scholarly journals Таксономічна характеристика РНК-геномних вірусів хребетних тварин і людини

2017 ◽  
Vol 19 (78) ◽  
pp. 30-35
Author(s):  
O.S. Kalinina
Keyword(s):  
Plasma Membrane ◽  
Golgi Complex ◽  
Viral Genome ◽  
Eriocheir Sinensis ◽  
Outer Membrane Lipoprotein ◽  
The Family ◽  
Membrane Lipoprotein ◽  
Family Rhabdoviridae ◽  
Size And Structure

The article presents a modern taxonomy and nomenclature of viruses of vertebrates animals and human based on information ICTV release 2016 (ratification 2017).  Described the basic criteria for the classification of viruses: characteristics of the viral genome, the mechanism of replication and virions structure. Viruses of vertebrates (1269 species) consist of 5 orders, 38 families, including 12 – DNA-genomic and 26 – RNA-genomic, 12 subfamilies and 233 genera. RNA-genomic viruses of vertebrates (679 species) classified of 4 orders, 26 families, 6 subfamilies and 119 genera. The order Mononegavirales has united family Paramyxoviridae, Pneumoviridae, Rhabdoviridae, Filoviridae, Bornaviridae, Nyamiviridae and Sunviridae, order Nidovirales – family Coronaviridae and Arteriviridae, order Bunyavirales –family Hantaviridae, Nairoviridae, Peribunyaviridae and Phenuiviridae, order Picornavirales – family Picornaviridae. Family Rhabdoviridae, Nodaviridae, Peribunyaviridae, Phenuiviridae, Reoviridae and Birnaviridae, except viruses of vertebrates, contain viruses of insects, and family Rhabdoviridae, Phenuiviridae and Reoviridae – viruses of plants. There is а one of «floating» genus Deltavirus, which is not included of families. The family Reoviridae includes the Eriocheir sinensis reovirus, and the family Birnaviridae – Tellina virus. Described the taxa of viruses: family, subfamily, genera, species. Named typical species genera of viruses. Characterized the basic taxonomic features of RNA-genomic vertebrates viruses of animals and human: the shape, size and structure of virions – the presence of outer membrane lipoprotein, capsid symmetry type (spiral, icosahedral), the structure of the viral RNA (the number of threads, conformation, fragmentation, polarity). The attention to virus reproduction features. Replication of most RNA-genomic viruses occurs in cells of the cytoplasm, except for the representatives of the families Bornaviridae, Nyamiviridae, Orthomyxoviridae, Retroviridae and «floating» genus Deltavirus, which are replicated in the nucleus. Output of the progeny virions in simply organized viruses is due to cell destruction, and in most of the complexly organized viruses – plasma membrane buds, as well as through the membranes of the Golgi complex or the endoplasmic net in combination with exocytosis (Peribunyaviridae, Hantaviridae, Nairoviridae, Phenuiviridae, Flaviviridae, Coronaviridae, Arteriviridae). 

scholarly journals ТАКСОНОМІЧНА ХАРАКТЕРИСТИКА ДНК-ГЕНОМНИХ ВІРУСІВ ХРЕБЕТНИХ ТВАРИН І ЛЮДИНИ

2016 ◽  
Vol 18 (2(66)) ◽  
pp. 83-88
Author(s):  
O.S. Kalinina
Keyword(s):  
Cell Membrane ◽  
Outer Membrane ◽  
Viral Genome ◽  
Structural Organization ◽  
Symmetry Type ◽  
Outer Membrane Lipoprotein ◽  
Membrane Lipoprotein ◽  
Size And Structure

