9 results on '"Yotoko K"'
Search Results
2. Malaria parasites (Apicomplexa, Haematozoea) and their relationships with their hosts: is there an evolutionary cost for the specialization?
- Author
-
Yotoko, K. S. C., primary and Elisei, C., additional
- Published
- 2006
- Full Text
- View/download PDF
3. Ethanol Fuel Improves Pitfall Traps Through Rapid Sinking and Death of Captured Orthopterans.
- Author
-
SZINWELSKI, N., YOTOKO, K. S. C., SOLAR, R., SELEME, L. R., and SPERBER, C. F.
- Subjects
ETHANOL as fuel ,ANIMAL welfare ,ORTHOPTERA ,INSECTS ,STATISTICAL sampling - Abstract
The choice of killing solutions for pitfall traps can influence sampling and is highly dependent on the objectives of each study. It is becoming increasingly common, however, and is more environmentally friendly, to use the same organisms to extract information for different kinds of studies. The killing solution should, therefore, be able to sample local active organisms, as well as maintain the integrity of their organs, tissues, and macromolecules. In a previous work, we showed that using ethanol fuel as a killing solution maintains the integrity of the specimens and enhances the Orthoptera richness and abundance of samples. In the current study, we evaluated two explanations for this pattern. We set up a field experiment to test whether ethanol fuel is attractive for orthopterans, and we investigated in the laboratory whether individuals of Gryllus sp. sink or die faster in ethanol fuel than in other killing solutions. Our results allowed us to refute the hypotheses of attraction caused by ethanol fuel and showed that the higher sampling efficiency of ethanol fuel is directly linked to the specimens sinking and dying faster than in other killing solutions. Thus, in addition to taxonomic, anatomical, and molecular studies, we recommend ethanol fuel for sampling organisms active in the litter in ecological studies. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
4. A phylogenomic appraisal of the evolutionary relationship of Mycoplasmas
- Author
-
Yotoko, K. S. C. and Sandro Bonatto
5. Evolution and Diversity of Semaphorins and Plexins in Choanoflagellates.
- Author
-
Junqueira Alves C, Silva Ladeira J, Hannah T, Pedroso Dias RJ, Zabala Capriles PV, Yotoko K, Zou H, and Friedel RH
- Subjects
- Animals, Axon Guidance, Biodiversity, Biological Evolution, Cell Adhesion Molecules chemistry, Cell Adhesion Molecules metabolism, Choanoflagellata classification, Ligands, Models, Molecular, Nerve Tissue Proteins chemistry, Nerve Tissue Proteins metabolism, Phylogeny, Protein Conformation, Protein Domains, Receptors, Cell Surface genetics, Cell Adhesion Molecules genetics, Choanoflagellata genetics, Choanoflagellata metabolism, Nerve Tissue Proteins genetics, Semaphorins genetics, Semaphorins metabolism
- Abstract
Semaphorins and plexins are cell surface ligand/receptor proteins that affect cytoskeletal dynamics in metazoan cells. Interestingly, they are also present in Choanoflagellata, a class of unicellular heterotrophic flagellates that forms the phylogenetic sister group to Metazoa. Several members of choanoflagellates are capable of forming transient colonies, whereas others reside solitary inside exoskeletons; their molecular diversity is only beginning to emerge. Here, we surveyed genomics data from 22 choanoflagellate species and detected semaphorin/plexin pairs in 16 species. Choanoflagellate semaphorins (Sema-FN1) contain several domain features distinct from metazoan semaphorins, including an N-terminal Reeler domain that may facilitate dimer stabilization, an array of fibronectin type III domains, a variable serine/threonine-rich domain that is a potential site for O-linked glycosylation, and a SEA domain that can undergo autoproteolysis. In contrast, choanoflagellate plexins (Plexin-1) harbor a domain arrangement that is largely identical to metazoan plexins. Both Sema-FN1 and Plexin-1 also contain a short homologous motif near the C-terminus, likely associated with a shared function. Three-dimensional molecular models revealed a highly conserved structural architecture of choanoflagellate Plexin-1 as compared to metazoan plexins, including similar predicted conformational changes in a segment that is involved in the activation of the intracellular Ras-GAP domain. The absence of semaphorins and plexins in several choanoflagellate species did not appear to correlate with unicellular versus colonial lifestyle or ecological factors such as fresh versus salt water environment. Together, our findings support a conserved mechanism of semaphorin/plexin proteins in regulating cytoskeletal dynamics in unicellular and multicellular organisms., (© The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.)
