Detection Of Prevalent Strain Of Ppr Virus And Efficacy Of Imported Live Attenuated Ppr Vaccine In Local Goat In Pakistan (Record no. 7421)
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| fixed length control field | 05094nam a22002057a 4500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20160212094346.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 160212b2015 xxu||||| |||| 00| 0 eng d |
| 041 ## - LANGUAGE CODE | |
| Language code of text/sound track or separate title | eng |
| 082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER | |
| Classification number | 2381-T |
| 100 ## - MAIN ENTRY--AUTHOR NAME | |
| Personal name | Iqra Javaid (2008-VA-76) |
| 110 ## - MAIN ENTRY--CORPORATE NAME | |
| Location of meeting | Prof.Dr. Aneela Zameer Durani |
| 245 ## - TITLE STATEMENT | |
| Title | Detection Of Prevalent Strain Of Ppr Virus And Efficacy Of Imported Live Attenuated Ppr Vaccine In Local Goat In Pakistan |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT) | |
| Year of publication | 2015. |
| 300 ## - PHYSICAL DESCRIPTION | |
| Number of Pages | 69p.; |
| 502 ## - DISSERTATION NOTE | |
| Dissertation note | Peste des petits ruminants (PPR) is a viral, extremely transmissible disease with 100% and 90% of morbidity and death rate in small ruminants (Singh et al. 2004; Singh et al. 2009). The morbillivirus of the family Paramyxoviridae is responsible for its etiology (Barrett et al. 2005). The clinical signs of Peste des petits ruminants (PPR) are severe pyrexia, oculo-nasal discharge, necrotizing and erosive stomatitis, enteritis and pneumonia (Dhar et al. 2002) and is also accompanied by decrease in lymphocyte count (Rajak et al. 2005). Peste des petits ruminants (PPR) produces a major impact on the economy of the country (Zahur et al. 2009). Because of huge economic blow, the Peste des petits ruminants (PPR) imposes a major limitation on sheep and goat production (Asim et al. 2009; Abubakar and Munir. 2014). The homologous Peste des Petits Ruminants (PPRV) vaccines using Nigeria 75/1 strain of the virus are being manufactured in Pakistan (Asim et al. 2009). The Advance Studies in Vaccinology and Biotechnology Center (CASVAB) University of Baluchistan, Quetta, with the help of Vero cell line manufactured the freeze dried and tissue culture based PPR virus (PPR 75-1) vaccine (Abbas et al. 2011). The homologous and Vero cell based live attenuated PPR vaccine having origin of Indian virus isolate “PPRV-Sungri/96”is being manufactured in India for immunization against Peste des Petits Ruminants (PPR) disease (Sreenivasa et al. 2000). Twenty goats of different age, breed and sex were examined for the presence of PPR disease during this study. About 2-3 ml of saliva was collected from oral cavity of twenty PPR suspected goats in falcon tubes, signifying PPR disease. The extraction of RNA from the samples was done by trizole method and the concentration was measured by nanodrop. The extracted samples were then subjected to one step RT-PCR and then the PCR products were sent for sequencing to detect the PPRV strain under field conditions. To study immunogenic behavior of Raksha PPR (Sungri 96), total of forty (40) goats free from peste des petits ruminants virus (PPR-V) were selected for the experimental study. The Group A comprising of twenty (20) goats of age (06 months-01 Year) were further subdivided into two groups i.e subgroup A1 comprising of 10 goats to which Raksha PPR vaccine (Sungri 96) was administered and other ten of sub-group A2 served as control. Similarly the Group B possessing twenty (20) goats of age (01 Year - 02 Year) were further subdivided into two sub-groups i.e subgroup B1 comprising of 10 goats to which Raksha PPR vaccine (Sungri 96) was administered and other ten of sub-group B2 served as control. The RNA concentration was different in all twenty saliva samples when measured by nanodrop. Only five (5) samples out of total twenty (20), saliva samples from PPR suspected goats, were positive through RT-PCR and yielded an amplified product of 351bp. The five amplicons were sent for sequencing and the phylogenetic tree was constructed. The tree demonstrated that the Pakistani strains of PPRV clustered into lineage IV showing similarity with the isolates from China, Kurdistan, Iran and Bangladesh. It was revealed that the that the animals (1 year to 2year old ) vaccinated with Raksha PPR (Sungri 96) displayed the significantly higher mean antibody titers than the mean antibody titers shown by vaccinated animals of age (6 months to 1 year) at zero, 7th, 14th, 28th, 48th day post vaccination respectively. On statistical analysis of data, the results were significant (p<0.05). The present study revealed the presence of lineage IV in Pakistan. This will help to plan proper control strategies against this deadly viral disease. Currently the Nigeria75/1 vaccine is being used in Pakistan which clusters in lineage II while Pakistani field isolates fall under lineage IV. So it is very important to immunize the animals with lineage specific vaccine like Raksha PPR (Sungri 96) manufactured by IVRI, India. This study reported the strong association of age and PPR vaccination titer in goats. Our findings concluded that the strong immune response was shown by adult animals against PPRV vaccine as compared to young stock. The results of present research project were mostly similar with the findings of other scientists. The results of this study were analyzed by one way ANOVA for independent samples. |
| 650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical Term | Department of Clinical Medicine |
| 700 ## - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Dr.M. Hassan Saleem |
| 700 ## - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Dr. Imran Altaf |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
| Koha item type | Thesis |
| Damaged status | Collection code | Permanent Location | Current Location | Shelving location | Date acquired | Full call number | Accession Number | Koha item type |
|---|---|---|---|---|---|---|---|---|
| Veterinary Science | UVAS Library | UVAS Library | Thesis Section | 2016-02-12 | 2381-T | 2381-T | Thesis |