scholarly journals Development and Evaluation of a Live Attenuated Egg-Based Camelpox Vaccine

2021 ◽  
Vol 8 ◽  
Author(s):  
Kuandyk Zhugunissov ◽  
Sanat Kilibayev ◽  
Muratbay Mambetaliyev ◽  
Kunsulu Zakarya ◽  
Markhabat Kassenov ◽  
...  
Keyword(s):  
Virus Strain ◽  
Wild Type Strain ◽  
Protective Efficacy ◽  
Chorioallantoic Membrane ◽  
Economic Loss ◽  
Viral Disease ◽  
Wild Type ◽  
Post Vaccination ◽  
Chicken Eggs ◽  
Embryonated Chicken

Camelpox is an infectious viral disease of camels reported in all the camel-breeding areas of Africa, north of the equator, the Middle East and Asia. It causes huge economic loss to the camel industry. We developed a live camelpox virus vaccine candidate using an attenuated strain and evaluated its safety, immunogenicity and protective efficacy in camels. The attenuated virus strain was generated from the camelpox wild-type strain M-96 by 40 consecutive passages on the chorioallantoic membrane of 11-day-old embryonated chicken eggs, henceforth called KM-40 strain. Reversion to virulence of the KM-40 strain was evaluated in camels by three serial passages, confirmed its inability to revert to virulence and its overdose administration was also found safe. Studies of immunogenicity and protective efficacy of the candidate vaccine KM-40 strain in camels was carried out using the dose of 5 x 104.0 EID50. Our data showed complete protection against the challenge infection using the virulent wild-type camelpox virus strain M-96 (dose of 105.0 EID50) which was evaluated at 1, 3, 6 and 12 months post vaccination. In summary, our candidate live attenuated egg-based camelpox vaccine strain KM-40 was found safe, protective, and thus has the potential to use safely in field conditions.

scholarly journals Safety and Protective Efficacy of Intramuscular Vaccination with a Live aroA Derivative of Pasteurella multocida B:2 against Experimental Hemorrhagic Septicemia in Calves

2007 ◽  
Vol 75 (12) ◽  
pp. 5837-5844 ◽  
Author(s):  
Mark P. Dagleish ◽  
J. Christopher Hodgson ◽  
Saeed Ataei ◽  
Anna Finucane ◽  
Jeanie Finlayson ◽  
...  
Keyword(s):  
Pasteurella Multocida ◽  
Wild Type Strain ◽  
Protective Efficacy ◽  
Vaccine Dose ◽  
Immunoglobulin M ◽  
Wild Type ◽  
Amyloid A ◽  
Challenge Control ◽  
Temperature Responses ◽  
Dose Dependent

ABSTRACT Three groups of five calves, namely, V1, V2, and V3, were immunized intramuscularly at 4 and 8 weeks of age with ca. 109, 108, and 107 CFU, respectively, of a derivative of Pasteurella multocida B:2 wild-type strain 85020 containing a deletion in the aroA gene (strain JRMT12). The first and second vaccinations resulted in significantly (P < 0.01) higher rectal temperature responses in groups V1 and V2 than in group V3. Serum immunoglobulin M (IgM) and IgG titers did not increase in any group until after the second vaccination and were then significantly higher in groups V1 and V2 than in group V3 (P = 0.001 for both IgM and IgG). All vaccinated groups and three unvaccinated challenge control calves (group CC) were injected subcutaneously at 10 weeks of age with ca. 107 CFU of strain 85020. Vaccinated calves survived the challenge, but two CC animals developed clinical disease and were killed for humane reasons. After challenge, mean serum amyloid A concentrations were significantly higher (P < 0.001) in the CC group than in the vaccinated groups. Postmortem examination revealed that calves in the CC group showed the most extensive range of bacteriologically positive tissues and gross and histopathological lesions. Overall, a clear dose-dependent response was present, with those receiving a higher vaccine dose being less affected clinically, bacteriologically, and pathologically by the wild-type challenge. The V2 treatment appeared to give the best combination of high immune response, protection, and safety.

scholarly journals Immunogenicity and Protective Efficacy in Mice of Influenza B Virus Vaccines Grown in Mammalian Cells or Embryonated Chicken Eggs

1998 ◽  
Vol 72 (5) ◽  
pp. 4472-4477 ◽  
Author(s):  
I. V. Alymova ◽  
S. Kodihalli ◽  
E. A. Govorkova ◽  
B. Fanget ◽  
C. Gerdil ◽  
...  
Keyword(s):  
Mammalian Cell ◽  
Mammalian Cells ◽  
Neutralizing Antibodies ◽  
Protective Efficacy ◽  
Influenza B Virus ◽  
Influenza B ◽  
Homologous Antigen ◽  
B Virus ◽  
Chicken Eggs ◽  
Embryonated Chicken

