Ecology, seasonality and host preferences of Austrian Phlebotomus (Transphlebotomus) mascittii Grassi, 1908, populations
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
DOC Fellowship
Österreichischen Akademie der Wissenschaften
BIOCEV CZ.1.05/1.1.00/02.0109
Interreg
CZ.02.1.01/0.0/0.0/16_019/0000759
Interreg
PubMed
34051839
PubMed Central
PMC8164323
DOI
10.1186/s13071-021-04787-2
PII: 10.1186/s13071-021-04787-2
Knihovny.cz E-zdroje
- Klíčová slova
- Blood meal, Central Europe, Climate, MALDI-TOF, Phlebotomine sand fly,
- MeSH
- ekologie * MeSH
- hmyz - vektory * parazitologie MeSH
- koně MeSH
- kur domácí MeSH
- Leishmania infantum MeSH
- Phlebotomus * genetika MeSH
- Psychodidae MeSH
- retrospektivní studie MeSH
- roční období * MeSH
- sekvenční analýza DNA MeSH
- spektrometrie hmotnostní - ionizace laserem za účasti matrice MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Evropa MeSH
- Rakousko MeSH
BACKGROUND: Sand flies are principal vectors of the protozoan parasites Leishmania spp. and are widely distributed in all warmer regions of the world, including the Mediterranean parts of Europe. In Central European countries, the sand fly fauna is still under investigation. Phlebotomus mascittii, a suspected but unproven vector of Leishmania infantum, is regarded as the most widely distributed species in Europe. However, many aspects of its biology and ecology remain poorly known. The aim of this study was to provide new data on the biology and ecology of Ph. mascittii in Austria to better understand its current distribution and potential dispersal. METHODS: Sand flies were collected by CDC light traps at four localities in Austria for 11 (2018) and 15 weeks (2019) during the active sand fly season. Climatic parameters (temperature, relative humidity, barometric pressure and wind speed) were retrospectively obtained for the trapping periods. Sand flies were identified by a combined approach (morphology, DNA barcoding, MALDI-TOF protein profiling), and blood meals of engorged females were analysed by DNA sequencing and MALDI-TOF mass spectrometry. RESULTS: In total, 450 individuals of Ph. mascittii were caught. Activity was observed to start at the beginning of June and end at the end of August with peaks in mid-July at three locations and early August at one location. Increased activity was associated with relatively high temperatures and humidity. Also, more individuals were caught on nights with low barometric pressure. Analysis of five identified blood meals revealed chicken (Gallus gallus) and equine (Equus spp.) hosts. Sand fly abundance was generally associated with availability of hosts. CONCLUSION: This study reports unexpectedly high numbers of Ph. mascittii at selected Austrian localities and provides the first detailed analysis of its ecology to date. Temperature and humidity were shown to be good predictors for sand fly activity. Blood meal analyses support the assumption that Ph. mascittii feeds on mammals as well as birds. The study significantly contributes to understanding the ecology of this sand fly species in Central Europe and facilitates prospective entomological surveys.
