Research Topics
| T TakimotoSummaryAffiliation: St. Jude Children's Research Hospital Country: USA Publications
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Detail Information
Publications
Molecular cloning and expression of human parainfluenza virus type 1 L geneT Takimoto
Department of Virology and Molecular Biology, St Jude Children s Research Hospital, 332 N Lauderdale, Memphis, TN 38105, USA
Virus Res 70:45-53. 2000..These results indicate that the protein encoded by the cloned hPIV1 L gene was biologically functional and that the hPIV1 polymerase complex recognized SV transcription initiation and termination sequences to produce viral transcripts...
Role of matrix and fusion proteins in budding of Sendai virusT Takimoto
Department of Virology and Molecular Biology, St Jude Children s Research Hospital, Memphis, Tennessee 38105, USA
J Virol 75:11384-91. 2001..Our results indicate that both M and F proteins are able to drive the budding of SV and propose the possible role of actin in the budding process...
Role of the hemagglutinin-neuraminidase protein in the mechanism of paramyxovirus-cell membrane fusionToru Takimoto
Department of Infectious Diseases, St Jude Children s Research Hospital, 332 N Lauderdale, Memphis, TN 38105, USA
J Virol 76:13028-33. 2002....
Nucleocapsid incorporation into parainfluenza virus is regulated by specific interaction with matrix proteinE C Coronel
Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA
J Virol 75:1117-23. 2001..Using SV-hPIV1 chimera NP cDNAs, we found that the C-terminal domain of the NP protein (amino acids 420 to 466) is responsible for the interaction with M...
Two regions of the P protein are required to be active with the L protein for human parainfluenza virus type 1 RNA polymerase activityT Bousse
Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, 332 N. Lauderdale St, Memphis, Tennessee 38105-2794, USA
Virology 283:306-14. 2001..Our results indicate that in addition to a P--L binding domain, hPIV1 L requires a specific region on P protein to be biologically functional as a polymerase...
Receptor specificities of human respirovirusesT Suzuki
Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105
J Virol 75:4604-13. 2001..These findings provide important information that can be used to develop inhibitors that prevent human parainfluenza virus infection...
The novel parainfluenza virus hemagglutinin-neuraminidase inhibitor BCX 2798 prevents lethal synergism between a paramyxovirus and Streptococcus pneumoniaeIrina V Alymova
Department of Infectious Diseases, St. Jude Children's Research Hospital, 332 N. Lauderdale, Memphis, TN 38105-2794, USA
Antimicrob Agents Chemother 49:398-405. 2005..Prophylaxis of parainfluenza virus infections with antivirals might be an effective strategy for prevention of secondary bacterial complications in humans...
A recombinant Sendai virus is controlled by CD4+ effector T cells responding to a secreted human immunodeficiency virus type 1 envelope glycoproteinScott A Brown
Department of Immunology, Memphis, TN 38105, USA
J Virol 81:12535-42. 2007....
Respiratory syncytial virus (RSV) fusion protein expressed by recombinant Sendai virus elicits B-cell and T-cell responses in cotton rats and confers protection against RSV subtypes A and BXiaoyan Zhan
Department of Infectious Diseases, St Jude Children s Research Hospital, 332N Lauderdale, Memphis, TN 38105, United States
Vaccine 25:8782-93. 2007..Together, experimental results encourage promotion of this recombinant SV construct as a vaccine candidate for the prevention of RSV in humans...
Biological significance of the second receptor binding site of Newcastle disease virus hemagglutinin-neuraminidase proteinTatiana L Bousse
Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, USA
J Virol 78:13351-5. 2004..Furthermore, the mutations at Arg516 slowed the growth rate of virus in tissue culture cells. These results suggest that the second binding site facilitates virus infection and growth by enhancing the fusion promotion activity of the HN...
