Hostname: page-component-848d4c4894-xm8r8 Total loading time: 0 Render date: 2024-06-21T21:20:19.027Z Has data issue: false hasContentIssue false

Effect of environmental variables and their interaction on gordiid hairworm larvae (Nematomorpha)

Published online by Cambridge University Press:  23 August 2021

C.L. Achiorno*
Affiliation:
Centro de Estudios Parasitológicos y de Vectores (CEPAVE), Universidad Nacional de La Plata (CCT La Plata-CONICET-UNLP), La Plata, 1900Buenos Aires, Argentina
G. Minardi
Affiliation:
Centro de Estudios Parasitológicos y de Vectores (CEPAVE), Universidad Nacional de La Plata (CCT La Plata-CONICET-UNLP), La Plata, 1900Buenos Aires, Argentina Facultad de Ciencias Económicas, Universidad Nacional de La Plata, La Plata, 1900Buenos Aires, Argentina
L. Ferrari
Affiliation:
Programa de Ecofisiología Aplicada (PRODEA), Instituto de Ecología y Desarrollo Sustentable (INEDES) UNLu–CONICET y Departamento de Ciencias Básicas. Universidad Nacional de Luján, Luján, 6700Buenos Aires, Argentina
*
Author for correspondence: C. Achiorno, E-mail: achiorno@cepave.edu.ar

Abstract

The different stages of the life cycle of parasites are important components of ecosystems. Changes in environmental conditions may affect free-living stages, host–parasite interactions and ecosystem functioning. The larvae of Chordodes nobilii, which belongs to the parasitic phylum Nematomorpha, are susceptible to extreme temperatures and different pollutants, but the effects of pH and moderate temperature variations have not been evaluated yet. Our objective was to assess the effect of temperature, pH and their interaction on the infectivity of C. nobilii larvae to Aedes aegypti larvae over time. Larvae were treated with factorial combinations of temperature (18, 23 and 28°C), pH (7, 8 and 9) and time periods (24 and 48 h). Results show a highly significant interaction among all variables. The highest infectivity was recorded at 18°C and pH 7 at 24 and 48 h, and the lowest one at 28°C and pH 8 at 24 and 48 h. Infectivity differed significantly among the three temperatures only at pH 8 and 48 h, decreasing with increasing temperature. Our study is the first report of the effect of pH on a Nematomorpha species and suggests that the infectivity of C. nobilii larvae may be affected negatively by an increase in temperature and its interaction with pH and time. Since parasites must be considered for a better understanding of the effects of stressors on freshwater ecosystems, our results may help in the design and analysis of studies of anthropogenic impact.

