Microphallus piriformes (Odhner, 1905)

Repkin, Egor A., Maltseva, Arina L., Varfolomeeva, Marina A., Aianka, Roman V., Mikhailova, Natalia A. & Granovitch, Andrei I., 2020, Genetic and morphological variation of metacercariae of Microphallus piriformes (Trematoda, Microphallidae): Effects of paraxenia and geographic location, International Journal for Parasitology: Parasites and Wildlife 11, pp. 235-245 : 238

publication ID

https://doi.org/ 10.1016/j.ijppaw.2020.02.004

persistent identifier

https://treatment.plazi.org/id/03C5A354-FFBD-6D78-1C2C-F90C6FAAC561

treatment provided by

Felipe

scientific name

Microphallus piriformes
status

 

3.2. Genetic polymorphism in populations of M. piriformes View in CoL . COI

COI gene proved to be rather polymorphic in M. piriformes : among 64 samples sequenced we have found 29 different haplotypes of COI fragment; three were observed most often. The Bayesian inference based on COI-sequences ( Fig. 3 View Fig ) implies a limited gene flow between populations of the White and Barents Seas, as there are several location-specific clades on the tree, e.g., clades including samples exclusively from ether Korga-islet (White Sea) or Kiberg (Barents Sea).

Strong effect of geographic location on haplotypes distribution is obvious also in the haplotypes network ( Fig. 4A View Fig ): although most often haplotypes were detected in all three examined regions, there were also many location-specific haplotypes, including several singletons, clustering according geographic region. As evidenced by both the Bayesian inference ( Fig. 3 View Fig ) and haplotypes network ( Fig. 4B View Fig ) there was no detectable population subdivision based on host species: haplotypes of M. piriformes parasitizing hosts of different species were interspersed after both analyses.

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