Molecular and computational investigation of the skin microbiota associated with Pityriasis infection / (Record no. 175210)

MARC details
000 -LEADER
fixed length control field 06916namaa22004451i 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GICUC
005 - أخر تعامل مع التسجيلة
control field 20251026135809.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 251026s2025 ua a|||frm||| 000 0 eng d
040 ## - CATALOGING SOURCE
Original cataloguing agency EG-GICUC
Language of cataloging eng
Transcribing agency EG-GICUC
Modifying agency EG-GICUC
Description conventions rda
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title eng
Language code of summary or abstract eng
-- ara
049 ## - Acquisition Source
Acquisition Source Deposit
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.01
092 ## - LOCALLY ASSIGNED DEWEY CALL NUMBER (OCLC)
Classification number 616.01
Edition number 21
097 ## - Degree
Degree M.Sc
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Local Call Number Cai01.08.06.M.Sc.2025.Mo.M
100 0# - MAIN ENTRY--PERSONAL NAME
Authority record control number or standard number Mohamed Taha Abdelaziz,
Preparation preparation.
245 10 - TITLE STATEMENT
Title Molecular and computational investigation of the skin microbiota associated with Pityriasis infection /
Statement of responsibility, etc. by Mohamed Taha Abdelaziz ; Supervision Dr. Ramy Karam Aziz, Dr. Mariam Hassan Haikal, Dr. Dalia Ali Eldamacy.
246 15 - VARYING FORM OF TITLE
Title proper/short title دراسات جزيئية وحاسوبية للتجمعات الميكروبية الجلدية المرتبطة بعدوي النخالية المبرقشة
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 2025.
300 ## - PHYSICAL DESCRIPTION
Extent 72 pages :
Other physical details illustrations ;
Dimensions 25 cm. +
Accompanying material CD.
336 ## - CONTENT TYPE
Content type term text
Source rda content
337 ## - MEDIA TYPE
Media type term Unmediated
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term volume
Source rdacarrier
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc)-Cairo University, 2025.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Bibliography: pages 61-72.
520 #3 - SUMMARY, ETC.
Summary, etc. Pityriasis versicolor is a superficial fungal infection that causes skin pigmentation lesions, mostly without any severe symptoms but with a high prevalence and incidence of recurrence. An altered skin microbial community with an increase in Malassezia species, predominately Malassezia furfur, together with the transformation of those pityrosporum Malassezia to their mycelial form, are reported as the main cause of the disease. Despite the substantial advances in studying the human skin microbiome over the past two decades, the distribution of M. furfur in different skin microbiomes, and the involvement of the skin bacteriome in pityriasis versicolor are not conclusive. This study was initiated to systematically determine the distribution of M. furfur in sequenced skin metagenomes and to experimentally investigate its association with skin bacteriome profiles, which may provide clues to the role of skin microbiota balance in the treatment of pityriasis versicolor. First, publicly available skin metagenomes were computationally analyzed to systematically determine the distribution of M. furfur and its relative abundance at different skin sites. Using BLASTN to map newly proposed marker genes to representative metagenomic datasets allowed the estimation of M. furfur relative abundance, which indicated a relative enrichment of M. furfur in retro auricular crease, antecubital fossa, and forehead samples. Among skin categories, sebaceous areas were the most significantly enriched in M. furfur, while in terms of exposure/occlusion, exposed areas had the highest relative abundance. Second, an experimental case-control study investigated how the skin bacteriome, its dysbiosis, and fungal colonization might be related to pityriasis versicolor infection. The study was conducted on 20 skin swabs (taken from the neck to the subclavius area) from ten patients with pityriasis versicolor and six swabs from healthy volunteers (healthy controls). For each patient, one swab was taken from the lesion, while the other from a non-lesion area. The bacteriome of the 26 samples was profiled by 16S rRNA amplicon sequencing. Bioinformatics analysis indicated that samples from healthy control were more diverse and significantly differed (p-value < 0.05) in their bacterial composition from patients with pityriasis versicolor samples (lesion and non-lesion samples). Betaproteobacteria and Alphaproteobacteria had lower relative abundance in pityriasis versicolor patient skin, while Gammaproteobacteria was slightly more abundant. On the genus level, Ochrobactrum was relative more abundant in healthy skin samples, while Facklamia was relatively more abundant in lesion and non-lesion samples of patients with pityriasis versicolor. In conclusion, skin fungal alteration associated with pityriasis versicolor correlated with remarkable skin bacterial dysbiosis, not only in skin lesions, but also in the non-lesion areas. This finding suggests that bacterial dysbiosis may correlate with pityriasis versicolor infection and recurrence. Moreover, identifying commonly altered disease-associated bacterial taxa is a first step towards potential intervention to restore normal diversity, thus reducing the risk pityriasis versicolor and improving patient recovery.
