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نتائج البحث: 25 من أصل 170

دراسة التلازن لبعض ضمات الكوليرا المعزولة من مياه عراقية == A Study on Agglutination of Some Vibrio Cholerae Pacini Isolated From Iraqi Water

اسم المؤلف: ابراهيم محمد سعيد عبد الواحد شناوه
اسم المشرف: مها رؤوف السعد
الموضوع العام: علوم الحياة
السنة: 1976
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:

دراسة العلاقة بين الكوليراجين والسم المعوي التالف بالحرارة لبكتريا Escherichia Coli باستعمال بعض الاختبارات المصلية == Serological Study of The Relation Between Choleragen and Heat Labile Enterotoxin of Escherichia Coli

اسم المؤلف: بتول علي احمد الحيدري
اسم المشرف: مها رؤوف السعد
الموضوع العام: علوم الحياة
السنة: 1979
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:

عزل وتشخيص الاحياء المجهرية المستخدمة لوقود الطائرات النفاثة والسيطرة عليها بالمواد الكيمياوية == Isolation and Identification of Microorganisms Utilizing Jet Fuel and Control of Their Growth by Chemicals

اسم المؤلف: فادية فرج بني
اسم المشرف: ناصر عبد الحسين | الهام زكي سعيد
الموضوع العام: علوم الحياة
السنة: 1978
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:

الاستخلاص والتنقية الجزئية لحامض اللايبوتكويك من بكتيريا Enterococcus Faecalis لعزلات محلية من مصادر سريرية مختلفة == Extraction and Partial Purification of Lipoteichoic Acid From Enterococcus Faecalis Isolated From Different Local Clinical Specimens

اسم المؤلف: خمائل لطفي شاكر الطائي
اسم المشرف: لينه عبد الكريم | مي طالب فليح
الموضوع العام: علوم الحياة
السنة: 2006
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:

دراسة تنميط مستضدات كريات الدم البيضاء البشرية في حالات اضطرابات الغدة الدرقية المناعية للذات == Astudy of HlA Typing in Autoimmune Thyoid Disorders

اسم المؤلف: نوال محمد عتبة العقابي
اسم المشرف: مها رؤوف السعد | عبد الوهاب الشيخلي
الموضوع العام: علوم الحياة
السنة: 1998
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:

دراسة على السموم المعوية التالفة بالحرارة لبكتريا القولون Escherichia Coli الممرضة للامعاء المعزولة محليا

اسم المؤلف: ناهضة راضي الزاهد
اسم المشرف: مها رؤوف السعد
الموضوع العام: علوم الحياة
السنة: 1981
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:

استخدام الكحول المثيلي من قبل احياء مجهرية معزولة محليا

اسم المؤلف: ثامر عبد الرحمن عمران
اسم المشرف: ناصر عبد الحسين الهنداوي
الموضوع العام: علوم الحياة
السنة: 1980
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:

تاثير المقاومة للجنتامايسين على بكتريا P. Aeruginosa والبايوسين النقي

اسم المؤلف: ثامر محمد اسماعيل
اسم المشرف: فاروق ياس العاني | سامي عبد المهدي المظفر
الموضوع العام: علوم الحياة
السنة: 1983
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:

دراسة دور الجراثيم بتكوين بعض انواع حصى المرارة

اسم المؤلف: مثنى بديع فرحان العاني
الموضوع العام: علوم الحياة
السنة: 2002
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
مكان الجامعة: بغداد

تواجد وانتشار المجاميع المختلفة للكلوستريديوم بيرفرنجنز (ولشاى) في التربة المزروعة والمياه ومياه المجاري لمدينة بغداد

اسم المؤلف: شبر اسماعيل كاظم
الموضوع العام: علوم الحياة
السنة: 1974
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
مكان الجامعة: بغداد
الكلمات الدلالية:
  • كلوستريديوم بيرفرنجنز - البكتريات - اطروحات

Leptin Level in Obese Type 2 Diabetic Patients Treated with Metformin and / or without Insulin Therapy

اسم المؤلف: يقين حميد الموسوي
اسم المشرف: Sabah N. Alwachi | Isam N. Salman
الموضوع العام: علوم الحياة
السنة: 2009
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:

استخلاص و تنقية الالجنيت من عزلات بكتريا Pseudomonas aeruginosa ودراسة دوره في الامراضية == Extraction and purification of alginate from Pseudomonas aeruginosa isolates and study its role in pathogenesis

اسم المؤلف: لؤلؤه سعد زكي
اسم المشرف: رشید محجوب المصلح
الموضوع العام: علوم الحياة
السنة: 2009
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:

تاثير البروتين الرابط للGlucan (Glucan Binding Protein) في تكوين الغشاء الحيوي لبكتريا Streptococcus mutans وتعيين المثبطات الكيميائية له

اسم المؤلف: شيماء فؤاد رشيد الخزرجي
اسم المشرف: مي طالب فليح
الموضوع العام: علوم الحياة
السنة: 2010
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:

تاثير مستخلصات نبات عين البزون Catharanthus roseus في البكتريا المرضية المعزولة من الالتهابات الجلدية داخل وخارج الجسم الحي == In vitro and in vivo effect of Catharanthus roseus plant extracts on pathogenic bacteria isolated from skin infections

اسم المؤلف: عهود عبد الستارعبد الجبار المخزومي
اسم المشرف: عبد اللطيف محمد جواد | هند حسين عبيد
الموضوع العام: علوم الحياة
السنة: 2014
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:

دراسة التنميط الجيني وبعض عوامل الضراوة لبكتيريا Pseudomonas aeruginos == Study of Genotyping and Some Virulence Factors of Pseudomonas aeruginosa

اسم المؤلف: عباس فالح مهدي الارناؤوطي
اسم المشرف: رنا مجاهد عبد الله الشيخ
الموضوع العام: علوم الحياة
السنة: 2015
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:

دراسة لبعض عوامل الفوعة للعنقوديات السالبة لمخثر البلازما المعزولة من خمج الجلد من مستشفيات السليمانية == A study on some virulence factors of coagulase negative staphylococci isolated from skin infection in sullaimaniya hospitals

اسم المؤلف: نرمين نصر الدين فتحي
اسم المشرف: ﻤﻲ ﻁﺎﻟﺏ فليح
الموضوع العام: علوم الحياة
السنة: 2007
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Out of 110 clinical samples taken from different sources of burn and wound infections, 22 isolates (20%) of coagulase negative staphylococci (CNS) were isolated. The most common isolated species among CNS was S. epidermidis which was accounted for 11 isolates (50%), S. haemolyticus was the second with 3 isolates (13.64%), followed by S. hominis and S. sciuri with two isolates for each species (9.1%) and one isolate (4.54%) for each species including S. cohnii, S. lugdunensis, S. saprophyticus, S. xylosus. Some virulence factors of CNS were detected including the hemolysins, which were determined in 10 isolates (45.4%), lipase production in 15 isolates (68.1%), 9 isolates (81.8%) of S. epidermidis were positive for lipase activity, and the proteolytic isolates of CNS were 11 isolates (50%). The production of slime layer by Congo red agar method revealed 7 isolates (31.8%) of CNS and 3 isolates (27.2%) of slime layer - producing S. epidermidis, while production of this layer by tube method was determined in 2 isolates (18.18%) of 11 isolates of S. epidermidis. The ability of S. epidermidis to adhere to abiotic materials and biofilm formation in vitro was done by using polystyrene microtitre plates which appeared in 2 isolates (18.1%). Sensitivity test of the isolates using 18 antimicrobial agents showed that the vancomycin was the more effective on CNS which was susceptible to this antibiotic and reached to (90.9%), and the incidence resistance to β - lactams antibiotics was very obvious in cefotaxim (100%), penicillin (95.5%) and in amoxycillin (72%). The effect of subinhibitory concentration of antibiotics on the adherence ability of S. epidermidis was done and the results revealed that the clindamycin was the best antibiotic, while the vancomycin was the lees affecting on the adhering of S. epidermidis.