Sendai virus recombinant vaccine expressing hPIV-3 HN or F elicits protective immunity and combines with a second recombinant to prevent hPIV-1, hPIV-3 and RSV infectionsXiaoyan Zhan
Department of Infectious Diseases, St Jude Children s Research Hospital, Memphis, TN 38105, United States
Vaccine 26:3480-8. 2008..Results encourage the continued development of the candidate recombinant SeV vaccines to combat serious respiratory infections of children...
Efficacy of novel hemagglutinin-neuraminidase inhibitors BCX 2798 and BCX 2855 against human parainfluenza viruses in vitro and in vivoIrina V Alymova
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee 38105-2794, USA
Antimicrob Agents Chemother 48:1495-502. 2004..Together, our results indicate that BCX 2798 and BCX 2855 are effective inhibitors of parainfluenza virus HN and may limit parainfluenza virus infections in humans...
Second sialic acid binding site in Newcastle disease virus hemagglutinin-neuraminidase: implications for fusionViatcheslav Zaitsev
Centre for Biomolecular Sciences, University of St. Andrews, St. Andrews, Fife KY16 9ST, United Kingdom
J Virol 78:3733-41. 2004..Three different crystal forms of NDV HN now reveal identical tetrameric arrangements of HN monomers, perhaps indicative of the tetramer association found on the viral surface...
Probing the sialic acid binding site of the hemagglutinin-neuraminidase of Newcastle disease virus: identification of key amino acids involved in cell binding, catalysis, and fusionHelen Connaris
Centre for Biomolecular Sciences, University of St. Andrews, St. Andrews, Fife KY16 9ST, Scotland
J Virol 76:1816-24. 2002..These results further support the single-site model and suggest certain residues to be important for the triggering of fusion...
Recombinant Sendai virus as a novel vaccine candidate for respiratory syncytial virusToru Takimoto
Department of Microbiology and Immunology, University of Rochester, Rochester, New York, USA
Viral Immunol 18:255-66. 2005..Sendai virus may prove an enormously valuable vaccine platform, permitting the delivery of recombinants targeting important pediatric respiratory pathogens, RSV chief among them...
Human parainfluenza virus type 1 but not Sendai virus replicates in human respiratory cells despite IFN treatmentTatiana Bousse
Department of Microbiology and Immunology, University of Rochester Medical Center, 601 Elmwood Avenue, Box 672, NY 14642, USA
Virus Res 121:23-32. 2006..These results suggest that SeV is less effective than hPIV1 in overcoming antiviral activity in human cells, which could be one of the factors that restrict the host range of SeV...
Differentially regulated interferon response determines the outcome of Newcastle disease virus infection in normal and tumor cell linesSateesh Krishnamurthy
Department of Infectious Diseases, Mail Stop 330, St. Jude Children's Research Hospital, 332 N. Lauderdale, Memphis, TN 38105-2794, USA
J Virol 80:5145-55. 2006..The rapid spread of NDV in HT-1080 cells appears to be caused by their deficient expression of anti-NDV proteins upon exposure to IFN-beta...
Mutation at residue 523 creates a second receptor binding site on human parainfluenza virus type 1 hemagglutinin-neuraminidase proteinTatiana Bousse
Department of Microbiology and Immunology, University of Rochester Medical Center, 601 Elmwood Avenue, Rochester, NY 14642, USA
J Virol 80:9009-16. 2006..Our study indicates that the presence and requirement of a second binding site vary among paramyxoviruses...
The long noncoding region of the human parainfluenza virus type 1 f gene contributes to the read-through transcription at the m-f gene junctionTatiana Bousse
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA
J Virol 76:8244-51. 2002..These phenotypes seem to be responsible for the extended survival of mice infected with rSVhMFjCG...
Recombinant Sendai virus expressing the G glycoprotein of respiratory syncytial virus (RSV) elicits immune protection against RSVToru Takimoto
St. Jude Children's Research Hospital, 332 N. Lauderdale St, Memphis, TN 38105, USA
J Virol 78:6043-7. 2004..RSV G-recombinant SV is thus a promising live virus vaccine candidate for RSV...
