmania infantum, the dog acts as the main reservoir for the disease

  • QPCR from conjunctival swabs (CS quantitative PCR (qPCR)) and from buffy coat (BC qPCR) The presence of Leishmania parasites was assessed in the dogs assigned to all groups by qPCR both from conjunctival swabs (CS qPCR) and buffy coat (BC qPCR)

  • Our study confirmed that BC qPCR is not as accurate as CS qPCR as a tool to rule out suspected leishmaniasis infection

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Summary

Introduction

In leishmaniasis caused by Leishmania infantum, the dog acts as the main reservoir for the disease. PCR-based Leishmania detection in CanL using whole blood or buffy coat is not without difficulties [18] It showed results variability [23,26,27,28,29], and is considered of little diagnostic value [30]. The usefulness of CS has been evaluated in the early diagnosis of leishmaniasis, but few works investigated their utility in the therapy monitoring [13] This approach has not been thoroughly investigated as a possible tool that could help guide treatment decisions in borderline cases, when there is suspicion of disease relapse or comorbidity. We confirmed the usefulness of qPCR as a quantitative diagnostic tool using CS raw lysate samples as a source of DNA, in cases with borderline IFAT titres, suspected disease relapse or the presence of comorbidity. We identified the haematochemical parameters significantly associated with qPCR positive results

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