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DNA Barcoding Supports Identification of Malacobdella Species (Nemertea: Hoplonemertea)
Background Nemerteans of the genus Malacobdella live inside of the mantle cavity of marine bivalves. The genus currently contains only six species, five of which are host-specific and usually found in a single host species, while the sixth species, M. grossa , has a wide host range and has been foun...
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Published in: | Zoological Studies 2015-01, Vol.54 (1), p.102-110, Article 10 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background
Nemerteans of the genus
Malacobdella
live inside of the mantle cavity of marine bivalves. The genus currently contains only six species, five of which are host-specific and usually found in a single host species, while the sixth species,
M. grossa
, has a wide host range and has been found in 27 different bivalve species to date. The main challenge of
Malacobdella
species identification resides in the similarity of the external morphology between species (terminal sucker, gut undulations number, anus position and gonad colouration), and thus, the illustrations provided in the original descriptions do not allow reliable identification. In this article, we analyse the relationships among three species of
Malacobdella
:
M. arrokeana
,
M. japonica
and
M. grossa
, adding new data for the
M. grossa
and reporting the first for
M. japonica
, analysing 658 base pairs of the mitochondrial cytochrome
c
oxidase subunit I gene (
COI
). Based on these analyses, we present and discuss the potential of DNA barcoding for
Malacobdella
species identification.
Results
Sixty-four DNA barcoding fragments of the mitochondrial
COI
gene from three different
Malacobdella
species (
M. arrokeana
,
M. japonica and M. grossa
) are analysed (24 of them newly sequenced for this study, along with four outgroup specimens) and used to delineate species. Divergences, measured as uncorrected differences, between the three species were
M. arrokeana
-
M. grossa
11.73%,
M. arrokeana
-
M. japonica
10.62% and
M. grossa
-
M. japonica
10.97%. The mean intraspecific divergence within the ingroup species showed a patent gap with respect to the interspecific ones: 0.18% for
M. arrokeana
, 0.13% for
M. grossa
and 0.02% for
M. japonica
(ranges from 0 to 0.91%).
Conclusions
We conclude that there is a clear correspondence between the molecular data and distinguishing morphological characters. Our results thus indicate that some morphological characters are useful for species identification and support the potential of DNA barcoding for species identification in a taxonomic group with subtle morphological external differences. |
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ISSN: | 1021-5506 1810-522X 1810-522X |
DOI: | 10.1186/s40555-014-0086-3 |