تكون الغشاء الحيوي بوساطة Klebsiella pneumoniae الملوثة للمثبتات الخارجية ومقاومته لمضادات الحياة == Biofilm Formation by The External Fixators Contaminating Klebsiella pneumoniae and Its Antibiotic Resistance

اسم المؤلف: مروى حميد مطشر الخفاجي
اسم المشرف: مي طالب فليح
الموضوع العام: علوم الحياة
السنة: 2008
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: شخصت 98 عزلة بكتيرية منماة بظروف هوائية من مجموع 100 عينة سريرية ماخوذه من الاخماج المصاحبة للمثبتات الخارجية المستعملة في جراحة العظام والكسور. شكلت البكتريا السالبة لملون غرام اعلى نسبة 51% (50 عزلة) من المجموع الكلي للعزلات، في حين شكلت البكتريا الموجبة لملون غرام 49% (48 عزلة) منها ، وكانت بكتريا Klebsiella pneumoniae هي المسبب الاكثر شيوعا لهذه الاخماج اذ عزلت بنسبة 74% (37 عزلة) من المجموع الكلي للعزلات السالبة لملون غرام . اجري اختبار حساسية عزلات K. pneumoniae لمضادات الحياة ، وتبين ان العزلات جميعها كانت حساسة لمضاد Amikacin (100%) ، ومقاومة للمضادات : Ampicillin ، وCefalexine ، وCefalothin ، وCefotaxime ، وCiprofloxacin ، وRifampin بنسبة 100% ، وقد كانت نسبة مقاومتها لمضادات Ceftazidime ، وStreptomycin ، وTobramycin ، وGentamycin ، وNeomycin ، وNitrofurantoin ، وNorfloxacin ، وTetracycline ، وNalidixic acid 94.5% و86.5% و86.5% و67.5% و59.5% و37.8% و35.1% و32.5% و24.3% وعلى التوالي . تم تحديد التراكيز المثبطة الدنيا لعزلات بكتريا K. pneumoniae لمضادات الحياة Cefotaxime ، وCeftazidime ، وNalidixic acid ، وAmikacin فبلغت 1024 مايكروغرام/مليليتر، و128 مايكروغرام/مليليتر، و64 مايكروغرام/مليليتر، و16 مايكروغرام/مليليتر على التوالي للعزلة K13 ، و1024 مايكروغرام/مليليتر، و64 مايكروغرام/مليليتر، و16 مايكروغرام/مليليتر، و4 مايكروغرام/مليليتر على التوالي للعزلة K51 . كما تم تحديد التراكيز القاتلة الدنيا لهذه المضادات وتراوحت مابين اكثر من 1024 مايكروغرام/مليليتر، و1024 مايكروغرام/مليليتر، و128 مايكروغرام/مليليتر، و32 مايكروغرام/مليليتر، على التوالي للعزلة K13 ، واكثر من 1024 مايكروغرام/مليليتر، و256 مايكروغرام/مليليتر، و32 مايكروغرام/مليليتر، و8 مايكروغرام/مليليتر على التوالي للعزلة K51. تم التحري عن قابلية عزلات K. pneumoniae على انتاج الطبقة اللزجة ، واظهرت نتائج طريقة الفحص بالانابيب ان 83.8% (31عزلة) كانت منتجة للطبقة اللزجة ، في حين اظهرت طريقة احمر الكونغو ان 97.3% (36عزلة) كانت منتجة للطبقة اللزجة . تم التحري عن فوعة عزلات K. pneumoniae المعزولة من الاخماج المصاحبة للمثبتات الخارجية وذلك باختبار قابليتها لربط البنفسج البلوري وكانت العزلات جميعها فائعة (Virulent) . اختبرت قدرة عزلات K. pneumoniae على انتاج الغشاء الحيوي باستخدام اطباق المعايرة الدقيقة فاظهرت النتائج ان العزلات جميعها كانت منتجة للغشاء الحيوي لكن بدرجات سمك متفاوتة ، وتراوحت قيم الامتصاصية مابين (0.111 - 2.899)، وكانت العزلة K13 هي العزلة الاكثر فعالية في انتاج الغشاء الحيوي حيث سجلت اعلى قيمة امتصاصية 2.899 . اختبر تاثير التراكيز تحت المثبطة الدنيا من مضادات الحياة Cefotaxime ، وCeftazidime ، وNalidixic acid ، وAmikacin في الاغشية الحيوية المتكونة بفعل العزلتين K13وK51 في اطباق المعايرة الدقيقة باعمار مختلفة 24 ساعة و48 ساعة ، واظهرت النتائج ان هذه التراكيز ثبطت التصاق البكتريا على سطح البولي ستيرين مما ادى الى انفصال الغشاء الحيوي ، كما تبين ان الاغشية الحيوية الاقدم اكثر مقاومة للعوامل ضد الميكروبية . تم تحديد التراكيز المثبطة الدنيا للغشاء الحيوي واظهرت النتائج انها اكبر بثلاث او اربع مرات من التراكيز المثبطة الدنيا لعزلات K. pneumoniae العالقة في الوسط الزرعي | Out of 100 clinical samples taken from infected external fixation devices used in orthopedic surgery 98 bacterial isolates grown in aerobic conditions had been diagnosed. The higher ratio 51% (50 isolates) of the total number of the isolates occupied by gram negative bacteria while gram positive bacteria represented the rest 49% (48 isolate) , Klebsiella pneumoniae was the most common aetiological agent of these infections which accounted 74% (37 isolates) of the total number of gram negative bacterial isolates. The sensitivity test against different antibiotics was done. It was found that all K. pneumoniae isolates (100%) were sensitive to Amikacin and resistant to Ampicillin, Cefalexine, Cefalothin, Cefotaxime, Ciprofloxacin, and Rifampin . While their resistance percetage to the antibiotics Ceftazidime, Streptomycin, Tobramycin, Gentamycin, Neomycin, Nitrofurantoin, Norfloxacin, Tetracycline, and Nalidixic acid were 94.5% , 86.5% , 86.5% , 67.5% , 59.5% , 37.8% , 35.1% , 32.5% , 24.3% respectively. Minimum inhibitory concentrations to K. pneumoniae isolates had been determined for the antibiotics Cefotaxime, Ceftazidime, Nalidixic acid, and Amikacin , they were 1024 Mcg/ml , 128 Mcg/ml , 64 Mcg/ml , and 16 Mcg/ml respectively for the isolate K13 , and they were 1024 Mcg/ml , 64 Mcg/ml, 16 Mcg/ml, and 4 Mcg/ml respectively for the isolate K51. Minimum bactericidal concentrations for the same antibiotics had been estimated and they were higher than 1024 Mcg/ml, 1024 Mcg/ml, 128 Mcg/ml, and 32 Mcg/ml respectively for K13 isolate, and higher than 1024 Mcg/ml, 256 Mcg/ml, 32 Mcg/ml, and 8 Mcg/ml respectively for the isolate K51. The ability of K.pneumoniae isolates to produce slime layer was detected , the results revealed that 83.3% (31 isolates) were slime layer producers by tube method, while 97.3% (36 isolates) were slime producers by congo red method. The virulence of K.pneumoniae isolates isolated from external fixators infections had been detected via detection the crystal violet binding ability of these isolates, all the isolates were virulent. The ability of K.pneumoniae isolates to produce the biofilm had been tested by using microtiter plates , results revealed that all the isolates were biofilm producers with different thickness degrees, absorbance values rendered between (0.111 - 2.899) , K13 was the best biofilm producer isolate, it,s absorbance value was 2.899 . The effect of subinhibitory concentrations of the antibiotics Cefotaxime, Ceftazidime, Nalidixic acid, and Amikacin , on biofilms formed by K13 and K51 isolates in microtiterplates in different ages , 24 hr and 48 hr had been tested , results revealed that these concentrations inhibited bacterial adhesion on polysteren surface and consequently causes biofilm detachment , also it was demonstrated that aged biofilms are more resistant to antimicrobial agents . Minimum inhibitory concentrations for the biofilm had been estimated, and the results revealed that these concentrations were three to four times higher than minimum inhibitory concentrations for the planktonic K.pneumoniae isolates.