BioCeV Institute of Microbiology of the Czech Academy of Sciences Vestec Czech Republic
Department of Parasitology Faculty of Science Charles University Prague Czech Republic
Division of Science Research and Development Federal Ministry of Defence Vienna Austria
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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
Naucke TJ, Pesson B. Presence of Phlebotomus (Transphlebotomus) mascittii Grassi, 1908 (Diptera: Psychodidae) in Germany. Parasitol Res. 2000;86:335–336. doi: 10.1007/s004360050053. PubMed DOI
Naucke TJ, Lorentz S, Rauchenwald F, Aspöck H. Phlebotomus (Transphlebotomus) mascittii Grassi, 1908, in Carinthia: first record of the occurrence of sandflies in Austria (Diptera: psychodidae: Phlebotominae) Parasitol Res. 2011;109:1161–1164. doi: 10.1007/s00436-011-2361-0. PubMed DOI
Poeppl W, Obwaller AG, Weiler M, Burgmann H, Mooseder G, Lorentz S, et al. Emergence of sandflies (Phlebotominae) in Austria, a Central European country. Parasitol Res. 2013;112:4231–4237. doi: 10.1007/s00436-013-3615-9. PubMed DOI PMC
Kniha E, Dvořák V, Halada P, Milchram M, Obwaller AG, Kuhls K, et al. Integrative approach to Phlebotomus mascittii Grassi, 1908: first Record in Vienna with New Morphological and Molecular Insights. Pathogens. 2020;9:1032. doi: 10.3390/pathogens9121032. PubMed DOI PMC
Dvořák V, Hlavackova K, Kocisova A, Volf P. First record of Phlebotomus (Transphlebotomus) mascittii in Slovakia. Parasite. 2016;23:48. doi: 10.1051/parasite/2016061. PubMed DOI PMC
Grimm F, Gessler M, Jenni L. Aspects of sandfly biology in southern Switzerland. Med Vet Entomol. 1993;7:170–176. doi: 10.1111/j.1365-2915.1993.tb00671.x. PubMed DOI
Depaquit J, Naucke TJ, Schmitt C, Ferté H, Léger N. A molecular analysis of the subgenus Transphlebotomus Artemiev, 1984 (Phlebotomus, Diptera, Psychodidae) inferred from ND4 mtDNA with new northern records of Phlebotomus mascittii Grassi, 1908. Parasitol Res. 2005;95:113–116. doi: 10.1007/s00436-004-1254-x. PubMed DOI
Melaun C, Krüger A, Werblow A, Klimpel S. New record of the suspected leishmaniasis vector Phlebotomus (Transphlebotomus) mascittii Grassi, 1908 (Diptera: Psychodidae: Phlebotominae) - The northernmost phlebotomine sandfly occurrence in the Palearctic region. Parasitol Res. 2014;113:2295–2301. doi: 10.1007/s00436-014-3884-y. PubMed DOI
Berdjane-Brouk Z, Charrel RN, Bitam I, Hamrioui B, Izri A. Record of Phlebotomus (Transphlebotomus) mascittii Grassi, 1908 and Phlebotomus (Laroussius) chadli Rioux, Juminer & Gibily, 1966 female in Algeria. Parasite. 2011;18:337–339. doi: 10.1051/parasite/2011184337. PubMed DOI PMC
Dantas-Torres F, Tarallo VD, Latrofa MS, Falchi A, Lia RP, Otranto D. Ecology of phlebotomine sand flies and Leishmania infantum infection in a rural area of southern Italy. Acta Trop. 2014;137:67–73. doi: 10.1016/j.actatropica.2014.04.034. PubMed DOI
Bosnić S, Gradoni L, Khoury C, Maroli M. A review of leishmaniasis in Dalmatia (Croatia) and results from recent surveys on phlebotomine sandflies in three southern counties. Acta Trop. 2006;99:42–49. doi: 10.1016/j.actatropica.2006.06.009. PubMed DOI
Kasap OE, Dvořák V, Depaquit J, Alten B, Votypka J, Volf P. Phylogeography of the subgenus Transphlebotomus Artemiev with description of two new species, Phlebotomus anatolicus n. sp. and Phlebotomus killicki n. sp. Infect Genet Evol. 2015;34:467–79. doi: 10.1016/j.meegid.2015.05.025. PubMed DOI
Kasap OE, Alten B. Laboratory estimation of degree-day developmental requirements of Phlebotomus papatasi (Diptera: Psychodidae) J Vector Ecol. 2005;30:328–333. PubMed
Naucke TJ, Menn B, Massberg D, Lorentz S. Winter activity of Phlebotomus (Transphlebotomus) mascittii, Grassi 1908 (Diptera: Psychodidae) on the island of Corsica. Parasitol Res. 2008;103:477–479. doi: 10.1007/s00436-008-1002-8. PubMed DOI
Dvořák V, Shaw J, Volf P. Parasite Biology: The Vectors. In: Bruschi F, Gradoni L, editors. Leishmaniases Old Neglected Trop Dis. Springer: Cham; 2018.