Type
Research Paper
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Achiorno, CL (2011) Influencia de perturbaciones ambientales de origen antrópico sobre el ciclo de vida de Chordodes nobilii (Gordiida, Nematomorpha). PhD thesis, Universidad de La Plata, La Plata, Buenos Aires, Argentina.Google Scholar
Achiorno, CL, de Villalobos, C and Ferrari, L (2008a) Effect of extreme temperature on egg development, larval and adult survival of Chordodes nobilii Camerano, 1901 (Gordiida, Nematomorpha). Acta Parasitologica 53(4), 392396.CrossRefGoogle Scholar
Achiorno, CL, de Villalobos, C and Ferrari, L (2008b) Toxicity of the herbicide glyphosate to Chordodes nobilii (Gordiida, Nematomorpha). Chemosphere 71, 18161822.CrossRefGoogle Scholar
Achiorno, CL, de Villalobos, C and Ferrari, L (2009) Sensitivity of preparasitic stages of Chordodes nobilii (Gordiida, Nematomorpha) to malathion. Ecotoxicology 18(5), 594599.CrossRefGoogle ScholarPubMed
Achiorno, CL, de Villalobos, C and Ferrari, L (2010) Validation test with embryonic and larval stages of Chordodes nobilii (Gordiida, Nematomorpha): sensitivity to three reference toxicants. Chemosphere 81(2), 133140.CrossRefGoogle ScholarPubMed
Achiorno, CL, de Villalobos, C and Ferrari, L (2015) Susceptibility of preparasitic stages of Chordodes nobilii (Gordiida, Nematomorpha) to the fungicide carbendazim. Journal of Helminthology 89, 748754.CrossRefGoogle ScholarPubMed
Achiorno, CL, de Villalobos, C and Ferrari, L (2018) Susceptibility of Chordodes nobilii (Gordiida, Nematomorpha) to three pesticides: influence of the water used for dilution on endpoints in an ecotoxicity bioassay. Environmental Pollution 242B, 14271435.CrossRefGoogle Scholar
Álvarez, J, Martínez, AM, Ábalo, PO, Weis, CF and Fernández, SN (2018) Hydrochemistry and organic matter of the surface water in the upper basin of the sauce Grande River. Revista Estudios Ambientales 6(2), 2245.Google Scholar
Barata, C, Damasio, J, López, MA, Kuster, M, López de Alda, M, Barceló, D, Riva, MC and Raldúa, D (2007) Combined use of biomarkers and in situ bioassays in daphnia magna to monitor environmental hazards of pesticides in the field. Environmental Toxicology and Chemistry 26(2), 370.CrossRefGoogle ScholarPubMed
Berezina, NA (2001) Influence of ambient pH on freshwater invertebrates under experimental conditions. Russian Journal of Ecology 32, 343351.CrossRefGoogle Scholar
Bolek, MG, Rogers, E, Szmygiel, C, Shannon, RP, Doerfert-Schrader, WE, Schmidt-Rhaesa, A and Hanelt, B (2013) Survival of larval and cyst stages of gordiids (Nematomorpha) after exposure to freezing. The Journal of Parasitology 99(3), 397402.CrossRefGoogle ScholarPubMed
Bolek, MG, Schmidt-Rhaesa, A, De Villalobos, LC and Hanelt, B (2015) Phylum Nematomorpha. Chapter 15. pp. 303326 in Thorp, J and Rogers, DC (Eds) Ecology and general biology: Thorp and Covich's freshwater invertebrates. Academic Press.CrossRefGoogle Scholar
Bush, AO, Lafferty, KD, Lotsg, JM and Shotsak, AW (1997) Parasitology meets ecology on its own terms: Margolis et al. revisited. The Journal of Parasitology 83, 576583.CrossRefGoogle Scholar
Faraway, J (2016) Chapters 8, 9, 10. pp. 151236 in Extending the linear model with R. 2nd edn. Boca Raton, Chapman & Hall/CRC Press.Google Scholar
Hanelt, B, Thomas, F and Schmidt-Rhaesa, A (2005) Biology of the phylum Nematomorpha. Advances in Parasitology 59, 243305.CrossRefGoogle ScholarPubMed
Holt, R and Boulinier, T (2006) Ecosystems and parasitism: the spatial dimension. Chapter 5. pp. 6884 in Thomas, F, Renaud, F and Guégan, JF (Eds) Parasitism and ecosystems. New York, Oxford University Press. First published 2005, reprinted 2006.Google Scholar
Hothorn, T, Bretz, F and Westfall, P (2008) Simultaneous inference in general parametric models. Biometrical Journal 50(3), 346363.CrossRefGoogle ScholarPubMed
Hudson, P (2006) Parasites, diversity, and the ecosystem. Introduction. pp. 1321 in Thomas, F, Renaud, F and Guégan, JF (Eds) Parasitism and ecosystems. New York, Oxford University Press. First published 2005, reprinted 2006.Google Scholar
