UVAS Library

Your cart is empty.

Your search returned 3 results. Subscribe to this search

Not what you expected? Check for suggestions
Unhighlight Highlight
|
1.
No cover image available
Prevalence And Chemotherapy Of Argas Persicus In Rural Poultry At Lahore District

by Nazish Munawar | Prf.Dr. Azhar Maqbool | Dr.Aftab | Dr.Kamran Ashraf | Faculty of Veterinary Sciences.

Material type: book Book; Format: print Publisher: 2010Dissertation note: External parasites like ticks causes great economic losses in poultry in term of low productivity, anemia, and secondary bacterial infection. Keeping in view economical importance of this problem the project was designed to record the prevalence of Argas persicus in poultry and to treat the birds with different drugs. For this purpose indigenous poultry at Lahore was visited for the collection. Overall prevalence of tick infestation and identification of ticks was on the basis of their taxonomic characteristics. During the study period 5207 ticks were collected from five hundred birds. Three species of Argas were identified, 3316 were belonging to Argas Persicus (65.02%), 935 Argas reflexus (17.95%), (18.32%), 957 were Argas vespertilionis. Antigen was prepared from the mouth parts of ticks. Five hundred blood samples were taken from birds found positive. Sera were centerifuged and subjected to AGID test. Overall 19.4% prevalence of Argas persicus was recorded. Age -wise 8.19% and 25.8% prevalence was observed in chicks and adults respectively. The highest prevalence during spring was (26.8%) due to high humidity reason. One hundred layers were selected for therapeutic trials. These were randomly divided into 5 groups i.e., A, B, C, D and E. Birds in group A, B, C, D was treated with Cypermethrin, Ivermectin, Permethrin, and Dormectin respectively. Where as birds in group E was served as untreated control. Efficacy of drugs was calculated on the basis of reduction of ticks on the body of poultry. The efficacy of drug trial was noted in poultry subunits for a period of 15 days. The maximum control was achieved by Cypermethrin (90.7%), Ivermectin (90.35%), Dormectin (89.3%) and Permethrin (88.9%). The data were analyzed statistically by using NPar test, kruskal-Wallis test and Median test (Steel and Torrie 1989). Availability: Items available for loan: UVAS Library [Call number: 1084,T] (1).

Place hold Add to cart
2.
No cover image available
Genotyping Of Hydatid Cyst And Itd Prevalence In Cattle,Buffalo And Human Beings

by Muhammad Nauman Zahid | Prf.Dr. Azhar Maqbool | Dr.Aftab | Dr.kamran Ashraf | Faculty of Veterinary Sciences.

Material type: book Book; Format: print ; Nature of contents: biography; Literary form: Publisher: 2008Dissertation note: ACystic echinococcosis (CE) is the larval cystic stage (called echinococcal cysts) of a small taeniid-type tapeworm (Echinococcus granulosus) that may cause illness in intermediate hosts, generally herbivorous animals and people who are infected accidentally. Echinococcus granulosus has number of genetically distinct strains which are known to differ morphologically and epiderniologically. Out of 150 cattle and 150 buffalo examined only 42 Samples of hydatid cysts were collected from different organs i.e. livers, kidneys, lungs and hearts from Lahore abbatoir. From 42 positive samples, 25 cysts were found in cattle and 17 cysts were tound in buffalo. Prevalence of hydatidosis in cattle was recoreded as 16.66% and 11.33% in buffalo. Fertility and viability of the cysts was observed microscopically. Out of 25 cysts of cattle. nine were fertile and out of 17 cysts of buffalo, only five were fertile. Seroprevalence of hydatidosis in 150 butchers working in abattoir was also determined by the use of Latex agglutination test (LAT) kit for detection of hydatidosis. The prevalence of Echinococcus is 24% which was derived from serum analysis of butchers. DNA from hydatid cyst was extracted. Polymerase Chain Reaction was run on extracted DNA samples. Amplicon was run on 1% agarose for confirmation of size and specificity of product. Size of PCR product was approximately l300bp. Genotyping of Echinococcus granulosus was performed through Polymerase Chain Reaction- Restriction Fragment Length Polymorphism (PCR-RFLP). The PCR-RFLP analysis of CO I gene of Echinococus was performed to confirm the strain of Echinococcus in cattle .The data obtained was analysed and it was concluded that the G5 strain of echinococus is prevalent in Cattle in Punjab area. It is hoped that the findings of the present study will be helpful for further planning about the control of the disease and correlating the prevalence in cattles,buffalos and butchers from the zoonotic point of view. According to the results, the PCR-RFLP analysis of samples of patients suspected for Echinococejis is a promising diagnostic method and also confirms the type of Echinococcits prevalent in that area and also enables an early direct detection of parasite DNA. This effort is a step to minimize the losses produced by this disease. Availability: Items available for loan: UVAS Library [Call number: 1097,T] (1).