دور بروتين A المستخلص من جدران خلايا Staphylococcus aureus في امراضية البكتريا == Role of Staphylococcus aureus cell wall protein A in the pathogenesis of the bacteria

اسم المؤلف: سمير عبد الامير عبد علي علـش
اسم المشرف: رشيد محجوب مصلح | علي عبد الرحمن طه
الموضوع العام: علوم الحياة
السنة: 2008
الموضوع الدقيق: الاحياء المجهرية
الدرجة: دكتوراه
الجامعة: جامعة بغداد
اللغة: العربية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: ا عتمد في اجراء هذه الدراسة على 20 عزلة مرضية من بكتريا Staphylococcus aureus ا خذت من مختبر الصحة المركزي مشخصة باستعمال نظام ابي للعنقوديات (API - Staph . Ident . System) . ا عيد تشخيص جميع العزلات عن طريق استخدام الاختبارات الكيموحيويه من اجل التثبت بشكل دقيق من هويتها ، وقد جاءت العزلات جميعها متوافقة مع تشخيص مختبر الصحة المركزي . ا ستخدم اختبار التلازن الدموي ( (Haemagglutination test في التحري عن وجود بروتين A في عزلات S . aureus المشخصة جميعا ، وقد اظهر هذا الاختبار تباينا ملحوظا في نسبة امتلاك هذه العزلات لبروتين A . فقد برزت العزلات ذوات الارقام 1 ، و5 ، و6 ، و7 ، و9 بوصفها عزلات ذات محتوى عال من بروتين A . اما العزلات ذوات الارقام 8 ، و10 ، و11، و12، و13، و14 ، و15، و17، و18، و19 ، و20 ظهرت انها ذات محتوى متوسط من بروتين A . فقط العزلة ذات الرقم 16 ظهرت انها فقيرة المحتوى من بروتين A . بينما كشف ووفق الاختبار المستعمل عدم امتلاك العزلات 2، و3 ، و4 اي محتوى من بروتين A . ا نتخبت العزلة رقم ( 1 ) كعزلة مثالية من اجل انجاز هذه الدراسة لكونها تميزت بمحتوى عال من بروتين A فضلا عن انها تقدمت على بقية العزلات في اعطاء النتيجة الموجبة لاختبار انتاج انزيم Coagulase ، وكذلك في اظهار تحللا كاملا وشديدا في اختبار انتاج حالة الدم Hemolysin . ا ستخلص بروتين A الخام (Crude protein A) على مرحلتين . كانت المرحلة الاولى باتباع طريقة (Lind , (1974 ( طريقة التعليق بالصوديوم ازايد ) بوصفها طريقة سهلة وغير مكلفة في الحصول على مستخلص بروتين A المرتبط بجدار الخلية العنقودية للعزلة رقم ( 1 ) (Cell - bound protein A) بشكل كامل مع الحفاظ وبدرجة عالية على وحدة التركيب البنائي لبروتين A من اية تشوهات . اما المرحلة الثانية كانت باتباع طريقة ( Seki et al .,( 1985 طريقة مكملة للطريقة الاولى وذلك بترسيب بروتين A الطافي بكبريتات الامونيوم ( 85 % اشباع ) مع بقاء بروتين A المترسب محتفظا بفعاليته . ا دخل مستخلص بروتين A الخام عملية التنقية ( Purification) وهي كذلك كانت على مرحلتين . المرحله الاولى استخدمت فيها طريقة كروماتوغرافيا التبادل الايوني (Ion - exchange chromatography) بعمود ( DEAE - Cellulose ). اما المرحلة الاخرى فقد تضمنت استخدام طريقة كروماتوغرافيا الترشيح بالهلام (Gel - filtration chromatography) بعمود Sepharose CL - 6B) ) . انتهى استخدام الطريقتين في الحصول على مستخلص بروتين A منقى ( Purified protein A ) .ومن اجل التحري عن احتفاظ مستخلص بروتين A الخام والمنقى بفعاليته استخدم اختبار الانتشار المناعي الثنائي في الهلام الذي اعطى نتيجة موجبة بتكون الخطوط الترسيبية التي نتجت من تفاعل مستخلص بروتين A الخام والمنقى مع IgG لمصل دم خنزير غينيا .قدر تركيز مستخلصات بروتين A ( الخام والمنقى جزئيا والمنقى ) باتباع طريقةBradford, ( 1976 ) . حيث بلغت التراكيز 63 مايكروغرام / مليلتر لمستخلص بروتين A الخام ، و42 مايكروغرام / مليلتر لمستخلص بروتين A المنقى جزئيا ، و36 مايكروغرام / مليلتر لمستخلص بروتين A المنقى .تم استخدام الفئران البيض من نوع ( Balb C ) من اجل الوصول الى التاثيرات المرضية لمستخلص بروتين A المنقى . حيث حقن المستخلص بطريقة الحقن داخل البريتون Intraperitonial injection)) بعدد سبع حقنات ، وبمعدل 0.1 مليلتر لكل حقنة ( ذو التركيز 36 مايكروغرام / مليلتر ) ، يفصل بين حقنة واخرى يوم واحد . اظهرت مجموعة فئران البحث المحقونة ببروتين A المنقى على المستوى السريري خمولا عاما بدا واضحا بعد الحقنة السادسة . لم تظهر اية تغيرات مظهرية جلدية في مناطق الحقن كما لم تحدث وفيات . بعد قتل الفئران وتشريحها جميعا ا ستاصلت اعضاء القلب ، والطحال ، والكبد ، والكليتين ، والامعاء ، والمعدة ، واخيرا الرئة . وبالموازنة مع اعضاء فئران السيطرة لوحظ حدوث تضخم كبير في الطحال . كما اظهر الكبد تضخما ملحوظا وهذا سجل في الفئران المحقونة ببروتين A المنقى . لم يسجل حدوث تغيرات على المستوى المظهري في اعضاء القلب ، والامعاء ، والمعدة ولكن لوحظ وجود بقع سوداء اللون على السطح الخارجي لنسيج الكبد ، والكليتين ، وهو ايضا سجل في فئران الدراسة اجمع .اهم ما برز في هذه الدراسة هو حجم التاثير المرضي الذي اصاب عضو الرئة حيث ظهر بشكل غريب فقد بدا النسيج يميل الى السواد ببهوت وهو ما كان واضحا في سبعة من فئران الحقن ، اما الثلاثة الباقية شوهدت الرئة فيها خلال التشريح وهي مغطاة بعض من اجزائها بالدم .كشف الفحص النسيجي لاعضاء القلب ، والامعاء ، والمعدة عدم وجود اية تاثيرات مرضية ناتجة من حقن بروتين A المنقى . اما الطحال فقد شهد حدوث توسع كبير في منطقة اللب الابيض White Pulp)) مع احتقان دموي بارز وانتشار للخلايا المولدة للصفيحات الدموية (Megacaryocytes) . اما الكبد فقد برز فيه حدوث تلف بسيط (Mild degenerative change) في خلايا الكبد مع ارتشاح خلايا احادية النواة (Monocytes) خصوصا في المنطقة البوابية التي بدت متوسعة نوعا ما . كما لوحظ زيادة في خلايا كبفر ((Kupffer cells في عموم نسيج الكبد . الكليتين شهدت بروز زيادة في الخلايا المكونة للكبيبة الكلوية ( Glomeruli) والتي يطلق عليها ( Mesengial cells ) .عضو الرئة تضمن الفحص النسيجي له تاثيرات عدة وهي كما يلي : 1 - احتقانات دموية كبيرة ( Bloody congestions ) .2 - وذمة ( Oedema ) .3 - ارتشاح خلايا التهابية ( Inflammatory cells infiltration) .4 - توسع في الفسح القصبية ( Alveolar spaces) مكونا ما يسمى بظاهرة Emphysema)) اي انتفاخ حويصلات الرئة . بدت الرئة للفئران المحقونة جميعا ببروتين A المنقى اكثر الاعضاء التي اظهرت تضررا نسيجيا كبيرا موازنة بالضرر في بقية الاعضاء .