Abstract
BackgroundInfluenza virus isolation in embryonated chicken eggs (ECEs) is not applicable for rapid diagnosis, however it allows the recovery and propagation of the viable virus. A low number of infectious virus particles in the swabs, poor quality of samples or individual strain properties can lead to difficulties during the virus isolation process. We propose to utilize chorioallantoic membranes (CAM) of ECEs with the assistance of real-time RT PCR to facilitate equine influenza virus isolation.MethodsReal-time RT PCR was used to detect influenza virus genetic material in amniotic/allantoic fluids (AF) and CAM of ECEs. Haemagglutination assay was used for AF. We used highly diluted virus as a substitute of clinical specimen for ECEs inoculation.ResultsOur study demonstrated that real-time RT PCR testing of CAM homogenates was more useful than testing of AF for EIV detection in ECEs. Positive results from CAM allowed to select the embryos from those with haemagglutination assay (HA) - and real-time RT PCR-negative AF for further passages. Using homogenates of CAM for subsequent passages, we finally obtained HA-positive AF, which confirmed virus replication.ConclusionWe postulate that real-time RT PCR testing of CAM homogenates and their subsequent passages may facilitate the isolation of equine influenza viruses.
Highlights
Influenza virus isolation in embryonated chicken eggs (ECEs) is not applicable for rapid diagnosis, it allows the recovery and propagation of the viable virus
Virus isolation in embryonated chicken eggs (ECEs) or Madin-Darby canine kidney cells is not required for rapid diagnosis, it allows the recovery and propagation of the viable viral strains, which is essential for virus characterization
ECEs have been preferred for isolation of equine influenza virus (EIV) and some authors proved that ECEs were more effective for virus isolation than cell cultures [6]
Summary
Influenza virus isolation in embryonated chicken eggs (ECEs) is not applicable for rapid diagnosis, it allows the recovery and propagation of the viable virus. To HA of AF, we examined chorioallantoic membranes (CAM) and AF by rtRT PCR for the detection of M gene of influenza A virus. CAM homogenates from ECEs inoculated with highly-diluted EIV were
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.