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Gerricola queenslandensis n. g., n. sp., a new monorchiid trematode from the eastern Australian coast and its life cycle partially elucidated

Published online by Cambridge University Press:  08 June 2021

N.Q.-X. Wee*
Affiliation:
School of Biological Sciences, The University of Queensland, St Lucia, Brisbane, QLD4072, Australia
S.C. Cutmore
Affiliation:
School of Biological Sciences, The University of Queensland, St Lucia, Brisbane, QLD4072, Australia
T.H. Cribb
Affiliation:
School of Biological Sciences, The University of Queensland, St Lucia, Brisbane, QLD4072, Australia
*
Author for correspondence: N.Q.-X. Wee, E-mail: qi.wee@uqconnect.edu.au

Abstract

Of over 250 species of Monorchiidae Odhner, 1911, just four are known from gerreid fishes. Here, we report adult specimens of a new species infecting Gerres oyena (Forsskål) and Gerres subfasciatus Cuvier from off Heron Island and North Stradbroke Island, Queensland, Australia. The species is morphologically most similar to the concept of Lasiotocus Looss, 1907, which currently comprises eight species, in the possession of an unspined genital atrium, bipartite terminal organ, round oral sucker and unlobed ovary. However, phylogenetic analyses of the 28S ribosomal DNA gene region shows the species to be distantly related to the two sequenced species of LasiotocusLasiotocus mulli (Stossich, 1883) Odhner, 1911 and Lasiotocus trachinoti Overstreet & Brown, 1970 – and that it clearly requires a distinct genus; thus, we propose Gerricola queenslandensis n. g., n. sp. Morphologically, G. queenslandensis n. g., n. sp. differs significantly from L. mulli and L. trachinoti only in the possession of distinctly longer caeca, which terminate in the post-testicular region, and in the absence of a distinct gap in the terminal organ spines. The remaining species of Lasiotocus possess caeca that also terminate in the post-testicular region, which might warrant their transfer to Gerricola n. g. However, doubt about their monophyly due to a combination of significant morphological variation, a lack of information on some features and infection of a wide range of hosts, lead us to retain these taxa as species of Lasiotocus until molecular sequence data are available to better inform their phylogenetic and taxonomic positions. Sporocysts and cercariae of G. queenslandensis n. g., n. sp. were found in a lucinid bivalve, Codakia paytenorum (Iredale), from Heron Island. Sexual adult and intramolluscan stages were genetically matched with the ITS2 ribosomal DNA and cox1 mitochondrial DNA regions. This is the second record of the Lucinidae as a first intermediate host for the Monorchiidae. Additionally, we report sporocysts and cercariae of another monorchiid infection in a tellinid bivalve, Jactellina clathrata (Deshayes), from Heron Island. Molecular sequence data for this species do not match any sequenced species and phylogenetic analyses do not suggest any generic position.

