Hostname: page-component-848d4c4894-sjtt6 Total loading time: 0 Render date: 2024-06-30T19:00:21.508Z Has data issue: false hasContentIssue false

Description of Saccocoelioides miguelmontesi n. sp. (Digenea: Haploporidae) from characid fishes in the Iguazu River Basin based on morphological and molecular evidence

Published online by Cambridge University Press:  13 March 2024

M.M. Montes*
Affiliation:
Centro de Estudios Parasitológicos y Vectores (CEPAVE), Consejo Nacional de Investigaciones Científicas y Técnicas, Universidad Nacional de La Plata (CCT, CONICET-UNLP), La Plata, Buenos Aires, Argentina
Y. Croci
Affiliation:
Centro de Estudios Parasitológicos y Vectores (CEPAVE), Consejo Nacional de Investigaciones Científicas y Técnicas, Universidad Nacional de La Plata (CCT, CONICET-UNLP), La Plata, Buenos Aires, Argentina
J. Barneche
Affiliation:
Centro de Estudios Parasitológicos y Vectores (CEPAVE), Consejo Nacional de Investigaciones Científicas y Técnicas, Universidad Nacional de La Plata (CCT, CONICET-UNLP), La Plata, Buenos Aires, Argentina
W. Ferrari
Affiliation:
Instituto de Biotecnología Ambiental y Salud (INBIAS), Consejo Nacional de Investigaciones Científicas, Universidad Nacional de Rio Cuarto (CONICET-UNRC), Rio cuarto, Córdoba
G. Reig Cardarella
Affiliation:
Escuela de Tecnología Médica y Centro Integrativo de Biología y Química Aplicada (CIBQA), Universidad Bernardo O’ Higgins, Santiago de Chile, Chile
S. Martorelli
Affiliation:
Centro de Estudios Parasitológicos y Vectores (CEPAVE), Consejo Nacional de Investigaciones Científicas y Técnicas, Universidad Nacional de La Plata (CCT, CONICET-UNLP), La Plata, Buenos Aires, Argentina
*
Corresponding author: M.M. Montes; Email: martinmiguelmontes@gmail.com

Abstract

Here we describe a new species of the genus Saccocoelioides found parasitizing Astyanax dissimilis Garavello & Sampaio, Psalidodon bifasciatus (Garavello and Sampaio) and Bryconamericus ikaa Casciotta, Almirón & Azpelicueta from the Iguazu National Park, Misiones province, Argentina. Saccocoelioides miguelmontesi n. sp. was studied based on morphological and molecular (28S rDNA and COI mtDNA sequences) data. The COI mtDNA tree indicated that the specimens collected from the three fish hosts are conspecific, with an intragroup p-distance of 0%. The new species shows an intermediate morphological configuration between the diminutive and robust forms described for Saccocoelioides by Curran (2018). Although, in the 28S rDNA tree, it is placed in a well-supported clade with the two robust species analysed (S. elongatus and S. magnus; p-distance of 1 and 2%, respectively), it differs from the robust group by the range of body size, mature egg size, oral and ventral sucker size, sucker ratio, oral sucker to pharynx ratio, and post-cecal or post-testis/body length percentage. Our results led us to redefine the robust group as having eggs shorter or equal in length to the pharynx. Saccocoelioides miguelmontesi n. sp. the 10th species reported from Argentina and the 7th species within the robust group.

Type
Research Paper
Copyright
© The Author(s), 2024. 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

