Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

The development of a diagnostic gene chip for detecting five kinds of viruses in horses

View through CrossRef
AbstractThe highly conserved DNAs of Equine herpesvirus-1 (EHV-1), Equine arteritis virus (EAV), Equine influenza virus (EIV), Equine infectious anaemia virus (EIAV) and Eastern equine encephalomyelitis virus (EEEV) were acquired by molecular cloning, and spotted on the diagnostic gene chip. The cDNAs reverse-transcribed from RNAs of samples were labelled with Cy5-dUTP/Cy3-dUTP as fluorescent probes. Following specific hybridization of the deposited gene chip and labelled probes, fluorescence signals were scanned by laser scanner and the resulting image was analysed by QiamtArray software on a digital computer. The results showed that the prepared gene chip could detect and distinguish the five equine viruses. Its sensitivity was about 25 viral genome copies. The hybridization specificity was confirmed by the presence of red fluorescence signals on the corresponding sites with samples from the five relevant viruses in horses and by the absence of positive signals with the specimens from irrelevant viruses from other animals. Peripheral blood leucocytes (PBL) from some seropositive horses in post-arrival quarantine were negative according to virus isolation, but were positive for EHV-1 and EAV according to the gene chip technique. The overall results suggest that gene chips, which are quick, specific, sensitive and reliable, can provide a practical alternative for screening quarantined animals, and will be able to deal with a large number of animal samples within a very short period of time.
Title: The development of a diagnostic gene chip for detecting five kinds of viruses in horses
Description:
AbstractThe highly conserved DNAs of Equine herpesvirus-1 (EHV-1), Equine arteritis virus (EAV), Equine influenza virus (EIV), Equine infectious anaemia virus (EIAV) and Eastern equine encephalomyelitis virus (EEEV) were acquired by molecular cloning, and spotted on the diagnostic gene chip.
The cDNAs reverse-transcribed from RNAs of samples were labelled with Cy5-dUTP/Cy3-dUTP as fluorescent probes.
Following specific hybridization of the deposited gene chip and labelled probes, fluorescence signals were scanned by laser scanner and the resulting image was analysed by QiamtArray software on a digital computer.
The results showed that the prepared gene chip could detect and distinguish the five equine viruses.
Its sensitivity was about 25 viral genome copies.
The hybridization specificity was confirmed by the presence of red fluorescence signals on the corresponding sites with samples from the five relevant viruses in horses and by the absence of positive signals with the specimens from irrelevant viruses from other animals.
Peripheral blood leucocytes (PBL) from some seropositive horses in post-arrival quarantine were negative according to virus isolation, but were positive for EHV-1 and EAV according to the gene chip technique.
The overall results suggest that gene chips, which are quick, specific, sensitive and reliable, can provide a practical alternative for screening quarantined animals, and will be able to deal with a large number of animal samples within a very short period of time.

Related Results

Abstract 4146122: Potential Protective Roles of Clonal Hematopoiesis of Indeterminate Potential in Angina Pectoris
Abstract 4146122: Potential Protective Roles of Clonal Hematopoiesis of Indeterminate Potential in Angina Pectoris
Introduction: Clonal hematopoiesis of indeterminate potential (CHIP) poses strong relationship to the occurrence of cardiovascular diseases with the process of aging. I...
Expression and polymorphism of genes in gallstones
Expression and polymorphism of genes in gallstones
ABSTRACT Through the method of clinical case control study, to explore the expression and genetic polymorphism of KLF14 gene (rs4731702 and rs972283) and SR-B1 gene (rs...
Characterisation and zoonotic risk of tick viruses in public datasets
Characterisation and zoonotic risk of tick viruses in public datasets
AbstractTick-borne viruses remain a substantial zoonotic risk worldwide, so knowledge of the diversity of tick viruses has potential health consequences. Despite their importance, ...
Traumatic brain injury in horses: 34 cases (1994–2004)
Traumatic brain injury in horses: 34 cases (1994–2004)
Abstract Objective—To investigate the clinical, clinicopathologic, and diagnostic characteristics; treatment; and outcome associated with acute traumatic brain injury (TBI) in hors...
Characterisation of putative novel tick viruses and zoonotic risk prediction
Characterisation of putative novel tick viruses and zoonotic risk prediction
AbstractTick‐associated viruses remain a substantial zoonotic risk worldwide, so knowledge of the diversity of tick viruses has potential health consequences. Despite their importa...
An Efficient Interconnection System for Neural NOC Using Fault Tolerant Routing Method
An Efficient Interconnection System for Neural NOC Using Fault Tolerant Routing Method
Abstract Large scale Neural Network (NN) accelerators typically have multiple processing nodes that can be implemented as a multi-core chip, and can be organized on ...
Revealing RNA virus diversity and evolution in unicellular algae transcriptomes
Revealing RNA virus diversity and evolution in unicellular algae transcriptomes
Abstract Remarkably little is known about the diversity and evolution of RNA viruses in unicellular eukaryotes. We screened a total of 570 transcriptomes from the Ma...
Research on Analysis and Classification of Vulnerability of Electromagnetic Pulse with a STM32 Single-Chip Microcomputer
Research on Analysis and Classification of Vulnerability of Electromagnetic Pulse with a STM32 Single-Chip Microcomputer
With the continuous development of information technology, the performance of the entire traditional electrical system is gradually optimized. Nowadays, the single-chip technology ...

Back to Top