Kollaritsch H, Emminger W, Zaunschirm A, Aspöck H. Suspected Autochthonous Kala-azar in Austria. Lancet. 1989;1:901–902. doi: 10.1016/S0140-6736(89)92895-X. PubMed DOI
Bogdan C, Schönian G, Bañuls AL, Hide M, Pratlong F, Lorenz E, et al. Visceral leishmaniasis in a German child who had never entered a known endemic area: case report and review of the literature. Clin Infect Dis. 2001;32:302–306. doi: 10.1086/318476. PubMed DOI
Obwaller AG, Karakus M, Poeppl W, Töz S, Özbel Y, Aspöck H, et al. Could Phlebotomus mascittii play a role as a natural vector for Leishmania infantum? New data. Parasit Vectors; 2016;9:458. PubMed PMC
Zanet S, Sposimo P, Trisciuoglio A, Giannini F, Strumia F, Ferroglio E. Epidemiology of leishmania infantum, toxoplasma gondii, and neospora caninum in Rattus rattus in absence of domestic reservoir and definitive hosts. Vet Parasitol. 2014;199:247–249. doi: 10.1016/j.vetpar.2013.10.023. PubMed DOI
Lewis DJ. A taxonomic review of the genus Phlebotomus (Diptera: Psychodidae) Bull Br Museum Natural Hist. 1982;45:121–209.
Kniha E, Dvořák V, Milchram M, Obwaller A, Köhsler M, Pöppl W, et al. Phlebotomus (Adlerius) Simici Nitzulescu, 1931: first record in Austria and phylogenetic relationship with Other Adlerius Species. Parasit Vectors. BioMed Central; 2021;14:20. PubMed PMC
Dvořák V, Halada P, Hlacvackiva K, Dokianakis E, Antoniou M, Volf P. Identification of phlebotomine sand flies (Diptera: Psychodidae) by matrix-assisted laser desorption/ionization time of flight mass spectrometry. Parasit Vectors. 2014;7:1–7. doi: 10.1186/1756-3305-7-21. PubMed DOI PMC
Halada P, Hlavackova K, Risueño J, Berriatua E, Volf P, Dvořák V. Effect of trapping method on species identification of phlebotomine sandflies by MALDI-TOF MS protein profiling. Med Vet Entomol. 2018;32:388–392. doi: 10.1111/mve.12305. PubMed DOI
Haouas N, Pesson B, Boudabous R, Dedet JP, Babba H, Ravel C. Development of a molecular tool for the identification of leishmania reservoir hosts by blood meal analysis in the insect vectors. Am J Trop Med Hyg. 2007;77:1054–1059. doi: 10.4269/ajtmh.2007.77.1054. PubMed DOI
Hlavackova K, Dvořák V, Chaskopoulou A, Volf P, Halada P. A novel MALDI-TOF MS-based method for blood meal identification in insect vectors: a proof of concept study on phlebotomine sand flies. PLoS Negl Trop Dis. 2019;13:1–23. doi: 10.1371/journal.pntd.0007669. PubMed DOI PMC
R Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/. 2020.
Brooks ME, Kristensen K, van Benthem KJ, Magnusson A, Berg CW, Nielsen A, et al. glmmTMB balances speed and flexibility among packages for zero-inflated generalized linear mixed modeling. R J. 2017;9:378–400. doi: 10.32614/RJ-2017-066. DOI
Akaike H. Factor analysis and AIC. Psychometrika. 1987;52:317–332. doi: 10.1007/BF02294359. DOI
Hartig F. DHARMa: Residual Diagnostics for Hierarchical (Multi-Level / Mixed) Regression Models. R package version 0.3.0. https://CRAN.R-project.org/package=DHARMa. 2020.
Wickham H. ggplot2: Elegant Graphics for Data Analysis. New York: Springer-Verlag; 2016.
