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Phylogenetic and ecological factors affecting the sharing of helminths between native and introduced rodents in Central Chile

Published online by Cambridge University Press:  11 June 2018

Carlos Landaeta-Aqueveque ,
María del Rosario Robles ,
AnaLía Henríquez ,
Andrea Yáñez-Meza ,
Juana Paola Correa ,
Daniel González-Acuña  and
Pedro Eduardo Cattan
Carlos Landaeta-Aqueveque*
Affiliation:
Facultad de Ciencias Veterinarias, Universidad de Concepción. Vicente Méndez 595, Chillán, Chile
María del Rosario Robles
Affiliation:
Centro de Estudios Parasitológicos y de Vectores – Consejo Nacional de Investigaciones Científicas y Técnicas. Boulevard 120s/n entre av. 60 y calle 64 (1900), La Plata, Argentina
AnaLía Henríquez
Affiliation:
Facultad de Medicina Veterinaria, Universidad San Sebastián. Lientur 1457, Concepción, Chile
Andrea Yáñez-Meza
Affiliation:
Facultad de Ciencias, Universidad de Chile. Las Palmeras 3425, Santiago, Chile
Juana Paola Correa
Affiliation:
Facultad de Ciencias, Universidad de Chile. Las Palmeras 3425, Santiago, Chile
Daniel González-Acuña
Affiliation:
Facultad de Ciencias Veterinarias, Universidad de Concepción. Vicente Méndez 595, Chillán, Chile
Pedro Eduardo Cattan
Affiliation:
Facultad de Ciencias Veterinarias y Pecuarias, Universidad de Chile. Santa Rosa 11735, Santiago, Chile
*
Author for correspondence: Carlos Landaeta-Aqueveque, E-mail: [email protected]
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Abstract

In order to analyse the effect of hosts’ relationships and the helminthic load on the switching of parasites between native and introduced hosts, we sampled rodents belonging to two suborders from Central Chile. We compared the number of helminthic species shared between murids (introduced) and cricetid (native, same suborder) rodents to those shared between murids and hystricomorphs (native, different suborder), and we assessed the association between parasitic presence, abundance and geographical dispersion in source hosts to the presence and abundance in recipient hosts. Introduced rodent species shared more helminth species with cricetid rodents than with non-cricetids. Presence and abundance in recipient hosts was not associated with the prevalence and mean abundance in source hosts’ population. The mean abundance of parasites in source hosts throughout the territory and wider dispersion was positively associated with the likelihood of being shared with a recipient host. Closer relationships between native and introduced hosts and high parasitic abundance and dispersion could facilitate host switching of helminths between native and introduced rodents. This work provides the first documentation of the importance of parasitic abundance and dispersion on the switching of parasites between native and introduced hosts.

Keywords

Cricetidhelminthshostinvasivenativeparasitespillbackspilloverrodents
Type
Research Article
Information
Parasitology , Volume 145 , Issue 12 , October 2018 , pp. 1570 - 1576
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Copyright
Copyright © Cambridge University Press 2018 

