Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.735395
Title: Telithromycin : the first ketolide, the interactions and alterations
Author: Walsh, Fiona
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 2003
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Abstract:
Respiratory tract infections are a serious cause of morbidity and mortality throughout the world. The most frequent causes of infection are Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis and atypical pathogens such as Chlamydophila pneumoniae. These infections are treated traditionally with antimicrobial agents, mainly the penicillins and macro lides. However, the incidence of macrolide resistance has increased markedly over the past 10 years, particularly in France, Belgium and Italy. Therefore, new compounds like telithromycin, an erythromycin derivative called a ketolide (K), have been developed to overcome this problem. In this study, clinical isolates of S. pneumoniae, H. influenzae and M. catarrhalis were tested in vitro against a range of antimicrobial agents, including telithromycin, to investigate the efficacy of this new drug. Telithromycin showed excellent activity against S. pneumoniae, including macrolide resistant strains, but its activity was not as high against M. catarrhalis or H. influenzae. For M. catarrhalis the minimum inhibitory concentration (MIC) of telithromycin was similar to that of the macrolides. With regard to H. influenzae telithromycin had higher activity than erythromycin and clarithromycin. The ermB and mefA/E genes mediate resistance to macrolides in S. pneumoniae in most cases. The ermB gene confers resistance to macrolide, lincosamide and streptogramin B (MLSB) antimicrobial agents by methylation of part of their ribosomal binding site. The mefA/E gene mediates efflux of 14- and 15-membered macrolides. Recent investigations have also implicated mutations in the 23S rRNA site of MLSbK interactions with macrolide and, in certain cases, ketolide resistance. Alterations of two ribosomal proteins L4 and L22 have also been associated with increased MLSBK MICs and resistance. In this study in vitro mutants were generated from three S. pneumoniae strains, 02J1095 (ermB positive), 02J1175 {mefA/E positive) and NCTC 13593 (MLSBK sensitive), on telithromycin. The MICs of the final generation mutants of each parent were increased in comparison to the parent but only the mutants from the macrolide resistant parents, 02J1095 and 02J1175, were telithromycin resistant. In order to ascertain the mechanism used by these telithromycin resistant mutants to achieve resistance, the ermB gene and upstream region, the mefA/E gene, the 23 S rRNA genes encoding domains II and V and the L4 and L22 riboprotein genes were amplified by PCR and sequenced. No alterations were located in any of the genes of the 02J1175 mutants investigated. No changes were present in the ermB genes or upstream regions, the 23 S rRNA genes or the L4 or L22 riboprotein genes of the 02J1095 mutants except J III 8. J III 8 had a telithromycin MIC of > 32mg/L and was a second-generation mutant of 02J1095. In this strain two mutations were present. The first was a 94K to Q94 amino acid mutation in the L22 riboprotein. The second was a 208 base pair deletion in the upstream region of the ermB gene containing the control peptide and one of two ribosome-binding sites. This region controls the expression of the ermB gene and hence methylase production. These mutations either alone or together were not present in any other mutant. They have not been described previously in S. pneumoniae. These mutations, while novel, do not alone explain the development of telithromycin resistance in S. pneumoniae. They do however; give an insight into how telithromycin interacts with the ribosome and the potential mechanisms clinical isolates may develop when telithromycin is introduced into the community.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.735395  DOI: Not available
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