Hostname: page-component-cd9895bd7-mkpzs Total loading time: 0 Render date: 2024-12-26T07:39:50.231Z Has data issue: false hasContentIssue false

A new species of Raphidascaris (Nematoda: Raphidascarididae) infecting the fish Gymnogeophagus balzanii (Cichlidae) from the Pantanal wetlands, Brazil and a taxonomic update of the subgenera of Raphidascaris based on molecular phylogeny and morphology

Published online by Cambridge University Press:  21 December 2018

L.S. Malta
Affiliation:
Programa de Pós-Graduação em Biologia Animal, Instituto de Biociências, Universidade Federal de Mato Grosso do Sul, Av. Costa e Silva s/n°, CEP 79070-900, Campo Grande, MS, Brazil
F. Paiva
Affiliation:
Programa de Pós-Graduação em Biologia Animal, Instituto de Biociências, Universidade Federal de Mato Grosso do Sul, Av. Costa e Silva s/n°, CEP 79070-900, Campo Grande, MS, Brazil
C. Elisei
Affiliation:
Programa de Pós-Graduação em Biotecnologia, Universidade Católica Dom Bosco, Av. Tamandaré 6000, Jardim Seminário, Campo Grande, MS, Brazil
L.E.R. Tavares
Affiliation:
Programa de Pós-Graduação em Biologia Animal, Instituto de Biociências, Universidade Federal de Mato Grosso do Sul, Av. Costa e Silva s/n°, CEP 79070-900, Campo Grande, MS, Brazil
F.B. Pereira*
Affiliation:
Programa de Pós-Graduação em Biologia Animal, Instituto de Biociências, Universidade Federal de Mato Grosso do Sul, Av. Costa e Silva s/n°, CEP 79070-900, Campo Grande, MS, Brazil
*
Author for correspondence: F.B. Pereira E-mail: felipebisaggiop@hotmail.com

Abstract

Raphidascaris (Sprentascaris) andersoni n. sp. (Nematoda: Raphidascarididae) collected in the intestine of the humphead cichlid Gymnogeophagus balzanii (Perugia) from the Pantanal wetlands, State of Mato Grosso do Sul (Brazil) is described and genetically characterized. The new species differs from its congeners mainly by having a conspicuous papilla-like formation slightly anterior to the cloacal aperture. Furthermore, males of R. (S.) lanfrediae and R. (S.) mahnerti have caudal alae, and R. (S.) hypostomi and R. (S.) pimelodi lack lateral alae, whereas in the new species caudal alae are absent and lateral alae present. The remaining congeners, namely, R. (S.) marano and R. (S.) saltaensis differ from Raphidascaris (Sprentascaris) andersoni n. sp. mainly because males have three pairs of postcloacal papillae (vs five pairs). In the phylogenetic reconstructions, using three nuclear genetic markers (18S, ITS1-5.8S-ITS2 and 28S rDNA) and one mitochondrial (cox1 mtDNA), the new species was separated from other representatives of Raphidascarididae, and the absence of monophyly in Hysterothylacium and Raphidascaroides was confirmed. Moreover, the subgenera Sprentascaris and Ichthyascaris appeared to be monophyletic. Therefore, even though Raphidascaris (Raphidascaris) was apparently not monophyletic, the subgenera of Raphidascaris should be re-erected as valid genera. The updated diagnoses of Ichthyascaris, Raphidascaris and Sprentascaris are given. The present study represents the first parasitological survey in G. balzanii.