Andrade-Gómez, L, Pinacho-Pinacho, CD, García-Varela, M (2017). Molecular, morphological and ecological data of Saccocoelioides Szidat, 1954 (Digenea: Haploporidae) from Middle America supported the reallocation from Culuwiya cichlidorum to Saccocoelioides. Journal of Parasitology 103, 3, 257267. https://doi.org/10.1645/16-129.CrossRefGoogle ScholarPubMed
Andrade-Gómez, L, Pinacho-Pinacho, CD, Hernández-Orts, JS, Sereno-Uribe, AL, García-Varela, M (2017). Morphological and molecular analyses of a new species of Saccocoelioides Szidat, 1954 (Haploporidae Nicoll, 1914) in the fat sleeper Dormitator maculatus (Bloch) (Perciformes: Eleotridae) from the Gulf of Mexico. Journal of Helminthology 91, 4, 504516. https://doi.org/10.1017/S0022149X1600047X.CrossRefGoogle ScholarPubMed
Andrade-Gómez, L, Sereno-Uribe, AL, Garcia-Varela, M (2019). Description of a new species and understanding the genetic diversity of Saccocoelioides Szidat, 1954 (Haploporidae) in Middle America using mitochondrial and nuclear DNA sequences. Parasitology International 71, 8798. https://doi.org/10.1016/j.parint.2019.04.005.CrossRefGoogle ScholarPubMed
Andres, MJ, Curran, SS, Fayton, TJ, Pulis, EE, Overstreet, RM (2015). An additional genus and two additional species of Forticulcitinae (Digenea: Haploporidae). Folia Parasitologica 62, 025. https://doi.org/10.14411/fp.2015.025.CrossRefGoogle ScholarPubMed
Casciotta, J, Almirón, A, Ciotek, AL, Giorgis, P, Říčan, O, Piálek, L, Dragová, K, Croci, Y, Montes, M, Iwaszkiw, J, Puentes, A (2016). Visibilizando lo invisible. Un relevamiento de la diversidad de peces del Parque Nacional Iguazú, Misiones, Argentina. Revista Historia Natural 6, 2, 577.Google Scholar
Curran, SS, Pulis, EE, Andres, MJ, Overstreet, RM (2018). Two new species of Saccocoelioides (Digenea: Haploporidae) with phylogenetic analysis of the family, including species of Saccocoelioides from North, Middle, and South America. Journal of Parasitology 104, 3, 221239. https://doi.org/10.1645/17-189.CrossRefGoogle ScholarPubMed
Curran, SS, Tkach, VV and Overstreet, RM (2006). A review of Polylekithum Arnold, 1934 and its familial affinities using morphological and molecular data, with description of Polylekithum catahoulensis sp. nov. Acta Parasitologica 51, 238248.CrossRefGoogle Scholar
Katoh, K, Rozewicki, J, Yamada, KD (2019). MAFFT online service: Multiple sequence alignment, interactive sequence choice and visualization. Briefings in Bioinformatics 20, 4, 11601166. https://doi.org/10.1093/bib/bbx108.CrossRefGoogle ScholarPubMed
Kohn, A, Fernandes, BMM, Cohen, SC (2007). South American trematodes parasites of fishes. Rio de Janeiro: FIOCRUZ, Instituto Oswaldo Cruz.Google Scholar
Kumar, S, Stecher, G, Li, M, Knyaz, C, Tamura, K (2018). Mega X: Molecular evolutionary genetics analysis across computing platforms. Molecular Biology and Evolution 35, 6, 15471549. https://doi.org/10.1093/molbev/msy096.CrossRefGoogle ScholarPubMed
Lanfear, R, Calcott, B, Kainer, D, Mayer, C, Stamatakis, A (2014). Selecting optimal partitioning schemes for phylogenomic datasets. BMC Evolutionary Biology 14, 82. https://doi.org/10.1186/1471-2148-14-82.CrossRefGoogle ScholarPubMed
Lunaschi, LI (1984). Helminthos parásitos de peces de agua dulce de la Argentina I. Tres nuevas especies del genero Saccocoelioides Szidat, 1954 (Trematoda Haploporidae). Neotropica 30, 3142.Google Scholar
Martorelli, SR, Montes, MM, Barneche, J, Reig Cardarella, G, Curran, SS (2022). Saccocoelioides kirchneri n. sp. (Digenea: Haploporidae) from the killifish Cnesterodon decemmaculatus (Cyprinodontiformes: Poeciliidae) from Argentina, morphological and molecular description. Journal of Helminthology 96, e37. https://doi.org/10.1017/S0022149X22000165.CrossRefGoogle Scholar
Mirande, JM (2010). Phylogeny of the family Characidae (Teleostei: Characiformes): From characters to taxonomy. Neotropical Ichthyology 8, 3, 385568. https://doi.org/10.1590/S1679-62252010000300001.CrossRefGoogle Scholar