Lüdecke D. ggeffects: tidy data frames of marginal effects from regression models. J Open Source Softw. 2018;3:772. doi: 10.21105/joss.00772. DOI
Naucke TJ, Schmitt C. Is leishmaniasis becoming endemic in Germany? Int J Med Microbiol. 2004;293:179–181. PubMed
Oerther S, Jöst H, Heitmann A, Lühken R, Krüger A, Steinhausen I, et al. Phlebotomine sand flies in Southwest Germany: an update with records in new locations. Parasit Vectors. 2020;13:173. doi: 10.1186/s13071-020-04058-6. PubMed DOI PMC
Prudhomme J, Rahola N, Toty C, Cassan C, Roiz D, Vergnes B, et al. Ecology and spatiotemporal dynamics of sandflies in the Mediterranean Languedoc region (Roquedur area, Gard, France) Parasit Vectors. 2015;8:1–14. doi: 10.1186/s13071-015-1250-2. PubMed DOI PMC
Cazan CD, Păstrav IR, Györke A, Oguz G, Alten B, Mihalca AD. Seasonal dynamics of a population of Phlebotomus (Larroussius) perfiliewi Parrot, 1930 (Diptera: Psychodidae) in North-Eastern Romania. Parasitol Res. 2019;1930:1371–1384. doi: 10.1007/s00436-019-06296-9. PubMed DOI
Huemer H, Prudhomme J, Amaro F, Baklouti A, Walder G, Alten B, et al. Practical guidelines for studies on sandfly-borne phleboviruses: Part II: important points to consider for fieldwork and subsequent virological screening. Vector-Borne Zoonotic Dis. 2017;17:81–90. doi: 10.1089/vbz.2016.1965. PubMed DOI
Obwaller AG, Poeppl W, Naucke TJ, Luksch U, Mooseder G, Aspöck H, et al. Stable populations of sandflies (Phlebotominae) in Eastern Austria : a comparison of the trapping seasons 2012 and 2013. Trends Entomol. 2014;2:1–5.
Poeppl W, Obwaller AG, Weiler M, Burgmann H, Mooseder G, Lorentz S, et al. Emergence of sandflies (Phlebotominae) in Southern and Eastern Austria : results from entomologic field studies 2010–2012. 2012.
Knechtli R, Jenni L. Distribution and relative density of three sandfly (Diptera: Phlebotominae) species in southern Switzerland. Ann Parasitol Hum Comparée. 1989;64:53–63. doi: 10.1051/parasite/198964153. DOI
Kasap OE, Belen A, Kaynas S, Simsek FM, Biler L, Ata N, et al. Activity patterns of sand fly (Diptera: Psychodidae) species and comparative performance of different traps in an endemic cutaneous leishmaniasis focus in Cukurova Plain, Southern Anatolia. Turkey Acta Vet Brno. 2009;78:327–335. doi: 10.2754/avb200978020327. DOI
Tsirigotakis N, Pavlou C, Christodoulou V, Dokianakis E, Kourouniotis C, Alten B, et al. Phlebotomine sand flies (Diptera: Psychodidae) in the Greek Aegean Islands: ecological approaches. Parasit Vectors. 2018;11:1–14. doi: 10.1186/s13071-018-2680-4. PubMed DOI PMC
Dye C, Davies CR, Lainson R. Lutzomyia iongipalpis populations in Amazonian Brazil. Anim Behav. 1991;42:183–192. doi: 10.1016/S0003-3472(05)80549-4. DOI
Quinnell RJ, Dye C. Correlates of the peridomestic abundance of Lutzomyia longipalpis (Diptera: Psychodidae) in Amazonian Brazil. Med Vet Entomol. 1994;8:219–224. doi: 10.1111/j.1365-2915.1994.tb00502.x. PubMed DOI
Lawyer P, Killick-Kendrick M, Rowland T, Rowton E, Volf P. Laboratory colonization and mass rearing of phlebotomine sand flies (Diptera, Psychodidae). Parasite. EDP Sciences; 2017 (cited 2019 Apr 26);24:42. http://www.ncbi.nlm.nih.gov/pubmed/29139377. PubMed PMC