تم اجراء اختبار التحري عن السمية الخلوية لبروتين A المنقى باستخدام تقنية مزرعة الخطوط الخلوية الطبيعية ( Normal cell lines - culture ) حيث اعطى الاختبار نتيجة سالبة اي عدم امتلاك بروتين A المنقى تاثيرا سميا (Toxic effect) في الخلايا النامية . | This study dealt with ( 20 ) diagnosed isolates of Staphylococcus aureus by "API - Staph . Ident . System". which were taken from the central health laboratory . The diagnosis was repeated so as to confirm the identity of those isolates by using biochemical tests whose results were the same as those of the central health laboratory .The haemagglutination test was used to investigate the presence of protein ( A ) in all S . aureus isolates . The results markedly showed differences in content concerning the ratio of this protein , thus isolates numbered 1 , 5 , 6 , 7 and 9 gave high content of protein ( A ) , but the isolates numbered 8 , 10 , 11 , 12 , 13 , 14 , 15 , 17 , 18 , 19 and 20 gave medium content of protein ( A ) . Isolate numbered 16 was the only isolate that has low content of protein ( A ) . On the other hand , isolates numbered 2 , 3 and 4 gave no content of protein ( A) .The isolate number ( 1 )has been chosen as an optimal isolate to accomplish this study , Because of its high content of protein ( A ) , furthermore it was the best isolate in getting positive result concerning the test of coagulase production , and in giving a complete and intensive result concerning the test of hemolysin production . Crude protein ( A ) was extracted by two steps : Lind method ( Lind , 1974 . ) "Suspending in sodium azide" was followed at the first step as an easy and a cheap method in getting a thorough cell - bound protein ( A ) extracted from the isolate number ( 1 ) with high preservation of the structural unit without any deformation .The Seki et al .,( 1985 ) method was followed in the second step as a completion method to the first one , by the precipitate of the supernatant protein ( A ) using ammonium sulfate ( 85 % saturation ) . The function of precipitated protein ( A ) was perfect . In order to get a purified protein ( A ) extract from crude protein A , purification was accomplished by two steps : Ion - exchange chromatography by DEAE - cellulose column was used in the first step , While Gel - filtration chromatography by Sepharose CL - 6B column was used in the second step . Double immunodiffusion in gel was used to investigate the preservation of the crude and purified protein ( A ) with its full function . This test gave a positive result by forming the precipitate lines as a result of the interaction between protein ( A ) ( Crude and Purified ) and IgG of guinea pig sera .Bradford method was used to estimate protein ( A ) extracts concentration ( Crude , Partial purified , Purified ) . The estimation was 63 microgram / ml for crude extract , 42 microgram / ml for partial purified extract and 36 microgram / ml for purified extract .white mice ( Balb C ) were used to investigate the pathogenic effects of purified protein ( A ) . Intraperitonial injection method was used to inject 0.1 ml of 36 microgram / ml of purified protein ( A ) for 7 times with a one - day separating period . The injected mice with purified protein ( A ) showed general weakness which was very clear after the sixth injection . there were no phenotypic dermal change in the injection area , and no dead mice as well .After killing and dissecting of all the mice , the organs of heart , spleen , liver , kidney , intestine , stomach and lung were eradicated . There were a great enlargement in spleen and a little in liver in all injected mice in comparison with the control mice . No phenotypic changes appeared in heart , intestine and stomach , but black spots were shown on the outer surface of kidney and liver tissue which were presented in all the injected mice . The most important results in this study is the great size of pathogenic effects in lung . The shape of its tissue seemed strange and tended to be faint black with which was obvious in seven mice . The lung of the three others ( some parts ) showed during anatomy covered by blood .The histological check for heart , intestine and stomach showed no pathogenic effects resulted from protein ( A ) injection . In the spleen , there was a huge expanding in the white pulp region , with blood congestion while the spreading of megacaryocytes has increased . The liver showed mild degenerative change in liver cells with monocytes infiltration especially in the entrance region which appeared expanded . Also there was an increase in kupffer cells in all liver tissue .Kidney showed increase in mesengial cells which are concedered the forming units of glomeruli .The histological check of lung included the following : 1 - Bloody congestions .2 - Oedema .3 - Inflammatory cells infiltration .4 - Alveolar spaces expanding forming '' Emphysema '' .The lung was the most effected organ that showed tissue injury among other all organs . The normal cell lines - culture technique was followed to investigate cellular toxicity of the purified protein ( A ) which gave a negative result , that means , there was no toxic effect of purified protein ( A ) on the growth cells .