Lafferty, KD and Kuris, AM (2006) Parasitism and environmental disturbances. Chapter 7. pp. 113123 in Thomas, F, Renaud, F and Guégan, JF (Eds) Parasitism and ecosystems. New York, Oxford University Press. First published 2005, reprinted 2006.Google Scholar
Lagrue, C and Poulin, R (2015) Local diversity reduces infection risk across multiple freshwater host-parasite associations. Freshwater Biology 60, 24452454.CrossRefGoogle Scholar
Pietrock, M and Marcogliese, DJ (2003) Free-living endohelminth stages: at the mercy of environmental conditions. Trends in Parasitology 19(7), 293299.CrossRefGoogle Scholar
Poulin, R (2006) Global warming and temperature-mediated increases in cercarial emergence in trematode parasites. Parasitology 132, 143151.CrossRefGoogle ScholarPubMed
Prasopdee, S, Kulsantiwong, J, Sathavornmanee, T and Thitapakorn, V (2020) The effects of temperature and salinity on the longevity of Opisthorchis viverrini cercariae: a climate change concern. Journal of Helminthology 94, e165, 16.CrossRefGoogle ScholarPubMed
R Core Team (2020) R: a language and environment for statistical computing. Vienna, Austria, R Foundation for Statistical Computing. Available at https://www.R-project.org/.Google Scholar
Salmelin, J, Leppänen, MT, Karjalainen, AK, Vuori, K-M, Gerhardt, A and Hämäläinen, H (2016) Assessing ecotoxicity of biomining effluents in stream ecosystems by in situ invertebrate bioassays: a case study in Talvivaara, Finland. Environmental Toxicology and Chemistry 36(1), 147155.CrossRefGoogle ScholarPubMed
Sato, T, Watanabe, K, Kanaiwa, M, Niizuma, Y, Harada, Y and Laferty, KD (2011) Nematomorph parasites drive energy flow through a riparian ecosystem. Ecology 92, 201207.CrossRefGoogle ScholarPubMed
Schmidt-Rhaesa, A (2012) Nematomorpha. pp. 29145 in Schmidt-Rhaesa, A (Ed.) Handbook of zoology. Gastrotricha, Cycloneuralia and Gnathifera. Nematomorpha, Priapulida, Kinorhyncha and Loricifera, vol. 1. Berlin, De Gruyter.CrossRefGoogle Scholar
Scian, B (2010) Clima: Bahía blanca y el sudoeste bonaerense. pp. 2783 in Paoloni, JD (Ed.) Ambiente y recursos naturales del Partido de Bahía Blanca: clima, morfología, suelos y agua. Bahía Blanca, Argentina, Universidad Nacional del Sur.Google Scholar
Sures, B, Nachev, M, Selbach, C and Marcogliese, DJ (2017) Review parasite responses to pollution: what we know and where we go in ‘environmental parasitology’. Parasites & Vectors 10, 65.CrossRefGoogle ScholarPubMed
Thieltges, DW, Jensen, KT and Poulin, R (2008) The role of biotic factors in the transmission of free-living endohelminth stages. Parasitology 135, 407426.CrossRefGoogle ScholarPubMed
Tinsley, RC (2006) Parasitism and hostile environments. Chapter 6. pp. 85112 in Thomas, F, Renaud, F and Guégan, JF (Eds) Parasitism and ecosystems. New York, Oxford University Press. First published 2005, reprinted 2006.Google Scholar
Vidal-Martínez, VM, Pech, D, Sures, B, Purucker, ST and Poulin, R (2010) Review. Can parasites really reveal environmental impact? Trends in Parasitology 26(1), 4451.CrossRefGoogle ScholarPubMed
Weber, CI (1993) Methods for measuring the acute toxicity of effluents and receiving waters to freshwater and marine organisms. 4th edn. Cincinnati, Ohio, Environmental Monitoring systems Laboratory, US Environmental Protection Agency. EPA 00/4-90/027.Google Scholar
Williams, M (2019) The importance of parasites in the functioning of warming ecosystems. PhD thesis, School of Natural Sciences (Zoology), Trinity College Dublin, University of Dublin.Google Scholar
Zuur, A, Ieno, E, Walker, N, Saveliev, A and Graham, M (2009) Chapters 5, 9. pp. 101142 and 209–243 in Mixed effects models and extensions in ecology with R. New York, Springer.CrossRefGoogle Scholar
Supplementary material: File

Achiorno et al. supplementary material

Achiorno et al. supplementary material

Download Achiorno et al. supplementary material(File)
File 17.3 KB