Internal Morphology and Phylogenetic Position of (Pancrustacea: Rhizocephala), an Enigmatic Parasitic Barnacle.

is an enigmatic parasitic barnacle from the family Mycetomorphidae, known for its unclear phylogenetic position within Rhizocephala. Specimens of were collected from infected shrimps near the South Kuril Islands. Detailed morphological studies were conducted using histological techniques and scanning electron microscopy, and 18S rDNA sequences were used to resolve the phylogenetic position of within Rhizocephala.

Tricks of the puppet masters: morphological adaptations to the interaction with nervous system underlying host manipulation by rhizocephalan barnacle .

Background: Rhizocephalan interaction with their decapod hosts is a superb example of host manipulation. These parasites are able to alter the host's physiology and behavior. Host-parasite interaction is performed, presumably, special modified rootlets invading the ventral ganglions.

Functional role of lacunar and muscular systems in the externa of Peltogasterella gracilis (Cirripedia: Rhizocephala).

One of the most conspicuous traits of parasitic organisms is a well-developed reproductive system. In Rhizocephala ("Crustacea": Cirripedia) it is believed to be nested in the externa-a "reproductive part" located outside of the host. However, it is not clear how nutrients are transported to the externa.

The interna of the rhizocephalan Peltogaster reticulata: Comparative morphology and ultrastructure.

Specialized morphology of diverse parasitic crustaceans reflects their adaptations to an endoparasitic lifestyle. Rhizocephalan barnacles are one of the most highly modified obligatory parasites of other crustaceans. Comprehension of the functional morphology of rhizocephalans could elucidate the main evolutionary trends not only inside parasitic barnacles, but in parasitism as a whole.

Obtaining mice that carry human mitochondrial DNA transmitted to the progeny.

To study human diseases associated with mutations in mitochondrial DNA one needs an animal model in which the distribution of abnormal mtDNA and its impact on the phenotype might be followed. We isolated human mitochondria from HepG2 cell culture and microinjected them into murine zygotes, upon which those were transplanted to the pseudopregnant mice. PCR with species-specific primers allowed detecting human mtDNA in the tissues of 7-13-day embryos.

Persistence of human mitochondrial DNA throughout the development to the blastocyst of mouse zygotes microinjected with human mitochondria.

The conditions for transfer of human mitochondria into fertilised mouse ova were elaborated. Species-specific primers were designed to discriminate human mitochondrial DNA (mtDNA) and the endogenous mtDNA in the preimplantation embryos. Human mitochondria isolated from the HepG2 cell line were microinjected into murine zygotes, and the latter cultured for 96 h to the blastocyst stage.