دراسة بعض الجوانب المناعية والبكتريولوجية لمرضى ذات الرئة Pneumonia == Study Some Immunological And Bacteriological Aspects of Pneumonia Patients

اسم المؤلف: كرم رياض حسن الجراح
اسم المشرف: رسمية عبد ابو ريشة
الموضوع العام: علوم الحياة
السنة: 2014
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: جمعت 120 عينة قشع من اشخاص مصابين بمرض ذات الرئه للمدة من ايار 2013 الى شباط 2014 من ثلاثة مستشفيات في مدينة بغداد وشملت مستشفى اليرموك التعليمي, مستشفى دار التمريض الخاص, مستشفى بغداد التعليمي. شخصت العينات باستخدام الفحوص البايوكيميائية, نظامApi 20 E و| From May 2013 to Feburey 2014, 120 sputum and Aspiration samples of patients with pneumonia disease were collected from different hospitals in Baghdad included : Al Yarmouk Teaching Hospital, Hospital Nursing Home sector and Baghdad Teaching Hospital. All samples were diagnosed by biochemical tests, Api 20 E and Api20 strep. Systems, The results was found to be 28 isolates (23.3%) belong to K.pneumoniae, 26 isolates (21.7 %) belong to S.pneumonia while 66 isolates(55%) belong to causes : E.coli, Pseudomonas sp., Moraxella catrrhalis, S.pyogens, Monilia and S.aureus. From (55) blood samples of pneumonia patients and 30 blood samples from healthy individuals, number of white blood cell (Neutrophil) counts were measured, percentage of Neutrophil cell count in female (53%) higher than the cell count in male(47%). Some markers of pneumonia disease were studied such as ratio of infection between male and female, chronic and acute cases and smoker and non smoker, the results were showed the ratio of infection in female more than in male, (60%, 40%), respectively. And number of acute cases of pneumonia patients 41(74.55%) more than chronic cases 14(25.45%). While infection ratio in smoker patients more than nonsmoker patients at ratio 24(57.14%)18(42.86%), respectively. The result of interleukin - 8 level through acute and chronic phases in pneumonia patients sera was showed high level in patients compared with healthy persons (86.4403 ± 25.50919 vs. 58.7636 ± 4.73152 pg / ml, respectively) with a non significant difference statistically (P?0.05). Also in the age group (age 15 - 60years), The results showed the results interleukin 8 levels higher than the age groups of (2month - 3years) and (age 60 - 85) (93.63 ± 51.65, 68.88 ± 17.17, 65.68 ± 11.73 pg / ml, respectively) with non significant difference (P?0.05). The result of Leukotriene B4 level through acute and chronic phases in pneumonia patients sera showed high level in patients compared with healthy persons (36.00 ± 3, 82 vs. 25.96 ± 4.44 pg / ml, respectively) with a significant difference (P?0.05). Also in the age group (two months - 3 years) were showed the results interleukin 8 levels higher than the age groups (age 15 - 60) (age (60 - 85)(33.61 ± 11.06, 19.29 ± 4.67, 16.86 ± 4.51 pg / ml respectively) with no siginificant difference (P?0.05), the correlation coeifficient between interleukin - 8 and leukotriene B4 was (0.12) with no siginificant difference. The phagocytic activity was determined in pneumonia patients sera according to measurement C3 protein level through acute and chronic phases, the result were showed the ratio of C3 protein levels in healthy persons more than in patients (135.93 ± 12.74, 133.19 ± 12.01 pg / ml, respectively) with a difference was not significant statistically (P?0.05).

التمنيع باضداد الخمل النوع الاول المنتجة من بكتريا الاشريكية القولونية المسببة لالتهاب المجاري البولية ضد استيطان واصابة المثانة == Immunization With Type 1 Fimbriae of Uropathogenic Escherichia Coli Against Colonization And Infection of Bladder

اسم المؤلف: اروى علي شكر
اسم المشرف: رسمية عبد ابو ريشة
الموضوع العام: علوم الحياة
السنة: 2014
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Between September and November 2013 a total of 140 urine specimens obtained from patients in Al - Kadhmiah Teaching Hospital, Ibn - Al Naffees Teaching Hospital, and Educational Laboratories in Medical city. These midstream urine specimens were obtained from patients clinically suspected to have urinary tract infection (UTI) in sterilized containers. All specimens were processed immediately after collection.A total number of 140 specimens of mid - stream urine were collected from patients suffering urinary tract infection symptoms. These isolates were obtained from 41 male and 99 female patients. They were distributed in the age group of 5 - 60 years old. All specimens were identified using biochemical tests and API 20 E system. 60 (42.85%) of urine specimens was Escherichia coli and 15(10.71%) of specimens growth was Klebsiella spp. and 25(17.85%) growth was Proteus spp. and 40 (28.57%) was G+ve bacteria.The adherence ability of E.coli isolates were evaluated by using Congo red agar and detected their ability to produce biofilm by using methylene blue staining technique in polystyrene microtiter plates and then Optical density was determined at 580 nm.All sixty isolates of E.coli were grown on Congo red agar medium to detect their adherence ability. Twenty (33.3%) isolates were given negative result by forming pink colonies on congo red agar, were as, forty (66.6%) isolates were given positive result by forming black colonies with a dry crystalline. Three isolates give strong results E.coli (13, 8, and 40). Consistency indicated biofilm production by microtiter plate. E. coli 40 which isolated produced the thickest biofilm (O.D. : =3.17).Type 1 fimbriae expression by E.coli 40 isolate was detected by mannose - resistant hemagglutination (MRHA) of human blood group (O) IRBCs in the presence of 2% D - mannose. The isolate showed strong MRHA characteristics of type 1 fimbriae under microscope (40x). The E.coli E.40isolate which produced the thickest biofilm and gave strong MRHA was elected to be the source of type 1 fimbriae.Type 1 fimbriae was extracted by heating and mechanical shearing and partially purified by Ultracentrifugation (48, 000xg for 3hrs). SDS - PAGE with a molecular weight 20, 000 Dalton.Anti - type1 fimbriae antisera were prepared in rabbits. The specificity and titration of anti - type1fimbriae antibodies were determined using IgG protein by radial immunodiffusion plate and bacterial agglutination. IgG antibodies to fimbriae type 1 were also detected in rabbit sera from immunized rabbit and non - immunized. Immunized rabbit test 1 had increases in Fim1 - specific IgG antibodies (9.5) mg/dl. Immunized rabbit test 2 had increases in Fim1 - specific IgG antibodies (8.6) mg/dl. The non - immunized rabbit had no increase in absolute IgG antibodies to Fim1.The antisera agglutinated bacterial cells up to 1/80 dilution confirming the presence and titer of specific antibodies against type1 fimbriae.The microtiter plate method was applied to estimate the role of the prepared anti - type1fimbriae antibodies in reducing the biofilim formation by E.coli. Prevention of bacterial adherence and subsequent biofilm formation to polystyrene microtiter plate was studied by employing different dilutions (1/10, 1/20, 1/40, 1/80, 1/160, 1/320, 1/640) of rabbit sera containing anti - type 1 fimbriae antibodies. The maximum inhibition of biofilm formation in terms of optical density (580 nm) was found in lowest dilution (1/10) (highest concentration of Abs). However, the minimum inhibition was observed in highest dilution of rabbit antisera (1/640) (lowest concentration of Abs). Here the inhibition occurs in a dose dependent manner as the biofilm formation increased dramatically with increasing in antisera dilution. The results also showed that there is a significant difference(P<0.05) among data treated with sera and data without sera and among serial dilutions.General urine examination and culture for urine that absorbed from test 2 and control was done (GUE) show that pus cell in urine was (1 - 2/HPF). There was no growth of bacteria in urine culture.The Histological section show that the Control and test 1 rabbit (have been immunized with fimbriae and adjuvant and injected with E.coli intra muscular) and Test 2rabbit (that has been immunized with fimbriae and adjuvant and injected with E.coli directly in bladder has normal epithelial cells and mucosa.

