Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.755393
Title: Interactions between pathways of the complement system and Neisseria meningitidis
Author: Ageel, Homam Helal
ISNI:       0000 0004 7428 3883
Awarding Body: University of Leicester
Current Institution: University of Leicester
Date of Award: 2018
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Abstract:
Neisseria meningitidis is the main cause of bacterial meningitis among adults. It can also invade the blood stream causing systematic infection sepsis, which can lead to septic shock. The most frequently isolated strain associated with disease in the UK is the genogroup B strain MC58. The complement system is known to be an important part of the immune system. There are many reports of recurrent meningococcal infections in individuals with genetic mutations causing partial or total malfunction of the complement system. Two of the pathways of complement, the Lectin (LP) and Alternative (AP) pathways are activated by recognition molecules binding to components of the bacterial surface. These recognition molecules are collectin 11 (CL-11), Ficolins and Mannan-binding Lectins (MBL), associated with MBL-associated serine proteases (MASPs), which ultimately activate either the LP and/or the AP. It is unclear, however, which recognition molecules interact with N. meningitidis. Therefore, in-vitro studies of the interaction between different complement components and different clonal complexes of N. meningitidis were undertaken, via assays of C3 and C5b-9 deposition. It was found that CL-11 is the major recognition molecule for different clonal complexes of N. meningitidis genogroup B, while MBL is the major recognition molecule for genogroup Y. It was found also that the capsule and the phase variation of MC58 have no significant impact on its recognition. In-vivo, the effect of inhibition of MASP-2 or MASP-3 on the survival of animals vaccinated against genogroup B and infected with MC58 was also studied. Vaccination overcomes the effect of inhibition of the LP or the AP in infected mice.
Supervisor: Andrew, Peter ; Lynch, Nicholas Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.755393  DOI: Not available
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