Microbiological studies on clostridium species / Amira Ahmed Ghonemy Seoudi ; Supervised Kamelia Osman , Mahmoud Elhariri

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Amira Ahmed Ghonemy Seoudi

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TextLanguage: English Publication details: Cairo : Amira Ahmed Ghonemy Seoudi , 2020Description: 110 P. : charts , facsimiles ; 25cmOther title:

دراسات ميكروبيولوجية على انواع الكلوستريديوم [Added title page title]

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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Microbiology Summary: A total of 300 samples representing fecal samples from cows & buffloes showing enteric disorder symptoms suspected to be due to enterotoximeia were analyzed by conventional methods and polymerase chain reaction (PCR). C. perfringens was isolated at the rate of 13.3% from diseased animals, and its presence was confirmed by cultural & biochemical characterization. Multiplex PCR was performed to toxinotype of the 40 toxigenic isolates, and the result showed that all isolates were positive for the alpha toxin gene. Multiplex PCR was performed to phospholipase gene (plc) 28 sample were positive A three selected isolates were identified by sequence analysis of (plc) gene sequencing

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Item type	Current library	Home library	Call number	Copy number	Status	Date due	Barcode
Thesis	قاعة الرسائل الجامعية - الدور الاول	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.10.10.M.Sc.2020.Am.M (Browse shelf(Opens below))		Not for loan		01010110080794000
CD - Rom	مخـــزن الرســائل الجـــامعية - البدروم	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.10.10.M.Sc.2020.Am.M (Browse shelf(Opens below))	80794.CD	Not for loan		01020110080794000

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Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Microbiology

A total of 300 samples representing fecal samples from cows & buffloes showing enteric disorder symptoms suspected to be due to enterotoximeia were analyzed by conventional methods and polymerase chain reaction (PCR). C. perfringens was isolated at the rate of 13.3% from diseased animals, and its presence was confirmed by cultural & biochemical characterization. Multiplex PCR was performed to toxinotype of the 40 toxigenic isolates, and the result showed that all isolates were positive for the alpha toxin gene. Multiplex PCR was performed to phospholipase gene (plc) 28 sample were positive A three selected isolates were identified by sequence analysis of (plc) gene sequencing

Issued also as CD

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