Natural hybrid of Leishmania infantum/L. donovani: development in Phlebotomus tobbi, P. perniciosus and Lutzomyia longipalpis and comparison with non-hybrid strains differing in tissue tropism
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
26608249
PubMed Central
PMC4660806
DOI
10.1186/s13071-015-1217-3
PII: 10.1186/s13071-015-1217-3
Knihovny.cz E-zdroje
- MeSH
- gastrointestinální trakt parazitologie MeSH
- hmyz - vektory parazitologie MeSH
- králíci MeSH
- Leishmania infantum genetika růst a vývoj izolace a purifikace MeSH
- Leishmania major genetika růst a vývoj izolace a purifikace MeSH
- leishmanióza kožní epidemiologie parazitologie MeSH
- lidé MeSH
- Phlebotomus parazitologie MeSH
- Psychodidae parazitologie MeSH
- tropismus MeSH
- zvířata MeSH
- Check Tag
- králíci MeSH
- lidé MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Geografické názvy
- Turecko MeSH
BACKGROUND: Infection caused by parasites from L. donovani complex can manifest as a serious visceral disease or a self-healing milder cutaneous form. The different tropism and pathology in humans is caused by the interaction between parasites, host and vector determinants but the mechanisms are not well understood. In Cukurova region in Turkey we previously identified a major focus of cutaneous leishmaniasis caused by L. donovani/infantum hybrids (CUK strain) and isolated this parasite from the locally abundant sand fly, Phlebotomus tobbi. Here, we present the first experimental study with P. tobbi. We tested the susceptibility of this species to various Leishmania under laboratory conditions, characterized glycoproteins in the P. tobbi midgut putatively involved in parasite-vector interaction and compared the development of the CUK strain in the sand fly with one other dermotropic and three viscerotropic strains belonging to the L. donovani complex. METHODS: Females of laboratory reared P. tobbi, P. perniciosus and Lutzomyia longipalpis were infected using membrane feeding on rabbit blood containing promastigotes of various Leishmania species with different tropisms. The individual guts were checked microscopically for presence and localization of Leishmania parasites; the number of parasites was assessed more precisely by qPCR. In addition, glycosylation of midgut proteins of P. tobbi was studied by lectin blotting of midgut lysate with lectins specific for terminal sugars of N-type and O-type glycans. RESULTS: High infection rates, heavy parasite loads and late-stage infection with colonization of the stomodeal valve were observed in P. tobbi infected by Leishmania major or L. infantum CUK hybrid. In parallel, lectin blotting revealed the presence of O-glycosylated proteins in the P. tobbi midgut. In P. perniciosus and L. longipalpis all five Leishmania strains tested developed well. In both vectors, significantly higher parasite numbers were detected by qPCR for dermotropic L. donovani from Cyprus, however, in all other parameters studied, including localization of infection and colonization of stomodeal valve, dermotropic and viscerotropic strains were not significantly different. CONCLUSIONS: We showed high susceptibility of P. tobbi to various Leishmania spp. This, together with the presence of O-glycosylated midgut proteins in their midguts demonstrate that P. tobbi is a permissive vector. Two dermotropic and three viscerotropic strains from the L. donovani complex developed late-stage infections in natural L. infantum vectors, P. perniciosus and L. longipalpis and none of the parameters studied seem to be linked with different tropism of parasites in the vertebrate host.
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Antoniou M, Gramiccia M, Molina R, Dvorak V, Volf P. The role of indigenous phlebotomine sandflies and mammals in the spreading of leishmaniasis agents in the Mediterranean region. Euro Surveill. 2013;18:20540. doi: 10.2807/1560-7917.ES2013.18.30.20540. 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. 2012;27:123–47. doi: 10.1111/j.1365-2915.2012.01034.x. PubMed DOI
Kamhawi S. Phlebotomine sand flies and Leishmania parasites: friends or foes? Trends Parasitol. 2006;22:439–45. doi: 10.1016/j.pt.2006.06.012. PubMed DOI
Myskova J, Svobodova M, Beverley SM, Volf P. A lipophosphoglycan-independent development of Leishmania in permissive sand flies. Microbes Infect. 2007;9:317–24. doi: 10.1016/j.micinf.2006.12.010. PubMed DOI PMC
Volf P, Myskova J. Sand flies and Leishmania: specific versus permissive vectors. Trends Parasitol. 2007;23:91–2. doi: 10.1016/j.pt.2006.12.010. PubMed DOI PMC
Svobodova M, Alten B, Zídková L, Dvořák V, Hlavačková J, Myšková J, et al. Cutaneous leishmaniasis caused by Leishmania infantum transmitted by Phlebotomus tobbi. Int J Parasitol. 2009;39:251–6. doi: 10.1016/j.ijpara.2008.06.016. PubMed DOI
Gouzelou E, Haralambous C, Amro A, Mentis A, Pratlong F, Dedet J-P, et al. Multilocus Microsatellite Typing (MLMT) of Strains from Turkey and Cyprus Reveals a Novel Monophyletic L. donovani Sensu Lato Group. PLoS Negl Trop Dis. 2012;6:e1507. doi: 10.1371/journal.pntd.0001507. PubMed DOI PMC
Rogers MB, Downing T, Smith BA, Imamura H, Sanders M, Svobodova M, et al. Genomic confirmation of hybridisation and recent inbreeding in a vector-isolated Leishmania population. PLoS Genet. 2014;10 doi: 10.1371/journal.pgen.1004092. PubMed DOI PMC
Killick-Kendrick R. The biology and control of phlebotomine sand flies. Clin Dermatol. 1999;17:279–89. doi: 10.1016/S0738-081X(99)00046-2. PubMed DOI
Rioux JA, Legér N, Haddaa N, Gramiccia M, Jalouk L, Dereure J, et al. Naturelle de Phlebotomus tobbi (Diptera, Psychodidae) par Leishmania donovani s. st. (Kinetoplastida, Trypanosomatidae), en Syrie. Parassitologia. 1998;40:148.