- Published
- 2021
- Full Text
- View/download PDF
6. Origin and evolution of plexins, semaphorins, and Met receptor tyrosine kinases.
- Author
-
Junqueira Alves C, Yotoko K, Zou H, and Friedel RH
- Subjects
- Amino Acid Sequence genetics, Animals, Biological Evolution, Databases, Genetic, Humans, Protein Domains genetics, Receptors, Cell Surface genetics, Cell Adhesion Molecules genetics, Choanoflagellata genetics, Echinodermata genetics, Nerve Tissue Proteins genetics, Proto-Oncogene Proteins c-met genetics, Semaphorins genetics
- Abstract
The transition from unicellular to multicellular organisms poses the question as to when genes that regulate cell-cell interactions emerged during evolution. The receptor and ligand pairing of plexins and semaphorins regulates cellular interactions in a wide range of developmental and physiological contexts. We surveyed here genomes of unicellular eukaryotes and of non-bilaterian and bilaterian Metazoa and performed phylogenetic analyses to gain insight into the evolution of plexin and semaphorin families. Remarkably, we detected plexins and semaphorins in unicellular choanoflagellates, indicating their evolutionary origin in a common ancestor of Choanoflagellida and Metazoa. The plexin domain structure is conserved throughout all clades; in contrast, semaphorins are structurally diverse. Choanoflagellate semaphorins are transmembrane proteins with multiple fibronectin type III domains following the N-terminal Sema domain (termed Sema-FN). Other previously not yet described semaphorin classes include semaphorins of Ctenophora with tandem immunoglobulin domains (Sema-IG) and secreted semaphorins of Echinoderamata (Sema-SP, Sema-SI). Our study also identified Met receptor tyrosine kinases (RTKs), which carry a truncated plexin extracellular domain, in several bilaterian clades, indicating evolutionary origin in a common ancestor of Bilateria. In addition, a novel type of Met-like RTK with a complete plexin extracellular domain was detected in Lophotrochozoa and Echinodermata (termed Met-LP RTK). Our findings are consistent with an ancient function of plexins and semaphorins in regulating cytoskeletal dynamics and cell adhesion that predates their role as axon guidance molecules.
- Published
- 2019
- Full Text
- View/download PDF
7. Misguided phylogenetic comparisons using DGGE excised bands may contaminate public sequence databases.
- Author
-
Pylro VS, Morais DK, Kalks KH, Roesch LF, Hirsch PR, Tótola MR, and Yotoko K
- Subjects
- Bacteria classification, Bacteria isolation & purification, Genes, rRNA, Polymerase Chain Reaction methods, Bacteria genetics, Databases, Nucleic Acid standards, Denaturing Gradient Gel Electrophoresis methods, Phylogeny, RNA, Ribosomal, 16S genetics
- Abstract
Controversy surrounding bacterial phylogenies has become one of the most important challenges for microbial ecology. Comparative analyses with nucleotide databases and phylogenetic reconstruction of the amplified 16S rRNA genes from DGGE (Denaturing Gradient Gel Electrophoresis) excised bands have been used by several researchers for the identification of organisms in complex samples. Here, we individually analyzed DGGE-excised 16S rRNA gene bands from 10 certified bacterial strains of different species, and demonstrated that this kind of approach can deliver erroneous outcomes to researchers, besides causing/emphasizing errors in public databases., (Copyright © 2016 Elsevier B.V. All rights reserved.)
