Reproductive strategy of an isopod Onisocryptus ovalis,parasitizing a bioluminescent myodocope ostracod Vargula hilgendorfii

The functional morphology and the reproductive strategy of a parasitic isopod Onisocryptus ovalis in a bioluminescent ostracod Vargula hilgendorfii as its final host were studied based on video and SEM observations. During its lifetime, Onisocryptus ovalis dramatically metamorphoses several times, changing sex from male to female in the final host's carapace. At nearly the last ontogenetical stage, the parasite anchors its body with a pair of thoracopods to the posterodorsal region of the host ostracod's trunk and loses all the other appendages and thus its mobility as well. Thereafter, the parasite reverses bodily orientation during the final moulting so as to locate its mouth in the midst of the host eggs, and finally consumes them, leaving only the egg membrane. Such a mode of feeding of the parasite following the fixation of the body is interpreted in terms of the adaptation to escape elimination from the ostracod carapace by the host's cleaning appendages (the seventh limbs) and to obtain as much space as possible for the parasite's own eggs/embryos at the sacrifice of the mother's mobility. The synchronization between the timing of metamorphosis of the parasite and the reproductive cycle of the host animal can be expected to guarantee the parasite the opportunity to exploit sufficient nutrition from the eggs of the host.     

A bacterial polysaccharide biosynthesis-related gene inversely regulates larval settlement and metamorphosis of Mytilus coruscus

Abstract

Larval settlement and metamorphosis is essential for the development of marine invertebrates. Although polysaccharides are involved in larval settlement and metamorphosis of Mytilus coruscus, the molecular basis of polysaccharides underlying this progression remains largely unknown. Here, the roles of the polysaccharide biosynthesis-related gene 01912 of Pseudoalteromonas marina ECSMB14103 in the regulation of larval settlement and metamorphosis were examined by gene-knockout technique. Compared with biofilms (BFs) of the wild-type P. marina, Δ01912 BFs with a higher colanic acid (CA) content showed a higher inducing activity on larval settlement and metamorphosis. Deletion of the 01912 gene caused an increase in c-di-GMP levels, accompanied by a decrease in the motility, an increase in cell aggregation, and overproduction of CA. Thus, the bacterial polysaccharide biosynthesis-related gene 01912 may regulate mussel settlement by producing CA via the coordination of c-di-GMP. This work provides a deeper insight into the molecular mechanism of polysaccharides in modulating mussel settlement.     

Ancestral Role of Ecdysis-Related Neuropeptides in Animal Life Cycle Transitions

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Development of oral and branchial muscles in lancelet larvae of Branchiostoma japonicum

The perforated pharynx has generally been regarded as a shared characteristic of chordates. However, there still remains phylogenetic ambiguity between the cilia‐driven system in invertebrate chordates and the muscle‐driven system in vertebrates. Giant larvae of the genus Asymmetron were reported to develop an orobranchial musculature similar to that of vertebrates more than 100 years ago. This discovery might represent an evolutionary link for the chordate branchial system, but few investigations of the lancelet orobranchial musculature have been completed since. We studied staged larvae of a Japanese population of Branchiostoma japonicum to characterize the developmental property of the orobranchial musculature. The larval mouth and the unpaired primary gills develop well‐organized muscles. These muscles function only as obturators of the openings without antagonistic system. As the larval mouth enlarged posteriorly to the level of the ninth myomere, the oral musculature was fortified accordingly without segmental patterning. In contrast, the iterated branchial muscles coincided with the dorsal myomeric pattern before metamorphosis, but the pharynx was remodeled dynamically irrespective of the myomeric pattern during metamorphosis. The orobranchial musculature disappeared completely during metamorphosis, and adult muscles in the oral hood and velum, as well as on the pterygial coeloms developed independently. The lancelet orobranchial musculature is apparently a larval adaptation to prevent harmful intake. However, vestigial muscles appeared transiently with the secondary gill formation suggest a bilateral ancestral state of muscular gills, and a segmental pattern of developing branchial muscles without neural crest and placodal contributions is suggestive of a precursor of vertebrate branchiomeric pattern. J. Morphol. 275:465–477, 2014. © 2013 Wiley Periodicals, Inc.