- Open Access
Avian malaria parasites in the last supper: identifying encounters between parasites and the invasive Asian mosquito tiger and native mosquito species in Italy
© Martínez-de la Puente et al.; licensee BioMed Central. 2015
- Received: 15 November 2014
- Accepted: 17 January 2015
- Published: 28 January 2015
The invasive Asian tiger mosquito Aedes albopictus has dramatically expanded its distribution range, being catalogued as one of the world’s 100 worst invasive alien species. As vectors of pathogens, Ae. albopictus may create novel epidemiological scenarios in the invaded areas.
Here, the frequency of encounters of Ae. albopictus with the avian malaria parasite Plasmodium and the related Haemoproteus was studied in an area with established populations in northeastern Italy and compared with those from four native mosquito species, Anopheles maculipennis s.l., Culex hortensis, Culex pipiens, and Ochlerotatus caspius. The abdomens of mosquitoes with a recent blood meal were used to identify both the blood meal source and the parasites harboured.
Aedes albopictus had a clear antropophilic behaviour while An. maculipennis and Oc. caspius fed mainly on non-human mammals. Birds were the most common hosts of Cx. pipiens and reptiles of Cx. hortensis. Parasites were isolated from three mosquito species, with Cx. pipiens (30%) showing the highest parasite prevalence followed by Cx. hortensis (9%) and Ae. albopictus (5%).
These results are the first identifying the avian malaria parasites harboured by mosquitoes in Italy and represent the first evidence supporting that, although Ae. albopictus could be involved in the transmission of avian malaria parasites, the risk of avian malaria parasite spread by this invasive mosquito in Europe would be minimal.
- Aedes albopictus
- Avian diseases
- Culex pipiens
- West Nile virus
Establishment of exotic mosquitoes to new areas may create novel epidemiological scenarios with potential dramatic consequences for wildlife and human health . The invasive Asian tiger mosquito Aedes albopictus, indigenous to Southeast Asia, islands of the Western Pacific and Indian Ocean, has expanded its distribution range to Africa, Europe and the Americas [2,3]. In Europe, this species was first recorded in 1979 in Albania  and subsequently in Italy, France and other countries of the Mediterranean region and northern Europe [1,3]. Aedes albopictus is vector of a diversity of pathogens including flaviviruses (e.g., West Nile virus, Dengue virus), alphaviruses (e.g., Chikungunya virus), and other viruses and filarial worms [5,6]. In Europe, Ae. albopictus has been incriminated in the transmission of both introduced (Chikungunya and Dengue viruses) and endemic (Dirofilaria nematodes) pathogens [5,7].
Avian malaria parasites of the genus Plasmodium, and the relative haemosporidian Haemoproteus, produce pathogenic effects on both vertebrate and invertebrate hosts . Plasmodium parasites require the intervention of a mosquito vector to be transmitted from an infected bird to another individual. Haemoproteus parasites have a similar life cycle, requiring a biting midge Culicoides or louse flies instead of mosquitoes to be transmitted between birds . During a bite event a mosquito feeding on an infected bird is able to acquire the parasites contained in the blood. A number of mosquito species belonging to different genera such as Aedes, Anopheles and Culex, have been reported as potential vectors of avian malaria parasites . Although different factors may influence the subsequent development of parasites in the mosquito after blood ingestion , pathogen isolation of recent blood meals may provide valuable information on parasite-mosquito encounters and potential parasite transmission [11,12]. In this respect, the blood ingested by potential vectors can be used as a source of host DNA to identify both the feeding sources of mosquitoes  and the blood parasites reaching these potential vectors .
In spite of their importance on parasite transmission, only a handful of studies have identified the blood parasites interacting with wild mosquito populations in Europe [14-18], and, no previous study has tested for the presence of avian malaria parasites in invasive populations of the tiger mosquito Ae. albopictus. Here, two molecular approaches were used to identify both host and avian malaria parasites from blood contained in the mosquito’s abdomen following protocols described by Alcaide et al.  and Hellgren et al. , respectively. Samples from five different mosquito species collected in northeastern Italy were included in this study: the invasive Ae. albopictus, and the native Anopheles maculipennis s.l., Culex hortensis, Culex pipiens, and Ochlerotatus caspius.