- Published
- 2016
- Full Text
- View/download PDF
8. Classification and putative origins of Brazilian porcine circovirus 2 inferred through phylogenetic and phylogeographical approaches.
- Author
-
Chiarelli-Neto O, Yotoko KS, Vidigal PM, Silva FM, Castro LA, Fietto JL, Silva A Jr, and Almeida MR
- Subjects
- Animals, Brazil, Cloning, Molecular, DNA, Viral genetics, Genome, Viral, Geography, Haplotypes, Open Reading Frames, Porcine Postweaning Multisystemic Wasting Syndrome virology, Sequence Analysis, DNA, Swine virology, Circovirus classification, Circovirus genetics, Genetic Variation, Phylogeny
- Abstract
Porcine circovirus 2 (PCV2) is the major causative agent of postweaning multisystemic wasting syndrome (PMWS) and is associated with different syndromes affecting pigs. The PCV2 genome has three main open reading frames (ORFs) among which the ORF2 encodes the capsid protein. In this study, the ORF2 nucleotide sequences of 30 Brazilian isolates were analyzed. The sequences were compared to other GenBank sequences using phylogenic and phylogeographic approaches. Our results show high sequence variability in Brazil, since, in this work, the Brazilian isolates were classified into subgroup 1AB, 2D and 2, which reveals that the virus was introduced in Brazil more than once. On the other hand, most of Brazilian isolates seem to be derived from only one introduction. According to the data from the Pig Breeders' Association, the multiple introductions of the virus probably occurred through the import of animals with the asymptomatic form of the virus or through the import of contaminated semen. The results point to the necessity of implementing programs aimed at selecting sows in order to avoid the import of animals infected by Group 1 PCV2.
- Published
- 2009
- Full Text
- View/download PDF
9. Molecular characterization of Hepatozoon sp. from Brazilian dogs and its phylogenetic relationship with other Hepatozoon spp.
- Author
-
Forlano MD, Teixeira KR, Scofield A, Elisei C, Yotoko KS, Fernandes KR, Linhares GF, Ewing SA, and Massard CL
- Subjects
- Animals, Brazil epidemiology, Coccidiosis epidemiology, Coccidiosis parasitology, Dog Diseases epidemiology, Coccidia classification, Coccidia genetics, Coccidiosis veterinary, Dog Diseases parasitology, Dogs parasitology, Phylogeny
- Abstract
To characterize phylogenetically the species which causes canine hepatozoonosis at two rural areas of Rio de Janeiro State, Brazil, we used universal or Hepatozoon spp. primer sets for the 18S SSU rRNA coding region. DNA extracts were obtained from blood samples of thirteen dogs naturally infected, from four experimentally infected, and from five puppies infected by vertical transmission from a dam, that was experimentally infected. DNA of sporozoites of Hepatozoon americanum was used as positive control. The amplification of DNA extracts from blood of dogs infected with sporozoites of Hepatozoon spp. was observed in the presence of primers to 18S SSU rRNA gene of Hepatozoon spp., whereas DNA of H. americanum sporozoites was amplified in the presence of either universal or Hepatozoon spp.-specific primer sets; the amplified products were approximately 600bp in size. Cloned PCR products obtained from DNA extracts of blood from two dogs experimentally infected with Hepatozoon sp. were sequenced. The consensus sequence, derived from six sequence data sets, were blasted against sequences of 18S SSU rRNA of Hepatozoon spp. available at GenBank and aligned to homologous sequences to perform the phylogenetic analysis. This analysis clearly showed that our sequence clustered, independently of H. americanum sequences, within a group comprising other Hepatozoon canis sequences. Our results confirmed the hypothesis that the agent causing hepatozoonosis in the areas studied in Brazil is H. canis, supporting previous reports that were based on morphological and morphometric analyses.
- Published
- 2007
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.