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

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References

Andres, MJ, Pulis, EE, Curran, SS and Overstreet, RM (2018) On the systematics of some marine haploporids (Trematoda) with the description of a new species of Megasolena Linton, 1910. Parasitology International 67, 805815.CrossRefGoogle ScholarPubMed
Ankenbrand, MJ, Keller, A, Wolf, M, Schultz, J and Förster, F (2015) ITS2 database V: twice as much. Molecular Biology and Evolution 32, 30303032.CrossRefGoogle ScholarPubMed
Atopkin, DM, Besprozvannykh, VV, Ngo, HD, Van Ha, N, Van Tang, N, Ermolenko, AV and Beloded, AY (2017) Morphometric and molecular data of the two digenean species Lasiotocus lizae Liu, 2002 (Monorchiidae) and Paucivitellosus vietnamensis sp. n. (Bivesiculidae) from mullet fish in Tonkin Bay, Vietnam. Journal of Helminthology 91, 346355.CrossRefGoogle Scholar
Bagnato, E, Gilardoni, C, Pina, S, Rodrigues, P and Cremonte, F (2016) Redescription and life cycle of the monorchiid Postmonorcheides maclovini Szidat, 1950 (Digenea) from the Southwestern Atlantic Ocean: Morphological and molecular data. Parasitology International 65, 4449.CrossRefGoogle ScholarPubMed
Besprozvannykh, VV, Ermolenko, AV and Atopkin, DM (2012) The life cycle of Asymphylodora percotti sp. n. (Trematoda: Lissorchiidae) in the Russian southern Far east. Parasitology International 61, 235241.CrossRefGoogle Scholar
Bott, NJ, Healy, JM and Cribb, TH (2005) Patterns of digenean parasitism of bivalves from the Great Barrier Reef and associated waters. Marine and Freshwater Research 56, 387394.CrossRefGoogle Scholar
Cable, RM (1956) Marine cercariae of Puerto Rico. Scientific Survey of Puerto Rico and the Virgin Islands 16, 491577.Google Scholar
Cable, RM (1963) Marine cercariae from Curaçao and Jamaica. Zeitschrift für Parasitenkunde 23, 429469.CrossRefGoogle Scholar
Cremonte, F, Kroeck, MA and Martorelli, SR (2001) A new monorchiid cercaria (Digenea) parasitising the purple clam Amiantis purpurata (Bivalvia: Veneridae) in the southwest Atlantic Ocean, with notes on its gonadal effect. Folia Parasitologica 48, 217223.CrossRefGoogle Scholar
Cribb, TH and Bray, RA (2010) Gut wash, body soak, blender and heat-fixation: approaches to the effective collection, fixation and preservation of trematodes of fishes. Systematic Parasitology 76, 17.CrossRefGoogle ScholarPubMed
Cribb, TH, Anderson, GR, Adlard, RD and Bray, RA (1998) A DNA-based demonstration of a three-host life-cycle for the Bivesiculidae (Playtyhelminthes: Digenea). International Journal for Parasitology 28, 17911795.CrossRefGoogle Scholar
Cribb, TH, Wee, NQ-X, Bray, RA and Cutmore, SC (2018) Monorchis lewisi n. sp. (Trematoda: Monorchiidae) from the surf bream, Acanthopagrus australis (Sparidae), in Moreton Bay, Australia. Journal of Helminthology 92, 100108.CrossRefGoogle Scholar
Darriba, D, Taboada, GL, Doallo, R and Posada, D (2012) Jmodeltest 2: more models, new heuristics and parallel computing. Nature Methods 9, 772.CrossRefGoogle ScholarPubMed
Edgar, RC (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Research 32, 17921797.CrossRefGoogle ScholarPubMed
Froese, R and Pauly, D (2021) FishBase. Available at www.fishbase.org (accessed 1 January 2021).Google Scholar
Gilardoni, C, Carballo, MC and Cremonte, F (2013) The life cycle and geographical distribution of the monorchiid Proctotrema bartolii (Digenea) in the clam Darina solenoides from the Patagonian coast, Argentina. Journal of Helminthology 87, 392399.CrossRefGoogle ScholarPubMed
ICZN (2012) International Commission on Zoological Nomenclature: amendment of articles 8, 9, 10, 21 and 78 of the international code of zoological Nomenclature to expand and refine methods of publication. Bulletin of Zoological Nomenclature 69, 161169.CrossRefGoogle Scholar
Kearse, M, Moir, R, Wilson, A, et al. (2012) Geneious basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics 28, 16471649.CrossRefGoogle ScholarPubMed
Keller, A, Schleicher, T, Schultz, J, Müller, T, Dandekar, T and Wolf, M (2009) 5.8S-28S rRNA interaction and HMM-based ITS2 annotation. Gene 430, 5057.CrossRefGoogle ScholarPubMed