Mosquito sampling and morphological identification
Mosquitoes were collected from May to October 2012 using BG-sentinel traps baited with BG-lure and dry ice. Twenty traps in Veneto and ten in Trentino provinces operated once a week or two weeks for 24 hr, respectively. In Trentino mosquitoes were also collected using a motor-powered aspirator. Mosquitoes were morphologically identified following the keys of the Italian Culicidae adults  and preserved frozen (−20 or −80°C) until examination.
Blood meal source and parasite identification
DNA from the abdomen of blood-fed mosquitoes was individually isolated using the DNeasy Blood and Tissue® kit (QIAGEN, Hilden, Germany) following company specifications. This DNA extraction approach resulted in a higher efficacy of host identification than other protocols such as Hotshot . Vertebrate blood meal origin was identified using a nested-PCR approach  to amplify a 758-base pairs fragment of the mitochondrial cytochrome oxidase 1 (COI) gene. Both negative controls for PCR reactions (at least one per plate) and DNA extraction were included in the analysis. DNA was also used to identify the presence of Plasmodium and Haemoproteus parasites based on the amplification of a fragment of the mitochondrial Cytochrome b gene .
Positive amplifications were sequenced using the Big Dye 1.1 technology (Applied Biosystems). Labelled DNA fragments of positive PCR products were resolved with an ABI 3130xl automated sequencer (Applied Biosystems) using the same forward and reverse primers used in the nested-PCR amplification for the case of blood parasite identifications. For blood meal identifications, amplicons were sequenced in one direction using the primer BCRV2, except for the case of Ae. albopictus mosquitoes that were sequenced using the primer BCVINT-RV (see ). Sequences were edited using the software Sequencher™ v 4.9 (Gene Codes Corp., © 1991–2009, Ann Arbor, MI 48108, USA). Blood meal sequences were assigned to particular vertebrate species when agreement was ≥98% to sequences of known species in GenBank DNA sequence database (National Center for Biotechnology Information Blast) or the Barcode of Life Data Systems (BOLD). Parasite lineages were identified by comparison with sequences deposited in GenBank database. Statistical significance of differences in parasite prevalence was tested with statistical software JMP (version 9.0.1).
Blood meal source of mosquitoes in Italy
Homo sapiens (31)
Passer montanus (1)
Erinaceus europaeus (1)
Turdus merula (1)
Canis lupus familiares (3)
Gallus gallus (1)
Equus asinus (2)
Equus caballus (2)
Lepus europaeus (2)
Bos taurus (1)
Capra hircus (1)
Felis silvestris/catus (1)
Homo sapiens (1)
Vulpes vulpes (1)
Homo sapiens (1)
Podarcis muralis (7)
Homo sapiens (14)
Turdus merula (72)
Podarcis muralis (4)
Felis silvestris/catus (9)
Passer domesticus (26)
Lacerta spp. (1)
Canis lupus familiaris (5)
Gallus gallus (21)
Equus caballus (3)
Streptopelia decaocto (16)
Sus scrofa (3)
Columba livia (5)
Bos taurus (2)
Passer montanus (5)
Erinaceus europaeus (1)
Athene noctua (4)
Meleagris gallopavo (3)
Columba palumbus (3)
Pica pica (3)
Anas platyrhychos (2)
Sturnus vulgaris (2)
Accipiter nisus (1)
Cairina moschata (1)
Carduelis carduelis (1)
Gallinula chloropus (1)
Jynx torquilla (1)
Numida meleagris (1)
Nycticorax nycticorax (1)
Oriolus oriolus (1)
Parus major (1)
Phasianus colchinus (1)
Sylvia atricapilla (1)
Felis silvestris/catus (6)
Gallus gallus (1)
Equus asinus (3)
Equus caballus (2)
Bos taurus (1)
Canis lupus familiaris (1)
Homo sapiens (1)
Blood parasite lineages isolated from mosquito blood meals
Blood meal source of mosquitoes harbouring identified blood parasite lineages
Africa, Asia, Europe*
Africa, Asia, Europe
Asia, Europe, Oceanía**
Africa, America, Asia, Europe, Oceania
Africa, America, Asia, Europe, Oceanía
America, Asia, Europe
