Prevalence of Newcastle Disease Virus in Pakistan, its present status and future challenges

2021 ◽  
Vol 7 (2) ◽  

Newcastle disease is caused by Newcastle Disease Virus (NDV) leads to severe morbidity and mortality in poultry throughout the world and considered as lentogenic, mesogenic or velogenic based on the mean death of the chicken embryo. The NDV velogenic strain is deadly endemic in Pakistan. Poultry is considered as the second major industry in Pakistan having annual growth of 8-10%. Unfortunately, the increase of NDV cases leads to severe cost impact, loss of production and livelihood. This review highlights the current status and epidemiology of NDV in Pakistan. Various genotypes and sub-genotypes have been identified in Pakistan. Various ND cases have been reported in Pakistan which has very bad consequences on the economy and dealing of poultry products.

2014 ◽  
Vol 184 ◽  
pp. 71-81 ◽  
Author(s):  
Ketan Ganar ◽  
Moushumee Das ◽  
Sugandha Sinha ◽  
Sachin Kumar

2021 ◽  
Author(s):  
Tingyu Peng ◽  
Xusheng Qiu ◽  
Lei Tan ◽  
Shengqing Yu ◽  
Binghuan Yang ◽  
...  

The Newcastle disease virus (NDV) matrix (M) protein is the pivotal element for viral assembly, budding and proliferation. It traffics through the cellular nucleus but performs its primary function in the cytoplasm. To investigate the biological importance of M’s nuclear–cytoplasmic trafficking and the mechanism involved, the regulatory motif nuclear export signal (NES) and nuclear localization signal (NLS) were deeply analyzed. Here, two types of combined NLS and NES signals were identified within NDV-M. The Herts/33-type M was found to mediate efficient nuclear export and stable virus-like particle (VLP) release, while the LaSota-type M was mostly retained in the nuclei and showed retarded VLP production. Two critical residues, 247 and 263, within the motif were identified and associated with nuclear export efficiency. We identified, for the first time, residue 247 as an important monoubiquitination site, the modification of which regulates the nuclear–cytoplasmic trafficking of NDV-M. Subsequently, mutant LaSota strains were rescued via reverse genetics, which contained either single or double amino acid substitutions that were similar to the M of Herts/33. The rescued rLaSota strains rLaSota-R247K, -S263R, and -DM (double mutation) showed about twofold higher HA titers and 10-fold higher EID 50 titers than wild-type (wt) rLaSota. Further, the MDT and ICPI values of those recombinant viruses were slightly higher than that of wt rLaSota probably due to their higher proliferation rates. Our findings contribute to a better understanding of the molecular mechanism of the replication and pathogenicity of NDV, and even those of all other paramyxoviruses. It is beneficial for the development of vaccines and therapies for paramyxoviruses. Importance Newcastle disease virus (NDV) is a pathogen that is lethal to birds and causes heavy losses in the poultry industry worldwide. The World Organization for Animal Health (OIE) ranked ND as the third most significant poultry disease and the eighth most important wildlife disease in the World Livestock Disease Atlas in 2011. The matrix (M) protein of NDV is very important for viral assembly and maturation. It is interesting that M proteins enter the cellular nucleus before performing their primary function in the cytoplasm. We found that NDV-M has a combined nuclear import and export signal. The ubiquitin modification of a lysine residue within this signal is critical for quick, efficient nuclear export and subsequent viral production. Our findings shed new light on viral replication and opens up new possibilities for therapeutics against NDV and other paramyxoviruses; furthermore, we demonstrate a novel approach to improving paramyxovirus vaccines.


2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Egbal Sidahmed Abdelrahim Bilal ◽  
Iman Mohammed Elnasri ◽  
Aymen Mohamed Alhassan ◽  
Khalda Abdelaziz Khalifa ◽  
Jedddha Ibrahim Elhag ◽  
...  

The biological properties and pathogenicity of seven Newcastle disease virus field isolates were studied. These isolates were recovered from different outbreaks in Sudan (5 from chickens and 2 from pigeons) during 2008–2013. Based on intracerebral pathogenicity index, four NDV isolates were characterized as velogenic (their ICPI ranged 2.0–1.6) and three isolates were characterized as mesogenic (ICPI ranged 1.2–1.3). The mean death time for all isolates ranged from 54 to 76.8 hours. The elution time of the viruses from chicken erythrocytes and the ability to haemagglutinate mammalian red blood cells differed considerably in their reactions.


