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Diagnosis of acute and chronic schistosomiasis haematobium using purified 26 kDa schistosoma-specific protein / Manar Mahmoud Imam Ibrahim ; Supervised Azza Mohamed Elamir , Noha Ahmed Mahana , Neamat Amer

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Manar Mahmoud Imam Ibrahim , 2017Description: 79 P. : charts , facsimiles ; 30cmOther title:
  • تشخيص حالات بلهارسيا المجاري البوليه الحادة والمزمنه بإستخدام البروتين الخاص ( 26 كيلو دالتون) المنقي من ديدان البلهارسيا [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Zoology Summary: One of the world wide major public health problems is the schistosomiasis that is caused by Schistosoma (S.) heamatobium. It is also one of the main concerns for the public health community in Egypt. There are several immunodiagnostic methods used for that diagnosis of such disease, but some are more sensitive and specific than others. The purified 26 kDa Schistosoma-specific protein (PSPA-26) detection in serum samples is found out to be more valuable in diagnosis; it also helps in the early diagnosis which will lead to the early treatment before the irreversible damage takes place. PSPA-26 was purified from whole worms by DEAESephadex G-75 ion exchange chromatography and then was injected into rabbits to produce specific polyclonal antibodies(anti-PSPA-26 pAb)which is then used as a primary capture in the indirect ELISA technique to reveal its reactivity using infected human sera.The anti-PSPA-26 was then labeled with horse-radish peroxidase (HRP) and used as a secondary capture.Sandwich ELISA was done for serum samples of human and hamsters infected with S. heamatobium.The results revealed a sensitivity of 85% for human and 80% for hamster's samples,and a specificity of 95% for human and 91.1% for hamsters samples by comparing them with those infected with other parasites and control samples. Data obtained concluded that PSPA-26 antigen can be used as a diagnostic marker for S. haematobium infection using the sandwich ELISA which is cost effective and applicable technique
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.21.M.Sc.2017.Ma.D (Browse shelf(Opens below)) Not for loan 01010110075742000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.21.M.Sc.2017.Ma.D (Browse shelf(Opens below)) 75742.CD Not for loan 01020110075742000

Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Zoology

One of the world wide major public health problems is the schistosomiasis that is caused by Schistosoma (S.) heamatobium. It is also one of the main concerns for the public health community in Egypt. There are several immunodiagnostic methods used for that diagnosis of such disease, but some are more sensitive and specific than others. The purified 26 kDa Schistosoma-specific protein (PSPA-26) detection in serum samples is found out to be more valuable in diagnosis; it also helps in the early diagnosis which will lead to the early treatment before the irreversible damage takes place. PSPA-26 was purified from whole worms by DEAESephadex G-75 ion exchange chromatography and then was injected into rabbits to produce specific polyclonal antibodies(anti-PSPA-26 pAb)which is then used as a primary capture in the indirect ELISA technique to reveal its reactivity using infected human sera.The anti-PSPA-26 was then labeled with horse-radish peroxidase (HRP) and used as a secondary capture.Sandwich ELISA was done for serum samples of human and hamsters infected with S. heamatobium.The results revealed a sensitivity of 85% for human and 80% for hamster's samples,and a specificity of 95% for human and 91.1% for hamsters samples by comparing them with those infected with other parasites and control samples. Data obtained concluded that PSPA-26 antigen can be used as a diagnostic marker for S. haematobium infection using the sandwich ELISA which is cost effective and applicable technique

Issued also as CD

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