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References

Anderson, RC, Chabaud, AG and Willmott, S (2009) Keys to the Nematode Parasites of Vertebrates. CAB International, Wallingford.Google Scholar
Asakawa, M (2005) Perspectives of host-parasite relationships between rodents and nematodes in Japan. Mammal Study 30, S95–SS9.Google Scholar
Babero, BB and Cattan, PE (1975) Helmintofauna de Chile: III. Parasitos del roedor degu, Octodon degus Molina, 1782, con la descripcion de tres nuevas especies. Boletin Chileno de Parasitologia 30, 68–76.Google Scholar
Babero, BB, Cattan, PE and Cabello, C (1975) Trichuris bradleyi sp. n., a whipworm from Octodon degus in Chile. The Journal of Parasitology 61, 1061–1063.Google Scholar
Barrett, JL, Carlisle, MS and Prociv, P (2002) Neuro-angiostrongylosis in wild black and grey-headed flying foxes (Pteropus spp). Australian Veterinary Journal 80, 554–558.Google Scholar
Barton, DP (1997) Introduced animals and their parasites: the cane toad, Bufo marinus, in Australia. Australian Journal of Ecology 22, 316–324.Google Scholar
Bordes, F, Blasdell, K and Morand, S (2015) Transmission ecology of rodent-borne diseases: new frontiers. Integrative Zoology 10, 424–435.Google Scholar
Bush, AO, Lafferty, KD, Lotz, JMShostak, AW (1997) Parasitology meets ecology on its own terms: Margolis, et al. Revisited. The Journal of Parasitology 83, 575–583.Google Scholar
Digiani, MC, Landaeta-Aqueveque, C, Serran, PC and Notarnicola, J (2017) Pudicinae (Nematoda: Heligmonellidae) parasitic in endemic Chilean rodents (Caviomorpha: Octodontidae and Abrocomidae): description of a new species and emended description of Pudica degusi (Babero and Cattan) n. comb. The Journal of Parasitology 103, 736–746.Google Scholar
Grabner, DS, Weigand, AM, Leese, F, Winking, C, Hering, D, Tollrian, R and Sures, B (2015) Invaders, natives and their enemies: distribution patterns of amphipods and their microsporidian parasites in the Ruhr Metropolis, Germany. Parasites & Vectors 8, 1–15.Google Scholar
Harkema, R (1936) The parasites of some North Carolina rodents. Ecological Monographs 6, 151–232.Google Scholar
Hatcher, MJ, Dick, JTA and Dunn, AM (2012) Disease emergence and invasions. Functional Ecology 26, 1275–1287.Google Scholar
Jaksic, F (1998) Vertebrate invaders and their ecological impacts in Chile. Biodiversity & Conservation 7, 1427–1445.Google Scholar
Johnson, PTJ and Thieltges, DW (2010) Diversity, decoys and the dilution effect: how ecological communities affect disease risk. The Journal of Experimental Biology 213, 961–970.Google Scholar
Kataranovski, M, Mirkov, I, Belij, S, Popov, A, Petrović, Z, Gačić, Z and Kataranovski, D (2011) Intestinal helminths infection of rats (Ratus norvegicus) in the Belgrade area (Serbia): the effect of sex, age and habitat. Parasite: Journal de la Société Française de Parasitologie 18, 189.Google Scholar
Kelly, DW, Paterson, RA, Townsend, CR, Poulin, R and Tompkins, DM (2009) Parasite spillback: a neglected concept in invasion ecology? Ecology 90, 2047–2056.Google Scholar
Khalil, LF, Jones, A and Bray, TA (1994) Keys to the Cestode Parasites of Vertebrates. Wallingford: CAB International.Google Scholar
Klimpel, S, Förster, M and Schmahl, G (2007) Parasites of two abundant sympatric rodent species in relation to host phylogeny and ecology. Parasitology Research 100, 867–875.Google Scholar
Landaeta-Aqueveque, C, Robles, MDR and Cattan, PE (2007a) The community of gastrointestinal helminths in the housemouse, Mus musculus, in Santiago, Chile. Parasitología Latinoamericana 62, 165–169.Google Scholar
Landaeta-Aqueveque, C, Robles, MDR and Cattan, PE (2007b) Helmintofauna del roedor Abrothrix olivaceus (Sigmodontinae) en áreas sub-urbanas de Santiago de Chile. Parasitología Latinoamericana 62, 134–141.Google Scholar
Landaeta-Aqueveque, C, Henríquez, A and Cattan, PE (2014) Introduced species: domestic mammals are more significant transmitters of parasites to native mammals than are feral mammals. International Journal for Parasitology 44, 243–249.Google Scholar
Locke, S, Marcogliese, D and Tellervo Valtonen, E (2014) Vulnerability and diet breadth predict larval and adult parasite diversity in fish of the Bothnian Bay. Oecologia 174, 253–262.Google Scholar
Lockwood, JL, Cassey, P and Blackburn, T (2005) The role of propagule pressure in explaining species invasions. Trends in Ecology & Evolution 20, 223–228.Google Scholar
Loxton, KC, Lawton, C, Stafford, P and Holland, CV (2017) Parasite dynamics in an invaded ecosystem: helminth communities of native wood mice are impacted by the invasive bank vole. Parasitology 144, 1476–1489.Google Scholar
MacLeod, CJ, Paterson, AM, Tompkins, DM and Duncan, RP (2010) Parasites lost – do invaders miss the boat or drown on arrival? Ecology Letters 13, 516–527.Google Scholar
