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

. 2018 Jan 15 ; 11 (1) : 37. [epub] 20180115

Language English Country Great Britain, England Media electronic

Document type Journal Article, Research Support, Non-U.S. Gov't

Grant support
13-07 500S Czech Science Foundation (GACR) - International
204017/2012 University Research Centre (UNCE) - International

Links

PubMed 29335002
PubMed Central PMC5769529
DOI 10.1186/s13071-018-2613-2
PII: 10.1186/s13071-018-2613-2
Knihovny.cz E-resources

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.

See more in PubMed

Dostalova A, Volf P. Leishmania development in sand flies: parasite-vector interactions overview. Parasit Vectors. 2012;5:276. doi: 10.1186/1756-3305-5-276. PubMed DOI PMC

Kamhawi S. Phlebotomine sand flies and Leishmania parasites: friends or foes? Trends Parasitol. 2006;22:439–445. doi: 10.1016/j.pt.2006.06.012. PubMed DOI

Elnaiem DEA. Ecology and control of the sand fly vectors of Leishmania donovani in East Africa, with special emphasis on Phlebotomus orientalis. J Vector Ecol. 2011;36:S23–S31. doi: 10.1111/j.1948-7134.2011.00109.x. PubMed DOI

Maroli M, Feliciangeli MD, Bichaud L, Charrel RN, Gradoni L. Phlebotomine sandflies and the spreading of leishmaniases and other diseases of public health concern. Med Vet Entomol. 2013;27:123–147. doi: 10.1111/j.1365-2915.2012.01034.x. PubMed DOI

Ready PD. Biology of phlebotomine sand flies as vectors of disease agents. Annu Rev Entomol. 2013;58:227–250. doi: 10.1146/annurev-ento-120811-153557. PubMed DOI

Volf P, Myskova J. Sand flies and Leishmania: specific versus permissive vectors. Trends Parasitol. 2007;23:91–92. doi: 10.1016/j.pt.2006.12.010. PubMed DOI PMC

Dillon RJ, Ivens AC, Churcher C, Holroyd N, Quail MA, Rogers ME, et al. Analysis of ESTs from Lutzomyia longipalpis sand flies and their contribution toward understanding the insect-parasite relationship. Genomics. 2006;88:831–840. doi: 10.1016/j.ygeno.2006.06.011. PubMed DOI PMC

Ramalho-Ortigao M, Jochim RC, Anderson JM, Lawyer PG, Pham VM, Kamhawi S, Valenzuela JG. Exploring the midgut transcriptome of Phlebotomus papatasi: comparative analysis of expression profiles of sugar-fed, blood-fed and Leishmania major-infected sandflies. BMC Genomics. 2007;8:300. doi: 10.1186/1471-2164-8-300. PubMed DOI PMC

Jochim RC, Teixeira CR, Laughinghouse A, JB M, Oliveira F, Gomes RB, et al. The midgut transcriptome of Lutzomyia longipalpis: comparative analysis of cDNA libraries from sugar-fed, blood-fed, post-digested and Leishmania infantum chagasi-infected sand flies. BMC Genomics. 2008;9:15. doi: 10.1186/1471-2164-9-15. PubMed DOI PMC

Dillon RJ, Lane RP. Bloodmeal digestion in the midgut of Phlebotomus papatasi and Phlebotomus langeroni. Med Vet Entomol. 1993;7:225–232. doi: 10.1111/j.1365-2915.1993.tb00681.x. PubMed DOI

Telleria EL, de Araujo APO, Secundino NF, d'Avila-Levy CM, Traub-Cseko YM. Trypsin like serine proteases in Lutzomyia longipalpis - expression, activity and possible modulation by Leishmania infantum chagasi. PLoS One. 2010;5:e10697. doi: 10.1371/journal.pone.0010697. PubMed DOI PMC

Pruzinova K, Sadlova J, Seblova V, Homola M, Votypka J, Volf P. Comparison of bloodmeal digestion and the peritrophic matrix in four sand fly species differing in susceptibility to Leishmania donovani. PLoS One. 2015;10:e0128203. doi: 10.1371/journal.pone.0128203. PubMed DOI PMC

Pruzinova K, Votypka J, Volf P. The effect of avian blood on Leishmania development in Phlebotomus duboscqi. Parasit Vectors. 2013;6:254. doi: 10.1186/1756-3305-6-254. PubMed DOI PMC

Borovsky D, Schlein Y. Trypsin and chymotrypsin-like enzymes of the sandfly Phlebotomus papatasi infected with Leishmania and their possible role in vector competence. Med Vet Entomol. 1987;1:235–242. doi: 10.1111/j.1365-2915.1987.tb00349.x. PubMed DOI

Pimenta PFP, Modi GB, Pereira ST, Shahabuddin M, Sacks DL. Novel role for the peritrophic matrix in protecting Leishmania from the hydrolytic activities of the sand fly midgut. Parasitology. 1997;115:359–369. doi: 10.1017/S0031182097001510. PubMed DOI