Léger N, Depaquit J, Ferté H, Rioux JA, Gantier JC, Gramiccia M, et al. [Phlebotomine sandflies (Diptera-Psychodidae) of the isle of Cyprus. II--Isolation and typing of Leishmania (Leishmania infantum Nicolle, 1908 (zymodeme MON 1) from Phlebotomus (Larroussius) tobbi Adler and Theodor, 1930] Parasite. 2000;7:143–6. doi: 10.1051/parasite/2000072143. PubMed DOI
Ergunay K, Kasap OE, Orsten S, Oter K, Gunay F, Yoldar AZA, et al. Phlebovirus and Leishmania detection in sandflies from eastern Thrace and northern Cyprus. Parasit Vectors. 2014;7:575. doi: 10.1186/s13071-014-0575-6. PubMed DOI PMC
Rassi Y, Sanei Dehkordi A, Oshaghi MA, Abai MR, Mohtarami F, Enayati A, et al. First report on natural infection of the Phlebotomus tobbi by Leishmania infantum in northwestern Iran. Exp Parasitol. 2012;3:344–9. doi: 10.1016/j.exppara.2012.04.020. PubMed DOI
Oshaghi MA, Rassi Y, Hazratian T, Fallah E, Rafizadeh S. Natural infection of wild caught Phlebotomus tobbi to Leishmania infantum in East Azerbaijan province, northwestern Iran. J Vector Borne Dis. 2013;50:24–9. PubMed
Warburg A, Schlein Y. The effect of post-bloodmeal nutrition of Phlebotomus papatasi on the transmission of Leishmania major. Am J Trop Med Hyg. 1986;35:926–30. PubMed
Kimblin N, Peters N, Debrabant A, Secundino N, Egen J, Lawyer P, et al. Quantification of the infectious dose of Leishmania major transmitted to the skin by single sand flies. Proc Natl Acad Sci U S A. 2008;105:10125–30. doi: 10.1073/pnas.0802331105. PubMed DOI PMC
Maia C, Seblova V, Sadlova J, Votypka J, Volf P. Experimental transmission of Leishmania infantum by two major vectors: a comparison between a viscerotropic and a dermotropic strain. PLoS Negl Trop Dis. 2011;5 doi: 10.1371/journal.pntd.0001181. PubMed DOI PMC
Secundino NFC, de Freitas VC, Monteiro CC, Pires A-CAM, David BA, Pimenta PFP. The transmission of Leishmania infantum chagasi by the bite of the Lutzomyia longipalpis to two different vertebrates. Parasit Vectors. 2012;5:20. doi: 10.1186/1756-3305-5-20. PubMed DOI PMC
Antoniou M, Gramiccia M, Molina R, Dvorak V, Volf P. The role of indigenous phlebotomine sandflies and mammals in the spreading of leishmaniasis agents in the Mediterranean region. Eurosurveillance. 2013;18:1–9. doi: 10.2807/1560-7917.ES2013.18.30.20540. PubMed DOI
Maia C, Nunes M, Cristóvão J, Campino L. Experimental canine leishmaniasis: Clinical, parasitological and serological follow-up. Acta Trop. 2010;116:193–9. doi: 10.1016/j.actatropica.2010.08.001. PubMed DOI
Volf P, Volfova V. Establishment and maintenance of sand fly colonies. J Vector Ecol. 2011;36(Suppl 1):S1–9. doi: 10.1111/j.1948-7134.2011.00106.x. PubMed DOI
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;45:133–8. doi: 10.1093/jmedent/45.1.133. PubMed DOI
Mary C, Faraut F, Lascombe L, Dumon H. Quantification of Leishmania infantum DNA by a Real-Time PCR Assay with High Sensitivity. J Clin Microbiol. 2004;42:5249–55. doi: 10.1128/JCM.42.11.5249-5255.2004. PubMed DOI PMC
Dostálová 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
Sharon N, Lis H. Lectins. 2. The Netherlands: Springer: Dordrech; 2007. Specificity and affinity; pp. 63–103.