ABSTRACT The immunogenicity and protective efficacy of formalin-inactivated influenza B/Memphis/1/93 virus vaccines propagated exclusively in Vero cells, MDCK cells, or embryonated chicken eggs (hereafter referred to as eggs) were investigated. Mammalian cell-grown viruses differ from the egg-grown variant at amino acid position 198 (Pro/Thr) in the hemagglutinin gene. The level of neuraminidase activity was highest in egg-grown virus, while MDCK and Vero cell-derived viruses possessed 70 and 90% less activity, respectively. After boosting, each of the vaccines induced high levels of hemagglutinin-inhibiting, neuraminidase-inhibiting, and neutralizing antibodies that provided complete protection from MDCK-grown virus challenge. Mammalian cell-derived virus vaccines induced serum antibodies that were more cross-reactive, while those induced by egg-grown virus vaccines were more specific to the homologous antigen. Enzyme-linked immunospot analysis indicated that cell-grown virus vaccines induced high frequencies of immunoglobulin G (IgG)-producing cells directed against both cell- and egg-grown virus antigens, whereas egg-grown virus vaccine induced higher frequencies of IgG- and IgM-producing cells reacting with homologous antigen and low levels of IgG-producing cells reactive with cell-grown viruses. These studies indicate that influenza B virus variants selected in different host systems can elicit different immune responses, but these alterations had no detectable influence on the protective efficacy of the vaccines with the immunization protocol used in this study.

An Epidemiological Study of Sheep and Goat pox Outbreaks in the Sudan

Food Biology ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
Ahmed Zein Elabdeen Mahmoud ◽  
Abdelmalik Ibrahim Khalafalla ◽  
Muaz Magzob Abdellatif
Keyword(s):  
Virus Isolation ◽  
Chorioallantoic Membrane ◽  
Vero Cells ◽  
Fibroblast Cells ◽  
Chick Embryo Fibroblast ◽  
Chain Reaction ◽  
Polymerase Chain ◽  
Species Specific ◽  
Chicken Eggs ◽  
Embryonated Chicken

Sheep and goat pox Outbreaks occurred in different geographic areas of Sudan and most strikingly, were highly species specific. Two outbreaks in Gedarif State in June. 2013 affected no goats and outbreak in Khartoum state in March. 2015 affected no sheep despite communal herding; affected goats were vaccinated with 0240 strain. Clinically, the disease was characterized by fever, depression and eruption of generalized pox lesions. Mortality rate ranged between 5.2 and 6.7% with a mean of 6.1%. Isolation of viruses succeed on Lamb testes cell culture at passage four, the diseases were diagnosed using virus neutralisation test and polymerase chain reaction. Sheeppox and goatpox isolates grew well in lamb testes and Vero cells. In MDBK however, both viruses induced slight CPE that reached 60% in 9 days. On the other hand, both isolates induced no CPE in chick embryo fibroblast cells. Virus isolation attempts failed on chorioallantoic membrane of embryonated chicken eggs.

scholarly journals Characterization and Evaluation of a Salmonella enterica Serotype Senftenberg Mutant Created by Deletion of Virulence-Related Genes for Use as a Live Attenuated Vaccine

2016 ◽  
Vol 23 (10) ◽  
pp. 802-812 ◽  
Author(s):  
Nitin M. Kamble ◽  
John Hwa Lee
Keyword(s):  
Salmonella Enterica ◽  
Type Strain ◽  
Wild Type Strain ◽  
Protective Efficacy ◽  
Control Group ◽  
Intestinal Loop ◽  
Wild Type ◽  
Exchange Method ◽  
Content Type

ABSTRACTNatural infections of chickens withSalmonella entericasubsp.entericaserovar Senftenberg (S.Senftenberg) are characterized by low-level intestinal invasiveness and insignificant production of antibodies. In this study, we investigated the potential effects oflonandcpxRgene deletions on the invasiveness ofS. Senftenberg into the intestinal epithelium of chickens and its ability to induce an immune response, conferring protection againstS. Senftenberg infection. With the allelic exchange method, we developed JOL1596 (Δlon), JOL1571 (ΔcpxR), and JOL1587 (ΔlonΔcpxR) deletion mutants from wild-typeS. Senftenberg. Deletion of thelongene fromS. Senftenberg produced increased frequency of elongated cells, with significantly greater amounts of exopolysaccharide (EPS) than in thecpxR-deleted strain and the wild-type strain. Thein vivointestinal loop invasion assay showed a significant increase in epithelial invasiveness for JOL1596 (Δlon) and JOL1587 (ΔlonΔcpxR), compared to JOL1571 (ΔcpxR) and the wild-type strain. Furthermore, theS. Senftenberg wild-type and mutant strains were internalized at high levels inside activated abdominal macrophages from chicken. Thein vivoinoculation of JOL1587 (ΔlonΔcpxR) into chickens led to colonization of the liver, spleen, and cecum for a short time. Chickens inoculated with JOL1587 (ΔlonΔcpxR) showed significant increases in humoral, mucosal, and cellular immune responses specific toS. Senftenberg antigens. Postchallenge, compared to the control group, the JOL1587 (ΔlonΔcpxR)-inoculated chickens showed not only lower persistence but also faster clearance of wild-typeS. Senftenberg from the cecum. We conclude that the increased intestinal invasiveness and colonization of internal organs exhibited by JOL1587 (ΔlonΔcpxR) led to the establishment of immunogenicity and conferred protective efficacy againstS. Senftenberg infections in chickens.