Place hold Add to cart
3.
No cover image available
Detection Of Toxoplasma Gondii From Water And Matrices (Soil,Fruits &

by Adeela Ajmal | Prf.Dr. Azhar Maqbool | Dr. Kamran ashraf | Dr.Aftab ahmad | Faculty of Veterinary Sciences.

Material type: book Book; Format: print Publisher: 2010Dissertation note: Toxoplasmosis caused by Toxoplasma gondii is a widely distributed protozoan disease capable of infecting a variety of animal species. Felids, both domestic and wild, are capable of serving as definitive hosts, shedding T.gondii oocysts in their faeces. People acquire toxoplasmosis posnatally by ingesting T.gondii oocysts from contaminated environments or by consuming T.gondii tissue cysts in inadequately meat products, raw meat containing tissue cysts or by ingestion of resistant oocysts from environmental matrices (soil, water, fruits and vegetables). However, the impact of oocysts in toxoplasmosis epidemiology needs to be specified because they are suspected to be associated with T.gondii seroprevalence in some emerging outbreaks of acute toxoplasmosis in humans from soil or water. They are probably responsible for a significant part of infections in animals that could be later consumed by humans. Detection of Toxoplasma gondii oocysts in environmental samples is great challenge as this coccidian parasite can be responsible for severe infections in humans and animals via ingestion of a single oocyst from contaminated water, soil, fruits or vegetables. The present proposed study was designed to develop methods for the detection of oocysts from Water, soil, food and parks environment. The results of recovery test showed that it was possible to detect Tooplasma gondii parasite from water samples collected from various sources i e, drinking water from muncipility, lakes, pools, various reservoirs around farms and from tube wells. From the results ,The highest (13%) prevalence was reported from water around farms followed by lakes & pools (9%) then water reservoirs (7%) whereas the lowest from drinking water & tubewells i e 6 & 6 percent respectively. A total of 250 samples of fruits and vegetables were collected for detection of T. gondii . From the results, it was noted that overall prevalence of T. gondii infection was higher in vegetables i e 5.6 % than fruits (4 %). A total of 250 soil samples were collected from urban and rural areas. Of these 125 were from urban areas and 125 from rural areas. From the table-3 it was shown that the highest prevalence of T. gondii infection was noted in gardens and back yards of homes and gardens i e 20 & 20 % respectively. In these places cats often defecate and become a source of infection. Then followed by public enclosures where infection was 14.3%. The lowest i e 13.3% infection was noted at homes of urban areas. T. gondii infection in rural areas indicated that It was highest (20% ) in home back yards followed by homes (16.7%) then public enclosure (14.5%) whereas the lowest (13.3%) at gardens of rural areas. Availability: Items available for loan: UVAS Library [Call number: 1161,T] (1).

Place hold Add to cart

Implemented and Maintained by UVAS Library.
For any Suggestions/Query Contact to library or Email:rehana.kousar@uvas.edu.pk Phone:+91 99239068
Website/OPAC best viewed in Mozilla Browser in 1366X768 Resolution.