Avian Plasmodium and Haemoproteus parasites were isolated from three different mosquito species with clear differences in parasite prevalence. Culex pipiens showed, by far, the highest parasite prevalence, suggesting that this species probably play a central role in the transmission of blood parasites in the studied area. Molecular isolation of parasites from mosquitoes could be used to identify the occurrence of encounters between parasites and mosquitoes, although this not necessarily implies that insects are real vectors of the parasite lineages isolated, because the parasites can be unable to replicate in the salivary glands, that may be the case of Haemoproteus parasites . Although there is no previous information on the role of wild mosquitoes in the transmission of avian malaria parasites in Italy, recent studies have isolated Plasmodium parasites from Cx. pipiens mosquitoes captured in Czech Republic , Portugal , Switzerland [15,17], and Spain . Also, sporozoites of both Plasmodium relictum and Plasmodium vaughani, parasite lineages found in this study, have been previously isolated from Cx. pipiens mosquitoes [9,24]. Furthermore, the Plasmodium lineage LINN1 was isolated from whole un-engorged Cx. pipiens mosquitoes . Curiously, we isolated avian blood parasites from two mosquito abdomens containing a non-avian derived blood meal. This could be due to the occurrence of undetected mixed blood meals in the mosquito, the presence of avian parasites in the blood on these vertebrate hosts (see ) or simply the fact that parasites isolated were in the mosquito tissue but not in the blood meal . This last possibility is supported by the detection of parasite DNA in mosquitoes with no host identification due to degraded blood, and consequently where it is unlikely that the parasites detected come from the vertebrate blood.
The invasive mosquito Ae. albopictus preferably bites on mammals, especially on humans [27-29], which is clearly supported by results from this study. However, this species is able to feed on non-mammal species including birds, with birds compromising between 0.8 to 73.0% of the total blood meals identified in previous studies , potentially playing a role on the transmission of avian malaria parasites. Under laboratory conditions, development of avian Plasmodium sporozoites occurs in Ae. albopictus , see also . Furthermore, avian malaria parasites have been isolated from wild Ae. albopictus mosquitoes, but usually showing low prevalence of infection [32-34]. Also, some studies have reported the absence of Plasmodium in Ae. albopictus mosquitoes from Japan [27,35]. Overall, results from these studies together with those reported here support that Ae. albopictus could be involved in the transmission of avian malaria parasites, although the risk of parasite spread by this mosquito species in Europe would be minimal due to its low biting rate on birds.
The use of molecular tools on avian malaria studies has allowed the identification of a broad diversity of parasite lineages infecting birds in different areas and, as a result, it is possible to infer their current geographical distribution. Most of the parasite lineages isolated in this study are widespread, being isolated from birds from different countries of the old world (Table 3, see Malavi database ). However, although the same parasite cyt b lineage could be found in birds from both Europe and Africa, as in the case of the widespread Plasmodium SGS1, the characterization of highly variable genes (i.e. merozoite surface protein 1 gene, MSP1) provided strong evidence of parasite differentiation among continents, and consequently parasites with the same sequence of cytb may in fact correspond to different lineages with more reduced distribution areas affecting the inference of geographical areas of parasite transmission .
In conclusion, our results support that, the risk of spread of avian malaria parasites by the invasive mosquito Ae. albopictus in Europe would be minimal. However, its ability to transmit other pathogens of sanitary importance including viruses and nematodes support the necessity of setting up an active surveillance and control programme on this species . Further studies are necessary in order to identify those factors affecting infections by different avian pathogens (i.e., WNV and avian malaria parasites) in vertebrate  and invertebrate  hosts, which may determine parasite epidemiology.