Kumar, S, Stecher, G, Li, M, Knyaz, C and Tamura, K (2018) MEGA x: molecular evolutionary genetics analysis across computing platforms. Molecular Biology and Evolution 35, 15471549.CrossRefGoogle ScholarPubMed
Lamprell, K and Whitehead, T (1992) Bivalves of Australia, volume 1. Bathurst, Crawford House Press.Google Scholar
Littlewood, DTJ (1994) Molecular phylogenetics of cupped oysters based on partial 28S rRNA gene sequences. Molecular Phylogenetics and Evolution 3, 221229.CrossRefGoogle ScholarPubMed
Littlewood, DTJ, Rohde, K and Clough, KA (1997) Parasite speciation within or between host species? – phylogenetic evidence from site-specific polystome monogeneans. Parasitology 27, 12891297.Google ScholarPubMed
Littlewood, DTJ, Curini-Galletti, M and Herniou, EA (2000) The interrelationships of Proseriata (Platyhelminthes: Seriata) tested with molecules and morphology. Molecular Phylogenetics and Evolution 16, 449466.CrossRefGoogle ScholarPubMed
Machida, M (1973) Two new trematodes from the gerrid fish of bungo channel, Japan. Bulletin of the National Science Museum, Tokyo 18, 429435.Google Scholar
Machida, M (2011) Additional monorchiid digeneans (Trematoda) from fishes of Japanese and adjacent waters. Bulletin of the National Museum of Nature and Science, Series A 37, 18.Google Scholar
Madhavi, R (2008) Family Monorchiidae Odhner, 1911. pp. 145175 in Bray, RA, Gibson, DI and Jones, A (Eds) Keys to the Trematoda, volume 3. Wallingford-London, CAB International and Natural History Museum.CrossRefGoogle Scholar
Manter, HW (1942) Monorchiidae (Trematoda) from fishes of Tortugas, Florida. Transactions of the American Microscopical Society 61, 349360.CrossRefGoogle Scholar
Miller, MA, Pfeiler, E and Schwartz, T (2010) Creating the CIPRES science gateway for inference of large phylogenetic trees. In 2010 Gateway Computing Environments Workshop (GCE), New Orleans, LA, 1–8.CrossRefGoogle Scholar
Morgan, JA and Blair, D (1995) Nuclear rDNA ITS sequence variation in the trematode genus Choanosome: an aid to establishing relationships within the 37-collar-spine group. Parasitology 111, 609615.CrossRefGoogle Scholar
Nahhas, FM and Cable, RM (1964) Digenetic and aspidogastrid trematodes from marine fishes of curaçao and Jamaica. Tulane Studies in Zoology 11, 169228.CrossRefGoogle Scholar
Olson, PD, Cribb, TH, Tkach, VV, Bray, RA and Littlewood, DTJ (2003) Phylogeny and classification of the Digenea (Platyhelminthes: Trematoda). International Journal for Parasitology 33, 733755.CrossRefGoogle Scholar
Overstreet, RM (1969) Digenetic trematodes of marine teleost fishes from Biscayne Bay, Florida. Tulane Studies in Zoology and Botany 15, 119180.Google Scholar
Panyi, A (2020) Interrelationships among monorchiid trematodes with species emphasis on some northwestern Atlantic genera. Master's Thesis, The University of Southern Mississippi, Hattiesburg, Mississippi.Google Scholar
Panyi, AJ, Curran, SS and Overstreet, RM (2020) Phylogenetic affinity of Genolopa (Digenea: Monorchiidae) with descriptions of two new species. Diversity 12, 51.CrossRefGoogle Scholar
Petkevičiūtė, R, Stanevičiūtė, G and Stunžėnas, V (2020) Exploring species diversity of Lissorchiid trematodes (Digenea: Lissorchiidae) associated with the gravel snail, Lithoglyphus naticoides, in European freshwaters. Journal of Helminthology 94, 110.CrossRefGoogle ScholarPubMed
Pleijel, F, Jondelius, U, Norlinder, E, Nygren, A, Oxelman, B, Schander, C, Sundberg, P and Thollesson, M (2008) Phylogenies without roots? A plea for the use of vouchers in molecular phylogenetic studies. Molecular Phylogenetics and Evolution 48, 369371.CrossRefGoogle Scholar
Ronquist, F, Teslenko, M, van der Mark, P, et al. (2012) Mrbayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology 61, 539542.CrossRefGoogle ScholarPubMed
Searle, EL, Cutmore, SC and Cribb, TH (2014) Monorchiid trematodes of the painted sweetlips, Diagramma labiosum (Perciformes: Haemulidae), from the southern Great Barrier Reef, including a new genus and three new species. Systematic Parasitology 88, 195211.CrossRefGoogle Scholar
Siddiqi, AH and Cable, RM (1960) Digenetic trematodes of marine fishes of Puerto Rico. Scientific Survey of Porto Rico and the Virgin Islands 17, 257369.Google Scholar
