scholarly journals Evaluation of the effect of simultaneous infection with E. coli O2 and H9N2 influenza virus on inflammatory factors in broiler chickens

2014 ◽  
Vol 4 (2) ◽  
Author(s):  
Habiballah Dadras ◽  
Saeed Nazifi ◽  
Marzieh Shakibainia

This study was conducted to evaluate the effect of experimental infection with <em>Escherichia</em> coli O2 and H9N2 influenza virus on inflammato- ry factors in broiler <em>chickens</em>. A total of 120 one-day-old Cobb broiler chicks were divided randomly to 6 groups. Inoculation program with 109 EID50/bird of the A/Chicken/Iran/772/1998 (H9N2) virus and 109 CFU/mL/bird of <em>E. coli</em> O2 was carried out as follows: the chicks in group 1 were inoculated with virus and bacteria simultaneously on day 26, group 2 received virus on day 26 and then bacteria 3 days later, group 3 were inoculated with bacteria on day 23 and then virus on day 26, group 4 received only bacteria on day 26, group 5 were inoculated with only virus on day 26 and group 6 served as control. Serum samples were collected from wing vein at days 20, 30, and 40. Sera were examined for inflammatory mediators (TNF-a and INF-γ), acute phase reactants (haptoglobin and serum amyloid A) and gangliosides (total, lipid-bound and protein-bound sialic acids) using validated standard procedures. Among the measured parameters, serum gangliosides showed significant differences between the challenged and control groups in different days post inoculation (P&lt;0.05). Significant increase in serum concentrations of serum sialic acids was observed on the 30th day in challenged groups. Elevations were found in the concentrations of serum gangliosides on day 40 compared to their first concentrations. The most obvious increase in serum sialic acids was observed in group 1 challenged with avian influenza virus and <em>E. coli</em> O2 simultaneously. Bacterial infected group showed more significant changes in comparison with viral infected one. These findings suggest that serum sialic acids may be a useful indicator of H9N2 avian influenza virus and avian pathogenic <em>E. coli</em> O2 co-infection.

Author(s):  
V. Yu. Marchenko ◽  
N. I. Goncharova ◽  
V. A. Evseenko ◽  
I. M. Susloparov ◽  
E. V. Gavrilova ◽  
...  

Analyzed was modern epidemiological situation on highly pathogenic avian flu in 2018. Prognosis for possible further distribution of viruses in the territory of Russia was made. In 2018, the situation on highly pathogenic avian flu in Russia was challenging. This was due to the spread of the viruses clade 2.3.4.4, which caused multiple outbreaks among wild birds and poultry in European part of Russia. In addition, A/H5N6 avian influenza virus circulation was for the first time detected in the Saratov Region during routine avian influenza virus surveillance. In May, 2018 two different lineages of avian influenza A/H9N2 were isolated during the outbreaks that occurred at several poultry plants in Primorsk Territory and Amur Region of Russia. Subsequently, that virus subtype continued spreading in Russia, which was recorded by detection of the A/H9N2 influenza virus in wild birds in the Khabarovsk and Tomsk Regions of Russia. Thus, it is shown yet again that the territory of Russia plays an  important geographical role in the spread of avian influenza viruses.


Vaccines ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 791
Author(s):  
Sixin Zhang ◽  
Xinming Tang ◽  
Si Wang ◽  
Fangyun Shi ◽  
Chunhui Duan ◽  
...  

The potential of Eimeria parasites as live vaccine vectors has been reported with successful genetic manipulation on several species like E. tenella, E. mitis and E. necatrix. Among seven Eimeria species infecting chickens, E. acervulina is a highly prevalent, moderately pathogenic species. Thus, it is valuable for the study of transfection and for use as a potential as vaccine vector. In this study, a plasmid containing expression cassette with enhanced yellow fluorescent protein (EYFP), red fluorescent protein (RFP) and 12 copies of extracellular domain of H9N2 avian influenza virus M2 (M2e) protein was used for the transfection. Nucleofected sporozoites were inoculated into birds through wing vein. Recombinant E. acervulina oocysts with 0.1% EYFP+ and RFP+ populations were collected from the feces of the inoculated birds. The fluorescent rate of transgenic parasites reached over 95% after nine successive propagations with a pyrimethamine selection in vivo and fluorescent-activated cell sorting (FACS) of progeny oocysts. The expression of M2e in the transgenic parasites (EaM2e) was confirmed by Western blot and its cytoplasm localization in sporozoites was displayed by an indirect immunofluorescent assay (IFA). Meanwhile, we found that the fecundity of EaM2e was equivalent to that of wild type E. acervulina (EaWT). Taken together, the stable transfection of E. acervulina was successfully established. Future studies will focus on whether transgenic E. acervulina can serve as a live vaccine vector.


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