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العنوان
A study on phenotypic and genotypic characterization of enterobacteriaceae, including campylobacter species and helicobacter pylori Recovered from water reservoirs in the Giza Area /
الناشر
Nourhan Mohamed Abdelgelil Abousetta ,
المؤلف
Nourhan Mohamed Abdelgelil Abousetta
هيئة الاعداد
باحث / Nourhan Mohamed Abdelgelil Abousetta
مشرف / Mohammad Abd El-Halim Ramadan
مشرف / Omneya Mohamed Helmy
مشرف / Walaa Ahmed Al-Shareef
تاريخ النشر
2019
عدد الصفحات
170 P. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
العلوم الصيدلية
تاريخ الإجازة
23/11/2019
مكان الإجازة
جامعة القاهرة - كلية الصيدلة - Microbiology and Immunology
الفهرس
Only 14 pages are availabe for public view

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Abstract

Background: Epidemiological studies have proved an association between drinking water sources and the incidence of H. pylori and Campylobacter spp. infection in developing countries. Aim: To investigate the role of water reservoirs as a potential source of H. pylori and Campylobacter spp. infection in Giza area, Egypt. Methods: A total of 125 water samples, from drinking water reservoirs, were collected from 13 districts of Giza governorate, Egypt. Physicochemical properties of the collected water samples including turbidity, color, odor, pH and chloride ion were determined. The filters obtained from the filtration of water samples were inoculated on a panel of different culture media including selective columbia blood agar (SCBA), modified columbia urea agar (MCUA), modified charcoal cefoperazone deoxycholate agar (mCCDA); the recovered isolated colonies were further identified by confirmatory biochemical reactions, Microscan WalkAway system or MALDI-TOF MS. Water samples were cultured in selective brain heart infusion broth (BHIB) supplemented with 20% horse serum, and selective Bolton broth; genomic DNA was extracted from the incubated cultures using phenol/chloroform/isoamyl alcohol extraction method. DNeasy® PowerWater® Kit for genomic DNA extraction from filtered water samples was used. PCR was used for the detection of H. pylori by virulence genes namely: glmM, ureA, cagA, vacA and Campylobacter spp. by cadF gene. All PCR amplified products were further sequenced