Presented modern taxonomy and nomenclature of the DNA-genomic of viruses of vertebrates animals and humans in accordance with the information ICTV release 2015 (ratification 2016). Described the basic criteria for the classification of viruses: characteristics of the viral genome, the mechanism of replication and virions morphology. Viruses of vertebrates (1120 species) consist of 4 orders, 34 families (12 – DNA-genomic, 22 – RNA-genomic), 11 subfamilies and 219 genera. DNA-genomic viruses of vertebrates (546 species) classified in 1 orders, 12 families, 5 subfamilies and 113 genera. The order Herpesvirales has united family Herpesviridae and Alloherpesviridae. Family Poxviridae, Iridoviridae and Parvoviridae, except of viruses of vertebrates, contain viruses of insects. Described the taxa of viruses:family, subfamily, genera, species. Characterized the basic taxonomic features of DNA-genomic viruses of vertebrates: the shape, size and structure of virions – the presence of outer membrane lipoprotein, capsid symmetry type, the structure of the viral DN and the number of proteins. The attention is focused on the features of reproduction of viruses. The replication of majority DNA-genomic viruses of vertebrates occur in the nucleus of cells, except for members of families Poxviridae and Asfarviridae, which are replicate in the cytoplasm. Yield virions is done due to destruction of cells or budding through the cell membrane (sometimes in combination with exocytosis) depending on the structural organization of the virus.

scholarly journals Modern taxonomy of viruses of vertebrates

2020 ◽  
Vol 22 (98) ◽  
pp. 113-118
Author(s):  
O. S. Kalinina
Keyword(s):  
Reverse Transcription ◽  
Viral Genome ◽  
Eriocheir Sinensis ◽  
Dna And Rna ◽  
Shell Type ◽  
The Family ◽  
Family Rhabdoviridae ◽  
Shape And Size

The modern taxonomy of viruses of vertebrates is presented according to the information of ICTV issue 07.2019, ratification 03.2020. The leading criteria of taxonomy of viruses are named: type and structure of viral genome, mechanism of replication and morphology of virion. The periods of formation of taxonomic ranks of viruses are characterized: in 1966–1970 genera of viruses were formed, in 1971–1975 – families and subfamilies, since 1990 – orders, in 2018–2019 – realms, kingdoms, phylums, subphylums, classes, suborders, subgenеres. The nomenclature of viruses is described. Viruses belong to the Viruses domain. Viruses of vertebrates (1878 species) belong to 4 realms, 5 kingdoms, 10 phylums, 2 subphylums, 20 classes, 26 orders, 3 suborders, 45 families (of which 15 – DNA-genomic and 30 – RNA-genomic), 33 subfamilies, 345 genera and 49 subgenera. Taxonomic ranks of DNA- and RNA-genomic viruses of vertebrates are described. The DNA-genome family Anelloviridae and the unclassified RNA-genomic genus Deltavirus are not included in any realm. The family Birnaviridae is not classified within the kingdom Orthornavirae. The family of DNA-genomic Hepadnaviridae is included in the realm of RNA-containing viruses Riboviria on the grounds that the replication of hepadnaviruses occurs through the stage of RNA on the principle of reverse transcription, as in the family Retroviridae. The main taxonomic features of DNA- and RNA-genomic viruses of vertebrates are described: type and structure of viral genome (DNA or RNA, number of strands, conformation, fragmentation, polarity), shape and size of virions, presence of outer lipoprotein shell, type of capsid symmetry (spiral, iсosahedral). Some families, in addition to viruses of vertebrates, contain viruses of invertebrates and plants, in particular: families Poxviridae, Iridoviridae, Parvoviridae, Circoviridae, Smacoviridae, Genomoviridae, Rhabdoviridae, Nyamiviridae, Peribunyaviridae, Phenuiviridae, Nairoviviridae, Nodaviridae, Reoviridae and Birnaviridae – viruses of insects; families Genomoviridae, Rhabdoviridae, Phenuiviridae and Reoviridae – viruses of plants; family Nyamiviridae – viruses of nematodes, cestodes, sipunculidеs and echinoderms; family Rhabdoviridae – viruses of nematodes; family Reoviridae – Eriocheir sinensis reovirus; family Birnaviridae – viruses of tellines and rotifers.

scholarly journals Sequence Diversity of the oprI Gene, Coding for Major Outer Membrane Lipoprotein I, among rRNA Group I Pseudomonads

1998 ◽  
Vol 180 (24) ◽  
pp. 6551-6556 ◽  
Author(s):  
Daniel De Vos ◽  
Christiane Bouton ◽  
Alain Sarniguet ◽  
Paul De Vos ◽  
Marc Vauterin ◽  
...  
Keyword(s):  
Outer Membrane ◽  
The Other ◽  
Widespread Distribution ◽  
Phylogenetic Marker ◽  
Silent Substitution ◽  
Group I ◽  
Gene Coding ◽  
Outer Membrane Lipoprotein ◽  
Membrane Lipoprotein