Mirande, JM, Koerber, S (2020). Checklist of the freshwater fishes of Argentina. 2nd edition. (CLOFFAR-2). Ichthyological Contributions of PecesCriollos 72, 181.Google Scholar
Montes, MM, Barneche, J, Croci, Y, Rodriguez Gil, S, Curran, SS, Ferrari, W, Casciotta, JR, Martorelli, SR (2020). Prosthenhystera gattii n. sp. (Digenea: Callodistomidae), a gallbladder parasite of Bryconamericus ikaa from the lower Iguazú River, described based on combined molecular and morphological evidence. Journal of Helminthology 94, e151. https://doi.org/10.1017/S0022149X20000322.CrossRefGoogle Scholar
Montes, MM, Barneche, J, Croci, Y, Balcazar, D, Almirón, A, Martorelli, S, Pérez-Ponce de León, G (2021). Description of a new species of Auriculostoma (Digenea: Allocreadiidae) from Characidium heirmostigmata (Characiformes: Crenuchidae) from Argentina, using morphological and molecular data. Journal of Helminthology 95, e19. https://doi.org/10.1017/S0022149X21000109.CrossRefGoogle ScholarPubMed
Nei, M, Kumar, S (2000). Molecular Evolution and Phylogenetics. New York: Oxford University Press, 352 pp.CrossRefGoogle Scholar
Ostrowski de Nuñez, M, Arredondo, NJ, Gil de Pertierra, A (2017). Adult trematodes (Platyhelminthes) of freshwater fishes from Argentina: A checklist. Revue Suisse de Zoologie 124, 1, 91113. https://doi.org/10.5281/zenodo.322669.Google Scholar
Pritchard, MH, Kruse, GO (1982). The Collection and Preservation of Animal Parasites. Nebraska: University of Nebraska Press, 141 pp.Google Scholar
Ronquist, F, Teslenko, M, van der Mark, P, Ayres, DL, Darling, A, Höhna, S, Larget, B, Liu, L, Suchard, MA, Huelsenbeck, JP (2012). MrBayes 3.2: Efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology 61, 3, 539542. https://doi.org/10.1093/sysbio/sys029.CrossRefGoogle ScholarPubMed
Schneider, CA, Rasband, WS, Eliceiri, KW (2012). NIH Image to ImageJ: 25 years of image analysis. Nature Methods 9, 671675. https://doi.org/10.1038/nmeth.2089.CrossRefGoogle ScholarPubMed
Schwarz, G (1978). Estimating the dimension of a model. Annals of Statistics 6, 461464. http://doi.org/10.1214/aos/1176344136.CrossRefGoogle Scholar
Szidat, L (1970). Saccocoelioides octavus n. sp., una nueva especie del genero Saccocoelioides Szidat 1954 (Trematoda, Haploporinae Looss 1902). Revista del Museo Argentino de Ciencias Naturales “Bernardino Rivadavia” e Instituto Nacional de Investigación de las Ciencias Naturales Zoología 10, 87100.Google Scholar
Terán, GE, Benitez, MF, Mirande, JM (2020). Opening the Trojan horse: Phylogeny of Astyanax, two new genera and resurrection of Psalidodon (Teleostei: Characidae). Zoological Journal of the Linnean Society 190, 4, 12171234. https://doi.org/10.1093/zoolinnean/zlaa019.Google Scholar
Thatcher, VE (1999). Two new Haploporidae (Trematoda) of fishes from the Brazilian state of Rondônia. Acta Amazonica 29, 601605.CrossRefGoogle Scholar
Thatcher, VE, Jégu, M (1996). Intestinal helminths as population markers of the Amazonian fish Mylesinus paraschomburgkii, with descriptions of five new genera and seven new species of trematodes. Amazoniana 14, 143155.Google Scholar
Travassos, L, Teixeira de Freitas, JF, Kohn, A (1969). Trematodeos do Brasil. Memorias do Instituto Oswaldo Cruz 67, 1, 1886.Google Scholar
Tkach, VV, Littlewood, DTJ, Olson, PD, Kinsella, JM, Swiderski, Z (2003). Molecular phylogenetic analysis of the Microphalloidea Ward, 1901 (Trematoda: Digenea). Systematic Parasitolology 56, 1, 115. https://doi.org/10.1023/a:1025546001611.CrossRefGoogle ScholarPubMed
Van Steenkiste, N, Locke, SA, Castelin, M, Marcogliese, DJ, Abbott, CL (2015). New primers for DNA barcoding of digeneans and cestodes (Platyhelminthes). Molecular Ecology Resources 15, 4, 945952. https://doi.org/10.1111/1755-0998.12358.CrossRefGoogle ScholarPubMed