This study was funded by EU grants FP7-261391 EuroWestNile and FP7-261504 EDENext and the project CGL2012-30759 from the Spanish Ministry of Science and Innovation. This study is catalogued by the EDENext Steering Committee as EDENext301 (http://www.edenext.eu). The contents of this publication are the sole responsibility of the authors and don't necessarily reflect the views of the European Commission. JMP is currently supported by a Juan de la Cierva contract. JM was supported by an International Outgoing Fellowship (FP7-PEOPLE-2010; ADAPT-ENVGENOME; Grant Number 271485). AR, DA and GC were partially supported by the Italian Ministry of Health under the grant Aedespread (RF-2010-2318965). We thank Isabel Martín for their help in the laboratory.
- Medlock JM, Hansford KM, Schaffner F, Versteirt V, Hendrickx G, Zeller H, et al. A review of the invasive mosquitoes in Europe: ecology, public health risks, and control options. Vector Borne Zoonotic Dis. 2012;12:435–47.PubMed CentralView ArticlePubMedGoogle Scholar
- Gratz NG. Critical review of the vector status of Aedes albopictus. Med Vet Entomol. 2004;18:215–27.View ArticlePubMedGoogle Scholar
- Bonizzoni M, Gasperi G, Chen X, James AA. The invasive mosquito species Aedes albopictus: current knowledge and future perspectives. Trends Parasitol. 2013;29:460–8.PubMed CentralView ArticlePubMedGoogle Scholar
- Adhami J, Reiter P. Introduction and establishment of Aedes (Stegomyia) albopictus Skuse (Diptera: Culicidae) in Albania. J Am Mosq Control Assoc. 1998;14:340–3.PubMedGoogle Scholar
- Cancrini G, Frangipane di Regalbono A, Ricci I, Tessarin C, Gabrielli S, Pietrobelli M. Aedes albopictus is a natural vector of Dirofilaria immitis in Italy. Vet Parasitol. 2003;118:195–202.View ArticlePubMedGoogle Scholar
- Paupy C, Delatte H, Bagny L, Corbel V, Fontenille D. Aedes albopictus, an arbovirus vector: from the darkness to the light. Microbes Infect. 2009;11:1177–85.View ArticlePubMedGoogle Scholar
- Schaffner F, Medlock JM, Van Bortel W. Public health significance of invasive mosquitoes in Europe. Clin Microbiol Infect. 2013;19:685–92.View ArticlePubMedGoogle Scholar
- Valkiūnas G. Avian malaria parasites and other haemosporidia. Boca Ratón: CRC Press; 2005.Google Scholar
- Santiago-Alarcon D, Palinauskas V, Schaefer HM. Diptera vectors of avian Haemosporidian parasites: untangling parasite life cycles and their taxonomy. Biol Rev Camb Philos Soc. 2012;87:928–64.View ArticlePubMedGoogle Scholar
- Lefèvre T, Vantaux A, Dabiré KR, Mouline K, Cohuet A. Non-genetic determinants of mosquito competence for malaria parasites. PLoS Pathog. 2013;9:e1003365.PubMed CentralView ArticlePubMedGoogle Scholar
- Hellgren O, Bensch S, Malmqvist B. Bird hosts, blood parasites and their vectors—associations uncovered by molecular analyses of blackfly blood meals. Mol Ecol. 2008;17:1605–13.View ArticlePubMedGoogle Scholar
- Santiago-Alarcon D, Havelka P, Schaefer HM, Segelbacher G. Bloodmeal analysis reveals avian Plasmodium infections and broad host preferences of Culicoides (Diptera: Ceratopogonidae) vectors. PLoS ONE. 2012;7:e31098.PubMed CentralView ArticlePubMedGoogle Scholar