تاثير انزيم SNase المنقى من العنقودي في الغشاء الحياتي للايشيركية القولونية والكليبسيلا الرئوية == Impact of Snase Purified From Staphylococcus Aureus On Biofilm of Klebsiella Pneumoniae And Escherichia Coli

اسم المؤلف: هند تحسين ابراهيم
اسم المشرف: حارث جبار فهد المذخوري
الموضوع العام: علوم الحياة
السنة: 2014
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: SDS - PAGE showed that a single sharp band with an approximately 16.8 KDa molecular weight has been seen. A matter indicates that the enzyme is consistently pure. PCR technique was applied to approve the existence of nuc gene in S.aureus Nevertheless, only those which depicted positive results on DNase agar harboured nuc gene, as it is specified by single band appearance of nuc at assumed molecular weight (ca. 255 pb) of marker that being used. The current study findings highlighted the participation of SNase purified from S. aureus in significant (P< 0.05) preventing biofilm formation by E. coli and K. pneumoniae compared with untreated controls. Evidently, the inhibitory effect of SNase on biofilm formation is undoubtedly perceived, indicating the degradation of the structural major component of biofilm formation (i.e. extracellular DNA). Results revealed that SNase was able to significantly (P< 0.05) reduce the number of the uropathogens; E. coli and K. pneumoniae attached to the uroepithelial cells. 1 Chapter one : Introduction and literature Review 1. Introduction and Literature Review 1.1. Introduction Staphylococcus aureus is a persistent human pathogen that is responsible for a range of diseases that vary widely in clinical presentation and severity. The pathogenesis of S. aureus infection is a complex process involving a diverse array of secreted and surface - associated virulence determinants that are coordinately expressed at different stages of infection (Loughman et al., 2009). Escherichia coli is a genetically diverse species that causes a variety of infections which fulfill many or all of the proposed criteria for biofilmassociated infections (Kaper et al., 2004). Klebsiella pneumoniae is an opportunistic pathogen responsible for a wide range of nosocomial infections. One important factor associated with virulence in K. pneumoniae is its capacity to adhere to surfaces and form biofilms (Cruz et al., 2012). Bacteria often exist as sessile communities called biofilms which are exquisite structures caused by a genetically programmed developmental process. It is estimated that biofilms are involved in 65% of human bacterial infections, since cells in biofilms are 1000 times more resistant than cells in the planktonic state, making medical treatments fail (Shal? et al., 2011). Extracellular DNA (eDNA) plays a significant role in biofilm formation, as revealed by studies in several bacteria including E. coli (Nakao, 2012) and K. pneumoniae (Whitchurch et al., 2002); however, there is no definite proof on a cause - and - effect relationship between DNA release and biofilm formation (Beenken et al., 2012) or becomes a key component of the macromolecular scaffold in many different biofilms (Jakubovics et al., 2013). In rare cases eDNA has been shown to inhibit bacterial settlement. Therefore, it is possible that nuclease mediated eDNA degradation would therefore promote adhesion. Consequently, it is not clear whether microbial nucleases contribute to the gross biofilm structure in clinically relevant situations (Sheilds et al., 2013). 2 Chapter one : Introduction and literature Review All previous studies used both commercial bovine and recombinant human DNaseI in the disruption of medically important biofilms; whilst, extracellular nuclease of S. aureus (SNase) was used against biofilm of S. aureus themselves (Benenken et al., 2012b ; Kiedrowski et al., 2014). Thus, to date, the role of S. aureus exonucleases in biofilm of other bacteria remains unclear. However, in the present study SNase is used against biofilm of other bacterial species (viz. K. pneumoniae and E. coli). To address this, the following steps were undertaken : 1 - Investigating the negative impact of SNase extracted from S. aureus on K. pneumoniae and E.coli biofilm formation. 2 - Studying the preventive activity of SNase on the adherence of K. pneumoniae and E. coli on uroepithelial cell.

التحري عن بعـض عوامل الفوعة لبكتريا المكورات Enterococci المعوية المقاومة للمضاد الحيوي الفانكومايسين == Detection of Some Virulence Factors of Vancomycin - Resistant Enterococci

اسم المؤلف: حيدر صباح كاظم الخماسي
اسم المشرف: مي طالب فليح
الموضوع العام: علوم الحياة
السنة: 2014
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: تم الحصول على (20) عزله لبكتريا المكورات المعوية البرازية من اصل (135) عينة جمعت من مستشفى مدينة الطب ومستشفى الكندي وهي كما ياتي (15 عينة الادرار, 60 عينة دم, 50 عينة من قنوات الجذر للاسنان و10 عينة من الحروق).اختبرت الحساسية لهذه العزلات العشرون لـ 11 | Clinical sampling was carried out between September and December 2013, Twenty Enterococcus faecalis isolates were obtained from 135 clinical specimens. The samples included of patients in Medical City Hospital and Al - kindy Hospital (15 urine, 60 blood, 50 root canal and 10 wound swabs) Antibiotics susceptibility test for 20 isolates was done against 11 antibiotics, it was revealed that the isolates showed multi drug resistance were (18) isolates. The vancomycin susceptibility was determined by the minimum inhibitory concentration (MIC). Resistant and intermediate resistant to vancomycin was distributed among isolates at a ratio of 65% and 20%, respectively. Imipenem was found to be the most bactericidal agent against E. faecalis isolates E. faecalis virulence factors were detected phenotypically, The results showed that all isolates (100%) were hemolysin, protease and aggregation substance producer. 30% of isolates showed an ability to produce gelatinase. While (40.7%) of the isolates were a lipase producer. The results of the tube method showed that all E. faecalis isolates (100%) were slime layer and biofilm producer but the amount of adherent layer were different among the isolates ranged from strong to moderate and weak.The extracted DNA was subjected to Polymerase chain reaction (PCR) technique in a monoplex pattern to amplify the virulence factor Enterococcal Surface Protein (esp) which is chromosomal, results of this investigation showed that 20 (100%) E. faecalis isolates gave the amplicon size 933 base pair for the esp gene.The genetic determinants of Vancomycin - Resistant vanA and vanB genes were amplified using monoplex and multiplex PCR techniques in order to identify vancomycin resistant (van+) and sensitive (lacking van) among (13) E. faecalis. The vanA, vanB genes were detected in 11 and 4 E. faecalis isolates, respectively. The results of monoplex and multiplex PCR revealed that the molecular weight of vanA and vanB genes were 550 and nearly 600 bp, respectively. The results revealed that the vanA and vanB amplicons have a genetic variation in their molecular weight during the electrophoresis of PCR product.

