Paraphyly of Marimermithida refines primary routes of transition to parasitism in roundworms

Abstract Parasitic life-strategies in the phylum Nematoda (roundworms) are remarkably diverse and intricate in terms of evolution and taxonomy. By analysing novel rDNA data obtained on rare host-associated groups with unusual biology, we reveal paraphyly of the last major taxon with uncertain higher...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Zoological journal of the Linnean Society 2023-03, Vol.197 (4), p.909-923
Hauptverfasser: Tchesunov, Alexei V, Nikolaeva, Olga V, Rusin, Leonid Yu, Sanamyan, Nadezda P, Panina, Elena G, Miljutin, Dmitry M, Gorelysheva, Daria I, Pegova, Anna N, Khromova, Maria R, Mardashova, Maria V, Mikhailov, Kirill V, Yushin, Vladimir V, Petrov, Nikolai B, Lyubetsky, Vassily A, Nikitin, Mikhail A, Aleoshin, Vladimir V
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Abstract Parasitic life-strategies in the phylum Nematoda (roundworms) are remarkably diverse and intricate in terms of evolution and taxonomy. By analysing novel rDNA data obtained on rare host-associated groups with unusual biology, we reveal paraphyly of the last major taxon with uncertain higher-rank classification that united solely parasitic nematodes (Marimermithida) to show that primarily marine parasitism only emerged independently and repeatedly in a few free-living lineages. We report secondary seaward ingression of land-based parasites (Mermithida) via invading hosts in the subtidal zone to illustrate the host-borne scenario of oceanic fish and mammal colonization by primarily terrestrial parasites (Spiruria). We also present the first molecular data on marine nematodes from unicellular hosts (foraminiferan protozoans) to demonstrate the independent origins of exploitative nematode associations at a microscopic scale. We argue that, in contrast with primarily intestinal associations arising from saprotrophy and commensalism, non-intestinal host capture (colonization of host body cavity or internal organs) is likely to be a primary route of transition to truly exploitative parasitism in roundworms. Predispositions to host capture in nematode morphology, ecology and life cycles imply its evolution as part of innate pre-adaptations to crossing environmental boundaries to enable multiple successful transitions to parasitism in the phylum history.
ISSN:0024-4082
1096-3642
DOI:10.1093/zoolinnean/zlac070