- Alcaide M, Rico C, Ruiz S, Soriguer R, Muñoz J, Figuerola J. Disentangling vector-borne transmission networks: a universal DNA barcoding method to identify vertebrate hosts from arthropod bloodmeals. PLoS ONE. 2009;4:e7092.PubMed CentralView ArticlePubMedGoogle Scholar
- Ferraguti M, Martínez-de la Puente J, Muñoz J, Roiz D, Ruiz S, Soriguer R, et al. Avian Plasmodium in Culex and Ochlerotatus mosquitoes from Southern Spain: effects of season and host-feeding source on parasite dynamics. PLoS ONE. 2013;8:e66237.PubMed CentralView ArticlePubMedGoogle Scholar
- Glaizot O, Fumagalli L, Iritano K, Lalubin F, Van Rooyen J, Christe P. High prevalence and lineage diversity of avian malaria in wild populations of great tits (Parus major) and mosquitoes (Culex pipiens). PLoS ONE. 2012;7:e34964.PubMed CentralView ArticlePubMedGoogle Scholar
- Synek P, Munclinger P, Albrecht T, Votýpka J. Avian haemosporidians in haematophagous insects in the Czech Republic. Parasitol Res. 2013;112:839–45.View ArticlePubMedGoogle Scholar
- Lalubin F, Delédevant A, Glaizot O, Christe P. Temporal changes in mosquito abundance (Culex pipiens), avian malaria prevalence and lineage composition. Parasit Vectors. 2013;6:307.PubMed CentralView ArticlePubMedGoogle Scholar
- Ventim R, Ramos JA, Osorio H, Lopes RJ, Pérez-Tris J, Mendes L. Avian malaria infections in western European mosquitoes. Parasitol Res. 2012;111:637–45.View ArticlePubMedGoogle Scholar
- Hellgren O, Waldenstrom J, Bensch S. A new PCR assay for simultaneous studies of Leucocytozoon, Plasmodium and Haemoproteus from avian blood. J Parasitol. 2004;90:797–802.View ArticlePubMedGoogle Scholar
- Severini F, Toma L, Luca MD, Romi R. Identification of the adult stages of the Italian mosquitoes (Diptera, Culicidae). Fragm Entomol. 2009;41:213–372.Google Scholar
- Martínez-de la Puente J, Ruiz S, Soriguer R, Figuerola J. Effect of blood meal digestion and DNA extraction protocol on the success of blood meal source determination in the malaria vector Anopheles atroparvus. Malar J. 2013;12:109.PubMed CentralView ArticlePubMedGoogle Scholar
- Muñoz J, Eritja R, Alcaide M, Montalvo T, Soriguer RC, Figuerola J. Host-feeding patterns of native Culex pipiens and invasive Aedes albopictus mosquitoes (Diptera: Culicidae) in urban zones from Barcelona, Spain. J Med Entomol. 2011;48:956–60.View ArticleGoogle Scholar
- Valkiūnas G. Haemosporidian vector research: marriage of molecular and microscopical approaches is essential. Mol Ecol. 2011;20:3084–6.View ArticlePubMedGoogle Scholar
- Ziegyte R, Bernotienė R, Bukauskaitė D, Palinauskas V, Iezhova T, Valkiūnas G. Complete sporogony of Plasmodium relictum (lineages pSGS1 and pGRW11) in mosquito Culex pipiens pipiens form molestus, with implications to avian malaria epidemiology. J Parasitol. 2014;100:878–82.View ArticlePubMedGoogle Scholar
- Kimura M, Darbro JM, Harrington LC. Avian malaria parasites share congeneric mosquito vectors. J Parasitol. 2010;96:144–51.View ArticlePubMedGoogle Scholar
- Valkiūnas G, Kazlauskienė R, Bernotienė R, Palinauskas V, Iezhova TA. Abortive long-lasting sporogony of two Haemoproteus species (Haemosporida, Haemoproteidae) in the mosquito Ochlerotatus cantans, with perspectives on haemosporidian vector research. Parasitol Res. 2013;112:2159–69.View ArticlePubMedGoogle Scholar
