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. 2018 Jan 15;11(1):37.
doi: 10.1186/s13071-018-2613-2.

Leishmania mortality in sand fly blood meal is not species-specific and does not result from direct effect of proteinases

Affiliations

Leishmania mortality in sand fly blood meal is not species-specific and does not result from direct effect of proteinases

Katerina Pruzinova et al. Parasit Vectors. .

Abstract

Background: Leishmania development in sand flies is confined to the alimentary tract and is closely connected with blood meal digestion. Previously, it has been published that activities of sand fly midgut proteases are harmful to Leishmania, especially to amastigote-promastigote transition forms. However, our experiments with various Leishmania-sand fly pairs gave quite opposite results.

Methods: We evaluated the effect of semi-digested midgut content on different life stages of Leishmania donovani and Leishmania major in vitro. Various morphological forms of parasites, including macrophage-derived amastigotes and transition forms, were incubated 2 h with midguts dissected at various intervals (6-72 h) post-blood meal or with commercially available proteinase, and their viability was determined using flow cytometry. In parallel, using amastigote-initiated experimental infections, we compared development of L. donovani in sand flies that are either susceptible (Phlebotomus argentipes and P. orientalis) or refractory (P. papatasi and Sergentomyia schwetzi) to this parasite.

Results: In vitro, sand fly midgut homogenates affected L. major and L. donovani in a similar way; in all sand fly species, the most significant mortality effect was observed by the end of the blood meal digestion process. Surprisingly, the most susceptible Leishmania stages were promastigotes, while mortality of transforming parasites and amastigotes was significantly lower. Parasites were also susceptible to killing by rabbit blood in combination with proteinase, but resistant to proteinase itself. In vivo, L. donovani developed late-stage infections in both natural vectors; in P. argentipes the development was much faster than in P. orientalis. On the other hand, in refractory species P. papatasi and S. schwetzi, promastigotes survived activity of digestive enzymes but were lost during defecation.

Conclusions: We demonstrated that Leishmania transition forms are more resistant to the killing effect of semi-digested blood meal than 24 h-old promastigotes. Data suggest that Leishmania mortality is not caused directly by sand fly proteases, we assume that this mortality results from toxic products of blood meal digestion. Survival of L. donovani promastigotes in refractory sand flies until blood meal defecation, together with similar mortality of Leishmania parasites incubated in vitro with midgut homogenates of susceptible as well as refractory species, contradict the previously raised hypotheses about the role of midgut proteases in sand fly vector competence to Leishmania.

Keywords: Blood meal digestion; Leishmania donovani; Leishmania major; Phlebotomus; Proteases; Sand fly; Sergentomyia.

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Conflict of interest statement

Ethics approval

Animals used for maintenance of sand flies colonies were maintained and handled in the animal facility of Charles University in Prague in accordance with institutional guidelines and Czech legislation (Act No. 246/1992 and 359/2012 coll. on Protection of Animals against Cruelty in present statutes at large), which complies with all relevant EU guidelines for experimental animals. All experiments were approved by the Committee on the Ethics of Laboratory Experiments of the Charles University in Prague and were performed under the Certificate of Competency (Registration Number: CZ 03069).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
Different L. donovani stages incubated with sand fly midguts dissected at 24 h post-blood meal. Leishmania donovani amastigotes (0 h AMA), parasites within amastigote-promastigote transition (5 h AMA/PROMA) and promastigotes (24 h PROMA) were incubated in a microtiter plate for 2 h with saline or midguts of P. argentipes, P. orientalis, P. papatasi and S. schwetzi dissected at 24 h post-blood meal. As a positive control, parasites killed by 1% formaldehyde and permeabilised by 0.5% Triton X-100 were used
Fig. 2
Fig. 2
Different L. major stages incubated with sand fly midguts dissected at 24 h post-blood meal. Leishmania major amastigotes (0 h AMA), parasites within amastigote-promastigote transition (5 h AMA/PROMA) and promastigotes (24 h PROMA) were incubated in a microtiter plate for 2 h with saline or midguts of P. argentipes, P. orientalis, P. papatasi and S. schwetzi dissected at 24 h post-blood meal. As a positive control, parasites killed by 1% formaldehyde and permeabilised by 0.5% Triton X-100 were used
Fig. 3
Fig. 3
Promastigotes of L. donovani incubated with sand fly midguts dissected at different times post-blood meal and various controls. Leishmania donovani promastigotes (24 h after the releasing from macrophages) were incubated in a microtiter plate for 2 h with: a midguts of P. argentipes, P. orientalis, P. papatasi and S. schwetzi dissected at 6, 24, 32, 48 and 72 h post-blood meal; or b with saline, proteinase K (PK), rabbit blood, red cells of rabbit blood, human haemoglobin, blood + proteinase K, red cells + proteinase K and human haemoglobin + proteinase K. As a positive control, parasites killed by 1% formaldehyde and permeabilised by 0.5% Triton X-100 were used
Fig. 4
Fig. 4
Amastigote-initiated infections of L. donovani in four sand fly species: P. orientalis (ORI), P. argentipes (ARG), P. papatasi (PAP) and S. schwetzi (SER). a Rates and intensities of L. donovani infections. Numbers of dissected females are shown above bars. Differences between species were evaluated using Chi-square test: day 2 PBM, χ2 = 20.009, df = 9, P = 0.018; day 3 pbm, χ2 = 74.880, df = 9, P < 0.0001; day 6 pbm, χ2 = 255.6, df = 9, P < 0.0001; day 10 pbm, χ2 = 296.2, df = 9, P < 0.0001. b Location of L. donovani in infected sand flies. Differences between species were evaluated using Chi-square test: day 2 PBM, χ2 = 96.863, df = 9, P < 0.0001; day 3 pbm, χ2 = 121.7, df = 12, P < 0.0001; day 6 pbm, χ2 = 260.1, df = 15, P < 0.0001; day 10 pbm, χ2 = 301.6, df = 9, P < 0.0001. c Morphological forms of L. donovani in infected sand flies. The guts of infected females were sampled at 2, 3, 6 and 10 days pbm and parasite morphometry determined as described in methods. The percentage of each form found in infected flies at each time point is shown. Differences among lines were most significant during early infections; day 2 pbm, χ2 = 190.7, df = 9, P < 0.0001; day 3 pbm, χ2 = 196.5, df = 9, P < 0.0001; day 6 pbm, χ2 = 8.572, df = 2, P = 0.014; day 10 pbm, χ2 = 6.755, df = 2, P = 0. 034. Abbreviations: E.SP., endoperitrophic space, AMG, abdominal midgut; TMG, thoracic midgut; SV, stomodeal valve

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