2019 ◽  
Vol 12 (6) ◽  
pp. 758-764 ◽  
Author(s):  
Anak Agung Ayu Mirah Adi ◽  
I Nyoman Mantik Astawa ◽  
I Gusti Agung Arta Putra

Aim: This study aimed to prepare binary ethylenimine (BEI)-inactivated virulent Newcastle disease virus (NDV) vaccine and to examine their ability to induce a protective antibody response in commercial chickens. Materials and Methods: A virulent NDV field isolate Gianyar-1/AK/2014 was propagated in chicken-embryonated eggs and was then inactivated with BEI at a concentration of 4 mM. Three groups of chickens with low-level (2 log2 hemagglutination inhibition [HI] units) maternally derived antibodies against NDV were then immunized with the BEI-inactivated vaccine. A commercial live vaccine (LaSota strain) was used as positive control, and phosphate-buffered saline (PBS) was used as negative control. A challenge experiment with a virulent NDV of Tabanan-1/ARP/2017 was performed at 3 weeks post-vaccination. Results: At 2 weeks post-immunization, the mean titers of antibodies against NDV in serum samples of chickens immunized with 0.2 mL of BEI-inactivated NDV (Group I), with live commercial NDV vaccine (Group II) and with PBS (Group III) were 3±0.94 log2 HI units, 4.9±0.99 log2 HI unit, and 0.0±0.0 HI units, respectively. At week 3 post-immunization, the mean titers of the antibodies for the three groups were 5±1.09 log2 HI units, 6.9±0.32 log2 HI units, and 0.00 HI units, respectively. The antibody titer induced by inactivated NDV Gianyar-1/AK/2014 isolates examined at 2 and 3 weeks post-vaccination was still at a significantly (p<0.01) lower level as compared to those induced by commercial life vaccine. However, the challenge test with virulent NDV of Tabanan 1/ARP/2017 isolates showed that all immunized chickens (Group I and II) survived without exhibiting any clinical sign post-challenge with the protection rates of 100%, whereas all chickens injected with PBS (Group III) died with clinical signs of ND. Conclusion: This finding shows that the BEI-inactivated vaccines prepared using virulent NDV of Gianyar-1/AK/2014 strain was able to induce protective antibody response in chickens but still at a lower level than those induce by commercial live NDV vaccine.


2017 ◽  
Vol 9 (1) ◽  
Author(s):  
Oksana Blotska

ObjectiveA test kit for the detection of antibodies to Newcastle disease virus(NDV) based on haemagglutination inhibition (HI) assay has beendeveloped and introduced into practice for the first time in Ukraine.IntroductionNewcastle disease (ND) is the most important infectious viraldisease of poultry. The world-wide economic loss from it is 2-3billion USD per year. ND is reportable to the World Organizationfor Animal Health (OIE). ND is caused by virulent strains of avianParamyxoviruses belonging to type 1. Industrial poultry farmingis rapidly developing in Ukraine. Ornithological fauna of Ukraineincludes about four hundred species of birds, 207 of which nestwithin its borders. The territory of Ukraine transits 3 out of 14transcontinental global migration flows. The wild birds are themain natural reservoir of ND agents. It is necessary to control theintensity of post-vaccination immunity in poultry and the timing ofrevaccinations. OIE recommends enzyme linked immunosorbentassays (ELISA) and HI test for these purposes [1]. However, it shouldbe noted that HI test, possessing high specificity and sensitivity, ismuch cheaper. Therefore, it is the excellent means for ND timelysurveillance.MethodsDuring the development of a new diagnostic kit, we used thereference strain “La-Sota”, which was obtained from the NationalCenter of Microorganism Strains of Ukraine. We have producedhaemagglutinating antigen using embryonated SPF fowl eggs and10-11 day incubation. A dilution of the virus was inoculated in0.1 ml volumes into the allantoic cavity and incubated at 35-37° Cfor 80-96 hours. For the purpose of NDV inactivation, we usedaminoethyleneimine at the final concentration of 0.1%. Positive serumwas prepared by immunizing 60-day-old chickens with live virus onceand by inactivated virus twice with an interval of 2 weeks. Negativeserum was obtained from healthy birds that did not contain antibodiesto NDV. The investigated blood sera were inactivated by heating(56 C/30 minutes). Samples of 1% suspension of chicken erythrocytesin phosphate buffered saline (pH 7.0-7.1) were used in HI tests.ResultsThe specific haemagglutination activity of the obtained antigenamounted to 10-11 log2.The test was performed using the 4HA unitsof the antigen. Positive control serum activity was in the range of 7-9log2. Negative control serum did not give results of more than 2 log2.The estimation of the quality indexes of the components of thediagnostic test-kit was performed using harmonized methods. In orderto examine sensitivity and specificity of HI test kits, antigens and serafrom commercial diagnostic kits were used. Also, certified negativecontrol serum and samples of International Standard sera were used,which were obtained from reference laboratories, namely againstthe following pathogens: Avian Influenza A (H5), Avian InfluenzaA (H7), Egg Drop Syndrome'76 Virus, Paramyxoviruses of 2 and3 serotypes, Reovirus, Avian Infectious Laryngotracheitis, AvianInfectious Bronchitis Virus, Mycoplasma gallisepticum, and NDV.In order to ensure a high degree of specificity for the antigen,special attention was given to the selection of a stabilizer for freeze-drying (the subject of a patent).Comparison between the national diagnostic test kit for HI andcommercial ELISA kit (IDEXX) in the evaluation of humoralimmune response to ND in vaccinated chickens was investigatedby examining of serum samples (n=152). Statistical analysis of datashowed that the correlation coefficient for the results of both tests was0.92. The relative sensitivity of HI test kit was 93.5% and the relativespecificity - 91.5%.The developed test kit was successfully used for the examinationof field samples. We developed regulatory documents, completed theprocedure of validation and registration in Ukraine of the commercialHI test kit for the detection of antibodies to NDV.ConclusionsThe use of the national standardized diagnostic test kit based onHI for detection of antibodies to NDV allows assessing the post-vaccination antibodies level that helps to maintain the disease-freestatus of the Ukrainian poultry industry with regard to ND.


