Literature DB >> 11406144

An investigation of the co-evolutionary relationships between onchobothriid tapeworms and their elasmobranch hosts.

J N Caira1, K Jensen.   

Abstract

There is general consensus that the living elasmobranchs comprise a monophyletic taxon. There is evidence that, among tetraphyllidean tapeworms, the approximately 201 hooked species (Onchobothriidae) may also comprise a monophyletic group. Determinations of host specificity are contingent upon correct specific identifications. Since 1960, over 200 new elasmobranch species and over 100 new onchobothriid species have been described. Some confidence can be placed in host and parasite identifications of recent studies, but specific identifications provided in older literature in many cases are suspect. There is some consensus among published works on the phylogenetic relationships among elasmobranchs. Phylogenetic relationships among onchobothriids remain largely unresolved. Elasmobranchs have been poorly sampled for onchobothriids; records exist for approximately 20% of the 911 species and approximately 44% of the 170 elasmobranch genera. Onchobothriids are remarkably host specific, exhibiting essentially oioxenous specificity for their definitive hosts. Multiple onchobothriid species commonly parasitise the same host species; in some cases these are congeners, in other cases these are members of two different onchobothriid genera. There is substantial incongruence between available host and parasite phylogenies. For example, Acanthobothrium is by far the most ubiquitous onchobothriid genus, parasitising almost all orders of elasmobranchs known to host onchobothriids, yet, there is no evidence of major clades of Acanthobothrium corresponding to postulated major subgroupings of elasmobranchs (e.g. Galea and Squalea or sharks and rays). Potamotrygonocestus appears to be among the most basal onchobothriid groups, yet it parasitises one of the most derived elasmobranch groups (the freshwater stingray genus Potamotrygon). It appears that congeners parasitising the same host species are not necessarily each other's closest relatives. At this point the preliminary and limited available data suggest that, at least in this system, strict host specificity is not necessarily indicative of strict co-evolution. This study was extremely limited by the lack of available robust phylogenies for onchobothriids and elasmobranchs.

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Year:  2001        PMID: 11406144     DOI: 10.1016/s0020-7519(01)00206-5

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  9 in total

1.  A revision of Platybothrium Linton, 1890 (Tetraphyllidea: Onchobothriidae), with a phylogenetic analysis and comments on host-parasite associations.

Authors:  Claire J Healy
Journal:  Syst Parasitol       Date:  2003-10       Impact factor: 1.431

2.  Phylogenetic relationships of the monozoic tapeworms (Eucestoda: Caryophyllidea) inferred from morphological characters.

Authors:  Mikulás Oros; Vladimíra Hanzelová; Tomás Scholz; John S Mackiewicz
Journal:  Syst Parasitol       Date:  2008-03-29       Impact factor: 1.431

3.  Systematics and diversification of Anindobothrium Marques, Brooks & Lasso, 2001 (Eucestoda: Rhinebothriidea).

Authors:  Bruna Trevisan; Juliana F Primon; Fernando P L Marques
Journal:  PLoS One       Date:  2017-09-27       Impact factor: 3.240

4.  Determinants and consequences of interspecific body size variation in tetraphyllidean tapeworms.

Authors:  Haseeb Sajjad Randhawa; Robert Poulin
Journal:  Oecologia       Date:  2009-07-10       Impact factor: 3.225

5.  A new species of Potamotrygonocestus Brooks & Thorson, 1976 (Eucestoda: Tetraphyllidea) from Plesiotrygon iwamae Rosa, Castello & Thorson (Mylliobatoidea: Potamotrygonidae) and a redescription of Potamotrygonocestus chaoi Marques, Brooks & Araujo, 2003.

Authors:  N M Luchetti; F P L Marques; P Charvet-Almeida
Journal:  Syst Parasitol       Date:  2008-04-23       Impact factor: 1.431

6.  A revision of Megalonchos Baer & Euzet, 1962 (Tetraphyllidea: Onchobothriidae), with the description of two new species and transfer of two species to Biloculuncus Nasin, Caira & Euzet, 1997.

Authors:  J N Caira; F B Reyda; J D Mega
Journal:  Syst Parasitol       Date:  2007-04-11       Impact factor: 1.023

7.  Diversification and species boundaries of Rhinebothrium (Cestoda; Rhinebothriidea) in South American freshwater stingrays (Batoidea; Potamotrygonidae).

Authors:  Florian B Reyda; Fernando P L Marques
Journal:  PLoS One       Date:  2011-08-03       Impact factor: 3.240

8.  Threatened, host-specific affiliates of a red-listed host: Three new species of Acanthobothrium van Beneden, 1849 (Cestoda: Onchoproteocephalidea) from the endangered white skate, Rostroraja alba (Lacépède).

Authors:  Linda Van Der Spuy; Nico J Smit; Bjoern C Schaeffner
Journal:  Int J Parasitol Parasites Wildl       Date:  2021-12-28       Impact factor: 2.773

9.  Do the historical biogeography and evolutionary history of the digenean Margotrema spp. across central Mexico mirror those of their freshwater fish hosts (Goodeinae)?

Authors:  Andrés Martínez-Aquino; Fadia Sara Ceccarelli; Luis E Eguiarte; Ella Vázquez-Domínguez; Gerardo Pérez-Ponce de León
Journal:  PLoS One       Date:  2014-07-07       Impact factor: 3.240

  9 in total

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