scholarly journals Pathological Lesions in Chicken Embryo Caused by Newly Virulent Isolate of Newcastle Disease Virus (LESI PATOLOGIS PADA EMBRIO AYAM YANG DISEBABKAN ISOLAT VIRUS PENYAKIT TETELO TERBARU YANG VIRULEN)

2019 ◽  
Vol 20 (3) ◽  
pp. 337
Author(s):  
I Gede Hendra Prasetya Wicaksana ◽  
Anak Agung Ayu Mirah Adi ◽  
I Made Kardena
Keyword(s):  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Viral Disease ◽  
Economic Losses ◽  
Valuable Insight ◽  
Virulent Isolate ◽  
Hematoxylin And Eosin ◽  
Chicken Eggs ◽  
Embryonated Chicken

Newcastle disease is a pathogenic viral disease in poultry which is infectious and can cause massive economic losses. The disease is still endemic in Indonesia. To understand the pathogenesis and the distribution pattern of the virus in the tissues, pathological observation was evaluated using newly virulent isolate Newcastle disease virus (NDV) that was inoculated in embryonated chicken eggs. As many as seven embryonic chicken eggs aged 11 days and specific antibody negative against Newcastle disease, divided into two categories: inoculated with phosphate buffer saline and inoculated with isolates. Then the allantois fluid was tested using hemagglutination assay and hemagglutination inhibition tests to prove the infection serologically. The hearts, lungs, livers and small intestines of the inoculated products were collected and followed with the process of histopathological preparation using Hematoxylin and Eosin (HE) stain. The pathological analysis showed that all organs had necrosis, hemorrhages, inflammation, and congestion. Congestion and hemorrhages in the hearts only occurred at 60% of the samples. However, necrosis, hemorrhages, and inflammation that were observed in liver occurred at 60%, 40% and 60% of the samples, respectively. Furthermore, the hearts were edema, thinner in the heart muscle fibers; while in the lungs, proliferation of pneumocyte type II was founded. Our finding provided valuable insight into the pathology of a virulent isolate of NDV which is dominated by blood circulation disorders with necrosis and inflammation in the chicken’s embryos and have important implication for the future studies.

scholarly journals A Recombinant Newcastle Disease Virus with Low-Level V Protein Expression Is Immunogenic and Lacks Pathogenicity for Chicken Embryos

2001 ◽  
Vol 75 (1) ◽  
pp. 420-428 ◽  
Author(s):  
Teshome Mebatsion ◽  
Stefan Verstegen ◽  
Leonarda T. C. De Vaan ◽  
Angela Römer-Oberdörfer ◽  
Carla C. Schrier
Keyword(s):  
Newcastle Disease Virus ◽  
Newcastle Disease ◽  
Editing Site ◽  
Wild Type Virus ◽  
Type Virus ◽  
Wild Type ◽  
V Protein ◽  
P Gene ◽  
Chicken Eggs ◽  
Embryonated Chicken

ABSTRACT Newcastle disease virus (NDV) edits its P-gene mRNA by inserting a nontemplated G residue(s) at a conserved editing site (3′-UUUUUCCC-template strand). In the wild-type virus, three amino-coterminal P-gene-derived proteins, P, V, and W, are produced at frequencies of approximately 68, 29, and 2%, respectively. By applying the reverse genetics technique, editing-defective mutants were generated in cell culture. Compared to the wild-type virus, mutants lacking either six nucleotides of the conserved editing site or the unique C-terminal part of the V protein produced as much as 5,000-fold fewer infectious progeny in vitro or 200,000-fold fewer in 6-day-old embryonated chicken eggs. In addition, both mutants were unable to propagate in 9- to 11-day-old embryonated specific-pathogen-free (SPF) chicken eggs. In contrast, a mutant (NDV-P1) with one nucleotide substitution (UUCUUCCC) grew in eggs, albeit with a 100-fold-lower infectious titer than the parent virus. The modification in the first two mutants described above led to complete abolition of V expression, whereas in NDV-P1 the editing frequency was reduced to less than 2%, and as a result, V was expressed at a 20-fold-lower level. NDV-P1 showed markedly attenuated pathogenicity for SPF chicken embryos, unlike currently available ND vaccine strains. These findings indicate that the V protein of NDV has a dual function, playing a direct role in virus replication as well as serving as a virulence factor. Administration of NDV-P1 to 18-day-old embryonated chicken eggs hardly affected hatchability. Hatched chickens developed high levels of NDV-specific antibodies and were fully protected against lethal challenge, demonstrating the potential use of editing-defective recombinant NDV as a safe embryo vaccine.

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