Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marla Koster"'
Autor:
Elizabeth Ramirez-Medina, Lawrence K. Silbart, Teresa de los Santos, Ignacio Fernandez-Sainz, Steven M. Szczepanek, Ping Wu, Yelitza Y. Rodriguez, Tyler D Gavitt, Marla Koster
Publikováno v:
Vaccine. 37:3435-3442
Foot and Mouth Disease is a highly contagious and economically important disease of livestock. While vaccination is often effective at controlling viral spread, failures can occur due to strain mismatch or viral mutation. Foot and Mouth Disease Virus
Autor:
Ignacio Fernandez-Sainz, Teresa de los Santos, Marvin J. Grubman, Gisselle N. Medina, Marla Koster, Elizabeth Ramirez-Medina
Publikováno v:
Virology. 502:123-132
A human adenovirus (Ad5) vectored foot-and-mouth disease virus (FMDV) O1-Manisa subunit vaccine (Ad5-O1Man) was engineered to deliver FMDV O1-Manisa capsid and capsid-processing proteins. Swine inoculated with Ad5-O1Man developed an FMDV-specific hum
Autor:
T. de los Santos, Marla Koster, M. Hosamani, Suresh H. Basagoudanavar, B.P. Sreenivasa, Paramasivam Saravanan, Marvin J. Grubman, V.C. Dhanya, Steven J. Pauszek, Ramamurthy Venkataramanan, Luis L. Rodriguez, Jajati K. Mohapatra, R. P. Tamil Selvan
Publikováno v:
Veterinary microbiology. 203
Recombinant adenovirus-5 vectored foot-and-mouth disease constructs (Ad5- FMD) were made for three Indian vaccine virus serotypes O, A and Asia 1. Constructs co-expressing foot-and- mouth disease virus (FMDV) capsid and viral 3C protease sequences, w
Autor:
Fayna Diaz-San Segundo, Gisselle N. Medina, Marla Koster, Marvin J. Grubman, Elizabeth Ramirez-Medina, Teresa de los Santos, Lauro Velazquez-Salinas
Publikováno v:
Journal of virology. 90(3)
Codon bias deoptimization has been previously used to successfully attenuate human pathogens, including poliovirus, respiratory syncytial virus, and influenza virus. We have applied a similar technology to deoptimize the capsid-coding region (P1) of
Publikováno v:
Journal of Virology. 77:1621-1625
We have previously shown that replication of foot-and-mouth disease virus (FMDV) is highly sensitive to alpha/beta interferon (IFN-α/β). In the present study, we constructed recombinant, replication-defective human adenovirus type 5 vectors contain
Autor:
Marla Koster, Camila C. A. Dias, Teresa de los Santos, Marvin J. Grubman, James Zhu, Fayna Diaz-San Segundo
Publikováno v:
Journal of virology. 83(4)
The leader proteinase (L pro ) of foot-and-mouth disease virus (FMDV) is involved in antagonizing the innate immune response by blocking the expression of interferon (IFN) and by reducing the immediate-early induction of IFN-β mRNA and IFN-stimulate
Publikováno v:
Microscopy and Microanalysis. 13
Autor:
Traci Turecek, He Wang, Vladimir G. Andreyev, Teresa de los Santos, Mauro P. Moraes, Marvin J. Grubman, Marla Koster
Publikováno v:
Journal of Virology
Previously, we showed that type I interferon (alpha/beta interferon [IFN-α/β]) can inhibit foot-and-mouth disease virus (FMDV) replication in cell culture, and swine inoculated with 109PFU of human adenovirus type 5 expressing porcine IFN-α (Ad5-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccfc6f83f677352a365f59d7671f657b
https://europepmc.org/articles/PMC1933294/
https://europepmc.org/articles/PMC1933294/
Autor:
William T. Golde, Rudi Weiblen, Elida M. Bautista, Marla Koster, Sônia de Avila Botton, Marvin J. Grubman, Mário Celso Sperotto Brum
Publikováno v:
Vaccine. 24(17)
The adjuvant effect of porcine interferon alpha (pIFN-alpha) was examined in swine vaccinated with a replication-defective adenovirus containing foot-and-mouth disease virus (FMDV) A24 capsid and 3C proteinase coding regions (Ad5-A24). Groups of swin
Publikováno v:
Microscopy and Microanalysis. 11