Schlein Y, Jacobson RL. Resistance of Phlebotomus papatasi to infection with Leishmania donovani is modulated by components of the infective bloodmeal. Parasitology. 1998;117:467–473. doi: 10.1017/S0031182098003321. PubMed DOI

Schlein Y, Romano H. Leishmania major and Leishmania donovani - effects on proteolytic enzymes of Phlebotomus papatasi (Diptera, Psychodidae) Exp Parasitol. 1986;62:376–380. doi: 10.1016/0014-4894(86)90045-7. PubMed DOI

Seblova V, Volfova V, Dvorak V, Pruzinova K, Votypka J, Kassahun A, et al. Phlebotomus orientalis sand flies from two geographically distant Ethiopian localities: biology, genetic analyses and susceptibility to Leishmania donovani. PLoS Negl Trop Dis. 2013;7:e2187. doi: 10.1371/journal.pntd.0002187. PubMed DOI PMC

Hoogstraal H, Heyneman D. Leishmaniasis in Sudan Republic. 30. Final epidemiologic report. Am J Trop Med Hyg. 1969;18:1091–1210. doi: 10.4269/ajtmh.1969.18.1091. DOI

Sadlova J, Dvorak V, Seblova V, Warburg A, Votypka J, Volf P. Sergentomyia schwetzi is not a competent vector for Leishmania donovani and other Leishmania species pathogenic to humans. Parasit Vectors. 2013;6:186. doi: 10.1186/1756-3305-6-186. PubMed DOI PMC

Volf P, Volfova V. Establishment and maintenance of sand fly colonies. J Vector Ecol. 2011;36:S1–S9. doi: 10.1111/j.1948-7134.2011.00106.x. PubMed DOI

Chang KP. Human cutaneous Leishmania in a mouse macrophage line: propagation and isolation of intracellular parasites. Science. 1980;209:1240–2. PubMed

Myskova J, Votypka J, Volf P. Leishmania in sand flies: comparison of quantitative polymerase chain reaction with other techniques to determine the intensity of infection. J Med Entomol. 2008;45:133–138. doi: 10.1093/jmedent/45.1.133. PubMed DOI

Sadlova J, Myskova J, Lestinova T, Votypka J, Yeo M, Volf P. Leishmania donovani development in Phlebotomus argentipes: comparison of promastigote- and amastigote-initiated infections. Parasitology. 2017;144:403–410. doi: 10.1017/S0031182016002067. PubMed DOI PMC

Schlein Y, Jacobson RL. Hemoglobin inhibits the development of infective promastigotes and chitinase secretion in Leishmania major cultures. Parasitology. 1994;109:23–28. doi: 10.1017/S0031182000077726. PubMed DOI

Balla J, Vercellotti GM, Jeney V, Yachie A, Varga Z, Eaton JW, Balla G. Heme, heme oxygenase and ferritin in vascular endothelial cell injury. Mol Nutr Food Res. 2005;49:1030–1043. doi: 10.1002/mnfr.200500076. PubMed DOI

Dillon RJ, Lane RP. Influence of Leishmania infection on blood meal digestion in the sandflies Phlebotomus papatasi and Phlebotomus langeronia. Parasitol Res. 1993;79:492–496. doi: 10.1007/BF00931590. PubMed DOI

Doehl JS, Sadlova J, Aslan H, Pruzinova K, Metangmo S, Votypka J, et al. Leishmania HASP and SHERP genes are required for in vivo differentiation, parasite transmission and virulence attenuation in the host. PLoS Pathog. 2017;13:e1006130. PubMed PMC

Pascoa V, Oliveira PL, Dansa-Petretski M, Silva JR, Alvarenga PH, Jacobs-Lorena M, Lemos FJ. Aedes aegypti peritrophic matrix and its interaction with heme during blood digestion. Insect Biochem Molec. 2002;32:517–523. doi: 10.1016/S0965-1748(01)00130-8. PubMed DOI

Pimenta PFP, Saraiva EMB, Rowton E, Modi GB, Garraway LA, Beverley SM, et al. Evidence that the vectorial competence of phlebotomine sand flies for different species of Leishmanias.s. controlled by structural polymorphisms in the surface lipophosphoglycan. Proc Natl Acad Sci USA. 1994;91:9155–9. PubMed PMC

Kamhawi S, Ramalho-Ortigao M, Pham VM, Kumar S, Lawyer PG, Turco SJ, et al. A role for insect galectins in parasite survival. Cell. 2004;119:329–341. doi: 10.1016/j.cell.2004.10.009. PubMed DOI

Chajbullinova A, Votypka J, Sadlova J, Kvapilova K, Seblova V, Kreisinger J, et al. The development of Leishmania turanica in sand flies and competition with L. major. Parasit Vectors. 2012;5:219. doi: 10.1186/1756-3305-5-219. PubMed DOI PMC

Volf P, Nogueira PM, Myskova J, Turco SJ, Soares RP. Structural comparison of lipophosphoglycan from Leishmania turanica and L. major, two species transmitted by Phlebotomus papatasi. Parasitol Int. 2014;63:683–686. doi: 10.1016/j.parint.2014.05.004. PubMed DOI

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