Macneil, C, Fielding, NJ, Dick, JT, Briffa, M, Prenter, J, Hatcher, MJ and Dunn, AM (2003) An acanthocephalan parasite mediates intraguild predation between invasive and native freshwater amphipods (Crustacea). Freshwater Biology 48, 2085–2093.Google Scholar
Marangi, M, Zechini, B, Fileti, A, Quaranta, G and Aceti, A (2003) Hymenolepis diminuta infection in a child living in the urban area of Rome, Italy. Journal of Clinical Microbiology 41, 3994–3995.Google Scholar
Mastitsky, S and Veres, J (2010) Field evidence for a parasite spillback caused by exotic mollusc Dreissena polymorpha in an invaded lake. Parasitology Research 106, 667–675.Google Scholar
Milazzo, C, de Bellocq, JG, Cagnin, M, Casanova, JC, di Bella, C, Feliu, C and Santalla, F (2003) Helminths and ectoparasites of Rattus rattus and Mus musculus from Sicily, Italy. Comparative Parasitology 70, 199–204.Google Scholar
Morand, S, Bordes, F, CHEN, HW, Claude, J, Cosson, JF, Galan, M, Czirjak, GA, Greenwood, AD, Latinne, A, Michaux, J and Ribas, A (2015) Global parasite and Rattus rodent invasions: the consequences for rodent-borne diseases. Integrative Zoology 10, 409–423.Google Scholar
Muñoz-Pedreros, A. (2009). Orden rodentia. In Muñoz-Pedreros, A., Yáñez, J. (eds). Mamíferos de Chile, Valdivia: Editorial CEA, pp. 93–157.Google Scholar
Notarnicola, J and Navone, G (2011) Litomosoides pardinasi n. sp. (Nematoda, Onchocercidae) from two species of cricetid rodents in northern Patagonia, Argentina. Parasitology Research 108, 187–194.Google Scholar
Paterson, RA, Townsend, CR, Poulin, R and Tompkins, DM (2011) Introduced brown trout alternative acanthocephalan infections in native fish. Journal of Animal Ecology 80, 990–998.Google Scholar
Pisanu, B, Chapuis, JL and Durette-Desset, MC (2001) Helminths from introduced small mammals on Kerguelen, Crozet, and Amsterdam Islands (Southern Indian Ocean). The Journal of Parasitology 87, 1205–1208.Google Scholar
Pisanu, B, Lebailleux, L and Chapuis, JL (2009) Why do Siberian chipmunks Tamias sibiricus (Sciuridae) introduced in French forests acquired so few intestinal helminth species from native sympatric Murids? Parasitology Research 104, 709–714.Google Scholar
Quentin, JC (1975) Oxyure de Rongeurs: II. Essai de classification des oxyures Heteroxynematidae. Memoires Du Museum National D'histoire Naturelle, Zoologie Serie A 94, 51–96.Google Scholar
Robles, MDR, Navone, GT and Notarnicola, J (2006) A new species of Trichuris (Nematoda: Trichuridae) from Phyllotini rodents in Argentina. Journal of Parasitology 92, 100–104.Google Scholar
Romeo, C, Ferrari, N, Lanfranchi, P, Saino, N, Santicchia, F, Martinoli, A and Wauters, LA (2015) Biodiversity threats from outside to inside: effects of alien grey squirrel (Sciurus carolinensis) on helminth community of native red squirrel (Sciurus vulgaris). Parasitology Research 114, 2621–2628.Google Scholar
Smith, KF and Carpenter, SM (2006) Potential spread of introduced black rat (Rattus rattus) parasites to endemic deer mice (Peromyscus maniculatus) on the California Channel Islands. Diversity and Distributions 12, 742–748.Google Scholar
Sutton, C (1989) Contribution to the knowledge of Argentina's parasitological fauna XVII. Spirurida (Nematoda) from Neotropical Cricetidae: Physaloptera calnuensis n. sp. and Protospirura numidica criceticola Quentin, Karimi and Rodríguez De Almeida. Bulletin Du Museum National D'histoire Naturelle, Paris, 4° Série 11, 61–67.Google Scholar
Taraschewski, H (2006) Hosts and parasites as aliens. Journal of Helminthology 80, 99–128.Google Scholar
Tena, D, Simón, MP, Gimeno, C, Pomata, MTP, Illescas, S, Amondarain, I, González, A, Domínguez, J and Bisquert, J (1998) Human infection with Hymenolepis diminuta: case report from Spain. Journal of Clinical Microbiology 36, 2375–2376.Google Scholar
Tompkins, DM, White, AR and Boots, M (2003) Ecological replacement of native red squirrels by invasive greys driven by disease. Ecology Letters 6, 189–196.Google Scholar
Wells, K, O'Hara, RB, Morand, S, Lessard, JP and Ribas, A (2015) The importance of parasite geography and spillover effects for global patterns of host–parasite associations in two invasive species. Diversity and Distributions 21, 477–486.Google Scholar
Wilcove, DS and Master, LL (2005) How many endangered species are there in the United States? Frontiers in Ecology and the Environment 3, 414–420.Google Scholar
Woolhouse, ME, Dye, C, Etard, JF, Smith, T, Charlwood, JD, Garnett, GP, Hagan, P, Hii, JLK, Ndhlovu, PD, Quinnell, RJ and Watts, CH (1997) Heterogeneities in the transmission of infectious agents: implications for the design of control programs. Proceedings of the National Academy of Sciences 94, 338–342.Google Scholar
Young, H. S., Parker, I. M., Gilbert, G. S., Sofia Guerra, A. and Nunn, C. L. (2017). Introduced species, disease ecology, and biodiversity-disease relationships. Trends in Ecology & Evolution 32, 41–54.Google Scholar