Type
Research Paper
Copyright
Copyright © Cambridge University Press 2018 

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

Ailán-Choke, LG, Ramallo, G and Davies, D (2017) New species of Raphidascaris (Sprentascaris) (Nematoda: Anisakidae) in Rineloricaria steinbachi (Actinopterygii: Loricariidae) from Northwest Argentina. Zootaxa 4231, 129136.Google Scholar
Astrin, JJ, Zhoun, X and Misof, B (2013) The importance of biobanking in molecular taxonomy, with proposed definitions for vouchers in a molecular context. Zookeys 365, 6770.Google Scholar
Bruce, NL (1990) Hysterothylacium Ward and Magath, 1917, and Ichthyascaris Wu, 1949, ascaridoid nematodes from Australian demersal fishes. Memories of the Queensland Museum 28, 389426.Google Scholar
Bruce, NL, Adlard, RD and Cannon, LRG (1994) Synoptic checklist of ascaridoid parasites (Nematoda) from fish hosts. Invertebrate Taxonomy 8, 583674.Google Scholar
Chang, J-M, Di Tommaso, P and Notredame, C (2014) TCS: a new multiple sequence alignment reliability measure to estimate alignment accuracy and improve phylogenetic tree reconstruction. Molecular Biology and Evolution 31, 16251637.Google Scholar
Darriba, D et al. (2012) jModelTest 2: more models, new heuristics and parallel computing. Nature Methods 9, 772.Google Scholar
Froese, R and Pauly, D (Eds) (2018) FishBase. http//www.fishbase.org, version 06/2018 (accessed 17 October 2018).Google Scholar
Guindon, S and Gascuel, O (2003) A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Systematic Biology 52, 696704.Google Scholar
Huelsenbeck, JP and Ronquist, F (2001) MrBayes: Bayesian inference of phylogenetic trees. Bioinformatics 17, 754755.Google Scholar
Li, L, Liu, Y-Y and Zhang, L-P (2012a) Morphological and molecular evidence for a new species of the genus Raphidascaris (Nematoda: Anisakidae) from marine fishes from South China Sea. Parasitology Research 110, 14731479.Google Scholar
Li, L, Liu, Y-Y and Zhang, L-P (2012b) Morphological and molecular identification of Hysterothylacium longilabrum sp. nov. (Nematoda: Anisakidae) and larvae of different stages from marine fishes in the South China Sea. Parasitology Research 111, 767777.Google Scholar
Li, L et al. (2018) Molecular phylogeny and dating reveal a terrestrial origin in the early Carboniferous for ascaridoid nematodes. Systematic Biology 67, 888900.Google Scholar
Luque, JL et al. (2011) Checklist of Nematoda associated with the fishes of Brazil. Zootaxa 3082, 188.Google Scholar
Melo, MFC et al. (2011) Raphidascaris (Sprentascaris) lanfrediae sp. nov. (Nematoda: Anisakidae) from the fish Satanoperca jurupari (Osteichthyes: Cichlidae). Memórias do Instituto Oswaldo Cruz 106, 553556.Google Scholar
Moravec, F (1998) Nematodes of Freshwater Fishes of the Neotropical Region. Prague: Academia.Google Scholar
Moravec, F and Justine, J-L (2012) Raphidascaris (Ichthyascaris) etelidis n. sp. (Nematoda, Anisakidae), a new ascaridoid nematode from lutjanid fishes off New Caledonia. Zoosystema 34, 113121.Google Scholar
Moravec, F and Nagasawa, K (2002) Redescription of Raphidascaris gigi Fujita, 1928 (Nematoda: Anisakidae), a parasite of freshwater fishes in Japan. Systematic Parasitology 52, 193198.Google Scholar
Moravec, F, Kohn, A and Fernandes, BMM (1990) First record of Raphidascaris (Sprentascaris) hypostomi (Petter & Cassone, 1984) comb. n. and R. (S.) manherti (Petter & Cassone, 1984) comb. n. (Nematoda: Anisakidae) from Brazil with remarks on the taxonomic status of this genus Sprentascaris Petter et Cassone, 1984. Folia Parasitologica 37, 131140.Google Scholar
Nadler, SA and Hudspeth, DSS (1998) Ribosomal DNA and phylogeny of the Ascaridoidea (Nemata: Secernentea): implications for morphological evolution and classification. Molecular Phylogenetics Evolution 10, 221236.Google Scholar
Nadler, SA and Hudspeth, DSS (2000) Phylogeny of the Ascaridoidea (Nematoda: Ascaridida) based on three genes and morphology: hypotesis of strucutural and sequence evolution. Journal of Parasitology 86, 380393.Google Scholar
Notredame, C, Higgins, DG and Heringa, J (2000) T-Coffee: a novel method for fast and accurate multiple sequence alignment. Journal of Molecular Biology 302, 205217.Google Scholar
Pantoja, CS et al. (2015) Molecular and morphological characterization of anisakid nematode larvae from the sandperches Pseudopercis numida and Pinguipes brasilianus (Perciformes: Pinguipedidae). Journal of Parasitology 101, 492499.Google Scholar
Pereira, FB and Luque, JL (2017) An integrated phylogenetic analysis on ascaridoid nematodes (Anisakidae, Raphidascarididae), including further description and intraspecific variations of Raphidascaris (Sprentascaris) lanfrediae in freshwater fishes from Brazil. Parasitology International 66, 898904.Google Scholar
Pereira, FB et al. (2015) A morphological and molecular study of two species of Raphidascaroides Yamaguti, 1941 (Nematoda: Anisakidae), parasites of doradid catfish (Siluriformes) in South America, with a description of R. moraveci n. sp. Systematic Parasitology 91, 4961.Google Scholar
Pérez-i-García, D et al. (2015) Raphidascaris (Raphidascaris) macrouri n. sp. (Nematoda: Anisakidae) from two deep-sea macrourid fishes in the western Mediterranean: morphological and molecular characterisations. Parasitology International 64, 345352.Google Scholar
Petter, AJ (1995) Nématodes de Poissons du Paraguay. VIII. Habronematoidea, Dracunculoidea et Ascaridoidea. Revue Suisse de Zoologie 102, 89102.Google Scholar
Petter, AJ and Cassone, J (1984) Nématodes de Poissons du Paraguay; I. Ascaridoidea: Sprentascaris, n. gen. Revue Suisse de Zoologie 91, 617634.Google Scholar
Ramallo, G (2009) A new species of Raphidascaris (Sprentascaris) (Nematoda: Anisakidae) in Hypostomus cordovae (Pisces: Loricariidae) from Argentina. Zootaxa 2045, 6064.Google Scholar
Simsek, E et al. (2016) First molecular characterization of Raphidascaris acus Bloch, 1779 (Nematoda: Anisakidae) from European eels (Anguilla anguilla Linnaeus, 1758) caught off the Aegean Region Streams, Turkey. Journal of the Faculty of Veterinary Medicine, Kfkas University 22, 529532.Google Scholar
Xu, Z et al. (2012) Morphological and molecular characterization of Raphidascaris (Ichthyascaris) lophii (Wu, 1949) (Nematoda, Anisakidae) from marine fishes from China, with a key to the species of the subgenus Ichthyascaris. Acta Parasitologica 57, 316322.Google Scholar
Zago, AC et al. (2013) The helminth community of Geophagus proximus (Perciformes: Cichlidae) from a tributary of the Paraná River, Ilha Solteira Reservoir, São Paulo State, Brazil. Journal of Helminthology 87, 203211.Google Scholar
Supplementary material: PDF

Malta et al. supplementary material

Malta et al. supplementary material 1

Download Malta et al. supplementary material(PDF)
PDF 174.1 KB