الدور الوقائي لبكتريا البفديس ضد خمج الفئران ببكتريا الاشيريكيا القولونية المنتجة لذيفان الشيكا == The Protective Role of Probiotic Bifidobacterium Against Mice Infection With Shiga Toxin Producing E.Coli O157 : H7

اسم المؤلف: سمر مصطفى محمد
اسم المشرف: شادان عباس الوانداوي
الموضوع العام: علوم الحياة
السنة: 2014
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: Six Bifidobacterum isolates were isolated from fully breast - fed healthy infant faeces on reduced de Man Rogosa and sharp medium (MRS - C). Isolates identified on the basis of, colonial and microscopical properties, biochemical tests, and fructose - 6 - phosphate phosphoketolase enzyme (F6PPK) activity assay in cellular extracts. Carbohydrates fermentation profile used for identification of isolates to species level. All bacterial isolates diagnosed as Bifidobacterium genus where in this study B. adolescntis was the predominant species (50%), (B4, B5 and B6), followed by B. breve (B3), B. longum (B1) and B. dentium (B2) each one represent 16.67%.Bifidobacterium isolates were screened for their antagonistic effects against test organism, clinical isolate of shiga toxin producing E.coli O157 : H7 (STEC), using agar - well diffusion method. The isolates B3 and B6 showed clear inhibitory actions, 22 mm and 15 mm diameter of inhibitions zones, respectively. The rest of the tested isolates did not pronounce any inhibitory activity.B. breve in vivo antagonistic behavior and the possible protective effects against STEC was evaluated, using streptomycin treated murine model. Murine intestines was stably colonized orally with B. breve for 14 days, in conjunction mice were challenged orally with STEC, 103 CFU / mouse / day on day 8 of experiment. Bacterteriological analysis of mice faeces at time intervals, was indicated high levels of bacterial colonization were achieved in intestine by B. breve and STEC.Colonization of mice intestine by B. Breve did not inhibited STEC cells from proliferation during infection phase. Hence, the excretion level of STEC in faeces reached to 2.4 x 10 6 CFU/ g of faeces.STEC infected mice showed no severe clinical signs, characterized by hairloss, lethargy, paralysis of fore limbs, and shed of loose faeces. In the B. breve - colonized group, the mentioned clinical signs were almost completely inhibited, except the lethargic of some animals.Immunological studies showed an increase in the levels of sIgA by 2.7 - fold from that of blood IgA in B. breve - colonized mice while, reversed values were recorded in mice infected with STEC, blood IgA level was 1.95 - fold higher than that of sIgA.Histological changes in spleen, liver, kidney, and intestine tissues of mice were studied. The histological sections clarified the protective roles of B.breve, where no effective histological disorders were appeared in B.breve and STEC - colonized mice. In the STEC - infected mice, the pathological abnormalities within the kidney was the predominant, diagnozed as ulcers in the lining membranes, glomerular and tubular epithelium necrosis, without evidence of glomerular thrombi, mild damages was appeared in liver and spleen, and characteristic attaching and effacing (A / E) lesions appeared in the large intestine sections

التحري عن جين الاوتولايسين في المكورات العنقوديه البشروية المقاومة لمضاد الفانكومايسين == Autolysin Gene Detection In Vancomycin Resistant Staphylococcus Epidermidis

اسم المؤلف: مريم خميس عبد ربة بريس
اسم المشرف: مي طالب فليح
الموضوع العام: علوم الحياة
السنة: 2014
الموضوع الدقيق: الاحياء المجهرية
الدرجة: ماجستير
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: من مجموع مئة عينة سريرية جمعت من مصادر مختلفة شملت الحروق والدم والجروح ومسحات انفية, تمكنت 90 عزلة من النمو على اكار المانيتول الملحي , ومن بينهم 40(44.4 %) عزلة عائدة لبكتريا المكورات العنقودية المنتجة للانزيم المخثر للبلازما و50 (55.5%) عائدة لبكتريا ا | Out of one hundred clinical samples were taken from different sources which include burns, blood cultures, wounds and nasal swabs infections ; 90 isolates developed growth on mannitol salt agar. Among these, 40 (44.4%) were Coagulase positive (Staphylococcus aureus) isolates, 50 (55.5%) belong to coagulase negative staphylococci in which Staphylococcus epidermidis isolates were 30(60%). The pattern of antibiotic susceptibility of Staphylococcus epidermidis isolates to 12 antibotics (Amoxiclav, Ceftazidim, ciprofloxacin, clindamycin, Erythromycin, Gentamycin, Imipenime, Penicillin G, Tetracycline, Rifampin , Methicillin, and Vancomycin) were determined using disc diffusion method. The results revealed that resistance to Penicillin G10 and Amoxiclav (Amoxicillin - clavulanic acid) were 100%, Methicillin were 93%, Erythromycin were 90%, Gentamycin and Clindamycin were 70%, Tetracycline and ceftazidim were 75%, Ciproflaxacin were 60%, Rifampin were30%. 95% of S.epidermidis isolates were sensitive to Imipenim and 5% of them were intermediate resistant, while these isolates showed 90% sensitivity to vancomycin. 19 isolates were multidrug resistance. Minimum inhibitory concentration of S.epidermidis isolates to vancomycin, was determined. The results revealed that (12) S.epidermidis isolates (40 %) were vancomycin resistant, the MIC of them were between 256 ?g\ml and 32 ?g\ml, (4) S.epidermidis isolates (13.3%) were intermediate resistance, the MIC to 3 of them were 16 ?g\ml and the last was 8 ?g\ml. Some virulence factors of VRSE and VSSE were detected including the hemolysin, protease, lipase and urease. The S. epidermidis isolates were produce hemolysin, protases, lipase and urease, were 100%, 100%, 25%, 100% respectively in VRSE, while in VSSE 100%, 100%, 60%, 100% respectively. The isolates were subjected to polymerase chain reaction (PCR) technique in monoplex pattern to amplify resistant incoding gene : the vanA, vanB and autolysine gene aae gene. The results by this study showed that 12 (40%) S. epidermidis isolates gave the implicone size (1030 base pair) of the vanA gene. However the results of MIC and PCR were similar but no any isolates gave product for presence of vanB gene. All S.epidermidis were able to produce implicone size(858bp) of aae gene. The effect of vancomycin resistant S. epidermidis on cell autolysis activity was detected by whole cell autolytic assay.The results revealed that there was significant difference among three isolates, the VSSE isolate (S.epidermidis 22) have the highest autolytic activity in the presence of antibiotic, followed by the VRSE isolate (S. epidermidis 1) and the VISE isolate (S. epidermidis14) which was the lowest autolytic activity with the presence of antibiotic. The result of transmission electron microscope (TEM) showed that the VRSE isolates (S.epidermidis 1) have thicker cell wall followed by VISE (S.epidermidis 14) isolates.However, the VSSE (S.epidermidis 22) didn't showed any cell wall thickening.