- Kim KS, Tsuda Y, Yamada A. Bloodmeal identification and detection of avian malaria parasite from mosquitoes (Diptera: Culicidae) inhabiting coastal areas of Tokyo Bay, Japan. J Med Entomol. 2009;46:1230–4.View ArticlePubMedGoogle Scholar
- Sawabe K, Isawa H, Hoshino K, Sasaki T, Roychoudhury S, Higa Y, et al. Host-feeding habits of Culex pipiens and Aedes albopictus (Diptera: Culicidae) collected at the urban and suburban residential areas of Japan. Med Entomol. 2010;47:442–50.View ArticleGoogle Scholar
- Egizi A, Healy SP, Fonseca DM. Rapid blood meal scoring in anthropophilic Aedes albopictus and application of PCR blocking to avoid pseudogenes. Infect Genet Evol. 2013;16:122–8.View ArticlePubMedGoogle Scholar
- Faraji A, Egizi A, Fonseca DM, Unlu I, Crepeau T, Healy SP, et al. Comparative host feeding patterns of the Asian tiger mosquito, Aedes albopictus, in urban and suburban Northeastern USA and implications for disease transmission. PLoS Negl Trop Dis. 2014;8:e3037.PubMed CentralView ArticlePubMedGoogle Scholar
- LaPointe DA, Goff ML, Atkinson CT. Comparative susceptibility of introduced forest-dwelling mosquitoes in Hawaii to avian malaria, Plasmodium relictum. J Parasitol. 2005;91:843–9.View ArticlePubMedGoogle Scholar
- Ejiri H, Sato Y, Sasaki E, Sumiyama D, Tsuda Y, Sawabe K, et al. Detection of avian Plasmodium spp. DNA sequences from mosquitoes captured in Minami Daito Island of Japan. J Vet Med Sci. 2008;70:1205–10.View ArticlePubMedGoogle Scholar
- Tanigawa M, Sato Y, Ejiri H, Imura T, Chiba R, Yamamoto H, et al. Molecular identification of avian haemosporidia in wild birds and mosquitoes on Tsushima Island, Japan. J Vet Med Sci. 2013;2013(75):319–26.View ArticleGoogle Scholar
- Trout Fryxell R, Thompson Lewis T, Peace H, Hendricks BM, Paulsen D. Identification of avian malaria (Plasmodium sp.) and canine heartworm (Dirofilaria immitis) in the mosquitoes of Tennessee. J Parasitol. 2014;100:455–62.View ArticleGoogle Scholar
- Ejiri H, Sato Y, Sawai R, Sasaki E, Matsumoto R, Ueda M, et al. Prevalence of avian malaria parasite in mosquitoes collected at a zoological garden in Japan. Parasitol Res. 2009;105:629–33.View ArticlePubMedGoogle Scholar
- Bensch S, Hellgren O, Pérez-Tris J. MalAvi: a public database of malaria parasites and related haemosporidians in avian hosts based on mitochondrial cytochrome b lineages. Mol Ecol Res. 2009;9:1353–8.View ArticleGoogle Scholar
- Hellgren O, Atkinson CT, Bensch S, Albayrak T, Dimitrov D, Ewen JG, et al. Global phylogeography of the avian malaria pathogen Plasmodium relictum based on MSP1 allelic diversity. Ecography, in press.Google Scholar
- Medeiros MC, Anderson TK, Higashiguchi JM, Kitron UD, Walker ED, Brawn JD, et al. An inverse association between West Nile virus serostatus and avian malaria infection status. Parasit Vectors. 2014;7:415.PubMed CentralView ArticlePubMedGoogle Scholar
- Hughes T, Irwin P, Hofmeister E, Paskewitz SM. Occurrence of avian Plasmodium and West Nile Virus in Culex species in Wisconsin. J Am Mosq Control Assoc. 2010;26:24–31.View ArticlePubMedGoogle Scholar
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