Snyder, SD and Tkach, VV (2001) Phylogenetic and biogeographical relationships among some Holarctic frog lung flukes (Digenea: Haematoloechidae). Journal of Parasitology 87, 14331440.CrossRefGoogle Scholar
Sokolov, SG and Gordeev, II (2019) Asaccotrema vietnamiense n. gen.; n. sp. (Trematoa: Monorchioidea), a new aberrant representative of Lissorchiid trematodes from the sidestripe rasbora, Rasbora paviana Tirant (Actinopterygii: Cyprinidae), Vietnam. Zootaxa 4674, 451462.CrossRefGoogle Scholar
Sokolov, S, Voropaeva, E and Atopkin, D (2020) A new species of deropristid trematode from the sterlet Acipenser ruthenus (Actinopterygii: Acipenseridae) and revision of superfamily affiliation of the family Deropristidae. Zoological Journal of the Linnean Society 190, 448459.CrossRefGoogle Scholar
Stamatakis, A (2014) RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 30, 13121313.CrossRefGoogle ScholarPubMed
Swofford, DL (2002) PAUP*. Phylogenetic analyses using parsimony (*and other methods). Version 4.0b10. Sunderland, Massachusetts, Sinauer Associates.Google Scholar
Tkach, VV, Pawlowski, J, Mariauxc, J and Swiderski, Z (2001) Molecular phylogeny of the suborder Plagiorchiata and its position in the system of Digenea. pp. 186193 in Littlewood, DTJ and Bray, RA (Eds) Interrelationships of Platyhelminthes. London, Taylor & Francis.Google Scholar
Wallet, M and Kohn, A (1987) Trématodes parasites de poissons marins du littoral de Rio de Janeiro, Brésil. Memorias do Instituto Oswaldo Cruz 82, 2127s.CrossRefGoogle Scholar
Wee, NQ-X, Cribb, TH, Bray, RA and Cutmore, SC (2017a) Two known and one new species of Proctoeces from Australian teleosts: variable host-specificity for closely related species identified through multi-locus molecular data. Parasitology International 66, 1626.CrossRefGoogle Scholar
Wee, NQ-X, Cutmore, SC, Yong, RQ-Y and Cribb, TH (2017b) Two new and one known species of Tergestia Stossich, 1899 (Trematoda: Fellodistomidae) with novel molecular characterisation for the genus. Systematic Parasitology 94, 861874.CrossRefGoogle Scholar
Wee, NQ-X, Cutmore, SC and Cribb, TH (2018) Two monorchiid species from the freckled goatfish, Upeneus tragula (Perciformes: Mullidae), in Moreton Bay, Australia, including a proposal of a new genus. Systematic Parasitology 95, 353365.CrossRefGoogle Scholar
Wee, NQ-X, Cutmore, SC and Cribb, TH (2019) Four new monorchiids from the golden trevally, Gnathanodon speciosus (Forsskål) (Perciformes: Carangidae), in Moreton Bay, Australia. Systematic Parasitology 96, 265278.CrossRefGoogle Scholar
Wee, NQ-X, Cribb, TH, Cutmore, SC and Martin, SB (2020a) Retroporomonorchis pansho n. gen. n. sp., an unusual monorchiid trematode exploiting an atypical host. Systematic Parasitology 97, 441454.CrossRefGoogle Scholar
Wee, NQ-X, Crouch, K, Cutmore, SC and Cribb, TH (2020b) Pseudohurleytrema yolandae n. sp., the first monorchiid trematode reported from the Triacanthidae (Tetraodontiformes). Systematic Parasitology 97, 491500.CrossRefGoogle Scholar
Wee, NQ-X, Cutmore, SC, Pérez-del-Olmo, A and Cribb, TH (2020c) First steps to restructuring the problematic genus Lasiotocus Looss, 1907 (Digenea: Monorchiidae) with the proposal of four new genera. Parasitology International 79. doi: 10.1016/j.parint.2020.102164CrossRefGoogle Scholar
Wee, NQ-X, Cutmore, SC, Sasal, P and Cribb, TH (2020d) Three new species of Allobacciger Hafeezullah & Siddiqi, 1970 (Digenea: Monorchiidae) from Australia and French Polynesia. Marine Biodiversity 50. doi: 10.1007/s12526-019-01029-8sCrossRefGoogle Scholar
Xia, X (2018) DAMBE7: new and improved tools for data analysis in molecular biology and evolution. Molecular Biology and Evolution 35, 15501552.CrossRefGoogle ScholarPubMed
Xia, X and Lemey, P (2009) Assessing substitution saturation with DAMBE. pp. 615630 in Lemey, P, Salemi, M and Vandamme, A-M (Eds) The phylogenetic handbook: a practical approach to DNA and protein phylogeny. Cambridge, Cambridge University Press.CrossRefGoogle Scholar
Xia, X, Xie, Z, Salemi, M, Chen, L and Wang, Y (2003) An index of substitution saturation and its application. Molecular Phylogenetics and Evolution 26, 17.CrossRefGoogle ScholarPubMed