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Background <p>Leishmaniasis is a parasitic disease transmitted by female sand flies and caused by protozoan parasites of the genus&#xa0;<i>Leishmania</i>. Accurate quantification of parasite load within vectors is essential for understanding transmission dynamics and vector competence. This study compares two quantitative polymerase chain reaction (qPCR) methods for detecting and quantifying <i>Leishmania infantum</i> in three experimentally infected sand fly species (<i>Phlebotomus perniciosus</i>,&#xa0;<i>Phlebotomus argentipes</i>, and&#xa0;<i>Phlebotomus orientalis</i>).</p> Methods <p>One method targets kinetoplast minicircle DNA, which offers high sensitivity but limited quantitative precision, while the other targets the single-copy&#xa0;<i>Meta-1</i> gene, providing more precise quantification but reduced sensitivity in low-level infections.</p> Results <p>A positive correlation between the two molecular markers supports a combined approach to maximize both sensitivity and accuracy in surveillance and transmission studies. Following this methodological comparison, significant differences were observed in parasite proliferation among sand fly species and&#xa0;<i>L. infantum</i> strains, with&#xa0;<i>Ph. orientalis</i>&#xa0;confirmed as a highly competent vector for&#xa0;<i>Leishmania donovani</i> complex.</p> Conclusions <p>Together, these findings highlight that combining high-sensitivity (kinetoplast DNA [kDNA]) and single-copy (<i>Meta-1</i>) targets enables both accurate and sensitive quantification of <i>Leishmania</i> infections in sand flies, improving the assessment of parasite–vector interactions.</p> Graphical Abstract <p></p>

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Comparative quantification of Leishmania infantum in experimental phlebotomine sand fly infections using kDNA and single-copy Meta-1 gene qPCR assays

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年1月24日

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  • Stefania Porcelli,
  • Jorian Prudhomme,
  • Jovana Sádlová,
  • Barbora Bečvářová,
  • Petr Volf,
  • Jérôme Depaquit,
  • Florence Robert-Gangneux

摘要

Background

Leishmaniasis is a parasitic disease transmitted by female sand flies and caused by protozoan parasites of the genus Leishmania. Accurate quantification of parasite load within vectors is essential for understanding transmission dynamics and vector competence. This study compares two quantitative polymerase chain reaction (qPCR) methods for detecting and quantifying Leishmania infantum in three experimentally infected sand fly species (Phlebotomus perniciosus, Phlebotomus argentipes, and Phlebotomus orientalis).

Methods

One method targets kinetoplast minicircle DNA, which offers high sensitivity but limited quantitative precision, while the other targets the single-copy Meta-1 gene, providing more precise quantification but reduced sensitivity in low-level infections.

Results

A positive correlation between the two molecular markers supports a combined approach to maximize both sensitivity and accuracy in surveillance and transmission studies. Following this methodological comparison, significant differences were observed in parasite proliferation among sand fly species and L. infantum strains, with Ph. orientalis confirmed as a highly competent vector for Leishmania donovani complex.

Conclusions

Together, these findings highlight that combining high-sensitivity (kinetoplast DNA [kDNA]) and single-copy (Meta-1) targets enables both accurate and sensitive quantification of Leishmania infections in sand flies, improving the assessment of parasite–vector interactions.

Graphical Abstract