ABSTRACT The sequence of oprI, the gene coding for the major outer membrane lipoprotein I, was determined by PCR sequencing for representatives of 17 species of rRNA group I pseudomonads, with a special emphasis on Pseudomonas aeruginosa andPseudomonas fluorescens. Within the P. aeruginosa species, oprI sequences for 25 independent isolates were found to be identical, except for one silent substitution at position 96. The oprI sequences diverged more for the other rRNA group I pseudomonads (85 to 91% similarity with P. aeruginosa oprI). An accumulation of silent and also (but to a much lesser extent) nonsilent substitutions in the different sequences was found. A clustering according to the respective presence and/or positions of the HaeIII, PvuII, andSphI sites could also be obtained. A sequence cluster analysis showed a rather widespread distribution of P. fluorescens isolates. All other rRNA group I pseudomonads clustered in a manner that was in agreement with other studies, showing that the oprI gene can be useful as a complementary phylogenetic marker for classification of rRNA group I pseudomonads.

Three new species, two new genera, and new family Biphragmosagittidae (Сhaetognatha) from Southwest Pacific Ocean

2011 ◽  
Vol 20 (1) ◽  
pp. 161-173
Author(s):  
A.P. Kassatkina
Keyword(s):  
New Species ◽  
Type Species ◽  
Morphological Characters ◽  
The Body ◽  
New Order ◽  
New Genera ◽  
New Family ◽  
The Family ◽  
Three New Species

Resuming published and own data, a revision of classification of Chaetognatha is presented. The family Sagittidae Claus & Grobben, 1905 is given a rank of subclass, Sagittiones, characterised, in particular, by the presence of two pairs of sac-like gelatinous structures or two pairs of fins. Besides the order Aphragmophora Tokioka, 1965, it contains the new order Biphragmosagittiformes ord. nov., which is a unique group of Chaetognatha with an unusual combination of morphological characters: the transverse muscles present in both the trunk and the tail sections of the body; the seminal vesicles simple, without internal complex compartments; the presence of two pairs of lateral fins. The only family assigned to the new order, Biphragmosagittidae fam. nov., contains two genera. Diagnoses of the two new genera, Biphragmosagitta gen. nov. (type species B. tarasovi sp. nov. and B. angusticephala sp. nov.) and Biphragmofastigata gen. nov. (type species B. fastigata sp. nov.), detailed descriptions and pictures of the three new species are presented.

scholarly journals Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis

2005 ◽  
Vol 169 (2) ◽  
pp. 285-295 ◽  
Author(s):  
Daniela A. Sahlender ◽  
Rhys C. Roberts ◽  
Susan D. Arden ◽  
Giulietta Spudich ◽  
Marcus J. Taylor ◽  
...  
Keyword(s):  
Plasma Membrane ◽  
Rna Interference ◽  
Vesicular Stomatitis Virus ◽  
Protein Interaction ◽  
Golgi Complex ◽  
Myosin Vi ◽  
Binding Partner ◽  
Binding Partners ◽  
Vesicular Stomatitis ◽  
Golgi Organization

Myosin VI plays a role in the maintenance of Golgi morphology and in exocytosis. In a yeast 2-hybrid screen we identified optineurin as a binding partner for myosin VI at the Golgi complex and confirmed this interaction in a range of protein interaction studies. Both proteins colocalize at the Golgi complex and in vesicles at the plasma membrane. When optineurin is depleted from cells using RNA interference, myosin VI is lost from the Golgi complex, the Golgi is fragmented and exocytosis of vesicular stomatitis virus G-protein to the plasma membrane is dramatically reduced. Two further binding partners for optineurin have been identified: huntingtin and Rab8. We show that myosin VI and Rab8 colocalize around the Golgi complex and in vesicles at the plasma membrane and overexpression of constitutively active Rab8-Q67L recruits myosin VI onto Rab8-positive structures. These results show that optineurin links myosin VI to the Golgi complex and plays a central role in Golgi ribbon formation and exocytosis.

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