2014 ◽  
Vol 2014 ◽  
pp. 1-2
Author(s):  
Egbal Sidahmed Abdelrahim ◽  
Jedda Elhag

Two diseased red-headed lovebirds were presented for diagnosis to the Department of Avian Diseases and Diagnosis,Veterinary Research Institute, aged 37 days and 4 years. The symptoms were dyspnea, cyanosis of the comb, diarrhea, and fever. Postmortem lesions included pale liver and bloody enteritis. Newcastle disease virus was isolated from lungs, trachea, and intestines following inoculation in the allantoic cavity of 10-day-old fertile eggs; the NDV was identified by the means of HA&HI tests using specific NDV antisera (Lasota strain). The isolate agglutinated equine RBCs but failed to agglutinate sheep and bovine RBCs. The pathogenicity of the NDV isolate was studied, the mean death time was 96 hours, and the intracerebral pathogenicity index (ICPI) value was 0.9, indicating the isolate of lentogenic type.


1970 ◽  
Vol 2 (2) ◽  
pp. 113-116
Author(s):  
MA Amin ◽  
MM Amin ◽  
MSR Khan ◽  
KA Choudhury ◽  
MNA Siddiky ◽  
...  

Two isolates of Newcastle disease virus from two different caged birds, one from a parrot and another from a kakatoa were characterized during the period from July 2001 to October 2002. In HA tests both the isolates haemagglutinated chicken and guineapig erythrocytes but the parrot isolate was found refractory to bovine and equine erythrocytes and the kakatoa isolate to bovine erythrocytes. In elution tests, the parrot isolate was found to be a rapid eluter and the kakatoa isolate as slow eluter. Both the isolates were found to be heat-unstable in relation to haemagglutinating activity and embryo-infectivity. The mean death time (MDT) of the parrot and kakatoa isolates were 57.6 hours and 117.6 hours and the intracerebral pathogenicity indices (ICPl) were 1.58 and 0.45 respectively. So, the parrot isolate was found as the velogenic strain and the kakatoa isolate as the lentogenic strain of Newcastle disease virus.Key words: Caged bird; NDV; mean death time; ICPI; haemagglutination test. elution testdoi: 10.3329/bjvm.v2i2.2541Bangl. J. Vet. Med. (2004). 2 (2): 113-116


Author(s):  
Jacob Pitcovski ◽  
Ehud Shahar ◽  
Avigdor Cahaner

This chapter first illustrates how a large number of observations can inform the design of a particular experiment intended to test rigorously the causes of the observed associations. It does so through the discussion and analysis of two case studies drawn from experimental immunology: (i) the efficacy of vaccines for Newcastle disease virus in poultry, and (ii) cancer immunotherapy. It then shows that it is important when repeating experiments to reproduce not only the expected result (i.e., the estimated mean value) but also to reduce the variability in estimates of the mean. Reduction in overall variance can be accomplished both with more precise measurements and by accounting for additional sources of error (covariates or “nuisance” variables). When potentially important covariates are recorded during an experiment, they can be included in the analysis of the data and help to isolate the true “signal” of the experimental treatment from the “noise” of the experimental environment.


2016 ◽  
Vol 21 (1) ◽  
pp. 235-248
Author(s):  
Amani Saleh ◽  
Rola Ali ◽  
Mohamed Fawzy ◽  
Mokhtar Eltarabily

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