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dc.contributor.advisorHasanuzzaman, Md.
dc.contributor.advisorAhmed, Akash
dc.contributor.authorAlam, Jarifa
dc.contributor.authorFaruk, Ruhama Binte
dc.contributor.authorAnik, Kamrul Hasan
dc.date.accessioned2024-11-21T09:42:35Z
dc.date.available2024-11-21T09:42:35Z
dc.date.copyright©2024
dc.date.issued2024-08
dc.identifier.otherID 19126062
dc.identifier.otherID 19126063
dc.identifier.otherID 19126061
dc.identifier.urihttp://hdl.handle.net/10361/24814
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Science in Microbiology, 2024.en_US
dc.descriptionCatalogued from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 36-46).
dc.description.abstractAcinetobacter baumannii is an opportunistic pathogen that affects persons with weakened immune systems and causes nosocomial infections due to its antibiotic resistance. Because of the global proliferation of multidrug resistance bacteria and biofilm development-ability to survive on dry surfaces aid in proliferation in a variety of healthcare environments, this study focuses on identifying the relevant gene for biofilm development and antibiotic resistance. Acinetobacter baumannii clinical isolates (150) were recovered from BSMMU in Dhaka. For A. baumannii pure strain identification; Biochemical tests and PCR (Polymerase chain reaction) were performed and validated using Agarose gel-electrophoresis. After verifying pure strains, the antibiotic susceptibility test was performed using the Kirby-Bauer disc diffusion method and biofilm development was assessed using the 96-well microtiter plate method. Furthermore, PCR was used to screen both the carbapenem resistance gene and the biofilm generating gene. Out of 150 isolates, 109 were verified true positive with PCR analysis, enforcing additional research. AST was performed with medicines from several groups, the majority of them were MDR and mostly, Carbapenem resistant. PCR was performed for screening both MDR gene and biofilm producing gene, with 15.59% NDM gene being positive and the others yielding no significant results. Biofilm-related genes such as bap, blaPER-1, csuE, and ompA were reported to be frequent at 88.98%, 56.88%, 84.40%, and 83.48%, respectively, in all biofilm generating isolates (24.77%) strong, (33.02%) moderate, and (10.09%) weak, (31.19) % non-biofilm forming. Our study focused on the prevalence and antibiotic -resistant pattern of the MDR A. baumannii, which is more common in clinical isolates, as well as biofilm producing capability and Biofilm-forming genes. It appears that effective surveillance and control actions are required to halt the CRAB outbreak in our country and healthcare settings.en_US
dc.description.statementofresponsibilityJarifa Alam
dc.description.statementofresponsibilityRuhama Binte Faruk
dc.description.statementofresponsibilityKamrul Hasan Anik
dc.format.extent46 pages
dc.language.isoenen_US
dc.publisherBrac Universityen_US
dc.rightsBrac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subjectAcinetobacter baumanniien_US
dc.subjectOpportunistic pathogenen_US
dc.subjectAntibiotic resistanceen_US
dc.subjectCarbapenem resistant geneen_US
dc.subjectBiofilm formationen_US
dc.subjectBiofilm forming geneen_US
dc.subjectPCRen_US
dc.subjectMulti-drug resistanceen_US
dc.subject.lcshBiofilms--growth & development.
dc.subject.lcshDrug resistance in microorganisms.
dc.subject.lcshOpportunistic infections.
dc.titleDetection and characterization of antibiotic resistant and biofilm producing clinical isolates of Acinetobacter baumanniien_US
dc.typeThesisen_US
dc.contributor.departmentDepartment of Mathematics and Natural Sciences, Brac University
dc.description.degreeB.Sc. in Microbiology


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