تعدد الاشكال الوراثي للحركيات الخلوية وHLA - DQB1 في مرضى السل الرئوي == Genetic Polymorphisms of Cytokines And HLA - DQB1 In Pulmonary Tuberculosis Patients

اسم المؤلف: خلود كريم حسن
اسم المشرف: علي حسين ادحية
الموضوع العام: علوم الحياة
السنة: 2014
الموضوع الدقيق: الاحياء المجهرية
الدرجة: دكتوراه
الجامعة: جامعة بغداد
اللغة: الانكليزية
مكان الجامعة: بغداد
الصفحات الاولى:
المستخلص: The present study aimed to understand the correlation between serum level of nine cytokines (IL - 1?, IL - 1RA, IL - 2, IL - 4, IL - 6, IL - 10, IL - 12, IFN - ? and TNF - ?) and their genetic polymorphisms at 16 gene positions defined by sequence specific primer - polymerase chain reaction (SSP - PCR) in pulmonary tuberculosis (PTB) patients, and in addition HLA - DQB1 gene polymorphism was also defined by SSP - PCR to determine their role in susceptibility or resistance to M. tuberculosis. Finally, serum level of cortisol was also determined in the patients.Ninety four Iraqi Arabs PTB patients (70 males and 24 females) were enrolled in the study. They were referred to the Institute of Chest and Respiratory Diseases in Baghdad for diagnosis and treatment during the period May - October 2012. A control sample of 80 apparently healthy individuals was also included and matched patients for gender (60 males and 20 females) and ethnicity. The results are summarized in the following : 1. A significant increased serum level of IL - 1? (24.16 ± 8.82 vs. 3.20 ± 1.18 pg/ml), IL - 1RA (41.31 ± 6.64 vs. 16.85 ± 5.50 pg/ml), IL - 2 (17.63 ± 3.53 vs. 7.80 ± 1.10 pg/ml), IL - 4 (9.56 ± 2.60 vs. 3.81 ± 1.70 pg/ml), IL - 10 (34.49 ± 4.60 vs. 7.61 ± 1.70 pg/ml), IL - 12 (25.16 ± 5.85 vs. 7.70 ± 1.12 pg/ml) and TNF - ? (22.52 ± 4.41 vs. 4.97 ± 1.15 pg/ml) was recorded in PTB patients compared to controls. Also, Cortisol serum level was significantly increased in patients (215.47 ± 1.33 vs. 38.63 ± 1.74 ng/ml).2. Cytokine gene polymorphism analysis revealed that neither genotypes nor alleles of IL1A - 889, IL2 - 330, IL2+166, IL4 - 590, IL4 - 33, IL6+565, IL10 - 819, IL10 - 592, IL12B - 1188 and TNF - 238 genes showed a significant variation between PTB patients and controls. In contrast, the frequency of TT genotype of IL1RN gene at position mspal 11100 showed a significant (P = 0.004) increase in PTB patients compared to controls (65.9 vs. 43.7%). For IL4 - 1098, the frequency of TT genotype was also significantly (P = 0.048) increased inpatients (82.9 vs. 70.0%). At position - 174 of IL6 gene, a significant (P = 0.002) increased frequency of GG genotype was observed in patients (55.3 vs. 31.2%). For IL10 gene, only GG genotype at position IL10 - 1082 was observed with a significant (P = 0.045) increased frequency in patients (18.1 vs. 7.5%). At position - 308 of TNF gene, a significant (P = 6.9 x 10 - 5) decreased frequency of GG genotype was observed in patients (60.6 vs. 87.5%), while GA genotype was significantly (P = 1.3 x 10 - 4) increased (38.2 vs. 12.5%). Finally, the frequency of AA genotype of IFNG gene at position +874 demonstrated a significant (P = 0.006) increase in PTB patients (55.3%) compared to controls (33.7%).3. To determine the impact of cytokine genotypes on cytokines serum level, PTB patients and controls were distributed according to their serum level in the three genotypes of each cytokine. It was found that CC genotype of IL1RNmspal 11100 in patients was observed with the highest IL - 1RA level (52.16 ± 5.81 pg/ml) compared to TT (41.39 ± 3.23 pg/ml) or TC (38.10 ± 4.54 pg/ml) genotype. The TT genotype of IL2 at position - 330 also showed the highest level of IL - 2 (22.16 ± 4.31 pg/ml) compared to TG (17.59 ± 3.40 pg/ml) or GG (13.68 ± 3.53 pg/ml) genotype in patients. The IL4 - 1098 TT genotype showed the highest level of IL - 4 in patients (10.38 ± 2.21 pg/ml) compared to TG (6.09 ± 1.20 pg/ml) or GG (3.93 ± 0.80 pg/ml) genotype. For IL10 gene, the GG genotype of IL10 - 1082 recorded the highest level of IL - 10 (40.67 ± 2.96 pg/ml), which was significantly different from AA genotype (26.66 ± 5.65 pg/ml). At position - 308 of TNF gene, serum level of TNF - ? in GG genotype of patients demonstrated a significant increased mean compared to genotype GA (24.76 ± 1.30 vs. 19.15 ± 1.12 pg/ml). At position - 238, TNF GG genotype showed a significant increase level of TNF - ? (23.02 ± 2.91 pg/ml) in patients compared to AA genotype (17.18 ± 1.53 pg/ml) of patients. Finally, IFNG+874 AA genotype was observed with the highest IFN - ? level in patients (11.07 ± 1.12 pg/ml) compared to AT (7.97 ± 1.81 pg/ml)or TT (6.10 ± 2.20 pg/ml) genotype. In contrast, no such differences were observed in controls.4. Out of the five encountered HLA - DQB1 alleles, DQB1*03 showed a significant (P = 0.005) increased frequency in PTB patients compared to controls (71.3 vs. 50.0%). It was also observed that heterozygosity at such gene locus was significantly (P = 0.03) more frequent in patients than in controls (93.6 vs. 82.5%), while homozygosity was observed with a less percentage frequency in patients compared to controls (6.4 vs. 17.5%) and the difference was also significant (P = 0.03).Accordingly, it is possible to conclude that the cytokine profile was deviated in PTB patients, and such deviation was correlated with the genotypes of some cytokines, which might also together with HLA - DQB1polymorphism confer the individual an immunogenetic predisposition to develop M. tuberculosis infection.
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