520 #3 - SUMMARY, ETC.
Summary, etc. تحتوي الرسالة على اربعة فصول. الفصل الاول يتضمن مقدمة حول الطرق المختلفة لتشييد مشتقات الثيينو]٢,٣-د[بيريميدين، ومقدمة موجزة عن موت الخلايا المبرمج، وإنزيمات مستقبلات التيروزين كيناز، وموت الخلايا المبرمج، بالإضافة إلى النشاط المضاد للسرطان لمشتقات الثينوبيريميدين. الفصل الثاني يعرض أهداف البحث وعرض المخططات التي توضح الطرق العملية التي صممت للحصول على هذه المركبات.<br/> الفصل الثالث يتضمن المناقشة النظرية للجزء العملى، ومناقشة الأنشطة المضادة للسرطان والأنشطة الإنزيمية للمركبات الجديدة، ودراسة النمذجة الجزيئية، ومناقشة موجزة عن علاقة تركيب المركبات بفاعليتها. الفصل الرابع يشمل الخطوات العملية التي تم تنفيذها لتحضير المركبات الوسيطة والمستهدفة بالتفصيل، بالإضافة إلى خصائص المركبات التي تم تشييدها، وتحليل العناصر والبيانات الطيفية لهذه المركبات. هذا الفصل يغطي أيضا النشاط المضاد للسرطان في المختبر وفاعلية المركبات التي تم تشييدها حديثًا ضد إنزيم FLT-3 ، ونشاط موت الخلايا المبرمج للمركبات الأكثر فاعلية ودراسة النمذجة الجزيئية لها.
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Issues CD Issues also as CD.
546 ## - LANGUAGE NOTE
Text Language Text in English and abstract in Arabic & English.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Microbiology
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element الميكروبيولوجيا الطبية
653 #1 - INDEX TERM--UNCONTROLLED
Uncontrolled term 16S rRNA gene sequencing
-- BLASTN
-- Dysbiosis
-- Malassezia furfur
-- Metagenomics
-- Pityriasis versicolor
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Ramy Karam Aziz
Relator term thesis advisor.
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Mariam Hassan Haikal
Relator term thesis advisor.
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Dalia Ali Eldamacy
Relator term thesis advisor.
900 ## - Thesis Information
Grant date 01-01-2025
Supervisory body Ramy Karam Aziz
-- Mariam Hassan Haikal
-- Dalia Ali Eldamacy
Universities Cairo University
Faculties Faculty of Pharmacy
Department Department of Microbiology and Immunology
905 ## - Cataloger and Reviser Names
Cataloger Name Shimaa
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Thesis
Edition 21
Suppress in OPAC No
Holdings
Source of classification or shelving scheme Home library Current library Date acquired Inventory number Full call number Barcode Date last seen Effective from Koha item type
Dewey Decimal Classification المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 26.10.2025 92263 Cai01.08.06.M.Sc.2025.Mo.M 01010110092263000 26.10.2025 26.10.2025 Thesis
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