Killick-Kendrick R. Phlebotomine vectors of the leishmaniases: a review. Med Vet Entomol. 1990;4:1–24. doi: 10.1111/j.1365-2915.1990.tb00255.x. PubMed DOI
Velo E, Paparisto A, Bongiorno G, Di Muccio T, Khoury C, Bino S, et al. Entomological and parasitological study on phlebotomine sandflies in central and northern Albania. Parasite. 2005;12:45–9. doi: 10.1051/parasite/2005121045. PubMed DOI
McMahon-Pratt D, Alexander J. Does the Leishmania major paradigm of pathogenesis and protection hold for New World cutaneous leishmaniases or the visceral disease? Immunol Rev. 2004;201:206–24. doi: 10.1111/j.0105-2896.2004.00190.x. PubMed DOI
Zhang W-W, Matlashewski G. Screening Leishmania donovani-specific genes required for visceral infection. Mol Microbiol. 2010;77:505–17. doi: 10.1111/j.1365-2958.2010.07230.x. PubMed DOI
Gradoni L, Gramiccia M. Leishmania infantum tropism: strain genotype or host immune status? Parasitol Today. 1994;10:264–7. doi: 10.1016/0169-4758(94)90142-2. PubMed DOI
Lipoldová M, Demant P. Genetic susceptibility to infectious disease: lessons from mouse models of leishmaniasis. Nat Rev Genet. 2006;7:294–305. doi: 10.1038/nrg1832. PubMed DOI
McCall L-I, Zhang W-W, Matlashewski G. Determinants for the development of visceral leishmaniasis disease. PLoS Pathog. 2013;9 doi: 10.1371/journal.ppat.1003053. PubMed DOI PMC
Pratlong F, Dedet JP, Marty P, Portús M, Deniau M, Dereure J, et al. Leishmania-human immunodeficiency virus coinfection in the Mediterranean basin: isoenzymatic characterization of 100 isolates of the Leishmania infantum complex. J Infect Dis. 1995;172:323–6. doi: 10.1093/infdis/172.1.323. PubMed DOI
Gradoni L, Guaraldi G, Codeluppi M, Scalone A, Rivasi F. Gastric localization of Leishmania in a patient with acquired immunodeficiency syndrome. A case report. APMIS. 1995;103:25–8. doi: 10.1111/j.1699-0463.1995.tb01075.x. PubMed DOI
Votypka J, Kasap OE, Volf P, Kodym P, Alten B. Risk factors for cutaneous leishmaniasis in Cukurova region, Turkey. Trans R Soc Trop Med Hyg. 2012;106:186–90. doi: 10.1016/j.trstmh.2011.12.004. PubMed DOI
Louassini M, Adroher FJ, Foulquié MR, Benítez R. Investigations on the in vitro metacyclogenesis of a visceral and a cutaneous human strain of Leishmania infantum. Acta Trop. 1998;70:355–68. doi: 10.1016/S0001-706X(98)00041-2. PubMed DOI
Campos-Ponce M, Ponce C, Ponce E, Maingon RDC. Leishmania chagasi/infantum: further investigations on Leishmania tropisms in atypical cutaneous and visceral leishmaniasis foci in Central America. Exp Parasitol. 2005;109:209–19. doi: 10.1016/j.exppara.2004.11.013. PubMed DOI
Meddeb-Garnaoui A, Zrelli H, Dellagi K. Effects of tropism and virulence of Leishmania parasites on cytokine production by infected human monocytes. Clin Exp Immunol. 2009;155:199–206. doi: 10.1111/j.1365-2249.2008.03821.x. PubMed DOI PMC
Sulahian A, Garin YJ, Pratlong F, Dedet JP, Derouin F. Experimental pathogenicity of viscerotropic and dermotropic isolates of Leishmania infantum from immunocompromised and immunocompetent patients in a murine model. FEMS Immunol Med Microbiol. 1997;17:131–8. doi: 10.1111/j.1574-695X.1997.tb01005.x. PubMed DOI
Cunha J, Carrillo E, Sánchez C, Cruz I, Moreno J, Cordeiro-da-Silva A. Characterization of the biology and infectivity of Leishmania infantum viscerotropic and dermotropic strains isolated from HIV+ and HIV- patients in the murine model of visceral leishmaniasis. Parasit Vectors. 2013;6:122. doi: 10.1186/1756-3305-6-122. PubMed DOI PMC
Lutzomyia migonei is a permissive vector competent for Leishmania infantum