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1.
Viruses ; 16(6)2024 May 24.
Artículo en Inglés | MEDLINE | ID: mdl-38932126

RESUMEN

Pig farming has become a strategically significant and economically important industry across the globe. It is also a potentially vulnerable sector due to challenges posed by transboundary diseases in which viral infections are at the forefront. Among the porcine viral diseases, African swine fever, classical swine fever, foot and mouth disease, porcine reproductive and respiratory syndrome, pseudorabies, swine influenza, and transmissible gastroenteritis are some of the diseases that cause substantial economic losses in the pig industry. It is a well-established fact that vaccination is undoubtedly the most effective strategy to control viral infections in animals. From the period of Jenner and Pasteur to the recent new-generation technology era, the development of vaccines has contributed significantly to reducing the burden of viral infections on animals and humans. Inactivated and modified live viral vaccines provide partial protection against key pathogens. However, there is a need to improve these vaccines to address emerging infections more comprehensively and ensure their safety. The recent reports on new-generation vaccines against swine viruses like DNA, viral-vector-based replicon, chimeric, peptide, plant-made, virus-like particle, and nanoparticle-based vaccines are very encouraging. The current review gathers comprehensive information on the available vaccines and the future perspectives on porcine viral vaccines.


Asunto(s)
Enfermedades de los Porcinos , Vacunas Virales , Virosis , Animales , Porcinos , Vacunas Virales/inmunología , Enfermedades de los Porcinos/prevención & control , Enfermedades de los Porcinos/virología , Virosis/prevención & control , Virosis/veterinaria , Virosis/inmunología , Vacunación/veterinaria , Vacunas Atenuadas/inmunología , Vacunas de Productos Inactivados/inmunología , Virus/inmunología , Virus/genética
2.
Vis Comput ; 38(7): 2383-2416, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-33907343

RESUMEN

Human recognition systems based on biometrics are much in demand due to increasing concerns of security and privacy. The human ear is unique and useful for recognition. It offers numerous advantages over popular biometrics traits face, iris, and fingerprints. A lot of work has been attributed to ear biometric, and the existing methods have achieved remarkable success over constrained databases. However, in unconstrained environment, a significant level of difficulty is observed as the images experience various challenges. In this paper, we first have provided a comprehensive survey on ear biometric using a novel taxonomy. The survey includes in-depth details of databases, performance evaluation parameters, and existing approaches. We have introduced a new database, NITJEW, for evaluation of unconstrained ear detection and recognition. A modified deep learning models Faster-RCNN and VGG-19 are used for ear detection and ear recognition tasks, respectively. The benchmark comparative assessment of our database is performed with six existing popular databases. Lastly, we have provided insight into open-ended research problems worth examining in the near future. We hope that our work will be a stepping stone for new researchers in ear biometrics and helpful for further development.

3.
J Virol Methods ; 226: 60-6, 2015 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-26478540

RESUMEN

To develop reverse genetics system of RNA viruses, cloning of full-length viral genome is required which is often challenging due to many steps involved. In this study, we report cloning of full-length cDNA from an Indian field isolate (CSFV/IVRI/VB-131) of classical swine fever virus (CSFV) using in vitro overlap extension PCR and recombination which drastically reduced the number of cloning steps. The genome of CSFV was amplified in six overlapping cDNA fragments, linked by overlap extension PCR and cloned in a bacterial artificial chromosome (BAC) vector using in vitro recombination method to generate full-length cDNA clone. The full-length CSFV cDNA clone was found stable in E. coli Stellar and DH10B cells. The full-length RNA was transcribed in vitro using T7 RNA polymerase and transfected in PK15 cells using Neon-tip electroporator to rescue infectious CSFV. The progeny CSFV was propagated in PK15 cells and found indistinguishable from the parent virus. The expression of CSFV proteins were detected in cytoplasm of PK15 cells infected with progeny CSFV at 72 h post-infection. We concluded that the in vitro overlap extension PCR and recombination method is useful to construct stable full-length cDNA clone of RNA virus in BAC vector.


Asunto(s)
Virus de la Fiebre Porcina Clásica/genética , Clonación Molecular , Animales , Línea Celular , Cromosomas Artificiales Bacterianos , ADN Complementario , India , Porcinos , Transfección
4.
Genome Announc ; 2(5)2014 Oct 02.
Artículo en Inglés | MEDLINE | ID: mdl-25278522

RESUMEN

We report the complete genome sequence of an Indian field isolate of classical swine fever virus (CSFV) belonging to predominant subgenotype 1.1 prevalent in India. This report will help in understanding the molecular diversity of CSFV strains circulating worldwide and to select and develop a suitable vaccine candidate for classical swine fever (CSF) control in India.

5.
Biomed Res Int ; 2014: 496219, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24877102

RESUMEN

Crimean-Congo hemorrhagic fever (CCHF) is an emerging zoonotic disease in India and requires immediate detection of infection both for preventing further transmission and for controlling the infection. The present study describes development, optimization, and evaluation of a novel molecular beacon-based real-time RT-PCR assay for rapid, sensitive, and specific diagnosis of Crimean-Congo hemorrhagic fever virus (CCHFV). The developed assay was found to be a better alternative to the reported TaqMan assay for routine diagnosis of CCHF.


Asunto(s)
Virus de la Fiebre Hemorrágica de Crimea-Congo/genética , Fiebre Hemorrágica de Crimea/sangre , Fiebre Hemorrágica de Crimea/diagnóstico , ARN Viral/sangre , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos , Animales , Búfalos , Bovinos , Fiebre Hemorrágica de Crimea/genética , Humanos , India , ARN Viral/genética , Ovinos
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