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dc.contributor.advisorHossain, M. Mahboob
dc.contributor.advisorAhmed, Akash
dc.contributor.authorChowdhury, Melisha
dc.contributor.authorProva, Sadiba Salim
dc.date.accessioned2024-09-18T05:40:39Z
dc.date.available2024-09-18T05:40:39Z
dc.date.copyright2022
dc.date.issued2022-06
dc.identifier.otherID 17336001
dc.identifier.otherID 18136034
dc.identifier.urihttp://hdl.handle.net/10361/24115
dc.descriptionThis thesis submitted to the Department of Mathematics and Natural Sciences in partial fulfillment of the requirements for the degree of Bachelor of Science in Biotechnology, 2022.en_US
dc.descriptionCataloged from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 35-37).
dc.description.abstractAntibiotic resistance has become a matter of utmost concern. Many disease-causing pathogens are becoming resistant to multiple antibiotics, referred to as multi-drug resistant (MDR) bacteria. The purpose of this study is to know the immunity against MDR bacteria among normal healthy individuals. Bacterial samples were collected from tertiary care hospitals. Gram staining followed by biochemical tests were performed to confirm the identity of the four different organisms- Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus and Pseudomonas aeruginosa. After identification, antibiogram was performed to confirm that they are MDR bacteria. From normal individuals’ blood was collected and centrifuged at 4000 rpm for 10 min to obtain serum. All serum samples were incubated with four different bacterial suspensions. All sera samples were heated at 56℃ for 30 minutes to inactivate them and then incubated with bacterial suspension. Lastly, bacterial suspension was incubated with sera to which ethylene glycol-bis (β-aminoethyl ether)-N, N, N′, N′-tetraacetic acid (EGTA) had been added. This was done to inhibit the classical pathway of the complement system. For Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae and Staphylococcus aureus, 67.82%, 99.56%, 48.33% and 93.38% highest inhibition was observed respectively. No inhibition of bacterial growth was observed when treated with inactivated sera. Incubation with EGTA-added sera showed uncontrolled bacterial growth which suggests that the observed bactericidal effect of sera was due to the classical pathway and no other pathway of the complement system was involved.en_US
dc.description.statementofresponsibilityMelisha Chowdhury
dc.description.statementofresponsibilitySadiba Salim Prova
dc.format.extent44 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.subjectMultidrug resistanten_US
dc.subjectBacteriaen_US
dc.subjectEscherichia colien_US
dc.subjectKlebsiella pneumoniaeen_US
dc.subjectStaphylococcus aureusen_US
dc.subjectPseudomonas aeruginosaen_US
dc.subjectBlooden_US
dc.subjectSerumen_US
dc.subjectethylene glycol-bis (β-aminoethyl ether)-Nen_US
dc.subjectN, N′, N′-tetraacetic acid (EGTA)en_US
dc.subject.lcshDrug resistance
dc.titleSerum bactericidal activity against multi-drug resistant Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus, and Pseudomonas aeruginosaen_US
dc.typeThesisen_US
dc.contributor.departmentDepartment of Mathematics and Natural Sciences, Brac University
dc.description.degreeB. Biotechnology


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