Praprotnik E, Zupan S, Ivović V. Morphological and molecular identification of Phlebotomus mascittii Grassi, 1908 populations from Slovenia. J Med Entomol. 2019;56:565–568. doi: 10.1093/jme/tjy176. PubMed DOI
Alten B, Maia C, Afonso MO, Campino L, Jiménez M, González E, et al. Seasonal dynamics of phlebotomine sand fly species proven vectors of mediterranean leishmaniasis caused by leishmania infantum. PLoS Negl Trop Dis. 2016;10:1–22. doi: 10.1371/journal.pntd.0004458. PubMed DOI PMC
Ivović V, Patakakis M, Tselentis Y, Chaniotis B. Faunistic study of sandflies in Greece. Med Vet Entomol. 2007;21:121–124. doi: 10.1111/j.1365-2915.2006.00649.x. PubMed DOI
Tichy H, Kallina W. Insect hygroreceptor responses to continuous changes in humidity and air pressure. J Neurophysiol. 2010;103:3274–3286. doi: 10.1152/jn.01043.2009. PubMed DOI PMC
Herczeg T, Száz D, Blahó M, Barta A, Gyurkovszky M, Farkas R, et al. The effect of weather variables on the flight activity of horseflies (Diptera: Tabanidae) in the continental climate of Hungary. Parasitol Res. 2015;114:1087–1097. doi: 10.1007/s00436-014-4280-3. PubMed DOI
Carta S, Sanna D, Scarpa F, Varcasia A, Cavallo L, Meloni MP, et al. Species diversity and molecular insights into phlebotomine sand flies in Sardinia (Italy)—an endemic region for leishmaniasis. Parasitol Res Parasitology Research. 2020;119:63–73. doi: 10.1007/s00436-019-06528-y. PubMed DOI
Gálvez R, Descalzo MA, Miró G, Jiménez MI, Martín O, Dos Santos-Brandao F, et al. Seasonal trends and spatial relations between environmental/meteorological factors and leishmaniosis sand fly vector abundances in Central Spain. Acta Trop. 2010;115:95–102. doi: 10.1016/j.actatropica.2010.02.009. PubMed DOI
Baum M, de Castro EA, Pinto MC, Goulart TM, Baura W, do Klisiowicz DR, et al. Molecular detection of the blood meal source of sand flies (Diptera: Psychodidae) in a transmission area of American cutaneous leishmaniasis, Paraná State, Brazil. Acta Trop. 2015;143:8–12. PubMed
Lewis DJ. Phlebotomid sandflies. Bull World Health Organ. 1971;44:535–551. PubMed PMC
Leschnik M, Löwenstein M, Edelhofer R, Kirtz G. Imported non-endemic, arthropod-borne and parasitic infectious diseases in Austrian dogs. Wien Klin Wochenschr. 2008;120:59–62. doi: 10.1007/s00508-008-1077-3. PubMed DOI
Koehler K, Stechele M, Hetzel U, Domingo M, Schönian G, Zahner H, et al. Cutaneous leishmaniosis in a horse in southern Germany caused by Leishmania infantum. Vet Parasitol. 2002;109:9–17. doi: 10.1016/S0304-4017(02)00246-7. PubMed DOI
Müller N, Welle M, Lobsiger L, Stoffel MH, Boghenbor KK, Hilbe M, et al. Occurrence of Leishmania sp. in cutaneous lesions of horses in Central Europe. Vet Parasitol. 2009;166:346–51. doi: 10.1016/j.vetpar.2009.09.001. PubMed DOI
Lobsiger L, Müller N, Schweizer T, Frey CF, Wiederkehr D, Zumkehr B, et al. An autochthonous case of cutaneous bovine leishmaniasis in Switzerland. Vet Parasitol. 2010 (cited 2019 Nov 19);169:408–14. https://www.sciencedirect.com/science/article/pii/S0304401710000415. PubMed
Ecological setting of phlebotomine sand flies in the Republic of Kosovo